,Unnamed: 0.6,Unnamed: 0.5,Unnamed: 0.4,Unnamed: 0.3,Unnamed: 0.2,Unnamed: 0.1,Unnamed: 0,id,name,source,type,Inter_ID
0,0,0,0,0,0,0,0,MONDO:0003523,gastrin-producing neuroendocrine tumor,MONDO,disease,DISEASE_0
1,1,1,1,1,1,1,1,MONDO:0002586,thymus cancer,MONDO,disease,DISEASE_1
2,2,2,2,2,2,2,2,MONDO:0012991,Kahrizi syndrome,MONDO,disease,DISEASE_2
3,3,3,3,3,3,3,3,MONDO:0016557,leukonychia totalis,MONDO,disease,DISEASE_3
4,4,4,4,4,4,4,4,MONDO:0008862,3-methylcrotonyl-CoA carboxylase 2 deficiency,MONDO,disease,DISEASE_4
5,5,5,5,5,5,5,5,MONDO:0021918,arena syndrome,MONDO,disease,DISEASE_5
6,6,6,6,6,6,6,6,MONDO:0019917,maternal uniparental disomy of chromosome 20,MONDO,disease,DISEASE_6
7,7,7,7,7,7,7,7,MONDO:0009486,autosomal recessive Kenny-Caffey syndrome,MONDO,disease,DISEASE_7
8,8,8,8,8,8,8,8,MONDO:0005291_MONDO:0006779,brain aneurysm,MONDO_grouped,disease,DISEASE_8
9,9,9,9,9,9,9,9,MONDO:0044628,six2-related frontonasal dysplasia,MONDO,disease,DISEASE_9
10,10,10,10,10,10,10,10,MONDO:0042486_MONDO:0012405,"polyposis syndrome, hereditary mixed",MONDO_grouped,disease,DISEASE_10
11,11,11,11,11,11,11,11,MONDO:0011117,iris pigment epithelium anomalies,MONDO,disease,DISEASE_11
12,12,12,12,12,12,12,12,MONDO:0008501,Sturge-Weber syndrome,MONDO,disease,DISEASE_12
13,13,13,13,13,13,13,13,MONDO:0001827_MONDO:0005669,white piedra,MONDO_grouped,disease,DISEASE_13
14,14,14,14,14,14,14,14,MONDO:0021206_MONDO:0001212,chronic non-suppurative otitis media,MONDO_grouped,disease,DISEASE_14
15,15,15,15,15,15,15,15,MONDO:0016144,qualitative or quantitative defects of delta-sarcoglycan,MONDO,disease,DISEASE_15
16,16,16,16,16,16,16,16,MONDO:0005906,peritonsillar abscess,MONDO,disease,DISEASE_16
17,17,17,17,17,17,17,17,MONDO:0010444,X-linked dyserythropoetic anemia with abnormal platelets and neutropenia,MONDO,disease,DISEASE_17
18,18,18,18,18,18,18,18,MONDO:0017684,disorder of beta and omega amino acid metabolism,MONDO,disease,DISEASE_18
19,19,19,19,19,19,19,19,MONDO:0018039,selective IgM deficiency,MONDO,disease,DISEASE_19
20,20,20,20,20,20,20,20,MONDO:0010786,chronic diarrhea with villous atrophy,MONDO,disease,DISEASE_20
21,21,21,21,21,21,21,21,MONDO:0016978,poorly differentiated thymic neuroendocrine carcinoma,MONDO,disease,DISEASE_21
22,22,22,22,22,22,22,22,MONDO:0002295,skin glomus tumor,MONDO,disease,DISEASE_22
23,23,23,23,23,23,23,23,MONDO:0008497,Stormorken syndrome,MONDO,disease,DISEASE_23
24,24,24,24,24,24,24,24,MONDO:0002053,obsolete hypoglycemic coma,MONDO,disease,DISEASE_24
25,25,25,25,25,25,25,25,MONDO:0003518_MONDO:0003826,mediastinum teratoma,MONDO_grouped,disease,DISEASE_25
26,26,26,26,26,26,26,26,MONDO:0014097,congenital short bowel syndrome,MONDO,disease,DISEASE_26
27,27,27,27,27,27,27,27,MONDO:0016057,isolated encephalocele,MONDO,disease,DISEASE_27
28,28,28,28,28,28,28,28,MONDO:0022055,Calabro syndrome,MONDO,disease,DISEASE_28
29,29,29,29,29,29,29,29,MONDO:0016790,tricarboxylic acid cycle disorder,MONDO,disease,DISEASE_29
30,30,30,30,30,30,30,30,MONDO:0008947,bilateral striopallidodentate calcinosis,MONDO,disease,DISEASE_30
31,31,31,31,31,31,31,31,MONDO:0007361,C1 inhibitor deficiency,MONDO,disease,DISEASE_31
32,32,32,32,32,32,32,32,MONDO:0014605_MONDO:0032697_MONDO:0957553,Houge-Janssens syndrome,MONDO_grouped,disease,DISEASE_32
33,33,33,33,33,33,33,33,MONDO:0800154,inborn disorder of the metabolism of sulfur-containing amino acids and hydrogen sulfide,MONDO,disease,DISEASE_33
34,34,34,34,34,34,34,34,MONDO:0023018,dupont sellier chochillon syndrome,MONDO,disease,DISEASE_34
35,35,35,35,35,35,35,35,MONDO:0021095_MONDO:0956980,parkinsonian disorder,MONDO_grouped,disease,DISEASE_35
36,36,36,36,36,36,36,36,MONDO:0018635,idiopathic phalangeal acro-osteolysis,MONDO,disease,DISEASE_36
37,37,37,37,37,37,37,37,MONDO:0041295,acute papillary necrosis,MONDO,disease,DISEASE_37
38,38,38,38,38,38,38,38,MONDO:0003588,larynx liposarcoma,MONDO,disease,DISEASE_38
39,39,39,39,39,39,39,39,MONDO:0001324,obsolete hyperandrogenism,MONDO,disease,DISEASE_39
40,40,40,40,40,40,40,40,MONDO:0021287,carcinoma in situ of epiglottis,MONDO,disease,DISEASE_40
41,41,41,41,41,41,41,41,MONDO:0008248,pigmented purpuric eruption,MONDO,disease,DISEASE_41
42,42,42,42,42,42,42,42,MONDO:1011473,"amyloidosis, Japanese quail",MONDO,disease,DISEASE_42
43,43,43,43,43,43,43,43,MONDO:0011744,primary intraosseous venous malformation,MONDO,disease,DISEASE_43
44,44,44,44,44,44,44,44,MONDO:0003768,signet ring cell variant cervical mucinous adenocarcinoma,MONDO,disease,DISEASE_44
45,45,45,45,45,45,45,45,MONDO:1010784_MONDO:1012542,"pyoderma, dog",MONDO_grouped,disease,DISEASE_45
46,46,46,46,46,46,46,46,MONDO:0958177_MONDO:0009813,chronic recurrent multifocal osteomyelitis 3,MONDO_grouped,disease,DISEASE_46
47,47,47,47,47,47,47,47,MONDO:0020346,obsolete synaptic congenital myasthenic syndrome,MONDO,disease,DISEASE_47
48,48,48,48,48,48,48,48,MONDO:0010388,"rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked",MONDO,disease,DISEASE_48
49,49,49,49,49,49,49,49,MONDO:1011866_MONDO:1011894,"degenerative myeloencephalopathy, non-human animal",MONDO_grouped,disease,DISEASE_49
50,50,50,50,50,50,50,50,MONDO:0011873_MONDO:0009757_MONDO:0009756_MONDO:0011871_MONDO:0018982_MONDO:0001982_MONDO:0020384_MONDO:1010873,"Niemann-Pick disease,",MONDO_grouped,disease,DISEASE_50
51,51,51,51,51,51,51,51,MONDO:0006141,cervical villoglandular adenocarcinoma,MONDO,disease,DISEASE_51
52,52,52,52,52,52,52,52,MONDO:0002604,pericytic neoplasm,MONDO,disease,DISEASE_52
53,53,53,53,53,53,53,53,MONDO:0006875_MONDO:0001534,ocular hypertension,MONDO_grouped,disease,DISEASE_53
54,54,54,54,54,54,54,54,MONDO:0008810,familial apolipoprotein C-II deficiency,MONDO,disease,DISEASE_54
55,55,55,55,55,55,55,55,MONDO:0957452,segmental arterial mediolysis,MONDO,disease,DISEASE_55
56,56,56,56,56,56,56,56,MONDO:0016349_MONDO:0007741,congenital hydrocephalus,MONDO_grouped,disease,DISEASE_56
57,57,57,57,57,57,57,57,MONDO:0100134,"mitochondrial complex I deficiency, mitochondrial type",MONDO,disease,DISEASE_57
58,58,58,58,58,58,58,58,MONDO:0013368,mammary-digital-nail syndrome,MONDO,disease,DISEASE_58
59,59,59,59,59,59,59,59,MONDO:0018037,hyper-IgE syndrome,MONDO,disease,DISEASE_59
60,60,60,60,60,60,60,60,MONDO:0016353,palmoplantar keratoderma-spastic paralysis syndrome,MONDO,disease,DISEASE_60
61,61,61,61,61,61,61,61,MONDO:0013428_MONDO:0009143_MONDO:0013430_MONDO:0013431_MONDO:0014794_MONDO:0013432_MONDO:0014894_MONDO:0033046_MONDO:0016817,Meier-Gorlin syndrome,MONDO_grouped,disease,DISEASE_61
62,62,62,62,62,62,62,62,MONDO:0700154,canine rhabdomyosarcoma,MONDO,disease,DISEASE_62
63,63,63,63,63,63,63,63,MONDO:0010771,histiocytoid cardiomyopathy,MONDO,disease,DISEASE_63
64,64,64,64,64,64,64,64,MONDO:0000935,larynx squamous papilloma,MONDO,disease,DISEASE_64
65,65,65,65,65,65,65,65,MONDO:0035742,factor V short isoforms-related bleeding disorder,MONDO,disease,DISEASE_65
66,66,66,66,66,66,66,66,MONDO:1012493,"combined deficiency of factors VIII, IX, and X, horse",MONDO,disease,DISEASE_66
67,67,67,67,67,67,67,67,MONDO:0001574,capillary disorder,MONDO,disease,DISEASE_67
68,68,68,68,68,68,68,68,MONDO:0003296,cellular leiomyoma,MONDO,disease,DISEASE_68
69,69,69,69,69,69,69,69,MONDO:0001144_MONDO:0001145,partial third-nerve palsy,MONDO_grouped,disease,DISEASE_69
70,70,70,70,70,70,70,70,MONDO:0008395,Ruvalcaba syndrome,MONDO,disease,DISEASE_70
71,71,71,71,71,71,71,71,MONDO:0015176,undetermined colitis,MONDO,disease,DISEASE_71
72,72,72,72,72,72,72,72,MONDO:0021896,anterior spinal artery stroke,MONDO,disease,DISEASE_72
73,73,73,73,73,73,73,73,MONDO:0017319,hereditary elliptocytosis,MONDO,disease,DISEASE_73
74,74,74,74,74,74,74,74,MONDO:0006887,parametritis,MONDO,disease,DISEASE_74
75,75,75,75,75,75,75,75,MONDO:0004009,kidney pelvis sarcomatoid transitional cell carcinoma,MONDO,disease,DISEASE_75
76,76,76,76,76,76,76,76,MONDO:0000516,phalanx chondroma,MONDO,disease,DISEASE_76
77,77,77,77,77,77,77,77,MONDO:0013925_MONDO:0010185_MONDO:0010184_MONDO:0010657_MONDO:0100463_MONDO:0975798,"methylmalonic acidemia with homocystinuria, type cblJ",MONDO_grouped,disease,DISEASE_77
78,78,78,78,78,78,78,78,MONDO:0018566,short stature-advanced bone age-early-onset osteoarthritis syndrome,MONDO,disease,DISEASE_78
79,79,79,79,79,79,79,79,MONDO:0958269,isolated left bronchial isomerism,MONDO,disease,DISEASE_79
80,80,80,80,80,80,80,80,MONDO:0019413,ischio-vertebral syndrome,MONDO,disease,DISEASE_80
81,81,81,81,81,81,81,81,MONDO:0001400,schwannoma of ureter,MONDO,disease,DISEASE_81
82,82,82,82,82,82,82,82,MONDO:0001128,nasal cavity cancer,MONDO,disease,DISEASE_82
83,83,83,83,83,83,83,83,MONDO:1012379,"guttural pouch tympany, horse",MONDO,disease,DISEASE_83
84,84,84,84,84,84,84,84,MONDO:1010592_MONDO:1010595_MONDO:1010599,"hyperparathyroidism, domestic cat",MONDO_grouped,disease,DISEASE_84
85,85,85,85,85,85,85,85,MONDO:0100112,acyl-CoA binding domain containing protein 5 deficiency,MONDO,disease,DISEASE_85
86,86,86,86,86,86,86,86,MONDO:0016331,infantile systemic hyalinosis,MONDO,disease,DISEASE_86
87,87,87,87,87,87,87,87,MONDO:0015023,MYPN-related myopathy,MONDO,disease,DISEASE_87
88,88,88,88,88,88,88,88,MONDO:0958196_MONDO:0030005,"epilepsy, early-onset, 3, with or without developmental delay",MONDO_grouped,disease,DISEASE_88
89,89,89,89,89,89,89,89,MONDO:0019733,AFib amyloidosis,MONDO,disease,DISEASE_89
90,90,90,90,90,90,90,90,MONDO:0007444,"dermal Ridges, patternless",MONDO,disease,DISEASE_90
91,91,91,91,91,91,91,91,MONDO:0021239,urethra neoplasm,MONDO,disease,DISEASE_91
92,92,92,92,92,92,92,92,MONDO:1012066,"pituitary dwarfism, dog",MONDO,disease,DISEASE_92
93,93,93,93,93,93,93,93,MONDO:0000373,gall bladder carcinoma in situ,MONDO,disease,DISEASE_93
94,94,94,94,94,94,94,94,MONDO:0006741,encephalomalacia,MONDO,disease,DISEASE_94
95,95,95,95,95,95,95,95,MONDO:0008867,biliary atresia,MONDO,disease,DISEASE_95
96,96,96,96,96,96,96,96,MONDO:0010219,xylosidase deficiency,MONDO,disease,DISEASE_96
97,97,97,97,97,97,97,97,MONDO:0011690_MONDO:0007542,"Camurati-Engelmann disease, type 2",MONDO_grouped,disease,DISEASE_97
98,98,98,98,98,98,98,98,MONDO:0011161,sperm-specific antigen 1,MONDO,disease,DISEASE_98
99,99,99,99,99,99,99,99,MONDO:0011551,TH-deficient dopa-responsive dystonia,MONDO,disease,DISEASE_99
100,100,100,100,100,100,100,100,MONDO:0015065,"ileal neuroendocrine tumor, well differentiated, low or intermediate grade",MONDO,disease,DISEASE_100
101,101,101,101,101,101,101,101,MONDO:0003104,epicardium cancer,MONDO,disease,DISEASE_101
102,102,102,102,102,102,102,102,MONDO:0006924,Bartonellaceae infectious disease,MONDO,disease,DISEASE_102
103,103,103,103,103,103,103,103,MONDO:0010094,spondylocarpotarsal synostosis syndrome,MONDO,disease,DISEASE_103
104,104,104,104,104,104,104,104,MONDO:0018469,pulmonary non-tuberculous mycobacterial infection,MONDO,disease,DISEASE_104
105,105,105,105,105,105,105,105,MONDO:1010779,"alopecia areata, domestic cat",MONDO,disease,DISEASE_105
106,106,106,106,106,106,106,106,MONDO:0007417,Darier disease,MONDO,disease,DISEASE_106
107,107,107,107,107,107,107,107,MONDO:0006025,autosomal recessive disease,MONDO,disease,DISEASE_107
108,108,108,108,108,108,108,108,MONDO:0003014_MONDO:0004514,rhinitis,MONDO_grouped,disease,DISEASE_108
109,109,109,109,109,109,109,109,MONDO:0006061,cervical artery dissection,MONDO,disease,DISEASE_109
110,110,110,110,110,110,110,110,MONDO:0030503,"cholestasis, progressive familial intrahepatic, 7, with or without hearing loss",MONDO,disease,DISEASE_110
111,111,111,111,111,111,111,111,MONDO:0016843,20q13.33 microdeletion syndrome,MONDO,disease,DISEASE_111
112,112,112,112,112,112,112,112,MONDO:0019335,mild hyperphenylalaninemia,MONDO,disease,DISEASE_112
113,113,113,113,113,113,113,113,MONDO:0006882,orchitis,MONDO,disease,DISEASE_113
114,114,114,114,114,114,114,114,MONDO:0042974_MONDO:0100197_MONDO:0100203_MONDO:0100204_MONDO:0100205,parainfluenza virus type 3 infectious disease,MONDO_grouped,disease,DISEASE_114
115,115,115,115,115,115,115,115,MONDO:0006721,de Quervain disease,MONDO,disease,DISEASE_115
116,116,116,116,116,116,116,116,MONDO:1012410,"combined deficiency of factors IX and XII, domestic cat",MONDO,disease,DISEASE_116
117,117,117,117,117,117,117,117,MONDO:0019168_MONDO:0002922,pyomyositis,MONDO_grouped,disease,DISEASE_117
118,118,118,118,118,118,118,118,MONDO:0100146,ATP6AP2-related disorder,MONDO,disease,DISEASE_118
119,119,119,119,119,119,119,119,MONDO:0012941_MONDO:0008617_MONDO:0054849_MONDO:0009960_MONDO:0033643_MONDO:0013153_MONDO:0012831_MONDO:0012845_MONDO:0012875_MONDO:0011471_MONDO:0005265_MONDO:0012832_MONDO:0012610_MONDO:0012840_MONDO:0011087_MONDO:0011521_MONDO:0011661_MONDO:0011699_MONDO:0011700_MONDO:0011701_MONDO:0012040_MONDO:0012829_MONDO:0012837_MONDO:0012838_MONDO:0012841_MONDO:0012852_MONDO:0012886_MONDO:0012887_MONDO:0012940_MONDO:0012973_MONDO:0013012,inflammatory bowel disease,MONDO_grouped,disease,DISEASE_119
120,120,120,120,120,120,120,120,MONDO:0010258,MEHMO syndrome,MONDO,disease,DISEASE_120
121,121,121,121,121,121,121,121,MONDO:0003802,cornea cancer,MONDO,disease,DISEASE_121
122,122,122,122,122,122,122,122,MONDO:1011877,"exercise-induced collapse, non-human animal",MONDO,disease,DISEASE_122
123,123,123,123,123,123,123,123,MONDO:0012860,"thrombophilia due to protein C deficiency, autosomal recessive",MONDO,disease,DISEASE_123
124,124,124,124,124,124,124,124,MONDO:0019944,Eisenmenger syndrome,MONDO,disease,DISEASE_124
125,125,125,125,125,125,125,125,MONDO:0020331,indolent systemic mastocytosis,MONDO,disease,DISEASE_125
126,126,126,126,126,126,126,126,MONDO:0018537,squamous cell carcinoma of gallbladder and extrahepatic biliary tract,MONDO,disease,DISEASE_126
127,127,127,127,127,127,127,127,MONDO:0002786,diencephalic cancer,MONDO,disease,DISEASE_127
128,128,128,128,128,128,128,128,MONDO:0800105,catatonia,MONDO,disease,DISEASE_128
129,129,129,129,129,129,129,129,MONDO:0016644,logopenic progressive aphasia,MONDO,disease,DISEASE_129
130,130,130,130,130,130,130,130,MONDO:0006621,vulvar inverted follicular keratosis,MONDO,disease,DISEASE_130
131,131,131,131,131,131,131,131,MONDO:0001033,mycotic corneal ulcer,MONDO,disease,DISEASE_131
132,132,132,132,132,132,132,132,MONDO:0018162,neurometabolic disorder due to serine deficiency,MONDO,disease,DISEASE_132
133,133,133,133,133,133,133,133,MONDO:0010293,ectodermal dysplasia and immune deficiency,MONDO,disease,DISEASE_133
134,134,134,134,134,134,134,134,MONDO:0044619,propylthiouracil embryofetopathy,MONDO,disease,DISEASE_134
135,135,135,135,135,135,135,135,MONDO:0008211,"pseudoleprechaunism syndrome, Patterson type",MONDO,disease,DISEASE_135
136,136,136,136,136,136,136,136,MONDO:1011359,"subcutaneous tissue disorder, non-human animal",MONDO,disease,DISEASE_136
137,137,137,137,137,137,137,137,MONDO:0700118,proximal chromosome 18q deletion syndrome,MONDO,disease,DISEASE_137
138,138,138,138,138,138,138,138,MONDO:1011100_MONDO:1011101,"primary hyperoxaluria, AGXT-related, dog",MONDO_grouped,disease,DISEASE_138
139,139,139,139,139,139,139,139,MONDO:0001236,appendiceal neoplasm,MONDO,disease,DISEASE_139
140,140,140,140,140,140,140,140,MONDO:0009698,Unverricht-Lundborg syndrome,MONDO,disease,DISEASE_140
141,141,141,141,141,141,141,141,MONDO:0006850,maxillary sinus neoplasm,MONDO,disease,DISEASE_141
142,142,142,142,142,142,142,142,MONDO:0007435,dentatorubral-pallidoluysian atrophy,MONDO,disease,DISEASE_142
143,143,143,143,143,143,143,143,MONDO:0014266_MONDO:0012419_MONDO:0013406_MONDO:0012540_MONDO:0012767_MONDO:0014189_MONDO:0011285_MONDO:0007932_MONDO:0003004_MONDO:0005150_MONDO:0014207_MONDO:0012659_MONDO:0013420_MONDO:0013409_MONDO:0013416_MONDO:0012674,age related macular degeneration,MONDO_grouped,disease,DISEASE_143
144,144,144,144,144,144,144,144,MONDO:0008034,"muscular dystrophy, pseudohypertrophic, with Internalized capillaries",MONDO,disease,DISEASE_144
145,145,145,145,145,145,145,145,MONDO:0030603_MONDO:0030602,Klebsiella infectious disease,MONDO_grouped,disease,DISEASE_145
146,146,146,146,146,146,146,146,MONDO:0000777,gastrointestinal allergy,MONDO,disease,DISEASE_146
147,147,147,147,147,147,147,147,MONDO:0011237_MONDO:0011470,"hyperlipidemia, combined",MONDO_grouped,disease,DISEASE_147
148,148,148,148,148,148,148,148,MONDO:0012914,chromosome 1q21.1 deletion syndrome,MONDO,disease,DISEASE_148
149,149,149,149,149,149,149,149,MONDO:0011686,DNA ligase IV deficiency,MONDO,disease,DISEASE_149
150,150,150,150,150,150,150,150,MONDO:0018634,hereditary amyloidosis,MONDO,disease,DISEASE_150
151,151,151,151,151,151,151,151,MONDO:0016909,partial monosomy of the long arm of chromosome 10,MONDO,disease,DISEASE_151
152,152,152,152,152,152,152,152,MONDO:0024229,miliaria crystallina,MONDO,disease,DISEASE_152
153,153,153,153,153,153,153,153,MONDO:0002945,micronodular basal cell carcinoma,MONDO,disease,DISEASE_153
154,154,154,154,154,154,154,154,MONDO:0008678,Williams syndrome,MONDO,disease,DISEASE_154
155,155,155,155,155,155,155,155,MONDO:0006782,hemometra,MONDO,disease,DISEASE_155
156,156,156,156,156,156,156,156,MONDO:0000943,acute hydrops keratoconus,MONDO,disease,DISEASE_156
157,157,157,157,157,157,157,157,MONDO:0021179,proteostasis deficiencies,MONDO,disease,DISEASE_157
158,158,158,158,158,158,158,158,MONDO:0007894,Leri pleonosteosis,MONDO,disease,DISEASE_158
159,159,159,159,159,159,159,159,MONDO:0020427,Laubry-Pezzi syndrome,MONDO,disease,DISEASE_159
160,160,160,160,160,160,160,160,MONDO:0005891,ostertagiasis,MONDO,disease,DISEASE_160
161,161,161,161,161,161,161,161,MONDO:0012321_MONDO:0007088_MONDO:0007089_MONDO:0011194_MONDO:0011913_MONDO:0012153_MONDO:0011743_MONDO:0004975_MONDO:1011461_MONDO:0014265_MONDO:0010422_MONDO:0011561_MONDO:0011647_MONDO:0011777_MONDO:0012344_MONDO:0012609_MONDO:0012630_MONDO:0012631_MONDO:0014036_MONDO:0014316_MONDO:1011460_MONDO:1011463,Alzheimer disease,MONDO_grouped,disease,DISEASE_161
162,162,162,162,162,162,162,162,MONDO:0002316_MONDO:0002321,motor peripheral neuropathy,MONDO_grouped,disease,DISEASE_162
163,163,163,163,163,163,163,163,MONDO:0010791,"myoglobinuria, recurrent",MONDO,disease,DISEASE_163
164,164,164,164,164,164,164,164,MONDO:0021065,pleural neoplasm,MONDO,disease,DISEASE_164
165,165,165,165,165,165,165,165,MONDO:0100547,cardiogenetic disease,MONDO,disease,DISEASE_165
166,166,166,166,166,166,166,166,MONDO:0009916,"46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency",MONDO,disease,DISEASE_166
167,167,167,167,167,167,167,167,MONDO:0004313,gasserian ganglion meningioma,MONDO,disease,DISEASE_167
168,168,168,168,168,168,168,168,MONDO:0006138,cervical large cell neuroendocrine carcinoma,MONDO,disease,DISEASE_168
169,169,169,169,169,169,169,169,MONDO:0002633,cranial nerve neoplasm,MONDO,disease,DISEASE_169
170,170,170,170,170,170,170,170,MONDO:0015545,macrophage activation syndrome,MONDO,disease,DISEASE_170
171,171,171,171,171,171,171,171,MONDO:0020204,conjunctival tumor,MONDO,disease,DISEASE_171
172,172,172,172,172,172,172,172,MONDO:0020601,mosquito-borne viral encephalitis,MONDO,disease,DISEASE_172
173,173,173,173,173,173,173,173,MONDO:1012897,"short QT syndrome, KCNH2-related, rabbit",MONDO,disease,DISEASE_173
174,174,174,174,174,174,174,174,MONDO:0019776,obsolete Juberg-Marsidi syndrome,MONDO,disease,DISEASE_174
175,175,175,175,175,175,175,175,MONDO:0005946,rhinosporidiosis,MONDO,disease,DISEASE_175
176,176,176,176,176,176,176,176,MONDO:0015779,"45,X/46,XY mixed gonadal dysgenesis",MONDO,disease,DISEASE_176
177,177,177,177,177,177,177,177,MONDO:0022025,boylan dew greco syndrome,MONDO,disease,DISEASE_177
178,178,178,178,178,178,178,178,MONDO:1012020,"audiogenic seizure, rabbit",MONDO,disease,DISEASE_178
179,179,179,179,179,179,179,179,MONDO:0011154,"acrofacial dysostosis, Palagonia type",MONDO,disease,DISEASE_179
180,180,180,180,180,180,180,180,MONDO:0700111,"bacterial pneumonia, non-human animal",MONDO,disease,DISEASE_180
181,181,181,181,181,181,181,181,MONDO:0016357,dysplastic cortical hyperostosis,MONDO,disease,DISEASE_181
182,182,182,182,182,182,182,182,MONDO:0019053,peroxisomal disease,MONDO,disease,DISEASE_182
183,183,183,183,183,183,183,183,MONDO:0008718,Morvan syndrome,MONDO,disease,DISEASE_183
184,184,184,184,184,184,184,184,MONDO:0015665,scleromyxedema,MONDO,disease,DISEASE_184
185,185,185,185,185,185,185,185,MONDO:0008100,nipples inverted,MONDO,disease,DISEASE_185
186,186,186,186,186,186,186,186,MONDO:0015636,dirofilariasis,MONDO,disease,DISEASE_186
187,187,187,187,187,187,187,187,MONDO:0018025,chronic actinic dermatitis,MONDO,disease,DISEASE_187
188,188,188,188,188,188,188,188,MONDO:0017135_MONDO:0002017_MONDO:1010994,olivopontocerebellar atrophy-deafness syndrome,MONDO_grouped,disease,DISEASE_188
189,189,189,189,189,189,189,189,MONDO:1012059,"delta 9-tetrahydrocannabinol seizure, rabbit",MONDO,disease,DISEASE_189
190,190,190,190,190,190,190,190,MONDO:0001598,benign lymphoepithelial lesion of salivary gland,MONDO,disease,DISEASE_190
191,191,191,191,191,191,191,191,MONDO:1011946,"congenital joint laxity and dwarfism, non-human animal",MONDO,disease,DISEASE_191
192,192,192,192,192,192,192,192,MONDO:0005893,pancreatic endocrine carcinoma,MONDO,disease,DISEASE_192
193,193,193,193,193,193,193,193,MONDO:0010788_MONDO:1011286,Leber hereditary optic neuropathy,MONDO_grouped,disease,DISEASE_193
194,194,194,194,194,194,194,194,MONDO:0000668,autotopagnosia,MONDO,disease,DISEASE_194
195,195,195,195,195,195,195,195,MONDO:0003658,"B-cell lymphoma, unclassifiable, with features intermediate between diffuse large b-cell lymphoma and classical Hodgkin lymphoma",MONDO,disease,DISEASE_195
196,196,196,196,196,196,196,196,MONDO:0021681,sexually transmitted disease,MONDO,disease,DISEASE_196
197,197,197,197,197,197,197,197,MONDO:0035776,combined deficiency of factor VII and factor X,MONDO,disease,DISEASE_197
198,198,198,198,198,198,198,198,MONDO:0018019,lead poisoning,MONDO,disease,DISEASE_198
199,199,199,199,199,199,199,199,MONDO:0017746,atypical Rett syndrome,MONDO,disease,DISEASE_199
200,200,200,200,200,200,200,200,MONDO:0958347,isolated filum lipoma,MONDO,disease,DISEASE_200
201,201,201,201,201,201,201,201,MONDO:0012521,herpes simplex encephalitis,MONDO,disease,DISEASE_201
202,202,202,202,202,202,202,202,MONDO:0024627,phagocytic cell dysfunction,MONDO,disease,DISEASE_202
203,203,203,203,203,203,203,203,MONDO:0004987,urinary bladder neoplasm,MONDO,disease,DISEASE_203
204,204,204,204,204,204,204,204,MONDO:0016711,desmoplastic/nodular medulloblastoma,MONDO,disease,DISEASE_204
205,205,205,205,205,205,205,205,MONDO:0020420_MONDO:0957433,pulmonary branch stenosis,MONDO_grouped,disease,DISEASE_205
206,206,206,206,206,206,206,206,MONDO:0008214_MONDO:1010650_MONDO:1010651_MONDO:1010652,Pelger-Huet anomaly,MONDO_grouped,disease,DISEASE_206
207,207,207,207,207,207,207,207,MONDO:0700231_MONDO:0100484,TSPAN12-related exudative vitreoretinopathy,MONDO_grouped,disease,DISEASE_207
208,208,208,208,208,208,208,208,MONDO:0100317,deficiency of adenosine deaminase 2,MONDO,disease,DISEASE_208
209,209,209,209,209,209,209,209,MONDO:0971063,autosomal dominant dopa-responsive dystonia,MONDO,disease,DISEASE_209
210,210,210,210,210,210,210,210,MONDO:0971116,borderline vascular tumor,MONDO,disease,DISEASE_210
211,211,211,211,211,211,211,211,MONDO:0014235,chromosome 22q13 duplication syndrome,MONDO,disease,DISEASE_211
212,212,212,212,212,212,212,212,MONDO:0007604,femoral-facial syndrome,MONDO,disease,DISEASE_212
213,213,213,213,213,213,213,213,MONDO:0033548,"myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies",MONDO,disease,DISEASE_213
214,214,214,214,214,214,214,214,MONDO:0021231,retina neoplasm,MONDO,disease,DISEASE_214
215,215,215,215,215,215,215,215,MONDO:0022380,acute lymphoblastic leukemia congenital sporadic aniridia,MONDO,disease,DISEASE_215
216,216,216,216,216,216,216,216,MONDO:0025489,enzootic bovine leukosis,MONDO,disease,DISEASE_216
217,217,217,217,217,217,217,217,MONDO:0007633,"Friedreich ataxia, so-called, with optic atrophy and sensorineural deafness",MONDO,disease,DISEASE_217
218,218,218,218,218,218,218,218,MONDO:1010085,"factor XIII deficiency, non-human animal",MONDO,disease,DISEASE_218
219,219,219,219,219,219,219,219,MONDO:1012420,"brachygnathia, cardiomegaly and renal hypoplasia syndrome, sheep",MONDO,disease,DISEASE_219
220,220,220,220,220,220,220,220,MONDO:0011229,ethylmalonic encephalopathy,MONDO,disease,DISEASE_220
221,221,221,221,221,221,221,221,MONDO:0032785_MONDO:0014090_MONDO:0060550_MONDO:0009893_MONDO:0008266_MONDO:0011187_MONDO:0032603_MONDO:0029130_MONDO:0019673_MONDO:0019674_MONDO:0020927_MONDO:0011813_MONDO:0012059_MONDO:0017531_MONDO:0017532,"polydactyly, postaxial,",MONDO_grouped,disease,DISEASE_221
222,222,222,222,222,222,222,222,MONDO:0957463,primary bone and joint tuberculosis,MONDO,disease,DISEASE_222
223,223,223,223,223,223,223,223,MONDO:0014821,complex lethal osteochondrodysplasia,MONDO,disease,DISEASE_223
224,224,224,224,224,224,224,224,MONDO:1012397,"tomaculous neuropathy, cattle",MONDO,disease,DISEASE_224
225,225,225,225,225,225,225,225,MONDO:0001191,hirudiniasis,MONDO,disease,DISEASE_225
226,226,226,226,226,226,226,226,MONDO:0100010,disease of the tendon,MONDO,disease,DISEASE_226
227,227,227,227,227,227,227,227,MONDO:0957577,"variegate porphyria, childhood-onset",MONDO,disease,DISEASE_227
228,228,228,228,228,228,228,228,MONDO:0010682,"obsolete myoclonic epilepsy, progressive, X-linked",MONDO,disease,DISEASE_228
229,229,229,229,229,229,229,229,MONDO:0009099,nephrogenic diabetes insipidus-intracranial calcification syndrome,MONDO,disease,DISEASE_229
230,230,230,230,230,230,230,230,MONDO:0030971,immunodeficiency 78 with autoimmunity and developmental delay,MONDO,disease,DISEASE_230
231,231,231,231,231,231,231,231,MONDO:0003589_MONDO:0002634,liposarcoma of the ovary,MONDO_grouped,disease,DISEASE_231
232,232,232,232,232,232,232,232,MONDO:0100227,ALS2-related motor neuron disease,MONDO,disease,DISEASE_232
233,233,233,233,233,233,233,233,MONDO:0019351,isolated spina bifida,MONDO,disease,DISEASE_233
234,234,234,234,234,234,234,234,MONDO:1010147,"stiff skin syndrome, non-human animal",MONDO,disease,DISEASE_234
235,235,235,235,235,235,235,235,MONDO:8000011_MONDO:0030399_MONDO:0012317,"visceral neuropathy, familial, 1, autosomal recessive",MONDO_grouped,disease,DISEASE_235
236,236,236,236,236,236,236,236,MONDO:0014873,nevus comedonicus syndrome,MONDO,disease,DISEASE_236
237,237,237,237,237,237,237,237,MONDO:0017776,nocardiosis,MONDO,disease,DISEASE_237
238,238,238,238,238,238,238,238,MONDO:0005873,neuroaspergillosis,MONDO,disease,DISEASE_238
239,239,239,239,239,239,239,239,MONDO:0004577_MONDO:0023865,corneal ulcer,MONDO_grouped,disease,DISEASE_239
240,240,240,240,240,240,240,240,MONDO:0100293,diaphragmatic malformation,MONDO,disease,DISEASE_240
241,241,241,241,241,241,241,241,MONDO:0016459,2q23.1 microdeletion syndrome,MONDO,disease,DISEASE_241
242,242,242,242,242,242,242,242,MONDO:0018115,epidermal nevus syndrome,MONDO,disease,DISEASE_242
243,243,243,243,243,243,243,243,MONDO:0009633_MONDO:0016559,"microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma",MONDO_grouped,disease,DISEASE_243
244,244,244,244,244,244,244,244,MONDO:0014805,Hao-Fountain syndrome,MONDO,disease,DISEASE_244
245,245,245,245,245,245,245,245,MONDO:0015063,"duodenal neuroendocrine tumor, well differentiated, low or intermediate grade",MONDO,disease,DISEASE_245
246,246,246,246,246,246,246,246,MONDO:0023238,giant mammary hamartoma,MONDO,disease,DISEASE_246
247,247,247,247,247,247,247,247,MONDO:0800466,disorder of GNAS inactivation,MONDO,disease,DISEASE_247
248,248,248,248,248,248,248,248,MONDO:0019902,monosomy 13q34,MONDO,disease,DISEASE_248
249,249,249,249,249,249,249,249,MONDO:0005636,adenosarcoma,MONDO,disease,DISEASE_249
250,250,250,250,250,250,250,250,MONDO:0022754,chromosome 17p deletion,MONDO,disease,DISEASE_250
251,251,251,251,251,251,251,251,MONDO:0020001,respiratory or thoracic malformation,MONDO,disease,DISEASE_251
252,252,252,252,252,252,252,252,MONDO:0004295,asbestos-related lung carcinoma,MONDO,disease,DISEASE_252
253,253,253,253,253,253,253,253,MONDO:0018215,paraneoplastic neurologic syndrome,MONDO,disease,DISEASE_253
254,254,254,254,254,254,254,254,MONDO:0008630,"urinary bladder, atony of",MONDO,disease,DISEASE_254
255,255,255,255,255,255,255,255,MONDO:0024934,fish disease,MONDO,disease,DISEASE_255
256,256,256,256,256,256,256,256,MONDO:0010469,epsilon-trimethyllysine hydroxylase deficiency,MONDO,disease,DISEASE_256
257,257,257,257,257,257,257,257,MONDO:1011353,"radiculitis, non-human animal",MONDO,disease,DISEASE_257
258,258,258,258,258,258,258,258,MONDO:0005398,upper aerodigestive tract neoplasm,MONDO,disease,DISEASE_258
259,259,259,259,259,259,259,259,MONDO:1011418_MONDO:1010135,"porphyria, non-human animal",MONDO_grouped,disease,DISEASE_259
260,260,260,260,260,260,260,260,MONDO:0009451,Nezelof syndrome,MONDO,disease,DISEASE_260
261,261,261,261,261,261,261,261,MONDO:0958346,isolated transitional filum lipoma,MONDO,disease,DISEASE_261
262,262,262,262,262,262,262,262,MONDO:0002812_MONDO:0024330,infectious otitis interna,MONDO_grouped,disease,DISEASE_262
263,263,263,263,263,263,263,263,MONDO:0957421,borna virus encephalitis,MONDO,disease,DISEASE_263
264,264,264,264,264,264,264,264,MONDO:0013618,craniofacial anomalies and anterior segment dysgenesis syndrome,MONDO,disease,DISEASE_264
265,265,265,265,265,265,265,265,MONDO:1030005,mosaic SMO syndrome,MONDO,disease,DISEASE_265
266,266,266,266,266,266,266,266,MONDO:0020745,ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome,MONDO,disease,DISEASE_266
267,267,267,267,267,267,267,267,MONDO:0021251,endometrium neoplasm,MONDO,disease,DISEASE_267
268,268,268,268,268,268,268,268,MONDO:0010201,Winchester syndrome,MONDO,disease,DISEASE_268
269,269,269,269,269,269,269,269,MONDO:0023164,viral pericarditis,MONDO,disease,DISEASE_269
270,270,270,270,270,270,270,270,MONDO:0011007,diaphragmatic defect-limb deficiency-skull defect syndrome,MONDO,disease,DISEASE_270
271,271,271,271,271,271,271,271,MONDO:0014213,intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome,MONDO,disease,DISEASE_271
272,272,272,272,272,272,272,272,MONDO:0006210,fibrolamellar hepatocellular carcinoma,MONDO,disease,DISEASE_272
273,273,273,273,273,273,273,273,MONDO:0003386,bladder clear cell adenocarcinoma,MONDO,disease,DISEASE_273
274,274,274,274,274,274,274,274,MONDO:0021962,baetz-greenwalt syndrome,MONDO,disease,DISEASE_274
275,275,275,275,275,275,275,275,MONDO:0016842,paternal 20q13.2q13.3 microdeletion syndrome,MONDO,disease,DISEASE_275
276,276,276,276,276,276,276,276,MONDO:0009175,eosinophilic fasciitis,MONDO,disease,DISEASE_276
277,277,277,277,277,277,277,277,MONDO:0019690,filamin-related bone disorder,MONDO,disease,DISEASE_277
278,278,278,278,278,278,278,278,MONDO:0012209,branchiogenic deafness syndrome,MONDO,disease,DISEASE_278
279,279,279,279,279,279,279,279,MONDO:0014490,ketoacidosis due to monocarboxylate transporter-1 deficiency,MONDO,disease,DISEASE_279
280,280,280,280,280,280,280,280,MONDO:0015356,hereditary neoplastic syndrome,MONDO,disease,DISEASE_280
281,281,281,281,281,281,281,281,MONDO:0002028_MONDO:0001157_MONDO:0001159_MONDO:0001163_MONDO:0002027,personality disorder,MONDO_grouped,disease,DISEASE_281
282,282,282,282,282,282,282,282,MONDO:0001692,pedophilia,MONDO,disease,DISEASE_282
283,283,283,283,283,283,283,283,MONDO:0009170,endocardial fibroelastosis and coarctation of abdominal aorta,MONDO,disease,DISEASE_283
284,284,284,284,284,284,284,284,MONDO:0010062,spinocerebellar ataxia-dysmorphism syndrome,MONDO,disease,DISEASE_284
285,285,285,285,285,285,285,285,MONDO:0016184_MONDO:0016185,qualitative or quantitative defects of protein O-mannosyltransferase,MONDO_grouped,disease,DISEASE_285
286,286,286,286,286,286,286,286,MONDO:1010235_MONDO:1010303_MONDO:1011852_MONDO:1011869,"spinal muscular atrophy, non-human animal",MONDO_grouped,disease,DISEASE_286
287,287,287,287,287,287,287,287,MONDO:0001168_MONDO:0001169_MONDO:0001167,spastic hemiplegia,MONDO_grouped,disease,DISEASE_287
288,288,288,288,288,288,288,288,MONDO:0024770,"autoinflammatory syndrome, familial, X-linked, Behcet-like 2",MONDO,disease,DISEASE_288
289,289,289,289,289,289,289,289,MONDO:0009313,Grubben-de Cock-Borghgraef syndrome,MONDO,disease,DISEASE_289
290,290,290,290,290,290,290,290,MONDO:0005244,peripheral neuropathy,MONDO,disease,DISEASE_290
291,291,291,291,291,291,291,291,MONDO:0000244,endothrix infectious disease,MONDO,disease,DISEASE_291
292,292,292,292,292,292,292,292,MONDO:1011927,"pulmonary adenomatosis, non-human animal",MONDO,disease,DISEASE_292
293,293,293,293,293,293,293,293,MONDO:0002282,West Nile fever,MONDO,disease,DISEASE_293
294,294,294,294,294,294,294,294,MONDO:0100186,GTP cyclohydrolase I deficiency with hyperphenylalaninemia,MONDO,disease,DISEASE_294
295,295,295,295,295,295,295,295,MONDO:0021259,prostate neoplasm,MONDO,disease,DISEASE_295
296,296,296,296,296,296,296,296,MONDO:0001885,lateral cystocele,MONDO,disease,DISEASE_296
297,297,297,297,297,297,297,297,MONDO:0100453_MONDO:0100454_MONDO:0100441,GUCY2D-related recessive retinopathy,MONDO_grouped,disease,DISEASE_297
298,298,298,298,298,298,298,298,MONDO:0021084_MONDO:0005328_MONDO:0003382_MONDO:0001176_MONDO:0043885,vision disorder,MONDO_grouped,disease,DISEASE_298
299,299,299,299,299,299,299,299,MONDO:0016743,tumor of meninges,MONDO,disease,DISEASE_299
300,300,300,300,300,300,300,300,MONDO:0022714,chester porphyria,MONDO,disease,DISEASE_300
301,301,301,301,301,301,301,301,MONDO:0008705,lysosomal acid phosphatase deficiency,MONDO,disease,DISEASE_301
302,302,302,302,302,302,302,302,MONDO:0014382,Tatton-Brown-Rahman overgrowth syndrome,MONDO,disease,DISEASE_302
303,303,303,303,303,303,303,303,MONDO:0007872,LADD syndrome,MONDO,disease,DISEASE_303
304,304,304,304,304,304,304,304,MONDO:0023011,Wilson-Mikity syndrome,MONDO,disease,DISEASE_304
305,305,305,305,305,305,305,305,MONDO:0027677,isoniazid toxicity,MONDO,disease,DISEASE_305
306,306,306,306,306,306,306,306,MONDO:0004625_MONDO:0005913,phlebitis,MONDO_grouped,disease,DISEASE_306
307,307,307,307,307,307,307,307,MONDO:1011281,"achromatopsia, PDE6C-related, Rhesus monkey",MONDO,disease,DISEASE_307
308,308,308,308,308,308,308,308,MONDO:0013419,complement component C1s deficiency,MONDO,disease,DISEASE_308
309,309,309,309,309,309,309,309,MONDO:0018872_MONDO:0018004_MONDO:0020526_MONDO:0850267_MONDO:0971091,acute megakaryoblastic leukemia,MONDO_grouped,disease,DISEASE_309
310,310,310,310,310,310,310,310,MONDO:0700281,MYH10-related neurodevelopmental disorder with congenital anomalies,MONDO,disease,DISEASE_310
311,311,311,311,311,311,311,311,MONDO:0006451,thymic carcinoma,MONDO,disease,DISEASE_311
312,312,312,312,312,312,312,312,MONDO:0006736,dysplasia of cervix,MONDO,disease,DISEASE_312
313,313,313,313,313,313,313,313,MONDO:0014920_MONDO:0012162_MONDO:0008210_MONDO:0020381,patterned macular dystrophy,MONDO_grouped,disease,DISEASE_313
314,314,314,314,314,314,314,314,MONDO:0018961_MONDO:0023122,familial melanoma,MONDO_grouped,disease,DISEASE_314
315,315,315,315,315,315,315,315,MONDO:0975951,"spastic paraplegia, mitochondrial",MONDO,disease,DISEASE_315
316,316,316,316,316,316,316,316,MONDO:0004951,susceptibility to HIV infection,MONDO,disease,DISEASE_316
317,317,317,317,317,317,317,317,MONDO:1040007,hemihydranencephaly,MONDO,disease,DISEASE_317
318,318,318,318,318,318,318,318,MONDO:0017338,fatal multiple mitochondrial dysfunctions syndrome,MONDO,disease,DISEASE_318
319,319,319,319,319,319,319,319,MONDO:0018166,oral submucous fibrosis,MONDO,disease,DISEASE_319
320,320,320,320,320,320,320,320,MONDO:0006228,gastric papillary adenocarcinoma,MONDO,disease,DISEASE_320
321,321,321,321,321,321,321,321,MONDO:0008207,chondromalacia patellae,MONDO,disease,DISEASE_321
322,322,322,322,322,322,322,322,MONDO:0023267,goldstein hutt syndrome,MONDO,disease,DISEASE_322
323,323,323,323,323,323,323,323,MONDO:0008530,"teeth, odd shapes of",MONDO,disease,DISEASE_323
324,324,324,324,324,324,324,324,MONDO:0006950,retinal vasculitis,MONDO,disease,DISEASE_324
325,325,325,325,325,325,325,325,MONDO:0001286,exotropia,MONDO,disease,DISEASE_325
326,326,326,326,326,326,326,326,MONDO:0013909,"human herpesvirus 8, susceptibility to",MONDO,disease,DISEASE_326
327,327,327,327,327,327,327,327,MONDO:0009576,megalocornea,MONDO,disease,DISEASE_327
328,328,328,328,328,328,328,328,MONDO:1010212,"osteosarcoma, non-human animal",MONDO,disease,DISEASE_328
329,329,329,329,329,329,329,329,MONDO:0859158,"ataxia, intention tremor, and hypotonia syndrome, childhood-onset",MONDO,disease,DISEASE_329
330,330,330,330,330,330,330,330,MONDO:0019875,Beckwith-Wiedemann syndrome due to 11p15 microduplication,MONDO,disease,DISEASE_330
331,331,331,331,331,331,331,331,MONDO:0001592,prolapse of female genital organ,MONDO,disease,DISEASE_331
332,332,332,332,332,332,332,332,MONDO:0037744,neoplasm of retromolar area,MONDO,disease,DISEASE_332
333,333,333,333,333,333,333,333,MONDO:0001602,labia minora carcinoma,MONDO,disease,DISEASE_333
334,334,334,334,334,334,334,334,MONDO:0009030,"cranial nerves, recurrent paresis of",MONDO,disease,DISEASE_334
335,335,335,335,335,335,335,335,MONDO:0003252,granular cell cancer,MONDO,disease,DISEASE_335
336,336,336,336,336,336,336,336,MONDO:0010725,X-linked retinoschisis,MONDO,disease,DISEASE_336
337,337,337,337,337,337,337,337,MONDO:0020678,sensorineural hearing loss disorder,MONDO,disease,DISEASE_337
338,338,338,338,338,338,338,338,MONDO:0015604,middle ear anomaly,MONDO,disease,DISEASE_338
339,339,339,339,339,339,339,339,MONDO:0002319,phosphorus metabolism disease,MONDO,disease,DISEASE_339
340,340,340,340,340,340,340,340,MONDO:0006570,lichen disease,MONDO,disease,DISEASE_340
341,341,341,341,341,341,341,341,MONDO:0002429,idiopathic interstitial pneumonia,MONDO,disease,DISEASE_341
342,342,342,342,342,342,342,342,MONDO:0019433,oligoarticular juvenile idiopathic arthritis,MONDO,disease,DISEASE_342
343,343,343,343,343,343,343,343,MONDO:0015030,sclerosing perineurioma,MONDO,disease,DISEASE_343
344,344,344,344,344,344,344,344,MONDO:0022468,antigen-peptide-transporter 2 deficiency,MONDO,disease,DISEASE_344
345,345,345,345,345,345,345,345,MONDO:0015532,generalized eruptive histiocytosis,MONDO,disease,DISEASE_345
346,346,346,346,346,346,346,346,MONDO:0008083_MONDO:0008768,"ceroid lipofuscinosis, neuronal, 4 (Kufs type)",MONDO_grouped,disease,DISEASE_346
347,347,347,347,347,347,347,347,MONDO:0003076,unilateral retinoblastoma,MONDO,disease,DISEASE_347
348,348,348,348,348,348,348,348,MONDO:0016739,yolk sac tumor of central nervous system,MONDO,disease,DISEASE_348
349,349,349,349,349,349,349,349,MONDO:0958345,limited dorsal myeloschisis,MONDO,disease,DISEASE_349
350,350,350,350,350,350,350,350,MONDO:0006052,pulmonary tuberculosis,MONDO,disease,DISEASE_350
351,351,351,351,351,351,351,351,MONDO:0006432,stromal predominant kidney Wilms tumor,MONDO,disease,DISEASE_351
352,352,352,352,352,352,352,352,MONDO:0019545,systemic monochloroacetate poisoning,MONDO,disease,DISEASE_352
353,353,353,353,353,353,353,353,MONDO:0002696,Sertoli cell tumor,MONDO,disease,DISEASE_353
354,354,354,354,354,354,354,354,MONDO:0014889,"striatonigral degeneration, childhood-onset",MONDO,disease,DISEASE_354
355,355,355,355,355,355,355,355,MONDO:0957461,primary tuberculous lymphadenitis,MONDO,disease,DISEASE_355
356,356,356,356,356,356,356,356,MONDO:1010067,"omphalocele, non-human animal",MONDO,disease,DISEASE_356
357,357,357,357,357,357,357,357,MONDO:0017242,cutaneous collagenous vasculopathy,MONDO,disease,DISEASE_357
358,358,358,358,358,358,358,358,MONDO:0044344_MONDO:0044351,Schistosoma japonicum infectious disease,MONDO_grouped,disease,DISEASE_358
359,359,359,359,359,359,359,359,MONDO:0006491,vulvar lichen sclerosus,MONDO,disease,DISEASE_359
360,360,360,360,360,360,360,360,MONDO:0004842_MONDO:0006979,stomatitis,MONDO_grouped,disease,DISEASE_360
361,361,361,361,361,361,361,361,MONDO:0002265,stereotypic movement disorder,MONDO,disease,DISEASE_361
362,362,362,362,362,362,362,362,MONDO:0001935,neurogenic arthropathy,MONDO,disease,DISEASE_362
363,363,363,363,363,363,363,363,MONDO:0023212,Garret-Tripp syndrome,MONDO,disease,DISEASE_363
364,364,364,364,364,364,364,364,MONDO:0006000,tuberculous peritonitis,MONDO,disease,DISEASE_364
365,365,365,365,365,365,365,365,MONDO:0002746_MONDO:0006206_MONDO:0002833_MONDO:0003328_MONDO:0003503_MONDO:0006207_MONDO:0006208,fallopian tube adenocarcinoma,MONDO_grouped,disease,DISEASE_365
366,366,366,366,366,366,366,366,MONDO:0013579,methylmalonate semialdehyde dehydrogenase deficiency,MONDO,disease,DISEASE_366
367,367,367,367,367,367,367,367,MONDO:0012243,"B-cell immunodeficiency, distal limb anomalies, and urogenital malformations",MONDO,disease,DISEASE_367
368,368,368,368,368,368,368,368,MONDO:0005498,botulism,MONDO,disease,DISEASE_368
369,369,369,369,369,369,369,369,MONDO:0035404_MONDO:0035405,mucinous cystadenoma of childhood,MONDO_grouped,disease,DISEASE_369
370,370,370,370,370,370,370,370,MONDO:0031240,familial panic disorder,MONDO,disease,DISEASE_370
371,371,371,371,371,371,371,371,MONDO:0018144,obsolete congenital myasthenic syndromes with glycosylation defect,MONDO,disease,DISEASE_371
372,372,372,372,372,372,372,372,MONDO:0018305,chronic granulomatous disease,MONDO,disease,DISEASE_372
373,373,373,373,373,373,373,373,MONDO:0004628,gastroduodenitis,MONDO,disease,DISEASE_373
374,374,374,374,374,374,374,374,MONDO:1010419,"narcolepsy, domestic cat",MONDO,disease,DISEASE_374
375,375,375,375,375,375,375,375,MONDO:0017737,intermediate severe Salla disease,MONDO,disease,DISEASE_375
376,376,376,376,376,376,376,376,MONDO:0001716,corneal argyrosis,MONDO,disease,DISEASE_376
377,377,377,377,377,377,377,377,MONDO:0004243,vulvar proximal-type epithelioid sarcoma,MONDO,disease,DISEASE_377
378,378,378,378,378,378,378,378,MONDO:0006970,sialolithiasis,MONDO,disease,DISEASE_378
379,379,379,379,379,379,379,379,MONDO:1011895,"Guillain-Barr-like polyradiculoneuropathy, non-human animal",MONDO,disease,DISEASE_379
380,380,380,380,380,380,380,380,MONDO:0012038,speech-sound disorder,MONDO,disease,DISEASE_380
381,381,381,381,381,381,381,381,MONDO:0010673,"modifier, X-linked, for Neurofunctional defects",MONDO,disease,DISEASE_381
382,382,382,382,382,382,382,382,MONDO:0030983,"Waardenburg syndrome, IIa 2F",MONDO,disease,DISEASE_382
383,383,383,383,383,383,383,383,MONDO:0007600,primary Fanconi syndrome,MONDO,disease,DISEASE_383
384,384,384,384,384,384,384,384,MONDO:0002069,female breast axillary tail cancer,MONDO,disease,DISEASE_384
385,385,385,385,385,385,385,385,MONDO:0019034,accessory pancreas,MONDO,disease,DISEASE_385
386,386,386,386,386,386,386,386,MONDO:0011011,skeletal dysplasia-epilepsy-short stature syndrome,MONDO,disease,DISEASE_386
387,387,387,387,387,387,387,387,MONDO:0060782,premalignant hematological system disease,MONDO,disease,DISEASE_387
388,388,388,388,388,388,388,388,MONDO:0042969,partial duplication of the long arm of chromosome 12,MONDO,disease,DISEASE_388
389,389,389,389,389,389,389,389,MONDO:0006484,usual ductal breast hyperplasia,MONDO,disease,DISEASE_389
390,390,390,390,390,390,390,390,MONDO:0020071,infantile epilepsy syndrome,MONDO,disease,DISEASE_390
391,391,391,391,391,391,391,391,MONDO:0100482_MONDO:0100483,extensively drug-resistant tuberculosis,MONDO_grouped,disease,DISEASE_391
392,392,392,392,392,392,392,392,MONDO:0024270_MONDO:0024610,parasitic intestinal disorder,MONDO_grouped,disease,DISEASE_392
393,393,393,393,393,393,393,393,MONDO:0001632,intracranial arteriosclerosis,MONDO,disease,DISEASE_393
394,394,394,394,394,394,394,394,MONDO:0011523_MONDO:0014439_MONDO:0014440_MONDO:0014926_MONDO:0023670_MONDO:0008854_MONDO:0014432_MONDO:0014446_MONDO:0014445_MONDO:0014447_MONDO:0014433_MONDO:0014434_MONDO:0014444_MONDO:0014438_MONDO:0014437_MONDO:0014443_MONDO:0010832_MONDO:0014435_MONDO:0014441_MONDO:0014442_MONDO:0014436_MONDO:0044308_MONDO:0015229,Bardet-Biedl syndrome,MONDO_grouped,disease,DISEASE_394
395,395,395,395,395,395,395,395,MONDO:0003492,lacrimal gland squamous cell carcinoma,MONDO,disease,DISEASE_395
396,396,396,396,396,396,396,396,MONDO:0010831,familial caudal dysgenesis,MONDO,disease,DISEASE_396
397,397,397,397,397,397,397,397,MONDO:0009454_MONDO:0014828_MONDO:0013553_MONDO:0014829_MONDO:0000133,immunodeficiency-centromeric instability-facial anomalies syndrome,MONDO_grouped,disease,DISEASE_397
398,398,398,398,398,398,398,398,MONDO:0020389,pulmonary valve agenesis-ventricular septal defect-persistent ductus arteriosus syndrome,MONDO,disease,DISEASE_398
399,399,399,399,399,399,399,399,MONDO:0021486,benign neoplasm of ciliary body,MONDO,disease,DISEASE_399
400,400,400,400,400,400,400,400,MONDO:0011628,propionic acidemia,MONDO,disease,DISEASE_400
401,401,401,401,401,401,401,401,MONDO:0008675,Freeman-Sheldon syndrome,MONDO,disease,DISEASE_401
402,402,402,402,402,402,402,402,MONDO:0002863,rhabdomyosarcoma with mixed embryonal and alveolar features,MONDO,disease,DISEASE_402
403,403,403,403,403,403,403,403,MONDO:0024985_MONDO:0024913,sheep disease,MONDO_grouped,disease,DISEASE_403
404,404,404,404,404,404,404,404,MONDO:0021337,tonsil carcinoma,MONDO,disease,DISEASE_404
405,405,405,405,405,405,405,405,MONDO:0009704,"carnitine palmitoyl transferase II deficiency, myopathic form",MONDO,disease,DISEASE_405
406,406,406,406,406,406,406,406,MONDO:0010103,"teeth, fused",MONDO,disease,DISEASE_406
407,407,407,407,407,407,407,407,MONDO:0000208_MONDO:0014785_MONDO:0800450,"microcephaly, short stature, and impaired glucose metabolism",MONDO_grouped,disease,DISEASE_407
408,408,408,408,408,408,408,408,MONDO:1012533,"calvarial hyperostotic syndrome, lion",MONDO,disease,DISEASE_408
409,409,409,409,409,409,409,409,MONDO:0044626,female infertility due to oocyte meiotic arrest,MONDO,disease,DISEASE_409
410,410,410,410,410,410,410,410,MONDO:0011221,Weyers ulnar ray/oligodactyly syndrome,MONDO,disease,DISEASE_410
411,411,411,411,411,411,411,411,MONDO:0017861,ethylene glycol poisoning,MONDO,disease,DISEASE_411
412,412,412,412,412,412,412,412,MONDO:0003975,Littre gland carcinoma,MONDO,disease,DISEASE_412
413,413,413,413,413,413,413,413,MONDO:0007618,Eng-Strom syndrome,MONDO,disease,DISEASE_413
414,414,414,414,414,414,414,414,MONDO:0018460,Eales disease,MONDO,disease,DISEASE_414
415,415,415,415,415,415,415,415,MONDO:0003792_MONDO:0004436,ovarian carcinosarcoma,MONDO_grouped,disease,DISEASE_415
416,416,416,416,416,416,416,416,MONDO:0044745,nervous system injury,MONDO,disease,DISEASE_416
417,417,417,417,417,417,417,417,MONDO:0008213,pectus excavatum,MONDO,disease,DISEASE_417
418,418,418,418,418,418,418,418,MONDO:0023143,fetal enterovirus syndrome,MONDO,disease,DISEASE_418
419,419,419,419,419,419,419,419,MONDO:0957385,"dystonia 37, early-onset, with striatal lesions",MONDO,disease,DISEASE_419
420,420,420,420,420,420,420,420,MONDO:0032687,"intellectual developmental disorder with abnormal behavior, microcephaly, and short stature",MONDO,disease,DISEASE_420
421,421,421,421,421,421,421,421,MONDO:0005424_MONDO:0019147_MONDO:0016566,elephantiasis,MONDO_grouped,disease,DISEASE_421
422,422,422,422,422,422,422,422,MONDO:0013276,Reynolds syndrome,MONDO,disease,DISEASE_422
423,423,423,423,423,423,423,423,MONDO:0009920,Acrootoocular syndrome,MONDO,disease,DISEASE_423
424,424,424,424,424,424,424,424,MONDO:0042433,mycotic endocarditis,MONDO,disease,DISEASE_424
425,425,425,425,425,425,425,425,MONDO:0019641_MONDO:0019988_MONDO:0019989,Pauci-immune glomerulonephritis,MONDO_grouped,disease,DISEASE_425
426,426,426,426,426,426,426,426,MONDO:0013417,complement component 3 deficiency,MONDO,disease,DISEASE_426
427,427,427,427,427,427,427,427,MONDO:0015580,distal monosomy 7q36,MONDO,disease,DISEASE_427
428,428,428,428,428,428,428,428,MONDO:0010158,T-substance anomaly,MONDO,disease,DISEASE_428
429,429,429,429,429,429,429,429,MONDO:0012176,Emanuel syndrome,MONDO,disease,DISEASE_429
430,430,430,430,430,430,430,430,MONDO:0007766,Morgagni-Stewart-Morel syndrome,MONDO,disease,DISEASE_430
431,431,431,431,431,431,431,431,MONDO:0024880,metastatic malignant neoplasm,MONDO,disease,DISEASE_431
432,432,432,432,432,432,432,432,MONDO:1012023_MONDO:1012024,"distal axonopathy, domestic cat",MONDO_grouped,disease,DISEASE_432
433,433,433,433,433,433,433,433,MONDO:0001320,ring staphyloma,MONDO,disease,DISEASE_433
434,434,434,434,434,434,434,434,MONDO:0002836,urethra transitional cell carcinoma,MONDO,disease,DISEASE_434
435,435,435,435,435,435,435,435,MONDO:0008834,"asthma, nasal polyps, and aspirin intolerance",MONDO,disease,DISEASE_435
436,436,436,436,436,436,436,436,MONDO:0021208,endocrine alopecia,MONDO,disease,DISEASE_436
437,437,437,437,437,437,437,437,MONDO:0036696,spleen neoplasm,MONDO,disease,DISEASE_437
438,438,438,438,438,438,438,438,MONDO:0009398_MONDO:0013882_MONDO:0014780_MONDO:0013628_MONDO:0014457_MONDO:0014318,hyperphosphatasia with intellectual disability syndrome,MONDO_grouped,disease,DISEASE_438
439,439,439,439,439,439,439,439,MONDO:1010917_MONDO:1012175,"myopathy, dog",MONDO_grouped,disease,DISEASE_439
440,440,440,440,440,440,440,440,MONDO:1011671,"spinal dysraphism, non-human animal",MONDO,disease,DISEASE_440
441,441,441,441,441,441,441,441,MONDO:0007968,melanoma tumor antigen Gp90,MONDO,disease,DISEASE_441
442,442,442,442,442,442,442,442,MONDO:0001661,background diabetic retinopathy,MONDO,disease,DISEASE_442
443,443,443,443,443,443,443,443,MONDO:0015265_MONDO:0100127_MONDO:0800119_MONDO:0958127_MONDO:0958128,bronchiolitis obliterans syndrome,MONDO_grouped,disease,DISEASE_443
444,444,444,444,444,444,444,444,MONDO:0100335,local anesthetic poisoning,MONDO,disease,DISEASE_444
445,445,445,445,445,445,445,445,MONDO:0002885,erythrasma,MONDO,disease,DISEASE_445
446,446,446,446,446,446,446,446,MONDO:0017394,ketamine-induced biliary dilatation,MONDO,disease,DISEASE_446
447,447,447,447,447,447,447,447,MONDO:0001959_MONDO:0002106,labyrinthine bilateral reactive loss,MONDO_grouped,disease,DISEASE_447
448,448,448,448,448,448,448,448,MONDO:0018921,Meckel syndrome,MONDO,disease,DISEASE_448
449,449,449,449,449,449,449,449,MONDO:0014013,maternal riboflavin deficiency,MONDO,disease,DISEASE_449
450,450,450,450,450,450,450,450,MONDO:0005851,Miller Fisher syndrome,MONDO,disease,DISEASE_450
451,451,451,451,451,451,451,451,MONDO:0005334,hereditary nephritis,MONDO,disease,DISEASE_451
452,452,452,452,452,452,452,452,MONDO:0003017,malignant peritoneal solitary fibrous tumor,MONDO,disease,DISEASE_452
453,453,453,453,453,453,453,453,MONDO:0019815,accessory tricuspid valve tissue,MONDO,disease,DISEASE_453
454,454,454,454,454,454,454,454,MONDO:0021662,bile duct neoplasm,MONDO,disease,DISEASE_454
455,455,455,455,455,455,455,455,MONDO:0032571_MONDO:0008476_MONDO:0010248_MONDO:0011252_MONDO:0016761_MONDO:0100510_MONDO:0019675_MONDO:0018254,"spondyloepimetaphyseal dysplasia, Krakow type",MONDO_grouped,disease,DISEASE_455
456,456,456,456,456,456,456,456,MONDO:0006391,pyloric gland adenoma,MONDO,disease,DISEASE_456
457,457,457,457,457,457,457,457,MONDO:0011733_MONDO:0100226_MONDO:0800355,"parasomnia, sleep bruxism type",MONDO_grouped,disease,DISEASE_457
458,458,458,458,458,458,458,458,MONDO:0006847,malignant lymphatic vessel tumor,MONDO,disease,DISEASE_458
459,459,459,459,459,459,459,459,MONDO:0024861,mixed teratoma and seminoma,MONDO,disease,DISEASE_459
460,460,460,460,460,460,460,460,MONDO:0008021_MONDO:0012878_MONDO:0014048_MONDO:0014047_MONDO:0014046_MONDO:0014802_MONDO:0016063_MONDO:0014045,Cowden syndrome,MONDO_grouped,disease,DISEASE_460
461,461,461,461,461,461,461,461,MONDO:0003841,heart lipoma,MONDO,disease,DISEASE_461
462,462,462,462,462,462,462,462,MONDO:0017580,11p15.4 microduplication syndrome,MONDO,disease,DISEASE_462
463,463,463,463,463,463,463,463,MONDO:0043191,radial defect robin sequence,MONDO,disease,DISEASE_463
464,464,464,464,464,464,464,464,MONDO:0011248,distal monosomy 13q,MONDO,disease,DISEASE_464
465,465,465,465,465,465,465,465,MONDO:0001366,splenic sequestration,MONDO,disease,DISEASE_465
466,466,466,466,466,466,466,466,MONDO:0005292,colitis,MONDO,disease,DISEASE_466
467,467,467,467,467,467,467,467,MONDO:1010102,"porphyria cutanea tarda, non-human animal",MONDO,disease,DISEASE_467
468,468,468,468,468,468,468,468,MONDO:0007541,"endometriosis, susceptibility to, 1",MONDO,disease,DISEASE_468
469,469,469,469,469,469,469,469,MONDO:0006273,low grade fibromyxoid sarcoma with giant collagen rosettes,MONDO,disease,DISEASE_469
470,470,470,470,470,470,470,470,MONDO:0011372,microcephaly with simplified gyral pattern,MONDO,disease,DISEASE_470
471,471,471,471,471,471,471,471,MONDO:1012167_MONDO:1012168_MONDO:1012169_MONDO:1012170_MONDO:1012311,"lower motor neuron disease, dog",MONDO_grouped,disease,DISEASE_471
472,472,472,472,472,472,472,472,MONDO:1012431,"rod dysplasia, dog",MONDO,disease,DISEASE_472
473,473,473,473,473,473,473,473,MONDO:0002480,endometrioid tumor,MONDO,disease,DISEASE_473
474,474,474,474,474,474,474,474,MONDO:0700128,translocation Down syndrome,MONDO,disease,DISEASE_474
475,475,475,475,475,475,475,475,MONDO:0022993,dipsogenic diabetes insipidus,MONDO,disease,DISEASE_475
476,476,476,476,476,476,476,476,MONDO:0024476,epithelial neoplasm of rectum,MONDO,disease,DISEASE_476
477,477,477,477,477,477,477,477,MONDO:0005824,Legionnaires' disease,MONDO,disease,DISEASE_477
478,478,478,478,478,478,478,478,MONDO:0007535,"emphysema, hereditary pulmonary",MONDO,disease,DISEASE_478
479,479,479,479,479,479,479,479,MONDO:0012412,complement component 7 deficiency,MONDO,disease,DISEASE_479
480,480,480,480,480,480,480,480,MONDO:0850069,familial hyperinflammatory lymphoproliferative immunodeficiency,MONDO,disease,DISEASE_480
481,481,481,481,481,481,481,481,MONDO:0005153_MONDO:0005131_MONDO:0003238_MONDO:0002876_MONDO:0000549_MONDO:0002877_MONDO:0003459,cervical adenocarcinoma,MONDO_grouped,disease,DISEASE_481
482,482,482,482,482,482,482,482,MONDO:0018535,biliary cystadenocarcinoma,MONDO,disease,DISEASE_482
483,483,483,483,483,483,483,483,MONDO:0023388,pityriasis rotunda,MONDO,disease,DISEASE_483
484,484,484,484,484,484,484,484,MONDO:0014346_MONDO:0008676,white sponge nevus,MONDO_grouped,disease,DISEASE_484
485,485,485,485,485,485,485,485,MONDO:0033043,"spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy",MONDO,disease,DISEASE_485
486,486,486,486,486,486,486,486,MONDO:0005744,yolk sac tumor,MONDO,disease,DISEASE_486
487,487,487,487,487,487,487,487,MONDO:0002400,synovitis,MONDO,disease,DISEASE_487
488,488,488,488,488,488,488,488,MONDO:0010315,T-B+ severe combined immunodeficiency due to gamma chain deficiency,MONDO,disease,DISEASE_488
489,489,489,489,489,489,489,489,MONDO:0014795,"exercise intolerance, riboflavin-responsive",MONDO,disease,DISEASE_489
490,490,490,490,490,490,490,490,MONDO:0001352,round ligament malignant neoplasm,MONDO,disease,DISEASE_490
491,491,491,491,491,491,491,491,MONDO:1011098_MONDO:1011624,"alkaptonuria, domestic cat",MONDO_grouped,disease,DISEASE_491
492,492,492,492,492,492,492,492,MONDO:0009179_MONDO:0019310_MONDO:0015552_MONDO:0019522_MONDO:0019521_MONDO:0035349,recessive dystrophic epidermolysis bullosa,MONDO_grouped,disease,DISEASE_492
493,493,493,493,493,493,493,493,MONDO:0025412,feline panleukopenia,MONDO,disease,DISEASE_493
494,494,494,494,494,494,494,494,MONDO:0700101,"carcinoma, non-human animal",MONDO,disease,DISEASE_494
495,495,495,495,495,495,495,495,MONDO:0017276,frontotemporal dementia,MONDO,disease,DISEASE_495
496,496,496,496,496,496,496,496,MONDO:0015433,ring chromosome 17,MONDO,disease,DISEASE_496
497,497,497,497,497,497,497,497,MONDO:0022470,aortic dissection lentiginosis,MONDO,disease,DISEASE_497
498,498,498,498,498,498,498,498,MONDO:1011120,"orchitis, dog",MONDO,disease,DISEASE_498
499,499,499,499,499,499,499,499,MONDO:0003278,inner ear cancer,MONDO,disease,DISEASE_499
500,500,500,500,500,500,500,500,MONDO:0008155,osteomesopyknosis,MONDO,disease,DISEASE_500
501,501,501,501,501,501,501,501,MONDO:0008454_MONDO:1012486,spinal intradural arachnoid cysts,MONDO_grouped,disease,DISEASE_501
502,502,502,502,502,502,502,502,MONDO:0011367,"Acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia",MONDO,disease,DISEASE_502
503,503,503,503,503,503,503,503,MONDO:0016956,partial trisomy of the long arm of chromosome 5,MONDO,disease,DISEASE_503
504,504,504,504,504,504,504,504,MONDO:0017078,cephalocele,MONDO,disease,DISEASE_504
505,505,505,505,505,505,505,505,MONDO:0008035,"muscular hypoplasia, congenital universal, of Krabbe",MONDO,disease,DISEASE_505
506,506,506,506,506,506,506,506,MONDO:0060781,Preeyasombat-Varavithya syndrome,MONDO,disease,DISEASE_506
507,507,507,507,507,507,507,507,MONDO:0008526,talonavicular coalition,MONDO,disease,DISEASE_507
508,508,508,508,508,508,508,508,MONDO:0024306,acquired lactic acidosis,MONDO,disease,DISEASE_508
509,509,509,509,509,509,509,509,MONDO:0021076,pancreatic exocrine neoplasm,MONDO,disease,DISEASE_509
510,510,510,510,510,510,510,510,MONDO:0000376,respiratory system cancer,MONDO,disease,DISEASE_510
511,511,511,511,511,511,511,511,MONDO:0006963,sebaceous gland neoplasm,MONDO,disease,DISEASE_511
512,512,512,512,512,512,512,512,MONDO:0002982,peripheral primitive neuroectodermal tumor of soft tissues,MONDO,disease,DISEASE_512
513,513,513,513,513,513,513,513,MONDO:0025449,paratuberculosis,MONDO,disease,DISEASE_513
514,514,514,514,514,514,514,514,MONDO:0056806,non-small cell squamous lung carcinoma,MONDO,disease,DISEASE_514
515,515,515,515,515,515,515,515,MONDO:0018509,squamous cell carcinoma of the small intestine,MONDO,disease,DISEASE_515
516,516,516,516,516,516,516,516,MONDO:0957494,"autoinflammatory disease, multisystem, with immune dysregulation, X-linked",MONDO,disease,DISEASE_516
517,517,517,517,517,517,517,517,MONDO:0100554,hereditary narcolepsy,MONDO,disease,DISEASE_517
518,518,518,518,518,518,518,518,MONDO:0015272,camptodactyly-taurinuria syndrome,MONDO,disease,DISEASE_518
519,519,519,519,519,519,519,519,MONDO:1040054,DHDDS-CDG,MONDO,disease,DISEASE_519
520,520,520,520,520,520,520,520,MONDO:0013003,isolated congenital hypoglossia/aglossia,MONDO,disease,DISEASE_520
521,521,521,521,521,521,521,521,MONDO:0015400,frontonasal arteriovenous malformation,MONDO,disease,DISEASE_521
522,522,522,522,522,522,522,522,MONDO:0016052,atypical autism,MONDO,disease,DISEASE_522
523,523,523,523,523,523,523,523,MONDO:0009386,hyperlexia,MONDO,disease,DISEASE_523
524,524,524,524,524,524,524,524,MONDO:1010138,"pemphigus, non-human animal",MONDO,disease,DISEASE_524
525,525,525,525,525,525,525,525,MONDO:0004082,childhood immature teratoma of ovary,MONDO,disease,DISEASE_525
526,526,526,526,526,526,526,526,MONDO:0700000,ALG9-associated autosomal dominant polycystic kidney disease,MONDO,disease,DISEASE_526
527,527,527,527,527,527,527,527,MONDO:0018249,finger hyperphalangy - toe anomalies - severe pectus excavatum syndrome,MONDO,disease,DISEASE_527
528,528,528,528,528,528,528,528,MONDO:1010278,"persistent Mullerian duct syndrome, non-human animal",MONDO,disease,DISEASE_528
529,529,529,529,529,529,529,529,MONDO:0013511,"cyanosis, transient neonatal",MONDO,disease,DISEASE_529
530,530,530,530,530,530,530,530,MONDO:0012679_MONDO:0012676_MONDO:0957262_MONDO:0009818_MONDO:0012859_MONDO:0014040_MONDO:0009817_MONDO:0009816_MONDO:0009815_MONDO:0009810_MONDO:0019026_MONDO:0020645,autosomal recessive osteopetrosis,MONDO_grouped,disease,DISEASE_530
531,531,531,531,531,531,531,531,MONDO:0009391,hypermetabolism due to defect in mitochondria,MONDO,disease,DISEASE_531
532,532,532,532,532,532,532,532,MONDO:0859209,Zaki syndrome,MONDO,disease,DISEASE_532
533,533,533,533,533,533,533,533,MONDO:0008951,cerebrocortical degeneration of infancy,MONDO,disease,DISEASE_533
534,534,534,534,534,534,534,534,MONDO:1010731,"X-linked severe combined immunodeficiency disease, IL2RG-related, dog",MONDO,disease,DISEASE_534
535,535,535,535,535,535,535,535,MONDO:0850514,inclusion body myopathy and brain white matter abnormalities,MONDO,disease,DISEASE_535
536,536,536,536,536,536,536,536,MONDO:0008363,raindrop hypopigmentation,MONDO,disease,DISEASE_536
537,537,537,537,537,537,537,537,MONDO:0043185,pointer syndrome,MONDO,disease,DISEASE_537
538,538,538,538,538,538,538,538,MONDO:0001936,brawny scleritis,MONDO,disease,DISEASE_538
539,539,539,539,539,539,539,539,MONDO:1012758_MONDO:1012759_MONDO:1012778_MONDO:1012779_MONDO:1012780_MONDO:1012837,"junctional epidermolysis bullosa, ITGB4-related, cattle",MONDO_grouped,disease,DISEASE_539
540,540,540,540,540,540,540,540,MONDO:0015449,criss-cross heart,MONDO,disease,DISEASE_540
541,541,541,541,541,541,541,541,MONDO:0017456_MONDO:0017536,central polydactyly of fingers,MONDO_grouped,disease,DISEASE_541
542,542,542,542,542,542,542,542,MONDO:1010427,"atherosclerosis, golden hamster",MONDO,disease,DISEASE_542
543,543,543,543,543,543,543,543,MONDO:0004560,follicular infundibulum tumor,MONDO,disease,DISEASE_543
544,544,544,544,544,544,544,544,MONDO:0001057,malignant gastric granular cell tumor,MONDO,disease,DISEASE_544
545,545,545,545,545,545,545,545,MONDO:0008846,atransferrinemia,MONDO,disease,DISEASE_545
546,546,546,546,546,546,546,546,MONDO:0000338,variola major infectious disease,MONDO,disease,DISEASE_546
547,547,547,547,547,547,547,547,MONDO:0008475,spondylolisthesis,MONDO,disease,DISEASE_547
548,548,548,548,548,548,548,548,MONDO:0045049,hypermature cataract,MONDO,disease,DISEASE_548
549,549,549,549,549,549,549,549,MONDO:0016273,malignant germ cell tumor of corpus uteri,MONDO,disease,DISEASE_549
550,550,550,550,550,550,550,550,MONDO:0020580,germinomatous germ cell tumor,MONDO,disease,DISEASE_550
551,551,551,551,551,551,551,551,MONDO:1011733,"atopy, non-human animal",MONDO,disease,DISEASE_551
552,552,552,552,552,552,552,552,MONDO:0007777,hypotaurinemic retinal degeneration and cardiomyopathy,MONDO,disease,DISEASE_552
553,553,553,553,553,553,553,553,MONDO:0005514,nanophthalmia,MONDO,disease,DISEASE_553
554,554,554,554,554,554,554,554,MONDO:0011872_MONDO:0008962_MONDO:0012220_MONDO:0018306,Griscelli syndrome,MONDO_grouped,disease,DISEASE_554
555,555,555,555,555,555,555,555,MONDO:0008874,Bangstad syndrome,MONDO,disease,DISEASE_555
556,556,556,556,556,556,556,556,MONDO:0010537,Borjeson-Forssman-Lehmann syndrome,MONDO,disease,DISEASE_556
557,557,557,557,557,557,557,557,MONDO:0008744,alar cartilages hypoplasia-coloboma-telecanthus syndrome,MONDO,disease,DISEASE_557
558,558,558,558,558,558,558,558,MONDO:0013743,autosomal systemic lupus erythematosus type 16,MONDO,disease,DISEASE_558
559,559,559,559,559,559,559,559,MONDO:0018020_MONDO:0017638_MONDO:0800385,mercury poisoning,MONDO_grouped,disease,DISEASE_559
560,560,560,560,560,560,560,560,MONDO:0041996,thallium poisoning,MONDO,disease,DISEASE_560
561,561,561,561,561,561,561,561,MONDO:0958256,pyoderma gangrenosum-acne-hidradenitis suppurativa-ankylosing spondylitis syndrome,MONDO,disease,DISEASE_561
562,562,562,562,562,562,562,562,MONDO:0010988,aplasia cutis-myopia syndrome,MONDO,disease,DISEASE_562
563,563,563,563,563,563,563,563,MONDO:1012467,"postpartum dysgalactia syndrome, pig",MONDO,disease,DISEASE_563
564,564,564,564,564,564,564,564,MONDO:0027653,abacavir toxicity,MONDO,disease,DISEASE_564
565,565,565,565,565,565,565,565,MONDO:1011823_MONDO:1010226,"hemangiosarcoma, non-human animal",MONDO_grouped,disease,DISEASE_565
566,566,566,566,566,566,566,566,MONDO:0011256,"emphysema, congenital, with deafness, penoscrotal web, and intellectual disability",MONDO,disease,DISEASE_566
567,567,567,567,567,567,567,567,MONDO:0002483,breast myoepithelial tumor,MONDO,disease,DISEASE_567
568,568,568,568,568,568,568,568,MONDO:0014979,"myoclonus, intractable, neonatal",MONDO,disease,DISEASE_568
569,569,569,569,569,569,569,569,MONDO:0016306,"Niemann-Pick disease type C, severe perinatal form",MONDO,disease,DISEASE_569
570,570,570,570,570,570,570,570,MONDO:1010520,"cleft lip with or without cleft palate, dog",MONDO,disease,DISEASE_570
571,571,571,571,571,571,571,571,MONDO:0021072_MONDO:0000448,sympathetic paraganglioma,MONDO_grouped,disease,DISEASE_571
572,572,572,572,572,572,572,572,MONDO:0003045,anal gland neoplasm,MONDO,disease,DISEASE_572
573,573,573,573,573,573,573,573,MONDO:0018949,distal myopathy,MONDO,disease,DISEASE_573
574,574,574,574,574,574,574,574,MONDO:0800098,SNRNP200-related dominant retinopathy,MONDO,disease,DISEASE_574
575,575,575,575,575,575,575,575,MONDO:0044305_MONDO:0013976_MONDO:0013973_MONDO:0011177_MONDO:0013975_MONDO:0013974,"ectodermal dysplasia 13, hair/tooth type",MONDO_grouped,disease,DISEASE_575
576,576,576,576,576,576,576,576,MONDO:0004245,ependymal tumor of brain,MONDO,disease,DISEASE_576
577,577,577,577,577,577,577,577,MONDO:0004677,tinea nigra,MONDO,disease,DISEASE_577
578,578,578,578,578,578,578,578,MONDO:0032817,"neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies",MONDO,disease,DISEASE_578
579,579,579,579,579,579,579,579,MONDO:1010228,"Dandy-Walker syndrome, non-human animal",MONDO,disease,DISEASE_579
580,580,580,580,580,580,580,580,MONDO:0800126,dystrophic pulmonary ossification,MONDO,disease,DISEASE_580
581,581,581,581,581,581,581,581,MONDO:0020072,childhood-onset epilepsy syndrome,MONDO,disease,DISEASE_581
582,582,582,582,582,582,582,582,MONDO:1011201,"schmid metaphyseal chondrodysplasia dwarfism, pig",MONDO,disease,DISEASE_582
583,583,583,583,583,583,583,583,MONDO:0010522,X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2,MONDO,disease,DISEASE_583
584,584,584,584,584,584,584,584,MONDO:0013788_MONDO:0013935_MONDO:0011748_MONDO:0014001_MONDO:0012662_MONDO:0032841_MONDO:0010170_MONDO:0700087_MONDO:0010169_MONDO:0011558_MONDO:0010171_MONDO:0029141_MONDO:0011195_MONDO:0011186_MONDO:0010984_MONDO:0019501_MONDO:0016484_MONDO:0016485_MONDO:0010168_MONDO:0012968_MONDO:0100050,Usher syndrome,MONDO_grouped,disease,DISEASE_584
585,585,585,585,585,585,585,585,MONDO:0024877,clitoris neoplasm,MONDO,disease,DISEASE_585
586,586,586,586,586,586,586,586,MONDO:0008990,"cleft larynx, posterior",MONDO,disease,DISEASE_586
587,587,587,587,587,587,587,587,MONDO:0011121_MONDO:0032767_MONDO:0032771_MONDO:0013602_MONDO:0008192_MONDO:0007273_MONDO:0011544,paragangliomas,MONDO_grouped,disease,DISEASE_587
588,588,588,588,588,588,588,588,MONDO:0018018,wild type ATTR amyloidosis,MONDO,disease,DISEASE_588
589,589,589,589,589,589,589,589,MONDO:0044013_MONDO:0021742,puerperal disorder,MONDO_grouped,disease,DISEASE_589
590,590,590,590,590,590,590,590,MONDO:0030314,"inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive",MONDO,disease,DISEASE_590
591,591,591,591,591,591,591,591,MONDO:0958151,cepacia syndrome,MONDO,disease,DISEASE_591
592,592,592,592,592,592,592,592,MONDO:0002987,spongiotic dermatitis,MONDO,disease,DISEASE_592
593,593,593,593,593,593,593,593,MONDO:0006019,yaws,MONDO,disease,DISEASE_593
594,594,594,594,594,594,594,594,MONDO:0003477_MONDO:0004352_MONDO:0004361,brain stem ependymoma,MONDO_grouped,disease,DISEASE_594
595,595,595,595,595,595,595,595,MONDO:0043199,short limb dwarf lethal colavita kozlowski type,MONDO,disease,DISEASE_595
596,596,596,596,596,596,596,596,MONDO:0700081,newborn respiratory distress syndrome,MONDO,disease,DISEASE_596
597,597,597,597,597,597,597,597,MONDO:0001625,corpus luteum cyst,MONDO,disease,DISEASE_597
598,598,598,598,598,598,598,598,MONDO:0006094,Askin tumor,MONDO,disease,DISEASE_598
599,599,599,599,599,599,599,599,MONDO:0957388_MONDO:0014861_MONDO:0000213,"autoimmune disease, multisystem, infantile-onset",MONDO_grouped,disease,DISEASE_599
600,600,600,600,600,600,600,600,MONDO:0017617,acquired adult-onset immunodeficiency,MONDO,disease,DISEASE_600
601,601,601,601,601,601,601,601,MONDO:0019636,"renal agenesis, unilateral",MONDO,disease,DISEASE_601
602,602,602,602,602,602,602,602,MONDO:0035651,choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome,MONDO,disease,DISEASE_602
603,603,603,603,603,603,603,603,MONDO:0021457,benign neoplasm of pleura,MONDO,disease,DISEASE_603
604,604,604,604,604,604,604,604,MONDO:0011414,Peters anomaly,MONDO,disease,DISEASE_604
605,605,605,605,605,605,605,605,MONDO:0017376,reactive arthritis,MONDO,disease,DISEASE_605
606,606,606,606,606,606,606,606,MONDO:0957473,craniosynostosis-facial dysmorphism-chiari-1 malformation-developmental and language delay syndrome,MONDO,disease,DISEASE_606
607,607,607,607,607,607,607,607,MONDO:0006540,dyshidrosis,MONDO,disease,DISEASE_607
608,608,608,608,608,608,608,608,MONDO:0032909_MONDO:0859321,"mitochondrial complex 3 deficiency, nuclear",MONDO_grouped,disease,DISEASE_608
609,609,609,609,609,609,609,609,MONDO:0011503_MONDO:0013842_MONDO:0000193,cortisone reductase deficiency,MONDO_grouped,disease,DISEASE_609
610,610,610,610,610,610,610,610,MONDO:0007544,"eosinophilia, familial",MONDO,disease,DISEASE_610
611,611,611,611,611,611,611,611,MONDO:0011347,craniosynostosis with ectopia lentis,MONDO,disease,DISEASE_611
612,612,612,612,612,612,612,612,MONDO:0016781,maternal 14q32.2 microdeletion syndrome,MONDO,disease,DISEASE_612
613,613,613,613,613,613,613,613,MONDO:0850101,spitzoid melanoma,MONDO,disease,DISEASE_613
614,614,614,614,614,614,614,614,MONDO:0008766,amaurosis-hypertrichosis syndrome,MONDO,disease,DISEASE_614
615,615,615,615,615,615,615,615,MONDO:0023528,KSHV inflammatory cytokine syndrome,MONDO,disease,DISEASE_615
616,616,616,616,616,616,616,616,MONDO:0032816,"neurodevelopmental disorder with ataxia, hypotonia, and microcephaly",MONDO,disease,DISEASE_616
617,617,617,617,617,617,617,617,MONDO:0004215,cutaneous anthrax,MONDO,disease,DISEASE_617
618,618,618,618,618,618,618,618,MONDO:0005148_MONDO:0007454_MONDO:0012919_MONDO:0005147_MONDO:0011123_MONDO:0012921_MONDO:0011068_MONDO:0011168_MONDO:0010863_MONDO:0009100_MONDO:0010861_MONDO:0010862_MONDO:0010864_MONDO:0010950_MONDO:0011016_MONDO:0011033_MONDO:0011167_MONDO:0011302_MONDO:0011572_MONDO:0012422_MONDO:0012920_MONDO:0012961_MONDO:0013078_MONDO:1011598_MONDO:1011599,type 2 diabetes mellitus,MONDO_grouped,disease,DISEASE_618
619,619,619,619,619,619,619,619,MONDO:0015533,benign cephalic histiocytosis,MONDO,disease,DISEASE_619
620,620,620,620,620,620,620,620,MONDO:0009340,non-spherocytic hemolytic anemia due to hexokinase deficiency,MONDO,disease,DISEASE_620
621,621,621,621,621,621,621,621,MONDO:0015610,acquired aplastic anemia,MONDO,disease,DISEASE_621
622,622,622,622,622,622,622,622,MONDO:0015205,isolated lissencephaly type 1 without known genetic defects,MONDO,disease,DISEASE_622
623,623,623,623,623,623,623,623,MONDO:0002901,blood group incompatibility,MONDO,disease,DISEASE_623
624,624,624,624,624,624,624,624,MONDO:0004191_MONDO:0002396_MONDO:0006301,nephrogenic adenoma,MONDO_grouped,disease,DISEASE_624
625,625,625,625,625,625,625,625,MONDO:0014758_MONDO:0024558_MONDO:0011555,radioulnar synostosis with amegakaryocytic thrombocytopenia,MONDO_grouped,disease,DISEASE_625
626,626,626,626,626,626,626,626,MONDO:1010949,"non-hodgkin lymphoma, domestic cat",MONDO,disease,DISEASE_626
627,627,627,627,627,627,627,627,MONDO:0011729,"stroke, susceptibility to, 1",MONDO,disease,DISEASE_627
628,628,628,628,628,628,628,628,MONDO:0009162,Ellis-van Creveld syndrome,MONDO,disease,DISEASE_628
629,629,629,629,629,629,629,629,MONDO:0001132_MONDO:0001139,sexual sadism disorder,MONDO_grouped,disease,DISEASE_629
630,630,630,630,630,630,630,630,MONDO:0100552,ATTRV30M amyloidosis,MONDO,disease,DISEASE_630
631,631,631,631,631,631,631,631,MONDO:1011901,"white skin color and iridophoroma, non-human animal",MONDO,disease,DISEASE_631
632,632,632,632,632,632,632,632,MONDO:0007992,microcornea-glaucoma-absent frontal sinuses syndrome,MONDO,disease,DISEASE_632
633,633,633,633,633,633,633,633,MONDO:0011203,Pierre Robin sequence with pectus excavatum and rib and scapular anomalies,MONDO,disease,DISEASE_633
634,634,634,634,634,634,634,634,MONDO:0022999,distichiasis heart congenital anomalies,MONDO,disease,DISEASE_634
635,635,635,635,635,635,635,635,MONDO:1010937_MONDO:1010938,"lymphosarcoma, pig",MONDO_grouped,disease,DISEASE_635
636,636,636,636,636,636,636,636,MONDO:0015446,atypical coarctation of aorta,MONDO,disease,DISEASE_636
637,637,637,637,637,637,637,637,MONDO:0024522_MONDO:0013502_MONDO:0054765,"amyloidosis, primary localized cutaneous",MONDO_grouped,disease,DISEASE_637
638,638,638,638,638,638,638,638,MONDO:0020436,"atrial septal defect, sinus venosus type",MONDO,disease,DISEASE_638
639,639,639,639,639,639,639,639,MONDO:0003746_MONDO:0004086,ciliary body spindle cell melanoma,MONDO_grouped,disease,DISEASE_639
640,640,640,640,640,640,640,640,MONDO:1012711,"immunodeficiency syndrome, SLC5A3-related, horse",MONDO,disease,DISEASE_640
641,641,641,641,641,641,641,641,MONDO:0019518,Waardenburg-Shah syndrome,MONDO,disease,DISEASE_641
642,642,642,642,642,642,642,642,MONDO:0018493,malignant hyperthermia of anesthesia,MONDO,disease,DISEASE_642
643,643,643,643,643,643,643,643,MONDO:0016102_MONDO:0003334_MONDO:0018776_MONDO:0100169,subacute inflammatory demyelinating polyneuropathy,MONDO_grouped,disease,DISEASE_643
644,644,644,644,644,644,644,644,MONDO:0008740,agnathia-otocephaly complex,MONDO,disease,DISEASE_644
645,645,645,645,645,645,645,645,MONDO:0011861,breath-holding Spells,MONDO,disease,DISEASE_645
646,646,646,646,646,646,646,646,MONDO:0011972,ovarian hyperstimulation syndrome,MONDO,disease,DISEASE_646
647,647,647,647,647,647,647,647,MONDO:0005704,Ciliophora infectious disease,MONDO,disease,DISEASE_647
648,648,648,648,648,648,648,648,MONDO:0016748_MONDO:0003902,hemangioblastoma,MONDO_grouped,disease,DISEASE_648
649,649,649,649,649,649,649,649,MONDO:0023577,Krieble Bixler syndrome,MONDO,disease,DISEASE_649
650,650,650,650,650,650,650,650,MONDO:0010224,corpus callosum agenesis-abnormal genitalia syndrome,MONDO,disease,DISEASE_650
651,651,651,651,651,651,651,651,MONDO:0019845,iatrogenic or traumatic pituitary deficiency,MONDO,disease,DISEASE_651
652,652,652,652,652,652,652,652,MONDO:0060707,Ververi-Brady syndrome,MONDO,disease,DISEASE_652
653,653,653,653,653,653,653,653,MONDO:0009207,"factor V and factor VIII, combined deficiency of, with normal protein C and protein C inhibitor",MONDO,disease,DISEASE_653
654,654,654,654,654,654,654,654,MONDO:0016356,diffuse cutaneous systemic sclerosis,MONDO,disease,DISEASE_654
655,655,655,655,655,655,655,655,MONDO:0017039,drug or radiation exposure-related interstitial lung disease,MONDO,disease,DISEASE_655
656,656,656,656,656,656,656,656,MONDO:0021809,primary dysautonomia,MONDO,disease,DISEASE_656
657,657,657,657,657,657,657,657,MONDO:0100149,PNPLA6-related spastic paraplegia with or without ataxia,MONDO,disease,DISEASE_657
658,658,658,658,658,658,658,658,MONDO:0008051,tubular aggregate myopathy,MONDO,disease,DISEASE_658
659,659,659,659,659,659,659,659,MONDO:0011081,dislocation of the hip-dysmorphism syndrome,MONDO,disease,DISEASE_659
660,660,660,660,660,660,660,660,MONDO:0700137,bovine lymphosarcoma,MONDO,disease,DISEASE_660
661,661,661,661,661,661,661,661,MONDO:0014388,familial median cleft of the upper and lower lips,MONDO,disease,DISEASE_661
662,662,662,662,662,662,662,662,MONDO:0005512_MONDO:0003805_MONDO:0002112,malignant peritoneal mesothelioma,MONDO_grouped,disease,DISEASE_662
663,663,663,663,663,663,663,663,MONDO:0011759,Hurler-Scheie syndrome,MONDO,disease,DISEASE_663
664,664,664,664,664,664,664,664,MONDO:1011630,"congenital lethal spasms, non-human animal",MONDO,disease,DISEASE_664
665,665,665,665,665,665,665,665,MONDO:0006469,tibial adamantinoma,MONDO,disease,DISEASE_665
666,666,666,666,666,666,666,666,MONDO:0014179_MONDO:0014178,inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia,MONDO_grouped,disease,DISEASE_666
667,667,667,667,667,667,667,667,MONDO:0017365,"hereditary acrokeratotic poikiloderma, Weary type",MONDO,disease,DISEASE_667
668,668,668,668,668,668,668,668,MONDO:1012701_MONDO:1012702,"X-linked progressive retinal atrophy, type 3, dog",MONDO_grouped,disease,DISEASE_668
669,669,669,669,669,669,669,669,MONDO:0003675_MONDO:0003676,posterolateral myocardial infarction,MONDO_grouped,disease,DISEASE_669
670,670,670,670,670,670,670,670,MONDO:1011037,"oculocutaneous albinism, SLC45A2-related, Japanese medaka",MONDO,disease,DISEASE_670
671,671,671,671,671,671,671,671,MONDO:0000414,childhood electroclinical syndrome,MONDO,disease,DISEASE_671
672,672,672,672,672,672,672,672,MONDO:0012565_MONDO:0044325_MONDO:0014987_MONDO:0012186_MONDO:0014986_MONDO:0011584_MONDO:0013248_MONDO:0014985_MONDO:0012187_MONDO:0014638_MONDO:0010953_MONDO:0010351_MONDO:0013499_MONDO:0054748_MONDO:0014108_MONDO:0013566_MONDO:0013565_MONDO:0009215_MONDO:0009213_MONDO:0009214_MONDO:0011325,Fanconi anemia complementation group,MONDO_grouped,disease,DISEASE_672
673,673,673,673,673,673,673,673,MONDO:0008208,"patella, familial recurrent dislocation of",MONDO,disease,DISEASE_673
674,674,674,674,674,674,674,674,MONDO:0019954,pancreatic neuroendocrine tumor,MONDO,disease,DISEASE_674
675,675,675,675,675,675,675,675,MONDO:0017806,15q overgrowth syndrome,MONDO,disease,DISEASE_675
676,676,676,676,676,676,676,676,MONDO:0020710,amnionitis,MONDO,disease,DISEASE_676
677,677,677,677,677,677,677,677,MONDO:1012037,"cerebellar Purkinje cell degeneration, dog",MONDO,disease,DISEASE_677
678,678,678,678,678,678,678,678,MONDO:0017648,Sydenham chorea,MONDO,disease,DISEASE_678
679,679,679,679,679,679,679,679,MONDO:0001771,infective urethral stricture,MONDO,disease,DISEASE_679
680,680,680,680,680,680,680,680,MONDO:0700162,canine granular cell tumor,MONDO,disease,DISEASE_680
681,681,681,681,681,681,681,681,MONDO:0016142,qualitative or quantitative defects of beta-sarcoglycan,MONDO,disease,DISEASE_681
682,682,682,682,682,682,682,682,MONDO:0004111,refractory hematologic cancer,MONDO,disease,DISEASE_682
683,683,683,683,683,683,683,683,MONDO:0001185,dissociative amnesia,MONDO,disease,DISEASE_683
684,684,684,684,684,684,684,684,MONDO:0054842,polycystic kidney disease 6 with or without polycystic liver disease,MONDO,disease,DISEASE_684
685,685,685,685,685,685,685,685,MONDO:1011849,"myasthenia, non-human animal",MONDO,disease,DISEASE_685
686,686,686,686,686,686,686,686,MONDO:0006838,lupus vulgaris,MONDO,disease,DISEASE_686
687,687,687,687,687,687,687,687,MONDO:0008316,"thrombophilia due to protein C deficiency, autosomal dominant",MONDO,disease,DISEASE_687
688,688,688,688,688,688,688,688,MONDO:0010774,"striatonigral degeneration, infantile, mitochondrial",MONDO,disease,DISEASE_688
689,689,689,689,689,689,689,689,MONDO:0027767,partial lipodystrophy,MONDO,disease,DISEASE_689
690,690,690,690,690,690,690,690,MONDO:0001197,qualitative platelet defect,MONDO,disease,DISEASE_690
691,691,691,691,691,691,691,691,MONDO:0017068_MONDO:0017075,upper thoracic spina bifida aperta,MONDO_grouped,disease,DISEASE_691
692,692,692,692,692,692,692,692,MONDO:0023094,exogenous ochronosis,MONDO,disease,DISEASE_692
693,693,693,693,693,693,693,693,MONDO:0958120,autosomal dominant combined immunodeficiency due to ERBIN deficiency,MONDO,disease,DISEASE_693
694,694,694,694,694,694,694,694,MONDO:0013330,agenesis of the corpus callosum and congenital lymphedema,MONDO,disease,DISEASE_694
695,695,695,695,695,695,695,695,MONDO:0015369,Joubert syndrome and related disorders,MONDO,disease,DISEASE_695
696,696,696,696,696,696,696,696,MONDO:0100102_MONDO:0100103_MONDO:0100101_MONDO:0100104_MONDO:0008824,fetal akinesia deformation sequence,MONDO_grouped,disease,DISEASE_696
697,697,697,697,697,697,697,697,MONDO:1010667,"bleeding disorder P2RY12-related, dog",MONDO,disease,DISEASE_697
698,698,698,698,698,698,698,698,MONDO:0003584_MONDO:0001834,visual cortex disorder,MONDO_grouped,disease,DISEASE_698
699,699,699,699,699,699,699,699,MONDO:0008729,congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency,MONDO,disease,DISEASE_699
700,700,700,700,700,700,700,700,MONDO:0016155,qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan,MONDO,disease,DISEASE_700
701,701,701,701,701,701,701,701,MONDO:0019951,rigid spine syndrome,MONDO,disease,DISEASE_701
702,702,702,702,702,702,702,702,MONDO:0016321,pulmonary interstitial glycogenosis,MONDO,disease,DISEASE_702
703,703,703,703,703,703,703,703,MONDO:0859202,"developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities",MONDO,disease,DISEASE_703
704,704,704,704,704,704,704,704,MONDO:0002856_MONDO:0003026,gallbladder rhabdomyosarcoma,MONDO_grouped,disease,DISEASE_704
705,705,705,705,705,705,705,705,MONDO:0100200,microcephaly with intellectual disability,MONDO,disease,DISEASE_705
706,706,706,706,706,706,706,706,MONDO:0006720,"cystic, mucinous, and serous neoplasm",MONDO,disease,DISEASE_706
707,707,707,707,707,707,707,707,MONDO:0020648,rubella encephalitis,MONDO,disease,DISEASE_707
708,708,708,708,708,708,708,708,MONDO:0007019_MONDO:0006014,vulvovaginitis,MONDO_grouped,disease,DISEASE_708
709,709,709,709,709,709,709,709,MONDO:0056822,amyotonia congenita,MONDO,disease,DISEASE_709
710,710,710,710,710,710,710,710,MONDO:0020302,Angelman syndrome due to maternal 15q11q13 deletion,MONDO,disease,DISEASE_710
711,711,711,711,711,711,711,711,MONDO:0003786,childhood testicular choriocarcinoma,MONDO,disease,DISEASE_711
712,712,712,712,712,712,712,712,MONDO:0007159,arthrogryposis-like hand anomaly-sensorineural deafness syndrome,MONDO,disease,DISEASE_712
713,713,713,713,713,713,713,713,MONDO:0002220,tooth hard tissue disease,MONDO,disease,DISEASE_713
714,714,714,714,714,714,714,714,MONDO:0009714,myosclerosis,MONDO,disease,DISEASE_714
715,715,715,715,715,715,715,715,MONDO:0001342_MONDO:0015977,dysgammaglobulinemia,MONDO_grouped,disease,DISEASE_715
716,716,716,716,716,716,716,716,MONDO:0021033,herpes zoster dermatitis,MONDO,disease,DISEASE_716
717,717,717,717,717,717,717,717,MONDO:0009351,homocarnosinosis,MONDO,disease,DISEASE_717
718,718,718,718,718,718,718,718,MONDO:0009716,Richieri Costa-da Silva syndrome,MONDO,disease,DISEASE_718
719,719,719,719,719,719,719,719,MONDO:0021579,neoplasm of femur,MONDO,disease,DISEASE_719
720,720,720,720,720,720,720,720,MONDO:0020474,cheirospondyloenchondromatosis,MONDO,disease,DISEASE_720
721,721,721,721,721,721,721,721,MONDO:0001957,critical illness polyneuropathy,MONDO,disease,DISEASE_721
722,722,722,722,722,722,722,722,MONDO:0100387_MONDO:0100388_MONDO:0100389_MONDO:0100390,"acute myeloid leukemia, Monosomy",MONDO_grouped,disease,DISEASE_722
723,723,723,723,723,723,723,723,MONDO:0001297,cardiac tamponade,MONDO,disease,DISEASE_723
724,724,724,724,724,724,724,724,MONDO:1010791,"tricho-dento-osseous-like syndrome, cattle",MONDO,disease,DISEASE_724
725,725,725,725,725,725,725,725,MONDO:0023538,Kaplowitz-Bodurtha syndrome,MONDO,disease,DISEASE_725
726,726,726,726,726,726,726,726,MONDO:0002916,brainstem intraparenchymal clear cell meningioma,MONDO,disease,DISEASE_726
727,727,727,727,727,727,727,727,MONDO:0012668,Tented eyebrows,MONDO,disease,DISEASE_727
728,728,728,728,728,728,728,728,MONDO:0002783,Shwartzman phenomenon,MONDO,disease,DISEASE_728
729,729,729,729,729,729,729,729,MONDO:0000494,renal fibrosis,MONDO,disease,DISEASE_729
730,730,730,730,730,730,730,730,MONDO:0004901,lingual-facial-buccal dyskinesia,MONDO,disease,DISEASE_730
731,731,731,731,731,731,731,731,MONDO:0013298,chromosome 17q21.31 duplication syndrome,MONDO,disease,DISEASE_731
732,732,732,732,732,732,732,732,MONDO:0018311,acromelanosis,MONDO,disease,DISEASE_732
733,733,733,733,733,733,733,733,MONDO:0100500,Mendelian neurodevelopmental disorder,MONDO,disease,DISEASE_733
734,734,734,734,734,734,734,734,MONDO:0016955,partial duplication of the long arm of chromosome 4,MONDO,disease,DISEASE_734
735,735,735,735,735,735,735,735,MONDO:0018093_MONDO:0020731,arbovirus fever,MONDO_grouped,disease,DISEASE_735
736,736,736,736,736,736,736,736,MONDO:0035121,myeloid/lymphoid neoplasm associated with JAK2 rearrangement,MONDO,disease,DISEASE_736
737,737,737,737,737,737,737,737,MONDO:0014546,myopathy due to calsequestrin and SERCA1 protein overload,MONDO,disease,DISEASE_737
738,738,738,738,738,738,738,738,MONDO:0025130,swine vesicular disease,MONDO,disease,DISEASE_738
739,739,739,739,739,739,739,739,MONDO:1011860,"spastic syndrome, non-human animal",MONDO,disease,DISEASE_739
740,740,740,740,740,740,740,740,MONDO:0009706,hereditary myopathy with lactic acidosis due to ISCU deficiency,MONDO,disease,DISEASE_740
741,741,741,741,741,741,741,741,MONDO:0956986,solitary fibrous tumor/hemangiopericytoma,MONDO,disease,DISEASE_741
742,742,742,742,742,742,742,742,MONDO:0002358_MONDO:0002448_MONDO:0000934_MONDO:0003374,laryngeal carcinoma,MONDO_grouped,disease,DISEASE_742
743,743,743,743,743,743,743,743,MONDO:0004277,gonorrhea,MONDO,disease,DISEASE_743
744,744,744,744,744,744,744,744,MONDO:0004892,refractive error,MONDO,disease,DISEASE_744
745,745,745,745,745,745,745,745,MONDO:0700070_MONDO:0700068_MONDO:0700067_MONDO:0700066_MONDO:0700071_MONDO:0100530_MONDO:0700084_MONDO:0700069,myopathy caused by variation in POMT1,MONDO_grouped,disease,DISEASE_745
746,746,746,746,746,746,746,746,MONDO:1010984_MONDO:1010985_MONDO:1010986_MONDO:1010988_MONDO:1010989_MONDO:1010990_MONDO:1010991_MONDO:1010992_MONDO:1010993_MONDO:1012105_MONDO:1012106,"hydrocephalus, dog",MONDO_grouped,disease,DISEASE_746
747,747,747,747,747,747,747,747,MONDO:0005516_MONDO:0022723,osteochondrodysplasia,MONDO_grouped,disease,DISEASE_747
748,748,748,748,748,748,748,748,MONDO:0006097,atypical lipomatous tumor,MONDO,disease,DISEASE_748
749,749,749,749,749,749,749,749,MONDO:0017857,spina bifida-hypospadias syndrome,MONDO,disease,DISEASE_749
750,750,750,750,750,750,750,750,MONDO:0022862,Cormier Rustin Munnich syndrome,MONDO,disease,DISEASE_750
751,751,751,751,751,751,751,751,MONDO:0957462,primary pulmonary tuberculosis,MONDO,disease,DISEASE_751
752,752,752,752,752,752,752,752,MONDO:1010637,"factor XI deficiency, domestic cat",MONDO,disease,DISEASE_752
753,753,753,753,753,753,753,753,MONDO:0013578,DYRK1A-related intellectual disability syndrome,MONDO,disease,DISEASE_753
754,754,754,754,754,754,754,754,MONDO:0005250,placental villitis,MONDO,disease,DISEASE_754
755,755,755,755,755,755,755,755,MONDO:0021921,Arnold stickler bourne syndrome,MONDO,disease,DISEASE_755
756,756,756,756,756,756,756,756,MONDO:0008060_MONDO:0007867_MONDO:0007900_MONDO:0011595_MONDO:0013592_MONDO:0008798_MONDO:0011852_MONDO:0008125_MONDO:0007135,nonsyndromic congenital nail disorder,MONDO_grouped,disease,DISEASE_756
757,757,757,757,757,757,757,757,MONDO:0004636,lip carcinoma in situ,MONDO,disease,DISEASE_757
758,758,758,758,758,758,758,758,MONDO:0000633,sensory organ benign neoplasm,MONDO,disease,DISEASE_758
759,759,759,759,759,759,759,759,MONDO:0700054,microcephaly 6 with or without short stature,MONDO,disease,DISEASE_759
760,760,760,760,760,760,760,760,MONDO:1010728,"leukocyte adhesion deficiency, ITGB2-related, domestic cat",MONDO,disease,DISEASE_760
761,761,761,761,761,761,761,761,MONDO:0018679,primary cutaneous plasmacytosis,MONDO,disease,DISEASE_761
762,762,762,762,762,762,762,762,MONDO:1010027,"endocardial fibroelastosis, non-human animal",MONDO,disease,DISEASE_762
763,763,763,763,763,763,763,763,MONDO:0014606,intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome,MONDO,disease,DISEASE_763
764,764,764,764,764,764,764,764,MONDO:0014689,Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome,MONDO,disease,DISEASE_764
765,765,765,765,765,765,765,765,MONDO:1011303,"mammary gland disorder, non-human animal",MONDO,disease,DISEASE_765
766,766,766,766,766,766,766,766,MONDO:0017200,polycystic ovaries-urethral sphincter dysfunction syndrome,MONDO,disease,DISEASE_766
767,767,767,767,767,767,767,767,MONDO:0003637,clear cell-sugar-tumor of the lung,MONDO,disease,DISEASE_767
768,768,768,768,768,768,768,768,MONDO:1012919,"XY sex reversal, sdY-related, Chinook salmon",MONDO,disease,DISEASE_768
769,769,769,769,769,769,769,769,MONDO:0007753,Frey syndrome,MONDO,disease,DISEASE_769
770,770,770,770,770,770,770,770,MONDO:1011502,"Fanconi syndrome, cattle",MONDO,disease,DISEASE_770
771,771,771,771,771,771,771,771,MONDO:0024501,appendix neuroendocrine neoplasm,MONDO,disease,DISEASE_771
772,772,772,772,772,772,772,772,MONDO:0007756,hyperkeratosis lenticularis perstans,MONDO,disease,DISEASE_772
773,773,773,773,773,773,773,773,MONDO:0022622,congenital disorder of glycosylation syndrome type 4,MONDO,disease,DISEASE_773
774,774,774,774,774,774,774,774,MONDO:0004946_MONDO:0002909,hypoglycemia,MONDO_grouped,disease,DISEASE_774
775,775,775,775,775,775,775,775,MONDO:0018860,microlissencephaly-micromelia syndrome,MONDO,disease,DISEASE_775
776,776,776,776,776,776,776,776,MONDO:0007659,obsolete giant platelet syndrome with thrombocytopenia,MONDO,disease,DISEASE_776
777,777,777,777,777,777,777,777,MONDO:1011993,"lacrimal fistula, non-human animal",MONDO,disease,DISEASE_777
778,778,778,778,778,778,778,778,MONDO:0001807,obsolete familial combined hyperlipidemia,MONDO,disease,DISEASE_778
779,779,779,779,779,779,779,779,MONDO:0009542,lysine malabsorption syndrome,MONDO,disease,DISEASE_779
780,780,780,780,780,780,780,780,MONDO:0014294,chromosome 15q11.2 deletion syndrome,MONDO,disease,DISEASE_780
781,781,781,781,781,781,781,781,MONDO:0010600,"granulomatous disease, chronic, X-linked",MONDO,disease,DISEASE_781
782,782,782,782,782,782,782,782,MONDO:0011988,neutrophil immunodeficiency syndrome,MONDO,disease,DISEASE_782
783,783,783,783,783,783,783,783,MONDO:0011779,"laryngeal atresia, encephalocele, and limb deformities",MONDO,disease,DISEASE_783
784,784,784,784,784,784,784,784,MONDO:0002831,non-keratinizing sinonasal squamous cell carcinoma,MONDO,disease,DISEASE_784
785,785,785,785,785,785,785,785,MONDO:0008131_MONDO:0009788,"optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant",MONDO_grouped,disease,DISEASE_785
786,786,786,786,786,786,786,786,MONDO:0010130,dihydropyrimidine dehydrogenase deficiency,MONDO,disease,DISEASE_786
787,787,787,787,787,787,787,787,MONDO:0009822,otoonychoperoneal syndrome,MONDO,disease,DISEASE_787
788,788,788,788,788,788,788,788,MONDO:0003832,complement deficiency,MONDO,disease,DISEASE_788
789,789,789,789,789,789,789,789,MONDO:0850068,early-onset autoimmunity-autoinflammation-immunodeficiency syndrome,MONDO,disease,DISEASE_789
790,790,790,790,790,790,790,790,MONDO:0043862,voice disorders,MONDO,disease,DISEASE_790
791,791,791,791,791,791,791,791,MONDO:0006380,pleural sarcomatoid mesothelioma,MONDO,disease,DISEASE_791
792,792,792,792,792,792,792,792,MONDO:0021357,tumor of salivary gland,MONDO,disease,DISEASE_792
793,793,793,793,793,793,793,793,MONDO:0022510,atlanto-axial fusion,MONDO,disease,DISEASE_793
794,794,794,794,794,794,794,794,MONDO:0016750,microcephaly-cleft palate syndrome,MONDO,disease,DISEASE_794
795,795,795,795,795,795,795,795,MONDO:1010581,"familial goiter, bongo",MONDO,disease,DISEASE_795
796,796,796,796,796,796,796,796,MONDO:0015546,non-distal monosomy 10q,MONDO,disease,DISEASE_796
797,797,797,797,797,797,797,797,MONDO:1012333,"hemophagocytic syndrome, domestic cat",MONDO,disease,DISEASE_797
798,798,798,798,798,798,798,798,MONDO:0009797,orotic aciduria,MONDO,disease,DISEASE_798
799,799,799,799,799,799,799,799,MONDO:1012666,"hereditary footpad hyperkeratosis, FAM83G-related, dog",MONDO,disease,DISEASE_799
800,800,800,800,800,800,800,800,MONDO:0035153,male infertility due to acephalic spermatozoa,MONDO,disease,DISEASE_800
801,801,801,801,801,801,801,801,MONDO:0006522,acquired keratosis,MONDO,disease,DISEASE_801
802,802,802,802,802,802,802,802,MONDO:0014281,"cholangiocarcinoma, susceptibility to",MONDO,disease,DISEASE_802
803,803,803,803,803,803,803,803,MONDO:0002759,bladder verrucous carcinoma,MONDO,disease,DISEASE_803
804,804,804,804,804,804,804,804,MONDO:0030335,"diarrhea 12, with microvillus atrophy",MONDO,disease,DISEASE_804
805,805,805,805,805,805,805,805,MONDO:0019002,Lhermitte-Duclos disease,MONDO,disease,DISEASE_805
806,806,806,806,806,806,806,806,MONDO:0002732,lung benign neoplasm,MONDO,disease,DISEASE_806
807,807,807,807,807,807,807,807,MONDO:0018987,granulomatous mastitis,MONDO,disease,DISEASE_807
808,808,808,808,808,808,808,808,MONDO:0008332,platelet-type von Willebrand disease,MONDO,disease,DISEASE_808
809,809,809,809,809,809,809,809,MONDO:0005494,triple-negative breast carcinoma,MONDO,disease,DISEASE_809
810,810,810,810,810,810,810,810,MONDO:0000833,bone remodeling disease,MONDO,disease,DISEASE_810
811,811,811,811,811,811,811,811,MONDO:0004835,necrotizing fasciitis,MONDO,disease,DISEASE_811
812,812,812,812,812,812,812,812,MONDO:0004567,ileus,MONDO,disease,DISEASE_812
813,813,813,813,813,813,813,813,MONDO:0016970,partial trisomy of the long arm of chromosome 20,MONDO,disease,DISEASE_813
814,814,814,814,814,814,814,814,MONDO:0017998,PLA2G6-associated neurodegeneration,MONDO,disease,DISEASE_814
815,815,815,815,815,815,815,815,MONDO:0009187,celiac disease-epilepsy-cerebral calcification syndrome,MONDO,disease,DISEASE_815
816,816,816,816,816,816,816,816,MONDO:1012630_MONDO:1011265_MONDO:1012661_MONDO:1012722,"rod-cone dysplasia 1, PDE6B-related, dog",MONDO_grouped,disease,DISEASE_816
817,817,817,817,817,817,817,817,MONDO:1012192,"neurological syndrome, horse",MONDO,disease,DISEASE_817
818,818,818,818,818,818,818,818,MONDO:0009155,EEM syndrome,MONDO,disease,DISEASE_818
819,819,819,819,819,819,819,819,MONDO:0859290,familial apolipoprotein gene cluster deletion syndrome,MONDO,disease,DISEASE_819
820,820,820,820,820,820,820,820,MONDO:0010982,ichthyosis-intellectual disability syndrome with large keratohyalin granules in the skin,MONDO,disease,DISEASE_820
821,821,821,821,821,821,821,821,MONDO:0010606,"hernia, anterior diaphragmatic",MONDO,disease,DISEASE_821
822,822,822,822,822,822,822,822,MONDO:0010778,cyclic vomiting syndrome,MONDO,disease,DISEASE_822
823,823,823,823,823,823,823,823,MONDO:0005777,granuloma inguinale,MONDO,disease,DISEASE_823
824,824,824,824,824,824,824,824,MONDO:0009338,hepatic veno-occlusive disease-immunodeficiency syndrome,MONDO,disease,DISEASE_824
825,825,825,825,825,825,825,825,MONDO:0019158,tropical endomyocardial fibrosis,MONDO,disease,DISEASE_825
826,826,826,826,826,826,826,826,MONDO:0020533,streptobacillary rat-bite fever,MONDO,disease,DISEASE_826
827,827,827,827,827,827,827,827,MONDO:0009948,"pyropoikilocytosis, hereditary",MONDO,disease,DISEASE_827
828,828,828,828,828,828,828,828,MONDO:0700269,BRCA2-related cancer predisposition,MONDO,disease,DISEASE_828
829,829,829,829,829,829,829,829,MONDO:1012945,"cerebellar abiotrophy, VMP1-related, dog",MONDO,disease,DISEASE_829
830,830,830,830,830,830,830,830,MONDO:1011638,"attention deficit hyperactivity disorder, non-human animal",MONDO,disease,DISEASE_830
831,831,831,831,831,831,831,831,MONDO:0019868,mosaic trisomy 10,MONDO,disease,DISEASE_831
832,832,832,832,832,832,832,832,MONDO:0003548,adenosquamous breast carcinoma,MONDO,disease,DISEASE_832
833,833,833,833,833,833,833,833,MONDO:0957208,"pituitary hormone deficiency, combined or isolated, 8",MONDO,disease,DISEASE_833
834,834,834,834,834,834,834,834,MONDO:0006463,thyroid gland mucoepidermoid carcinoma,MONDO,disease,DISEASE_834
835,835,835,835,835,835,835,835,MONDO:0022094,Cartwright Nelson Fryns syndrome,MONDO,disease,DISEASE_835
836,836,836,836,836,836,836,836,MONDO:1012144_MONDO:1012149_MONDO:1012150_MONDO:1012151,"malignant hyperthermia, turkey",MONDO_grouped,disease,DISEASE_836
837,837,837,837,837,837,837,837,MONDO:1012606,"glycogen storage disease IV, domestic cat",MONDO,disease,DISEASE_837
838,838,838,838,838,838,838,838,MONDO:0007249,camptobrachydactyly,MONDO,disease,DISEASE_838
839,839,839,839,839,839,839,839,MONDO:0036779,axillary neoplasm,MONDO,disease,DISEASE_839
840,840,840,840,840,840,840,840,MONDO:1012298,"displaced abomasum, water buffalo",MONDO,disease,DISEASE_840
841,841,841,841,841,841,841,841,MONDO:1011021_MONDO:1012585_MONDO:1012789_MONDO:1012878,"spinocerebellar ataxia, CAPN1-related, dog",MONDO_grouped,disease,DISEASE_841
842,842,842,842,842,842,842,842,MONDO:1012015,"arthrogryposis and palatoschisis syndrome, cattle",MONDO,disease,DISEASE_842
843,843,843,843,843,843,843,843,MONDO:1012821,"hypotrichosis, HEPHL1-related, cattle",MONDO,disease,DISEASE_843
844,844,844,844,844,844,844,844,MONDO:1011870,"polioencephalomyelopathy, non-human animal",MONDO,disease,DISEASE_844
845,845,845,845,845,845,845,845,MONDO:1011751,"acrochordonous plaque, non-human animal",MONDO,disease,DISEASE_845
846,846,846,846,846,846,846,846,MONDO:0001998,Foster-Kennedy syndrome,MONDO,disease,DISEASE_846
847,847,847,847,847,847,847,847,MONDO:0001336_MONDO:0005439,familial hyperlipidemia,MONDO_grouped,disease,DISEASE_847
848,848,848,848,848,848,848,848,MONDO:0021229,ciliary body neoplasm,MONDO,disease,DISEASE_848
849,849,849,849,849,849,849,849,MONDO:0009476,atresia of small intestine,MONDO,disease,DISEASE_849
850,850,850,850,850,850,850,850,MONDO:0009402_MONDO:0100044_MONDO:0008715,acrofrontofacionasal dysostosis,MONDO_grouped,disease,DISEASE_850
851,851,851,851,851,851,851,851,MONDO:1011839,"degenerative myelopathy, non-human animal",MONDO,disease,DISEASE_851
852,852,852,852,852,852,852,852,MONDO:0015252,severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome,MONDO,disease,DISEASE_852
853,853,853,853,853,853,853,853,MONDO:0004314,malignant cutaneous granular cell skin tumor,MONDO,disease,DISEASE_853
854,854,854,854,854,854,854,854,MONDO:0012322_MONDO:0007999_MONDO:0030886_MONDO:0009349_MONDO:0007734_MONDO:0007733_MONDO:0013642_MONDO:0012562_MONDO:0012563_MONDO:0016296_MONDO:0011616_MONDO:0012267_MONDO:1010517_MONDO:1010518_MONDO:1010519,holoprosencephaly,MONDO_grouped,disease,DISEASE_854
855,855,855,855,855,855,855,855,MONDO:0024341,retinal cell neoplasm,MONDO,disease,DISEASE_855
856,856,856,856,856,856,856,856,MONDO:0007056,acroosteolysis,MONDO,disease,DISEASE_856
857,857,857,857,857,857,857,857,MONDO:0005572,polycythemia due to hypoxia,MONDO,disease,DISEASE_857
858,858,858,858,858,858,858,858,MONDO:0022643,carcinoma of the vocal tract,MONDO,disease,DISEASE_858
859,859,859,859,859,859,859,859,MONDO:0024316,physiological malfunction arising from mental factor,MONDO,disease,DISEASE_859
860,860,860,860,860,860,860,860,MONDO:0010085,Schilder disease,MONDO,disease,DISEASE_860
861,861,861,861,861,861,861,861,MONDO:0018320,primary microcephaly-mild intellectual disability-young-onset diabetes syndrome,MONDO,disease,DISEASE_861
862,862,862,862,862,862,862,862,MONDO:1011650,"pentalogy of Fallot, non-human animal",MONDO,disease,DISEASE_862
863,863,863,863,863,863,863,863,MONDO:0958183_MONDO:0958197_MONDO:0030309,"Leber-like hereditary optic neuropathy, autosomal recessive",MONDO_grouped,disease,DISEASE_863
864,864,864,864,864,864,864,864,MONDO:0008762,autosomal recessive Alport syndrome,MONDO,disease,DISEASE_864
865,865,865,865,865,865,865,865,MONDO:0005135_MONDO:0020947,parasitic infectious disease,MONDO_grouped,disease,DISEASE_865
866,866,866,866,866,866,866,866,MONDO:0957791,"neurodevelopmental disorder with motor regression, progressive spastic paraplegia, and oromotor dysfunction",MONDO,disease,DISEASE_866
867,867,867,867,867,867,867,867,MONDO:0021923,Arroyo Garcia Cimadevilla syndrome,MONDO,disease,DISEASE_867
868,868,868,868,868,868,868,868,MONDO:0005597,cystic renal cell carcinoma,MONDO,disease,DISEASE_868
869,869,869,869,869,869,869,869,MONDO:0005903,pericardial tuberculosis,MONDO,disease,DISEASE_869
870,870,870,870,870,870,870,870,MONDO:0007840,"internal carotid artery, spontaneous dissection of",MONDO,disease,DISEASE_870
871,871,871,871,871,871,871,871,MONDO:0850067,immune deficiency due to impaired neutrophil phagocytosis and migration,MONDO,disease,DISEASE_871
872,872,872,872,872,872,872,872,MONDO:0000751,cervical polyp,MONDO,disease,DISEASE_872
873,873,873,873,873,873,873,873,MONDO:0001792,epiphora due to insufficient drainage,MONDO,disease,DISEASE_873
874,874,874,874,874,874,874,874,MONDO:0007158,arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome,MONDO,disease,DISEASE_874
875,875,875,875,875,875,875,875,MONDO:1012936,"persistent truncus arteriosus, GATA6-related, cattle",MONDO,disease,DISEASE_875
876,876,876,876,876,876,876,876,MONDO:0020362,inverse Marcus-Gunn phenomenon,MONDO,disease,DISEASE_876
877,877,877,877,877,877,877,877,MONDO:0001208,acute respiratory failure,MONDO,disease,DISEASE_877
878,878,878,878,878,878,878,878,MONDO:1010830,"radial hemimelia, domestic cat",MONDO,disease,DISEASE_878
879,879,879,879,879,879,879,879,MONDO:0007467,"DNA, low-repetitive sequences of",MONDO,disease,DISEASE_879
880,880,880,880,880,880,880,880,MONDO:0002850_MONDO:0003021_MONDO:0003882,central nervous system rhabdomyosarcoma,MONDO_grouped,disease,DISEASE_880
881,881,881,881,881,881,881,881,MONDO:0011679,"craniosynostosis syndrome, autosomal recessive",MONDO,disease,DISEASE_881
882,882,882,882,882,882,882,882,MONDO:0005138,lung carcinoma,MONDO,disease,DISEASE_882
883,883,883,883,883,883,883,883,MONDO:0013577,Lipedema,MONDO,disease,DISEASE_883
884,884,884,884,884,884,884,884,MONDO:0003649,esophageal neuroendocrine tumor,MONDO,disease,DISEASE_884
885,885,885,885,885,885,885,885,MONDO:0009177,late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome,MONDO,disease,DISEASE_885
886,886,886,886,886,886,886,886,MONDO:0018102_MONDO:0004686,corneal dystrophy,MONDO_grouped,disease,DISEASE_886
887,887,887,887,887,887,887,887,MONDO:0008000_MONDO:0013344_MONDO:0011850_MONDO:0011845_MONDO:0011851_MONDO:0011847_MONDO:0012715_MONDO:0012440_MONDO:0012441_MONDO:0100246_MONDO:0012210_MONDO:0012303_MONDO:0012331,"migraine with or without aura, susceptibility to",MONDO_grouped,disease,DISEASE_887
888,888,888,888,888,888,888,888,MONDO:0019603,osteopenia-myopia-hearing loss-intellectual disability-facial dysmorphism syndrome,MONDO,disease,DISEASE_888
889,889,889,889,889,889,889,889,MONDO:0004264,acute gonococcal endometritis,MONDO,disease,DISEASE_889
890,890,890,890,890,890,890,890,MONDO:1011855_MONDO:1012220,"distal sensorimotor polyneuropathy, non-human animal",MONDO_grouped,disease,DISEASE_890
891,891,891,891,891,891,891,891,MONDO:0002875,parasitic ectoparasitic infectious disease,MONDO,disease,DISEASE_891
892,892,892,892,892,892,892,892,MONDO:0021246,pharynx neoplasm,MONDO,disease,DISEASE_892
893,893,893,893,893,893,893,893,MONDO:0008844,"Athrombia, essential",MONDO,disease,DISEASE_893
894,894,894,894,894,894,894,894,MONDO:0009305,granulocytopenia with immunoglobulin abnormality,MONDO,disease,DISEASE_894
895,895,895,895,895,895,895,895,MONDO:0002903,articulation disorder,MONDO,disease,DISEASE_895
896,896,896,896,896,896,896,896,MONDO:1010704,"glycogen storage disease, PYGM-related, sheep",MONDO,disease,DISEASE_896
897,897,897,897,897,897,897,897,MONDO:0971137,severe congenital myelofibrosis-pancytopenia-intellectual disability-neurologic and ophthalmic abnormalities syndrome,MONDO,disease,DISEASE_897
898,898,898,898,898,898,898,898,MONDO:0005672,blastomycosis,MONDO,disease,DISEASE_898
899,899,899,899,899,899,899,899,MONDO:0008491,stiff-person syndrome,MONDO,disease,DISEASE_899
900,900,900,900,900,900,900,900,MONDO:0004615,upper gum cancer,MONDO,disease,DISEASE_900
901,901,901,901,901,901,901,901,MONDO:0002109,pituitary cancer,MONDO,disease,DISEASE_901
902,902,902,902,902,902,902,902,MONDO:1010858,"lysosomal storage disease, emu",MONDO,disease,DISEASE_902
903,903,903,903,903,903,903,903,MONDO:0021408_MONDO:0021418_MONDO:0021420,polyp of frontal sinus,MONDO_grouped,disease,DISEASE_903
904,904,904,904,904,904,904,904,MONDO:0700216,RET fusion positive cancer,MONDO,disease,DISEASE_904
905,905,905,905,905,905,905,905,MONDO:0002343,splenic hemangioma,MONDO,disease,DISEASE_905
906,906,906,906,906,906,906,906,MONDO:0007702_MONDO:0015284_MONDO:0016432,heart-hand syndrome,MONDO_grouped,disease,DISEASE_906
907,907,907,907,907,907,907,907,MONDO:0400003,skeletal fluorosis,MONDO,disease,DISEASE_907
908,908,908,908,908,908,908,908,MONDO:0016167_MONDO:0003235,optic pathway glioma,MONDO_grouped,disease,DISEASE_908
909,909,909,909,909,909,909,909,MONDO:0006986,substernal goiter,MONDO,disease,DISEASE_909
910,910,910,910,910,910,910,910,MONDO:0005564,embryonal neoplasm,MONDO,disease,DISEASE_910
911,911,911,911,911,911,911,911,MONDO:0033925,pediatric-onset Graves disease,MONDO,disease,DISEASE_911
912,912,912,912,912,912,912,912,MONDO:0004718,xeroderma of eyelid,MONDO,disease,DISEASE_912
913,913,913,913,913,913,913,913,MONDO:0100176,AP-4 deficiency syndrome,MONDO,disease,DISEASE_913
914,914,914,914,914,914,914,914,MONDO:0010114,"thanatophoric dysplasia, Glasgow variant",MONDO,disease,DISEASE_914
915,915,915,915,915,915,915,915,MONDO:0054602_MONDO:0020790,"gaze palsy, familial horizontal, with progressive scoliosis",MONDO_grouped,disease,DISEASE_915
916,916,916,916,916,916,916,916,MONDO:0000234,Rickettsia parkeri spotted fever,MONDO,disease,DISEASE_916
917,917,917,917,917,917,917,917,MONDO:0006812,intracranial vasospasm,MONDO,disease,DISEASE_917
918,918,918,918,918,918,918,918,MONDO:0003069,suppurative lymphadenitis,MONDO,disease,DISEASE_918
919,919,919,919,919,919,919,919,MONDO:0007608,desmoid tumor,MONDO,disease,DISEASE_919
920,920,920,920,920,920,920,920,MONDO:0024864,medium/large size posterior uveal melanoma,MONDO,disease,DISEASE_920
921,921,921,921,921,921,921,921,MONDO:0002824,extrinsic cardiomyopathy,MONDO,disease,DISEASE_921
922,922,922,922,922,922,922,922,MONDO:0023035,Eagle syndrome,MONDO,disease,DISEASE_922
923,923,923,923,923,923,923,923,MONDO:0045024,cancer or benign tumor,MONDO,disease,DISEASE_923
924,924,924,924,924,924,924,924,MONDO:0002199,benign mixed tumor of the vulva,MONDO,disease,DISEASE_924
925,925,925,925,925,925,925,925,MONDO:0003688_MONDO:0006364,well differentiated papillary mesothelioma,MONDO_grouped,disease,DISEASE_925
926,926,926,926,926,926,926,926,MONDO:0019485,idiopathic hemiconvulsion-hemiplegia syndrome,MONDO,disease,DISEASE_926
927,927,927,927,927,927,927,927,MONDO:0007293_MONDO:0013016_MONDO:0009953_MONDO:0017570,leukocyte adhesion deficiency,MONDO_grouped,disease,DISEASE_927
928,928,928,928,928,928,928,928,MONDO:0005731,dipetalonemiasis,MONDO,disease,DISEASE_928
929,929,929,929,929,929,929,929,MONDO:0021836,Aksu von Stockhausen syndrome,MONDO,disease,DISEASE_929
930,930,930,930,930,930,930,930,MONDO:0018171,malignant germ cell tumor of ovary,MONDO,disease,DISEASE_930
931,931,931,931,931,931,931,931,MONDO:0005004_MONDO:0003426,clear cell adenocarcinoma,MONDO_grouped,disease,DISEASE_931
932,932,932,932,932,932,932,932,MONDO:0008160,osteosclerosis with ichthyosis and fractures,MONDO,disease,DISEASE_932
933,933,933,933,933,933,933,933,MONDO:0010265_MONDO:0020602_MONDO:0010731,Simpson-Golabi-Behmel syndrome,MONDO_grouped,disease,DISEASE_933
934,934,934,934,934,934,934,934,MONDO:1011227_MONDO:1011229_MONDO:1011231_MONDO:1011232,"entropion, horse",MONDO_grouped,disease,DISEASE_934
935,935,935,935,935,935,935,935,MONDO:0002096,malignant conjunctival melanoma,MONDO,disease,DISEASE_935
936,936,936,936,936,936,936,936,MONDO:0002813,lipomatous cancer,MONDO,disease,DISEASE_936
937,937,937,937,937,937,937,937,MONDO:0002472,carcinoma ex pleomorphic adenoma,MONDO,disease,DISEASE_937
938,938,938,938,938,938,938,938,MONDO:0017348,lymphoepithelial-like carcinoma,MONDO,disease,DISEASE_938
939,939,939,939,939,939,939,939,MONDO:0032690,"microcephaly, growth deficiency, seizures, and brain malformations",MONDO,disease,DISEASE_939
940,940,940,940,940,940,940,940,MONDO:0013696,chromosome 2p16.3 deletion syndrome,MONDO,disease,DISEASE_940
941,941,941,941,941,941,941,941,MONDO:0014219,"alacrima, achalasia, and intellectual disability syndrome",MONDO,disease,DISEASE_941
942,942,942,942,942,942,942,942,MONDO:0019499,Turner syndrome,MONDO,disease,DISEASE_942
943,943,943,943,943,943,943,943,MONDO:0010740,"taurodontism, microdontia, and dens invaginatus",MONDO,disease,DISEASE_943
944,944,944,944,944,944,944,944,MONDO:1011757,"sebaceous gland dysplasia, non-human animal",MONDO,disease,DISEASE_944
945,945,945,945,945,945,945,945,MONDO:0037739,benign neoplasm of cauda equina,MONDO,disease,DISEASE_945
946,946,946,946,946,946,946,946,MONDO:0009188,epilepsy-telangiectasia syndrome,MONDO,disease,DISEASE_946
947,947,947,947,947,947,947,947,MONDO:1010553,"patent urachus, white rhinoceros",MONDO,disease,DISEASE_947
948,948,948,948,948,948,948,948,MONDO:0016918,partial deletion of the long arm of chromosome 20,MONDO,disease,DISEASE_948
949,949,949,949,949,949,949,949,MONDO:0014596_MONDO:0019450_MONDO:0015034_MONDO:0015035_MONDO:0015036_MONDO:0015037_MONDO:0015038_MONDO:0015039_MONDO:1011022_MONDO:1011026,lissencephaly 7 with cerebellar hypoplasia,MONDO_grouped,disease,DISEASE_949
950,950,950,950,950,950,950,950,MONDO:0007170,atresia of external auditory canal and conductive deafness,MONDO,disease,DISEASE_950
951,951,951,951,951,951,951,951,MONDO:0023157,fibular hypoplasia scapulo pelvic dysplasia absent,MONDO,disease,DISEASE_951
952,952,952,952,952,952,952,952,MONDO:0021777,acute rheumatic heart disease,MONDO,disease,DISEASE_952
953,953,953,953,953,953,953,953,MONDO:0042495,arteriosclerotic retinopathy,MONDO,disease,DISEASE_953
954,954,954,954,954,954,954,954,MONDO:0003003,cervical alveolar soft part sarcoma,MONDO,disease,DISEASE_954
955,955,955,955,955,955,955,955,MONDO:0013672,chromosome 15q25 deletion syndrome,MONDO,disease,DISEASE_955
956,956,956,956,956,956,956,956,MONDO:0007675,"glutamic acid decarboxylase, brain, membrane form",MONDO,disease,DISEASE_956
957,957,957,957,957,957,957,957,MONDO:1011808,"Hodgkin disease, non-human animal",MONDO,disease,DISEASE_957
958,958,958,958,958,958,958,958,MONDO:0004208,superior vena cava leiomyosarcoma,MONDO,disease,DISEASE_958
959,959,959,959,959,959,959,959,MONDO:0018692,variably protease-sensitive prionopathy,MONDO,disease,DISEASE_959
960,960,960,960,960,960,960,960,MONDO:0004917,internal hordeolum,MONDO,disease,DISEASE_960
961,961,961,961,961,961,961,961,MONDO:0042497,mycotoxicosis,MONDO,disease,DISEASE_961
962,962,962,962,962,962,962,962,MONDO:1011937,"type-II collagen-immune complex arthritis, non-human animal",MONDO,disease,DISEASE_962
963,963,963,963,963,963,963,963,MONDO:0002988,cervix melanoma,MONDO,disease,DISEASE_963
964,964,964,964,964,964,964,964,MONDO:0017740_MONDO:0017741,disorder of protein N-glycosylation,MONDO_grouped,disease,DISEASE_964
965,965,965,965,965,965,965,965,MONDO:0005397,goiter,MONDO,disease,DISEASE_965
966,966,966,966,966,966,966,966,MONDO:0009851,"peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain",MONDO,disease,DISEASE_966
967,967,967,967,967,967,967,967,MONDO:0015308,laminopathy type Decaudain-Vigouroux,MONDO,disease,DISEASE_967
968,968,968,968,968,968,968,968,MONDO:1012776,"atherosclerosis, APOE-related, rabbit",MONDO,disease,DISEASE_968
969,969,969,969,969,969,969,969,MONDO:0019360_MONDO:0005947,rickettsialpox,MONDO_grouped,disease,DISEASE_969
970,970,970,970,970,970,970,970,MONDO:0014704,skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome,MONDO,disease,DISEASE_970
971,971,971,971,971,971,971,971,MONDO:0018861,Zellweger-like syndrome without peroxisomal anomalies,MONDO,disease,DISEASE_971
972,972,972,972,972,972,972,972,MONDO:0015740,trisomy 18p,MONDO,disease,DISEASE_972
973,973,973,973,973,973,973,973,MONDO:0017294,"glycerol kinase deficiency, infantile form",MONDO,disease,DISEASE_973
974,974,974,974,974,974,974,974,MONDO:0008965,CHARGE syndrome,MONDO,disease,DISEASE_974
975,975,975,975,975,975,975,975,MONDO:0017207,primary organ-specific lymphoma,MONDO,disease,DISEASE_975
976,976,976,976,976,976,976,976,MONDO:0007504,thickened earlobes-conductive deafness syndrome,MONDO,disease,DISEASE_976
977,977,977,977,977,977,977,977,MONDO:0021081,anti-NMDA receptor encephalitis,MONDO,disease,DISEASE_977
978,978,978,978,978,978,978,978,MONDO:0010412,X-linked intellectual disability-craniofacioskeletal syndrome,MONDO,disease,DISEASE_978
979,979,979,979,979,979,979,979,MONDO:0012621,deafness-infertility syndrome,MONDO,disease,DISEASE_979
980,980,980,980,980,980,980,980,MONDO:0008983,chromosomal instability with tissue-specific radiosensitivity,MONDO,disease,DISEASE_980
981,981,981,981,981,981,981,981,MONDO:0859285,"neurodevelopmental disorder with microcephaly, short stature, and speech delay",MONDO,disease,DISEASE_981
982,982,982,982,982,982,982,982,MONDO:0009264,gastroschisis,MONDO,disease,DISEASE_982
983,983,983,983,983,983,983,983,MONDO:0014299_MONDO:0007039_MONDO:0859764,LZTR1-related schwannomatosis,MONDO_grouped,disease,DISEASE_983
984,984,984,984,984,984,984,984,MONDO:0012295,complement component 5 deficiency,MONDO,disease,DISEASE_984
985,985,985,985,985,985,985,985,MONDO:0008488,holoprosencephaly-radial heart renal anomalies syndrome,MONDO,disease,DISEASE_985
986,986,986,986,986,986,986,986,MONDO:0020860,faucial diphtheria,MONDO,disease,DISEASE_986
987,987,987,987,987,987,987,987,MONDO:0032878,"neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia",MONDO,disease,DISEASE_987
988,988,988,988,988,988,988,988,MONDO:0043723,Monteggia's fracture,MONDO,disease,DISEASE_988
989,989,989,989,989,989,989,989,MONDO:0015624,diazoxide-sensitive diffuse hyperinsulinism,MONDO,disease,DISEASE_989
990,990,990,990,990,990,990,990,MONDO:0008870,"bird headed-dwarfism, Montreal type",MONDO,disease,DISEASE_990
991,991,991,991,991,991,991,991,MONDO:0012928_MONDO:0014568_MONDO:0012867_MONDO:0012766_MONDO:0013132_MONDO:0013239_MONDO:0011489_MONDO:0011785_MONDO:0011339_MONDO:0011862_MONDO:0014282_MONDO:0014020_MONDO:0010418_MONDO:0012643_MONDO:0010878_MONDO:0013342_MONDO:0014015_MONDO:0010044_MONDO:0014016_MONDO:0012213_MONDO:0014018_MONDO:0012256_MONDO:0013552_MONDO:0013551_MONDO:0008437_MONDO:0014304_MONDO:0008438_MONDO:0013048_MONDO:0013401_MONDO:0014305_MONDO:0014882_MONDO:0014024_MONDO:0012639_MONDO:0011445_MONDO:0014303_MONDO:0011532_MONDO:0014302_MONDO:0012181_MONDO:0012334_MONDO:0010046_MONDO:0011408_MONDO:0013165_MONDO:0011006_MONDO:0012453_MONDO:0012448_MONDO:0014295_MONDO:0010047_MONDO:0010733_MONDO:0012866_MONDO:0010287_MONDO:0011803_MONDO:0011992_MONDO:0013737_MONDO:0013179_MONDO:0010043_MONDO:0014729_MONDO:0012787_MONDO:0012476_MONDO:0014644_MONDO:0013962_MONDO:0011522_MONDO:0019064,hereditary spastic paraplegia,MONDO_grouped,disease,DISEASE_991
992,992,992,992,992,992,992,992,MONDO:0005468,hypotensive disorder,MONDO,disease,DISEASE_992
993,993,993,993,993,993,993,993,MONDO:0010467,Xq27.3q28 duplication syndrome,MONDO,disease,DISEASE_993
994,994,994,994,994,994,994,994,MONDO:0011854,"secretory diarrhea, myopathy, and deafness",MONDO,disease,DISEASE_994
995,995,995,995,995,995,995,995,MONDO:0016075,filariasis,MONDO,disease,DISEASE_995
996,996,996,996,996,996,996,996,MONDO:1010699,"glycogen storage disease, PFKM-related, dog",MONDO,disease,DISEASE_996
997,997,997,997,997,997,997,997,MONDO:0041751,multibacillary leprosy,MONDO,disease,DISEASE_997
998,998,998,998,998,998,998,998,MONDO:0600008,cytokine release syndrome,MONDO,disease,DISEASE_998
999,999,999,999,999,999,999,999,MONDO:0011042,Martinez-Frias syndrome,MONDO,disease,DISEASE_999
1000,1000,1000,1000,1000,1000,1000,1000,MONDO:1010795,"Ehlers-Danlos syndrome, classic-like, TNXB-related, dog",MONDO,disease,DISEASE_1000
1001,1001,1001,1001,1001,1001,1001,1001,MONDO:0016191,qualitative or quantitative defects of titin,MONDO,disease,DISEASE_1001
1002,1002,1002,1002,1002,1002,1002,1002,MONDO:0018203,LMNA-related cardiocutaneous progeria syndrome,MONDO,disease,DISEASE_1002
1003,1003,1003,1003,1003,1003,1003,1003,MONDO:0024271,intestinal helminthiasis,MONDO,disease,DISEASE_1003
1004,1004,1004,1004,1004,1004,1004,1004,MONDO:0023147,fetal parainfluenza virus type 3 syndrome,MONDO,disease,DISEASE_1004
1005,1005,1005,1005,1005,1005,1005,1005,MONDO:0005693,cauda equina syndrome,MONDO,disease,DISEASE_1005
1006,1006,1006,1006,1006,1006,1006,1006,MONDO:0012177,posterior column ataxia-retinitis pigmentosa syndrome,MONDO,disease,DISEASE_1006
1007,1007,1007,1007,1007,1007,1007,1007,MONDO:0018076,tuberculosis,MONDO,disease,DISEASE_1007
1008,1008,1008,1008,1008,1008,1008,1008,MONDO:0009954,Ramon syndrome,MONDO,disease,DISEASE_1008
1009,1009,1009,1009,1009,1009,1009,1009,MONDO:0700273,RAD51C-related cancer predisposition,MONDO,disease,DISEASE_1009
1010,1010,1010,1010,1010,1010,1010,1010,MONDO:0011574,"tetralogy of fallot syndrome, autosomal recessive",MONDO,disease,DISEASE_1010
1011,1011,1011,1011,1011,1011,1011,1011,MONDO:0010311,Becker muscular dystrophy,MONDO,disease,DISEASE_1011
1012,1012,1012,1012,1012,1012,1012,1012,MONDO:1012393,"growth-hormone deficiency dwarfism, dog",MONDO,disease,DISEASE_1012
1013,1013,1013,1013,1013,1013,1013,1013,MONDO:1010064_MONDO:1010065_MONDO:1010084_MONDO:1010087,anti-MDA5 dermatomyositis,MONDO_grouped,disease,DISEASE_1013
1014,1014,1014,1014,1014,1014,1014,1014,MONDO:0030991,bile acid conjugation defect 1,MONDO,disease,DISEASE_1014
1015,1015,1015,1015,1015,1015,1015,1015,MONDO:0019160,primary progressive freezing gait,MONDO,disease,DISEASE_1015
1016,1016,1016,1016,1016,1016,1016,1016,MONDO:0016164,herpetiform pemphigus,MONDO,disease,DISEASE_1016
1017,1017,1017,1017,1017,1017,1017,1017,MONDO:0010764,"hearing loss, Y-linked 1",MONDO,disease,DISEASE_1017
1018,1018,1018,1018,1018,1018,1018,1018,MONDO:0032684,"intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency",MONDO,disease,DISEASE_1018
1019,1019,1019,1019,1019,1019,1019,1019,MONDO:0014021,familial episodic pain syndrome with predominantly upper body involvement,MONDO,disease,DISEASE_1019
1020,1020,1020,1020,1020,1020,1020,1020,MONDO:0017787,erythroderma desquamativum,MONDO,disease,DISEASE_1020
1021,1021,1021,1021,1021,1021,1021,1021,MONDO:0020479,pituitary gigantism,MONDO,disease,DISEASE_1021
1022,1022,1022,1022,1022,1022,1022,1022,MONDO:0001802,acute tympanitis,MONDO,disease,DISEASE_1022
1023,1023,1023,1023,1023,1023,1023,1023,MONDO:0000491,limb ischemia,MONDO,disease,DISEASE_1023
1024,1024,1024,1024,1024,1024,1024,1024,MONDO:1012052,"contact activation defect, domestic cat",MONDO,disease,DISEASE_1024
1025,1025,1025,1025,1025,1025,1025,1025,MONDO:0007677_MONDO:0957268_MONDO:0002177,hyperglycinuria,MONDO_grouped,disease,DISEASE_1025
1026,1026,1026,1026,1026,1026,1026,1026,MONDO:0017504,"apodia, unilateral",MONDO,disease,DISEASE_1026
1027,1027,1027,1027,1027,1027,1027,1027,MONDO:0060666,"hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome",MONDO,disease,DISEASE_1027
1028,1028,1028,1028,1028,1028,1028,1028,MONDO:0019810,toxic epidermal necrolysis,MONDO,disease,DISEASE_1028
1029,1029,1029,1029,1029,1029,1029,1029,MONDO:0005866,Mycobacterium avium complex disease,MONDO,disease,DISEASE_1029
1030,1030,1030,1030,1030,1030,1030,1030,MONDO:0008712,acrocraniofacial dysostosis,MONDO,disease,DISEASE_1030
1031,1031,1031,1031,1031,1031,1031,1031,MONDO:0006904,phimosis,MONDO,disease,DISEASE_1031
1032,1032,1032,1032,1032,1032,1032,1032,MONDO:0014163_MONDO:0014042_MONDO:0012285_MONDO:0011403_MONDO:0014152_MONDO:0018901_MONDO:0800350_MONDO:0800351_MONDO:0800346,left ventricular noncompaction,MONDO_grouped,disease,DISEASE_1032
1033,1033,1033,1033,1033,1033,1033,1033,MONDO:1010213_MONDO:1010222_MONDO:1011819,"chronic monocytic leukemia, non-human animal",MONDO_grouped,disease,DISEASE_1033
1034,1034,1034,1034,1034,1034,1034,1034,MONDO:0024473,Astrakhan spotted fever,MONDO,disease,DISEASE_1034
1035,1035,1035,1035,1035,1035,1035,1035,MONDO:0700267,BARD1-related cancer predisposition,MONDO,disease,DISEASE_1035
1036,1036,1036,1036,1036,1036,1036,1036,MONDO:0018850,proliferating trichilemmal cyst,MONDO,disease,DISEASE_1036
1037,1037,1037,1037,1037,1037,1037,1037,MONDO:0958351,hemi-myeloschisis,MONDO,disease,DISEASE_1037
1038,1038,1038,1038,1038,1038,1038,1038,MONDO:0971115,benign vascular tumor,MONDO,disease,DISEASE_1038
1039,1039,1039,1039,1039,1039,1039,1039,MONDO:0044336,colorectal signet ring cell carcinoma,MONDO,disease,DISEASE_1039
1040,1040,1040,1040,1040,1040,1040,1040,MONDO:0006033,diffuse intrinsic pontine glioma,MONDO,disease,DISEASE_1040
1041,1041,1041,1041,1041,1041,1041,1041,MONDO:0021224,iris neoplasm,MONDO,disease,DISEASE_1041
1042,1042,1042,1042,1042,1042,1042,1042,MONDO:0013957,Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency,MONDO,disease,DISEASE_1042
1043,1043,1043,1043,1043,1043,1043,1043,MONDO:0017045,neuroectodermal-endocrine syndrome,MONDO,disease,DISEASE_1043
1044,1044,1044,1044,1044,1044,1044,1044,MONDO:0003976_MONDO:0004400,malignant type AB thymoma,MONDO_grouped,disease,DISEASE_1044
1045,1045,1045,1045,1045,1045,1045,1045,MONDO:0040871_MONDO:0040872,psychogenic polydipsia,MONDO_grouped,disease,DISEASE_1045
1046,1046,1046,1046,1046,1046,1046,1046,MONDO:0004824,neonatal candidiasis,MONDO,disease,DISEASE_1046
1047,1047,1047,1047,1047,1047,1047,1047,MONDO:0022846,congenital nonhemolytic jaundice,MONDO,disease,DISEASE_1047
1048,1048,1048,1048,1048,1048,1048,1048,MONDO:1010437_MONDO:1010915,"cardiomyopathy, golden hamster",MONDO_grouped,disease,DISEASE_1048
1049,1049,1049,1049,1049,1049,1049,1049,MONDO:0100531_MONDO:0800318,"Emery-Dreifuss muscular dystrophy 1, X-linked",MONDO_grouped,disease,DISEASE_1049
1050,1050,1050,1050,1050,1050,1050,1050,MONDO:0013076_MONDO:0012149_MONDO:0012150_MONDO:0012151_MONDO:0012152_MONDO:0012862_MONDO:0012863,"attention deficit-hyperactivity disorder, susceptibility to",MONDO_grouped,disease,DISEASE_1050
1051,1051,1051,1051,1051,1051,1051,1051,MONDO:0009863,BH4-deficient hyperphenylalaninemia A,MONDO,disease,DISEASE_1051
1052,1052,1052,1052,1052,1052,1052,1052,MONDO:0008615,tune deafness,MONDO,disease,DISEASE_1052
1053,1053,1053,1053,1053,1053,1053,1053,MONDO:0010569,X-linked complicated corpus callosum dysgenesis,MONDO,disease,DISEASE_1053
1054,1054,1054,1054,1054,1054,1054,1054,MONDO:0007098,ACys amyloidosis,MONDO,disease,DISEASE_1054
1055,1055,1055,1055,1055,1055,1055,1055,MONDO:1010073,"factor XI deficiency, non-human animal",MONDO,disease,DISEASE_1055
1056,1056,1056,1056,1056,1056,1056,1056,MONDO:0014338,IL21-related infantile inflammatory bowel disease,MONDO,disease,DISEASE_1056
1057,1057,1057,1057,1057,1057,1057,1057,MONDO:0007124,ankyloblepharon-ectodermal defects-cleft lip/palate syndrome,MONDO,disease,DISEASE_1057
1058,1058,1058,1058,1058,1058,1058,1058,MONDO:1012584,"arachnomelia syndrome, SUOX-related, cattle",MONDO,disease,DISEASE_1058
1059,1059,1059,1059,1059,1059,1059,1059,MONDO:1012590,"oculocutaneous albinism, TYR-related, water buffalo",MONDO,disease,DISEASE_1059
1060,1060,1060,1060,1060,1060,1060,1060,MONDO:0018941,furuncular myiasis,MONDO,disease,DISEASE_1060
1061,1061,1061,1061,1061,1061,1061,1061,MONDO:0012830,chromosome 10q23 deletion syndrome,MONDO,disease,DISEASE_1061
1062,1062,1062,1062,1062,1062,1062,1062,MONDO:0800407,NYX-related retinopathy,MONDO,disease,DISEASE_1062
1063,1063,1063,1063,1063,1063,1063,1063,MONDO:0000375,bronchus carcinoma in situ,MONDO,disease,DISEASE_1063
1064,1064,1064,1064,1064,1064,1064,1064,MONDO:0000715,lymph node adenoid cystic carcinoma,MONDO,disease,DISEASE_1064
1065,1065,1065,1065,1065,1065,1065,1065,MONDO:0002522,tenosynovial giant cell tumor,MONDO,disease,DISEASE_1065
1066,1066,1066,1066,1066,1066,1066,1066,MONDO:0021510,benign neoplasm of prostate,MONDO,disease,DISEASE_1066
1067,1067,1067,1067,1067,1067,1067,1067,MONDO:1012301_MONDO:1012302,"spondylosis deformans, dog",MONDO_grouped,disease,DISEASE_1067
1068,1068,1068,1068,1068,1068,1068,1068,MONDO:0100429_MONDO:0013995_MONDO:0007829,intrahepatic cholestasis of pregnancy,MONDO_grouped,disease,DISEASE_1068
1069,1069,1069,1069,1069,1069,1069,1069,MONDO:0006309,mucinous gastric adenocarcinoma,MONDO,disease,DISEASE_1069
1070,1070,1070,1070,1070,1070,1070,1070,MONDO:0600017_MONDO:0600018_MONDO:0600019,acinar dysplasia caused by mutation in FGF10,MONDO_grouped,disease,DISEASE_1070
1071,1071,1071,1071,1071,1071,1071,1071,MONDO:0009230,"fibrosclerosis, multifocal",MONDO,disease,DISEASE_1071
1072,1072,1072,1072,1072,1072,1072,1072,MONDO:0001732,trigonitis,MONDO,disease,DISEASE_1072
1073,1073,1073,1073,1073,1073,1073,1073,MONDO:0006436,submandibular gland adenoid cystic carcinoma,MONDO,disease,DISEASE_1073
1074,1074,1074,1074,1074,1074,1074,1074,MONDO:0024320,inner ear neoplasm,MONDO,disease,DISEASE_1074
1075,1075,1075,1075,1075,1075,1075,1075,MONDO:0003717_MONDO:0003776,renal pelvis papillary tumor,MONDO_grouped,disease,DISEASE_1075
1076,1076,1076,1076,1076,1076,1076,1076,MONDO:0019013,non-histaminic angioedema,MONDO,disease,DISEASE_1076
1077,1077,1077,1077,1077,1077,1077,1077,MONDO:0003551,thymic adenosquamous carcinoma,MONDO,disease,DISEASE_1077
1078,1078,1078,1078,1078,1078,1078,1078,MONDO:1012863,"epilepsy, mitochondrial dysfunction and neurodegeneration, PITRM1-related, dog",MONDO,disease,DISEASE_1078
1079,1079,1079,1079,1079,1079,1079,1079,MONDO:0009395,hyperostosis corticalis generalisata,MONDO,disease,DISEASE_1079
1080,1080,1080,1080,1080,1080,1080,1080,MONDO:0009027,"cramps, familial adolescent",MONDO,disease,DISEASE_1080
1081,1081,1081,1081,1081,1081,1081,1081,MONDO:0011721,distal myopathy with anterior tibial onset,MONDO,disease,DISEASE_1081
1082,1082,1082,1082,1082,1082,1082,1082,MONDO:0017691,erythrocyte galactose epimerase deficiency,MONDO,disease,DISEASE_1082
1083,1083,1083,1083,1083,1083,1083,1083,MONDO:0012191,hepatoencephalopathy due to combined oxidative phosphorylation defect type 1,MONDO,disease,DISEASE_1083
1084,1084,1084,1084,1084,1084,1084,1084,MONDO:0001533,pes anserinus tendinitis or bursitis,MONDO,disease,DISEASE_1084
1085,1085,1085,1085,1085,1085,1085,1085,MONDO:0022946,deafness progressive cataract autosomal dominant,MONDO,disease,DISEASE_1085
1086,1086,1086,1086,1086,1086,1086,1086,MONDO:0007180,"Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities",MONDO,disease,DISEASE_1086
1087,1087,1087,1087,1087,1087,1087,1087,MONDO:0008738,"aganglionosis, total intestinal",MONDO,disease,DISEASE_1087
1088,1088,1088,1088,1088,1088,1088,1088,MONDO:1010806,"polydactyly, alpaca",MONDO,disease,DISEASE_1088
1089,1089,1089,1089,1089,1089,1089,1089,MONDO:0032892,structural brain anomalies with impaired intellectual development and craniosynostosis,MONDO,disease,DISEASE_1089
1090,1090,1090,1090,1090,1090,1090,1090,MONDO:0006275,lung giant cell carcinoma,MONDO,disease,DISEASE_1090
1091,1091,1091,1091,1091,1091,1091,1091,MONDO:0011310,"long chain fatty acids, defect in transport of",MONDO,disease,DISEASE_1091
1092,1092,1092,1092,1092,1092,1092,1092,MONDO:0018847,omphalomesenteric cyst,MONDO,disease,DISEASE_1092
1093,1093,1093,1093,1093,1093,1093,1093,MONDO:0030866,"neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities",MONDO,disease,DISEASE_1093
1094,1094,1094,1094,1094,1094,1094,1094,MONDO:0008583,inherited torticollis,MONDO,disease,DISEASE_1094
1095,1095,1095,1095,1095,1095,1095,1095,MONDO:0800311,"vas deferens, congenital unilateral aplasia of",MONDO,disease,DISEASE_1095
1096,1096,1096,1096,1096,1096,1096,1096,MONDO:0035666,acute transverse myelitis with anti-MOG antibodies,MONDO,disease,DISEASE_1096
1097,1097,1097,1097,1097,1097,1097,1097,MONDO:0001686,anatomical narrow angle borderline glaucoma,MONDO,disease,DISEASE_1097
1098,1098,1098,1098,1098,1098,1098,1098,MONDO:1011314,"disorder of glycosylation, non-human animal",MONDO,disease,DISEASE_1098
1099,1099,1099,1099,1099,1099,1099,1099,MONDO:0002656,skin carcinoma,MONDO,disease,DISEASE_1099
1100,1100,1100,1100,1100,1100,1100,1100,MONDO:1011906,"hemolytic uremic syndrome, non-human animal",MONDO,disease,DISEASE_1100
1101,1101,1101,1101,1101,1101,1101,1101,MONDO:0023102,facio skeletal genital syndrome rippberger type,MONDO,disease,DISEASE_1101
1102,1102,1102,1102,1102,1102,1102,1102,MONDO:1011329,"keratoconjunctivitis, non-human animal",MONDO,disease,DISEASE_1102
1103,1103,1103,1103,1103,1103,1103,1103,MONDO:0004131,anal verrucous carcinoma,MONDO,disease,DISEASE_1103
1104,1104,1104,1104,1104,1104,1104,1104,MONDO:0013970,branched-chain keto acid dehydrogenase kinase deficiency,MONDO,disease,DISEASE_1104
1105,1105,1105,1105,1105,1105,1105,1105,MONDO:0016530,laryngocele,MONDO,disease,DISEASE_1105
1106,1106,1106,1106,1106,1106,1106,1106,MONDO:0002957,sarcomatoid basal cell carcinoma,MONDO,disease,DISEASE_1106
1107,1107,1107,1107,1107,1107,1107,1107,MONDO:0003764,pediatric leptomeningeal melanoma,MONDO,disease,DISEASE_1107
1108,1108,1108,1108,1108,1108,1108,1108,MONDO:0003663,uterine ligament endometrioid adenocarcinoma,MONDO,disease,DISEASE_1108
1109,1109,1109,1109,1109,1109,1109,1109,MONDO:0035667_MONDO:0035668,isolated optic neuritis without anti-MOG antibodies,MONDO_grouped,disease,DISEASE_1109
1110,1110,1110,1110,1110,1110,1110,1110,MONDO:0009471,"intrinsic factor and r binder, combined congenital deficiency of",MONDO,disease,DISEASE_1110
1111,1111,1111,1111,1111,1111,1111,1111,MONDO:0018247,CADDS,MONDO,disease,DISEASE_1111
1112,1112,1112,1112,1112,1112,1112,1112,MONDO:0010157,Tryptophanuria with dwarfism,MONDO,disease,DISEASE_1112
1113,1113,1113,1113,1113,1113,1113,1113,MONDO:0018097,infantile spasms,MONDO,disease,DISEASE_1113
1114,1114,1114,1114,1114,1114,1114,1114,MONDO:0010366_MONDO:0010318_MONDO:0010297_MONDO:0010590_MONDO:0010316_MONDO:0002010,FG syndrome,MONDO_grouped,disease,DISEASE_1114
1115,1115,1115,1115,1115,1115,1115,1115,MONDO:0000393,partial fetal alcohol syndrome,MONDO,disease,DISEASE_1115
1116,1116,1116,1116,1116,1116,1116,1116,MONDO:0013533,hyperlipidemia due to hepatic triglyceride lipase deficiency,MONDO,disease,DISEASE_1116
1117,1117,1117,1117,1117,1117,1117,1117,MONDO:0008347,obsolete idiopathic and/or familial pulmonary arterial hypertension,MONDO,disease,DISEASE_1117
1118,1118,1118,1118,1118,1118,1118,1118,MONDO:0000813,cardiac tuberculosis,MONDO,disease,DISEASE_1118
1119,1119,1119,1119,1119,1119,1119,1119,MONDO:0022205,pustular psoriasis,MONDO,disease,DISEASE_1119
1120,1120,1120,1120,1120,1120,1120,1120,MONDO:0016302_MONDO:0016303_MONDO:0020385,isolated congenitally uncorrected transposition of the great arteries,MONDO_grouped,disease,DISEASE_1120
1121,1121,1121,1121,1121,1121,1121,1121,MONDO:0008397,aplasia of lacrimal and salivary glands,MONDO,disease,DISEASE_1121
1122,1122,1122,1122,1122,1122,1122,1122,MONDO:0007988_MONDO:0016660,autosomal dominant primary microcephaly,MONDO_grouped,disease,DISEASE_1122
1123,1123,1123,1123,1123,1123,1123,1123,MONDO:0013190_MONDO:0013187,"factor XIII, b subunit, deficiency",MONDO_grouped,disease,DISEASE_1123
1124,1124,1124,1124,1124,1124,1124,1124,MONDO:0006121,calcifying fibrous tumor,MONDO,disease,DISEASE_1124
1125,1125,1125,1125,1125,1125,1125,1125,MONDO:0017872,Lujo hemorrhagic fever,MONDO,disease,DISEASE_1125
1126,1126,1126,1126,1126,1126,1126,1126,MONDO:0014421,glucocorticoid resistance,MONDO,disease,DISEASE_1126
1127,1127,1127,1127,1127,1127,1127,1127,MONDO:0007363,congenital contractural arachnodactyly,MONDO,disease,DISEASE_1127
1128,1128,1128,1128,1128,1128,1128,1128,MONDO:0003762,malignant leptomeningeal tumor,MONDO,disease,DISEASE_1128
1129,1129,1129,1129,1129,1129,1129,1129,MONDO:0016796,"mitochondrial DNA depletion syndrome, encephalomyopathic form",MONDO,disease,DISEASE_1129
1130,1130,1130,1130,1130,1130,1130,1130,MONDO:0018780,congenital generalized hypercontractile muscle stiffness syndrome,MONDO,disease,DISEASE_1130
1131,1131,1131,1131,1131,1131,1131,1131,MONDO:0018830,Kimura disease,MONDO,disease,DISEASE_1131
1132,1132,1132,1132,1132,1132,1132,1132,MONDO:1012754,"ptosis, intellectual disability, retarded growth and mortality syndrome, UBE3B-related, cattle",MONDO,disease,DISEASE_1132
1133,1133,1133,1133,1133,1133,1133,1133,MONDO:0018408,cystic echinococcosis,MONDO,disease,DISEASE_1133
1134,1134,1134,1134,1134,1134,1134,1134,MONDO:0008853,Barber-Say syndrome,MONDO,disease,DISEASE_1134
1135,1135,1135,1135,1135,1135,1135,1135,MONDO:0100059,hypereosinophilia of undetermined significance,MONDO,disease,DISEASE_1135
1136,1136,1136,1136,1136,1136,1136,1136,MONDO:0004008,flat ductal epithelial atypia,MONDO,disease,DISEASE_1136
1137,1137,1137,1137,1137,1137,1137,1137,MONDO:0011684_MONDO:0700077,vitiligo-associated multiple autoimmune disease susceptibility,MONDO_grouped,disease,DISEASE_1137
1138,1138,1138,1138,1138,1138,1138,1138,MONDO:0800439_MONDO:1040018,syndromic complex neurodevelopmental disorder,MONDO_grouped,disease,DISEASE_1138
1139,1139,1139,1139,1139,1139,1139,1139,MONDO:0017258,idiopathic panuveitis,MONDO,disease,DISEASE_1139
1140,1140,1140,1140,1140,1140,1140,1140,MONDO:0023510,Jaffer-Beighton syndrome,MONDO,disease,DISEASE_1140
1141,1141,1141,1141,1141,1141,1141,1141,MONDO:0013580,pyruvate dehydrogenase E1-beta deficiency,MONDO,disease,DISEASE_1141
1142,1142,1142,1142,1142,1142,1142,1142,MONDO:0021381,neoplasm of pericardium,MONDO,disease,DISEASE_1142
1143,1143,1143,1143,1143,1143,1143,1143,MONDO:0020468,paternal uniparental disomy of chromosome 13,MONDO,disease,DISEASE_1143
1144,1144,1144,1144,1144,1144,1144,1144,MONDO:0800147,hemophagocytic lymphohistiocytosis due to RhoG deficiency,MONDO,disease,DISEASE_1144
1145,1145,1145,1145,1145,1145,1145,1145,MONDO:0015041,myelodysplastic syndrome with excess blasts-2,MONDO,disease,DISEASE_1145
1146,1146,1146,1146,1146,1146,1146,1146,MONDO:0019407,"microcephalic osteodysplastic dysplasia, Saul-Wilson type",MONDO,disease,DISEASE_1146
1147,1147,1147,1147,1147,1147,1147,1147,MONDO:1010430_MONDO:1010431_MONDO:1010432,"atherosclerosis, dog",MONDO_grouped,disease,DISEASE_1147
1148,1148,1148,1148,1148,1148,1148,1148,MONDO:0001824_MONDO:0003335_MONDO:0021718_MONDO:0004224_MONDO:0004372_MONDO:0006645,polyneuropathy,MONDO_grouped,disease,DISEASE_1148
1149,1149,1149,1149,1149,1149,1149,1149,MONDO:0400004,phrynoderma,MONDO,disease,DISEASE_1149
1150,1150,1150,1150,1150,1150,1150,1150,MONDO:0017682,intellectual disability-polydactyly-uncombable hair syndrome,MONDO,disease,DISEASE_1150
1151,1151,1151,1151,1151,1151,1151,1151,MONDO:0013856,"hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, intellectual disability, and recurrent inflammatory episodes",MONDO,disease,DISEASE_1151
1152,1152,1152,1152,1152,1152,1152,1152,MONDO:0850420,acute necrotizing pancreatitis,MONDO,disease,DISEASE_1152
1153,1153,1153,1153,1153,1153,1153,1153,MONDO:0006714,coronary aneurysm,MONDO,disease,DISEASE_1153
1154,1154,1154,1154,1154,1154,1154,1154,MONDO:0850333_MONDO:0850335,IDH-wildtype anaplastic astrocytoma,MONDO_grouped,disease,DISEASE_1154
1155,1155,1155,1155,1155,1155,1155,1155,MONDO:0010792,lethal infantile mitochondrial myopathy,MONDO,disease,DISEASE_1155
1156,1156,1156,1156,1156,1156,1156,1156,MONDO:0016007,cocaine embryofetopathy,MONDO,disease,DISEASE_1156
1157,1157,1157,1157,1157,1157,1157,1157,MONDO:0016065,cleft palate-short stature-vertebral anomalies syndrome,MONDO,disease,DISEASE_1157
1158,1158,1158,1158,1158,1158,1158,1158,MONDO:0019817,congenital mitral valve insufficiency and/or stenosis,MONDO,disease,DISEASE_1158
1159,1159,1159,1159,1159,1159,1159,1159,MONDO:0002357,hepatic flexure cancer,MONDO,disease,DISEASE_1159
1160,1160,1160,1160,1160,1160,1160,1160,MONDO:0020737,"optic atrophy 10 with or without ataxia, intellectual disability, and seizures",MONDO,disease,DISEASE_1160
1161,1161,1161,1161,1161,1161,1161,1161,MONDO:0017831_MONDO:0017830,mild Canavan disease,MONDO_grouped,disease,DISEASE_1161
1162,1162,1162,1162,1162,1162,1162,1162,MONDO:0006372,pituicytoma,MONDO,disease,DISEASE_1162
1163,1163,1163,1163,1163,1163,1163,1163,MONDO:0004884_MONDO:0000941,eye degenerative disorder,MONDO_grouped,disease,DISEASE_1163
1164,1164,1164,1164,1164,1164,1164,1164,MONDO:0010457,Ogden syndrome,MONDO,disease,DISEASE_1164
1165,1165,1165,1165,1165,1165,1165,1165,MONDO:0018359,neonatal dermatomyositis,MONDO,disease,DISEASE_1165
1166,1166,1166,1166,1166,1166,1166,1166,MONDO:0021023,complete androgen insensitivity syndrome,MONDO,disease,DISEASE_1166
1167,1167,1167,1167,1167,1167,1167,1167,MONDO:0008259,familial spontaneous pneumothorax,MONDO,disease,DISEASE_1167
1168,1168,1168,1168,1168,1168,1168,1168,MONDO:0006858,mouth disorder,MONDO,disease,DISEASE_1168
1169,1169,1169,1169,1169,1169,1169,1169,MONDO:0015158,unexplained periodic fever syndrome,MONDO,disease,DISEASE_1169
1170,1170,1170,1170,1170,1170,1170,1170,MONDO:1012012,"aniridia with cataract, horse",MONDO,disease,DISEASE_1170
1171,1171,1171,1171,1171,1171,1171,1171,MONDO:1010264_MONDO:1010265_MONDO:1010266_MONDO:1010268,"renal hypoplasia, non-human animal",MONDO_grouped,disease,DISEASE_1171
1172,1172,1172,1172,1172,1172,1172,1172,MONDO:0010035,Smith-Lemli-Opitz syndrome,MONDO,disease,DISEASE_1172
1173,1173,1173,1173,1173,1173,1173,1173,MONDO:0003501,external ear squamous cell carcinoma,MONDO,disease,DISEASE_1173
1174,1174,1174,1174,1174,1174,1174,1174,MONDO:0008510,symphalangism with multiple anomalies of hands and feet,MONDO,disease,DISEASE_1174
1175,1175,1175,1175,1175,1175,1175,1175,MONDO:1011311_MONDO:1011365_MONDO:1011364_MONDO:1011666,"digestive system disorder, non-human animal",MONDO_grouped,disease,DISEASE_1175
1176,1176,1176,1176,1176,1176,1176,1176,MONDO:0043424_MONDO:0004335_MONDO:0044991,digestive system infectious disorder,MONDO_grouped,disease,DISEASE_1176
1177,1177,1177,1177,1177,1177,1177,1177,MONDO:0000291,granulomatous amebic encephalitis,MONDO,disease,DISEASE_1177
1178,1178,1178,1178,1178,1178,1178,1178,MONDO:0008130,ophthalmoplegia-intellectual disability-lingua scrotalis syndrome,MONDO,disease,DISEASE_1178
1179,1179,1179,1179,1179,1179,1179,1179,MONDO:1011713,"malignant hyperthermia, non-human animal",MONDO,disease,DISEASE_1179
1180,1180,1180,1180,1180,1180,1180,1180,MONDO:0008382,"retinoschisis, autosomal dominant",MONDO,disease,DISEASE_1180
1181,1181,1181,1181,1181,1181,1181,1181,MONDO:0033630,neurodevelopmental disorder with speech impairment and dysmorphic facies,MONDO,disease,DISEASE_1181
1182,1182,1182,1182,1182,1182,1182,1182,MONDO:1011275,"glaucoma, LTBP2-related, domestic cat",MONDO,disease,DISEASE_1182
1183,1183,1183,1183,1183,1183,1183,1183,MONDO:0007820,fused mandibular incisors,MONDO,disease,DISEASE_1183
1184,1184,1184,1184,1184,1184,1184,1184,MONDO:0040675_MONDO:0002062,myofibroblastoma,MONDO_grouped,disease,DISEASE_1184
1185,1185,1185,1185,1185,1185,1185,1185,MONDO:0014239,testicular anomalies with or without congenital heart disease,MONDO,disease,DISEASE_1185
1186,1186,1186,1186,1186,1186,1186,1186,MONDO:0013222_MONDO:0024545_MONDO:0013221,Miyoshi muscular dystrophy,MONDO_grouped,disease,DISEASE_1186
1187,1187,1187,1187,1187,1187,1187,1187,MONDO:0006189,eccrine porocarcinoma,MONDO,disease,DISEASE_1187
1188,1188,1188,1188,1188,1188,1188,1188,MONDO:0005394_MONDO:0002679_MONDO:0006686,brain infarction,MONDO_grouped,disease,DISEASE_1188
1189,1189,1189,1189,1189,1189,1189,1189,MONDO:0000290,primary amebic meningoencephalitis,MONDO,disease,DISEASE_1189
1190,1190,1190,1190,1190,1190,1190,1190,MONDO:0020048,internal carotid agenesis,MONDO,disease,DISEASE_1190
1191,1191,1191,1191,1191,1191,1191,1191,MONDO:1011367_MONDO:1012969_MONDO:1011318,"vision disorder, non-human animal",MONDO_grouped,disease,DISEASE_1191
1192,1192,1192,1192,1192,1192,1192,1192,MONDO:0010507,Xq25 microduplication syndrome,MONDO,disease,DISEASE_1192
1193,1193,1193,1193,1193,1193,1193,1193,MONDO:0006250,ileal neuroendocrine tumor G1,MONDO,disease,DISEASE_1193
1194,1194,1194,1194,1194,1194,1194,1194,MONDO:0014025,lower motor neuron syndrome with late-adult onset,MONDO,disease,DISEASE_1194
1195,1195,1195,1195,1195,1195,1195,1195,MONDO:0015756,myeloid hemopathy,MONDO,disease,DISEASE_1195
1196,1196,1196,1196,1196,1196,1196,1196,MONDO:0956969,chronic inducible urticaria,MONDO,disease,DISEASE_1196
1197,1197,1197,1197,1197,1197,1197,1197,MONDO:0008811,XK aprosencephaly,MONDO,disease,DISEASE_1197
1198,1198,1198,1198,1198,1198,1198,1198,MONDO:0007254,breast cancer,MONDO,disease,DISEASE_1198
1199,1199,1199,1199,1199,1199,1199,1199,MONDO:0006608_MONDO:0006609,seborrheic dermatitis,MONDO_grouped,disease,DISEASE_1199
1200,1200,1200,1200,1200,1200,1200,1200,MONDO:0100545_MONDO:0024257_MONDO:0100546,hereditary neurological disease,MONDO_grouped,disease,DISEASE_1200
1201,1201,1201,1201,1201,1201,1201,1201,MONDO:0017748,inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation,MONDO,disease,DISEASE_1201
1202,1202,1202,1202,1202,1202,1202,1202,MONDO:0015434,ring chromosome 18,MONDO,disease,DISEASE_1202
1203,1203,1203,1203,1203,1203,1203,1203,MONDO:0017591,combined pulmonary fibrosis-emphysema syndrome,MONDO,disease,DISEASE_1203
1204,1204,1204,1204,1204,1204,1204,1204,MONDO:0019878,3q26 microduplication syndrome,MONDO,disease,DISEASE_1204
1205,1205,1205,1205,1205,1205,1205,1205,MONDO:0000947,psychosexual disorder,MONDO,disease,DISEASE_1205
1206,1206,1206,1206,1206,1206,1206,1206,MONDO:0006633,acalculous cholecystitis,MONDO,disease,DISEASE_1206
1207,1207,1207,1207,1207,1207,1207,1207,MONDO:0016202,autosomal dominant rhegmatogenous retinal detachment,MONDO,disease,DISEASE_1207
1208,1208,1208,1208,1208,1208,1208,1208,MONDO:0001790,spinal cord lipoma,MONDO,disease,DISEASE_1208
1209,1209,1209,1209,1209,1209,1209,1209,MONDO:1012804,"hereditary nonpolyposis colorectal cancer, MSH6-related, rhesus monkey",MONDO,disease,DISEASE_1209
1210,1210,1210,1210,1210,1210,1210,1210,MONDO:0011191,capillary infantile hemangioma,MONDO,disease,DISEASE_1210
1211,1211,1211,1211,1211,1211,1211,1211,MONDO:0009124,Dubowitz syndrome,MONDO,disease,DISEASE_1211
1212,1212,1212,1212,1212,1212,1212,1212,MONDO:1010054_MONDO:1010055_MONDO:1010056_MONDO:1011945_MONDO:1011678,"hyperparathyroidism, non-human animal",MONDO_grouped,disease,DISEASE_1212
1213,1213,1213,1213,1213,1213,1213,1213,MONDO:0010480,"anemia, nonspherocytic hemolytic, due to G6PD deficiency",MONDO,disease,DISEASE_1213
1214,1214,1214,1214,1214,1214,1214,1214,MONDO:0030457,immunodeficiency 87 and autoimmunity,MONDO,disease,DISEASE_1214
1215,1215,1215,1215,1215,1215,1215,1215,MONDO:0002958,signet ring basal cell carcinoma,MONDO,disease,DISEASE_1215
1216,1216,1216,1216,1216,1216,1216,1216,MONDO:0032673_MONDO:0975875_MONDO:0032938_MONDO:0968977,"basal ganglia calcification, idiopathic, 7, autosomal recessive",MONDO_grouped,disease,DISEASE_1216
1217,1217,1217,1217,1217,1217,1217,1217,MONDO:0002254,syndromic disease,MONDO,disease,DISEASE_1217
1218,1218,1218,1218,1218,1218,1218,1218,MONDO:0007226,brachydactyly-nystagmus-cerebellar ataxia syndrome,MONDO,disease,DISEASE_1218
1219,1219,1219,1219,1219,1219,1219,1219,MONDO:0007244,Caffey disease,MONDO,disease,DISEASE_1219
1220,1220,1220,1220,1220,1220,1220,1220,MONDO:0005124,leprosy,MONDO,disease,DISEASE_1220
1221,1221,1221,1221,1221,1221,1221,1221,MONDO:0800319_MONDO:0800320,"cone dystrophy 5, X-linked",MONDO_grouped,disease,DISEASE_1221
1222,1222,1222,1222,1222,1222,1222,1222,MONDO:0018342,Joubert syndrome with Jeune asphyxiating thoracic dystrophy,MONDO,disease,DISEASE_1222
1223,1223,1223,1223,1223,1223,1223,1223,MONDO:0007100,familial amyloid neuropathy,MONDO,disease,DISEASE_1223
1224,1224,1224,1224,1224,1224,1224,1224,MONDO:0024346,pityriasis amiantacea,MONDO,disease,DISEASE_1224
1225,1225,1225,1225,1225,1225,1225,1225,MONDO:0008878,"bone dysplasia, lethal Holmgren type",MONDO,disease,DISEASE_1225
1226,1226,1226,1226,1226,1226,1226,1226,MONDO:0020707,central hearing loss,MONDO,disease,DISEASE_1226
1227,1227,1227,1227,1227,1227,1227,1227,MONDO:0002956,skin cystic basal cell carcinoma,MONDO,disease,DISEASE_1227
1228,1228,1228,1228,1228,1228,1228,1228,MONDO:0010555_MONDO:0014743_MONDO:0020603_MONDO:0008972_MONDO:0010823_MONDO:0009112_MONDO:0007321_MONDO:0015776_MONDO:0015775_MONDO:0019701_MONDO:0010556,X-linked chondrodysplasia punctata,MONDO_grouped,disease,DISEASE_1228
1229,1229,1229,1229,1229,1229,1229,1229,MONDO:0007437_MONDO:0007436_MONDO:0015613,dentin dysplasia,MONDO_grouped,disease,DISEASE_1229
1230,1230,1230,1230,1230,1230,1230,1230,MONDO:0008494,cryohydrocytosis,MONDO,disease,DISEASE_1230
1231,1231,1231,1231,1231,1231,1231,1231,MONDO:0017055,mycophenolate mofetil embryopathy,MONDO,disease,DISEASE_1231
1232,1232,1232,1232,1232,1232,1232,1232,MONDO:0001382,hepatorenal syndrome,MONDO,disease,DISEASE_1232
1233,1233,1233,1233,1233,1233,1233,1233,MONDO:0016264_MONDO:0005543_MONDO:0021176_MONDO:0021177,autoimmune hepatitis,MONDO_grouped,disease,DISEASE_1233
1234,1234,1234,1234,1234,1234,1234,1234,MONDO:0012329,short stature and Facioauriculothoracic malformations,MONDO,disease,DISEASE_1234
1235,1235,1235,1235,1235,1235,1235,1235,MONDO:1010863,"alpha-mannosidosis, domestic guinea pig",MONDO,disease,DISEASE_1235
1236,1236,1236,1236,1236,1236,1236,1236,MONDO:0010751,unique green phenomenon,MONDO,disease,DISEASE_1236
1237,1237,1237,1237,1237,1237,1237,1237,MONDO:0014292,leukoencephalopathy with mild cerebellar ataxia and white matter edema,MONDO,disease,DISEASE_1237
1238,1238,1238,1238,1238,1238,1238,1238,MONDO:0002140,vagina sarcoma,MONDO,disease,DISEASE_1238
1239,1239,1239,1239,1239,1239,1239,1239,MONDO:0016655,6p22 microdeletion syndrome,MONDO,disease,DISEASE_1239
1240,1240,1240,1240,1240,1240,1240,1240,MONDO:0020694,salivary gland epithelial myoepithelial carcinoma,MONDO,disease,DISEASE_1240
1241,1241,1241,1241,1241,1241,1241,1241,MONDO:0001791,neonatal urinary tract infectious disease,MONDO,disease,DISEASE_1241
1242,1242,1242,1242,1242,1242,1242,1242,MONDO:0022568,bidirectional tachycardia,MONDO,disease,DISEASE_1242
1243,1243,1243,1243,1243,1243,1243,1243,MONDO:1011079,"urolithiasis, domestic ferret",MONDO,disease,DISEASE_1243
1244,1244,1244,1244,1244,1244,1244,1244,MONDO:0018371,nebulin-related early-onset distal myopathy,MONDO,disease,DISEASE_1244
1245,1245,1245,1245,1245,1245,1245,1245,MONDO:0100085,cancer of long bone of upper limb,MONDO,disease,DISEASE_1245
1246,1246,1246,1246,1246,1246,1246,1246,MONDO:0015355_MONDO:0015352_MONDO:0018894,distal hereditary motor neuropathy,MONDO_grouped,disease,DISEASE_1246
1247,1247,1247,1247,1247,1247,1247,1247,MONDO:0016719,microcephaly-seizures-intellectual disability-heart disease syndrome,MONDO,disease,DISEASE_1247
1248,1248,1248,1248,1248,1248,1248,1248,MONDO:0015690,myeloid neoplasm associated with PDGFRB rearrangement,MONDO,disease,DISEASE_1248
1249,1249,1249,1249,1249,1249,1249,1249,MONDO:0004248_MONDO:0004249_MONDO:0004263,pediatric infratentorial ependymoma,MONDO_grouped,disease,DISEASE_1249
1250,1250,1250,1250,1250,1250,1250,1250,MONDO:1010304,"synovial chondromatosis, non-human animal",MONDO,disease,DISEASE_1250
1251,1251,1251,1251,1251,1251,1251,1251,MONDO:0017610_MONDO:0015550_MONDO:1011499_MONDO:0011869,epidermolysis bullosa simplex,MONDO_grouped,disease,DISEASE_1251
1252,1252,1252,1252,1252,1252,1252,1252,MONDO:0009061_MONDO:1010544_MONDO:1010545,cystic fibrosis,MONDO_grouped,disease,DISEASE_1252
1253,1253,1253,1253,1253,1253,1253,1253,MONDO:0007517,ectrodactyly-cleft palate syndrome,MONDO,disease,DISEASE_1253
1254,1254,1254,1254,1254,1254,1254,1254,MONDO:0001217_MONDO:0020843,pseudomembranous conjunctivitis,MONDO_grouped,disease,DISEASE_1254
1255,1255,1255,1255,1255,1255,1255,1255,MONDO:0015845,uterine cervical aplasia and agenesis,MONDO,disease,DISEASE_1255
1256,1256,1256,1256,1256,1256,1256,1256,MONDO:1011541,"ichthyosis, cattle",MONDO,disease,DISEASE_1256
1257,1257,1257,1257,1257,1257,1257,1257,MONDO:0003509,pineal region choriocarcinoma,MONDO,disease,DISEASE_1257
1258,1258,1258,1258,1258,1258,1258,1258,MONDO:1011236,"microphthalmia, water buffalo",MONDO,disease,DISEASE_1258
1259,1259,1259,1259,1259,1259,1259,1259,MONDO:0958259,dysraphism with stalk,MONDO,disease,DISEASE_1259
1260,1260,1260,1260,1260,1260,1260,1260,MONDO:0100177,"allergic rhinitis, susceptibility to",MONDO,disease,DISEASE_1260
1261,1261,1261,1261,1261,1261,1261,1261,MONDO:0007143,aortic arch anomaly-facial dysmorphism-intellectual disability syndrome,MONDO,disease,DISEASE_1261
1262,1262,1262,1262,1262,1262,1262,1262,MONDO:0800369,"parkinson disease 19B, early-onset",MONDO,disease,DISEASE_1262
1263,1263,1263,1263,1263,1263,1263,1263,MONDO:0015248,ataxia-photosensitivity-short stature syndrome,MONDO,disease,DISEASE_1263
1264,1264,1264,1264,1264,1264,1264,1264,MONDO:0975758,microvenular haemangioma,MONDO,disease,DISEASE_1264
1265,1265,1265,1265,1265,1265,1265,1265,MONDO:0006859_MONDO:0005858_MONDO:0002398_MONDO:0003886,mucinous cystadenoma,MONDO_grouped,disease,DISEASE_1265
1266,1266,1266,1266,1266,1266,1266,1266,MONDO:0007043_MONDO:0019661_MONDO:0019659_MONDO:0019660,Pfeiffer syndrome,MONDO_grouped,disease,DISEASE_1266
1267,1267,1267,1267,1267,1267,1267,1267,MONDO:0032838,"neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies",MONDO,disease,DISEASE_1267
1268,1268,1268,1268,1268,1268,1268,1268,MONDO:1011080_MONDO:1011046_MONDO:1011078_MONDO:1011081_MONDO:1011082_MONDO:1011083_MONDO:1011084_MONDO:1011085_MONDO:1011086,"urolithiasis, domestic cat",MONDO_grouped,disease,DISEASE_1268
1269,1269,1269,1269,1269,1269,1269,1269,MONDO:0033809,isolated blepharochalasis,MONDO,disease,DISEASE_1269
1270,1270,1270,1270,1270,1270,1270,1270,MONDO:0020456,pleuro-pericardial cyst,MONDO,disease,DISEASE_1270
1271,1271,1271,1271,1271,1271,1271,1271,MONDO:0011025,Cayman type cerebellar ataxia,MONDO,disease,DISEASE_1271
1272,1272,1272,1272,1272,1272,1272,1272,MONDO:0700107,"chromosome 19q13.11 deletion syndrome, distal",MONDO,disease,DISEASE_1272
1273,1273,1273,1273,1273,1273,1273,1273,MONDO:0000382,respiratory system benign neoplasm,MONDO,disease,DISEASE_1273
1274,1274,1274,1274,1274,1274,1274,1274,MONDO:0019004,kidney Wilms tumor,MONDO,disease,DISEASE_1274
1275,1275,1275,1275,1275,1275,1275,1275,MONDO:0012762_MONDO:0014191_MONDO:0011484_MONDO:0013529_MONDO:0013966_MONDO:0017990_MONDO:0800374,catecholaminergic polymorphic ventricular tachycardia,MONDO_grouped,disease,DISEASE_1275
1276,1276,1276,1276,1276,1276,1276,1276,MONDO:0016489,delta-beta-thalassemia,MONDO,disease,DISEASE_1276
1277,1277,1277,1277,1277,1277,1277,1277,MONDO:0018946,rhombencephalosynapsis,MONDO,disease,DISEASE_1277
1278,1278,1278,1278,1278,1278,1278,1278,MONDO:0016904,partial deletion of the long arm of chromosome 5,MONDO,disease,DISEASE_1278
1279,1279,1279,1279,1279,1279,1279,1279,MONDO:0100340_MONDO:0011175_MONDO:0100339,Friedreich ataxia,MONDO_grouped,disease,DISEASE_1279
1280,1280,1280,1280,1280,1280,1280,1280,MONDO:0005191_MONDO:0024879,metastatic melanoma,MONDO_grouped,disease,DISEASE_1280
1281,1281,1281,1281,1281,1281,1281,1281,MONDO:0006190,endolymphatic sac tumor,MONDO,disease,DISEASE_1281
1282,1282,1282,1282,1282,1282,1282,1282,MONDO:0019470,aggressive NK-cell leukemia,MONDO,disease,DISEASE_1282
1283,1283,1283,1283,1283,1283,1283,1283,MONDO:0005852,mitral valve stenosis,MONDO,disease,DISEASE_1283
1284,1284,1284,1284,1284,1284,1284,1284,MONDO:0015990,"focal, segmental or multifocal dystonia",MONDO,disease,DISEASE_1284
1285,1285,1285,1285,1285,1285,1285,1285,MONDO:0014379_MONDO:0035706,ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder,MONDO_grouped,disease,DISEASE_1285
1286,1286,1286,1286,1286,1286,1286,1286,MONDO:0008324,pseudoarthrogryposis,MONDO,disease,DISEASE_1286
1287,1287,1287,1287,1287,1287,1287,1287,MONDO:1012658,"retinal degeneration, CEP290-related, domestic cat",MONDO,disease,DISEASE_1287
1288,1288,1288,1288,1288,1288,1288,1288,MONDO:0020532,spirillary rat-bite fever,MONDO,disease,DISEASE_1288
1289,1289,1289,1289,1289,1289,1289,1289,MONDO:1011754,"reactive perforating collagenosis, non-human animal",MONDO,disease,DISEASE_1289
1290,1290,1290,1290,1290,1290,1290,1290,MONDO:0019199,interstitial granulomatous dermatitis with arthritis,MONDO,disease,DISEASE_1290
1291,1291,1291,1291,1291,1291,1291,1291,MONDO:0000396,spastic cerebral palsy,MONDO,disease,DISEASE_1291
1292,1292,1292,1292,1292,1292,1292,1292,MONDO:0015097,aortic valve dysplasia,MONDO,disease,DISEASE_1292
1293,1293,1293,1293,1293,1293,1293,1293,MONDO:0008685,Wolff-Parkinson-White syndrome,MONDO,disease,DISEASE_1293
1294,1294,1294,1294,1294,1294,1294,1294,MONDO:0858960,spindle cell oncocytoma,MONDO,disease,DISEASE_1294
1295,1295,1295,1295,1295,1295,1295,1295,MONDO:0700131_MONDO:1010209,"sarcoma, non-human animal",MONDO_grouped,disease,DISEASE_1295
1296,1296,1296,1296,1296,1296,1296,1296,MONDO:0019437,enthesitis-related juvenile idiopathic arthritis,MONDO,disease,DISEASE_1296
1297,1297,1297,1297,1297,1297,1297,1297,MONDO:0001310,Bowman's membrane folds or rupture,MONDO,disease,DISEASE_1297
1298,1298,1298,1298,1298,1298,1298,1298,MONDO:0003555,Bartholin gland adenosquamous carcinoma,MONDO,disease,DISEASE_1298
1299,1299,1299,1299,1299,1299,1299,1299,MONDO:0011512,Brooke-Spiegler syndrome,MONDO,disease,DISEASE_1299
1300,1300,1300,1300,1300,1300,1300,1300,MONDO:0000446,midface dysplasia,MONDO,disease,DISEASE_1300
1301,1301,1301,1301,1301,1301,1301,1301,MONDO:0001427,Dieulafoy lesion,MONDO,disease,DISEASE_1301
1302,1302,1302,1302,1302,1302,1302,1302,MONDO:0010781,"ataxia and polyneuropathy, adult-onset",MONDO,disease,DISEASE_1302
1303,1303,1303,1303,1303,1303,1303,1303,MONDO:0018760,DeSanto-Shinawi syndrome,MONDO,disease,DISEASE_1303
1304,1304,1304,1304,1304,1304,1304,1304,MONDO:0700064,aneuploidy,MONDO,disease,DISEASE_1304
1305,1305,1305,1305,1305,1305,1305,1305,MONDO:0016827,myopathy-growth delay-intellectual disability-hypospadias syndrome,MONDO,disease,DISEASE_1305
1306,1306,1306,1306,1306,1306,1306,1306,MONDO:0010734,"spatial visualization, aptitude for",MONDO,disease,DISEASE_1306
1307,1307,1307,1307,1307,1307,1307,1307,MONDO:0001337,inflamed seborrheic keratosis,MONDO,disease,DISEASE_1307
1308,1308,1308,1308,1308,1308,1308,1308,MONDO:1012677,"Waardenburg syndrome, MITF-related, golden hamster",MONDO,disease,DISEASE_1308
1309,1309,1309,1309,1309,1309,1309,1309,MONDO:0002055_MONDO:0004420,benign eccrine breast spiradenoma,MONDO_grouped,disease,DISEASE_1309
1310,1310,1310,1310,1310,1310,1310,1310,MONDO:1012920,"abdominal hernia, TWIST1-related, cattle",MONDO,disease,DISEASE_1310
1311,1311,1311,1311,1311,1311,1311,1311,MONDO:0016234,obsolete rare arteriovenous malformation,MONDO,disease,DISEASE_1311
1312,1312,1312,1312,1312,1312,1312,1312,MONDO:0001921,chronic atticoantral disease,MONDO,disease,DISEASE_1312
1313,1313,1313,1313,1313,1313,1313,1313,MONDO:0000761,syndrome caused by partial chromosomal deletion,MONDO,disease,DISEASE_1313
1314,1314,1314,1314,1314,1314,1314,1314,MONDO:0015394,nasal encephalocele,MONDO,disease,DISEASE_1314
1315,1315,1315,1315,1315,1315,1315,1315,MONDO:0014826,obsolete nucleoside diphosphate-linked moiety X Motif 15 deficiency,MONDO,disease,DISEASE_1315
1316,1316,1316,1316,1316,1316,1316,1316,MONDO:0003117,somatoform disorder,MONDO,disease,DISEASE_1316
1317,1317,1317,1317,1317,1317,1317,1317,MONDO:0009106,diastematomyelia,MONDO,disease,DISEASE_1317
1318,1318,1318,1318,1318,1318,1318,1318,MONDO:0021495,benign neoplasm of sublingual gland,MONDO,disease,DISEASE_1318
1319,1319,1319,1319,1319,1319,1319,1319,MONDO:0025381,avian leukosis,MONDO,disease,DISEASE_1319
1320,1320,1320,1320,1320,1320,1320,1320,MONDO:0800034,MELAS syndrome caused by mutation in MTTH,MONDO,disease,DISEASE_1320
1321,1321,1321,1321,1321,1321,1321,1321,MONDO:0859164,osteootohepatoenteric syndrome,MONDO,disease,DISEASE_1321
1322,1322,1322,1322,1322,1322,1322,1322,MONDO:0008832,right atrial isomerism,MONDO,disease,DISEASE_1322
1323,1323,1323,1323,1323,1323,1323,1323,MONDO:0002660,blepharochalasis,MONDO,disease,DISEASE_1323
1324,1324,1324,1324,1324,1324,1324,1324,MONDO:0003867_MONDO:0016745,diffuse meningeal melanocytosis,MONDO_grouped,disease,DISEASE_1324
1325,1325,1325,1325,1325,1325,1325,1325,MONDO:0024356,primary central sleep apnea syndrome,MONDO,disease,DISEASE_1325
1326,1326,1326,1326,1326,1326,1326,1326,MONDO:0010531,contractures-ectodermal dysplasia-cleft lip/palate syndrome,MONDO,disease,DISEASE_1326
1327,1327,1327,1327,1327,1327,1327,1327,MONDO:0036042,KAT6B-related multiple congenital anomalies syndrome,MONDO,disease,DISEASE_1327
1328,1328,1328,1328,1328,1328,1328,1328,MONDO:0019897,distal monosomy 12q,MONDO,disease,DISEASE_1328
1329,1329,1329,1329,1329,1329,1329,1329,MONDO:0010789,MELAS syndrome,MONDO,disease,DISEASE_1329
1330,1330,1330,1330,1330,1330,1330,1330,MONDO:0006352,paranasal sinus adenoid cystic carcinoma,MONDO,disease,DISEASE_1330
1331,1331,1331,1331,1331,1331,1331,1331,MONDO:0000754_MONDO:0015382,anal fistula,MONDO_grouped,disease,DISEASE_1331
1332,1332,1332,1332,1332,1332,1332,1332,MONDO:0000245,tinea imbricata,MONDO,disease,DISEASE_1332
1333,1333,1333,1333,1333,1333,1333,1333,MONDO:0016825,mitochondrial myopathy-lactic acidosis-deafness syndrome,MONDO,disease,DISEASE_1333
1334,1334,1334,1334,1334,1334,1334,1334,MONDO:0100550,orbital myositis,MONDO,disease,DISEASE_1334
1335,1335,1335,1335,1335,1335,1335,1335,MONDO:0014166_MONDO:0010438_MONDO:0019533_MONDO:0100244,paroxysmal nocturnal hemoglobinuria,MONDO_grouped,disease,DISEASE_1335
1336,1336,1336,1336,1336,1336,1336,1336,MONDO:0000301,ophthalmomyiasis,MONDO,disease,DISEASE_1336
1337,1337,1337,1337,1337,1337,1337,1337,MONDO:0016880,partial deletion of chromosome 18,MONDO,disease,DISEASE_1337
1338,1338,1338,1338,1338,1338,1338,1338,MONDO:0016294,Hirschsprung disease-type D brachydactyly syndrome,MONDO,disease,DISEASE_1338
1339,1339,1339,1339,1339,1339,1339,1339,MONDO:0859346,mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition,MONDO,disease,DISEASE_1339
1340,1340,1340,1340,1340,1340,1340,1340,MONDO:0800492,variable-age onset focal epilepsy syndrome,MONDO,disease,DISEASE_1340
1341,1341,1341,1341,1341,1341,1341,1341,MONDO:0017232,recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome,MONDO,disease,DISEASE_1341
1342,1342,1342,1342,1342,1342,1342,1342,MONDO:0015907,epimetaphyseal skeletal dysplasia,MONDO,disease,DISEASE_1342
1343,1343,1343,1343,1343,1343,1343,1343,MONDO:0019327,phakomatosis spilorosea,MONDO,disease,DISEASE_1343
1344,1344,1344,1344,1344,1344,1344,1344,MONDO:0023540,Kashani-Strom-Utley syndrome,MONDO,disease,DISEASE_1344
1345,1345,1345,1345,1345,1345,1345,1345,MONDO:0032933,"chromosome 1p36.33 duplication syndrome, atad3 gene cluster, autosomal dominant",MONDO,disease,DISEASE_1345
1346,1346,1346,1346,1346,1346,1346,1346,MONDO:1011542,"ichthyosis, greater kudu",MONDO,disease,DISEASE_1346
1347,1347,1347,1347,1347,1347,1347,1347,MONDO:0002741_MONDO:0021629_MONDO:0003626_MONDO:0200000,uterine ligament adenocarcinoma,MONDO_grouped,disease,DISEASE_1347
1348,1348,1348,1348,1348,1348,1348,1348,MONDO:0008038,ataxia-pancytopenia syndrome,MONDO,disease,DISEASE_1348
1349,1349,1349,1349,1349,1349,1349,1349,MONDO:0030308,immunodeficiency 82 with systemic inflammation,MONDO,disease,DISEASE_1349
1350,1350,1350,1350,1350,1350,1350,1350,MONDO:1010313,"spondylocostal dysostosis, autosomal recessive, non-human animal",MONDO,disease,DISEASE_1350
1351,1351,1351,1351,1351,1351,1351,1351,MONDO:0012328,trichilemmal cyst,MONDO,disease,DISEASE_1351
1352,1352,1352,1352,1352,1352,1352,1352,MONDO:1012177_MONDO:1012178_MONDO:1012179_MONDO:1012181,"myoclonus epilepsy of Lafora, fennec fox",MONDO_grouped,disease,DISEASE_1352
1353,1353,1353,1353,1353,1353,1353,1353,MONDO:0010643,acute leukemia,MONDO,disease,DISEASE_1353
1354,1354,1354,1354,1354,1354,1354,1354,MONDO:0020431,juxtaposition of the atrial appendages,MONDO,disease,DISEASE_1354
1355,1355,1355,1355,1355,1355,1355,1355,MONDO:0003744,spindle cell intraocular melanoma,MONDO,disease,DISEASE_1355
1356,1356,1356,1356,1356,1356,1356,1356,MONDO:1010615,"congenital adrenal hypoplasia, crab-eating macaque",MONDO,disease,DISEASE_1356
1357,1357,1357,1357,1357,1357,1357,1357,MONDO:0004833,plantar fasciitis,MONDO,disease,DISEASE_1357
1358,1358,1358,1358,1358,1358,1358,1358,MONDO:1010319,"coloboma, non-human animal",MONDO,disease,DISEASE_1358
1359,1359,1359,1359,1359,1359,1359,1359,MONDO:0037745,fibromyxoid tumor,MONDO,disease,DISEASE_1359
1360,1360,1360,1360,1360,1360,1360,1360,MONDO:0009930,obsolete pulmonary arteriovenous malformation,MONDO,disease,DISEASE_1360
1361,1361,1361,1361,1361,1361,1361,1361,MONDO:0019042,multiple congenital anomalies/dysmorphic syndrome,MONDO,disease,DISEASE_1361
1362,1362,1362,1362,1362,1362,1362,1362,MONDO:0007414,Gorham-Stout disease,MONDO,disease,DISEASE_1362
1363,1363,1363,1363,1363,1363,1363,1363,MONDO:0003635,sebaceous breast carcinoma,MONDO,disease,DISEASE_1363
1364,1364,1364,1364,1364,1364,1364,1364,MONDO:0008407,"neurogenic scapuloperoneal syndrome, Kaeser type",MONDO,disease,DISEASE_1364
1365,1365,1365,1365,1365,1365,1365,1365,MONDO:0007717,hemoglobin--variants for which the chain carrying the mutation 1S unknown or uncertain,MONDO,disease,DISEASE_1365
1366,1366,1366,1366,1366,1366,1366,1366,MONDO:0100301,"hemangioma, capillary infantile, susceptibility to",MONDO,disease,DISEASE_1366
1367,1367,1367,1367,1367,1367,1367,1367,MONDO:0012198,PCWH syndrome,MONDO,disease,DISEASE_1367
1368,1368,1368,1368,1368,1368,1368,1368,MONDO:0957266,RECON progeroid syndrome,MONDO,disease,DISEASE_1368
1369,1369,1369,1369,1369,1369,1369,1369,MONDO:0003192_MONDO:0004005_MONDO:0001992_MONDO:0003191_MONDO:0003610_MONDO:0003893_MONDO:0004006,rete ovarii neoplasm,MONDO_grouped,disease,DISEASE_1369
1370,1370,1370,1370,1370,1370,1370,1370,MONDO:0002185,hyperostosis,MONDO,disease,DISEASE_1370
1371,1371,1371,1371,1371,1371,1371,1371,MONDO:0043207,urethral obstruction sequence,MONDO,disease,DISEASE_1371
1372,1372,1372,1372,1372,1372,1372,1372,MONDO:1011048,"nephrotic syndrome, domestic cat",MONDO,disease,DISEASE_1372
1373,1373,1373,1373,1373,1373,1373,1373,MONDO:0017697,"glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form",MONDO,disease,DISEASE_1373
1374,1374,1374,1374,1374,1374,1374,1374,MONDO:0035875,ivermectin toxicity,MONDO,disease,DISEASE_1374
1375,1375,1375,1375,1375,1375,1375,1375,MONDO:0008469,spondyloepimetaphyseal dysplasia-hypotrichosis syndrome,MONDO,disease,DISEASE_1375
1376,1376,1376,1376,1376,1376,1376,1376,MONDO:0015015_MONDO:0013439_MONDO:0009339_MONDO:0008967_MONDO:0014564_MONDO:0011906_MONDO:0018841,congenital bile acid synthesis defect,MONDO_grouped,disease,DISEASE_1376
1377,1377,1377,1377,1377,1377,1377,1377,MONDO:1011933,"pulmonary surfactant metabolism dysfunction, non-human animal",MONDO,disease,DISEASE_1377
1378,1378,1378,1378,1378,1378,1378,1378,MONDO:0859004,invasive scopulariopsis infection,MONDO,disease,DISEASE_1378
1379,1379,1379,1379,1379,1379,1379,1379,MONDO:0002646,viral laryngitis,MONDO,disease,DISEASE_1379
1380,1380,1380,1380,1380,1380,1380,1380,MONDO:0002531,skin neoplasm,MONDO,disease,DISEASE_1380
1381,1381,1381,1381,1381,1381,1381,1381,MONDO:0009192,Wolcott-Rallison syndrome,MONDO,disease,DISEASE_1381
1382,1382,1382,1382,1382,1382,1382,1382,MONDO:0010891,lethal hemolytic anemia-genital anomalies syndrome,MONDO,disease,DISEASE_1382
1383,1383,1383,1383,1383,1383,1383,1383,MONDO:0000807,latex allergy,MONDO,disease,DISEASE_1383
1384,1384,1384,1384,1384,1384,1384,1384,MONDO:0012854,bilateral microtia-deafness-cleft palate syndrome,MONDO,disease,DISEASE_1384
1385,1385,1385,1385,1385,1385,1385,1385,MONDO:0018734,verrucous hemangioma,MONDO,disease,DISEASE_1385
1386,1386,1386,1386,1386,1386,1386,1386,MONDO:0022500,arthrogryposis multiplex congenita CNS calcification,MONDO,disease,DISEASE_1386
1387,1387,1387,1387,1387,1387,1387,1387,MONDO:0007389_MONDO:0000359,spondylocostal dysostosis 5,MONDO_grouped,disease,DISEASE_1387
1388,1388,1388,1388,1388,1388,1388,1388,MONDO:0004403,childhood precursor T-lymphoblastic lymphoma/leukemia,MONDO,disease,DISEASE_1388
1389,1389,1389,1389,1389,1389,1389,1389,MONDO:0008737_MONDO:0018060,congenital afibrinogenemia,MONDO_grouped,disease,DISEASE_1389
1390,1390,1390,1390,1390,1390,1390,1390,MONDO:0013607,monocytopenia with susceptibility to infections,MONDO,disease,DISEASE_1390
1391,1391,1391,1391,1391,1391,1391,1391,MONDO:0010273,"lymphoma, Hodgkin, X-linked pseudoautosomal",MONDO,disease,DISEASE_1391
1392,1392,1392,1392,1392,1392,1392,1392,MONDO:0001910,ochronosis disorder,MONDO,disease,DISEASE_1392
1393,1393,1393,1393,1393,1393,1393,1393,MONDO:0100537,"plasminogen deficiency, type II",MONDO,disease,DISEASE_1393
1394,1394,1394,1394,1394,1394,1394,1394,MONDO:0001681_MONDO:0001682,diphtheritic cystitis,MONDO_grouped,disease,DISEASE_1394
1395,1395,1395,1395,1395,1395,1395,1395,MONDO:0010811_MONDO:1010962,benign prostatic hyperplasia,MONDO_grouped,disease,DISEASE_1395
1396,1396,1396,1396,1396,1396,1396,1396,MONDO:0003753,nasal vestibule squamous papilloma,MONDO,disease,DISEASE_1396
1397,1397,1397,1397,1397,1397,1397,1397,MONDO:0016852,paternal uniparental disomy of chromosome X,MONDO,disease,DISEASE_1397
1398,1398,1398,1398,1398,1398,1398,1398,MONDO:0020755,obsolete heart block,MONDO,disease,DISEASE_1398
1399,1399,1399,1399,1399,1399,1399,1399,MONDO:0044705,paranasal sinus squamous cell carcinoma,MONDO,disease,DISEASE_1399
1400,1400,1400,1400,1400,1400,1400,1400,MONDO:1011878,"sensory ataxic neuropathy, non-human animal",MONDO,disease,DISEASE_1400
1401,1401,1401,1401,1401,1401,1401,1401,MONDO:0024890,pineal parenchymal cell neoplasm,MONDO,disease,DISEASE_1401
1402,1402,1402,1402,1402,1402,1402,1402,MONDO:1010287,"pulmonary hypertension, non-human animal",MONDO,disease,DISEASE_1402
1403,1403,1403,1403,1403,1403,1403,1403,MONDO:0008876,Bloom syndrome,MONDO,disease,DISEASE_1403
1404,1404,1404,1404,1404,1404,1404,1404,MONDO:0010330,obsolete primary ciliary dyskinesia-retinitis pigmentosa syndrome,MONDO,disease,DISEASE_1404
1405,1405,1405,1405,1405,1405,1405,1405,MONDO:0007735,congenital Horner syndrome,MONDO,disease,DISEASE_1405
1406,1406,1406,1406,1406,1406,1406,1406,MONDO:0003661,breast lymphoma,MONDO,disease,DISEASE_1406
1407,1407,1407,1407,1407,1407,1407,1407,MONDO:0018687,progressive muscular atrophy,MONDO,disease,DISEASE_1407
1408,1408,1408,1408,1408,1408,1408,1408,MONDO:0009614,"methylmalonic aciduria, cblB type",MONDO,disease,DISEASE_1408
1409,1409,1409,1409,1409,1409,1409,1409,MONDO:0035449,atelencephaly,MONDO,disease,DISEASE_1409
1410,1410,1410,1410,1410,1410,1410,1410,MONDO:1011816,"lymphoproliferative disease, non-human animal",MONDO,disease,DISEASE_1410
1411,1411,1411,1411,1411,1411,1411,1411,MONDO:0003195,peritoneal serous adenocarcinoma,MONDO,disease,DISEASE_1411
1412,1412,1412,1412,1412,1412,1412,1412,MONDO:0023208,Fuqua Berkovitz syndrome,MONDO,disease,DISEASE_1412
1413,1413,1413,1413,1413,1413,1413,1413,MONDO:0021580,neoplasm of jaw,MONDO,disease,DISEASE_1413
1414,1414,1414,1414,1414,1414,1414,1414,MONDO:0009181,"epidermolysis bullosa simplex 5B, with muscular dystrophy",MONDO,disease,DISEASE_1414
1415,1415,1415,1415,1415,1415,1415,1415,MONDO:0000553_MONDO:0002923,uterine corpus endometrial carcinoma,MONDO_grouped,disease,DISEASE_1415
1416,1416,1416,1416,1416,1416,1416,1416,MONDO:0023170,focal or multifocal malformations in neuronal migration,MONDO,disease,DISEASE_1416
1417,1417,1417,1417,1417,1417,1417,1417,MONDO:0019405,facial onset sensory and motor neuronopathy,MONDO,disease,DISEASE_1417
1418,1418,1418,1418,1418,1418,1418,1418,MONDO:1012747,"canine hereditary ataxia, RAB24-related, dog",MONDO,disease,DISEASE_1418
1419,1419,1419,1419,1419,1419,1419,1419,MONDO:0002172,otosalpingitis,MONDO,disease,DISEASE_1419
1420,1420,1420,1420,1420,1420,1420,1420,MONDO:0019879,distal trisomy 4q,MONDO,disease,DISEASE_1420
1421,1421,1421,1421,1421,1421,1421,1421,MONDO:0014498_MONDO:0007349_MONDO:0012724_MONDO:0013766_MONDO:0018768,familial cold autoinflammatory syndrome,MONDO_grouped,disease,DISEASE_1421
1422,1422,1422,1422,1422,1422,1422,1422,MONDO:0006426,spinal cord primitive neuroectodermal tumor,MONDO,disease,DISEASE_1422
1423,1423,1423,1423,1423,1423,1423,1423,MONDO:0002534,fallopian tube papilloma,MONDO,disease,DISEASE_1423
1424,1424,1424,1424,1424,1424,1424,1424,MONDO:0009399,"hyperphosphatemia, polyuria, and seizures",MONDO,disease,DISEASE_1424
1425,1425,1425,1425,1425,1425,1425,1425,MONDO:0017876,Venezuelan hemorrhagic fever,MONDO,disease,DISEASE_1425
1426,1426,1426,1426,1426,1426,1426,1426,MONDO:0007388,congenitally short costocoracoid ligament,MONDO,disease,DISEASE_1426
1427,1427,1427,1427,1427,1427,1427,1427,MONDO:0025667,limbal stem cell deficiency,MONDO,disease,DISEASE_1427
1428,1428,1428,1428,1428,1428,1428,1428,MONDO:0800032,MELAS syndrome caused by mutation in MTTL1,MONDO,disease,DISEASE_1428
1429,1429,1429,1429,1429,1429,1429,1429,MONDO:0009612,methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency,MONDO,disease,DISEASE_1429
1430,1430,1430,1430,1430,1430,1430,1430,MONDO:0015759,B-cell non-Hodgkin lymphoma,MONDO,disease,DISEASE_1430
1431,1431,1431,1431,1431,1431,1431,1431,MONDO:0017306,disorder of phenylalanine metabolism,MONDO,disease,DISEASE_1431
1432,1432,1432,1432,1432,1432,1432,1432,MONDO:0100448,RAB28-related retinopathy,MONDO,disease,DISEASE_1432
1433,1433,1433,1433,1433,1433,1433,1433,MONDO:0000415,adolescence-adult electroclinical syndrome,MONDO,disease,DISEASE_1433
1434,1434,1434,1434,1434,1434,1434,1434,MONDO:0001628,tinea unguium,MONDO,disease,DISEASE_1434
1435,1435,1435,1435,1435,1435,1435,1435,MONDO:0001641_MONDO:0001072,severe pre-eclampsia,MONDO_grouped,disease,DISEASE_1435
1436,1436,1436,1436,1436,1436,1436,1436,MONDO:0100298,abdominal wall malformation,MONDO,disease,DISEASE_1436
1437,1437,1437,1437,1437,1437,1437,1437,MONDO:1012960_MONDO:1011889,"hereditary cerebellar ataxia, non-human animal",MONDO_grouped,disease,DISEASE_1437
1438,1438,1438,1438,1438,1438,1438,1438,MONDO:0021499,benign neoplasm of cerebellum,MONDO,disease,DISEASE_1438
1439,1439,1439,1439,1439,1439,1439,1439,MONDO:0957403,periodic fever syndrome of childhood,MONDO,disease,DISEASE_1439
1440,1440,1440,1440,1440,1440,1440,1440,MONDO:0859297,neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities,MONDO,disease,DISEASE_1440
1441,1441,1441,1441,1441,1441,1441,1441,MONDO:0018576,non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy,MONDO,disease,DISEASE_1441
1442,1442,1442,1442,1442,1442,1442,1442,MONDO:0000639,cartilage cancer,MONDO,disease,DISEASE_1442
1443,1443,1443,1443,1443,1443,1443,1443,MONDO:0004459,bladder hepatoid adenocarcinoma,MONDO,disease,DISEASE_1443
1444,1444,1444,1444,1444,1444,1444,1444,MONDO:0035362,TRIM22-related inflammatory bowel disease,MONDO,disease,DISEASE_1444
1445,1445,1445,1445,1445,1445,1445,1445,MONDO:0800381,"46,XX true hermaphroditism, SRY-positive",MONDO,disease,DISEASE_1445
1446,1446,1446,1446,1446,1446,1446,1446,MONDO:1012832,"palmoplantar hyperkeratosis, DSG1-related, dog",MONDO,disease,DISEASE_1446
1447,1447,1447,1447,1447,1447,1447,1447,MONDO:0001680_MONDO:0001779,vaginal mullerian papilloma,MONDO_grouped,disease,DISEASE_1447
1448,1448,1448,1448,1448,1448,1448,1448,MONDO:0001897_MONDO:0003567,bilateral hyperactive labyrinth,MONDO_grouped,disease,DISEASE_1448
1449,1449,1449,1449,1449,1449,1449,1449,MONDO:0013532,protein Z deficiency,MONDO,disease,DISEASE_1449
1450,1450,1450,1450,1450,1450,1450,1450,MONDO:0043152,negative rheumatoid factor polyarthritis,MONDO,disease,DISEASE_1450
1451,1451,1451,1451,1451,1451,1451,1451,MONDO:0014935_MONDO:0024550_MONDO:0015942,frontometaphyseal dysplasia,MONDO_grouped,disease,DISEASE_1451
1452,1452,1452,1452,1452,1452,1452,1452,MONDO:0013536,heme oxygenase 1 deficiency,MONDO,disease,DISEASE_1452
1453,1453,1453,1453,1453,1453,1453,1453,MONDO:1011745,"comedo syndrome, non-human animal",MONDO,disease,DISEASE_1453
1454,1454,1454,1454,1454,1454,1454,1454,MONDO:0010325,"X-linked intellectual disability, Stocco dos Santos type",MONDO,disease,DISEASE_1454
1455,1455,1455,1455,1455,1455,1455,1455,MONDO:0018066,trisomy X,MONDO,disease,DISEASE_1455
1456,1456,1456,1456,1456,1456,1456,1456,MONDO:0015390,proboscis lateralis,MONDO,disease,DISEASE_1456
1457,1457,1457,1457,1457,1457,1457,1457,MONDO:0007830,insensitivity to pain with hyperplastic Myelinopathy,MONDO,disease,DISEASE_1457
1458,1458,1458,1458,1458,1458,1458,1458,MONDO:0700027,chromosome X disorder,MONDO,disease,DISEASE_1458
1459,1459,1459,1459,1459,1459,1459,1459,MONDO:0009760,Norman-Roberts syndrome,MONDO,disease,DISEASE_1459
1460,1460,1460,1460,1460,1460,1460,1460,MONDO:0850115,early-onset obesity-hyperphagia-severe developmental delay syndrome,MONDO,disease,DISEASE_1460
1461,1461,1461,1461,1461,1461,1461,1461,MONDO:0971049,single isolated optic neuritis,MONDO,disease,DISEASE_1461
1462,1462,1462,1462,1462,1462,1462,1462,MONDO:0005201,restrictive cardiomyopathy,MONDO,disease,DISEASE_1462
1463,1463,1463,1463,1463,1463,1463,1463,MONDO:0021506,benign neoplasm of spinal cord,MONDO,disease,DISEASE_1463
1464,1464,1464,1464,1464,1464,1464,1464,MONDO:0032485_MONDO:0032919_MONDO:0032795,intellectual developmental disorder,MONDO_grouped,disease,DISEASE_1464
1465,1465,1465,1465,1465,1465,1465,1465,MONDO:1010839,"gangliosidosis, emu",MONDO,disease,DISEASE_1465
1466,1466,1466,1466,1466,1466,1466,1466,MONDO:0009608,methionine malabsorption syndrome,MONDO,disease,DISEASE_1466
1467,1467,1467,1467,1467,1467,1467,1467,MONDO:0007200,blepharonasofacial malformation syndrome,MONDO,disease,DISEASE_1467
1468,1468,1468,1468,1468,1468,1468,1468,MONDO:0018930,monosomy 21,MONDO,disease,DISEASE_1468
1469,1469,1469,1469,1469,1469,1469,1469,MONDO:0017377,preaxial polydactyly-colobomata-intellectual disability syndrome,MONDO,disease,DISEASE_1469
1470,1470,1470,1470,1470,1470,1470,1470,MONDO:0017213,postorgasmic illness syndrome,MONDO,disease,DISEASE_1470
1471,1471,1471,1471,1471,1471,1471,1471,MONDO:0958096,monomorphic epitheliotropic intestinal T-cell lymphoma,MONDO,disease,DISEASE_1471
1472,1472,1472,1472,1472,1472,1472,1472,MONDO:0859575_MONDO:0859576_MONDO:0859393,Atelis syndrome,MONDO_grouped,disease,DISEASE_1472
1473,1473,1473,1473,1473,1473,1473,1473,MONDO:0006067,acinar prostate mucinous adenocarcinoma,MONDO,disease,DISEASE_1473
1474,1474,1474,1474,1474,1474,1474,1474,MONDO:0010884,"muscular dystrophy, scapulohumeral",MONDO,disease,DISEASE_1474
1475,1475,1475,1475,1475,1475,1475,1475,MONDO:0000646,ovarian benign neoplasm,MONDO,disease,DISEASE_1475
1476,1476,1476,1476,1476,1476,1476,1476,MONDO:0016256,Hennekam syndrome,MONDO,disease,DISEASE_1476
1477,1477,1477,1477,1477,1477,1477,1477,MONDO:0017983,humero-radio-ulnar synostosis,MONDO,disease,DISEASE_1477
1478,1478,1478,1478,1478,1478,1478,1478,MONDO:0004334,non-functional pancreatic neuroendocrine tumor,MONDO,disease,DISEASE_1478
1479,1479,1479,1479,1479,1479,1479,1479,MONDO:0008310,Hutchinson-Gilford progeria syndrome,MONDO,disease,DISEASE_1479
1480,1480,1480,1480,1480,1480,1480,1480,MONDO:0004318,pulmonary type ovarian small cell carcinoma,MONDO,disease,DISEASE_1480
1481,1481,1481,1481,1481,1481,1481,1481,MONDO:0002750,bladder colloid adenocarcinoma,MONDO,disease,DISEASE_1481
1482,1482,1482,1482,1482,1482,1482,1482,MONDO:0007102,amyotrophic dystonic paraplegia,MONDO,disease,DISEASE_1482
1483,1483,1483,1483,1483,1483,1483,1483,MONDO:0019325,phakomatosis cesioflammea,MONDO,disease,DISEASE_1483
1484,1484,1484,1484,1484,1484,1484,1484,MONDO:0015466,cranio-osteoarthropathy,MONDO,disease,DISEASE_1484
1485,1485,1485,1485,1485,1485,1485,1485,MONDO:0011169,keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome,MONDO,disease,DISEASE_1485
1486,1486,1486,1486,1486,1486,1486,1486,MONDO:0000151,symphalangism,MONDO,disease,DISEASE_1486
1487,1487,1487,1487,1487,1487,1487,1487,MONDO:0021516,benign neoplasm of glottis,MONDO,disease,DISEASE_1487
1488,1488,1488,1488,1488,1488,1488,1488,MONDO:0015640,benign infantile seizures associated with mild gastroenteritis,MONDO,disease,DISEASE_1488
1489,1489,1489,1489,1489,1489,1489,1489,MONDO:0017885_MONDO:0006701,chromophobe renal cell carcinoma,MONDO_grouped,disease,DISEASE_1489
1490,1490,1490,1490,1490,1490,1490,1490,MONDO:0008238,"phosphatase, acid, of tissues",MONDO,disease,DISEASE_1490
1491,1491,1491,1491,1491,1491,1491,1491,MONDO:0015763,mosaic trisomy 2,MONDO,disease,DISEASE_1491
1492,1492,1492,1492,1492,1492,1492,1492,MONDO:0025351,"multiple congenital anomalies-neurodevelopmental syndrome, X-linked",MONDO,disease,DISEASE_1492
1493,1493,1493,1493,1493,1493,1493,1493,MONDO:0024382,"circadian rhythm sleep disorder, shift work type",MONDO,disease,DISEASE_1493
1494,1494,1494,1494,1494,1494,1494,1494,MONDO:0007106,anal sphincter dysplasia,MONDO,disease,DISEASE_1494
1495,1495,1495,1495,1495,1495,1495,1495,MONDO:1030011,paroxysmal atrial fibrillation,MONDO,disease,DISEASE_1495
1496,1496,1496,1496,1496,1496,1496,1496,MONDO:0700266,paraneoplastic cutaneous syndrome,MONDO,disease,DISEASE_1496
1497,1497,1497,1497,1497,1497,1497,1497,MONDO:1012682_MONDO:1012708_MONDO:1012709,"multifocal retinopathy 1, BEST1-related, dog",MONDO_grouped,disease,DISEASE_1497
1498,1498,1498,1498,1498,1498,1498,1498,MONDO:0000626,vestibular gland benign neoplasm,MONDO,disease,DISEASE_1498
1499,1499,1499,1499,1499,1499,1499,1499,MONDO:0012494,testicular microlithiasis,MONDO,disease,DISEASE_1499
1500,1500,1500,1500,1500,1500,1500,1500,MONDO:0014063_MONDO:0014496_MONDO:0014364_MONDO:0014194_MONDO:0007415_MONDO:0014066_MONDO:0014065_MONDO:0014356_MONDO:0014064_MONDO:0020811,mitochondrial complex III deficiency nuclear,MONDO_grouped,disease,DISEASE_1500
1501,1501,1501,1501,1501,1501,1501,1501,MONDO:0008402,cleft palate-large ears-small head syndrome,MONDO,disease,DISEASE_1501
1502,1502,1502,1502,1502,1502,1502,1502,MONDO:0004205,lymphohistiocytoid mesothelioma,MONDO,disease,DISEASE_1502
1503,1503,1503,1503,1503,1503,1503,1503,MONDO:0007029,branchio-oto-renal syndrome,MONDO,disease,DISEASE_1503
1504,1504,1504,1504,1504,1504,1504,1504,MONDO:0010217,de Sanctis-Cacchione syndrome,MONDO,disease,DISEASE_1504
1505,1505,1505,1505,1505,1505,1505,1505,MONDO:0005611,bladder transitional cell carcinoma,MONDO,disease,DISEASE_1505
1506,1506,1506,1506,1506,1506,1506,1506,MONDO:0010611,X-linked hydrocephalus with stenosis of the aqueduct of Sylvius,MONDO,disease,DISEASE_1506
1507,1507,1507,1507,1507,1507,1507,1507,MONDO:0005112,malignant pleural mesothelioma,MONDO,disease,DISEASE_1507
1508,1508,1508,1508,1508,1508,1508,1508,MONDO:0037870,valine metabolism disease,MONDO,disease,DISEASE_1508
1509,1509,1509,1509,1509,1509,1509,1509,MONDO:0859250,"neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures",MONDO,disease,DISEASE_1509
1510,1510,1510,1510,1510,1510,1510,1510,MONDO:1012634_MONDO:1012715,"XX difference of sexual development, domestic cat",MONDO_grouped,disease,DISEASE_1510
1511,1511,1511,1511,1511,1511,1511,1511,MONDO:0004338,retinal cell cancer,MONDO,disease,DISEASE_1511
1512,1512,1512,1512,1512,1512,1512,1512,MONDO:0014706_MONDO:0013751_MONDO:0007411,"cutis laxa, autosomal dominant",MONDO_grouped,disease,DISEASE_1512
1513,1513,1513,1513,1513,1513,1513,1513,MONDO:1010216,"embryonal rhabdomyosarcoma, non-human animal",MONDO,disease,DISEASE_1513
1514,1514,1514,1514,1514,1514,1514,1514,MONDO:0011671_MONDO:0011299_MONDO:0011487_MONDO:0015548,Huntington disease-like,MONDO_grouped,disease,DISEASE_1514
1515,1515,1515,1515,1515,1515,1515,1515,MONDO:0004495,myotonic cataract,MONDO,disease,DISEASE_1515
1516,1516,1516,1516,1516,1516,1516,1516,MONDO:1011147_MONDO:1011148_MONDO:1011149,"achondroplasia, dog",MONDO_grouped,disease,DISEASE_1516
1517,1517,1517,1517,1517,1517,1517,1517,MONDO:1011996,"ocular melanosis, non-human animal",MONDO,disease,DISEASE_1517
1518,1518,1518,1518,1518,1518,1518,1518,MONDO:0015555,plaque-form urticaria pigmentosa,MONDO,disease,DISEASE_1518
1519,1519,1519,1519,1519,1519,1519,1519,MONDO:1011415_MONDO:1010092_MONDO:1010093_MONDO:1011903,"amyloidosis, non-human animal",MONDO_grouped,disease,DISEASE_1519
1520,1520,1520,1520,1520,1520,1520,1520,MONDO:0005836,male reproductive organ cancer,MONDO,disease,DISEASE_1520
1521,1521,1521,1521,1521,1521,1521,1521,MONDO:1010017_MONDO:1010023,"patent ductus arteriosus, non-human animal",MONDO_grouped,disease,DISEASE_1521
1522,1522,1522,1522,1522,1522,1522,1522,MONDO:0008095,nevus anemicus,MONDO,disease,DISEASE_1522
1523,1523,1523,1523,1523,1523,1523,1523,MONDO:0020367_MONDO:0005338_MONDO:1012498,juvenile open angle glaucoma,MONDO_grouped,disease,DISEASE_1523
1524,1524,1524,1524,1524,1524,1524,1524,MONDO:0002657,breast disorder,MONDO,disease,DISEASE_1524
1525,1525,1525,1525,1525,1525,1525,1525,MONDO:0044333,alcohol-induced Wernicke-Korsakoff's syndrome,MONDO,disease,DISEASE_1525
1526,1526,1526,1526,1526,1526,1526,1526,MONDO:0014662_MONDO:0016319_MONDO:0958106,congenital insensitivity to pain-hypohidrosis syndrome,MONDO_grouped,disease,DISEASE_1526
1527,1527,1527,1527,1527,1527,1527,1527,MONDO:0004981_MONDO:1010498_MONDO:1010499,atrial fibrillation,MONDO_grouped,disease,DISEASE_1527
1528,1528,1528,1528,1528,1528,1528,1528,MONDO:0019556,pressure-induced localized lipoatrophy,MONDO,disease,DISEASE_1528
1529,1529,1529,1529,1529,1529,1529,1529,MONDO:0700075,congenital muscular dystrophy caused by variation in POMGNT2,MONDO,disease,DISEASE_1529
1530,1530,1530,1530,1530,1530,1530,1530,MONDO:0012512,fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3,MONDO,disease,DISEASE_1530
1531,1531,1531,1531,1531,1531,1531,1531,MONDO:0858939,"diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype",MONDO,disease,DISEASE_1531
1532,1532,1532,1532,1532,1532,1532,1532,MONDO:0018029,congenital factor XIII deficiency,MONDO,disease,DISEASE_1532
1533,1533,1533,1533,1533,1533,1533,1533,MONDO:0009095,"dermatoosteolysis, Kirghizian type",MONDO,disease,DISEASE_1533
1534,1534,1534,1534,1534,1534,1534,1534,MONDO:0014402,severe neurodegenerative syndrome with lipodystrophy,MONDO,disease,DISEASE_1534
1535,1535,1535,1535,1535,1535,1535,1535,MONDO:0004442,testis polyembryoma,MONDO,disease,DISEASE_1535
1536,1536,1536,1536,1536,1536,1536,1536,MONDO:0008651,vertebral hypoplasia with lumbar kyphosis,MONDO,disease,DISEASE_1536
1537,1537,1537,1537,1537,1537,1537,1537,MONDO:0000775_MONDO:0700226,drug allergy,MONDO_grouped,disease,DISEASE_1537
1538,1538,1538,1538,1538,1538,1538,1538,MONDO:0004642,tonsillar pillar cancer,MONDO,disease,DISEASE_1538
1539,1539,1539,1539,1539,1539,1539,1539,MONDO:0958344,spinal dermal sinus,MONDO,disease,DISEASE_1539
1540,1540,1540,1540,1540,1540,1540,1540,MONDO:1011722,"cytochrome B-related exercise intolerance, non-human animal",MONDO,disease,DISEASE_1540
1541,1541,1541,1541,1541,1541,1541,1541,MONDO:0009869,isolated Pierre-Robin syndrome,MONDO,disease,DISEASE_1541
1542,1542,1542,1542,1542,1542,1542,1542,MONDO:0014700,Au-Kline syndrome,MONDO,disease,DISEASE_1542
1543,1543,1543,1543,1543,1543,1543,1543,MONDO:0015292,endotheliitis,MONDO,disease,DISEASE_1543
1544,1544,1544,1544,1544,1544,1544,1544,MONDO:0008485,sebocystomatosis,MONDO,disease,DISEASE_1544
1545,1545,1545,1545,1545,1545,1545,1545,MONDO:0016037,superficial Fibromatosis,MONDO,disease,DISEASE_1545
1546,1546,1546,1546,1546,1546,1546,1546,MONDO:0008380_MONDO:0016707,retinoblastoma,MONDO_grouped,disease,DISEASE_1546
1547,1547,1547,1547,1547,1547,1547,1547,MONDO:0009663,mucus inspissation of respiratory tract,MONDO,disease,DISEASE_1547
1548,1548,1548,1548,1548,1548,1548,1548,MONDO:0021805,"acromesomelic dysplasia, Campailla Martinelli type",MONDO,disease,DISEASE_1548
1549,1549,1549,1549,1549,1549,1549,1549,MONDO:0800427,"dengue hemorrhagic fever, susceptibility to",MONDO,disease,DISEASE_1549
1550,1550,1550,1550,1550,1550,1550,1550,MONDO:0800137,early-onset pulmonary and cutaneous vasculitis,MONDO,disease,DISEASE_1550
1551,1551,1551,1551,1551,1551,1551,1551,MONDO:0009978,retinal degeneration-nanophthalmos-glaucoma syndrome,MONDO,disease,DISEASE_1551
1552,1552,1552,1552,1552,1552,1552,1552,MONDO:1010872_MONDO:1012618_MONDO:1012665,"mucopolysaccharidosis, GUSB-related, domestic cat",MONDO_grouped,disease,DISEASE_1552
1553,1553,1553,1553,1553,1553,1553,1553,MONDO:1011354,"reproductive system disorder, non-human animal",MONDO,disease,DISEASE_1553
1554,1554,1554,1554,1554,1554,1554,1554,MONDO:0010111,odontotrichomelic syndrome,MONDO,disease,DISEASE_1554
1555,1555,1555,1555,1555,1555,1555,1555,MONDO:1012266,"androgen insensitivity syndrome, horse",MONDO,disease,DISEASE_1555
1556,1556,1556,1556,1556,1556,1556,1556,MONDO:0005025_MONDO:0006669,endocarditis,MONDO_grouped,disease,DISEASE_1556
1557,1557,1557,1557,1557,1557,1557,1557,MONDO:0017716,disorder of carnitine cycle and carnitine transport,MONDO,disease,DISEASE_1557
1558,1558,1558,1558,1558,1558,1558,1558,MONDO:0040677,invasive carcinoma,MONDO,disease,DISEASE_1558
1559,1559,1559,1559,1559,1559,1559,1559,MONDO:0000273,Kunjin virus infectous disease,MONDO,disease,DISEASE_1559
1560,1560,1560,1560,1560,1560,1560,1560,MONDO:1011635,"familial convulsions and ataxia, non-human animal",MONDO,disease,DISEASE_1560
1561,1561,1561,1561,1561,1561,1561,1561,MONDO:0008429,Singleton-Merten dysplasia,MONDO,disease,DISEASE_1561
1562,1562,1562,1562,1562,1562,1562,1562,MONDO:0009251,"fructose-1,6-bisphosphatase deficiency",MONDO,disease,DISEASE_1562
1563,1563,1563,1563,1563,1563,1563,1563,MONDO:0016959,partial duplication of the long arm of chromosome 8,MONDO,disease,DISEASE_1563
1564,1564,1564,1564,1564,1564,1564,1564,MONDO:0006135,cervical clear cell adenocarcinoma,MONDO,disease,DISEASE_1564
1565,1565,1565,1565,1565,1565,1565,1565,MONDO:0033562,"neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotonia",MONDO,disease,DISEASE_1565
1566,1566,1566,1566,1566,1566,1566,1566,MONDO:1010700,"maple syrup urine disease, BCKDHA-related, cattle",MONDO,disease,DISEASE_1566
1567,1567,1567,1567,1567,1567,1567,1567,MONDO:0003490,ampulla of vater squamous cell carcinoma,MONDO,disease,DISEASE_1567
1568,1568,1568,1568,1568,1568,1568,1568,MONDO:0009721,Nathalie syndrome,MONDO,disease,DISEASE_1568
1569,1569,1569,1569,1569,1569,1569,1569,MONDO:1010500,"Wolff-Parkinson-White syndrome, cattle",MONDO,disease,DISEASE_1569
1570,1570,1570,1570,1570,1570,1570,1570,MONDO:0009877,Laron syndrome,MONDO,disease,DISEASE_1570
1571,1571,1571,1571,1571,1571,1571,1571,MONDO:0033810,isolated iridoschisis,MONDO,disease,DISEASE_1571
1572,1572,1572,1572,1572,1572,1572,1572,MONDO:0003952,adult central nervous system choriocarcinoma,MONDO,disease,DISEASE_1572
1573,1573,1573,1573,1573,1573,1573,1573,MONDO:0800406_MONDO:0100438,ABCA4-related retinopathy,MONDO_grouped,disease,DISEASE_1573
1574,1574,1574,1574,1574,1574,1574,1574,MONDO:0006629_MONDO:0005416_MONDO:0006630_MONDO:0006631_MONDO:0006632_MONDO:1011159_MONDO:1011162_MONDO:1011163_MONDO:1011164_MONDO:1011165,"osteoarthritis, hip",MONDO_grouped,disease,DISEASE_1574
1575,1575,1575,1575,1575,1575,1575,1575,MONDO:0000339,spinal polio,MONDO,disease,DISEASE_1575
1576,1576,1576,1576,1576,1576,1576,1576,MONDO:0031061,"nephrotic syndrome, IIa 26",MONDO,disease,DISEASE_1576
1577,1577,1577,1577,1577,1577,1577,1577,MONDO:0017738,lysosomal glycogen storage disease,MONDO,disease,DISEASE_1577
1578,1578,1578,1578,1578,1578,1578,1578,MONDO:0042982,GATA2 deficiency with susceptibility to MDS/AML,MONDO,disease,DISEASE_1578
1579,1579,1579,1579,1579,1579,1579,1579,MONDO:0009171,"endothelial dystrophy, congenital hereditary, with nail hypoplasia",MONDO,disease,DISEASE_1579
1580,1580,1580,1580,1580,1580,1580,1580,MONDO:0009879,short stature due to growth hormone qualitative anomaly,MONDO,disease,DISEASE_1580
1581,1581,1581,1581,1581,1581,1581,1581,MONDO:0800481,oral fibroma,MONDO,disease,DISEASE_1581
1582,1582,1582,1582,1582,1582,1582,1582,MONDO:0002382,benign mesenchymoma,MONDO,disease,DISEASE_1582
1583,1583,1583,1583,1583,1583,1583,1583,MONDO:0016850,atypical Norrie disease due to monosomy Xp11.3,MONDO,disease,DISEASE_1583
1584,1584,1584,1584,1584,1584,1584,1584,MONDO:0010799,"deafness, aminoglycoside-induced",MONDO,disease,DISEASE_1584
1585,1585,1585,1585,1585,1585,1585,1585,MONDO:0013034_MONDO:0011881,keratosis palmoplantaris striata,MONDO_grouped,disease,DISEASE_1585
1586,1586,1586,1586,1586,1586,1586,1586,MONDO:1012555_MONDO:1012556_MONDO:1012557,"mitral valve dysplasia, domestic cat",MONDO_grouped,disease,DISEASE_1586
1587,1587,1587,1587,1587,1587,1587,1587,MONDO:0009064,ocular cystinosis,MONDO,disease,DISEASE_1587
1588,1588,1588,1588,1588,1588,1588,1588,MONDO:0021193_MONDO:0017046,neuroepithelial neoplasm,MONDO_grouped,disease,DISEASE_1588
1589,1589,1589,1589,1589,1589,1589,1589,MONDO:0958264,infectious scleritis,MONDO,disease,DISEASE_1589
1590,1590,1590,1590,1590,1590,1590,1590,MONDO:0006165,colorectal squamous cell carcinoma,MONDO,disease,DISEASE_1590
1591,1591,1591,1591,1591,1591,1591,1591,MONDO:0024666,benign epithelial skin neoplasm,MONDO,disease,DISEASE_1591
1592,1592,1592,1592,1592,1592,1592,1592,MONDO:0008505,"surface antigen, glycoprotein 75",MONDO,disease,DISEASE_1592
1593,1593,1593,1593,1593,1593,1593,1593,MONDO:0017435,popliteal pterygium syndrome,MONDO,disease,DISEASE_1593
1594,1594,1594,1594,1594,1594,1594,1594,MONDO:0002064_MONDO:0003024,breast angiomatosis,MONDO_grouped,disease,DISEASE_1594
1595,1595,1595,1595,1595,1595,1595,1595,MONDO:0030707,Trichomonas balanoposthitis,MONDO,disease,DISEASE_1595
1596,1596,1596,1596,1596,1596,1596,1596,MONDO:1011300,"acute disease, non-human animal",MONDO,disease,DISEASE_1596
1597,1597,1597,1597,1597,1597,1597,1597,MONDO:0009519,letterer-Siwe disease,MONDO,disease,DISEASE_1597
1598,1598,1598,1598,1598,1598,1598,1598,MONDO:1010416_MONDO:1010417,"myoclonus, horse",MONDO_grouped,disease,DISEASE_1598
1599,1599,1599,1599,1599,1599,1599,1599,MONDO:0041052,postherpetic neuralgia,MONDO,disease,DISEASE_1599
1600,1600,1600,1600,1600,1600,1600,1600,MONDO:1011124,"persistent Mullerian duct syndrome, goat",MONDO,disease,DISEASE_1600
1601,1601,1601,1601,1601,1601,1601,1601,MONDO:0018380,idiopathic avascular necrosis,MONDO,disease,DISEASE_1601
1602,1602,1602,1602,1602,1602,1602,1602,MONDO:0005154_MONDO:0005240,liver disorder,MONDO_grouped,disease,DISEASE_1602
1603,1603,1603,1603,1603,1603,1603,1603,MONDO:0011664,immunodeficiency due to CD25 deficiency,MONDO,disease,DISEASE_1603
1604,1604,1604,1604,1604,1604,1604,1604,MONDO:0020443,absence of innominate vein,MONDO,disease,DISEASE_1604
1605,1605,1605,1605,1605,1605,1605,1605,MONDO:0015351,neuropathy with hearing impairment,MONDO,disease,DISEASE_1605
1606,1606,1606,1606,1606,1606,1606,1606,MONDO:0003350,granular cell leiomyosarcoma,MONDO,disease,DISEASE_1606
1607,1607,1607,1607,1607,1607,1607,1607,MONDO:0005796,HIV enteropathy,MONDO,disease,DISEASE_1607
1608,1608,1608,1608,1608,1608,1608,1608,MONDO:0018056_MONDO:0016769,bullous lichen planus,MONDO_grouped,disease,DISEASE_1608
1609,1609,1609,1609,1609,1609,1609,1609,MONDO:0017701,"glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form",MONDO,disease,DISEASE_1609
1610,1610,1610,1610,1610,1610,1610,1610,MONDO:1011959,"growth-hormone deficiency dwarfism,, non-human animal",MONDO,disease,DISEASE_1610
1611,1611,1611,1611,1611,1611,1611,1611,MONDO:0010676,"muscular dystrophy, Hemizygous lethal type",MONDO,disease,DISEASE_1611
1612,1612,1612,1612,1612,1612,1612,1612,MONDO:0009844,pellagra-like syndrome,MONDO,disease,DISEASE_1612
1613,1613,1613,1613,1613,1613,1613,1613,MONDO:0001274,anal spasm,MONDO,disease,DISEASE_1613
1614,1614,1614,1614,1614,1614,1614,1614,MONDO:1010931,"polymyositis, dog",MONDO,disease,DISEASE_1614
1615,1615,1615,1615,1615,1615,1615,1615,MONDO:0022896,craniosynostosis contractures cleft,MONDO,disease,DISEASE_1615
1616,1616,1616,1616,1616,1616,1616,1616,MONDO:0017856,X-linked spasticity-intellectual disability-epilepsy syndrome,MONDO,disease,DISEASE_1616
1617,1617,1617,1617,1617,1617,1617,1617,MONDO:0018182,bullous impetigo,MONDO,disease,DISEASE_1617
1618,1618,1618,1618,1618,1618,1618,1618,MONDO:0001177,anorectal stricture,MONDO,disease,DISEASE_1618
1619,1619,1619,1619,1619,1619,1619,1619,MONDO:1010927_MONDO:1010928,"congenital pseudomyotonia, dog",MONDO_grouped,disease,DISEASE_1619
1620,1620,1620,1620,1620,1620,1620,1620,MONDO:0020547,chronic graft versus host disease,MONDO,disease,DISEASE_1620
1621,1621,1621,1621,1621,1621,1621,1621,MONDO:0700336,peritoneal carcinomatosis,MONDO,disease,DISEASE_1621
1622,1622,1622,1622,1622,1622,1622,1622,MONDO:0017917,maternally-inherited spastic paraplegia,MONDO,disease,DISEASE_1622
1623,1623,1623,1623,1623,1623,1623,1623,MONDO:0004387,luteoma of pregnancy,MONDO,disease,DISEASE_1623
1624,1624,1624,1624,1624,1624,1624,1624,MONDO:0015476,cysts and fistulae of the face and oral cavity,MONDO,disease,DISEASE_1624
1625,1625,1625,1625,1625,1625,1625,1625,MONDO:0008198,parietal foramina with cleidocranial dysplasia,MONDO,disease,DISEASE_1625
1626,1626,1626,1626,1626,1626,1626,1626,MONDO:0020363,honey-droplet corneal dystrophy,MONDO,disease,DISEASE_1626
1627,1627,1627,1627,1627,1627,1627,1627,MONDO:0020769_MONDO:0020763_MONDO:0020774,Menke-Hennekam syndrome,MONDO_grouped,disease,DISEASE_1627
1628,1628,1628,1628,1628,1628,1628,1628,MONDO:0024503,digestive system neuroendocrine neoplasm,MONDO,disease,DISEASE_1628
1629,1629,1629,1629,1629,1629,1629,1629,MONDO:0021364,neoplasm of oropharynx,MONDO,disease,DISEASE_1629
1630,1630,1630,1630,1630,1630,1630,1630,MONDO:1010110,"hyperphosphatemia, non-human animal",MONDO,disease,DISEASE_1630
1631,1631,1631,1631,1631,1631,1631,1631,MONDO:0007373,"corneal degeneration, ribbonlike, with deafness",MONDO,disease,DISEASE_1631
1632,1632,1632,1632,1632,1632,1632,1632,MONDO:0018586,zinc-responsive necrolytic acral erythema,MONDO,disease,DISEASE_1632
1633,1633,1633,1633,1633,1633,1633,1633,MONDO:0017995,spondylocostal dysostosis-hypospadias-intellectual disability syndrome,MONDO,disease,DISEASE_1633
1634,1634,1634,1634,1634,1634,1634,1634,MONDO:0016502,Hermansky-Pudlak syndrome without pulmonary fibrosis,MONDO,disease,DISEASE_1634
1635,1635,1635,1635,1635,1635,1635,1635,MONDO:0016574,hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome,MONDO,disease,DISEASE_1635
1636,1636,1636,1636,1636,1636,1636,1636,MONDO:0014231,juvenile onset Parkinson disease 19A,MONDO,disease,DISEASE_1636
1637,1637,1637,1637,1637,1637,1637,1637,MONDO:0013374,supernumerary der(22)t(8;22) syndrome,MONDO,disease,DISEASE_1637
1638,1638,1638,1638,1638,1638,1638,1638,MONDO:0030921,"intellectual disability, autosomal dominant 55, with seizures",MONDO,disease,DISEASE_1638
1639,1639,1639,1639,1639,1639,1639,1639,MONDO:0016354,xeroderma pigmentosum-Cockayne syndrome complex,MONDO,disease,DISEASE_1639
1640,1640,1640,1640,1640,1640,1640,1640,MONDO:0004089,basaloid carcinoma of the penis,MONDO,disease,DISEASE_1640
1641,1641,1641,1641,1641,1641,1641,1641,MONDO:0019553,drug-induced localized lipodystrophy,MONDO,disease,DISEASE_1641
1642,1642,1642,1642,1642,1642,1642,1642,MONDO:0001059,gastric lymphoma,MONDO,disease,DISEASE_1642
1643,1643,1643,1643,1643,1643,1643,1643,MONDO:0012291_MONDO:1012130,immunoglobulin A deficiency,MONDO_grouped,disease,DISEASE_1643
1644,1644,1644,1644,1644,1644,1644,1644,MONDO:0009919,peroxisomal acyl-CoA oxidase deficiency,MONDO,disease,DISEASE_1644
1645,1645,1645,1645,1645,1645,1645,1645,MONDO:0020424,intramural coronary arterial course,MONDO,disease,DISEASE_1645
1646,1646,1646,1646,1646,1646,1646,1646,MONDO:1011316,"disorder of visual system, non-human animal",MONDO,disease,DISEASE_1646
1647,1647,1647,1647,1647,1647,1647,1647,MONDO:0700083,reciprocal translocation down syndrome,MONDO,disease,DISEASE_1647
1648,1648,1648,1648,1648,1648,1648,1648,MONDO:0011262,"camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye",MONDO,disease,DISEASE_1648
1649,1649,1649,1649,1649,1649,1649,1649,MONDO:0008698,achalasia,MONDO,disease,DISEASE_1649
1650,1650,1650,1650,1650,1650,1650,1650,MONDO:0044644,congenital agenesis of the scrotum,MONDO,disease,DISEASE_1650
1651,1651,1651,1651,1651,1651,1651,1651,MONDO:0004156,pancreatic mucinous cystadenocarcinoma,MONDO,disease,DISEASE_1651
1652,1652,1652,1652,1652,1652,1652,1652,MONDO:0002734,anal mucinous adenocarcinoma,MONDO,disease,DISEASE_1652
1653,1653,1653,1653,1653,1653,1653,1653,MONDO:0013829_MONDO:0010909_MONDO:0013834_MONDO:0015797,UV-sensitive syndrome,MONDO_grouped,disease,DISEASE_1653
1654,1654,1654,1654,1654,1654,1654,1654,MONDO:0000945,venous insufficiency,MONDO,disease,DISEASE_1654
1655,1655,1655,1655,1655,1655,1655,1655,MONDO:0007208,Boomerang dysplasia,MONDO,disease,DISEASE_1655
1656,1656,1656,1656,1656,1656,1656,1656,MONDO:0043240,hemophilic arthropathy,MONDO,disease,DISEASE_1656
1657,1657,1657,1657,1657,1657,1657,1657,MONDO:0009928,pulmonary alveolar microlithiasis,MONDO,disease,DISEASE_1657
1658,1658,1658,1658,1658,1658,1658,1658,MONDO:0016526,trisomy 9p,MONDO,disease,DISEASE_1658
1659,1659,1659,1659,1659,1659,1659,1659,MONDO:0019101,retinal capillary malformation,MONDO,disease,DISEASE_1659
1660,1660,1660,1660,1660,1660,1660,1660,MONDO:0800145,non-severe combined immunodeficiency due to polymerase delta deficiency,MONDO,disease,DISEASE_1660
1661,1661,1661,1661,1661,1661,1661,1661,MONDO:0016411,hypothyroidism due to deficient transcription factors involved in pituitary development or function,MONDO,disease,DISEASE_1661
1662,1662,1662,1662,1662,1662,1662,1662,MONDO:0001042,patellar tendinitis,MONDO,disease,DISEASE_1662
1663,1663,1663,1663,1663,1663,1663,1663,MONDO:1011904,"chronic interstitial nephropathy, non-human animal",MONDO,disease,DISEASE_1663
1664,1664,1664,1664,1664,1664,1664,1664,MONDO:0040998,Pasteurella multocida infectious disease,MONDO,disease,DISEASE_1664
1665,1665,1665,1665,1665,1665,1665,1665,MONDO:0022615,burn goodship syndrome,MONDO,disease,DISEASE_1665
1666,1666,1666,1666,1666,1666,1666,1666,MONDO:0021385_MONDO:0024658_MONDO:0002665_MONDO:0003090_MONDO:0006203_MONDO:0000978_MONDO:0003286_MONDO:0003377_MONDO:0004250_MONDO:0004462,extrahepatic bile duct neoplasm,MONDO_grouped,disease,DISEASE_1666
1667,1667,1667,1667,1667,1667,1667,1667,MONDO:0024300_MONDO:0000044,hypophosphatemic rickets,MONDO_grouped,disease,DISEASE_1667
1668,1668,1668,1668,1668,1668,1668,1668,MONDO:0005117_MONDO:0024459,Aeromonas hydrophila infectious disease,MONDO_grouped,disease,DISEASE_1668
1669,1669,1669,1669,1669,1669,1669,1669,MONDO:0007948,marfanoid hypermobility syndrome,MONDO,disease,DISEASE_1669
1670,1670,1670,1670,1670,1670,1670,1670,MONDO:0011644,pars planitis,MONDO,disease,DISEASE_1670
1671,1671,1671,1671,1671,1671,1671,1671,MONDO:0014953,gnb5-related intellectual disability-cardiac arrhythmia syndrome,MONDO,disease,DISEASE_1671
1672,1672,1672,1672,1672,1672,1672,1672,MONDO:0032796,"hyper-IgE recurrent infection syndrome 4, autosomal recessive",MONDO,disease,DISEASE_1672
1673,1673,1673,1673,1673,1673,1673,1673,MONDO:0006527,anhidrosis,MONDO,disease,DISEASE_1673
1674,1674,1674,1674,1674,1674,1674,1674,MONDO:0002760,bladder squamous cell carcinoma,MONDO,disease,DISEASE_1674
1675,1675,1675,1675,1675,1675,1675,1675,MONDO:0004439,periocular meningioma,MONDO,disease,DISEASE_1675
1676,1676,1676,1676,1676,1676,1676,1676,MONDO:0004199,vulvar keratinizing squamous cell carcinoma,MONDO,disease,DISEASE_1676
1677,1677,1677,1677,1677,1677,1677,1677,MONDO:0016382,hereditary poikiloderma,MONDO,disease,DISEASE_1677
1678,1678,1678,1678,1678,1678,1678,1678,MONDO:0100236,LTBP2-related ocular dysgenesis,MONDO,disease,DISEASE_1678
1679,1679,1679,1679,1679,1679,1679,1679,MONDO:0001715,basilar artery occlusion,MONDO,disease,DISEASE_1679
1680,1680,1680,1680,1680,1680,1680,1680,MONDO:0001046,imperforate anus,MONDO,disease,DISEASE_1680
1681,1681,1681,1681,1681,1681,1681,1681,MONDO:0008783,Tangier disease,MONDO,disease,DISEASE_1681
1682,1682,1682,1682,1682,1682,1682,1682,MONDO:1011670,"spina bifida with raduschisis, non-human animal",MONDO,disease,DISEASE_1682
1683,1683,1683,1683,1683,1683,1683,1683,MONDO:0008722,short chain acyl-CoA dehydrogenase deficiency,MONDO,disease,DISEASE_1683
1684,1684,1684,1684,1684,1684,1684,1684,MONDO:0004936,uterine inversion,MONDO,disease,DISEASE_1684
1685,1685,1685,1685,1685,1685,1685,1685,MONDO:0043465,achlorhydria,MONDO,disease,DISEASE_1685
1686,1686,1686,1686,1686,1686,1686,1686,MONDO:0001007,chronic meningitis,MONDO,disease,DISEASE_1686
1687,1687,1687,1687,1687,1687,1687,1687,MONDO:0021534,rectal neuroendocrine tumor G1,MONDO,disease,DISEASE_1687
1688,1688,1688,1688,1688,1688,1688,1688,MONDO:0010127_MONDO:0006456_MONDO:0016974_MONDO:0016975_MONDO:0002588_MONDO:0006458_MONDO:0006459,thymoma,MONDO_grouped,disease,DISEASE_1688
1689,1689,1689,1689,1689,1689,1689,1689,MONDO:0001701_MONDO:0001916,gastrointestinal anthrax,MONDO_grouped,disease,DISEASE_1689
1690,1690,1690,1690,1690,1690,1690,1690,MONDO:0001898,optic choroid disorder,MONDO,disease,DISEASE_1690
1691,1691,1691,1691,1691,1691,1691,1691,MONDO:0700243_MONDO:0700244,CACNA1F-related retinopathy,MONDO_grouped,disease,DISEASE_1691
1692,1692,1692,1692,1692,1692,1692,1692,MONDO:0007709_MONDO:0008979_MONDO:0958186_MONDO:0957317,"hematuria, benign familial",MONDO_grouped,disease,DISEASE_1692
1693,1693,1693,1693,1693,1693,1693,1693,MONDO:1012732,"difference of sexual development, DMRT1-related, Japanese medaka",MONDO,disease,DISEASE_1693
1694,1694,1694,1694,1694,1694,1694,1694,MONDO:1012577,"neurocristopathy, CHD7-related, cattle",MONDO,disease,DISEASE_1694
1695,1695,1695,1695,1695,1695,1695,1695,MONDO:0004293,supraglottis squamous cell carcinoma,MONDO,disease,DISEASE_1695
1696,1696,1696,1696,1696,1696,1696,1696,MONDO:0037002,benign phyllodes tumor,MONDO,disease,DISEASE_1696
1697,1697,1697,1697,1697,1697,1697,1697,MONDO:1030015,acquired porphyria,MONDO,disease,DISEASE_1697
1698,1698,1698,1698,1698,1698,1698,1698,MONDO:0007464,obsolete isolated distichiasis,MONDO,disease,DISEASE_1698
1699,1699,1699,1699,1699,1699,1699,1699,MONDO:0015674_MONDO:0019261_MONDO:0850001,late infantile neuronal ceroid lipofuscinosis,MONDO_grouped,disease,DISEASE_1699
1700,1700,1700,1700,1700,1700,1700,1700,MONDO:0005175,aggressive insulitis,MONDO,disease,DISEASE_1700
1701,1701,1701,1701,1701,1701,1701,1701,MONDO:0005751,epidemic pleurodynia,MONDO,disease,DISEASE_1701
1702,1702,1702,1702,1702,1702,1702,1702,MONDO:0017284,Xp22.13p22.2 duplication syndrome,MONDO,disease,DISEASE_1702
1703,1703,1703,1703,1703,1703,1703,1703,MONDO:0011663,juvenile primary lateral sclerosis,MONDO,disease,DISEASE_1703
1704,1704,1704,1704,1704,1704,1704,1704,MONDO:0023209,galactorrhoea-hyperprolactinaemia,MONDO,disease,DISEASE_1704
1705,1705,1705,1705,1705,1705,1705,1705,MONDO:0006367,pharyngeal adenoid cystic carcinoma,MONDO,disease,DISEASE_1705
1706,1706,1706,1706,1706,1706,1706,1706,MONDO:0009149,ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome,MONDO,disease,DISEASE_1706
1707,1707,1707,1707,1707,1707,1707,1707,MONDO:0022293,vascular disorder of penis,MONDO,disease,DISEASE_1707
1708,1708,1708,1708,1708,1708,1708,1708,MONDO:1010673_MONDO:1010674,"thrombopathia, RASGRP2-related, dog",MONDO_grouped,disease,DISEASE_1708
1709,1709,1709,1709,1709,1709,1709,1709,MONDO:0024430,allesthesia,MONDO,disease,DISEASE_1709
1710,1710,1710,1710,1710,1710,1710,1710,MONDO:0016462,isolated agammaglobulinemia,MONDO,disease,DISEASE_1710
1711,1711,1711,1711,1711,1711,1711,1711,MONDO:0010232,"intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked",MONDO,disease,DISEASE_1711
1712,1712,1712,1712,1712,1712,1712,1712,MONDO:0015696,Good syndrome,MONDO,disease,DISEASE_1712
1713,1713,1713,1713,1713,1713,1713,1713,MONDO:0022456,ankle defects short stature,MONDO,disease,DISEASE_1713
1714,1714,1714,1714,1714,1714,1714,1714,MONDO:0016930,partial trisomy/tetrasomy of chromosome 9,MONDO,disease,DISEASE_1714
1715,1715,1715,1715,1715,1715,1715,1715,MONDO:0004804_MONDO:0004800,dacryoadenitis,MONDO_grouped,disease,DISEASE_1715
1716,1716,1716,1716,1716,1716,1716,1716,MONDO:0021143,melanocytic neoplasm,MONDO,disease,DISEASE_1716
1717,1717,1717,1717,1717,1717,1717,1717,MONDO:0016784,obsolete gestational trophoblastic disease,MONDO,disease,DISEASE_1717
1718,1718,1718,1718,1718,1718,1718,1718,MONDO:0015525,congenital pseudoarthrosis of the limbs,MONDO,disease,DISEASE_1718
1719,1719,1719,1719,1719,1719,1719,1719,MONDO:0003639,lung hilum neoplasm,MONDO,disease,DISEASE_1719
1720,1720,1720,1720,1720,1720,1720,1720,MONDO:0005989_MONDO:0005697,toxoplasmosis,MONDO_grouped,disease,DISEASE_1720
1721,1721,1721,1721,1721,1721,1721,1721,MONDO:0005227,abscess,MONDO,disease,DISEASE_1721
1722,1722,1722,1722,1722,1722,1722,1722,MONDO:0018059,meningococcal meningitis,MONDO,disease,DISEASE_1722
1723,1723,1723,1723,1723,1723,1723,1723,MONDO:0043277,mosaic trisomy 6,MONDO,disease,DISEASE_1723
1724,1724,1724,1724,1724,1724,1724,1724,MONDO:0001721,urethral intrinsic sphincter deficiency,MONDO,disease,DISEASE_1724
1725,1725,1725,1725,1725,1725,1725,1725,MONDO:0013037,Giacheti syndrome,MONDO,disease,DISEASE_1725
1726,1726,1726,1726,1726,1726,1726,1726,MONDO:0000631,bone benign neoplasm,MONDO,disease,DISEASE_1726
1727,1727,1727,1727,1727,1727,1727,1727,MONDO:0004770_MONDO:0001210,exophthalmos,MONDO_grouped,disease,DISEASE_1727
1728,1728,1728,1728,1728,1728,1728,1728,MONDO:0006901,peritoneal neoplasm,MONDO,disease,DISEASE_1728
1729,1729,1729,1729,1729,1729,1729,1729,MONDO:0034150,idiopathic gastroparesis,MONDO,disease,DISEASE_1729
1730,1730,1730,1730,1730,1730,1730,1730,MONDO:0013196_MONDO:0012249_MONDO:0013710_MONDO:0013699_MONDO:0007356_MONDO:0005835,Lynch syndrome,MONDO_grouped,disease,DISEASE_1730
1731,1731,1731,1731,1731,1731,1731,1731,MONDO:1011467_MONDO:1011466_MONDO:1011471_MONDO:1010683_MONDO:1010684_MONDO:1010686_MONDO:1010688_MONDO:1010690_MONDO:1010691_MONDO:1010692_MONDO:1010693_MONDO:1010695_MONDO:1011470_MONDO:1012009_MONDO:1012011,"amyloidosis, dog",MONDO_grouped,disease,DISEASE_1731
1732,1732,1732,1732,1732,1732,1732,1732,MONDO:0014956,Chitayat syndrome,MONDO,disease,DISEASE_1732
1733,1733,1733,1733,1733,1733,1733,1733,MONDO:0018587,non-recovering obstetric brachial plexus lesion,MONDO,disease,DISEASE_1733
1734,1734,1734,1734,1734,1734,1734,1734,MONDO:0700180,feline bronchioloalveolar lung carcinoma,MONDO,disease,DISEASE_1734
1735,1735,1735,1735,1735,1735,1735,1735,MONDO:0021389,neoplasm of aortic body,MONDO,disease,DISEASE_1735
1736,1736,1736,1736,1736,1736,1736,1736,MONDO:1010267_MONDO:1010260,"urolithiasis, non-human animal",MONDO_grouped,disease,DISEASE_1736
1737,1737,1737,1737,1737,1737,1737,1737,MONDO:0002196,perinatal intestinal perforation,MONDO,disease,DISEASE_1737
1738,1738,1738,1738,1738,1738,1738,1738,MONDO:0011086,"severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive",MONDO,disease,DISEASE_1738
1739,1739,1739,1739,1739,1739,1739,1739,MONDO:0000987,cholesterolosis of gallbladder,MONDO,disease,DISEASE_1739
1740,1740,1740,1740,1740,1740,1740,1740,MONDO:0009131,Riley-Day syndrome,MONDO,disease,DISEASE_1740
1741,1741,1741,1741,1741,1741,1741,1741,MONDO:0018225,ALK-positive large B-cell lymphoma,MONDO,disease,DISEASE_1741
1742,1742,1742,1742,1742,1742,1742,1742,MONDO:0003861,vulvar eccrine adenocarcinoma,MONDO,disease,DISEASE_1742
1743,1743,1743,1743,1743,1743,1743,1743,MONDO:0000341,paralytic poliomyelitis,MONDO,disease,DISEASE_1743
1744,1744,1744,1744,1744,1744,1744,1744,MONDO:0017112_MONDO:0017113,isolated unilateral hemispheric cerebellar hypoplasia,MONDO_grouped,disease,DISEASE_1744
1745,1745,1745,1745,1745,1745,1745,1745,MONDO:1011639,"generalized myoclonic epilepsy with photosensitivity, non-human animal",MONDO,disease,DISEASE_1745
1746,1746,1746,1746,1746,1746,1746,1746,MONDO:0015027_MONDO:0016390_MONDO:0016365,familial isolated hyperparathyroidism,MONDO_grouped,disease,DISEASE_1746
1747,1747,1747,1747,1747,1747,1747,1747,MONDO:0002045,communicating hydrocephalus,MONDO,disease,DISEASE_1747
1748,1748,1748,1748,1748,1748,1748,1748,MONDO:0000144_MONDO:0800310,"pregnancy loss, recurrent",MONDO_grouped,disease,DISEASE_1748
1749,1749,1749,1749,1749,1749,1749,1749,MONDO:0022891,craniosynostosis Maroteaux Fonfria type,MONDO,disease,DISEASE_1749
1750,1750,1750,1750,1750,1750,1750,1750,MONDO:0033968,immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome,MONDO,disease,DISEASE_1750
1751,1751,1751,1751,1751,1751,1751,1751,MONDO:0001349,odontoclasia,MONDO,disease,DISEASE_1751
1752,1752,1752,1752,1752,1752,1752,1752,MONDO:0010070,"brachyolmia type 1, Hobaek type",MONDO,disease,DISEASE_1752
1753,1753,1753,1753,1753,1753,1753,1753,MONDO:0013246,"fatty liver disease, nonalcoholic, susceptibility to, 2",MONDO,disease,DISEASE_1753
1754,1754,1754,1754,1754,1754,1754,1754,MONDO:0700043,syndrome caused by partial chromosomal duplication of the short arm of chromosome 9,MONDO,disease,DISEASE_1754
1755,1755,1755,1755,1755,1755,1755,1755,MONDO:0014258,congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome,MONDO,disease,DISEASE_1755
1756,1756,1756,1756,1756,1756,1756,1756,MONDO:0017713_MONDO:0019223,disorder of fatty acid oxidation and ketogenesis,MONDO_grouped,disease,DISEASE_1756
1757,1757,1757,1757,1757,1757,1757,1757,MONDO:0005730,Dictyocaulus infectious disease,MONDO,disease,DISEASE_1757
1758,1758,1758,1758,1758,1758,1758,1758,MONDO:0019451,chronic neutrophilic leukemia,MONDO,disease,DISEASE_1758
1759,1759,1759,1759,1759,1759,1759,1759,MONDO:0021082,Meckel diverticulum neoplasm,MONDO,disease,DISEASE_1759
1760,1760,1760,1760,1760,1760,1760,1760,MONDO:1011761,"naked foal syndrome, non-human animal",MONDO,disease,DISEASE_1760
1761,1761,1761,1761,1761,1761,1761,1761,MONDO:0000926,eye accommodation disease,MONDO,disease,DISEASE_1761
1762,1762,1762,1762,1762,1762,1762,1762,MONDO:0010928,"dwarfism, familial, with muscle spasms",MONDO,disease,DISEASE_1762
1763,1763,1763,1763,1763,1763,1763,1763,MONDO:0009137,dysmyelination with jaundice,MONDO,disease,DISEASE_1763
1764,1764,1764,1764,1764,1764,1764,1764,MONDO:0010552,"Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia cutis congenita",MONDO,disease,DISEASE_1764
1765,1765,1765,1765,1765,1765,1765,1765,MONDO:0004298,stomach disorder,MONDO,disease,DISEASE_1765
1766,1766,1766,1766,1766,1766,1766,1766,MONDO:0002218,temporal lobe cancer,MONDO,disease,DISEASE_1766
1767,1767,1767,1767,1767,1767,1767,1767,MONDO:1012600_MONDO:1012773,"cystinuria, SLC3A1-related, domestic cat",MONDO_grouped,disease,DISEASE_1767
1768,1768,1768,1768,1768,1768,1768,1768,MONDO:0005160_MONDO:0005350,aortic aneurysm,MONDO_grouped,disease,DISEASE_1768
1769,1769,1769,1769,1769,1769,1769,1769,MONDO:0019479_MONDO:0700147,histiocytic sarcoma,MONDO_grouped,disease,DISEASE_1769
1770,1770,1770,1770,1770,1770,1770,1770,MONDO:0018301,interstitial cystitis,MONDO,disease,DISEASE_1770
1771,1771,1771,1771,1771,1771,1771,1771,MONDO:0018818,facial diplegia with paresthesias,MONDO,disease,DISEASE_1771
1772,1772,1772,1772,1772,1772,1772,1772,MONDO:0012258,"epidermolysis bullosa simplex 2E, with migratory circinate erythema",MONDO,disease,DISEASE_1772
1773,1773,1773,1773,1773,1773,1773,1773,MONDO:0002414,gastric hemangioma,MONDO,disease,DISEASE_1773
1774,1774,1774,1774,1774,1774,1774,1774,MONDO:1012537,"hypopigmentation and deafness, pig",MONDO,disease,DISEASE_1774
1775,1775,1775,1775,1775,1775,1775,1775,MONDO:0018919,McCune-Albright syndrome,MONDO,disease,DISEASE_1775
1776,1776,1776,1776,1776,1776,1776,1776,MONDO:0009575,thiamine-responsive megaloblastic anemia syndrome,MONDO,disease,DISEASE_1776
1777,1777,1777,1777,1777,1777,1777,1777,MONDO:0000901,relapsed/refractory diffuse large B-cell lymphoma,MONDO,disease,DISEASE_1777
1778,1778,1778,1778,1778,1778,1778,1778,MONDO:0021060,RASopathy,MONDO,disease,DISEASE_1778
1779,1779,1779,1779,1779,1779,1779,1779,MONDO:0009344,Hirschsprung disease-nail hypoplasia-dysmorphism syndrome,MONDO,disease,DISEASE_1779
1780,1780,1780,1780,1780,1780,1780,1780,MONDO:0056798,disorder of appendix,MONDO,disease,DISEASE_1780
1781,1781,1781,1781,1781,1781,1781,1781,MONDO:0004175,mucin-rich endometrial endometrioid adenocarcinoma,MONDO,disease,DISEASE_1781
1782,1782,1782,1782,1782,1782,1782,1782,MONDO:0007179,autoimmune disease,MONDO,disease,DISEASE_1782
1783,1783,1783,1783,1783,1783,1783,1783,MONDO:0800201,"baldness, male pattern",MONDO,disease,DISEASE_1783
1784,1784,1784,1784,1784,1784,1784,1784,MONDO:0004485,interstitial myocarditis,MONDO,disease,DISEASE_1784
1785,1785,1785,1785,1785,1785,1785,1785,MONDO:0019452,"myeloproliferative neoplasm, unclassifiable",MONDO,disease,DISEASE_1785
1786,1786,1786,1786,1786,1786,1786,1786,MONDO:0008920,"carnitine deficiency, myopathic",MONDO,disease,DISEASE_1786
1787,1787,1787,1787,1787,1787,1787,1787,MONDO:0006102,basaloid carcinoma,MONDO,disease,DISEASE_1787
1788,1788,1788,1788,1788,1788,1788,1788,MONDO:0002378_MONDO:0004096_MONDO:0010921,dermoid cyst,MONDO_grouped,disease,DISEASE_1788
1789,1789,1789,1789,1789,1789,1789,1789,MONDO:0010196,Werner syndrome,MONDO,disease,DISEASE_1789
1790,1790,1790,1790,1790,1790,1790,1790,MONDO:1012350,"polioencephalomyelopathy, dog",MONDO,disease,DISEASE_1790
1791,1791,1791,1791,1791,1791,1791,1791,MONDO:0006897_MONDO:0043314,periapical granuloma,MONDO_grouped,disease,DISEASE_1791
1792,1792,1792,1792,1792,1792,1792,1792,MONDO:0016414,"hypotrichosis-intellectual disability, Lopes type",MONDO,disease,DISEASE_1792
1793,1793,1793,1793,1793,1793,1793,1793,MONDO:0021474,benign neoplasm of ear,MONDO,disease,DISEASE_1793
1794,1794,1794,1794,1794,1794,1794,1794,MONDO:0005787,hepatic tuberculosis,MONDO,disease,DISEASE_1794
1795,1795,1795,1795,1795,1795,1795,1795,MONDO:0009038,craniosynostosis-fibular aplasia syndrome,MONDO,disease,DISEASE_1795
1796,1796,1796,1796,1796,1796,1796,1796,MONDO:0003719,renal pelvis neoplasm,MONDO,disease,DISEASE_1796
1797,1797,1797,1797,1797,1797,1797,1797,MONDO:0024674,Pancoast syndrome,MONDO,disease,DISEASE_1797
1798,1798,1798,1798,1798,1798,1798,1798,MONDO:0020120_MONDO:0003939,skeletal muscle disorder,MONDO_grouped,disease,DISEASE_1798
1799,1799,1799,1799,1799,1799,1799,1799,MONDO:0019072_MONDO:0006757,intrahepatic cholestasis,MONDO_grouped,disease,DISEASE_1799
1800,1800,1800,1800,1800,1800,1800,1800,MONDO:0002640,optic nerve neoplasm,MONDO,disease,DISEASE_1800
1801,1801,1801,1801,1801,1801,1801,1801,MONDO:0016053,isolated cerebellar vermis hypoplasia,MONDO,disease,DISEASE_1801
1802,1802,1802,1802,1802,1802,1802,1802,MONDO:0023961,"visceral neuropathy, familial",MONDO,disease,DISEASE_1802
1803,1803,1803,1803,1803,1803,1803,1803,MONDO:0000957,lacrimal passage granuloma,MONDO,disease,DISEASE_1803
1804,1804,1804,1804,1804,1804,1804,1804,MONDO:0022687_MONDO:0004742_MONDO:0022685,cerebellar degeneration,MONDO_grouped,disease,DISEASE_1804
1805,1805,1805,1805,1805,1805,1805,1805,MONDO:0008941,hepatic fibrosis-renal cysts-intellectual disability syndrome,MONDO,disease,DISEASE_1805
1806,1806,1806,1806,1806,1806,1806,1806,MONDO:0005503,developmental disorder of mental health,MONDO,disease,DISEASE_1806
1807,1807,1807,1807,1807,1807,1807,1807,MONDO:0007403_MONDO:0018686_MONDO:0007012_MONDO:0034976,inherited Creutzfeldt-Jakob disease,MONDO_grouped,disease,DISEASE_1807
1808,1808,1808,1808,1808,1808,1808,1808,MONDO:0019681,juvenile sialidosis type 2,MONDO,disease,DISEASE_1808
1809,1809,1809,1809,1809,1809,1809,1809,MONDO:0010940,inherited susceptibility to asthma,MONDO,disease,DISEASE_1809
1810,1810,1810,1810,1810,1810,1810,1810,MONDO:0011134,Curry-Jones syndrome,MONDO,disease,DISEASE_1810
1811,1811,1811,1811,1811,1811,1811,1811,MONDO:0006031,chronic rhinosinusitis,MONDO,disease,DISEASE_1811
1812,1812,1812,1812,1812,1812,1812,1812,MONDO:0011648,radiation-induced meningioma,MONDO,disease,DISEASE_1812
1813,1813,1813,1813,1813,1813,1813,1813,MONDO:0001053,acute infection of pinna,MONDO,disease,DISEASE_1813
1814,1814,1814,1814,1814,1814,1814,1814,MONDO:0009045,cataract-nephropathy-encephalopathy syndrome,MONDO,disease,DISEASE_1814
1815,1815,1815,1815,1815,1815,1815,1815,MONDO:0021323,malignant neoplasm of chest wall,MONDO,disease,DISEASE_1815
1816,1816,1816,1816,1816,1816,1816,1816,MONDO:1010120,sudden unexpected death in pediatrics,MONDO,disease,DISEASE_1816
1817,1817,1817,1817,1817,1817,1817,1817,MONDO:0008739,agenesis of cerebral white matter,MONDO,disease,DISEASE_1817
1818,1818,1818,1818,1818,1818,1818,1818,MONDO:0006726,diaphragmatic eventration,MONDO,disease,DISEASE_1818
1819,1819,1819,1819,1819,1819,1819,1819,MONDO:0022509,asternia,MONDO,disease,DISEASE_1819
1820,1820,1820,1820,1820,1820,1820,1820,MONDO:0014574,peeling skin-leukonuchia-acral punctate keratoses-cheilitis-knuckle pads syndrome,MONDO,disease,DISEASE_1820
1821,1821,1821,1821,1821,1821,1821,1821,MONDO:1011813,"sarcoid, non-human animal",MONDO,disease,DISEASE_1821
1822,1822,1822,1822,1822,1822,1822,1822,MONDO:0020213,stromal corneal dystrophy,MONDO,disease,DISEASE_1822
1823,1823,1823,1823,1823,1823,1823,1823,MONDO:0019637_MONDO:1011063,renal hypoplasia,MONDO_grouped,disease,DISEASE_1823
1824,1824,1824,1824,1824,1824,1824,1824,MONDO:0014990_MONDO:0020736_MONDO:0014989_MONDO:0008621,uncombable hair syndrome,MONDO_grouped,disease,DISEASE_1824
1825,1825,1825,1825,1825,1825,1825,1825,MONDO:0957990,Tan-Almurshedi syndrome,MONDO,disease,DISEASE_1825
1826,1826,1826,1826,1826,1826,1826,1826,MONDO:0010166,ulnar agenesis and endocardial fibroelastosis,MONDO,disease,DISEASE_1826
1827,1827,1827,1827,1827,1827,1827,1827,MONDO:0006797,hypertensive retinopathy,MONDO,disease,DISEASE_1827
1828,1828,1828,1828,1828,1828,1828,1828,MONDO:0016812,dopa-responsive dystonia,MONDO,disease,DISEASE_1828
1829,1829,1829,1829,1829,1829,1829,1829,MONDO:0004652_MONDO:0006012,bacterial pneumonia,MONDO_grouped,disease,DISEASE_1829
1830,1830,1830,1830,1830,1830,1830,1830,MONDO:1011421,"complement component 3 deficiency, non-human animal",MONDO,disease,DISEASE_1830
1831,1831,1831,1831,1831,1831,1831,1831,MONDO:0859331,Rabin-Pappas syndrome,MONDO,disease,DISEASE_1831
1832,1832,1832,1832,1832,1832,1832,1832,MONDO:0044744,prekallikrein deficiency,MONDO,disease,DISEASE_1832
1833,1833,1833,1833,1833,1833,1833,1833,MONDO:0008575_MONDO:0003969_MONDO:0001225,nicotine dependence,MONDO_grouped,disease,DISEASE_1833
1834,1834,1834,1834,1834,1834,1834,1834,MONDO:0012214_MONDO:0040502_MONDO:0011826_MONDO:0013874_MONDO:0024536,glucocorticoid deficiency,MONDO_grouped,disease,DISEASE_1834
1835,1835,1835,1835,1835,1835,1835,1835,MONDO:0001850,female breast lower-outer quadrant cancer,MONDO,disease,DISEASE_1835
1836,1836,1836,1836,1836,1836,1836,1836,MONDO:0002918,clear cell meningioma,MONDO,disease,DISEASE_1836
1837,1837,1837,1837,1837,1837,1837,1837,MONDO:0859085,"neurodevelopmental disorder with gait disturbance, dysmorphic facies, and behavioral abnormalities, X-linked",MONDO,disease,DISEASE_1837
1838,1838,1838,1838,1838,1838,1838,1838,MONDO:1012216,"platelet function defect, cattle",MONDO,disease,DISEASE_1838
1839,1839,1839,1839,1839,1839,1839,1839,MONDO:0010328,alpha-thalassemia-myelodysplastic syndrome,MONDO,disease,DISEASE_1839
1840,1840,1840,1840,1840,1840,1840,1840,MONDO:0008142,"Thiemann disease, familial form",MONDO,disease,DISEASE_1840
1841,1841,1841,1841,1841,1841,1841,1841,MONDO:0008566_MONDO:0011653_MONDO:0014682_MONDO:0014681_MONDO:0008567,"thyroid cancer, nonmedullary",MONDO_grouped,disease,DISEASE_1841
1842,1842,1842,1842,1842,1842,1842,1842,MONDO:0012133,"lateral semicircular canal malformation, familial, with external and middle ear abnormalities",MONDO,disease,DISEASE_1842
1843,1843,1843,1843,1843,1843,1843,1843,MONDO:0016475,Beckwith-Wiedemann syndrome due to imprinting defect of 11p15,MONDO,disease,DISEASE_1843
1844,1844,1844,1844,1844,1844,1844,1844,MONDO:0958137,early-onset autoimmune disorder due to DOCK11 partial deficiency,MONDO,disease,DISEASE_1844
1845,1845,1845,1845,1845,1845,1845,1845,MONDO:0030346,"ciliary dyskinesia, primary, 47, and lissencephaly",MONDO,disease,DISEASE_1845
1846,1846,1846,1846,1846,1846,1846,1846,MONDO:0008666,volvulus of midgut,MONDO,disease,DISEASE_1846
1847,1847,1847,1847,1847,1847,1847,1847,MONDO:0012171,marfanoid habitus with situs inversus,MONDO,disease,DISEASE_1847
1848,1848,1848,1848,1848,1848,1848,1848,MONDO:0043094,"ichthyosis, follicular",MONDO,disease,DISEASE_1848
1849,1849,1849,1849,1849,1849,1849,1849,MONDO:0001714,bejel,MONDO,disease,DISEASE_1849
1850,1850,1850,1850,1850,1850,1850,1850,MONDO:0018480,"carcinoma of esophagus, salivary gland type",MONDO,disease,DISEASE_1850
1851,1851,1851,1851,1851,1851,1851,1851,MONDO:0022654,cardiomyopathy hypogonadism collagenoma syndrome,MONDO,disease,DISEASE_1851
1852,1852,1852,1852,1852,1852,1852,1852,MONDO:0003525,pancreatic gastrin-producing neuroendocrine tumor,MONDO,disease,DISEASE_1852
1853,1853,1853,1853,1853,1853,1853,1853,MONDO:0019246,inborn disorder of lysosomal amino acid transport,MONDO,disease,DISEASE_1853
1854,1854,1854,1854,1854,1854,1854,1854,MONDO:0010916_MONDO:0054743_MONDO:0044327,polycystic kidney disease 3 with or without polycystic liver disease,MONDO_grouped,disease,DISEASE_1854
1855,1855,1855,1855,1855,1855,1855,1855,MONDO:0007211,brachydactyly-arterial hypertension syndrome,MONDO,disease,DISEASE_1855
1856,1856,1856,1856,1856,1856,1856,1856,MONDO:0021116,luminal A breast carcinoma,MONDO,disease,DISEASE_1856
1857,1857,1857,1857,1857,1857,1857,1857,MONDO:0032836,Weiss-Kruszka syndrome,MONDO,disease,DISEASE_1857
1858,1858,1858,1858,1858,1858,1858,1858,MONDO:0008589,"tremor of intention, ataxia, and lipofuscinosis",MONDO,disease,DISEASE_1858
1859,1859,1859,1859,1859,1859,1859,1859,MONDO:0016162_MONDO:0013907_MONDO:0017091,bilateral frontal polymicrogyria,MONDO_grouped,disease,DISEASE_1859
1860,1860,1860,1860,1860,1860,1860,1860,MONDO:0023573,Kozlowski Warren Fisher syndrome,MONDO,disease,DISEASE_1860
1861,1861,1861,1861,1861,1861,1861,1861,MONDO:0800501,developmental and/or epileptic encephalopathy with spike-wave activation in sleep,MONDO,disease,DISEASE_1861
1862,1862,1862,1862,1862,1862,1862,1862,MONDO:0005696,central nervous system tuberculosis,MONDO,disease,DISEASE_1862
1863,1863,1863,1863,1863,1863,1863,1863,MONDO:0044983,benign lipomatous neoplasm,MONDO,disease,DISEASE_1863
1864,1864,1864,1864,1864,1864,1864,1864,MONDO:0017615_MONDO:0019448_MONDO:0015637,benign familial infantile epilepsy,MONDO_grouped,disease,DISEASE_1864
1865,1865,1865,1865,1865,1865,1865,1865,MONDO:0011596_MONDO:0011597_MONDO:0011598_MONDO:0011608_MONDO:0011609_MONDO:0013107_MONDO:0013294_MONDO:0013295_MONDO:0100181_MONDO:1010743,"dermatitis, atopic",MONDO_grouped,disease,DISEASE_1865
1866,1866,1866,1866,1866,1866,1866,1866,MONDO:0024277_MONDO:0004877,neonatal thrombocytopenia,MONDO_grouped,disease,DISEASE_1866
1867,1867,1867,1867,1867,1867,1867,1867,MONDO:0006622,vulvar seborrheic keratosis,MONDO,disease,DISEASE_1867
1868,1868,1868,1868,1868,1868,1868,1868,MONDO:0859152,neurodevelopmental disorder with cerebellar atrophy and motor dysfunction,MONDO,disease,DISEASE_1868
1869,1869,1869,1869,1869,1869,1869,1869,MONDO:1010231,"Huntington disease, non-human animal",MONDO,disease,DISEASE_1869
1870,1870,1870,1870,1870,1870,1870,1870,MONDO:0007193_MONDO:0005388_MONDO:0013079_MONDO:0013080_MONDO:0013636_MONDO:0013637,primary biliary cholangitis,MONDO_grouped,disease,DISEASE_1870
1871,1871,1871,1871,1871,1871,1871,1871,MONDO:0043073,Zadik-Barak-Levin syndrome,MONDO,disease,DISEASE_1871
1872,1872,1872,1872,1872,1872,1872,1872,MONDO:0004229,acantholytic variant squamous cell breast carcinoma,MONDO,disease,DISEASE_1872
1873,1873,1873,1873,1873,1873,1873,1873,MONDO:0003905,"ovarian yolk sac tumor, glandular pattern",MONDO,disease,DISEASE_1873
1874,1874,1874,1874,1874,1874,1874,1874,MONDO:0021202,allergic otitis media,MONDO,disease,DISEASE_1874
1875,1875,1875,1875,1875,1875,1875,1875,MONDO:0021680_MONDO:0001316_MONDO:0001667_MONDO:0005972,streptococcal infection,MONDO_grouped,disease,DISEASE_1875
1876,1876,1876,1876,1876,1876,1876,1876,MONDO:0018354,Prader-Willi-like syndrome,MONDO,disease,DISEASE_1876
1877,1877,1877,1877,1877,1877,1877,1877,MONDO:0007799,hypophosphatemic bone disease,MONDO,disease,DISEASE_1877
1878,1878,1878,1878,1878,1878,1878,1878,MONDO:0022435,Mauriac syndrome,MONDO,disease,DISEASE_1878
1879,1879,1879,1879,1879,1879,1879,1879,MONDO:1010797,"Ehlers-Danlos syndrome, classic type, COL5A2-related, dog",MONDO,disease,DISEASE_1879
1880,1880,1880,1880,1880,1880,1880,1880,MONDO:0016874,partial deletion of chromosome 9,MONDO,disease,DISEASE_1880
1881,1881,1881,1881,1881,1881,1881,1881,MONDO:0975759,acquired elastotic haemangioma,MONDO,disease,DISEASE_1881
1882,1882,1882,1882,1882,1882,1882,1882,MONDO:0008580,"toes, space between first and second",MONDO,disease,DISEASE_1882
1883,1883,1883,1883,1883,1883,1883,1883,MONDO:0859082,"thrombophilia, X-linked, due to factor 8 defect",MONDO,disease,DISEASE_1883
1884,1884,1884,1884,1884,1884,1884,1884,MONDO:0008532,teeth present at birth,MONDO,disease,DISEASE_1884
1885,1885,1885,1885,1885,1885,1885,1885,MONDO:0007320,chondrocalcinosis due to apatite crystal deposition,MONDO,disease,DISEASE_1885
1886,1886,1886,1886,1886,1886,1886,1886,MONDO:0014449,congenital analbuminemia,MONDO,disease,DISEASE_1886
1887,1887,1887,1887,1887,1887,1887,1887,MONDO:0021167,myositis disease,MONDO,disease,DISEASE_1887
1888,1888,1888,1888,1888,1888,1888,1888,MONDO:0003023,aorta angiosarcoma,MONDO,disease,DISEASE_1888
1889,1889,1889,1889,1889,1889,1889,1889,MONDO:0019984,renal tubular dysgenesis due to twin-twin transfusion,MONDO,disease,DISEASE_1889
1890,1890,1890,1890,1890,1890,1890,1890,MONDO:0016837,16p13.11 microduplication syndrome,MONDO,disease,DISEASE_1890
1891,1891,1891,1891,1891,1891,1891,1891,MONDO:0015374_MONDO:0003346_MONDO:0100248,primary central nervous system vasculitis,MONDO_grouped,disease,DISEASE_1891
1892,1892,1892,1892,1892,1892,1892,1892,MONDO:0018713,retiform hemangioendothelioma,MONDO,disease,DISEASE_1892
1893,1893,1893,1893,1893,1893,1893,1893,MONDO:0008692,abetalipoproteinemia,MONDO,disease,DISEASE_1893
1894,1894,1894,1894,1894,1894,1894,1894,MONDO:0014262,Rienhoff syndrome,MONDO,disease,DISEASE_1894
1895,1895,1895,1895,1895,1895,1895,1895,MONDO:0007463,distal osteosclerosis,MONDO,disease,DISEASE_1895
1896,1896,1896,1896,1896,1896,1896,1896,MONDO:1011288,"night blindness, cattle",MONDO,disease,DISEASE_1896
1897,1897,1897,1897,1897,1897,1897,1897,MONDO:1012290,"chronic active hepatitis, dog",MONDO,disease,DISEASE_1897
1898,1898,1898,1898,1898,1898,1898,1898,MONDO:0009632,"microphthalmia with hyperopia, retinal degeneration, macrophakia, and dental anomalies",MONDO,disease,DISEASE_1898
1899,1899,1899,1899,1899,1899,1899,1899,MONDO:0018369,immature ovarian teratoma,MONDO,disease,DISEASE_1899
1900,1900,1900,1900,1900,1900,1900,1900,MONDO:0002232,nasal cavity disorder,MONDO,disease,DISEASE_1900
1901,1901,1901,1901,1901,1901,1901,1901,MONDO:0006254,intestinal type adenocarcinoma,MONDO,disease,DISEASE_1901
1902,1902,1902,1902,1902,1902,1902,1902,MONDO:0011719,gastrointestinal stromal tumor,MONDO,disease,DISEASE_1902
1903,1903,1903,1903,1903,1903,1903,1903,MONDO:0957545_MONDO:0014095_MONDO:0013147_MONDO:0030680_MONDO:0011094_MONDO:0011567_MONDO:0013848_MONDO:0013371_MONDO:0011425_MONDO:0012808_MONDO:0013198_MONDO:0013339_MONDO:0013373_MONDO:0014073_MONDO:0011095_MONDO:0971175_MONDO:0013211_MONDO:0030366_MONDO:0013261_MONDO:0011003_MONDO:0032592_MONDO:0010542_MONDO:0014396_MONDO:0013262_MONDO:0010951_MONDO:0011482_MONDO:0012364_MONDO:0011840_MONDO:0859358_MONDO:0012062_MONDO:0011400_MONDO:0030887_MONDO:0957984_MONDO:0013030_MONDO:0012704_MONDO:0014100_MONDO:0012667_MONDO:0007269_MONDO:0013168_MONDO:0012362_MONDO:0013479_MONDO:0011702_MONDO:0012745_MONDO:0012744_MONDO:0859381_MONDO:0011541_MONDO:0012746_MONDO:0030300_MONDO:1010448_MONDO:1010451_MONDO:1010452_MONDO:0800368_MONDO:0800367_MONDO:1010447_MONDO:1010450,"cardiomyopathy, dilated",MONDO_grouped,disease,DISEASE_1903
1904,1904,1904,1904,1904,1904,1904,1904,MONDO:0007911,"lipoprotein, variant of beta",MONDO,disease,DISEASE_1904
1905,1905,1905,1905,1905,1905,1905,1905,MONDO:1010533,"gingival hypertrophy, dog",MONDO,disease,DISEASE_1905
1906,1906,1906,1906,1906,1906,1906,1906,MONDO:0958265,idiopathic scleritis,MONDO,disease,DISEASE_1906
1907,1907,1907,1907,1907,1907,1907,1907,MONDO:0002981,peripheral primitive neuroectodermal tumor of bone,MONDO,disease,DISEASE_1907
1908,1908,1908,1908,1908,1908,1908,1908,MONDO:0019177,odontoleukodystrophy,MONDO,disease,DISEASE_1908
1909,1909,1909,1909,1909,1909,1909,1909,MONDO:0975957,"telangiectasia, impaired intellectual development, microcephaly, metaphyseal dysplasia, eye abnormalities, and short stature",MONDO,disease,DISEASE_1909
1910,1910,1910,1910,1910,1910,1910,1910,MONDO:0000811,anomalous left coronary artery from the pulmonary artery,MONDO,disease,DISEASE_1910
1911,1911,1911,1911,1911,1911,1911,1911,MONDO:0958164,poorly differentiated chordoma,MONDO,disease,DISEASE_1911
1912,1912,1912,1912,1912,1912,1912,1912,MONDO:0019976,dementia pugilistica,MONDO,disease,DISEASE_1912
1913,1913,1913,1913,1913,1913,1913,1913,MONDO:0009598,metaphyseal chondrodysplasia-retinitis pigmentosa syndrome,MONDO,disease,DISEASE_1913
1914,1914,1914,1914,1914,1914,1914,1914,MONDO:0800027_MONDO:0030634_MONDO:0030796,"leukoencephalopathy, diffuse hereditary, with spheroids",MONDO_grouped,disease,DISEASE_1914
1915,1915,1915,1915,1915,1915,1915,1915,MONDO:0008061,nail-patella syndrome,MONDO,disease,DISEASE_1915
1916,1916,1916,1916,1916,1916,1916,1916,MONDO:0011812,Duane-radial ray syndrome,MONDO,disease,DISEASE_1916
1917,1917,1917,1917,1917,1917,1917,1917,MONDO:0007864,angioosteohypertrophic syndrome,MONDO,disease,DISEASE_1917
1918,1918,1918,1918,1918,1918,1918,1918,MONDO:0011736,Cree intellectual disability syndrome,MONDO,disease,DISEASE_1918
1919,1919,1919,1919,1919,1919,1919,1919,MONDO:0010397,severe neonatal-onset encephalopathy with microcephaly,MONDO,disease,DISEASE_1919
1920,1920,1920,1920,1920,1920,1920,1920,MONDO:0100501,body-stalk anomaly,MONDO,disease,DISEASE_1920
1921,1921,1921,1921,1921,1921,1921,1921,MONDO:0019883,distal trisomy 9q,MONDO,disease,DISEASE_1921
1922,1922,1922,1922,1922,1922,1922,1922,MONDO:0957563,"cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay",MONDO,disease,DISEASE_1922
1923,1923,1923,1923,1923,1923,1923,1923,MONDO:0036501,refractory malignant neoplasm,MONDO,disease,DISEASE_1923
1924,1924,1924,1924,1924,1924,1924,1924,MONDO:0024685,Philadelphia-positive myelogenous leukemia,MONDO,disease,DISEASE_1924
1925,1925,1925,1925,1925,1925,1925,1925,MONDO:0001272,functional diarrhea,MONDO,disease,DISEASE_1925
1926,1926,1926,1926,1926,1926,1926,1926,MONDO:0002889,orbital cancer,MONDO,disease,DISEASE_1926
1927,1927,1927,1927,1927,1927,1927,1927,MONDO:0003133,exudative glomerulonephritis,MONDO,disease,DISEASE_1927
1928,1928,1928,1928,1928,1928,1928,1928,MONDO:0018656,tremor-ataxia-central hypomyelination syndrome,MONDO,disease,DISEASE_1928
1929,1929,1929,1929,1929,1929,1929,1929,MONDO:0011289,apraxia of eyelid opening,MONDO,disease,DISEASE_1929
1930,1930,1930,1930,1930,1930,1930,1930,MONDO:0002953,skin infiltrative basal cell carcinoma,MONDO,disease,DISEASE_1930
1931,1931,1931,1931,1931,1931,1931,1931,MONDO:0032741,neurodevelopmental disorder with impaired speech and hyperkinetic movements,MONDO,disease,DISEASE_1931
1932,1932,1932,1932,1932,1932,1932,1932,MONDO:0000750,dental abscess,MONDO,disease,DISEASE_1932
1933,1933,1933,1933,1933,1933,1933,1933,MONDO:0002664,extrahepatic bile duct signet ring cell carcinoma,MONDO,disease,DISEASE_1933
1934,1934,1934,1934,1934,1934,1934,1934,MONDO:0002209,heel spur,MONDO,disease,DISEASE_1934
1935,1935,1935,1935,1935,1935,1935,1935,MONDO:0006784,hemorrhagic disease of newborn,MONDO,disease,DISEASE_1935
1936,1936,1936,1936,1936,1936,1936,1936,MONDO:0015157,human herpesvirus 8-related tumor,MONDO,disease,DISEASE_1936
1937,1937,1937,1937,1937,1937,1937,1937,MONDO:0007676,glutathione transferase activity toward trans-stilbene oxide,MONDO,disease,DISEASE_1937
1938,1938,1938,1938,1938,1938,1938,1938,MONDO:0013116,congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome,MONDO,disease,DISEASE_1938
1939,1939,1939,1939,1939,1939,1939,1939,MONDO:0020393,discrete fibromuscular subaortic stenosis,MONDO,disease,DISEASE_1939
1940,1940,1940,1940,1940,1940,1940,1940,MONDO:0004331,bladder urachal adenocarcinoma,MONDO,disease,DISEASE_1940
1941,1941,1941,1941,1941,1941,1941,1941,MONDO:0007431,dens in dente and palatal invaginations,MONDO,disease,DISEASE_1941
1942,1942,1942,1942,1942,1942,1942,1942,MONDO:0002409_MONDO:0021944,auditory system disorder,MONDO_grouped,disease,DISEASE_1942
1943,1943,1943,1943,1943,1943,1943,1943,MONDO:0030835,"developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy",MONDO,disease,DISEASE_1943
1944,1944,1944,1944,1944,1944,1944,1944,MONDO:0054813_MONDO:0971044,"Ehlers-Danlos syndrome, classic-like",MONDO_grouped,disease,DISEASE_1944
1945,1945,1945,1945,1945,1945,1945,1945,MONDO:0019623,hereditary angioedema,MONDO,disease,DISEASE_1945
1946,1946,1946,1946,1946,1946,1946,1946,MONDO:0971108,common arterial trunk with pulmonary dominance and interrupted aortic arch,MONDO,disease,DISEASE_1946
1947,1947,1947,1947,1947,1947,1947,1947,MONDO:0009918,"fundus dystrophy, pseudoinflammatory, recessive form",MONDO,disease,DISEASE_1947
1948,1948,1948,1948,1948,1948,1948,1948,MONDO:0008632,"urticaria, aquagenic",MONDO,disease,DISEASE_1948
1949,1949,1949,1949,1949,1949,1949,1949,MONDO:0010591,fingerprint body myopathy,MONDO,disease,DISEASE_1949
1950,1950,1950,1950,1950,1950,1950,1950,MONDO:0957464,primary cutaneous tuberculosis,MONDO,disease,DISEASE_1950
1951,1951,1951,1951,1951,1951,1951,1951,MONDO:0100065,TH-deficient infantile parkinsonism and motor delay,MONDO,disease,DISEASE_1951
1952,1952,1952,1952,1952,1952,1952,1952,MONDO:0020697,lung epithelial-myoepithelial carcinoma,MONDO,disease,DISEASE_1952
1953,1953,1953,1953,1953,1953,1953,1953,MONDO:0006304,minor salivary gland adenocarcinoma,MONDO,disease,DISEASE_1953
1954,1954,1954,1954,1954,1954,1954,1954,MONDO:1010906_MONDO:1010907_MONDO:1012182,"central core myopathy, dog",MONDO_grouped,disease,DISEASE_1954
1955,1955,1955,1955,1955,1955,1955,1955,MONDO:0024656,colorectal lymphoma,MONDO,disease,DISEASE_1955
1956,1956,1956,1956,1956,1956,1956,1956,MONDO:0015806_MONDO:0015805,adult intestinal botulism,MONDO_grouped,disease,DISEASE_1956
1957,1957,1957,1957,1957,1957,1957,1957,MONDO:0800474,SOX3-related X-linked pituitary hormone deficiency with or without intellectual developmental disorder,MONDO,disease,DISEASE_1957
1958,1958,1958,1958,1958,1958,1958,1958,MONDO:0006452,thymic sarcomatoid carcinoma,MONDO,disease,DISEASE_1958
1959,1959,1959,1959,1959,1959,1959,1959,MONDO:0016249,hereditary site-specific ovarian cancer syndrome,MONDO,disease,DISEASE_1959
1960,1960,1960,1960,1960,1960,1960,1960,MONDO:0008239,phosphoglucomutase 4,MONDO,disease,DISEASE_1960
1961,1961,1961,1961,1961,1961,1961,1961,MONDO:0014522,retinal dystrophy and obesity,MONDO,disease,DISEASE_1961
1962,1962,1962,1962,1962,1962,1962,1962,MONDO:1011717,"pulmonary hypoplasia with anasarca, non-human animal",MONDO,disease,DISEASE_1962
1963,1963,1963,1963,1963,1963,1963,1963,MONDO:0018515,squamous cell carcinoma of rectum,MONDO,disease,DISEASE_1963
1964,1964,1964,1964,1964,1964,1964,1964,MONDO:0019622,non-specific interstitial pneumonia,MONDO,disease,DISEASE_1964
1965,1965,1965,1965,1965,1965,1965,1965,MONDO:0004555,kidney angiomyolipoma,MONDO,disease,DISEASE_1965
1966,1966,1966,1966,1966,1966,1966,1966,MONDO:0017231,erythropoietic uroporphyria associated with myeloid malignancy,MONDO,disease,DISEASE_1966
1967,1967,1967,1967,1967,1967,1967,1967,MONDO:0009226_MONDO:0013795_MONDO:0016068,fibrochondrogenesis,MONDO_grouped,disease,DISEASE_1967
1968,1968,1968,1968,1968,1968,1968,1968,MONDO:0000648,nervous system benign neoplasm,MONDO,disease,DISEASE_1968
1969,1969,1969,1969,1969,1969,1969,1969,MONDO:0006262,lacrimal gland adenoid cystic carcinoma,MONDO,disease,DISEASE_1969
1970,1970,1970,1970,1970,1970,1970,1970,MONDO:0000618,Her2-receptor negative breast cancer,MONDO,disease,DISEASE_1970
1971,1971,1971,1971,1971,1971,1971,1971,MONDO:0032591,"hyperparathyroidism, transient neonatal",MONDO,disease,DISEASE_1971
1972,1972,1972,1972,1972,1972,1972,1972,MONDO:0054695,"myopathy, centronuclear, 6, with fiber-type disproportion",MONDO,disease,DISEASE_1972
1973,1973,1973,1973,1973,1973,1973,1973,MONDO:0012508,agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome,MONDO,disease,DISEASE_1973
1974,1974,1974,1974,1974,1974,1974,1974,MONDO:0002327,intracranial cavernous angioma,MONDO,disease,DISEASE_1974
1975,1975,1975,1975,1975,1975,1975,1975,MONDO:0003244,central nervous system mesenchymal non-meningothelial tumor,MONDO,disease,DISEASE_1975
1976,1976,1976,1976,1976,1976,1976,1976,MONDO:0011240,megalencephaly-capillary malformation-polymicrogyria syndrome,MONDO,disease,DISEASE_1976
1977,1977,1977,1977,1977,1977,1977,1977,MONDO:0003280,swayback,MONDO,disease,DISEASE_1977
1978,1978,1978,1978,1978,1978,1978,1978,MONDO:0002535,verrucous papilloma,MONDO,disease,DISEASE_1978
1979,1979,1979,1979,1979,1979,1979,1979,MONDO:0957281,"nemaline myopathy 5B, autosomal recessive, childhood-onset",MONDO,disease,DISEASE_1979
1980,1980,1980,1980,1980,1980,1980,1980,MONDO:1011714,"hypocatalasia, non-human animal",MONDO,disease,DISEASE_1980
1981,1981,1981,1981,1981,1981,1981,1981,MONDO:0007534,Beckwith-Wiedemann syndrome,MONDO,disease,DISEASE_1981
1982,1982,1982,1982,1982,1982,1982,1982,MONDO:0008978,chordoma,MONDO,disease,DISEASE_1982
1983,1983,1983,1983,1983,1983,1983,1983,MONDO:0018854,acquired purpura fulminans,MONDO,disease,DISEASE_1983
1984,1984,1984,1984,1984,1984,1984,1984,MONDO:0035882,chronic intervillositis of unknown etiology,MONDO,disease,DISEASE_1984
1985,1985,1985,1985,1985,1985,1985,1985,MONDO:1011343,"perceptual disorders, non-human animal",MONDO,disease,DISEASE_1985
1986,1986,1986,1986,1986,1986,1986,1986,MONDO:0020283_MONDO:0002661_MONDO:0017255,uveitis,MONDO_grouped,disease,DISEASE_1986
1987,1987,1987,1987,1987,1987,1987,1987,MONDO:1011411,"Von Willebrand disease, non-human animal",MONDO,disease,DISEASE_1987
1988,1988,1988,1988,1988,1988,1988,1988,MONDO:0012253,"multiple epiphyseal dysplasia, with severe proximal femoral dysplasia",MONDO,disease,DISEASE_1988
1989,1989,1989,1989,1989,1989,1989,1989,MONDO:0005489,dyslexia,MONDO,disease,DISEASE_1989
1990,1990,1990,1990,1990,1990,1990,1990,MONDO:0016332,hypertrophic cardiomyopathy due to intensive athletic training,MONDO,disease,DISEASE_1990
1991,1991,1991,1991,1991,1991,1991,1991,MONDO:0003289,deep leiomyoma,MONDO,disease,DISEASE_1991
1992,1992,1992,1992,1992,1992,1992,1992,MONDO:0015830_MONDO:0015831,partial bilateral aplasia of the mullerian ducts,MONDO_grouped,disease,DISEASE_1992
1993,1993,1993,1993,1993,1993,1993,1993,MONDO:0016545,leukoencephalopathy-palmoplantar keratoderma syndrome,MONDO,disease,DISEASE_1993
1994,1994,1994,1994,1994,1994,1994,1994,MONDO:0004486_MONDO:0004538,endocervical type cervical adenomyoma,MONDO_grouped,disease,DISEASE_1994
1995,1995,1995,1995,1995,1995,1995,1995,MONDO:1010882,"GM2 gangliosidosis, springbok",MONDO,disease,DISEASE_1995
1996,1996,1996,1996,1996,1996,1996,1996,MONDO:0004719,hard palate cancer,MONDO,disease,DISEASE_1996
1997,1997,1997,1997,1997,1997,1997,1997,MONDO:0021476,benign neoplasm of tongue,MONDO,disease,DISEASE_1997
1998,1998,1998,1998,1998,1998,1998,1998,MONDO:0971103,Nicolau syndrome,MONDO,disease,DISEASE_1998
1999,1999,1999,1999,1999,1999,1999,1999,MONDO:0034991,intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome,MONDO,disease,DISEASE_1999
2000,2000,2000,2000,2000,2000,2000,2000,MONDO:0001118,Queensland tick typhus,MONDO,disease,DISEASE_2000
2001,2001,2001,2001,2001,2001,2001,2001,MONDO:0010010,Schinzel-Giedion syndrome,MONDO,disease,DISEASE_2001
2002,2002,2002,2002,2002,2002,2002,2002,MONDO:0007473,Duane retraction syndrome,MONDO,disease,DISEASE_2002
2003,2003,2003,2003,2003,2003,2003,2003,MONDO:0009014_MONDO:0000733,cornea plana 2,MONDO_grouped,disease,DISEASE_2003
2004,2004,2004,2004,2004,2004,2004,2004,MONDO:0002174,preretinal fibrosis,MONDO,disease,DISEASE_2004
2005,2005,2005,2005,2005,2005,2005,2005,MONDO:0800458,NR2F2 related multiple congenital anomalies/dysmorphic syndrome,MONDO,disease,DISEASE_2005
2006,2006,2006,2006,2006,2006,2006,2006,MONDO:0042912,Schlegelberger-Grote syndrome,MONDO,disease,DISEASE_2006
2007,2007,2007,2007,2007,2007,2007,2007,MONDO:0001066_MONDO:0001067,late yaws,MONDO_grouped,disease,DISEASE_2007
2008,2008,2008,2008,2008,2008,2008,2008,MONDO:0045012_MONDO:0019256,steroid metabolism disease,MONDO_grouped,disease,DISEASE_2008
2009,2009,2009,2009,2009,2009,2009,2009,MONDO:0010097,Tatsumi factor deficiency,MONDO,disease,DISEASE_2009
2010,2010,2010,2010,2010,2010,2010,2010,MONDO:0008812,AREDYLD syndrome,MONDO,disease,DISEASE_2010
2011,2011,2011,2011,2011,2011,2011,2011,MONDO:0003362_MONDO:0003600,cutaneous leiomyosarcoma,MONDO_grouped,disease,DISEASE_2011
2012,2012,2012,2012,2012,2012,2012,2012,MONDO:0006987_MONDO:1010426_MONDO:1010480,subvalvular aortic stenosis,MONDO_grouped,disease,DISEASE_2012
2013,2013,2013,2013,2013,2013,2013,2013,MONDO:0007093,hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism,MONDO,disease,DISEASE_2013
2014,2014,2014,2014,2014,2014,2014,2014,MONDO:0020088,familial partial lipodystrophy,MONDO,disease,DISEASE_2014
2015,2015,2015,2015,2015,2015,2015,2015,MONDO:0023227,gestational diabetes insipidus,MONDO,disease,DISEASE_2015
2016,2016,2016,2016,2016,2016,2016,2016,MONDO:0022745,mixed dust pneumoconiosis,MONDO,disease,DISEASE_2016
2017,2017,2017,2017,2017,2017,2017,2017,MONDO:1012484,"hoof wall separation syndrome, horse",MONDO,disease,DISEASE_2017
2018,2018,2018,2018,2018,2018,2018,2018,MONDO:0044014,postpartum thyroiditis,MONDO,disease,DISEASE_2018
2019,2019,2019,2019,2019,2019,2019,2019,MONDO:0008201,Perry syndrome,MONDO,disease,DISEASE_2019
2020,2020,2020,2020,2020,2020,2020,2020,MONDO:0100160,alcoholic ketoacidosis,MONDO,disease,DISEASE_2020
2021,2021,2021,2021,2021,2021,2021,2021,MONDO:0001252,Plummer disease,MONDO,disease,DISEASE_2021
2022,2022,2022,2022,2022,2022,2022,2022,MONDO:0016016,toluene embryopathy,MONDO,disease,DISEASE_2022
2023,2023,2023,2023,2023,2023,2023,2023,MONDO:0004700,parotid gland cancer,MONDO,disease,DISEASE_2023
2024,2024,2024,2024,2024,2024,2024,2024,MONDO:0003301,dartoic leiomyoma,MONDO,disease,DISEASE_2024
2025,2025,2025,2025,2025,2025,2025,2025,MONDO:0004732,kidney carcinoma in situ,MONDO,disease,DISEASE_2025
2026,2026,2026,2026,2026,2026,2026,2026,MONDO:0003822,non-invasive bladder papillary urothelial neoplasm,MONDO,disease,DISEASE_2026
2027,2027,2027,2027,2027,2027,2027,2027,MONDO:0850223,Libman-Sacks endocarditis,MONDO,disease,DISEASE_2027
2028,2028,2028,2028,2028,2028,2028,2028,MONDO:0009703,myopathy with abnormal lipid metabolism,MONDO,disease,DISEASE_2028
2029,2029,2029,2029,2029,2029,2029,2029,MONDO:0007901,levator-medial rectus synkinesis,MONDO,disease,DISEASE_2029
2030,2030,2030,2030,2030,2030,2030,2030,MONDO:0850130,gastroesophageal adenocarcinoma,MONDO,disease,DISEASE_2030
2031,2031,2031,2031,2031,2031,2031,2031,MONDO:0009381_MONDO:1012609_MONDO:1012611,"hyperbilirubinemia, conjugated,",MONDO_grouped,disease,DISEASE_2031
2032,2032,2032,2032,2032,2032,2032,2032,MONDO:0011313_MONDO:0014408_MONDO:0014407,megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome,MONDO_grouped,disease,DISEASE_2032
2033,2033,2033,2033,2033,2033,2033,2033,MONDO:0017389,tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria,MONDO,disease,DISEASE_2033
2034,2034,2034,2034,2034,2034,2034,2034,MONDO:0020467,mosaic monosomy X,MONDO,disease,DISEASE_2034
2035,2035,2035,2035,2035,2035,2035,2035,MONDO:0022812,complement receptor deficiency,MONDO,disease,DISEASE_2035
2036,2036,2036,2036,2036,2036,2036,2036,MONDO:0006685,brain hypoxia - ischemia,MONDO,disease,DISEASE_2036
2037,2037,2037,2037,2037,2037,2037,2037,MONDO:0019436,psoriasis-related juvenile idiopathic arthritis,MONDO,disease,DISEASE_2037
2038,2038,2038,2038,2038,2038,2038,2038,MONDO:0025459,rinderpest,MONDO,disease,DISEASE_2038
2039,2039,2039,2039,2039,2039,2039,2039,MONDO:1010036,"frontonasal dysplasia, non-human animal",MONDO,disease,DISEASE_2039
2040,2040,2040,2040,2040,2040,2040,2040,MONDO:0010129,thymic-renal-anal-lung dysplasia,MONDO,disease,DISEASE_2040
2041,2041,2041,2041,2041,2041,2041,2041,MONDO:0700158,canine pancreatic carcinoma,MONDO,disease,DISEASE_2041
2042,2042,2042,2042,2042,2042,2042,2042,MONDO:0004047,sphenoidal sinus neoplasm,MONDO,disease,DISEASE_2042
2043,2043,2043,2043,2043,2043,2043,2043,MONDO:0006834,lip cancer,MONDO,disease,DISEASE_2043
2044,2044,2044,2044,2044,2044,2044,2044,MONDO:0019633,relapsing fever,MONDO,disease,DISEASE_2044
2045,2045,2045,2045,2045,2045,2045,2045,MONDO:0017449,split hand,MONDO,disease,DISEASE_2045
2046,2046,2046,2046,2046,2046,2046,2046,MONDO:0017399,"frontotemporal dementia, right temporal atrophy variant",MONDO,disease,DISEASE_2046
2047,2047,2047,2047,2047,2047,2047,2047,MONDO:0023250,global disaccharide intolerance,MONDO,disease,DISEASE_2047
2048,2048,2048,2048,2048,2048,2048,2048,MONDO:0008609,Tristichiasis,MONDO,disease,DISEASE_2048
2049,2049,2049,2049,2049,2049,2049,2049,MONDO:0014200,aldosterone-producing adenoma with seizures and neurological abnormalities,MONDO,disease,DISEASE_2049
2050,2050,2050,2050,2050,2050,2050,2050,MONDO:0041086,mixed anxiety and depressive disorder,MONDO,disease,DISEASE_2050
2051,2051,2051,2051,2051,2051,2051,2051,MONDO:0008673,"acrofacial dysostosis, Weyers type",MONDO,disease,DISEASE_2051
2052,2052,2052,2052,2052,2052,2052,2052,MONDO:1010756_MONDO:1010786_MONDO:1010787_MONDO:1012712_MONDO:1012786_MONDO:1012893,"ichthyosis TGM1-related, dog",MONDO_grouped,disease,DISEASE_2052
2053,2053,2053,2053,2053,2053,2053,2053,MONDO:0000702,microscopic colitis,MONDO,disease,DISEASE_2053
2054,2054,2054,2054,2054,2054,2054,2054,MONDO:1011210,"GAPO syndrome, pig",MONDO,disease,DISEASE_2054
2055,2055,2055,2055,2055,2055,2055,2055,MONDO:0016846,distal 22q11.2 microduplication syndrome,MONDO,disease,DISEASE_2055
2056,2056,2056,2056,2056,2056,2056,2056,MONDO:0037251_MONDO:0001367,congestive splenomegaly,MONDO_grouped,disease,DISEASE_2056
2057,2057,2057,2057,2057,2057,2057,2057,MONDO:1010898,"sphingomyelinase deficiency, cattle",MONDO,disease,DISEASE_2057
2058,2058,2058,2058,2058,2058,2058,2058,MONDO:0001446,low compliance bladder,MONDO,disease,DISEASE_2058
2059,2059,2059,2059,2059,2059,2059,2059,MONDO:0009625_MONDO:0020762_MONDO:0017868,diencephalic-mesencephalic junction dysplasia syndrome,MONDO_grouped,disease,DISEASE_2059
2060,2060,2060,2060,2060,2060,2060,2060,MONDO:0017628,myospherulosis,MONDO,disease,DISEASE_2060
2061,2061,2061,2061,2061,2061,2061,2061,MONDO:1012576,"hypohidrotic ectodermal dysplasia, non-human animal",MONDO,disease,DISEASE_2061
2062,2062,2062,2062,2062,2062,2062,2062,MONDO:0018942,macrophagic myofasciitis,MONDO,disease,DISEASE_2062
2063,2063,2063,2063,2063,2063,2063,2063,MONDO:0005912,phencyclidine abuse,MONDO,disease,DISEASE_2063
2064,2064,2064,2064,2064,2064,2064,2064,MONDO:0016204,idiopathic copper-associated cirrhosis,MONDO,disease,DISEASE_2064
2065,2065,2065,2065,2065,2065,2065,2065,MONDO:0005103,well-differentiated liposarcoma,MONDO,disease,DISEASE_2065
2066,2066,2066,2066,2066,2066,2066,2066,MONDO:0020401,congenital unguarded mitral orifice,MONDO,disease,DISEASE_2066
2067,2067,2067,2067,2067,2067,2067,2067,MONDO:0012386,trichoscyphodysplasia,MONDO,disease,DISEASE_2067
2068,2068,2068,2068,2068,2068,2068,2068,MONDO:0043172,pfeiffer rockelein syndrome,MONDO,disease,DISEASE_2068
2069,2069,2069,2069,2069,2069,2069,2069,MONDO:0956975_MONDO:0956976,T2-high asthma,MONDO_grouped,disease,DISEASE_2069
2070,2070,2070,2070,2070,2070,2070,2070,MONDO:0008361,"radius, aplasia of, with cleft lip/palate",MONDO,disease,DISEASE_2070
2071,2071,2071,2071,2071,2071,2071,2071,MONDO:0009306,combined immunodeficiency with skin granulomas,MONDO,disease,DISEASE_2071
2072,2072,2072,2072,2072,2072,2072,2072,MONDO:0850110,melanoma in congenital melanocytic nevus,MONDO,disease,DISEASE_2072
2073,2073,2073,2073,2073,2073,2073,2073,MONDO:0014185,chromosome 3q13.31 deletion syndrome,MONDO,disease,DISEASE_2073
2074,2074,2074,2074,2074,2074,2074,2074,MONDO:0013069,"autosomal recessive optic atrophy, OPA7 type",MONDO,disease,DISEASE_2074
2075,2075,2075,2075,2075,2075,2075,2075,MONDO:0017918,white matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome,MONDO,disease,DISEASE_2075
2076,2076,2076,2076,2076,2076,2076,2076,MONDO:0850015,selective intrauterine growth restriction,MONDO,disease,DISEASE_2076
2077,2077,2077,2077,2077,2077,2077,2077,MONDO:0015326,night blindness-skeletal anomalies-dysmorphism syndrome,MONDO,disease,DISEASE_2077
2078,2078,2078,2078,2078,2078,2078,2078,MONDO:0008065,"nasal groove, familial transverse",MONDO,disease,DISEASE_2078
2079,2079,2079,2079,2079,2079,2079,2079,MONDO:0008991,Verloove Vanhorick-Brubakk syndrome,MONDO,disease,DISEASE_2079
2080,2080,2080,2080,2080,2080,2080,2080,MONDO:0009516,absence deformity of leg-cataract syndrome,MONDO,disease,DISEASE_2080
2081,2081,2081,2081,2081,2081,2081,2081,MONDO:0019532_MONDO:0016450,"autoimmune hemolytic anemia, warm type",MONDO_grouped,disease,DISEASE_2081
2082,2082,2082,2082,2082,2082,2082,2082,MONDO:1010330,"keratitis, non-human animal",MONDO,disease,DISEASE_2082
2083,2083,2083,2083,2083,2083,2083,2083,MONDO:0019340_MONDO:1010735,scleroderma,MONDO_grouped,disease,DISEASE_2083
2084,2084,2084,2084,2084,2084,2084,2084,MONDO:0024575,pregnancy disorder,MONDO,disease,DISEASE_2084
2085,2085,2085,2085,2085,2085,2085,2085,MONDO:0016905,partial deletion of the long arm of chromosome 6,MONDO,disease,DISEASE_2085
2086,2086,2086,2086,2086,2086,2086,2086,MONDO:0006841,lymphangioendothelioma,MONDO,disease,DISEASE_2086
2087,2087,2087,2087,2087,2087,2087,2087,MONDO:0016966,partial trisomy of the long arm of chromosome 16,MONDO,disease,DISEASE_2087
2088,2088,2088,2088,2088,2088,2088,2088,MONDO:1010046,"patent urachus, non-human animal",MONDO,disease,DISEASE_2088
2089,2089,2089,2089,2089,2089,2089,2089,MONDO:0009899,"polyhydramnios, chronic idiopathic",MONDO,disease,DISEASE_2089
2090,2090,2090,2090,2090,2090,2090,2090,MONDO:0100345,lactose intolerance,MONDO,disease,DISEASE_2090
2091,2091,2091,2091,2091,2091,2091,2091,MONDO:1012623,"X-linked canine shaking pup, PLP1-related, dog",MONDO,disease,DISEASE_2091
2092,2092,2092,2092,2092,2092,2092,2092,MONDO:0001862,malignant visceral pleura tumor,MONDO,disease,DISEASE_2092
2093,2093,2093,2093,2093,2093,2093,2093,MONDO:0004817,non-secretory plasma cell myeloma,MONDO,disease,DISEASE_2093
2094,2094,2094,2094,2094,2094,2094,2094,MONDO:0003973_MONDO:0004541,tubular variant testicular seminoma,MONDO_grouped,disease,DISEASE_2094
2095,2095,2095,2095,2095,2095,2095,2095,MONDO:0013692,BAP1-related tumor predisposition syndrome,MONDO,disease,DISEASE_2095
2096,2096,2096,2096,2096,2096,2096,2096,MONDO:0019939,early-onset schizophrenia,MONDO,disease,DISEASE_2096
2097,2097,2097,2097,2097,2097,2097,2097,MONDO:0000540,small intestinal neuroendocrine tumor G1,MONDO,disease,DISEASE_2097
2098,2098,2098,2098,2098,2098,2098,2098,MONDO:0010596,"membranoproliferative glomerulonephritis, X-linked",MONDO,disease,DISEASE_2098
2099,2099,2099,2099,2099,2099,2099,2099,MONDO:0014131,hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome,MONDO,disease,DISEASE_2099
2100,2100,2100,2100,2100,2100,2100,2100,MONDO:1010215,"familial adenomatous polyposis, non-human animal",MONDO,disease,DISEASE_2100
2101,2101,2101,2101,2101,2101,2101,2101,MONDO:1012258,"spinal dysplasia, domestic cat",MONDO,disease,DISEASE_2101
2102,2102,2102,2102,2102,2102,2102,2102,MONDO:0005925,pneumonic pasteurellosis,MONDO,disease,DISEASE_2102
2103,2103,2103,2103,2103,2103,2103,2103,MONDO:0008795,aniridia-cerebellar ataxia-intellectual disability syndrome,MONDO,disease,DISEASE_2103
2104,2104,2104,2104,2104,2104,2104,2104,MONDO:0008934,cerebellar ataxia-ectodermal dysplasia syndrome,MONDO,disease,DISEASE_2104
2105,2105,2105,2105,2105,2105,2105,2105,MONDO:0001341,selective IgA deficiency disease,MONDO,disease,DISEASE_2105
2106,2106,2106,2106,2106,2106,2106,2106,MONDO:0012548,Kostmann syndrome,MONDO,disease,DISEASE_2106
2107,2107,2107,2107,2107,2107,2107,2107,MONDO:0008586,esophageal atresia/tracheoesophageal fistula,MONDO,disease,DISEASE_2107
2108,2108,2108,2108,2108,2108,2108,2108,MONDO:0010187_MONDO:0011837,"vitamin K-dependent clotting factors, combined deficiency of,",MONDO_grouped,disease,DISEASE_2108
2109,2109,2109,2109,2109,2109,2109,2109,MONDO:0007539,"encephalopathy, recurrent, of childhood",MONDO,disease,DISEASE_2109
2110,2110,2110,2110,2110,2110,2110,2110,MONDO:1010133,"acrodermatitis enteropathica, non-human animal",MONDO,disease,DISEASE_2110
2111,2111,2111,2111,2111,2111,2111,2111,MONDO:0009835,subacute sclerosing panencephalitis,MONDO,disease,DISEASE_2111
2112,2112,2112,2112,2112,2112,2112,2112,MONDO:0022330,4-hydroxyphenylacetic aciduria,MONDO,disease,DISEASE_2112
2113,2113,2113,2113,2113,2113,2113,2113,MONDO:1011011,"Horner syndrome, horse",MONDO,disease,DISEASE_2113
2114,2114,2114,2114,2114,2114,2114,2114,MONDO:0700057,neurological pain disorder,MONDO,disease,DISEASE_2114
2115,2115,2115,2115,2115,2115,2115,2115,MONDO:0011796,"epilepsy, partial, with pericentral spikes",MONDO,disease,DISEASE_2115
2116,2116,2116,2116,2116,2116,2116,2116,MONDO:1011459,"ligneous membranitis, non-human animal",MONDO,disease,DISEASE_2116
2117,2117,2117,2117,2117,2117,2117,2117,MONDO:0013886,cerebellar dysfunction with variable cognitive and behavioral abnormalities,MONDO,disease,DISEASE_2117
2118,2118,2118,2118,2118,2118,2118,2118,MONDO:0010889,arterial dissection-lentiginosis syndrome,MONDO,disease,DISEASE_2118
2119,2119,2119,2119,2119,2119,2119,2119,MONDO:0019458,acute basophilic leukemia,MONDO,disease,DISEASE_2119
2120,2120,2120,2120,2120,2120,2120,2120,MONDO:0013969_MONDO:0014684_MONDO:0014728_MONDO:0013977_MONDO:0014547_MONDO:0014397_MONDO:0014525_MONDO:0012510_MONDO:0013986_MONDO:0013987_MONDO:0014190_MONDO:0013306_MONDO:0012534_MONDO:0014398_MONDO:0014636_MONDO:0013811_MONDO:0014856_MONDO:0013570,combined oxidative phosphorylation defect,MONDO_grouped,disease,DISEASE_2120
2121,2121,2121,2121,2121,2121,2121,2121,MONDO:0002277,arteriosclerosis disorder,MONDO,disease,DISEASE_2121
2122,2122,2122,2122,2122,2122,2122,2122,MONDO:0015441,ring chromosome 7,MONDO,disease,DISEASE_2122
2123,2123,2123,2123,2123,2123,2123,2123,MONDO:0003699,phobic disorder,MONDO,disease,DISEASE_2123
2124,2124,2124,2124,2124,2124,2124,2124,MONDO:0019786,severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia,MONDO,disease,DISEASE_2124
2125,2125,2125,2125,2125,2125,2125,2125,MONDO:0020413,encircling double aortic arch,MONDO,disease,DISEASE_2125
2126,2126,2126,2126,2126,2126,2126,2126,MONDO:0004053,bartholin gland squamous cell carcinoma,MONDO,disease,DISEASE_2126
2127,2127,2127,2127,2127,2127,2127,2127,MONDO:0000489,diabetic encephalopathy,MONDO,disease,DISEASE_2127
2128,2128,2128,2128,2128,2128,2128,2128,MONDO:0005318,canker sore,MONDO,disease,DISEASE_2128
2129,2129,2129,2129,2129,2129,2129,2129,MONDO:1012207_MONDO:1012208_MONDO:1012209_MONDO:1012210_MONDO:1012211,"perosomus elumbis, dog",MONDO_grouped,disease,DISEASE_2129
2130,2130,2130,2130,2130,2130,2130,2130,MONDO:0000652,integumentary system benign neoplasm,MONDO,disease,DISEASE_2130
2131,2131,2131,2131,2131,2131,2131,2131,MONDO:0005776,gnathomiasis,MONDO,disease,DISEASE_2131
2132,2132,2132,2132,2132,2132,2132,2132,MONDO:0000467_MONDO:0000468_MONDO:0000466,second-degree atrioventricular block,MONDO_grouped,disease,DISEASE_2132
2133,2133,2133,2133,2133,2133,2133,2133,MONDO:0013982_MONDO:0013983_MONDO:0009147,"ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant",MONDO_grouped,disease,DISEASE_2133
2134,2134,2134,2134,2134,2134,2134,2134,MONDO:0100053,anaphylaxis,MONDO,disease,DISEASE_2134
2135,2135,2135,2135,2135,2135,2135,2135,MONDO:0045016,cholesterol catabolic process disease,MONDO,disease,DISEASE_2135
2136,2136,2136,2136,2136,2136,2136,2136,MONDO:0049221,"myopia 26, X-linked, female-limited",MONDO,disease,DISEASE_2136
2137,2137,2137,2137,2137,2137,2137,2137,MONDO:0006330,ossifying fibromyxoid tumor,MONDO,disease,DISEASE_2137
2138,2138,2138,2138,2138,2138,2138,2138,MONDO:0971172,"neurodevelopmental disorder with hypotonia, brain anomalies, distinctive facies, and absent language",MONDO,disease,DISEASE_2138
2139,2139,2139,2139,2139,2139,2139,2139,MONDO:0000519,corpus callosum oligodendroglioma,MONDO,disease,DISEASE_2139
2140,2140,2140,2140,2140,2140,2140,2140,MONDO:0020662,borderline ovarian serous tumor,MONDO,disease,DISEASE_2140
2141,2141,2141,2141,2141,2141,2141,2141,MONDO:0858967,"primary intracranial sarcoma, DICER1-mutant",MONDO,disease,DISEASE_2141
2142,2142,2142,2142,2142,2142,2142,2142,MONDO:0013320,chromosome 16p12.2-p11.2 deletion syndrome,MONDO,disease,DISEASE_2142
2143,2143,2143,2143,2143,2143,2143,2143,MONDO:0975756,reactive angioendotheliomatosis,MONDO,disease,DISEASE_2143
2144,2144,2144,2144,2144,2144,2144,2144,MONDO:0800433_MONDO:0800434_MONDO:0800435,"ovarian cancer, familial, susceptibility to",MONDO_grouped,disease,DISEASE_2144
2145,2145,2145,2145,2145,2145,2145,2145,MONDO:0002736,ampulla of vater mucinous adenocarcinoma,MONDO,disease,DISEASE_2145
2146,2146,2146,2146,2146,2146,2146,2146,MONDO:1011694,"thrombasthenia, non-human animal",MONDO,disease,DISEASE_2146
2147,2147,2147,2147,2147,2147,2147,2147,MONDO:0002134,physiological sexual disorder,MONDO,disease,DISEASE_2147
2148,2148,2148,2148,2148,2148,2148,2148,MONDO:0017513,"split foot, unilateral",MONDO,disease,DISEASE_2148
2149,2149,2149,2149,2149,2149,2149,2149,MONDO:0017871,bilateral massive adrenal hemorrhage,MONDO,disease,DISEASE_2149
2150,2150,2150,2150,2150,2150,2150,2150,MONDO:0018875,Li-Fraumeni syndrome,MONDO,disease,DISEASE_2150
2151,2151,2151,2151,2151,2151,2151,2151,MONDO:0006071,adenofibroma,MONDO,disease,DISEASE_2151
2152,2152,2152,2152,2152,2152,2152,2152,MONDO:0859229,"cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism",MONDO,disease,DISEASE_2152
2153,2153,2153,2153,2153,2153,2153,2153,MONDO:0859211,neurodevelopmental disorder with hyperkinetic movements and dyskinesia,MONDO,disease,DISEASE_2153
2154,2154,2154,2154,2154,2154,2154,2154,MONDO:0024262,massive neonatal aspiration syndrome,MONDO,disease,DISEASE_2154
2155,2155,2155,2155,2155,2155,2155,2155,MONDO:0000703_MONDO:0043355,collagenous colitis,MONDO_grouped,disease,DISEASE_2155
2156,2156,2156,2156,2156,2156,2156,2156,MONDO:1010922,"myotonic dystrophy, Japanese quail",MONDO,disease,DISEASE_2156
2157,2157,2157,2157,2157,2157,2157,2157,MONDO:0019225,disorder of gluconeogenesis,MONDO,disease,DISEASE_2157
2158,2158,2158,2158,2158,2158,2158,2158,MONDO:0001383,degenerative myopia,MONDO,disease,DISEASE_2158
2159,2159,2159,2159,2159,2159,2159,2159,MONDO:1011610,"vitamin-K-dependent blood coagulation factors deficiency, sheep",MONDO,disease,DISEASE_2159
2160,2160,2160,2160,2160,2160,2160,2160,MONDO:0005940_MONDO:0005658,respirovirus infectious disease,MONDO_grouped,disease,DISEASE_2160
2161,2161,2161,2161,2161,2161,2161,2161,MONDO:0002451,benign prostate phyllodes tumor,MONDO,disease,DISEASE_2161
2162,2162,2162,2162,2162,2162,2162,2162,MONDO:0024419,enthesitis,MONDO,disease,DISEASE_2162
2163,2163,2163,2163,2163,2163,2163,2163,MONDO:0012131,"metaphyseal undermodeling, spondylar dysplasia, and overgrowth",MONDO,disease,DISEASE_2163
2164,2164,2164,2164,2164,2164,2164,2164,MONDO:0002984,reticulohistiocytic granuloma,MONDO,disease,DISEASE_2164
2165,2165,2165,2165,2165,2165,2165,2165,MONDO:0016727,extraventricular neurocytoma,MONDO,disease,DISEASE_2165
2166,2166,2166,2166,2166,2166,2166,2166,MONDO:0014643,congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome,MONDO,disease,DISEASE_2166
2167,2167,2167,2167,2167,2167,2167,2167,MONDO:0012218,"dandy-walker malformation with occipital cephalocele, autosomal dominant",MONDO,disease,DISEASE_2167
2168,2168,2168,2168,2168,2168,2168,2168,MONDO:0006497,cerebral palsy,MONDO,disease,DISEASE_2168
2169,2169,2169,2169,2169,2169,2169,2169,MONDO:1011735,"dermal allergy, non-human animal",MONDO,disease,DISEASE_2169
2170,2170,2170,2170,2170,2170,2170,2170,MONDO:0021201,skin infection,MONDO,disease,DISEASE_2170
2171,2171,2171,2171,2171,2171,2171,2171,MONDO:0000009,"inherited bleeding disorder, platelet-type",MONDO,disease,DISEASE_2171
2172,2172,2172,2172,2172,2172,2172,2172,MONDO:1011211,"coloboma, snow leopard",MONDO,disease,DISEASE_2172
2173,2173,2173,2173,2173,2173,2173,2173,MONDO:0006363,peritoneal multicystic mesothelioma,MONDO,disease,DISEASE_2173
2174,2174,2174,2174,2174,2174,2174,2174,MONDO:0001915,orbital cyst,MONDO,disease,DISEASE_2174
2175,2175,2175,2175,2175,2175,2175,2175,MONDO:0002971_MONDO:0005208,amelanotic melanoma,MONDO_grouped,disease,DISEASE_2175
2176,2176,2176,2176,2176,2176,2176,2176,MONDO:0032572,"cardiac, facial, and digital anomalies with developmental delay",MONDO,disease,DISEASE_2176
2177,2177,2177,2177,2177,2177,2177,2177,MONDO:1012816,"lipid malabsorption, ACSL5-related, dog",MONDO,disease,DISEASE_2177
2178,2178,2178,2178,2178,2178,2178,2178,MONDO:0700021,chromosome 14 disorder,MONDO,disease,DISEASE_2178
2179,2179,2179,2179,2179,2179,2179,2179,MONDO:0003438,combined small cell lung carcinoma,MONDO,disease,DISEASE_2179
2180,2180,2180,2180,2180,2180,2180,2180,MONDO:0859748,grade II lymphomatoid granulomatosis,MONDO,disease,DISEASE_2180
2181,2181,2181,2181,2181,2181,2181,2181,MONDO:0013767_MONDO:0011158_MONDO:0011804_MONDO:0011383_MONDO:0017979,autoimmune lymphoproliferative syndrome,MONDO_grouped,disease,DISEASE_2181
2182,2182,2182,2182,2182,2182,2182,2182,MONDO:0000976,paratesticular lipoma,MONDO,disease,DISEASE_2182
2183,2183,2183,2183,2183,2183,2183,2183,MONDO:0008335,short stature-craniofacial anomalies-genital hypoplasia syndrome,MONDO,disease,DISEASE_2183
2184,2184,2184,2184,2184,2184,2184,2184,MONDO:0032774,"cerebellar, ocular, craniofacial, and genital syndrome",MONDO,disease,DISEASE_2184
2185,2185,2185,2185,2185,2185,2185,2185,MONDO:0018815,aneurysmal bone cyst,MONDO,disease,DISEASE_2185
2186,2186,2186,2186,2186,2186,2186,2186,MONDO:0700254,paraneoplastic gastrointestinal syndrome,MONDO,disease,DISEASE_2186
2187,2187,2187,2187,2187,2187,2187,2187,MONDO:0020304_MONDO:0020305,isochromosomy,MONDO_grouped,disease,DISEASE_2187
2188,2188,2188,2188,2188,2188,2188,2188,MONDO:1012520_MONDO:1012521_MONDO:1012528,"bilateral deafness and vestibular dysfunction, dog",MONDO_grouped,disease,DISEASE_2188
2189,2189,2189,2189,2189,2189,2189,2189,MONDO:0004773,iridocyclitis,MONDO,disease,DISEASE_2189
2190,2190,2190,2190,2190,2190,2190,2190,MONDO:0023255,glossopalatine ankylosis micrognathia ear anomalies,MONDO,disease,DISEASE_2190
2191,2191,2191,2191,2191,2191,2191,2191,MONDO:0019848,posterior hypospadias,MONDO,disease,DISEASE_2191
2192,2192,2192,2192,2192,2192,2192,2192,MONDO:0016693,subependymal giant cell astrocytoma,MONDO,disease,DISEASE_2192
2193,2193,2193,2193,2193,2193,2193,2193,MONDO:0017719,gangliosidosis,MONDO,disease,DISEASE_2193
2194,2194,2194,2194,2194,2194,2194,2194,MONDO:0005326,sunburn,MONDO,disease,DISEASE_2194
2195,2195,2195,2195,2195,2195,2195,2195,MONDO:0004777,acute laryngitis,MONDO,disease,DISEASE_2195
2196,2196,2196,2196,2196,2196,2196,2196,MONDO:0003847,hereditary disease,MONDO,disease,DISEASE_2196
2197,2197,2197,2197,2197,2197,2197,2197,MONDO:0022737,choroideremia hypopituitarism,MONDO,disease,DISEASE_2197
2198,2198,2198,2198,2198,2198,2198,2198,MONDO:0002135,optic nerve disorder,MONDO,disease,DISEASE_2198
2199,2199,2199,2199,2199,2199,2199,2199,MONDO:1012568,"congenital mast cell tumor, cattle",MONDO,disease,DISEASE_2199
2200,2200,2200,2200,2200,2200,2200,2200,MONDO:0004153,childhood central nervous system embryonal carcinoma,MONDO,disease,DISEASE_2200
2201,2201,2201,2201,2201,2201,2201,2201,MONDO:0009975,reticulum cell sarcoma,MONDO,disease,DISEASE_2201
2202,2202,2202,2202,2202,2202,2202,2202,MONDO:0019321,atypical Werner syndrome,MONDO,disease,DISEASE_2202
2203,2203,2203,2203,2203,2203,2203,2203,MONDO:0859232,neurodevelopmental disorder with central hypotonia and dysmorphic facies,MONDO,disease,DISEASE_2203
2204,2204,2204,2204,2204,2204,2204,2204,MONDO:0007303,cervical rib disease,MONDO,disease,DISEASE_2204
2205,2205,2205,2205,2205,2205,2205,2205,MONDO:0023655,"immunodeficiency 14b, autosomal recessive",MONDO,disease,DISEASE_2205
2206,2206,2206,2206,2206,2206,2206,2206,MONDO:0014791,Luscan-Lumish syndrome,MONDO,disease,DISEASE_2206
2207,2207,2207,2207,2207,2207,2207,2207,MONDO:0025494,porcine reproductive and respiratory syndrome,MONDO,disease,DISEASE_2207
2208,2208,2208,2208,2208,2208,2208,2208,MONDO:0007961,"megalencephaly, autosomal dominant",MONDO,disease,DISEASE_2208
2209,2209,2209,2209,2209,2209,2209,2209,MONDO:0060768,gingival fibroepithelial polyp,MONDO,disease,DISEASE_2209
2210,2210,2210,2210,2210,2210,2210,2210,MONDO:0003243,hepatocellular clear cell carcinoma,MONDO,disease,DISEASE_2210
2211,2211,2211,2211,2211,2211,2211,2211,MONDO:0100105,brain small vessel disease 3,MONDO,disease,DISEASE_2211
2212,2212,2212,2212,2212,2212,2212,2212,MONDO:0006329,olfactory neuroblastoma,MONDO,disease,DISEASE_2212
2213,2213,2213,2213,2213,2213,2213,2213,MONDO:0006036,granulosa cell tumor,MONDO,disease,DISEASE_2213
2214,2214,2214,2214,2214,2214,2214,2214,MONDO:0006321,non-functioning adrenal cortex adenoma,MONDO,disease,DISEASE_2214
2215,2215,2215,2215,2215,2215,2215,2215,MONDO:0004328,maxillary sinus adenocarcinoma,MONDO,disease,DISEASE_2215
2216,2216,2216,2216,2216,2216,2216,2216,MONDO:0042233,disseminated candidiasis,MONDO,disease,DISEASE_2216
2217,2217,2217,2217,2217,2217,2217,2217,MONDO:0800437_MONDO:0100292_MONDO:0031415,Carey-Fineman-Ziter syndrome,MONDO_grouped,disease,DISEASE_2217
2218,2218,2218,2218,2218,2218,2218,2218,MONDO:0000989,mumps infectious disease,MONDO,disease,DISEASE_2218
2219,2219,2219,2219,2219,2219,2219,2219,MONDO:0001770,gastrin secretion abnormality,MONDO,disease,DISEASE_2219
2220,2220,2220,2220,2220,2220,2220,2220,MONDO:0004145,meningothelial meningioma,MONDO,disease,DISEASE_2220
2221,2221,2221,2221,2221,2221,2221,2221,MONDO:0015247,opsoclonus-myoclonus syndrome,MONDO,disease,DISEASE_2221
2222,2222,2222,2222,2222,2222,2222,2222,MONDO:0017791,high bone mass osteogenesis imperfecta,MONDO,disease,DISEASE_2222
2223,2223,2223,2223,2223,2223,2223,2223,MONDO:0005453_MONDO:0000577_MONDO:0022357,congenital heart disease,MONDO_grouped,disease,DISEASE_2223
2224,2224,2224,2224,2224,2224,2224,2224,MONDO:0044083,alternariosis,MONDO,disease,DISEASE_2224
2225,2225,2225,2225,2225,2225,2225,2225,MONDO:0006143,cervical squamous cell carcinoma,MONDO,disease,DISEASE_2225
2226,2226,2226,2226,2226,2226,2226,2226,MONDO:0006935_MONDO:0017870,pulmonary subvalvular stenosis,MONDO_grouped,disease,DISEASE_2226
2227,2227,2227,2227,2227,2227,2227,2227,MONDO:0043892,prosthesis-related infectious disease,MONDO,disease,DISEASE_2227
2228,2228,2228,2228,2228,2228,2228,2228,MONDO:0032807,neurodevelopmental disorder with visual defects and brain anomalies,MONDO,disease,DISEASE_2228
2229,2229,2229,2229,2229,2229,2229,2229,MONDO:0002771,pulmonary fibrosis,MONDO,disease,DISEASE_2229
2230,2230,2230,2230,2230,2230,2230,2230,MONDO:0000672,form agnosia,MONDO,disease,DISEASE_2230
2231,2231,2231,2231,2231,2231,2231,2231,MONDO:0013803,leukoencephalopathy with calcifications and cysts,MONDO,disease,DISEASE_2231
2232,2232,2232,2232,2232,2232,2232,2232,MONDO:0018083,transient tyrosinemia of the newborn,MONDO,disease,DISEASE_2232
2233,2233,2233,2233,2233,2233,2233,2233,MONDO:1012094,"granule cell type cerebellar hypoplasia, dog",MONDO,disease,DISEASE_2233
2234,2234,2234,2234,2234,2234,2234,2234,MONDO:0016889,partial deletion of the short arm of chromosome 7,MONDO,disease,DISEASE_2234
2235,2235,2235,2235,2235,2235,2235,2235,MONDO:0003701,thyroid gland diffuse sclerosing papillary carcinoma,MONDO,disease,DISEASE_2235
2236,2236,2236,2236,2236,2236,2236,2236,MONDO:0009467,natal teeth-intestinal pseudoobstruction-patent ductus syndrome,MONDO,disease,DISEASE_2236
2237,2237,2237,2237,2237,2237,2237,2237,MONDO:0007724,hirsutism-skeletal dysplasia-intellectual disability syndrome,MONDO,disease,DISEASE_2237
2238,2238,2238,2238,2238,2238,2238,2238,MONDO:0005695,central nervous system AIDS arteritis,MONDO,disease,DISEASE_2238
2239,2239,2239,2239,2239,2239,2239,2239,MONDO:1012548,"dynamic laryngeal collapse, horse",MONDO,disease,DISEASE_2239
2240,2240,2240,2240,2240,2240,2240,2240,MONDO:0008171_MONDO:0024647,nephrolithiasis,MONDO_grouped,disease,DISEASE_2240
2241,2241,2241,2241,2241,2241,2241,2241,MONDO:0004223,polyp of middle ear,MONDO,disease,DISEASE_2241
2242,2242,2242,2242,2242,2242,2242,2242,MONDO:0015388,polyrrhinia,MONDO,disease,DISEASE_2242
2243,2243,2243,2243,2243,2243,2243,2243,MONDO:0018425,Huntington disease-like syndrome due to C9ORF72 expansions,MONDO,disease,DISEASE_2243
2244,2244,2244,2244,2244,2244,2244,2244,MONDO:0010735,Kennedy disease,MONDO,disease,DISEASE_2244
2245,2245,2245,2245,2245,2245,2245,2245,MONDO:0019893,distal monosomy 19p13.3,MONDO,disease,DISEASE_2245
2246,2246,2246,2246,2246,2246,2246,2246,MONDO:1012363,"myopathy of the diaphragmatic muscles, cattle",MONDO,disease,DISEASE_2246
2247,2247,2247,2247,2247,2247,2247,2247,MONDO:0700094,unbalanced Robertsonian translocation Down syndrome,MONDO,disease,DISEASE_2247
2248,2248,2248,2248,2248,2248,2248,2248,MONDO:1011783,"alpha fucosidosis, non-human animal",MONDO,disease,DISEASE_2248
2249,2249,2249,2249,2249,2249,2249,2249,MONDO:0003801,corneal intraepithelial neoplasm,MONDO,disease,DISEASE_2249
2250,2250,2250,2250,2250,2250,2250,2250,MONDO:0010055,spinal muscular atrophy with microcephaly and mental subnormality,MONDO,disease,DISEASE_2250
2251,2251,2251,2251,2251,2251,2251,2251,MONDO:0018765,cryptogenic multifocal ulcerous stenosing enteritis,MONDO,disease,DISEASE_2251
2252,2252,2252,2252,2252,2252,2252,2252,MONDO:0020419_MONDO:0800133,pulmonary artery hypoplasia,MONDO_grouped,disease,DISEASE_2252
2253,2253,2253,2253,2253,2253,2253,2253,MONDO:0002520_MONDO:0971154,hepatic porphyria,MONDO_grouped,disease,DISEASE_2253
2254,2254,2254,2254,2254,2254,2254,2254,MONDO:1010220,"ameloblastoma, non-human animal",MONDO,disease,DISEASE_2254
2255,2255,2255,2255,2255,2255,2255,2255,MONDO:0032879,"megabladder, congenital",MONDO,disease,DISEASE_2255
2256,2256,2256,2256,2256,2256,2256,2256,MONDO:0020454_MONDO:0020455,congenital complete agenesis of pericardium,MONDO_grouped,disease,DISEASE_2256
2257,2257,2257,2257,2257,2257,2257,2257,MONDO:0019093,immunodeficiency due to selective anti-polysaccharide antibody deficiency,MONDO,disease,DISEASE_2257
2258,2258,2258,2258,2258,2258,2258,2258,MONDO:0004874,ganglion or cyst of synovium/tendon/bursa,MONDO,disease,DISEASE_2258
2259,2259,2259,2259,2259,2259,2259,2259,MONDO:1012934,"deafness, EPS8L2-related, dog",MONDO,disease,DISEASE_2259
2260,2260,2260,2260,2260,2260,2260,2260,MONDO:0001588,chronic lacrimal gland enlargement,MONDO,disease,DISEASE_2260
2261,2261,2261,2261,2261,2261,2261,2261,MONDO:0017457_MONDO:0017535_MONDO:0017537_MONDO:0017538,Preaxial polydactyly of toes,MONDO_grouped,disease,DISEASE_2261
2262,2262,2262,2262,2262,2262,2262,2262,MONDO:0700178,feline oral squamous cell carcinoma,MONDO,disease,DISEASE_2262
2263,2263,2263,2263,2263,2263,2263,2263,MONDO:0800033,MELAS syndrome caused by mutation in MTTQ,MONDO,disease,DISEASE_2263
2264,2264,2264,2264,2264,2264,2264,2264,MONDO:0800135,congenital emphysematous lung disease due to Filamin A loss-of-function variant,MONDO,disease,DISEASE_2264
2265,2265,2265,2265,2265,2265,2265,2265,MONDO:0015573_MONDO:0005282_MONDO:0015574_MONDO:0044113,subacute cutaneous lupus erythematosus,MONDO_grouped,disease,DISEASE_2265
2266,2266,2266,2266,2266,2266,2266,2266,MONDO:0009769,oculo-palato-cerebral syndrome,MONDO,disease,DISEASE_2266
2267,2267,2267,2267,2267,2267,2267,2267,MONDO:0001568,mixed receptive-expressive language disorder,MONDO,disease,DISEASE_2267
2268,2268,2268,2268,2268,2268,2268,2268,MONDO:0011253,craniomicromelic syndrome,MONDO,disease,DISEASE_2268
2269,2269,2269,2269,2269,2269,2269,2269,MONDO:0019840,acropectororenal dysplasia,MONDO,disease,DISEASE_2269
2270,2270,2270,2270,2270,2270,2270,2270,MONDO:0009923,"46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency",MONDO,disease,DISEASE_2270
2271,2271,2271,2271,2271,2271,2271,2271,MONDO:0012772,Stevenson-Carey syndrome,MONDO,disease,DISEASE_2271
2272,2272,2272,2272,2272,2272,2272,2272,MONDO:0011637,Sener syndrome,MONDO,disease,DISEASE_2272
2273,2273,2273,2273,2273,2273,2273,2273,MONDO:0004290,subglottis verrucous carcinoma,MONDO,disease,DISEASE_2273
2274,2274,2274,2274,2274,2274,2274,2274,MONDO:0004879,senile atrophy of choroid,MONDO,disease,DISEASE_2274
2275,2275,2275,2275,2275,2275,2275,2275,MONDO:0006676,beriberi,MONDO,disease,DISEASE_2275
2276,2276,2276,2276,2276,2276,2276,2276,MONDO:0044956,paranasal sinus mucoepidermoid carcinoma,MONDO,disease,DISEASE_2276
2277,2277,2277,2277,2277,2277,2277,2277,MONDO:0004701,uterine polyp,MONDO,disease,DISEASE_2277
2278,2278,2278,2278,2278,2278,2278,2278,MONDO:0003632,endocervicitis,MONDO,disease,DISEASE_2278
2279,2279,2279,2279,2279,2279,2279,2279,MONDO:0800118,visceral botryomycosis,MONDO,disease,DISEASE_2279
2280,2280,2280,2280,2280,2280,2280,2280,MONDO:0010893_MONDO:0007783_MONDO:0007939_MONDO:0007940_MONDO:0011163_MONDO:0800188_MONDO:0011164,"malignant hyperthermia, susceptibility to",MONDO_grouped,disease,DISEASE_2280
2281,2281,2281,2281,2281,2281,2281,2281,MONDO:0018495,X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome,MONDO,disease,DISEASE_2281
2282,2282,2282,2282,2282,2282,2282,2282,MONDO:0006806,intermediate uveitis,MONDO,disease,DISEASE_2282
2283,2283,2283,2283,2283,2283,2283,2283,MONDO:0013009,Megarbane-Jalkh syndrome,MONDO,disease,DISEASE_2283
2284,2284,2284,2284,2284,2284,2284,2284,MONDO:0010793,"nephropathy, chronic tubulointerstitial",MONDO,disease,DISEASE_2284
2285,2285,2285,2285,2285,2285,2285,2285,MONDO:1010653_MONDO:1010654_MONDO:1010655_MONDO:1010656,"polycythemia, dog",MONDO_grouped,disease,DISEASE_2285
2286,2286,2286,2286,2286,2286,2286,2286,MONDO:1010788,"Ehlers-Danlos syndrome, kyphoscoliotic type, PLOD1-related, horse",MONDO,disease,DISEASE_2286
2287,2287,2287,2287,2287,2287,2287,2287,MONDO:0004619,measles,MONDO,disease,DISEASE_2287
2288,2288,2288,2288,2288,2288,2288,2288,MONDO:0030018_MONDO:0968982,autoinflammation with episodic fever and lymphadenopathy,MONDO_grouped,disease,DISEASE_2288
2289,2289,2289,2289,2289,2289,2289,2289,MONDO:0035008,isolated splenic vein thrombosis,MONDO,disease,DISEASE_2289
2290,2290,2290,2290,2290,2290,2290,2290,MONDO:1012526,"bilateral corneal stromal loss, horse",MONDO,disease,DISEASE_2290
2291,2291,2291,2291,2291,2291,2291,2291,MONDO:0027026,Buschke Lowenstein tumor,MONDO,disease,DISEASE_2291
2292,2292,2292,2292,2292,2292,2292,2292,MONDO:0011130,"sebaceous gland hyperplasia, familial presenile",MONDO,disease,DISEASE_2292
2293,2293,2293,2293,2293,2293,2293,2293,MONDO:0010849,"palmoplantar keratoderma, Bothnian type",MONDO,disease,DISEASE_2293
2294,2294,2294,2294,2294,2294,2294,2294,MONDO:0020604,X-linked dominant disease,MONDO,disease,DISEASE_2294
2295,2295,2295,2295,2295,2295,2295,2295,MONDO:0024292,gastrointestinal polyp,MONDO,disease,DISEASE_2295
2296,2296,2296,2296,2296,2296,2296,2296,MONDO:1012440,"lethal multi-organ developmental dysplasia, cattle",MONDO,disease,DISEASE_2296
2297,2297,2297,2297,2297,2297,2297,2297,MONDO:0015279,chronic mucocutaneous candidiasis,MONDO,disease,DISEASE_2297
2298,2298,2298,2298,2298,2298,2298,2298,MONDO:0001877,infertility due to extratesticular cause,MONDO,disease,DISEASE_2298
2299,2299,2299,2299,2299,2299,2299,2299,MONDO:0019139_MONDO:0035735_MONDO:0035736,acquired hemophilia,MONDO_grouped,disease,DISEASE_2299
2300,2300,2300,2300,2300,2300,2300,2300,MONDO:1012503_MONDO:1012502_MONDO:1012504_MONDO:1012505,"hydrallantois, cattle",MONDO_grouped,disease,DISEASE_2300
2301,2301,2301,2301,2301,2301,2301,2301,MONDO:0012323,lethal acantholytic epidermolysis bullosa,MONDO,disease,DISEASE_2301
2302,2302,2302,2302,2302,2302,2302,2302,MONDO:0008482,Sprengel deformity,MONDO,disease,DISEASE_2302
2303,2303,2303,2303,2303,2303,2303,2303,MONDO:0010794,NARP syndrome,MONDO,disease,DISEASE_2303
2304,2304,2304,2304,2304,2304,2304,2304,MONDO:0009600,"metaphyseal dysplasia, anetoderma, and optic atrophy",MONDO,disease,DISEASE_2304
2305,2305,2305,2305,2305,2305,2305,2305,MONDO:0002707,breast mucinous carcinoma,MONDO,disease,DISEASE_2305
2306,2306,2306,2306,2306,2306,2306,2306,MONDO:0003240_MONDO:0003393,thyroid gland disorder,MONDO_grouped,disease,DISEASE_2306
2307,2307,2307,2307,2307,2307,2307,2307,MONDO:0013693_MONDO:0014481_MONDO:0017411,"inflammatory skin and bowel disease, neonatal",MONDO_grouped,disease,DISEASE_2307
2308,2308,2308,2308,2308,2308,2308,2308,MONDO:0015672,diprosopus,MONDO,disease,DISEASE_2308
2309,2309,2309,2309,2309,2309,2309,2309,MONDO:0000572,recombinase activating gene 1 deficiency,MONDO,disease,DISEASE_2309
2310,2310,2310,2310,2310,2310,2310,2310,MONDO:0008056_MONDO:0011266_MONDO:0016107,myotonic dystrophy,MONDO_grouped,disease,DISEASE_2310
2311,2311,2311,2311,2311,2311,2311,2311,MONDO:1011419,"glycogen storage disease, non-human animal",MONDO,disease,DISEASE_2311
2312,2312,2312,2312,2312,2312,2312,2312,MONDO:0010583,"Dyggve-Melchior-Clausen syndrome, X-linked",MONDO,disease,DISEASE_2312
2313,2313,2313,2313,2313,2313,2313,2313,MONDO:0017944,invasive non-typhoidal salmonellosis,MONDO,disease,DISEASE_2313
2314,2314,2314,2314,2314,2314,2314,2314,MONDO:0008015,motion sickness,MONDO,disease,DISEASE_2314
2315,2315,2315,2315,2315,2315,2315,2315,MONDO:0100566,myoclonic epilepsy in infancy,MONDO,disease,DISEASE_2315
2316,2316,2316,2316,2316,2316,2316,2316,MONDO:0970964,myelic limited dorsal malformation,MONDO,disease,DISEASE_2316
2317,2317,2317,2317,2317,2317,2317,2317,MONDO:0002273_MONDO:0037829,plasma protein metabolism disease,MONDO_grouped,disease,DISEASE_2317
2318,2318,2318,2318,2318,2318,2318,2318,MONDO:0018314,infantile-onset mesial temporal lobe epilepsy with severe cognitive regression,MONDO,disease,DISEASE_2318
2319,2319,2319,2319,2319,2319,2319,2319,MONDO:0005459,human African trypanosomiasis,MONDO,disease,DISEASE_2319
2320,2320,2320,2320,2320,2320,2320,2320,MONDO:0001089_MONDO:0001090,acute inferolateral myocardial infarction,MONDO_grouped,disease,DISEASE_2320
2321,2321,2321,2321,2321,2321,2321,2321,MONDO:1011931,"upper airway syndrome, non-human animal",MONDO,disease,DISEASE_2321
2322,2322,2322,2322,2322,2322,2322,2322,MONDO:1010409_MONDO:1010413_MONDO:1010414_MONDO:1010415,"epilepsy, chicken",MONDO_grouped,disease,DISEASE_2322
2323,2323,2323,2323,2323,2323,2323,2323,MONDO:0009710,Thomsen and Becker disease,MONDO,disease,DISEASE_2323
2324,2324,2324,2324,2324,2324,2324,2324,MONDO:0005048,pancreatic insulin-producing neuroendocrine tumor,MONDO,disease,DISEASE_2324
2325,2325,2325,2325,2325,2325,2325,2325,MONDO:0014784,severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome,MONDO,disease,DISEASE_2325
2326,2326,2326,2326,2326,2326,2326,2326,MONDO:0007175,"PR interval, variation in",MONDO,disease,DISEASE_2326
2327,2327,2327,2327,2327,2327,2327,2327,MONDO:0002558,melanotic neurilemmoma,MONDO,disease,DISEASE_2327
2328,2328,2328,2328,2328,2328,2328,2328,MONDO:0015730,mosaic trisomy 17,MONDO,disease,DISEASE_2328
2329,2329,2329,2329,2329,2329,2329,2329,MONDO:0007232,autosomal dominant brachyolmia,MONDO,disease,DISEASE_2329
2330,2330,2330,2330,2330,2330,2330,2330,MONDO:0017878,Chapare hemorrhagic fever,MONDO,disease,DISEASE_2330
2331,2331,2331,2331,2331,2331,2331,2331,MONDO:0019098_MONDO:1010069_MONDO:1010625_MONDO:1010626_MONDO:1010663_MONDO:1010664,autoimmune thrombocytopenia,MONDO_grouped,disease,DISEASE_2331
2332,2332,2332,2332,2332,2332,2332,2332,MONDO:1011891,"cervical vertebral compressive myelopathy, non-human animal",MONDO,disease,DISEASE_2332
2333,2333,2333,2333,2333,2333,2333,2333,MONDO:0011421_MONDO:0957254_MONDO:0957255_MONDO:0014091_MONDO:0013546_MONDO:0013547,"mitochondrial complex V (ATP synthase) deficiency, nuclear",MONDO_grouped,disease,DISEASE_2333
2334,2334,2334,2334,2334,2334,2334,2334,MONDO:0005223,acute myeloid leukemia with minimal differentiation,MONDO,disease,DISEASE_2334
2335,2335,2335,2335,2335,2335,2335,2335,MONDO:0035124,"linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies",MONDO,disease,DISEASE_2335
2336,2336,2336,2336,2336,2336,2336,2336,MONDO:0021011,hereditary progressive chorea without dementia,MONDO,disease,DISEASE_2336
2337,2337,2337,2337,2337,2337,2337,2337,MONDO:0000766,corneal endothelial dystrophy,MONDO,disease,DISEASE_2337
2338,2338,2338,2338,2338,2338,2338,2338,MONDO:0026727,Shukla-Vernon syndrome,MONDO,disease,DISEASE_2338
2339,2339,2339,2339,2339,2339,2339,2339,MONDO:0008066,"nasal hyperpigmentation, familial transverse",MONDO,disease,DISEASE_2339
2340,2340,2340,2340,2340,2340,2340,2340,MONDO:0005885_MONDO:0000958_MONDO:0044690,optic neuritis,MONDO_grouped,disease,DISEASE_2340
2341,2341,2341,2341,2341,2341,2341,2341,MONDO:1012566,"corneal sequestra, domestic cat",MONDO,disease,DISEASE_2341
2342,2342,2342,2342,2342,2342,2342,2342,MONDO:0009941,obsolete Pygmy,MONDO,disease,DISEASE_2342
2343,2343,2343,2343,2343,2343,2343,2343,MONDO:1011202_MONDO:1011209_MONDO:1012944,"amelogenesis imperfecta, ENAM-related, dog",MONDO_grouped,disease,DISEASE_2343
2344,2344,2344,2344,2344,2344,2344,2344,MONDO:0021105,NAFLD1,MONDO,disease,DISEASE_2344
2345,2345,2345,2345,2345,2345,2345,2345,MONDO:0859478_MONDO:0024773_MONDO:0957202_MONDO:0859477_MONDO:0025354_MONDO:0056795_MONDO:0010647_MONDO:0970943,"spermatogenic failure, X-linked",MONDO_grouped,disease,DISEASE_2345
2346,2346,2346,2346,2346,2346,2346,2346,MONDO:0014809,DDX41-related hematologic malignancy predisposition syndrome,MONDO,disease,DISEASE_2346
2347,2347,2347,2347,2347,2347,2347,2347,MONDO:0850050,congenital aphakia-iris hypoplasia-microphthalmia-microcornea syndrome,MONDO,disease,DISEASE_2347
2348,2348,2348,2348,2348,2348,2348,2348,MONDO:0005070,neoplasm,MONDO,disease,DISEASE_2348
2349,2349,2349,2349,2349,2349,2349,2349,MONDO:0002047,pulmonary systemic sclerosis,MONDO,disease,DISEASE_2349
2350,2350,2350,2350,2350,2350,2350,2350,MONDO:0800035,MELAS syndrome caused by mutation in MTTK,MONDO,disease,DISEASE_2350
2351,2351,2351,2351,2351,2351,2351,2351,MONDO:0000307,parasitic Ichthyosporea infectious disease,MONDO,disease,DISEASE_2351
2352,2352,2352,2352,2352,2352,2352,2352,MONDO:0015102,non-secreting chemodectoma,MONDO,disease,DISEASE_2352
2353,2353,2353,2353,2353,2353,2353,2353,MONDO:0030798,immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias,MONDO,disease,DISEASE_2353
2354,2354,2354,2354,2354,2354,2354,2354,MONDO:0008161,otodental syndrome,MONDO,disease,DISEASE_2354
2355,2355,2355,2355,2355,2355,2355,2355,MONDO:0002083,Richter syndrome,MONDO,disease,DISEASE_2355
2356,2356,2356,2356,2356,2356,2356,2356,MONDO:1010620_MONDO:1010621,"omphalocele, horse",MONDO_grouped,disease,DISEASE_2356
2357,2357,2357,2357,2357,2357,2357,2357,MONDO:0002191,syringoma,MONDO,disease,DISEASE_2357
2358,2358,2358,2358,2358,2358,2358,2358,MONDO:0700218,group B streptococcal infection,MONDO,disease,DISEASE_2358
2359,2359,2359,2359,2359,2359,2359,2359,MONDO:0000253,piedra,MONDO,disease,DISEASE_2359
2360,2360,2360,2360,2360,2360,2360,2360,MONDO:0011504,NDE1-related microhydranencephaly,MONDO,disease,DISEASE_2360
2361,2361,2361,2361,2361,2361,2361,2361,MONDO:0060745,intellectual developmental disorder with or without epilepsy or cerebellar ataxia,MONDO,disease,DISEASE_2361
2362,2362,2362,2362,2362,2362,2362,2362,MONDO:0060502,"neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies",MONDO,disease,DISEASE_2362
2363,2363,2363,2363,2363,2363,2363,2363,MONDO:1011186_MONDO:1011187_MONDO:1011188,"scoliosis, chicken",MONDO_grouped,disease,DISEASE_2363
2364,2364,2364,2364,2364,2364,2364,2364,MONDO:0700265,paraneoplastic rheumatic syndrome,MONDO,disease,DISEASE_2364
2365,2365,2365,2365,2365,2365,2365,2365,MONDO:0007261,Carabelli anomaly of maxillary molar teeth,MONDO,disease,DISEASE_2365
2366,2366,2366,2366,2366,2366,2366,2366,MONDO:0021761,acral dysostosis dyserythropoiesis syndrome,MONDO,disease,DISEASE_2366
2367,2367,2367,2367,2367,2367,2367,2367,MONDO:0005362,erectile dysfunction,MONDO,disease,DISEASE_2367
2368,2368,2368,2368,2368,2368,2368,2368,MONDO:0000153,transposition of the great arteries,MONDO,disease,DISEASE_2368
2369,2369,2369,2369,2369,2369,2369,2369,MONDO:0018316,fatal post-viral neurodegenerative disorder,MONDO,disease,DISEASE_2369
2370,2370,2370,2370,2370,2370,2370,2370,MONDO:1012933_MONDO:1012941,"cleft primary palate, ESRP2-related, chicken",MONDO_grouped,disease,DISEASE_2370
2371,2371,2371,2371,2371,2371,2371,2371,MONDO:0032660,"spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant",MONDO,disease,DISEASE_2371
2372,2372,2372,2372,2372,2372,2372,2372,MONDO:0005654_MONDO:0005655,ascariasis,MONDO_grouped,disease,DISEASE_2372
2373,2373,2373,2373,2373,2373,2373,2373,MONDO:1012032,"brachycephalic airway obstruction syndrome, dog",MONDO,disease,DISEASE_2373
2374,2374,2374,2374,2374,2374,2374,2374,MONDO:0020760,skin squamous cell carcinoma in situ,MONDO,disease,DISEASE_2374
2375,2375,2375,2375,2375,2375,2375,2375,MONDO:0011145,colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome,MONDO,disease,DISEASE_2375
2376,2376,2376,2376,2376,2376,2376,2376,MONDO:0015749,6q16 deletion syndrome,MONDO,disease,DISEASE_2376
2377,2377,2377,2377,2377,2377,2377,2377,MONDO:0600029,restrictive pulmonary disease,MONDO,disease,DISEASE_2377
2378,2378,2378,2378,2378,2378,2378,2378,MONDO:1011668,"perosomus elumbis, non-human animal",MONDO,disease,DISEASE_2378
2379,2379,2379,2379,2379,2379,2379,2379,MONDO:0800391,EYS-related retinopathy,MONDO,disease,DISEASE_2379
2380,2380,2380,2380,2380,2380,2380,2380,MONDO:0008225,normokalemic periodic paralysis,MONDO,disease,DISEASE_2380
2381,2381,2381,2381,2381,2381,2381,2381,MONDO:0003421_MONDO:0004302,mixed cell adenoma,MONDO_grouped,disease,DISEASE_2381
2382,2382,2382,2382,2382,2382,2382,2382,MONDO:0700059,"Actinobacillus infectious disease, non-human animal",MONDO,disease,DISEASE_2382
2383,2383,2383,2383,2383,2383,2383,2383,MONDO:0956984,YAP1-MAMLD1 fusion-positive supratentorial ependymoma,MONDO,disease,DISEASE_2383
2384,2384,2384,2384,2384,2384,2384,2384,MONDO:0007533_MONDO:0054780_MONDO:0012731,elliptocytosis,MONDO_grouped,disease,DISEASE_2384
2385,2385,2385,2385,2385,2385,2385,2385,MONDO:1010203_MONDO:1011952_MONDO:1011872,"polymyositis, non-human animal",MONDO_grouped,disease,DISEASE_2385
2386,2386,2386,2386,2386,2386,2386,2386,MONDO:0017772,oral erosive lichen,MONDO,disease,DISEASE_2386
2387,2387,2387,2387,2387,2387,2387,2387,MONDO:0010882,aphalangy-syndactyly-microcephaly syndrome,MONDO,disease,DISEASE_2387
2388,2388,2388,2388,2388,2388,2388,2388,MONDO:0001073,idiopathic progressive polyneuropathy,MONDO,disease,DISEASE_2388
2389,2389,2389,2389,2389,2389,2389,2389,MONDO:0800409,"ventricular fibrillation during myocardial infarction, susceptibility to",MONDO,disease,DISEASE_2389
2390,2390,2390,2390,2390,2390,2390,2390,MONDO:1040035,LRIT3-related retinopathy,MONDO,disease,DISEASE_2390
2391,2391,2391,2391,2391,2391,2391,2391,MONDO:1010798,"Ehlers-Danlos syndrome, classic type, COL5A2-related, cattle",MONDO,disease,DISEASE_2391
2392,2392,2392,2392,2392,2392,2392,2392,MONDO:0003925,ethmoid sinus inverted papilloma,MONDO,disease,DISEASE_2392
2393,2393,2393,2393,2393,2393,2393,2393,MONDO:0018633,20q11.2 microdeletion syndrome,MONDO,disease,DISEASE_2393
2394,2394,2394,2394,2394,2394,2394,2394,MONDO:0016083,FLOTCH syndrome,MONDO,disease,DISEASE_2394
2395,2395,2395,2395,2395,2395,2395,2395,MONDO:0015100,aregenerative anemia,MONDO,disease,DISEASE_2395
2396,2396,2396,2396,2396,2396,2396,2396,MONDO:0004580_MONDO:0001451_MONDO:0001455_MONDO:0001539,retinal degeneration,MONDO_grouped,disease,DISEASE_2396
2397,2397,2397,2397,2397,2397,2397,2397,MONDO:0011370_MONDO:0010819_MONDO:0019353,Stargardt disease,MONDO_grouped,disease,DISEASE_2397
2398,2398,2398,2398,2398,2398,2398,2398,MONDO:0019082_MONDO:1010771,bullous pemphigoid,MONDO_grouped,disease,DISEASE_2398
2399,2399,2399,2399,2399,2399,2399,2399,MONDO:0044675,LRP5-related primary osteoporosis,MONDO,disease,DISEASE_2399
2400,2400,2400,2400,2400,2400,2400,2400,MONDO:0017334,12q15q21.1 microdeletion syndrome,MONDO,disease,DISEASE_2400
2401,2401,2401,2401,2401,2401,2401,2401,MONDO:0005311_MONDO:0000980,atherosclerosis,MONDO_grouped,disease,DISEASE_2401
2402,2402,2402,2402,2402,2402,2402,2402,MONDO:0011565_MONDO:0005066_MONDO:1011557_MONDO:1011558,metabolic syndrome,MONDO_grouped,disease,DISEASE_2402
2403,2403,2403,2403,2403,2403,2403,2403,MONDO:0005613,mesonephric adenocarcinoma,MONDO,disease,DISEASE_2403
2404,2404,2404,2404,2404,2404,2404,2404,MONDO:0019788,non-secreting paraganglioma,MONDO,disease,DISEASE_2404
2405,2405,2405,2405,2405,2405,2405,2405,MONDO:0001618,balanoposthitis,MONDO,disease,DISEASE_2405
2406,2406,2406,2406,2406,2406,2406,2406,MONDO:0030330_MONDO:0007270_MONDO:0012900_MONDO:0012306_MONDO:0800371,"cardiomyopathy, familial restrictive",MONDO_grouped,disease,DISEASE_2406
2407,2407,2407,2407,2407,2407,2407,2407,MONDO:0009480,Joubert syndrome with oculorenal defect,MONDO,disease,DISEASE_2407
2408,2408,2408,2408,2408,2408,2408,2408,MONDO:1011696,"stomatocytosis and gastrits, non-human animal",MONDO,disease,DISEASE_2408
2409,2409,2409,2409,2409,2409,2409,2409,MONDO:0013357,"chromosome 17q11.2 deletion syndrome, 1.4Mb",MONDO,disease,DISEASE_2409
2410,2410,2410,2410,2410,2410,2410,2410,MONDO:0014992_MONDO:0013527_MONDO:0030031_MONDO:0015148_MONDO:0015146,lissencephaly,MONDO_grouped,disease,DISEASE_2410
2411,2411,2411,2411,2411,2411,2411,2411,MONDO:0007793,hypochondroplasia,MONDO,disease,DISEASE_2411
2412,2412,2412,2412,2412,2412,2412,2412,MONDO:0100513,TRAF3 haploinsufficiency,MONDO,disease,DISEASE_2412
2413,2413,2413,2413,2413,2413,2413,2413,MONDO:0016002_MONDO:0013800,"Ehlers-Danlos syndrome, kyphoscoliotic",MONDO_grouped,disease,DISEASE_2413
2414,2414,2414,2414,2414,2414,2414,2414,MONDO:0957960,Long-Olsen-Distelmaier syndrome,MONDO,disease,DISEASE_2414
2415,2415,2415,2415,2415,2415,2415,2415,MONDO:0001595,choreatic disease,MONDO,disease,DISEASE_2415
2416,2416,2416,2416,2416,2416,2416,2416,MONDO:0011996_MONDO:0006115_MONDO:0004653,"chronic myelogenous leukemia, BCR-ABL1 positive",MONDO_grouped,disease,DISEASE_2416
2417,2417,2417,2417,2417,2417,2417,2417,MONDO:0043131,Michels Caskey syndrome,MONDO,disease,DISEASE_2417
2418,2418,2418,2418,2418,2418,2418,2418,MONDO:0002416,ethmoid sinus squamous cell carcinoma,MONDO,disease,DISEASE_2418
2419,2419,2419,2419,2419,2419,2419,2419,MONDO:0001744_MONDO:0001742,angle-closure glaucoma,MONDO_grouped,disease,DISEASE_2419
2420,2420,2420,2420,2420,2420,2420,2420,MONDO:0005023,ductal breast carcinoma in situ,MONDO,disease,DISEASE_2420
2421,2421,2421,2421,2421,2421,2421,2421,MONDO:0800499,childhood-onset idiopathic generalized epilepsy syndrome,MONDO,disease,DISEASE_2421
2422,2422,2422,2422,2422,2422,2422,2422,MONDO:1011916,"Meckel-like hepatorenal fibrocystic dysplasia syndrome, non-human animal",MONDO,disease,DISEASE_2422
2423,2423,2423,2423,2423,2423,2423,2423,MONDO:0015274,chronic beryllium disease,MONDO,disease,DISEASE_2423
2424,2424,2424,2424,2424,2424,2424,2424,MONDO:0016780,paternal 14q32.2 microdeletion syndrome,MONDO,disease,DISEASE_2424
2425,2425,2425,2425,2425,2425,2425,2425,MONDO:0002553,cerebellopontine angle tumor,MONDO,disease,DISEASE_2425
2426,2426,2426,2426,2426,2426,2426,2426,MONDO:0011426,aceruloplasminemia,MONDO,disease,DISEASE_2426
2427,2427,2427,2427,2427,2427,2427,2427,MONDO:0016480,silver-Russell syndrome due to an imprinting defect of 11p15,MONDO,disease,DISEASE_2427
2428,2428,2428,2428,2428,2428,2428,2428,MONDO:0020414,persistent fifth aortic arch,MONDO,disease,DISEASE_2428
2429,2429,2429,2429,2429,2429,2429,2429,MONDO:1012340,"chronic valvular disease, dog",MONDO,disease,DISEASE_2429
2430,2430,2430,2430,2430,2430,2430,2430,MONDO:1011197,"inherited rickets, DMP1-related, sheep",MONDO,disease,DISEASE_2430
2431,2431,2431,2431,2431,2431,2431,2431,MONDO:0013217_MONDO:0031071_MONDO:0007110_MONDO:0012529_MONDO:0013216_MONDO:0044309_MONDO:0014245_MONDO:0044310_MONDO:0012937_MONDO:0032669_MONDO:0032670_MONDO:0012938_MONDO:0032668_MONDO:0012939_MONDO:0012925_MONDO:0014394_MONDO:0012924_MONDO:0013964_MONDO:0015253_MONDO:0011636_MONDO:1011491,Diamond-Blackfan anemia,MONDO_grouped,disease,DISEASE_2431
2432,2432,2432,2432,2432,2432,2432,2432,MONDO:0011583,"cerebral amyloid angiopathy, APP-related",MONDO,disease,DISEASE_2432
2433,2433,2433,2433,2433,2433,2433,2433,MONDO:0021447,benign neoplasm of testis,MONDO,disease,DISEASE_2433
2434,2434,2434,2434,2434,2434,2434,2434,MONDO:1012135,"immunoglobulin M deficiency, horse",MONDO,disease,DISEASE_2434
2435,2435,2435,2435,2435,2435,2435,2435,MONDO:0003647,atrophic flaccid tympanic membrane,MONDO,disease,DISEASE_2435
2436,2436,2436,2436,2436,2436,2436,2436,MONDO:0005189,internal carotid artery stenosis,MONDO,disease,DISEASE_2436
2437,2437,2437,2437,2437,2437,2437,2437,MONDO:0023007,Drachtman Weinblatt Sitarz syndrome,MONDO,disease,DISEASE_2437
2438,2438,2438,2438,2438,2438,2438,2438,MONDO:0008157,Buschke-Ollendorff syndrome,MONDO,disease,DISEASE_2438
2439,2439,2439,2439,2439,2439,2439,2439,MONDO:0002623_MONDO:0003587,pediatric osteosarcoma,MONDO_grouped,disease,DISEASE_2439
2440,2440,2440,2440,2440,2440,2440,2440,MONDO:0043839,ulcer disease,MONDO,disease,DISEASE_2440
2441,2441,2441,2441,2441,2441,2441,2441,MONDO:1011256_MONDO:1011257_MONDO:1011260_MONDO:1011261,"achromatopsia, CNGB3-related, dog",MONDO_grouped,disease,DISEASE_2441
2442,2442,2442,2442,2442,2442,2442,2442,MONDO:0011496,mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis,MONDO,disease,DISEASE_2442
2443,2443,2443,2443,2443,2443,2443,2443,MONDO:0002590,combined thymoma,MONDO,disease,DISEASE_2443
2444,2444,2444,2444,2444,2444,2444,2444,MONDO:0019201,thyrotoxic periodic paralysis,MONDO,disease,DISEASE_2444
2445,2445,2445,2445,2445,2445,2445,2445,MONDO:0012589,Pitt-Hopkins syndrome,MONDO,disease,DISEASE_2445
2446,2446,2446,2446,2446,2446,2446,2446,MONDO:0016214,pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome,MONDO,disease,DISEASE_2446
2447,2447,2447,2447,2447,2447,2447,2447,MONDO:0021513,benign neoplasm of tonsil,MONDO,disease,DISEASE_2447
2448,2448,2448,2448,2448,2448,2448,2448,MONDO:0100465,complex neurodevelopmental disorder with or without congenital anomalies,MONDO,disease,DISEASE_2448
2449,2449,2449,2449,2449,2449,2449,2449,MONDO:0009174,protein-losing enteropathy,MONDO,disease,DISEASE_2449
2450,2450,2450,2450,2450,2450,2450,2450,MONDO:0045043,disorder of uterine broad ligament,MONDO,disease,DISEASE_2450
2451,2451,2451,2451,2451,2451,2451,2451,MONDO:0019584,localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms,MONDO,disease,DISEASE_2451
2452,2452,2452,2452,2452,2452,2452,2452,MONDO:0004766,status asthmaticus,MONDO,disease,DISEASE_2452
2453,2453,2453,2453,2453,2453,2453,2453,MONDO:1011602,"type 2 diabetes mellitus, Chinese hamster",MONDO,disease,DISEASE_2453
2454,2454,2454,2454,2454,2454,2454,2454,MONDO:0013144,hereditary antithrombin deficiency,MONDO,disease,DISEASE_2454
2455,2455,2455,2455,2455,2455,2455,2455,MONDO:0021074,precancerous condition,MONDO,disease,DISEASE_2455
2456,2456,2456,2456,2456,2456,2456,2456,MONDO:1012186_MONDO:1012188_MONDO:1012187_MONDO:1012238,"nephropathy, dog",MONDO_grouped,disease,DISEASE_2456
2457,2457,2457,2457,2457,2457,2457,2457,MONDO:0001769,acquired tear duct stenosis,MONDO,disease,DISEASE_2457
2458,2458,2458,2458,2458,2458,2458,2458,MONDO:0001643,exophthalmic ophthalmoplegia,MONDO,disease,DISEASE_2458
2459,2459,2459,2459,2459,2459,2459,2459,MONDO:0018979,multifocal motor neuropathy,MONDO,disease,DISEASE_2459
2460,2460,2460,2460,2460,2460,2460,2460,MONDO:0010773,mitochondrial myopathy with diabetes,MONDO,disease,DISEASE_2460
2461,2461,2461,2461,2461,2461,2461,2461,MONDO:0700108,"prion disease, non-human animal",MONDO,disease,DISEASE_2461
2462,2462,2462,2462,2462,2462,2462,2462,MONDO:0014232,"craniosynostosis 5, susceptibility to",MONDO,disease,DISEASE_2462
2463,2463,2463,2463,2463,2463,2463,2463,MONDO:0030750_MONDO:0030749_MONDO:0030768_MONDO:0030747_MONDO:0030748_MONDO:0030746,"epidermolysis bullosa, junctional 4, intermediate",MONDO_grouped,disease,DISEASE_2463
2464,2464,2464,2464,2464,2464,2464,2464,MONDO:0003955,juvenile breast papillomatosis,MONDO,disease,DISEASE_2464
2465,2465,2465,2465,2465,2465,2465,2465,MONDO:1011850,"necrotising myelopathy, non-human animal",MONDO,disease,DISEASE_2465
2466,2466,2466,2466,2466,2466,2466,2466,MONDO:0859207,neurodevelopmental disorder with hypotonia and gross motor and speech delay,MONDO,disease,DISEASE_2466
2467,2467,2467,2467,2467,2467,2467,2467,MONDO:0014080,osteosclerotic metaphyseal dysplasia,MONDO,disease,DISEASE_2467
2468,2468,2468,2468,2468,2468,2468,2468,MONDO:0001658,nontoxic goiter,MONDO,disease,DISEASE_2468
2469,2469,2469,2469,2469,2469,2469,2469,MONDO:0016168,cryopyrin-associated periodic syndrome,MONDO,disease,DISEASE_2469
2470,2470,2470,2470,2470,2470,2470,2470,MONDO:0800124,Lane Hamilton syndrome,MONDO,disease,DISEASE_2470
2471,2471,2471,2471,2471,2471,2471,2471,MONDO:0020513,spermatocytic seminoma,MONDO,disease,DISEASE_2471
2472,2472,2472,2472,2472,2472,2472,2472,MONDO:0004750_MONDO:0001276,language disorder,MONDO_grouped,disease,DISEASE_2472
2473,2473,2473,2473,2473,2473,2473,2473,MONDO:0011995,cataract - congenital heart disease - neural tube defect syndrome,MONDO,disease,DISEASE_2473
2474,2474,2474,2474,2474,2474,2474,2474,MONDO:0003264,basosquamous carcinoma,MONDO,disease,DISEASE_2474
2475,2475,2475,2475,2475,2475,2475,2475,MONDO:0001444,Chagas disease,MONDO,disease,DISEASE_2475
2476,2476,2476,2476,2476,2476,2476,2476,MONDO:0060662,Diamond-Blackfan anemia-like,MONDO,disease,DISEASE_2476
2477,2477,2477,2477,2477,2477,2477,2477,MONDO:0004186,cranial nodular fasciitis,MONDO,disease,DISEASE_2477
2478,2478,2478,2478,2478,2478,2478,2478,MONDO:0008688,WT limb-blood syndrome,MONDO,disease,DISEASE_2478
2479,2479,2479,2479,2479,2479,2479,2479,MONDO:0019818,cleft mitral valve,MONDO,disease,DISEASE_2479
2480,2480,2480,2480,2480,2480,2480,2480,MONDO:0043317,amyopathic dermatomyositis,MONDO,disease,DISEASE_2480
2481,2481,2481,2481,2481,2481,2481,2481,MONDO:1010446,"dilated cardiomyopathy, sea otter",MONDO,disease,DISEASE_2481
2482,2482,2482,2482,2482,2482,2482,2482,MONDO:0010421,Bruton-type agammaglobulinemia,MONDO,disease,DISEASE_2482
2483,2483,2483,2483,2483,2483,2483,2483,MONDO:0006893,Pasteurella hemorrhagic septicemia,MONDO,disease,DISEASE_2483
2484,2484,2484,2484,2484,2484,2484,2484,MONDO:0858950,traumatic brain injury,MONDO,disease,DISEASE_2484
2485,2485,2485,2485,2485,2485,2485,2485,MONDO:1012511,"generalized myoclonic epilepsy with photosensitivity, dog",MONDO,disease,DISEASE_2485
2486,2486,2486,2486,2486,2486,2486,2486,MONDO:0018926,human prion disease,MONDO,disease,DISEASE_2486
2487,2487,2487,2487,2487,2487,2487,2487,MONDO:0600001,glutaminase deficiency,MONDO,disease,DISEASE_2487
2488,2488,2488,2488,2488,2488,2488,2488,MONDO:0002286,renal artery disease,MONDO,disease,DISEASE_2488
2489,2489,2489,2489,2489,2489,2489,2489,MONDO:0015741,distal trisomy 18q,MONDO,disease,DISEASE_2489
2490,2490,2490,2490,2490,2490,2490,2490,MONDO:0001130,nasal cavity lymphoma,MONDO,disease,DISEASE_2490
2491,2491,2491,2491,2491,2491,2491,2491,MONDO:0003773,intracerebral cystic meningioma,MONDO,disease,DISEASE_2491
2492,2492,2492,2492,2492,2492,2492,2492,MONDO:0011038,cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome,MONDO,disease,DISEASE_2492
2493,2493,2493,2493,2493,2493,2493,2493,MONDO:0009792,ichthyosis-oral and digital anomalies syndrome,MONDO,disease,DISEASE_2493
2494,2494,2494,2494,2494,2494,2494,2494,MONDO:0001929_MONDO:0004786,ascending cholangitis,MONDO_grouped,disease,DISEASE_2494
2495,2495,2495,2495,2495,2495,2495,2495,MONDO:0004868_MONDO:0003060,biliary tract disorder,MONDO_grouped,disease,DISEASE_2495
2496,2496,2496,2496,2496,2496,2496,2496,MONDO:1010596_MONDO:1010597,"hyperthyroidism, horse",MONDO_grouped,disease,DISEASE_2496
2497,2497,2497,2497,2497,2497,2497,2497,MONDO:0045003,scrotal disorder,MONDO,disease,DISEASE_2497
2498,2498,2498,2498,2498,2498,2498,2498,MONDO:0010597,glutamyl ribose-5-phosphate storage disease,MONDO,disease,DISEASE_2498
2499,2499,2499,2499,2499,2499,2499,2499,MONDO:0800001,"delayed sleep phase syndrome, susceptibility to",MONDO,disease,DISEASE_2499
2500,2500,2500,2500,2500,2500,2500,2500,MONDO:0011052,amelia cleft lip palate hydrocephalus iris coloboma,MONDO,disease,DISEASE_2500
2501,2501,2501,2501,2501,2501,2501,2501,MONDO:0054559_MONDO:0030043_MONDO:0030437_MONDO:0030423_MONDO:0859357_MONDO:0859356_MONDO:0014904_MONDO:0012123_MONDO:0026729_MONDO:0957820_MONDO:0800044_MONDO:0008909_MONDO:0957540_MONDO:0026765_MONDO:0030770_MONDO:0015286_MONDO:0005500_MONDO:0005501_MONDO:0031376_MONDO:0800353_MONDO:0975846,"congenital disorder of glycosylation,",MONDO_grouped,disease,DISEASE_2501
2502,2502,2502,2502,2502,2502,2502,2502,MONDO:0008980,ataxia-hypogonadism-choroidal dystrophy syndrome,MONDO,disease,DISEASE_2502
2503,2503,2503,2503,2503,2503,2503,2503,MONDO:0007111_MONDO:0012194_MONDO:0032891_MONDO:0010468_MONDO:0012053_MONDO:0012443_MONDO:0012752_MONDO:0012810_MONDO:0012811_MONDO:0012949_MONDO:0012950_MONDO:0013654,"aneurysm, intracranial berry",MONDO_grouped,disease,DISEASE_2503
2504,2504,2504,2504,2504,2504,2504,2504,MONDO:0020317_MONDO:0044923,acute myeloid leukemia with 11q23 abnormalities,MONDO_grouped,disease,DISEASE_2504
2505,2505,2505,2505,2505,2505,2505,2505,MONDO:0100528,Hao-Fountain syndrome due to 16p13.2 microdeletion,MONDO,disease,DISEASE_2505
2506,2506,2506,2506,2506,2506,2506,2506,MONDO:0007931_MONDO:0024561_MONDO:0007933_MONDO:0014508_MONDO:0014509_MONDO:0000390,vitelliform macular dystrophy,MONDO_grouped,disease,DISEASE_2506
2507,2507,2507,2507,2507,2507,2507,2507,MONDO:0004857_MONDO:0100011,tendinitis,MONDO_grouped,disease,DISEASE_2507
2508,2508,2508,2508,2508,2508,2508,2508,MONDO:0016779_MONDO:0100499_MONDO:0100507,multiple congenital anomalies due to 14q32.2 maternally expressed gene defect,MONDO_grouped,disease,DISEASE_2508
2509,2509,2509,2509,2509,2509,2509,2509,MONDO:0030930,neurodevelopmental disorder with or without early-onset generalized epilepsy,MONDO,disease,DISEASE_2509
2510,2510,2510,2510,2510,2510,2510,2510,MONDO:0008064,"nasal bones, absence of",MONDO,disease,DISEASE_2510
2511,2511,2511,2511,2511,2511,2511,2511,MONDO:0002118,urinary system disorder,MONDO,disease,DISEASE_2511
2512,2512,2512,2512,2512,2512,2512,2512,MONDO:0005993,Trichomonas vaginitis urogenital infection,MONDO,disease,DISEASE_2512
2513,2513,2513,2513,2513,2513,2513,2513,MONDO:0017991,Takayasu arteritis,MONDO,disease,DISEASE_2513
2514,2514,2514,2514,2514,2514,2514,2514,MONDO:1010834_MONDO:1010835_MONDO:1010836,"Wilson disease, pig",MONDO_grouped,disease,DISEASE_2514
2515,2515,2515,2515,2515,2515,2515,2515,MONDO:0043361,May-Thurner syndrome,MONDO,disease,DISEASE_2515
2516,2516,2516,2516,2516,2516,2516,2516,MONDO:0001061,pylorus cancer,MONDO,disease,DISEASE_2516
2517,2517,2517,2517,2517,2517,2517,2517,MONDO:0019338_MONDO:0006611,sarcoidosis,MONDO_grouped,disease,DISEASE_2517
2518,2518,2518,2518,2518,2518,2518,2518,MONDO:0011136,Quebec platelet disorder,MONDO,disease,DISEASE_2518
2519,2519,2519,2519,2519,2519,2519,2519,MONDO:0033170,statin toxicity,MONDO,disease,DISEASE_2519
2520,2520,2520,2520,2520,2520,2520,2520,MONDO:0023679,hematohidrosis,MONDO,disease,DISEASE_2520
2521,2521,2521,2521,2521,2521,2521,2521,MONDO:0000530,rectum adenoma,MONDO,disease,DISEASE_2521
2522,2522,2522,2522,2522,2522,2522,2522,MONDO:0012721_MONDO:0030936_MONDO:0014521_MONDO:0014685_MONDO:0014545_MONDO:0013526_MONDO:0030034_MONDO:0012904_MONDO:0018126_MONDO:0020074,progressive myoclonic epilepsy,MONDO_grouped,disease,DISEASE_2522
2523,2523,2523,2523,2523,2523,2523,2523,MONDO:0021643,mesenteric varices,MONDO,disease,DISEASE_2523
2524,2524,2524,2524,2524,2524,2524,2524,MONDO:1012416,"Kurosawa and Kusanagi hypercholesterolaemia, rabbit",MONDO,disease,DISEASE_2524
2525,2525,2525,2525,2525,2525,2525,2525,MONDO:0015021,"hypotonia, ataxia, and delayed development syndrome",MONDO,disease,DISEASE_2525
2526,2526,2526,2526,2526,2526,2526,2526,MONDO:0010959,van den Ende-Gupta syndrome,MONDO,disease,DISEASE_2526
2527,2527,2527,2527,2527,2527,2527,2527,MONDO:0006132,cervical adenoid basal carcinoma,MONDO,disease,DISEASE_2527
2528,2528,2528,2528,2528,2528,2528,2528,MONDO:0001571,gynecomastia disorder,MONDO,disease,DISEASE_2528
2529,2529,2529,2529,2529,2529,2529,2529,MONDO:0007178,aurocephalosyndactyly,MONDO,disease,DISEASE_2529
2530,2530,2530,2530,2530,2530,2530,2530,MONDO:1010957,"colorectal cancer, MLH1-related, Rhesus monkey",MONDO,disease,DISEASE_2530
2531,2531,2531,2531,2531,2531,2531,2531,MONDO:0008062_MONDO:0012179_MONDO:0013652_MONDO:0021107_MONDO:1010418_MONDO:1010420_MONDO:1010421,narcolepsy,MONDO_grouped,disease,DISEASE_2531
2532,2532,2532,2532,2532,2532,2532,2532,MONDO:1012265,"androgen insensitivity syndrome, domestic cat",MONDO,disease,DISEASE_2532
2533,2533,2533,2533,2533,2533,2533,2533,MONDO:0008184,"pancreas, dorsal, agenesis of",MONDO,disease,DISEASE_2533
2534,2534,2534,2534,2534,2534,2534,2534,MONDO:0003182,anterior horn disorder,MONDO,disease,DISEASE_2534
2535,2535,2535,2535,2535,2535,2535,2535,MONDO:0022739,Christian Demyer Franken syndrome,MONDO,disease,DISEASE_2535
2536,2536,2536,2536,2536,2536,2536,2536,MONDO:1012061,"dermatosis vegetans, pig",MONDO,disease,DISEASE_2536
2537,2537,2537,2537,2537,2537,2537,2537,MONDO:0007635,Frasier syndrome,MONDO,disease,DISEASE_2537
2538,2538,2538,2538,2538,2538,2538,2538,MONDO:0011419,camera-Marugo-Cohen syndrome,MONDO,disease,DISEASE_2538
2539,2539,2539,2539,2539,2539,2539,2539,MONDO:0024876,tendon sheath disorder,MONDO,disease,DISEASE_2539
2540,2540,2540,2540,2540,2540,2540,2540,MONDO:0800066,polydactyly-syndactyly-triphalangism,MONDO,disease,DISEASE_2540
2541,2541,2541,2541,2541,2541,2541,2541,MONDO:0017076,posterior meningocele,MONDO,disease,DISEASE_2541
2542,2542,2542,2542,2542,2542,2542,2542,MONDO:0019036,amoebiasis due to free-living amoebae,MONDO,disease,DISEASE_2542
2543,2543,2543,2543,2543,2543,2543,2543,MONDO:1011942,"autosomal dwarfism, non-human animal",MONDO,disease,DISEASE_2543
2544,2544,2544,2544,2544,2544,2544,2544,MONDO:0008381,dominant pericentral pigmentary retinopathy,MONDO,disease,DISEASE_2544
2545,2545,2545,2545,2545,2545,2545,2545,MONDO:0018597,plastic bronchitis,MONDO,disease,DISEASE_2545
2546,2546,2546,2546,2546,2546,2546,2546,MONDO:0009018,central cloudy dystrophy of François,MONDO,disease,DISEASE_2546
2547,2547,2547,2547,2547,2547,2547,2547,MONDO:1011183_MONDO:1011184_MONDO:1011185,"vitamin D dependent rickets, CYP27B1-related, dog",MONDO_grouped,disease,DISEASE_2547
2548,2548,2548,2548,2548,2548,2548,2548,MONDO:0013858,pontine tegmental cap dysplasia,MONDO,disease,DISEASE_2548
2549,2549,2549,2549,2549,2549,2549,2549,MONDO:0006393,rectal traditional serrated adenoma,MONDO,disease,DISEASE_2549
2550,2550,2550,2550,2550,2550,2550,2550,MONDO:0003614,intravenous leiomyomatosis,MONDO,disease,DISEASE_2550
2551,2551,2551,2551,2551,2551,2551,2551,MONDO:0005774,glanders,MONDO,disease,DISEASE_2551
2552,2552,2552,2552,2552,2552,2552,2552,MONDO:0009118,disseminated sclerosis with narcolepsy,MONDO,disease,DISEASE_2552
2553,2553,2553,2553,2553,2553,2553,2553,MONDO:0011048,epilepsy-microcephaly-skeletal dysplasia syndrome,MONDO,disease,DISEASE_2553
2554,2554,2554,2554,2554,2554,2554,2554,MONDO:0015060,mosaic trisomy 3,MONDO,disease,DISEASE_2554
2555,2555,2555,2555,2555,2555,2555,2555,MONDO:0034092,optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome,MONDO,disease,DISEASE_2555
2556,2556,2556,2556,2556,2556,2556,2556,MONDO:0008249,pilonidal sinus,MONDO,disease,DISEASE_2556
2557,2557,2557,2557,2557,2557,2557,2557,MONDO:0957210,neurooculorenal syndrome,MONDO,disease,DISEASE_2557
2558,2558,2558,2558,2558,2558,2558,2558,MONDO:0003648,tympanic membrane disorder,MONDO,disease,DISEASE_2558
2559,2559,2559,2559,2559,2559,2559,2559,MONDO:1010808_MONDO:1010809_MONDO:1010810_MONDO:1010811_MONDO:1010813_MONDO:1010814_MONDO:1010819_MONDO:1010820_MONDO:1010821,"polydactyly, rock pigeon",MONDO_grouped,disease,DISEASE_2559
2560,2560,2560,2560,2560,2560,2560,2560,MONDO:1012616,"microphthalmia-4, chicken",MONDO,disease,DISEASE_2560
2561,2561,2561,2561,2561,2561,2561,2561,MONDO:0100276,disorder of defective peroxisomal and mitochondrial fission,MONDO,disease,DISEASE_2561
2562,2562,2562,2562,2562,2562,2562,2562,MONDO:0957541,"neurodevelopmental disorder with hypotonia and speech delay, with or without seizures",MONDO,disease,DISEASE_2562
2563,2563,2563,2563,2563,2563,2563,2563,MONDO:0044881,hematopoietic and lymphoid cell neoplasm,MONDO,disease,DISEASE_2563
2564,2564,2564,2564,2564,2564,2564,2564,MONDO:0011014_MONDO:0020555_MONDO:0020556_MONDO:0020557,pleuropulmonary blastoma,MONDO_grouped,disease,DISEASE_2564
2565,2565,2565,2565,2565,2565,2565,2565,MONDO:0019784,12q14 microdeletion syndrome,MONDO,disease,DISEASE_2565
2566,2566,2566,2566,2566,2566,2566,2566,MONDO:0859564_MONDO:0859390,"epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features",MONDO_grouped,disease,DISEASE_2566
2567,2567,2567,2567,2567,2567,2567,2567,MONDO:0002466,eye carcinoma,MONDO,disease,DISEASE_2567
2568,2568,2568,2568,2568,2568,2568,2568,MONDO:0009431_MONDO:0012795,hereditary hypophosphatemic rickets with hypercalciuria,MONDO_grouped,disease,DISEASE_2568
2569,2569,2569,2569,2569,2569,2569,2569,MONDO:0017181,hypnic headache,MONDO,disease,DISEASE_2569
2570,2570,2570,2570,2570,2570,2570,2570,MONDO:0006733,dry eye syndrome,MONDO,disease,DISEASE_2570
2571,2571,2571,2571,2571,2571,2571,2571,MONDO:0002436,nasal disorder,MONDO,disease,DISEASE_2571
2572,2572,2572,2572,2572,2572,2572,2572,MONDO:0009368_MONDO:0014049,urofacial syndrome,MONDO_grouped,disease,DISEASE_2572
2573,2573,2573,2573,2573,2573,2573,2573,MONDO:8000003,streptococcus pneumoniae discitis,MONDO,disease,DISEASE_2573
2574,2574,2574,2574,2574,2574,2574,2574,MONDO:0001561,pyloric stenosis,MONDO,disease,DISEASE_2574
2575,2575,2575,2575,2575,2575,2575,2575,MONDO:0003918,angiomatous meningioma,MONDO,disease,DISEASE_2575
2576,2576,2576,2576,2576,2576,2576,2576,MONDO:1010155,"cutis laxa, non-human animal",MONDO,disease,DISEASE_2576
2577,2577,2577,2577,2577,2577,2577,2577,MONDO:0002666,pancreatic signet ring cell adenocarcinoma,MONDO,disease,DISEASE_2577
2578,2578,2578,2578,2578,2578,2578,2578,MONDO:0009549,severe early-childhood-onset retinal dystrophy,MONDO,disease,DISEASE_2578
2579,2579,2579,2579,2579,2579,2579,2579,MONDO:0005058_MONDO:0003291_MONDO:0002624_MONDO:0003347_MONDO:0003348_MONDO:0003353_MONDO:0003373,leiomyosarcoma,MONDO_grouped,disease,DISEASE_2579
2580,2580,2580,2580,2580,2580,2580,2580,MONDO:0016292,nodular neuronal heterotopia,MONDO,disease,DISEASE_2580
2581,2581,2581,2581,2581,2581,2581,2581,MONDO:0850065,neonatal-onset severe multisystemic autoinflammatory disease with increased IL18,MONDO,disease,DISEASE_2581
2582,2582,2582,2582,2582,2582,2582,2582,MONDO:0958205,Yuksel-Vogel-Bauer syndrome,MONDO,disease,DISEASE_2582
2583,2583,2583,2583,2583,2583,2583,2583,MONDO:0035293,streptococcus pneumoniae-associated hemolytic uremic syndrome,MONDO,disease,DISEASE_2583
2584,2584,2584,2584,2584,2584,2584,2584,MONDO:0018443,FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome,MONDO,disease,DISEASE_2584
2585,2585,2585,2585,2585,2585,2585,2585,MONDO:0002353,glottis neoplasm,MONDO,disease,DISEASE_2585
2586,2586,2586,2586,2586,2586,2586,2586,MONDO:0008819,"arteriosclerosis, severe juvenile",MONDO,disease,DISEASE_2586
2587,2587,2587,2587,2587,2587,2587,2587,MONDO:0005728,diaphragm disorder,MONDO,disease,DISEASE_2587
2588,2588,2588,2588,2588,2588,2588,2588,MONDO:0700161,canine gastrointestinal stromal tumor,MONDO,disease,DISEASE_2588
2589,2589,2589,2589,2589,2589,2589,2589,MONDO:0013273,chromosome 16p13.3 duplication syndrome,MONDO,disease,DISEASE_2589
2590,2590,2590,2590,2590,2590,2590,2590,MONDO:0006949,retinal drusen,MONDO,disease,DISEASE_2590
2591,2591,2591,2591,2591,2591,2591,2591,MONDO:0017594,indolent B-cell non-Hodgkin lymphoma,MONDO,disease,DISEASE_2591
2592,2592,2592,2592,2592,2592,2592,2592,MONDO:0002067,female breast upper-inner quadrant cancer,MONDO,disease,DISEASE_2592
2593,2593,2593,2593,2593,2593,2593,2593,MONDO:0022904,cryofibrinogenemia,MONDO,disease,DISEASE_2593
2594,2594,2594,2594,2594,2594,2594,2594,MONDO:0005194,Rotavirus infection,MONDO,disease,DISEASE_2594
2595,2595,2595,2595,2595,2595,2595,2595,MONDO:0034971,isolated congenital entropion,MONDO,disease,DISEASE_2595
2596,2596,2596,2596,2596,2596,2596,2596,MONDO:0003653,stork bite,MONDO,disease,DISEASE_2596
2597,2597,2597,2597,2597,2597,2597,2597,MONDO:0020464,euryblepharon,MONDO,disease,DISEASE_2597
2598,2598,2598,2598,2598,2598,2598,2598,MONDO:0006468,thyroid gland undifferentiated (anaplastic) carcinoma,MONDO,disease,DISEASE_2598
2599,2599,2599,2599,2599,2599,2599,2599,MONDO:0010134,Pendred syndrome,MONDO,disease,DISEASE_2599
2600,2600,2600,2600,2600,2600,2600,2600,MONDO:0003714,bladder urachal squamous cell carcinoma,MONDO,disease,DISEASE_2600
2601,2601,2601,2601,2601,2601,2601,2601,MONDO:0043455,humoral hypercalcemia of malignancy,MONDO,disease,DISEASE_2601
2602,2602,2602,2602,2602,2602,2602,2602,MONDO:0007832,interferon antiviral depressor,MONDO,disease,DISEASE_2602
2603,2603,2603,2603,2603,2603,2603,2603,MONDO:0032889,Poirier-Bienvenu neurodevelopmental syndrome,MONDO,disease,DISEASE_2603
2604,2604,2604,2604,2604,2604,2604,2604,MONDO:0002641,subclavian artery aneurysm,MONDO,disease,DISEASE_2604
2605,2605,2605,2605,2605,2605,2605,2605,MONDO:0009929_MONDO:0013712_MONDO:0024465_MONDO:0010424_MONDO:1012534,"surfactant metabolism dysfunction, pulmonary",MONDO_grouped,disease,DISEASE_2605
2606,2606,2606,2606,2606,2606,2606,2606,MONDO:0007433,dementia/parkinsonism with non-Alzheimer amyloid plaques,MONDO,disease,DISEASE_2606
2607,2607,2607,2607,2607,2607,2607,2607,MONDO:0019900,non-distal monosomy 12q,MONDO,disease,DISEASE_2607
2608,2608,2608,2608,2608,2608,2608,2608,MONDO:0002219,paraurethral gland neoplasm,MONDO,disease,DISEASE_2608
2609,2609,2609,2609,2609,2609,2609,2609,MONDO:0017992,autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis,MONDO,disease,DISEASE_2609
2610,2610,2610,2610,2610,2610,2610,2610,MONDO:0003821,ovarian biphasic or triphasic teratoma,MONDO,disease,DISEASE_2610
2611,2611,2611,2611,2611,2611,2611,2611,MONDO:0800178,platinum-induced ototoxicity,MONDO,disease,DISEASE_2611
2612,2612,2612,2612,2612,2612,2612,2612,MONDO:0018616,central serous chorioretinopathy,MONDO,disease,DISEASE_2612
2613,2613,2613,2613,2613,2613,2613,2613,MONDO:0012611,"polyhydramnios, megalencephaly, and symptomatic epilepsy",MONDO,disease,DISEASE_2613
2614,2614,2614,2614,2614,2614,2614,2614,MONDO:1012865,"deafness, KLF7-related, dog",MONDO,disease,DISEASE_2614
2615,2615,2615,2615,2615,2615,2615,2615,MONDO:0007778,obsolete hypertelorism,MONDO,disease,DISEASE_2615
2616,2616,2616,2616,2616,2616,2616,2616,MONDO:1010247_MONDO:1011888,"lissencephaly and cerebellar hypoplasia, non-human animal",MONDO_grouped,disease,DISEASE_2616
2617,2617,2617,2617,2617,2617,2617,2617,MONDO:0022771,circumscribed disseminated keratosis Jadassohn lew type,MONDO,disease,DISEASE_2617
2618,2618,2618,2618,2618,2618,2618,2618,MONDO:0975836,Karayol-Borroto-Haghshenas neurodevelopmental syndrome,MONDO,disease,DISEASE_2618
2619,2619,2619,2619,2619,2619,2619,2619,MONDO:0003895,periosteal osteogenic sarcoma,MONDO,disease,DISEASE_2619
2620,2620,2620,2620,2620,2620,2620,2620,MONDO:0024286,benign blood vessel neoplasm,MONDO,disease,DISEASE_2620
2621,2621,2621,2621,2621,2621,2621,2621,MONDO:0008069_MONDO:1012293,"necrotizing encephalomyelopathy, subacute, of Leigh, adult",MONDO_grouped,disease,DISEASE_2621
2622,2622,2622,2622,2622,2622,2622,2622,MONDO:0023472,chondrodysplasia situs inversus imperforate anus polydactyly,MONDO,disease,DISEASE_2622
2623,2623,2623,2623,2623,2623,2623,2623,MONDO:0017612_MONDO:1010751_MONDO:1011547,junctional epidermolysis bullosa,MONDO_grouped,disease,DISEASE_2623
2624,2624,2624,2624,2624,2624,2624,2624,MONDO:0003942,eosinophilic variant of chromophobe renal cell carcinoma,MONDO,disease,DISEASE_2624
2625,2625,2625,2625,2625,2625,2625,2625,MONDO:0000004,adrenocortical insufficiency,MONDO,disease,DISEASE_2625
2626,2626,2626,2626,2626,2626,2626,2626,MONDO:0006581,miliaria rubra,MONDO,disease,DISEASE_2626
2627,2627,2627,2627,2627,2627,2627,2627,MONDO:0013934,combined immunodeficiency due to STK4 deficiency,MONDO,disease,DISEASE_2627
2628,2628,2628,2628,2628,2628,2628,2628,MONDO:0008816_MONDO:0007316_MONDO:0000115_MONDO:0022715_MONDO:0022716,Chiari malformation,MONDO_grouped,disease,DISEASE_2628
2629,2629,2629,2629,2629,2629,2629,2629,MONDO:0019171,familial long QT syndrome,MONDO,disease,DISEASE_2629
2630,2630,2630,2630,2630,2630,2630,2630,MONDO:0002931,conjunctivochalasis,MONDO,disease,DISEASE_2630
2631,2631,2631,2631,2631,2631,2631,2631,MONDO:0003388,ampulla of vater clear cell adenocarcinoma,MONDO,disease,DISEASE_2631
2632,2632,2632,2632,2632,2632,2632,2632,MONDO:0007305,cervical vertebral dysplasia,MONDO,disease,DISEASE_2632
2633,2633,2633,2633,2633,2633,2633,2633,MONDO:0010903,"craniosynostosis, Adelaide type",MONDO,disease,DISEASE_2633
2634,2634,2634,2634,2634,2634,2634,2634,MONDO:0006833,lingual goiter,MONDO,disease,DISEASE_2634
2635,2635,2635,2635,2635,2635,2635,2635,MONDO:0007127,diffuse idiopathic skeletal hyperostosis,MONDO,disease,DISEASE_2635
2636,2636,2636,2636,2636,2636,2636,2636,MONDO:0009253,Fryns syndrome,MONDO,disease,DISEASE_2636
2637,2637,2637,2637,2637,2637,2637,2637,MONDO:0008883,"brachydactyly, type A2, with microcephaly",MONDO,disease,DISEASE_2637
2638,2638,2638,2638,2638,2638,2638,2638,MONDO:1011450,"xanthinuria, non-human animal",MONDO,disease,DISEASE_2638
2639,2639,2639,2639,2639,2639,2639,2639,MONDO:0003581,ovarian embryonal carcinoma,MONDO,disease,DISEASE_2639
2640,2640,2640,2640,2640,2640,2640,2640,MONDO:0008984,ciliary discoordination due to random ciliary orientation,MONDO,disease,DISEASE_2640
2641,2641,2641,2641,2641,2641,2641,2641,MONDO:0010745,beta-thalassemia-X-linked thrombocytopenia syndrome,MONDO,disease,DISEASE_2641
2642,2642,2642,2642,2642,2642,2642,2642,MONDO:0011696_MONDO:0011695,"melanoma, uveal, susceptibility to",MONDO_grouped,disease,DISEASE_2642
2643,2643,2643,2643,2643,2643,2643,2643,MONDO:0006159,colorectal gastrointestinal stromal tumor,MONDO,disease,DISEASE_2643
2644,2644,2644,2644,2644,2644,2644,2644,MONDO:0004957,mucinous adenocarcinoma,MONDO,disease,DISEASE_2644
2645,2645,2645,2645,2645,2645,2645,2645,MONDO:0014009_MONDO:0014010_MONDO:0011218_MONDO:0014011_MONDO:0011485_MONDO:0009443_MONDO:0015018_MONDO:0009439_MONDO:0009441_MONDO:0012847_MONDO:0011680_MONDO:0013495_MONDO:0011026_MONDO:0033092_MONDO:0009209_MONDO:0033091_MONDO:0017265,autosomal recessive congenital ichthyosis,MONDO_grouped,disease,DISEASE_2645
2646,2646,2646,2646,2646,2646,2646,2646,MONDO:0020672,vascular occlusion disorder,MONDO,disease,DISEASE_2646
2647,2647,2647,2647,2647,2647,2647,2647,MONDO:0010477,"blepharophimosis - intellectual disability syndrome, MKB type",MONDO,disease,DISEASE_2647
2648,2648,2648,2648,2648,2648,2648,2648,MONDO:0030876_MONDO:0030877_MONDO:0031386,cardioacrofacial dysplasia,MONDO_grouped,disease,DISEASE_2648
2649,2649,2649,2649,2649,2649,2649,2649,MONDO:0009287,glycogen storage disease due to glucose-6-phosphatase deficiency type IA,MONDO,disease,DISEASE_2649
2650,2650,2650,2650,2650,2650,2650,2650,MONDO:0035605,B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality,MONDO,disease,DISEASE_2650
2651,2651,2651,2651,2651,2651,2651,2651,MONDO:0003453,conjunctival intraepithelial neoplasm,MONDO,disease,DISEASE_2651
2652,2652,2652,2652,2652,2652,2652,2652,MONDO:0016705,angiocentric glioma,MONDO,disease,DISEASE_2652
2653,2653,2653,2653,2653,2653,2653,2653,MONDO:0009921,holoprosencephaly-postaxial polydactyly syndrome,MONDO,disease,DISEASE_2653
2654,2654,2654,2654,2654,2654,2654,2654,MONDO:0859278,"keratoderma-ichthyosis-deafness syndrome, autosomal recessive",MONDO,disease,DISEASE_2654
2655,2655,2655,2655,2655,2655,2655,2655,MONDO:0000979,pinta disease,MONDO,disease,DISEASE_2655
2656,2656,2656,2656,2656,2656,2656,2656,MONDO:0009375,"hymen, imperforate",MONDO,disease,DISEASE_2656
2657,2657,2657,2657,2657,2657,2657,2657,MONDO:0014151,"pulmonary hypertension, neonatal, susceptibility to",MONDO,disease,DISEASE_2657
2658,2658,2658,2658,2658,2658,2658,2658,MONDO:1012500,"subclinical hypomagnesemia, cattle",MONDO,disease,DISEASE_2658
2659,2659,2659,2659,2659,2659,2659,2659,MONDO:0008968,"cholestasis with gallstone, ataxia, and visual disturbance",MONDO,disease,DISEASE_2659
2660,2660,2660,2660,2660,2660,2660,2660,MONDO:0030990,Kohlschutter-Tonz syndrome-like,MONDO,disease,DISEASE_2660
2661,2661,2661,2661,2661,2661,2661,2661,MONDO:0011654,"intellectual disability, microcephaly, growth retardation, joint contractures, and facial dysmorphism",MONDO,disease,DISEASE_2661
2662,2662,2662,2662,2662,2662,2662,2662,MONDO:0006392,rectal hyperplastic polyp,MONDO,disease,DISEASE_2662
2663,2663,2663,2663,2663,2663,2663,2663,MONDO:0016046,familial clubfoot with or without associated lower limb anomalies,MONDO,disease,DISEASE_2663
2664,2664,2664,2664,2664,2664,2664,2664,MONDO:0006984,subdural empyema,MONDO,disease,DISEASE_2664
2665,2665,2665,2665,2665,2665,2665,2665,MONDO:0700150,canine mastocytoma,MONDO,disease,DISEASE_2665
2666,2666,2666,2666,2666,2666,2666,2666,MONDO:0026419,obsolete isolated corpus callosum agenesis,MONDO,disease,DISEASE_2666
2667,2667,2667,2667,2667,2667,2667,2667,MONDO:0004882,angioid streaks of choroid,MONDO,disease,DISEASE_2667
2668,2668,2668,2668,2668,2668,2668,2668,MONDO:0022333,5-nucleotidase syndrome,MONDO,disease,DISEASE_2668
2669,2669,2669,2669,2669,2669,2669,2669,MONDO:0002966,splenic manifestation of prolymphocytic leukemia,MONDO,disease,DISEASE_2669
2670,2670,2670,2670,2670,2670,2670,2670,MONDO:0003190_MONDO:0003189_MONDO:0003423,middle ear carcinoma,MONDO_grouped,disease,DISEASE_2670
2671,2671,2671,2671,2671,2671,2671,2671,MONDO:0016958,partial duplication of the long arm of chromosome 7,MONDO,disease,DISEASE_2671
2672,2672,2672,2672,2672,2672,2672,2672,MONDO:0005279,pulmonary embolism,MONDO,disease,DISEASE_2672
2673,2673,2673,2673,2673,2673,2673,2673,MONDO:0006573,lipodystrophy,MONDO,disease,DISEASE_2673
2674,2674,2674,2674,2674,2674,2674,2674,MONDO:0022893_MONDO:0022895,craniosynostosis arthrogryposis cleft palate,MONDO_grouped,disease,DISEASE_2674
2675,2675,2675,2675,2675,2675,2675,2675,MONDO:0014380,colobomatous microphthalmia-rhizomelic dysplasia syndrome,MONDO,disease,DISEASE_2675
2676,2676,2676,2676,2676,2676,2676,2676,MONDO:1011110,"cryptorchidism, puma",MONDO,disease,DISEASE_2676
2677,2677,2677,2677,2677,2677,2677,2677,MONDO:1012090,"gastric dilatation volvulus syndrome, maned wolf",MONDO,disease,DISEASE_2677
2678,2678,2678,2678,2678,2678,2678,2678,MONDO:0017874,Argentine hemorrhagic fever,MONDO,disease,DISEASE_2678
2679,2679,2679,2679,2679,2679,2679,2679,MONDO:0005586,head and neck neoplasm,MONDO,disease,DISEASE_2679
2680,2680,2680,2680,2680,2680,2680,2680,MONDO:0011931,"ovarian cancer, susceptibility to, 1",MONDO,disease,DISEASE_2680
2681,2681,2681,2681,2681,2681,2681,2681,MONDO:1012378,"hereditary pancreatitis, dog",MONDO,disease,DISEASE_2681
2682,2682,2682,2682,2682,2682,2682,2682,MONDO:0018794,cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder,MONDO,disease,DISEASE_2682
2683,2683,2683,2683,2683,2683,2683,2683,MONDO:0016060_MONDO:0019764_MONDO:0017220_MONDO:0019761_MONDO:0019762_MONDO:0019763,laryngotracheoesophageal cleft,MONDO_grouped,disease,DISEASE_2683
2684,2684,2684,2684,2684,2684,2684,2684,MONDO:0007384,congenital trigeminal anesthesia,MONDO,disease,DISEASE_2684
2685,2685,2685,2685,2685,2685,2685,2685,MONDO:0015383,cervicofacial fibrochondroma,MONDO,disease,DISEASE_2685
2686,2686,2686,2686,2686,2686,2686,2686,MONDO:0007715,hemolytic poikilocytic anemia due to reduced ankyrin binding sites,MONDO,disease,DISEASE_2686
2687,2687,2687,2687,2687,2687,2687,2687,MONDO:0007765,hyperostosis cranialis interna,MONDO,disease,DISEASE_2687
2688,2688,2688,2688,2688,2688,2688,2688,MONDO:0010898,autosomal dominant epilepsy with auditory features,MONDO,disease,DISEASE_2688
2689,2689,2689,2689,2689,2689,2689,2689,MONDO:0004942,orbit lymphoma,MONDO,disease,DISEASE_2689
2690,2690,2690,2690,2690,2690,2690,2690,MONDO:1010070,"Chediak-Higashi syndrome, non-human animal",MONDO,disease,DISEASE_2690
2691,2691,2691,2691,2691,2691,2691,2691,MONDO:0012729_MONDO:0033483_MONDO:0012353_MONDO:0054802_MONDO:0054801,"erythrocytosis, familial",MONDO_grouped,disease,DISEASE_2691
2692,2692,2692,2692,2692,2692,2692,2692,MONDO:0006188,EBV-positive T-cell lymphoproliferative disorder of childhood,MONDO,disease,DISEASE_2692
2693,2693,2693,2693,2693,2693,2693,2693,MONDO:0011798,"hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration",MONDO,disease,DISEASE_2693
2694,2694,2694,2694,2694,2694,2694,2694,MONDO:0006865,necrotizing ulcerative gingivitis,MONDO,disease,DISEASE_2694
2695,2695,2695,2695,2695,2695,2695,2695,MONDO:1010503_MONDO:1010504_MONDO:1010505_MONDO:1010506_MONDO:1010507,"endocardial fibroelastosis, dog",MONDO_grouped,disease,DISEASE_2695
2696,2696,2696,2696,2696,2696,2696,2696,MONDO:0004662,heterophyiasis,MONDO,disease,DISEASE_2696
2697,2697,2697,2697,2697,2697,2697,2697,MONDO:0021645_MONDO:0021644,esophageal varices with bleeding,MONDO_grouped,disease,DISEASE_2697
2698,2698,2698,2698,2698,2698,2698,2698,MONDO:0006111,bladder flat intraepithelial lesion,MONDO,disease,DISEASE_2698
2699,2699,2699,2699,2699,2699,2699,2699,MONDO:0003813,ovarian papillary tumor,MONDO,disease,DISEASE_2699
2700,2700,2700,2700,2700,2700,2700,2700,MONDO:0016865,Kleefstra syndrome due to a point mutation,MONDO,disease,DISEASE_2700
2701,2701,2701,2701,2701,2701,2701,2701,MONDO:0021345,carcinoma of pharynx,MONDO,disease,DISEASE_2701
2702,2702,2702,2702,2702,2702,2702,2702,MONDO:1011005_MONDO:1011006,"leukodystrophy, dog",MONDO_grouped,disease,DISEASE_2702
2703,2703,2703,2703,2703,2703,2703,2703,MONDO:0030875_MONDO:0007105_MONDO:0030872_MONDO:0014395_MONDO:0014641_MONDO:0013501_MONDO:0014640_MONDO:0010936_MONDO:0030923,frontotemporal dementia and/or amyotrophic lateral sclerosis,MONDO_grouped,disease,DISEASE_2703
2704,2704,2704,2704,2704,2704,2704,2704,MONDO:1012199,"ocular squamous cell carcinoma, sheep",MONDO,disease,DISEASE_2704
2705,2705,2705,2705,2705,2705,2705,2705,MONDO:0014959,"mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant",MONDO,disease,DISEASE_2705
2706,2706,2706,2706,2706,2706,2706,2706,MONDO:0009334,hemolytic anemia with thermal sensitivity of red cells,MONDO,disease,DISEASE_2706
2707,2707,2707,2707,2707,2707,2707,2707,MONDO:0700142,canine hemangiosarcoma,MONDO,disease,DISEASE_2707
2708,2708,2708,2708,2708,2708,2708,2708,MONDO:0021245,oral cavity neoplasm,MONDO,disease,DISEASE_2708
2709,2709,2709,2709,2709,2709,2709,2709,MONDO:0004674,chorioretinitis,MONDO,disease,DISEASE_2709
2710,2710,2710,2710,2710,2710,2710,2710,MONDO:0009578,neurocutaneous melanocytosis,MONDO,disease,DISEASE_2710
2711,2711,2711,2711,2711,2711,2711,2711,MONDO:0007895,"platyspondylic dysplasia, Torrance type",MONDO,disease,DISEASE_2711
2712,2712,2712,2712,2712,2712,2712,2712,MONDO:1010668,"factor XIII deficiency, cattle",MONDO,disease,DISEASE_2712
2713,2713,2713,2713,2713,2713,2713,2713,MONDO:0025356,"azoospermia, obstructive, with nephrolithiasis",MONDO,disease,DISEASE_2713
2714,2714,2714,2714,2714,2714,2714,2714,MONDO:1012549,"asymmetrical occipital condylar dysplasia, sheep",MONDO,disease,DISEASE_2714
2715,2715,2715,2715,2715,2715,2715,2715,MONDO:0001753,female infertility of uterine origin,MONDO,disease,DISEASE_2715
2716,2716,2716,2716,2716,2716,2716,2716,MONDO:0011406,"cholesteatoma, congenital",MONDO,disease,DISEASE_2716
2717,2717,2717,2717,2717,2717,2717,2717,MONDO:1012328,"cutaneous and renal vasculopathy, dog",MONDO,disease,DISEASE_2717
2718,2718,2718,2718,2718,2718,2718,2718,MONDO:0008542,tetralogy of fallot,MONDO,disease,DISEASE_2718
2719,2719,2719,2719,2719,2719,2719,2719,MONDO:0700222,disease related to hematopoietic stem cell transplant,MONDO,disease,DISEASE_2719
2720,2720,2720,2720,2720,2720,2720,2720,MONDO:0016857,blepharophimosis-epicanthus inversus-ptosis due to 3q23 rearrangement syndrome,MONDO,disease,DISEASE_2720
2721,2721,2721,2721,2721,2721,2721,2721,MONDO:0005898,paronychia,MONDO,disease,DISEASE_2721
2722,2722,2722,2722,2722,2722,2722,2722,MONDO:0009320,Hall-Riggs syndrome,MONDO,disease,DISEASE_2722
2723,2723,2723,2723,2723,2723,2723,2723,MONDO:0000739,uvulitis,MONDO,disease,DISEASE_2723
2724,2724,2724,2724,2724,2724,2724,2724,MONDO:0009940,pycnodysostosis,MONDO,disease,DISEASE_2724
2725,2725,2725,2725,2725,2725,2725,2725,MONDO:0003640,verruciform xanthoma of skin,MONDO,disease,DISEASE_2725
2726,2726,2726,2726,2726,2726,2726,2726,MONDO:0003881,vulvar apocrine adenocarcinoma,MONDO,disease,DISEASE_2726
2727,2727,2727,2727,2727,2727,2727,2727,MONDO:0014118,congenital neutropenia-myelofibrosis-nephromegaly syndrome,MONDO,disease,DISEASE_2727
2728,2728,2728,2728,2728,2728,2728,2728,MONDO:0003596_MONDO:0005238,spindle cell liposarcoma,MONDO_grouped,disease,DISEASE_2728
2729,2729,2729,2729,2729,2729,2729,2729,MONDO:1010040,"pyloric stenosis, non-human animal",MONDO,disease,DISEASE_2729
2730,2730,2730,2730,2730,2730,2730,2730,MONDO:0001819,multiple cranial nerve palsy,MONDO,disease,DISEASE_2730
2731,2731,2731,2731,2731,2731,2731,2731,MONDO:0017711,pancreatic colipase deficiency,MONDO,disease,DISEASE_2731
2732,2732,2732,2732,2732,2732,2732,2732,MONDO:0008195,paramyotonia congenita of Von Eulenburg,MONDO,disease,DISEASE_2732
2733,2733,2733,2733,2733,2733,2733,2733,MONDO:0004909,urethral gland abscess,MONDO,disease,DISEASE_2733
2734,2734,2734,2734,2734,2734,2734,2734,MONDO:0004227,epididymal adenomatoid tumor,MONDO,disease,DISEASE_2734
2735,2735,2735,2735,2735,2735,2735,2735,MONDO:0009108,hyperdibasic aminoaciduria type 1,MONDO,disease,DISEASE_2735
2736,2736,2736,2736,2736,2736,2736,2736,MONDO:0043101,hypothalamic dysfunction,MONDO,disease,DISEASE_2736
2737,2737,2737,2737,2737,2737,2737,2737,MONDO:0019196,Foix-Alajouanine syndrome,MONDO,disease,DISEASE_2737
2738,2738,2738,2738,2738,2738,2738,2738,MONDO:0019980_MONDO:0019645,"renal hypoplasia, bilateral",MONDO_grouped,disease,DISEASE_2738
2739,2739,2739,2739,2739,2739,2739,2739,MONDO:0000432,lymphoplasmacytic lymphoma,MONDO,disease,DISEASE_2739
2740,2740,2740,2740,2740,2740,2740,2740,MONDO:0018683,acquired ichthyosis,MONDO,disease,DISEASE_2740
2741,2741,2741,2741,2741,2741,2741,2741,MONDO:0013329_MONDO:0017382,familial clubfoot due to 17q23.1q23.2 microduplication,MONDO_grouped,disease,DISEASE_2741
2742,2742,2742,2742,2742,2742,2742,2742,MONDO:0004665,nodular sclerosis classical Hodgkin lymphoma,MONDO,disease,DISEASE_2742
2743,2743,2743,2743,2743,2743,2743,2743,MONDO:0000891,mixed fibrolamellar hepatocellular carcinoma,MONDO,disease,DISEASE_2743
2744,2744,2744,2744,2744,2744,2744,2744,MONDO:0020307,self-limited epilepsy with autonomic seizures,MONDO,disease,DISEASE_2744
2745,2745,2745,2745,2745,2745,2745,2745,MONDO:0030674_MONDO:0800025_MONDO:0030639,Teebi hypertelorism syndrome,MONDO_grouped,disease,DISEASE_2745
2746,2746,2746,2746,2746,2746,2746,2746,MONDO:0012082_MONDO:0012079_MONDO:0012119_MONDO:0012377,"asperger syndrome, susceptibility to",MONDO_grouped,disease,DISEASE_2746
2747,2747,2747,2747,2747,2747,2747,2747,MONDO:0010077,spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome,MONDO,disease,DISEASE_2747
2748,2748,2748,2748,2748,2748,2748,2748,MONDO:0015169,chronic diarrhea due to glucoamylase deficiency,MONDO,disease,DISEASE_2748
2749,2749,2749,2749,2749,2749,2749,2749,MONDO:0007882,lattice degeneration of retina leading to retinal detachment,MONDO,disease,DISEASE_2749
2750,2750,2750,2750,2750,2750,2750,2750,MONDO:0011490,diffuse panbronchiolitis,MONDO,disease,DISEASE_2750
2751,2751,2751,2751,2751,2751,2751,2751,MONDO:0022071,carbon baby syndrome,MONDO,disease,DISEASE_2751
2752,2752,2752,2752,2752,2752,2752,2752,MONDO:0003064,inverted transitional cell papilloma,MONDO,disease,DISEASE_2752
2753,2753,2753,2753,2753,2753,2753,2753,MONDO:0020373_MONDO:0020378_MONDO:0018610,early-onset anterior polar cataract,MONDO_grouped,disease,DISEASE_2753
2754,2754,2754,2754,2754,2754,2754,2754,MONDO:0014742_MONDO:0011220,"Parkinson disease 22, autosomal dominant",MONDO_grouped,disease,DISEASE_2754
2755,2755,2755,2755,2755,2755,2755,2755,MONDO:0006500,hemangioma,MONDO,disease,DISEASE_2755
2756,2756,2756,2756,2756,2756,2756,2756,MONDO:0012292_MONDO:0012488,"hepatitis C virus, susceptibility",MONDO_grouped,disease,DISEASE_2756
2757,2757,2757,2757,2757,2757,2757,2757,MONDO:0002729,rhabdoid tumor of the kidney,MONDO,disease,DISEASE_2757
2758,2758,2758,2758,2758,2758,2758,2758,MONDO:0000369,abdominal tuberculosis,MONDO,disease,DISEASE_2758
2759,2759,2759,2759,2759,2759,2759,2759,MONDO:1010062,"congenital adrenal hyperplasia due to 11-beta hydroxylase deficiency, non-human animal",MONDO,disease,DISEASE_2759
2760,2760,2760,2760,2760,2760,2760,2760,MONDO:0016032_MONDO:0017484_MONDO:0017485,femoral agenesis/hypoplasia,MONDO_grouped,disease,DISEASE_2760
2761,2761,2761,2761,2761,2761,2761,2761,MONDO:0003211,nasal cavity adenocarcinoma,MONDO,disease,DISEASE_2761
2762,2762,2762,2762,2762,2762,2762,2762,MONDO:0000837,bone resorption disease,MONDO,disease,DISEASE_2762
2763,2763,2763,2763,2763,2763,2763,2763,MONDO:0017343,Epstein-Barr virus-associated malignant lymphoproliferative disorder,MONDO,disease,DISEASE_2763
2764,2764,2764,2764,2764,2764,2764,2764,MONDO:0001665,oculoglandular tularemia,MONDO,disease,DISEASE_2764
2765,2765,2765,2765,2765,2765,2765,2765,MONDO:0014651,acrofacial dysostosis Cincinnati type,MONDO,disease,DISEASE_2765
2766,2766,2766,2766,2766,2766,2766,2766,MONDO:0030974_MONDO:0030935_MONDO:0030937,"mitochondrial complex 2 deficiency, nuclear",MONDO_grouped,disease,DISEASE_2766
2767,2767,2767,2767,2767,2767,2767,2767,MONDO:1011069,"urolithiasis, Javan langur",MONDO,disease,DISEASE_2767
2768,2768,2768,2768,2768,2768,2768,2768,MONDO:0006866_MONDO:0018326,neonatal myasthenia gravis,MONDO_grouped,disease,DISEASE_2768
2769,2769,2769,2769,2769,2769,2769,2769,MONDO:0000521,salivary gland carcinoma,MONDO,disease,DISEASE_2769
2770,2770,2770,2770,2770,2770,2770,2770,MONDO:1012519,"lethal acrodermatitis, dog",MONDO,disease,DISEASE_2770
2771,2771,2771,2771,2771,2771,2771,2771,MONDO:0100077,congenital alveolar dysplasia,MONDO,disease,DISEASE_2771
2772,2772,2772,2772,2772,2772,2772,2772,MONDO:0013199_MONDO:0008612_MONDO:0001734,tuberous sclerosis,MONDO_grouped,disease,DISEASE_2772
2773,2773,2773,2773,2773,2773,2773,2773,MONDO:0007651,gastrocutaneous syndrome,MONDO,disease,DISEASE_2773
2774,2774,2774,2774,2774,2774,2774,2774,MONDO:0015275_MONDO:0015273,partial atrioventricular canal,MONDO_grouped,disease,DISEASE_2774
2775,2775,2775,2775,2775,2775,2775,2775,MONDO:0007937_MONDO:0012717_MONDO:0009550_MONDO:0013480,renal hypomagnesemia,MONDO_grouped,disease,DISEASE_2775
2776,2776,2776,2776,2776,2776,2776,2776,MONDO:0015465_MONDO:0009031,craniometaphyseal dysplasia,MONDO_grouped,disease,DISEASE_2776
2777,2777,2777,2777,2777,2777,2777,2777,MONDO:1012860,"abnormal gait, retinal dysplasia, cataracts, RORB-related, rabbit",MONDO,disease,DISEASE_2777
2778,2778,2778,2778,2778,2778,2778,2778,MONDO:0006766,gait apraxia,MONDO,disease,DISEASE_2778
2779,2779,2779,2779,2779,2779,2779,2779,MONDO:0018277_MONDO:0011306,obsolete congenital muscular dystrophy with cerebellar involvement,MONDO_grouped,disease,DISEASE_2779
2780,2780,2780,2780,2780,2780,2780,2780,MONDO:0005659_MONDO:1011131_MONDO:1011132,atrophic rhinitis,MONDO_grouped,disease,DISEASE_2780
2781,2781,2781,2781,2781,2781,2781,2781,MONDO:0032675,"myasthenic syndrome, congenital, 25, presynaptic",MONDO,disease,DISEASE_2781
2782,2782,2782,2782,2782,2782,2782,2782,MONDO:0024285,epsilon-heavy chain disease,MONDO,disease,DISEASE_2782
2783,2783,2783,2783,2783,2783,2783,2783,MONDO:0011979,adult-onset foveomacular vitelliform dystrophy,MONDO,disease,DISEASE_2783
2784,2784,2784,2784,2784,2784,2784,2784,MONDO:0021902,aortopulmonary window,MONDO,disease,DISEASE_2784
2785,2785,2785,2785,2785,2785,2785,2785,MONDO:1012869,"long QT syndrome, KCNH2-related, rabbit",MONDO,disease,DISEASE_2785
2786,2786,2786,2786,2786,2786,2786,2786,MONDO:1012031,"congenital blindness, pig",MONDO,disease,DISEASE_2786
2787,2787,2787,2787,2787,2787,2787,2787,MONDO:0030449,"hearing loss, autosomal recessive 118, with cochlear aplasia",MONDO,disease,DISEASE_2787
2788,2788,2788,2788,2788,2788,2788,2788,MONDO:0023003,double fingernail of fifth finger,MONDO,disease,DISEASE_2788
2789,2789,2789,2789,2789,2789,2789,2789,MONDO:1011966_MONDO:1012485,"skeletal dysplasia with craniofacial deformity and disproportionate dwarfism, non-human animal",MONDO_grouped,disease,DISEASE_2789
2790,2790,2790,2790,2790,2790,2790,2790,MONDO:0011053,intellectual disability-sparse hair-brachydactyly syndrome,MONDO,disease,DISEASE_2790
2791,2791,2791,2791,2791,2791,2791,2791,MONDO:1012466,"perinatal weak calf syndrome, cattle",MONDO,disease,DISEASE_2791
2792,2792,2792,2792,2792,2792,2792,2792,MONDO:0013576,recurrent infections associated with rare immunoglobulin isotypes deficiency,MONDO,disease,DISEASE_2792
2793,2793,2793,2793,2793,2793,2793,2793,MONDO:0017533_MONDO:0017534,"postaxial polydactyly type B, unilateral",MONDO_grouped,disease,DISEASE_2793
2794,2794,2794,2794,2794,2794,2794,2794,MONDO:0000397_MONDO:0700283,ataxic cerebral palsy,MONDO_grouped,disease,DISEASE_2794
2795,2795,2795,2795,2795,2795,2795,2795,MONDO:1010905,"deficiency of uridine monophosphate synthase, cattle",MONDO,disease,DISEASE_2795
2796,2796,2796,2796,2796,2796,2796,2796,MONDO:0021925,tracheobronchitis,MONDO,disease,DISEASE_2796
2797,2797,2797,2797,2797,2797,2797,2797,MONDO:0005574,tauopathy,MONDO,disease,DISEASE_2797
2798,2798,2798,2798,2798,2798,2798,2798,MONDO:0015414,paramedian nasal cleft,MONDO,disease,DISEASE_2798
2799,2799,2799,2799,2799,2799,2799,2799,MONDO:0011908_MONDO:0018871_MONDO:0020311,juvenile myelomonocytic leukemia,MONDO_grouped,disease,DISEASE_2799
2800,2800,2800,2800,2800,2800,2800,2800,MONDO:0005530,opiate dependence,MONDO,disease,DISEASE_2800
2801,2801,2801,2801,2801,2801,2801,2801,MONDO:0000372,pharynx carcinoma in situ,MONDO,disease,DISEASE_2801
2802,2802,2802,2802,2802,2802,2802,2802,MONDO:0033532,Suleiman-El-Hattab syndrome,MONDO,disease,DISEASE_2802
2803,2803,2803,2803,2803,2803,2803,2803,MONDO:0014941,"arthrogryposis, distal, with impaired proprioception and touch",MONDO,disease,DISEASE_2803
2804,2804,2804,2804,2804,2804,2804,2804,MONDO:1012250,"spastic lameness, cattle",MONDO,disease,DISEASE_2804
2805,2805,2805,2805,2805,2805,2805,2805,MONDO:0022930,Dandy-Walker malformation with nasopharyngeal teratoma and diaphragmatic hernia,MONDO,disease,DISEASE_2805
2806,2806,2806,2806,2806,2806,2806,2806,MONDO:1011953_MONDO:1011984_MONDO:1011967,"spinal dysplasia, non-human animal",MONDO_grouped,disease,DISEASE_2806
2807,2807,2807,2807,2807,2807,2807,2807,MONDO:0007581,"exchondrosis of pinna, posterior",MONDO,disease,DISEASE_2807
2808,2808,2808,2808,2808,2808,2808,2808,MONDO:0700103,"nutritional deficiency disease, non-human animal",MONDO,disease,DISEASE_2808
2809,2809,2809,2809,2809,2809,2809,2809,MONDO:0017450,split foot,MONDO,disease,DISEASE_2809
2810,2810,2810,2810,2810,2810,2810,2810,MONDO:1010789_MONDO:1012027,"stiff skin syndrome, dog",MONDO_grouped,disease,DISEASE_2810
2811,2811,2811,2811,2811,2811,2811,2811,MONDO:0004133,pituitary gland mixed eosinophil-basophil adenoma,MONDO,disease,DISEASE_2811
2812,2812,2812,2812,2812,2812,2812,2812,MONDO:0010678,"muscular dystrophy, progressive Pectorodorsal",MONDO,disease,DISEASE_2812
2813,2813,2813,2813,2813,2813,2813,2813,MONDO:0008679_MONDO:0008680_MONDO:0011112_MONDO:0011056_MONDO:0014779_MONDO:0008683_MONDO:0006058_MONDO:1011619_MONDO:1011620_MONDO:1011621_MONDO:1011622,Wilms tumor,MONDO_grouped,disease,DISEASE_2813
2814,2814,2814,2814,2814,2814,2814,2814,MONDO:1010099,"pyruvate kinase deficiency of erythrocyte, non-human animal",MONDO,disease,DISEASE_2814
2815,2815,2815,2815,2815,2815,2815,2815,MONDO:0004543,enteric pattern testicular yolk sac tumor,MONDO,disease,DISEASE_2815
2816,2816,2816,2816,2816,2816,2816,2816,MONDO:0013825_MONDO:0000824,congenital diarrhea 6,MONDO_grouped,disease,DISEASE_2816
2817,2817,2817,2817,2817,2817,2817,2817,MONDO:0013296,myeloid neoplasm associated with FGFR1 rearrangement,MONDO,disease,DISEASE_2817
2818,2818,2818,2818,2818,2818,2818,2818,MONDO:0006856,mesothelial neoplasm,MONDO,disease,DISEASE_2818
2819,2819,2819,2819,2819,2819,2819,2819,MONDO:0012262_MONDO:0011181_MONDO:0014538_MONDO:0021083_MONDO:0007614_MONDO:0800209,"fibrosis of extraocular muscles, congenital",MONDO_grouped,disease,DISEASE_2819
2820,2820,2820,2820,2820,2820,2820,2820,MONDO:0043352,fournier gangrene,MONDO,disease,DISEASE_2820
2821,2821,2821,2821,2821,2821,2821,2821,MONDO:1011273_MONDO:1012703_MONDO:1012743_MONDO:1012749_MONDO:1012753_MONDO:1012765_MONDO:1012833_MONDO:1012838_MONDO:1012842_MONDO:1012861,"progressive retinal atrophy, TTC8-related, dog",MONDO_grouped,disease,DISEASE_2821
2822,2822,2822,2822,2822,2822,2822,2822,MONDO:0958241,"cardiomyopathy, familial hypertrophic, 30, atrial",MONDO,disease,DISEASE_2822
2823,2823,2823,2823,2823,2823,2823,2823,MONDO:1010815,"polydactyly, Arabian camel",MONDO,disease,DISEASE_2823
2824,2824,2824,2824,2824,2824,2824,2824,MONDO:1010286,"pneumothorax, non-human animal",MONDO,disease,DISEASE_2824
2825,2825,2825,2825,2825,2825,2825,2825,MONDO:0006198,endometrial squamous cell carcinoma,MONDO,disease,DISEASE_2825
2826,2826,2826,2826,2826,2826,2826,2826,MONDO:0009419,Woodhouse-Sakati syndrome,MONDO,disease,DISEASE_2826
2827,2827,2827,2827,2827,2827,2827,2827,MONDO:0006995,tethered spinal cord syndrome,MONDO,disease,DISEASE_2827
2828,2828,2828,2828,2828,2828,2828,2828,MONDO:0002837,sarcomatoid transitional cell carcinoma,MONDO,disease,DISEASE_2828
2829,2829,2829,2829,2829,2829,2829,2829,MONDO:1011828,"cancer, non-human animal",MONDO,disease,DISEASE_2829
2830,2830,2830,2830,2830,2830,2830,2830,MONDO:0060577,"neurodevelopmental disorder with microcephaly, ataxia, and seizures",MONDO,disease,DISEASE_2830
2831,2831,2831,2831,2831,2831,2831,2831,MONDO:0019318,inflammatory linear verrucous epidermal nevus,MONDO,disease,DISEASE_2831
2832,2832,2832,2832,2832,2832,2832,2832,MONDO:0019157,myelodysplastic syndrome with ring sideroblasts,MONDO,disease,DISEASE_2832
2833,2833,2833,2833,2833,2833,2833,2833,MONDO:0035173,9q21.13 microdeletion syndrome,MONDO,disease,DISEASE_2833
2834,2834,2834,2834,2834,2834,2834,2834,MONDO:0021571_MONDO:0007462_MONDO:0012956_MONDO:0012957_MONDO:0012958_MONDO:0013893,"multiple sclerosis, susceptibility to",MONDO_grouped,disease,DISEASE_2834
2835,2835,2835,2835,2835,2835,2835,2835,MONDO:0024249,pityriasis lichenoides,MONDO,disease,DISEASE_2835
2836,2836,2836,2836,2836,2836,2836,2836,MONDO:0012182_MONDO:0012468,"skeletal dysplasia, rhizomelic, with retinitis pigmentosa",MONDO_grouped,disease,DISEASE_2836
2837,2837,2837,2837,2837,2837,2837,2837,MONDO:1011763,"lethal acrodermatitis, non-human animal",MONDO,disease,DISEASE_2837
2838,2838,2838,2838,2838,2838,2838,2838,MONDO:0006612,steroid lipomatosis,MONDO,disease,DISEASE_2838
2839,2839,2839,2839,2839,2839,2839,2839,MONDO:0010379,Brunner syndrome,MONDO,disease,DISEASE_2839
2840,2840,2840,2840,2840,2840,2840,2840,MONDO:0018837,postinfectious vasculitis,MONDO,disease,DISEASE_2840
2841,2841,2841,2841,2841,2841,2841,2841,MONDO:0019632,Lyme disease,MONDO,disease,DISEASE_2841
2842,2842,2842,2842,2842,2842,2842,2842,MONDO:0001830,somatization disorder,MONDO,disease,DISEASE_2842
2843,2843,2843,2843,2843,2843,2843,2843,MONDO:0005800,hordeolum,MONDO,disease,DISEASE_2843
2844,2844,2844,2844,2844,2844,2844,2844,MONDO:0007624,Flynn-Aird syndrome,MONDO,disease,DISEASE_2844
2845,2845,2845,2845,2845,2845,2845,2845,MONDO:0018031,granulomatous slack skin disease,MONDO,disease,DISEASE_2845
2846,2846,2846,2846,2846,2846,2846,2846,MONDO:1010025,"Wolff-Parkinson-White syndrome, non-human animal",MONDO,disease,DISEASE_2846
2847,2847,2847,2847,2847,2847,2847,2847,MONDO:0020699,biotin metabolic disease,MONDO,disease,DISEASE_2847
2848,2848,2848,2848,2848,2848,2848,2848,MONDO:0005108_MONDO:0005113_MONDO:0005550_MONDO:0024352,viral infectious disease,MONDO_grouped,disease,DISEASE_2848
2849,2849,2849,2849,2849,2849,2849,2849,MONDO:0001319,bladder lateral wall cancer,MONDO,disease,DISEASE_2849
2850,2850,2850,2850,2850,2850,2850,2850,MONDO:0004125_MONDO:0003379,rectum leiomyoma,MONDO_grouped,disease,DISEASE_2850
2851,2851,2851,2851,2851,2851,2851,2851,MONDO:0017322,disorders of vitamin D metabolism,MONDO,disease,DISEASE_2851
2852,2852,2852,2852,2852,2852,2852,2852,MONDO:0006752,Erysipelothrix rhusiopathiae infectious disease,MONDO,disease,DISEASE_2852
2853,2853,2853,2853,2853,2853,2853,2853,MONDO:0013735,microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome,MONDO,disease,DISEASE_2853
2854,2854,2854,2854,2854,2854,2854,2854,MONDO:0044885,tonsillar lipoma,MONDO,disease,DISEASE_2854
2855,2855,2855,2855,2855,2855,2855,2855,MONDO:0020702_MONDO:0044742,autosomal dominant epidermolytic ichthyosis,MONDO_grouped,disease,DISEASE_2855
2856,2856,2856,2856,2856,2856,2856,2856,MONDO:0022822,congenital cardiovascular shunt,MONDO,disease,DISEASE_2856
2857,2857,2857,2857,2857,2857,2857,2857,MONDO:0004746,myopathy of extraocular muscle,MONDO,disease,DISEASE_2857
2858,2858,2858,2858,2858,2858,2858,2858,MONDO:0007182_MONDO:0017174_MONDO:0017176_MONDO:0017175_MONDO:0042964,Machado-Joseph disease,MONDO_grouped,disease,DISEASE_2858
2859,2859,2859,2859,2859,2859,2859,2859,MONDO:0001825_MONDO:0004204_MONDO:0004267,squamous papilloma,MONDO_grouped,disease,DISEASE_2859
2860,2860,2860,2860,2860,2860,2860,2860,MONDO:0010775_MONDO:0009982,retinitis pigmentosa-deafness syndrome,MONDO_grouped,disease,DISEASE_2860
2861,2861,2861,2861,2861,2861,2861,2861,MONDO:0018899,posterior cortical atrophy,MONDO,disease,DISEASE_2861
2862,2862,2862,2862,2862,2862,2862,2862,MONDO:0060583,platelet abnormalities with eosinophilia and immune-mediated inflammatory disease,MONDO,disease,DISEASE_2862
2863,2863,2863,2863,2863,2863,2863,2863,MONDO:0006184,ductal breast carcinoma in situ and lobular carcinoma in situ,MONDO,disease,DISEASE_2863
2864,2864,2864,2864,2864,2864,2864,2864,MONDO:0023016,duplication of leg mirror foot,MONDO,disease,DISEASE_2864
2865,2865,2865,2865,2865,2865,2865,2865,MONDO:0008778,"amyloidosis, cutaneous bullous",MONDO,disease,DISEASE_2865
2866,2866,2866,2866,2866,2866,2866,2866,MONDO:0041850,pneumonia caused by gram negative bacteria,MONDO,disease,DISEASE_2866
2867,2867,2867,2867,2867,2867,2867,2867,MONDO:0022901,Crohn disease of the esophagus,MONDO,disease,DISEASE_2867
2868,2868,2868,2868,2868,2868,2868,2868,MONDO:0025129,swine erysipelas,MONDO,disease,DISEASE_2868
2869,2869,2869,2869,2869,2869,2869,2869,MONDO:0015244_MONDO:0020047_MONDO:0018218,autosomal recessive cerebellar ataxia,MONDO_grouped,disease,DISEASE_2869
2870,2870,2870,2870,2870,2870,2870,2870,MONDO:0957224,congenital myopathy 21 with early respiratory failure,MONDO,disease,DISEASE_2870
2871,2871,2871,2871,2871,2871,2871,2871,MONDO:0100302,LADD syndrome 1,MONDO,disease,DISEASE_2871
2872,2872,2872,2872,2872,2872,2872,2872,MONDO:0004690,tonsillar fossa cancer,MONDO,disease,DISEASE_2872
2873,2873,2873,2873,2873,2873,2873,2873,MONDO:0018962,common mesentery,MONDO,disease,DISEASE_2873
2874,2874,2874,2874,2874,2874,2874,2874,MONDO:0017598,primary cutaneous anaplastic large cell lymphoma,MONDO,disease,DISEASE_2874
2875,2875,2875,2875,2875,2875,2875,2875,MONDO:0024311,cancer affecting bone of limb skeleton,MONDO,disease,DISEASE_2875
2876,2876,2876,2876,2876,2876,2876,2876,MONDO:1011727,"immunoglobulin G deficiency, non-human animal",MONDO,disease,DISEASE_2876
2877,2877,2877,2877,2877,2877,2877,2877,MONDO:0004183_MONDO:0001408,axonal neuropathy,MONDO_grouped,disease,DISEASE_2877
2878,2878,2878,2878,2878,2878,2878,2878,MONDO:0859177,VISS syndrome,MONDO,disease,DISEASE_2878
2879,2879,2879,2879,2879,2879,2879,2879,MONDO:0013992,obesity due to leptin receptor gene deficiency,MONDO,disease,DISEASE_2879
2880,2880,2880,2880,2880,2880,2880,2880,MONDO:0006350,papillary transitional cell carcinoma,MONDO,disease,DISEASE_2880
2881,2881,2881,2881,2881,2881,2881,2881,MONDO:0045018,creatine biosynthetic process disease,MONDO,disease,DISEASE_2881
2882,2882,2882,2882,2882,2882,2882,2882,MONDO:0100194,pregnancy associated osteoporosis,MONDO,disease,DISEASE_2882
2883,2883,2883,2883,2883,2883,2883,2883,MONDO:0016122,periodic paralysis,MONDO,disease,DISEASE_2883
2884,2884,2884,2884,2884,2884,2884,2884,MONDO:8000010,antiphospholipid syndrome,MONDO,disease,DISEASE_2884
2885,2885,2885,2885,2885,2885,2885,2885,MONDO:0003959,breast large cell neuroendocrine carcinoma,MONDO,disease,DISEASE_2885
2886,2886,2886,2886,2886,2886,2886,2886,MONDO:0042499,benign familial neonatal-infantile seizures 1,MONDO,disease,DISEASE_2886
2887,2887,2887,2887,2887,2887,2887,2887,MONDO:0800063,primordial dwarfism and slender bone disorder,MONDO,disease,DISEASE_2887
2888,2888,2888,2888,2888,2888,2888,2888,MONDO:0015588,limbic encephalitis,MONDO,disease,DISEASE_2888
2889,2889,2889,2889,2889,2889,2889,2889,MONDO:0010683,X-linked myotubular myopathy,MONDO,disease,DISEASE_2889
2890,2890,2890,2890,2890,2890,2890,2890,MONDO:0001776,prostate calculus,MONDO,disease,DISEASE_2890
2891,2891,2891,2891,2891,2891,2891,2891,MONDO:0009881,pituitary dwarfism with large sella turcica,MONDO,disease,DISEASE_2891
2892,2892,2892,2892,2892,2892,2892,2892,MONDO:0006471,tracheal adenoid cystic carcinoma,MONDO,disease,DISEASE_2892
2893,2893,2893,2893,2893,2893,2893,2893,MONDO:0003062,intestinal benign neoplasm,MONDO,disease,DISEASE_2893
2894,2894,2894,2894,2894,2894,2894,2894,MONDO:0001438,postinflammatory pulmonary fibrosis,MONDO,disease,DISEASE_2894
2895,2895,2895,2895,2895,2895,2895,2895,MONDO:0009142,dystonia with Ringbinden,MONDO,disease,DISEASE_2895
2896,2896,2896,2896,2896,2896,2896,2896,MONDO:0019114,psychogenic movement disorders,MONDO,disease,DISEASE_2896
2897,2897,2897,2897,2897,2897,2897,2897,MONDO:0004657,disseminated chorioretinitis,MONDO,disease,DISEASE_2897
2898,2898,2898,2898,2898,2898,2898,2898,MONDO:0000936_MONDO:0000937,syphilitic meningitis,MONDO_grouped,disease,DISEASE_2898
2899,2899,2899,2899,2899,2899,2899,2899,MONDO:1011939,"brachygnathia superior and degenerative joint disease, non-human animal",MONDO,disease,DISEASE_2899
2900,2900,2900,2900,2900,2900,2900,2900,MONDO:0021512,benign neoplasm of thymus,MONDO,disease,DISEASE_2900
2901,2901,2901,2901,2901,2901,2901,2901,MONDO:0008663,snowflake vitreoretinal degeneration,MONDO,disease,DISEASE_2901
2902,2902,2902,2902,2902,2902,2902,2902,MONDO:0033954,monoclonal mast cell activation syndrome,MONDO,disease,DISEASE_2902
2903,2903,2903,2903,2903,2903,2903,2903,MONDO:0004358,subglottis carcinoma,MONDO,disease,DISEASE_2903
2904,2904,2904,2904,2904,2904,2904,2904,MONDO:0019668,adenoma of pancreas,MONDO,disease,DISEASE_2904
2905,2905,2905,2905,2905,2905,2905,2905,MONDO:0004658,breast carcinoma in situ,MONDO,disease,DISEASE_2905
2906,2906,2906,2906,2906,2906,2906,2906,MONDO:0002949,morpheaform basal cell carcinoma,MONDO,disease,DISEASE_2906
2907,2907,2907,2907,2907,2907,2907,2907,MONDO:0014006,Schuurs-Hoeijmakers syndrome,MONDO,disease,DISEASE_2907
2908,2908,2908,2908,2908,2908,2908,2908,MONDO:0005293,flatfoot,MONDO,disease,DISEASE_2908
2909,2909,2909,2909,2909,2909,2909,2909,MONDO:0010703,ornithine carbamoyltransferase deficiency,MONDO,disease,DISEASE_2909
2910,2910,2910,2910,2910,2910,2910,2910,MONDO:0004458,bladder mixed adenocarcinoma,MONDO,disease,DISEASE_2910
2911,2911,2911,2911,2911,2911,2911,2911,MONDO:0004865,blue drum syndrome,MONDO,disease,DISEASE_2911
2912,2912,2912,2912,2912,2912,2912,2912,MONDO:1011646_MONDO:1012327,"persistent truncus arteriosus with ventricular septal defect and patent foramen ovale, non-human animal",MONDO_grouped,disease,DISEASE_2912
2913,2913,2913,2913,2913,2913,2913,2913,MONDO:0014944,short stature-brachydactyly-obesity-global developmental delay syndrome,MONDO,disease,DISEASE_2913
2914,2914,2914,2914,2914,2914,2914,2914,MONDO:0000254,cutaneous mycosis,MONDO,disease,DISEASE_2914
2915,2915,2915,2915,2915,2915,2915,2915,MONDO:1011249,"retinoschisis, dog",MONDO,disease,DISEASE_2915
2916,2916,2916,2916,2916,2916,2916,2916,MONDO:0016174,obsolete paraneoplastic sensory ganglionopathy,MONDO,disease,DISEASE_2916
2917,2917,2917,2917,2917,2917,2917,2917,MONDO:0100115,acute flaccid myelitis,MONDO,disease,DISEASE_2917
2918,2918,2918,2918,2918,2918,2918,2918,MONDO:0025370,obsolete urogenital neoplasm,MONDO,disease,DISEASE_2918
2919,2919,2919,2919,2919,2919,2919,2919,MONDO:1011555,"mast cell tumor, dog",MONDO,disease,DISEASE_2919
2920,2920,2920,2920,2920,2920,2920,2920,MONDO:0003277,malignant ear neoplasm,MONDO,disease,DISEASE_2920
2921,2921,2921,2921,2921,2921,2921,2921,MONDO:0005481,contact dermatitis due to nickel,MONDO,disease,DISEASE_2921
2922,2922,2922,2922,2922,2922,2922,2922,MONDO:0008450_MONDO:0015304,spinal arachnoiditis,MONDO_grouped,disease,DISEASE_2922
2923,2923,2923,2923,2923,2923,2923,2923,MONDO:0015697,immunoglobulin heavy chain deficiency,MONDO,disease,DISEASE_2923
2924,2924,2924,2924,2924,2924,2924,2924,MONDO:0010384_MONDO:0010423_MONDO:0010458,"hypospadias 1, X-linked",MONDO_grouped,disease,DISEASE_2924
2925,2925,2925,2925,2925,2925,2925,2925,MONDO:0002121_MONDO:0002128,mononeuritis simplex,MONDO_grouped,disease,DISEASE_2925
2926,2926,2926,2926,2926,2926,2926,2926,MONDO:0008425,"omphalocele syndrome, Shprintzen-Goldberg type",MONDO,disease,DISEASE_2926
2927,2927,2927,2927,2927,2927,2927,2927,MONDO:0017217,visceral calciphylaxis,MONDO,disease,DISEASE_2927
2928,2928,2928,2928,2928,2928,2928,2928,MONDO:0021577,malignant mediastinal neural neoplasm,MONDO,disease,DISEASE_2928
2929,2929,2929,2929,2929,2929,2929,2929,MONDO:0008320,Protrusio acetabuli,MONDO,disease,DISEASE_2929
2930,2930,2930,2930,2930,2930,2930,2930,MONDO:0010808,fatal familial insomnia,MONDO,disease,DISEASE_2930
2931,2931,2931,2931,2931,2931,2931,2931,MONDO:0006889,paraphimosis,MONDO,disease,DISEASE_2931
2932,2932,2932,2932,2932,2932,2932,2932,MONDO:0014334,severe combined immunodeficiency due to LCK deficiency,MONDO,disease,DISEASE_2932
2933,2933,2933,2933,2933,2933,2933,2933,MONDO:0002340,tactile epilepsy,MONDO,disease,DISEASE_2933
2934,2934,2934,2934,2934,2934,2934,2934,MONDO:0024250,acute lichenoid pityriasis,MONDO,disease,DISEASE_2934
2935,2935,2935,2935,2935,2935,2935,2935,MONDO:1012473,"medial coronoid disease, dog",MONDO,disease,DISEASE_2935
2936,2936,2936,2936,2936,2936,2936,2936,MONDO:0859615,"diffuse astrocytoma, MYB- or MYBL1-altered",MONDO,disease,DISEASE_2936
2937,2937,2937,2937,2937,2937,2937,2937,MONDO:0011335_MONDO:0010075_MONDO:0032724_MONDO:0007738,spondyloepimetaphyseal dysplasia with multiple dislocations,MONDO_grouped,disease,DISEASE_2937
2938,2938,2938,2938,2938,2938,2938,2938,MONDO:0006408,sex hormone-producing adrenal cortex adenoma,MONDO,disease,DISEASE_2938
2939,2939,2939,2939,2939,2939,2939,2939,MONDO:0009646,monosomy 7 myelodysplasia and leukemia syndrome 1,MONDO,disease,DISEASE_2939
2940,2940,2940,2940,2940,2940,2940,2940,MONDO:0007680,multinodular goiter-cystic kidney-polydactyly syndrome,MONDO,disease,DISEASE_2940
2941,2941,2941,2941,2941,2941,2941,2941,MONDO:0005436,postoperative ventricular dysfunction,MONDO,disease,DISEASE_2941
2942,2942,2942,2942,2942,2942,2942,2942,MONDO:0010145,"tibia, absence of, with congenital deafness",MONDO,disease,DISEASE_2942
2943,2943,2943,2943,2943,2943,2943,2943,MONDO:0030062,"arrhythmogenic right ventricular dysplasia, familial, 14",MONDO,disease,DISEASE_2943
2944,2944,2944,2944,2944,2944,2944,2944,MONDO:0011949,Thai symphalangism syndrome,MONDO,disease,DISEASE_2944
2945,2945,2945,2945,2945,2945,2945,2945,MONDO:0018763,tubulinopathy-associated dysgyria,MONDO,disease,DISEASE_2945
2946,2946,2946,2946,2946,2946,2946,2946,MONDO:0024344,pityriasis folliculorum,MONDO,disease,DISEASE_2946
2947,2947,2947,2947,2947,2947,2947,2947,MONDO:0007720,"hernia, double inguinal",MONDO,disease,DISEASE_2947
2948,2948,2948,2948,2948,2948,2948,2948,MONDO:1010930,"myotubular myopathy 1, domestic cat",MONDO,disease,DISEASE_2948
2949,2949,2949,2949,2949,2949,2949,2949,MONDO:0033946,hereditary angioedema with C1Inh deficiency,MONDO,disease,DISEASE_2949
2950,2950,2950,2950,2950,2950,2950,2950,MONDO:0013598,myostatin-related muscle hypertrophy,MONDO,disease,DISEASE_2950
2951,2951,2951,2951,2951,2951,2951,2951,MONDO:0031280,Stuve-Wiedemann syndrome,MONDO,disease,DISEASE_2951
2952,2952,2952,2952,2952,2952,2952,2952,MONDO:0009737_MONDO:1010838,galactosialidosis,MONDO_grouped,disease,DISEASE_2952
2953,2953,2953,2953,2953,2953,2953,2953,MONDO:0009047,cryptorchidism,MONDO,disease,DISEASE_2953
2954,2954,2954,2954,2954,2954,2954,2954,MONDO:0020809,benign sertoli cell tumor,MONDO,disease,DISEASE_2954
2955,2955,2955,2955,2955,2955,2955,2955,MONDO:1011337_MONDO:1011881,"neurocristopathy, non-human animal",MONDO_grouped,disease,DISEASE_2955
2956,2956,2956,2956,2956,2956,2956,2956,MONDO:1011879_MONDO:1012391,"necrotizing meningoencephalitis, non-human animal",MONDO_grouped,disease,DISEASE_2956
2957,2957,2957,2957,2957,2957,2957,2957,MONDO:0007590,hemifacial hypertrophy,MONDO,disease,DISEASE_2957
2958,2958,2958,2958,2958,2958,2958,2958,MONDO:0000923,interstitial emphysema,MONDO,disease,DISEASE_2958
2959,2959,2959,2959,2959,2959,2959,2959,MONDO:0006406,sarcomatoid carcinoma,MONDO,disease,DISEASE_2959
2960,2960,2960,2960,2960,2960,2960,2960,MONDO:0011030,"epithelial basolateral chloride conductance regulator, rabbit, homolog of",MONDO,disease,DISEASE_2960
2961,2961,2961,2961,2961,2961,2961,2961,MONDO:0004038,dental enamel hypoplasia,MONDO,disease,DISEASE_2961
2962,2962,2962,2962,2962,2962,2962,2962,MONDO:0018807,idiopathic ductopenia,MONDO,disease,DISEASE_2962
2963,2963,2963,2963,2963,2963,2963,2963,MONDO:0017140,L1 syndrome,MONDO,disease,DISEASE_2963
2964,2964,2964,2964,2964,2964,2964,2964,MONDO:0001045,intestinal atresia,MONDO,disease,DISEASE_2964
2965,2965,2965,2965,2965,2965,2965,2965,MONDO:0007482,dyschondrosteosis-nephritis syndrome,MONDO,disease,DISEASE_2965
2966,2966,2966,2966,2966,2966,2966,2966,MONDO:0007835,intussusception,MONDO,disease,DISEASE_2966
2967,2967,2967,2967,2967,2967,2967,2967,MONDO:1010916,"myopathy, chicken",MONDO,disease,DISEASE_2967
2968,2968,2968,2968,2968,2968,2968,2968,MONDO:0026777,VEXAS syndrome,MONDO,disease,DISEASE_2968
2969,2969,2969,2969,2969,2969,2969,2969,MONDO:0010198,Wernicke-Korsakoff syndrome,MONDO,disease,DISEASE_2969
2970,2970,2970,2970,2970,2970,2970,2970,MONDO:0008793,"angiomatosis, diffuse Corticomeningeal, of Divry and van Bogaert",MONDO,disease,DISEASE_2970
2971,2971,2971,2971,2971,2971,2971,2971,MONDO:0010855,short tarsus-absence of lower eyelashes syndrome,MONDO,disease,DISEASE_2971
2972,2972,2972,2972,2972,2972,2972,2972,MONDO:0016814,maternally-inherited Leigh syndrome,MONDO,disease,DISEASE_2972
2973,2973,2973,2973,2973,2973,2973,2973,MONDO:0013098_MONDO:0850094,noise induced hearing loss,MONDO_grouped,disease,DISEASE_2973
2974,2974,2974,2974,2974,2974,2974,2974,MONDO:0003655,cerebral lymphoma,MONDO,disease,DISEASE_2974
2975,2975,2975,2975,2975,2975,2975,2975,MONDO:0004840,non-congenital cyst of kidney,MONDO,disease,DISEASE_2975
2976,2976,2976,2976,2976,2976,2976,2976,MONDO:0004050,telangiectatic osteogenic sarcoma,MONDO,disease,DISEASE_2976
2977,2977,2977,2977,2977,2977,2977,2977,MONDO:1010310,"schmid metaphyseal chondrodysplasia dwarfism, non-human animal",MONDO,disease,DISEASE_2977
2978,2978,2978,2978,2978,2978,2978,2978,MONDO:0859296,"neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss",MONDO,disease,DISEASE_2978
2979,2979,2979,2979,2979,2979,2979,2979,MONDO:0024664,"hypertension, pregnancy-induced",MONDO,disease,DISEASE_2979
2980,2980,2980,2980,2980,2980,2980,2980,MONDO:0006976,somatostatinoma,MONDO,disease,DISEASE_2980
2981,2981,2981,2981,2981,2981,2981,2981,MONDO:0010153,trichoodontoonychial dysplasia,MONDO,disease,DISEASE_2981
2982,2982,2982,2982,2982,2982,2982,2982,MONDO:0012929,Compton-North congenital myopathy,MONDO,disease,DISEASE_2982
2983,2983,2983,2983,2983,2983,2983,2983,MONDO:0000147,polyposis,MONDO,disease,DISEASE_2983
2984,2984,2984,2984,2984,2984,2984,2984,MONDO:0045011,keratinization disease,MONDO,disease,DISEASE_2984
2985,2985,2985,2985,2985,2985,2985,2985,MONDO:0016448,pseudoxanthoma elasticum-like papillary dermal elastolysis,MONDO,disease,DISEASE_2985
2986,2986,2986,2986,2986,2986,2986,2986,MONDO:0017384,acute generalized exanthematous pustulosis,MONDO,disease,DISEASE_2986
2987,2987,2987,2987,2987,2987,2987,2987,MONDO:8000005,fungal discitis,MONDO,disease,DISEASE_2987
2988,2988,2988,2988,2988,2988,2988,2988,MONDO:1012407,"acral mutilation syndrome, dog",MONDO,disease,DISEASE_2988
2989,2989,2989,2989,2989,2989,2989,2989,MONDO:0012043,Reis-Bucklers corneal dystrophy,MONDO,disease,DISEASE_2989
2990,2990,2990,2990,2990,2990,2990,2990,MONDO:0015453,Cogan syndrome,MONDO,disease,DISEASE_2990
2991,2991,2991,2991,2991,2991,2991,2991,MONDO:0021518,benign neoplasm of hard palate,MONDO,disease,DISEASE_2991
2992,2992,2992,2992,2992,2992,2992,2992,MONDO:0012297_MONDO:0008444,"spastic paraplegia, optic atropy, and neuropathy",MONDO_grouped,disease,DISEASE_2992
2993,2993,2993,2993,2993,2993,2993,2993,MONDO:0008243_MONDO:0010269,Pick disease,MONDO_grouped,disease,DISEASE_2993
2994,2994,2994,2994,2994,2994,2994,2994,MONDO:0023017,duplication of the thumb unilateral biphalangeal,MONDO,disease,DISEASE_2994
2995,2995,2995,2995,2995,2995,2995,2995,MONDO:0034556,vibratory angioedema,MONDO,disease,DISEASE_2995
2996,2996,2996,2996,2996,2996,2996,2996,MONDO:0859347,"neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities",MONDO,disease,DISEASE_2996
2997,2997,2997,2997,2997,2997,2997,2997,MONDO:0971050,relapsing isolated optic neuritis,MONDO,disease,DISEASE_2997
2998,2998,2998,2998,2998,2998,2998,2998,MONDO:0007154,arteriovenous malformations of the brain,MONDO,disease,DISEASE_2998
2999,2999,2999,2999,2999,2999,2999,2999,MONDO:0011228,"creases, infra-auricular cutaneous, with tall stature and advanced bone age",MONDO,disease,DISEASE_2999
3000,3000,3000,3000,3000,3000,3000,3000,MONDO:0005518_MONDO:0002768,pseudohermaphroditism,MONDO_grouped,disease,DISEASE_3000
3001,3001,3001,3001,3001,3001,3001,3001,MONDO:0012064,choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome,MONDO,disease,DISEASE_3001
3002,3002,3002,3002,3002,3002,3002,3002,MONDO:0017613,intellectual disability-hypotonia-skin hyperpigmentation syndrome,MONDO,disease,DISEASE_3002
3003,3003,3003,3003,3003,3003,3003,3003,MONDO:0016058_MONDO:0043969,paroxysmal dystonia,MONDO_grouped,disease,DISEASE_3003
3004,3004,3004,3004,3004,3004,3004,3004,MONDO:0850353,castration-resistant prostate carcinoma,MONDO,disease,DISEASE_3004
3005,3005,3005,3005,3005,3005,3005,3005,MONDO:0008787,microcytic anemia with liver iron overload,MONDO,disease,DISEASE_3005
3006,3006,3006,3006,3006,3006,3006,3006,MONDO:0010777,"cardiomyopathy, infantile hypertrophic",MONDO,disease,DISEASE_3006
3007,3007,3007,3007,3007,3007,3007,3007,MONDO:0700020,chromosome 13 disorder,MONDO,disease,DISEASE_3007
3008,3008,3008,3008,3008,3008,3008,3008,MONDO:0023197,frontonasal dysplasia Klippel feil syndrome,MONDO,disease,DISEASE_3008
3009,3009,3009,3009,3009,3009,3009,3009,MONDO:0006150,colon Burkitt lymphoma,MONDO,disease,DISEASE_3009
3010,3010,3010,3010,3010,3010,3010,3010,MONDO:0957919,Lui-Jee-Baron syndrome,MONDO,disease,DISEASE_3010
3011,3011,3011,3011,3011,3011,3011,3011,MONDO:0003689_MONDO:0001115_MONDO:0017182,familial hemolytic anemia,MONDO_grouped,disease,DISEASE_3011
3012,3012,3012,3012,3012,3012,3012,3012,MONDO:0024248,obsolete pityriasis,MONDO,disease,DISEASE_3012
3013,3013,3013,3013,3013,3013,3013,3013,MONDO:0009436,congenital hypothalamic hamartoma syndrome,MONDO,disease,DISEASE_3013
3014,3014,3014,3014,3014,3014,3014,3014,MONDO:1012003,"corneal sequestra, non-human animal",MONDO,disease,DISEASE_3014
3015,3015,3015,3015,3015,3015,3015,3015,MONDO:1011729,"immunoglobulin M deficiency, non-human animal",MONDO,disease,DISEASE_3015
3016,3016,3016,3016,3016,3016,3016,3016,MONDO:0008135,optic atrophy 13 with retinal and foveal abnormalities,MONDO,disease,DISEASE_3016
3017,3017,3017,3017,3017,3017,3017,3017,MONDO:0021375,tumor of duodenum,MONDO,disease,DISEASE_3017
3018,3018,3018,3018,3018,3018,3018,3018,MONDO:0009212,congenital factor X deficiency,MONDO,disease,DISEASE_3018
3019,3019,3019,3019,3019,3019,3019,3019,MONDO:0000250,osmotic diarrheal disease,MONDO,disease,DISEASE_3019
3020,3020,3020,3020,3020,3020,3020,3020,MONDO:0001468,synovial plica syndrome,MONDO,disease,DISEASE_3020
3021,3021,3021,3021,3021,3021,3021,3021,MONDO:0011455,"lissencephaly, familial, with cleft palate and cerebellar hypoplasia",MONDO,disease,DISEASE_3021
3022,3022,3022,3022,3022,3022,3022,3022,MONDO:0021280,mucoepidermoid carcinoma of parotid gland,MONDO,disease,DISEASE_3022
3023,3023,3023,3023,3023,3023,3023,3023,MONDO:0006130,central nervous system neoplasm,MONDO,disease,DISEASE_3023
3024,3024,3024,3024,3024,3024,3024,3024,MONDO:1012322_MONDO:1012323_MONDO:1012324,"laryngeal paralysis, dog",MONDO_grouped,disease,DISEASE_3024
3025,3025,3025,3025,3025,3025,3025,3025,MONDO:0019396,collagen type III glomerulopathy,MONDO,disease,DISEASE_3025
3026,3026,3026,3026,3026,3026,3026,3026,MONDO:0009693_MONDO:0004819,plasma cell myeloma,MONDO_grouped,disease,DISEASE_3026
3027,3027,3027,3027,3027,3027,3027,3027,MONDO:0005813,interdigitating dendritic cell sarcoma,MONDO,disease,DISEASE_3027
3028,3028,3028,3028,3028,3028,3028,3028,MONDO:0700208_MONDO:0700095,"Caliciviridae infectious disease, non-human animal",MONDO_grouped,disease,DISEASE_3028
3029,3029,3029,3029,3029,3029,3029,3029,MONDO:0018274,GM3 synthase deficiency,MONDO,disease,DISEASE_3029
3030,3030,3030,3030,3030,3030,3030,3030,MONDO:0007650,MALT lymphoma,MONDO,disease,DISEASE_3030
3031,3031,3031,3031,3031,3031,3031,3031,MONDO:0022572,bilateral renal agenesis dominant type,MONDO,disease,DISEASE_3031
3032,3032,3032,3032,3032,3032,3032,3032,MONDO:0016470,Ehlers-Danlos/osteogenesis imperfecta syndrome,MONDO,disease,DISEASE_3032
3033,3033,3033,3033,3033,3033,3033,3033,MONDO:1010224,"benign prostatic hyperplasia, non-human animal",MONDO,disease,DISEASE_3033
3034,3034,3034,3034,3034,3034,3034,3034,MONDO:0021098,papillomatosis,MONDO,disease,DISEASE_3034
3035,3035,3035,3035,3035,3035,3035,3035,MONDO:0005615,plasmacytoma,MONDO,disease,DISEASE_3035
3036,3036,3036,3036,3036,3036,3036,3036,MONDO:0011385,intervertebral disk degenerative disorder,MONDO,disease,DISEASE_3036
3037,3037,3037,3037,3037,3037,3037,3037,MONDO:1011825,"choroid plexus tumour, non-human animal",MONDO,disease,DISEASE_3037
3038,3038,3038,3038,3038,3038,3038,3038,MONDO:0022907,cutaneous sclerosis,MONDO,disease,DISEASE_3038
3039,3039,3039,3039,3039,3039,3039,3039,MONDO:0007700,hawkinsinuria,MONDO,disease,DISEASE_3039
3040,3040,3040,3040,3040,3040,3040,3040,MONDO:0022655,cardiomyopathy hypogonadism metabolic anomalies,MONDO,disease,DISEASE_3040
3041,3041,3041,3041,3041,3041,3041,3041,MONDO:0004351,intraocular lymphoma,MONDO,disease,DISEASE_3041
3042,3042,3042,3042,3042,3042,3042,3042,MONDO:0004728,diabetic macular edema,MONDO,disease,DISEASE_3042
3043,3043,3043,3043,3043,3043,3043,3043,MONDO:0700199,sheep lung adenocarcinoma,MONDO,disease,DISEASE_3043
3044,3044,3044,3044,3044,3044,3044,3044,MONDO:0006711,constrictive pericarditis,MONDO,disease,DISEASE_3044
3045,3045,3045,3045,3045,3045,3045,3045,MONDO:0020402,congenital accessory mitral valve tissue,MONDO,disease,DISEASE_3045
3046,3046,3046,3046,3046,3046,3046,3046,MONDO:1040029,Sharpin-related autoinflammatory syndrome,MONDO,disease,DISEASE_3046
3047,3047,3047,3047,3047,3047,3047,3047,MONDO:0011723,hemifacial myohyperplasia,MONDO,disease,DISEASE_3047
3048,3048,3048,3048,3048,3048,3048,3048,MONDO:0100235,FOXC1-related anterior segment dysgenesis,MONDO,disease,DISEASE_3048
3049,3049,3049,3049,3049,3049,3049,3049,MONDO:0018123,intellectual disability-obesity-brain malformations-facial dysmorphism syndrome,MONDO,disease,DISEASE_3049
3050,3050,3050,3050,3050,3050,3050,3050,MONDO:0008915,dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome,MONDO,disease,DISEASE_3050
3051,3051,3051,3051,3051,3051,3051,3051,MONDO:0009637,inborn mitochondrial myopathy,MONDO,disease,DISEASE_3051
3052,3052,3052,3052,3052,3052,3052,3052,MONDO:0001510,lateral displacement of eye,MONDO,disease,DISEASE_3052
3053,3053,3053,3053,3053,3053,3053,3053,MONDO:0024507_MONDO:0014937_MONDO:0014938_MONDO:0019172,aniridia,MONDO_grouped,disease,DISEASE_3053
3054,3054,3054,3054,3054,3054,3054,3054,MONDO:0023076_MONDO:0850048,eosinophilic pustular folliculitis,MONDO_grouped,disease,DISEASE_3054
3055,3055,3055,3055,3055,3055,3055,3055,MONDO:0009534_MONDO:0009536,chronic mucocutaneous candidiasis due to inhibition of lymphoblastic transformation,MONDO_grouped,disease,DISEASE_3055
3056,3056,3056,3056,3056,3056,3056,3056,MONDO:1012681,"cone-rod dystrophy, RPGRIP1-related and MAP9-related, dog",MONDO,disease,DISEASE_3056
3057,3057,3057,3057,3057,3057,3057,3057,MONDO:1012801,"Leigh syndrome, SURF1-related, pig",MONDO,disease,DISEASE_3057
3058,3058,3058,3058,3058,3058,3058,3058,MONDO:0010579,X-linked corneal dermoid,MONDO,disease,DISEASE_3058
3059,3059,3059,3059,3059,3059,3059,3059,MONDO:0004198,"testicular yolk sac tumor, solid pattern",MONDO,disease,DISEASE_3059
3060,3060,3060,3060,3060,3060,3060,3060,MONDO:0006517,childhood malignant neoplasm,MONDO,disease,DISEASE_3060
3061,3061,3061,3061,3061,3061,3061,3061,MONDO:0016858_MONDO:0016859,blepharophimosis-epicanthus inversus-ptosis due to a point mutation syndrome,MONDO_grouped,disease,DISEASE_3061
3062,3062,3062,3062,3062,3062,3062,3062,MONDO:0000541,jejunal adenocarcinoma,MONDO,disease,DISEASE_3062
3063,3063,3063,3063,3063,3063,3063,3063,MONDO:0002536,skin papilloma,MONDO,disease,DISEASE_3063
3064,3064,3064,3064,3064,3064,3064,3064,MONDO:0008724,"adducted thumbs-arthrogryposis syndrome, Christian type",MONDO,disease,DISEASE_3064
3065,3065,3065,3065,3065,3065,3065,3065,MONDO:0017800,pseudo-Meigs syndrome,MONDO,disease,DISEASE_3065
3066,3066,3066,3066,3066,3066,3066,3066,MONDO:0007620,fish eye disease,MONDO,disease,DISEASE_3066
3067,3067,3067,3067,3067,3067,3067,3067,MONDO:0011362,"myopathy, myofibrillar, 9, with early respiratory failure",MONDO,disease,DISEASE_3067
3068,3068,3068,3068,3068,3068,3068,3068,MONDO:0031030,"immunodeficiency 107, susceptibility to invasive staphylococcus aureus infection",MONDO,disease,DISEASE_3068
3069,3069,3069,3069,3069,3069,3069,3069,MONDO:0006938,pyelitis,MONDO,disease,DISEASE_3069
3070,3070,3070,3070,3070,3070,3070,3070,MONDO:0002304,protein S deficiency,MONDO,disease,DISEASE_3070
3071,3071,3071,3071,3071,3071,3071,3071,MONDO:1012748_MONDO:1012762_MONDO:1012840_MONDO:1012905,"polyneuropathy, ARHGEF10-related, dog",MONDO_grouped,disease,DISEASE_3071
3072,3072,3072,3072,3072,3072,3072,3072,MONDO:0015856,syndromic breast hypoplasia/aplasia,MONDO,disease,DISEASE_3072
3073,3073,3073,3073,3073,3073,3073,3073,MONDO:1012928,"Alzheimer disease, APP-related, Rhesus monkey",MONDO,disease,DISEASE_3073
3074,3074,3074,3074,3074,3074,3074,3074,MONDO:0859080,"intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies",MONDO,disease,DISEASE_3074
3075,3075,3075,3075,3075,3075,3075,3075,MONDO:0013213,"hearing loss, cisplatin-induced, susceptibility to",MONDO,disease,DISEASE_3075
3076,3076,3076,3076,3076,3076,3076,3076,MONDO:0024182_MONDO:0024183,dry beriberi,MONDO_grouped,disease,DISEASE_3076
3077,3077,3077,3077,3077,3077,3077,3077,MONDO:0000629,cardiovascular organ benign neoplasm,MONDO,disease,DISEASE_3077
3078,3078,3078,3078,3078,3078,3078,3078,MONDO:1010277,"orchitis, non-human animal",MONDO,disease,DISEASE_3078
3079,3079,3079,3079,3079,3079,3079,3079,MONDO:0032716,"leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate",MONDO,disease,DISEASE_3079
3080,3080,3080,3080,3080,3080,3080,3080,MONDO:0016026,infant epilepsy with migrant focal crisis,MONDO,disease,DISEASE_3080
3081,3081,3081,3081,3081,3081,3081,3081,MONDO:0018621,lymphoplasmacytic lymphoma without IgM production,MONDO,disease,DISEASE_3081
3082,3082,3082,3082,3082,3082,3082,3082,MONDO:0004481,pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma,MONDO,disease,DISEASE_3082
3083,3083,3083,3083,3083,3083,3083,3083,MONDO:0037807,glycerol metabolism disease,MONDO,disease,DISEASE_3083
3084,3084,3084,3084,3084,3084,3084,3084,MONDO:0042488,Cestode infectious disease,MONDO,disease,DISEASE_3084
3085,3085,3085,3085,3085,3085,3085,3085,MONDO:0023199,frontonasal dysplasia phocomelic upper limbs,MONDO,disease,DISEASE_3085
3086,3086,3086,3086,3086,3086,3086,3086,MONDO:0859178,"developmental delay, impaired speech, and behavioral abnormalities",MONDO,disease,DISEASE_3086
3087,3087,3087,3087,3087,3087,3087,3087,MONDO:0003659,pediatric lymphoma,MONDO,disease,DISEASE_3087
3088,3088,3088,3088,3088,3088,3088,3088,MONDO:0017225,null syndrome,MONDO,disease,DISEASE_3088
3089,3089,3089,3089,3089,3089,3089,3089,MONDO:0011118,bilineal acute myeloid leukemia,MONDO,disease,DISEASE_3089
3090,3090,3090,3090,3090,3090,3090,3090,MONDO:1010793,"Ehlers-Danlos syndrome, classic type, COL5A1-related, dog",MONDO,disease,DISEASE_3090
3091,3091,3091,3091,3091,3091,3091,3091,MONDO:0017728,"Tay-Sachs disease, B1 variant",MONDO,disease,DISEASE_3091
3092,3092,3092,3092,3092,3092,3092,3092,MONDO:0006848,marasmus,MONDO,disease,DISEASE_3092
3093,3093,3093,3093,3093,3093,3093,3093,MONDO:1011567,"neurofibromatosis, teleost fishes",MONDO,disease,DISEASE_3093
3094,3094,3094,3094,3094,3094,3094,3094,MONDO:0004528,lymph node palisaded myofibroblastoma,MONDO,disease,DISEASE_3094
3095,3095,3095,3095,3095,3095,3095,3095,MONDO:0030528,immunodeficiency 93 and hypertrophic cardiomyopathy,MONDO,disease,DISEASE_3095
3096,3096,3096,3096,3096,3096,3096,3096,MONDO:0010944,mitochondrial import-stimulating factor,MONDO,disease,DISEASE_3096
3097,3097,3097,3097,3097,3097,3097,3097,MONDO:0019240,sterol biosynthesis disorder,MONDO,disease,DISEASE_3097
3098,3098,3098,3098,3098,3098,3098,3098,MONDO:0017934,aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome,MONDO,disease,DISEASE_3098
3099,3099,3099,3099,3099,3099,3099,3099,MONDO:0034978,isolated foveal hypoplasia,MONDO,disease,DISEASE_3099
3100,3100,3100,3100,3100,3100,3100,3100,MONDO:1012902,"hair shaft dysplasia, DSG4-related, domestic cat",MONDO,disease,DISEASE_3100
3101,3101,3101,3101,3101,3101,3101,3101,MONDO:0020684_MONDO:0014954,"Ehlers-Danlos syndrome, periodontal",MONDO_grouped,disease,DISEASE_3101
3102,3102,3102,3102,3102,3102,3102,3102,MONDO:0018317,growth retardation-mild developmental delay-chronic hepatitis syndrome,MONDO,disease,DISEASE_3102
3103,3103,3103,3103,3103,3103,3103,3103,MONDO:0100290,colon serrated polyposis,MONDO,disease,DISEASE_3103
3104,3104,3104,3104,3104,3104,3104,3104,MONDO:0002927_MONDO:0006427_MONDO:0000962,spindle cell sarcoma,MONDO_grouped,disease,DISEASE_3104
3105,3105,3105,3105,3105,3105,3105,3105,MONDO:1011613,"Von Willebrand disease, domestic cat",MONDO,disease,DISEASE_3105
3106,3106,3106,3106,3106,3106,3106,3106,MONDO:0016699,myxopapillary ependymoma,MONDO,disease,DISEASE_3106
3107,3107,3107,3107,3107,3107,3107,3107,MONDO:0011219,Fried's tooth and nail syndrome,MONDO,disease,DISEASE_3107
3108,3108,3108,3108,3108,3108,3108,3108,MONDO:0011801_MONDO:0018996_MONDO:0020770_MONDO:0020771,"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy",MONDO_grouped,disease,DISEASE_3108
3109,3109,3109,3109,3109,3109,3109,3109,MONDO:0015278,familial pancreatic carcinoma,MONDO,disease,DISEASE_3109
3110,3110,3110,3110,3110,3110,3110,3110,MONDO:1012018,"atopy, domestic cat",MONDO,disease,DISEASE_3110
3111,3111,3111,3111,3111,3111,3111,3111,MONDO:0009329_MONDO:0020713_MONDO:0009937,pulmonary venoocclusive disease,MONDO_grouped,disease,DISEASE_3111
3112,3112,3112,3112,3112,3112,3112,3112,MONDO:0018267,combined cervical dystonia,MONDO,disease,DISEASE_3112
3113,3113,3113,3113,3113,3113,3113,3113,MONDO:0006139,cervical metaplasia,MONDO,disease,DISEASE_3113
3114,3114,3114,3114,3114,3114,3114,3114,MONDO:0004751,disease of orbital part of eye adnexa,MONDO,disease,DISEASE_3114
3115,3115,3115,3115,3115,3115,3115,3115,MONDO:0008107,"nystagmus, hereditary vertical",MONDO,disease,DISEASE_3115
3116,3116,3116,3116,3116,3116,3116,3116,MONDO:0019215,classic organic aciduria,MONDO,disease,DISEASE_3116
3117,3117,3117,3117,3117,3117,3117,3117,MONDO:1012226_MONDO:1012227_MONDO:1012228,"progressive retinal atrophy, dog",MONDO_grouped,disease,DISEASE_3117
3118,3118,3118,3118,3118,3118,3118,3118,MONDO:0007707,hemangiomas of small intestine,MONDO,disease,DISEASE_3118
3119,3119,3119,3119,3119,3119,3119,3119,MONDO:0025478,"venereal tumors, veterinary",MONDO,disease,DISEASE_3119
3120,3120,3120,3120,3120,3120,3120,3120,MONDO:0009636,mitochondrial DNA depletion syndrome 3 (hepatocerebral type),MONDO,disease,DISEASE_3120
3121,3121,3121,3121,3121,3121,3121,3121,MONDO:0021106,laminopathy,MONDO,disease,DISEASE_3121
3122,3122,3122,3122,3122,3122,3122,3122,MONDO:0012791,"mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria",MONDO,disease,DISEASE_3122
3123,3123,3123,3123,3123,3123,3123,3123,MONDO:0003185,adenoid cystic breast carcinoma,MONDO,disease,DISEASE_3123
3124,3124,3124,3124,3124,3124,3124,3124,MONDO:0008655,"vestibulocochlear dysfunction, progressive",MONDO,disease,DISEASE_3124
3125,3125,3125,3125,3125,3125,3125,3125,MONDO:0000487,hemidystonia,MONDO,disease,DISEASE_3125
3126,3126,3126,3126,3126,3126,3126,3126,MONDO:0003337,acute hemorrhagic encephalitis,MONDO,disease,DISEASE_3126
3127,3127,3127,3127,3127,3127,3127,3127,MONDO:0001137,Murray valley encephalitis,MONDO,disease,DISEASE_3127
3128,3128,3128,3128,3128,3128,3128,3128,MONDO:1011707,"congenital dyserythropoietic anemia, non-human animal",MONDO,disease,DISEASE_3128
3129,3129,3129,3129,3129,3129,3129,3129,MONDO:0003227,prosopagnosia,MONDO,disease,DISEASE_3129
3130,3130,3130,3130,3130,3130,3130,3130,MONDO:0016915,partial deletion of the long arm of chromosome 17,MONDO,disease,DISEASE_3130
3131,3131,3131,3131,3131,3131,3131,3131,MONDO:0004266,anal gland adenocarcinoma,MONDO,disease,DISEASE_3131
3132,3132,3132,3132,3132,3132,3132,3132,MONDO:0012259,colloid cysts of third ventricle,MONDO,disease,DISEASE_3132
3133,3133,3133,3133,3133,3133,3133,3133,MONDO:0007518,"edema, familial idiopathic, prepubertal",MONDO,disease,DISEASE_3133
3134,3134,3134,3134,3134,3134,3134,3134,MONDO:0003590,fibroblastic liposarcoma,MONDO,disease,DISEASE_3134
3135,3135,3135,3135,3135,3135,3135,3135,MONDO:0859276,primordial dwarfism-immunodeficiency-lipodystrophy syndrome,MONDO,disease,DISEASE_3135
3136,3136,3136,3136,3136,3136,3136,3136,MONDO:0016120,myotonic syndrome,MONDO,disease,DISEASE_3136
3137,3137,3137,3137,3137,3137,3137,3137,MONDO:0004423,central nervous system extraskeletal osteosarcoma,MONDO,disease,DISEASE_3137
3138,3138,3138,3138,3138,3138,3138,3138,MONDO:0009947,glutathione synthetase deficiency with 5-oxoprolinuria,MONDO,disease,DISEASE_3138
3139,3139,3139,3139,3139,3139,3139,3139,MONDO:0030873,cardiofacioneurodevelopmental syndrome,MONDO,disease,DISEASE_3139
3140,3140,3140,3140,3140,3140,3140,3140,MONDO:1012799,"skeletal dysplasia, FGF4-retrogene-related, dog",MONDO,disease,DISEASE_3140
3141,3141,3141,3141,3141,3141,3141,3141,MONDO:0024633,hypertensive nephropathy,MONDO,disease,DISEASE_3141
3142,3142,3142,3142,3142,3142,3142,3142,MONDO:0008558,autoimmune thrombocytopenic purpura,MONDO,disease,DISEASE_3142
3143,3143,3143,3143,3143,3143,3143,3143,MONDO:0011267,"intellectual disability, severe, with spasticity and pigmentary tapetoretinal degeneration",MONDO,disease,DISEASE_3143
3144,3144,3144,3144,3144,3144,3144,3144,MONDO:0016092,serous or mucinous cystadenoma of childhood,MONDO,disease,DISEASE_3144
3145,3145,3145,3145,3145,3145,3145,3145,MONDO:0002649,scrotum Paget disease,MONDO,disease,DISEASE_3145
3146,3146,3146,3146,3146,3146,3146,3146,MONDO:0005052,irritable bowel syndrome,MONDO,disease,DISEASE_3146
3147,3147,3147,3147,3147,3147,3147,3147,MONDO:1012212_MONDO:1012213_MONDO:1012214_MONDO:1012215,"persistent right aortic arch, dog",MONDO_grouped,disease,DISEASE_3147
3148,3148,3148,3148,3148,3148,3148,3148,MONDO:0021317,cancer of cerebellum,MONDO,disease,DISEASE_3148
3149,3149,3149,3149,3149,3149,3149,3149,MONDO:0021166,inflammatory disease,MONDO,disease,DISEASE_3149
3150,3150,3150,3150,3150,3150,3150,3150,MONDO:1011248,"strabismus, domestic cat",MONDO,disease,DISEASE_3150
3151,3151,3151,3151,3151,3151,3151,3151,MONDO:0007638,fucosidase regulator,MONDO,disease,DISEASE_3151
3152,3152,3152,3152,3152,3152,3152,3152,MONDO:0005300,chronic kidney disease,MONDO,disease,DISEASE_3152
3153,3153,3153,3153,3153,3153,3153,3153,MONDO:0010871,succinic acidemia,MONDO,disease,DISEASE_3153
3154,3154,3154,3154,3154,3154,3154,3154,MONDO:1011654,"facial digital syndrome, non-human animal",MONDO,disease,DISEASE_3154
3155,3155,3155,3155,3155,3155,3155,3155,MONDO:0017269,X-linked ichthyosis syndrome,MONDO,disease,DISEASE_3155
3156,3156,3156,3156,3156,3156,3156,3156,MONDO:0000661,alexithymia,MONDO,disease,DISEASE_3156
3157,3157,3157,3157,3157,3157,3157,3157,MONDO:0005841,maxillary neoplasm,MONDO,disease,DISEASE_3157
3158,3158,3158,3158,3158,3158,3158,3158,MONDO:1011692,"protein C deficiency, non-human animal",MONDO,disease,DISEASE_3158
3159,3159,3159,3159,3159,3159,3159,3159,MONDO:0009066_MONDO:0100151_MONDO:0018467,juvenile nephropathic cystinosis,MONDO_grouped,disease,DISEASE_3159
3160,3160,3160,3160,3160,3160,3160,3160,MONDO:0001476_MONDO:1011218,coloboma,MONDO_grouped,disease,DISEASE_3160
3161,3161,3161,3161,3161,3161,3161,3161,MONDO:0006398,retroperitoneal inflammatory myofibroblastic tumor,MONDO,disease,DISEASE_3161
3162,3162,3162,3162,3162,3162,3162,3162,MONDO:0001239,anemia of prematurity,MONDO,disease,DISEASE_3162
3163,3163,3163,3163,3163,3163,3163,3163,MONDO:0015420,cleft lip and alveolus,MONDO,disease,DISEASE_3163
3164,3164,3164,3164,3164,3164,3164,3164,MONDO:0001220_MONDO:1010600_MONDO:1010598,hypoparathyroidism,MONDO_grouped,disease,DISEASE_3164
3165,3165,3165,3165,3165,3165,3165,3165,MONDO:0021146,headache disorder,MONDO,disease,DISEASE_3165
3166,3166,3166,3166,3166,3166,3166,3166,MONDO:0003953,pediatric CNS choriocarcinoma,MONDO,disease,DISEASE_3166
3167,3167,3167,3167,3167,3167,3167,3167,MONDO:0016731_MONDO:0022963_MONDO:0022965,desmoplastic infantile astrocytoma/ganglioglioma,MONDO_grouped,disease,DISEASE_3167
3168,3168,3168,3168,3168,3168,3168,3168,MONDO:0018813,high grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement,MONDO,disease,DISEASE_3168
3169,3169,3169,3169,3169,3169,3169,3169,MONDO:0021147,disorder of development or morphogenesis,MONDO,disease,DISEASE_3169
3170,3170,3170,3170,3170,3170,3170,3170,MONDO:0003749_MONDO:0004189,esophageal disorder,MONDO_grouped,disease,DISEASE_3170
3171,3171,3171,3171,3171,3171,3171,3171,MONDO:0100213,"IFAP syndrome 1, with or without BRESHECK syndrome",MONDO,disease,DISEASE_3171
3172,3172,3172,3172,3172,3172,3172,3172,MONDO:0010617,male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome,MONDO,disease,DISEASE_3172
3173,3173,3173,3173,3173,3173,3173,3173,MONDO:0013582_MONDO:0859329_MONDO:0009759_MONDO:0054736_MONDO:0000141,mosaic variegated aneuploidy syndrome,MONDO_grouped,disease,DISEASE_3173
3174,3174,3174,3174,3174,3174,3174,3174,MONDO:0021279,mucoepidermoid carcinoma of submandibular gland,MONDO,disease,DISEASE_3174
3175,3175,3175,3175,3175,3175,3175,3175,MONDO:0016220,congenital temporomandibular joint ankylosis,MONDO,disease,DISEASE_3175
3176,3176,3176,3176,3176,3176,3176,3176,MONDO:0800470,TUBB4A-related neurologic disorder,MONDO,disease,DISEASE_3176
3177,3177,3177,3177,3177,3177,3177,3177,MONDO:0003806,thyroid hyalinizing trabecular adenoma,MONDO,disease,DISEASE_3177
3178,3178,3178,3178,3178,3178,3178,3178,MONDO:0008513_MONDO:0011984_MONDO:0021651_MONDO:0012447,synpolydactyly,MONDO_grouped,disease,DISEASE_3178
3179,3179,3179,3179,3179,3179,3179,3179,MONDO:0014737_MONDO:0008493_MONDO:0017910,dehydrated hereditary stomatocytosis 2,MONDO_grouped,disease,DISEASE_3179
3180,3180,3180,3180,3180,3180,3180,3180,MONDO:0007323,Chondronectin,MONDO,disease,DISEASE_3180
3181,3181,3181,3181,3181,3181,3181,3181,MONDO:0012336_MONDO:0011547_MONDO:0012437_MONDO:0007278_MONDO:0007288_MONDO:0007284_MONDO:0012701_MONDO:0011104_MONDO:0010948_MONDO:0012688_MONDO:0014111_MONDO:0011413_MONDO:0014110_MONDO:0013411_MONDO:0007281_MONDO:0014075_MONDO:0007290_MONDO:0012527_MONDO:0011162_MONDO:0007280_MONDO:0013067_MONDO:0011591,cataract 22 multiple types,MONDO_grouped,disease,DISEASE_3181
3182,3182,3182,3182,3182,3182,3182,3182,MONDO:0016437,late-onset focal dermal elastosis,MONDO,disease,DISEASE_3182
3183,3183,3183,3183,3183,3183,3183,3183,MONDO:0054868,meconium ileus,MONDO,disease,DISEASE_3183
3184,3184,3184,3184,3184,3184,3184,3184,MONDO:0006539,diffuse lipomatosis,MONDO,disease,DISEASE_3184
3185,3185,3185,3185,3185,3185,3185,3185,MONDO:0022096,pyogenic granuloma,MONDO,disease,DISEASE_3185
3186,3186,3186,3186,3186,3186,3186,3186,MONDO:0001373,urinary bladder posterior wall cancer,MONDO,disease,DISEASE_3186
3187,3187,3187,3187,3187,3187,3187,3187,MONDO:0008037,myelinated optic nerve fibers,MONDO,disease,DISEASE_3187
3188,3188,3188,3188,3188,3188,3188,3188,MONDO:0014247,familial episodic pain syndrome with predominantly lower limb involvement,MONDO,disease,DISEASE_3188
3189,3189,3189,3189,3189,3189,3189,3189,MONDO:0000997_MONDO:0001392,monocular esotropia,MONDO_grouped,disease,DISEASE_3189
3190,3190,3190,3190,3190,3190,3190,3190,MONDO:0859304,"neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction",MONDO,disease,DISEASE_3190
3191,3191,3191,3191,3191,3191,3191,3191,MONDO:0012156,"myasthenic syndrome, congenital, 1B, fast-channel",MONDO,disease,DISEASE_3191
3192,3192,3192,3192,3192,3192,3192,3192,MONDO:0016778,iatrogenic botulism,MONDO,disease,DISEASE_3192
3193,3193,3193,3193,3193,3193,3193,3193,MONDO:0019955,GRFoma,MONDO,disease,DISEASE_3193
3194,3194,3194,3194,3194,3194,3194,3194,MONDO:0024565,ectodermal dysplasia-syndactyly syndrome 1,MONDO,disease,DISEASE_3194
3195,3195,3195,3195,3195,3195,3195,3195,MONDO:0024905,bird disease,MONDO,disease,DISEASE_3195
3196,3196,3196,3196,3196,3196,3196,3196,MONDO:0025510,"pythiosis, non-human animal",MONDO,disease,DISEASE_3196
3197,3197,3197,3197,3197,3197,3197,3197,MONDO:0013340_MONDO:0859183_MONDO:0012466_MONDO:0011896_MONDO:0013653_MONDO:0975748,"Parkinson disease 5, autosomal dominant, susceptibility to",MONDO_grouped,disease,DISEASE_3197
3198,3198,3198,3198,3198,3198,3198,3198,MONDO:0007670,hypotrichosis-lymphedema-telangiectasia syndrome (grouping),MONDO,disease,DISEASE_3198
3199,3199,3199,3199,3199,3199,3199,3199,MONDO:0018154,Madelung deformity,MONDO,disease,DISEASE_3199
3200,3200,3200,3200,3200,3200,3200,3200,MONDO:0800373,carbon monoxide poisoning,MONDO,disease,DISEASE_3200
3201,3201,3201,3201,3201,3201,3201,3201,MONDO:0013755,PYCR1-related de Barsy syndrome,MONDO,disease,DISEASE_3201
3202,3202,3202,3202,3202,3202,3202,3202,MONDO:0019609,Zellweger spectrum disorders,MONDO,disease,DISEASE_3202
3203,3203,3203,3203,3203,3203,3203,3203,MONDO:0018122,digital anomalies-intellectual disability-short stature syndrome,MONDO,disease,DISEASE_3203
3204,3204,3204,3204,3204,3204,3204,3204,MONDO:0022013,Boerhaave syndrome,MONDO,disease,DISEASE_3204
3205,3205,3205,3205,3205,3205,3205,3205,MONDO:0005017,diffuse gastric adenocarcinoma,MONDO,disease,DISEASE_3205
3206,3206,3206,3206,3206,3206,3206,3206,MONDO:0800424,"colorectal cancer, susceptibility to, on chromosome 15",MONDO,disease,DISEASE_3206
3207,3207,3207,3207,3207,3207,3207,3207,MONDO:1010442,"cardiomyopathy, domestic cat",MONDO,disease,DISEASE_3207
3208,3208,3208,3208,3208,3208,3208,3208,MONDO:0008933,cephalin lipidosis,MONDO,disease,DISEASE_3208
3209,3209,3209,3209,3209,3209,3209,3209,MONDO:0003467,mediastinum synovial sarcoma,MONDO,disease,DISEASE_3209
3210,3210,3210,3210,3210,3210,3210,3210,MONDO:0018327,glomus tumor,MONDO,disease,DISEASE_3210
3211,3211,3211,3211,3211,3211,3211,3211,MONDO:0004597,pulmonary embolism and infarction,MONDO,disease,DISEASE_3211
3212,3212,3212,3212,3212,3212,3212,3212,MONDO:0029143,intellectual developmental disorder with hypertelorism and distinctive facies,MONDO,disease,DISEASE_3212
3213,3213,3213,3213,3213,3213,3213,3213,MONDO:0006737,dystocia,MONDO,disease,DISEASE_3213
3214,3214,3214,3214,3214,3214,3214,3214,MONDO:0012089,ichthyosis prematurity syndrome,MONDO,disease,DISEASE_3214
3215,3215,3215,3215,3215,3215,3215,3215,MONDO:0009415,"hypoglycemia, leucine-induced",MONDO,disease,DISEASE_3215
3216,3216,3216,3216,3216,3216,3216,3216,MONDO:0025488,"leukemia, feline",MONDO,disease,DISEASE_3216
3217,3217,3217,3217,3217,3217,3217,3217,MONDO:0019372,solitary bone cyst,MONDO,disease,DISEASE_3217
3218,3218,3218,3218,3218,3218,3218,3218,MONDO:1011584,"paroxysmal nocturnal hemoglobinuria, Rhesus monkey",MONDO,disease,DISEASE_3218
3219,3219,3219,3219,3219,3219,3219,3219,MONDO:0007690,aromatase excess syndrome,MONDO,disease,DISEASE_3219
3220,3220,3220,3220,3220,3220,3220,3220,MONDO:0017560,congenital genu recurvatum,MONDO,disease,DISEASE_3220
3221,3221,3221,3221,3221,3221,3221,3221,MONDO:0018883,Berardinelli-Seip congenital lipodystrophy,MONDO,disease,DISEASE_3221
3222,3222,3222,3222,3222,3222,3222,3222,MONDO:1012529,"recurrent inflammatory pulmonary disease, dog",MONDO,disease,DISEASE_3222
3223,3223,3223,3223,3223,3223,3223,3223,MONDO:0010118,inherited threoninemia,MONDO,disease,DISEASE_3223
3224,3224,3224,3224,3224,3224,3224,3224,MONDO:0100042,cardiac conduction defect,MONDO,disease,DISEASE_3224
3225,3225,3225,3225,3225,3225,3225,3225,MONDO:0100278,alanine glyoxylate aminotransferase deficiency,MONDO,disease,DISEASE_3225
3226,3226,3226,3226,3226,3226,3226,3226,MONDO:0018503,"carcinoma of stomach, salivary gland type",MONDO,disease,DISEASE_3226
3227,3227,3227,3227,3227,3227,3227,3227,MONDO:0015341,congenital panfollicular nevus,MONDO,disease,DISEASE_3227
3228,3228,3228,3228,3228,3228,3228,3228,MONDO:0800215,"multicentric Castleman disease, susceptibility to",MONDO,disease,DISEASE_3228
3229,3229,3229,3229,3229,3229,3229,3229,MONDO:0017137,onchocerciasis,MONDO,disease,DISEASE_3229
3230,3230,3230,3230,3230,3230,3230,3230,MONDO:0016683,gliomatosis cerebri,MONDO,disease,DISEASE_3230
3231,3231,3231,3231,3231,3231,3231,3231,MONDO:0036870,lymphatic vessel neoplasm,MONDO,disease,DISEASE_3231
3232,3232,3232,3232,3232,3232,3232,3232,MONDO:0010005,saccharopinuria,MONDO,disease,DISEASE_3232
3233,3233,3233,3233,3233,3233,3233,3233,MONDO:0100404,"acute myeloid leukemia, MLL gene rearrangement",MONDO,disease,DISEASE_3233
3234,3234,3234,3234,3234,3234,3234,3234,MONDO:0008164_MONDO:0957928_MONDO:0012797_MONDO:0012697_MONDO:0968980_MONDO:0012696_MONDO:0011999_MONDO:0014264_MONDO:0005349_MONDO:0011586_MONDO:0012121,otosclerosis,MONDO_grouped,disease,DISEASE_3234
3235,3235,3235,3235,3235,3235,3235,3235,MONDO:0003863,malignant melanocytic neoplasm of the peripheral nerve sheath,MONDO,disease,DISEASE_3235
3236,3236,3236,3236,3236,3236,3236,3236,MONDO:0000400,mixed cerebral palsy,MONDO,disease,DISEASE_3236
3237,3237,3237,3237,3237,3237,3237,3237,MONDO:0008981,infantile choroidocerebral calcification syndrome,MONDO,disease,DISEASE_3237
3238,3238,3238,3238,3238,3238,3238,3238,MONDO:0022818,congenital aneurysms of the great vessels,MONDO,disease,DISEASE_3238
3239,3239,3239,3239,3239,3239,3239,3239,MONDO:0100569_MONDO:0800469_MONDO:0100570,ACD-related short telomere syndrome,MONDO_grouped,disease,DISEASE_3239
3240,3240,3240,3240,3240,3240,3240,3240,MONDO:0021025,"cirrhosis, familial, with antigenemia",MONDO,disease,DISEASE_3240
3241,3241,3241,3241,3241,3241,3241,3241,MONDO:1011961,"brachygnathia, cardiomegaly and renal hypoplasia syndrome, non-human animal",MONDO,disease,DISEASE_3241
3242,3242,3242,3242,3242,3242,3242,3242,MONDO:0011427,"Ascaris lumbricoides infection, susceptibility to",MONDO,disease,DISEASE_3242
3243,3243,3243,3243,3243,3243,3243,3243,MONDO:0700186_MONDO:0700188,feline histiocytic sarcoma,MONDO_grouped,disease,DISEASE_3243
3244,3244,3244,3244,3244,3244,3244,3244,MONDO:0025102,monkey disease,MONDO,disease,DISEASE_3244
3245,3245,3245,3245,3245,3245,3245,3245,MONDO:0003528,Volkmann contracture,MONDO,disease,DISEASE_3245
3246,3246,3246,3246,3246,3246,3246,3246,MONDO:0007225,fibular aplasia-ectrodactyly syndrome,MONDO,disease,DISEASE_3246
3247,3247,3247,3247,3247,3247,3247,3247,MONDO:0008103,"noduli Cutanei, multiple, with urinary tract abnormalities",MONDO,disease,DISEASE_3247
3248,3248,3248,3248,3248,3248,3248,3248,MONDO:0003471_MONDO:0003482,Pediculus humanus capitis infestation,MONDO_grouped,disease,DISEASE_3248
3249,3249,3249,3249,3249,3249,3249,3249,MONDO:0018227,hypocomplementemic urticarial vasculitis,MONDO,disease,DISEASE_3249
3250,3250,3250,3250,3250,3250,3250,3250,MONDO:0012825_MONDO:0003681_MONDO:0003899_MONDO:0004392,extraskeletal myxoid chondrosarcoma,MONDO_grouped,disease,DISEASE_3250
3251,3251,3251,3251,3251,3251,3251,3251,MONDO:0005230,cellulitis,MONDO,disease,DISEASE_3251
3252,3252,3252,3252,3252,3252,3252,3252,MONDO:0010687,"nephrolithiasis, X-linked recessive, with renal failure",MONDO,disease,DISEASE_3252
3253,3253,3253,3253,3253,3253,3253,3253,MONDO:0022936,de Hauwere Leroy adriaenssens syndrome,MONDO,disease,DISEASE_3253
3254,3254,3254,3254,3254,3254,3254,3254,MONDO:0008240,6-phosphogluconolactonase deficiency,MONDO,disease,DISEASE_3254
3255,3255,3255,3255,3255,3255,3255,3255,MONDO:0017573,"46,XX disorder of sex development-anorectal anomalies syndrome",MONDO,disease,DISEASE_3255
3256,3256,3256,3256,3256,3256,3256,3256,MONDO:0003531_MONDO:0003450,papillary eccrine carcinoma,MONDO_grouped,disease,DISEASE_3256
3257,3257,3257,3257,3257,3257,3257,3257,MONDO:0010956,"enamel hypoplasia, cataracts, and aqueductal stenosis",MONDO,disease,DISEASE_3257
3258,3258,3258,3258,3258,3258,3258,3258,MONDO:0003414,skin pilomatrix carcinoma,MONDO,disease,DISEASE_3258
3259,3259,3259,3259,3259,3259,3259,3259,MONDO:0700206_MONDO:0700072_MONDO:0700214_MONDO:0700202,"Parvoviridae infectious disease, non-human animal",MONDO_grouped,disease,DISEASE_3259
3260,3260,3260,3260,3260,3260,3260,3260,MONDO:0006640,adrenal gland hyperfunction,MONDO,disease,DISEASE_3260
3261,3261,3261,3261,3261,3261,3261,3261,MONDO:1012114_MONDO:1012115_MONDO:1012116_MONDO:1012117,"congenital hypomyelinogenesis, dog",MONDO_grouped,disease,DISEASE_3261
3262,3262,3262,3262,3262,3262,3262,3262,MONDO:0008212,Pechet factor deficiency,MONDO,disease,DISEASE_3262
3263,3263,3263,3263,3263,3263,3263,3263,MONDO:0002351,glottis cancer,MONDO,disease,DISEASE_3263
3264,3264,3264,3264,3264,3264,3264,3264,MONDO:0001152_MONDO:0021702,amnestic disorder,MONDO_grouped,disease,DISEASE_3264
3265,3265,3265,3265,3265,3265,3265,3265,MONDO:0800300,black locks with albinism and deafness syndrome,MONDO,disease,DISEASE_3265
3266,3266,3266,3266,3266,3266,3266,3266,MONDO:0008974,Greenberg dysplasia,MONDO,disease,DISEASE_3266
3267,3267,3267,3267,3267,3267,3267,3267,MONDO:0012727,mucocutaneous lymph node syndrome,MONDO,disease,DISEASE_3267
3268,3268,3268,3268,3268,3268,3268,3268,MONDO:0100449,FLVCR1-related retinopathy with or without ataxia,MONDO,disease,DISEASE_3268
3269,3269,3269,3269,3269,3269,3269,3269,MONDO:1010616,"congenital dyshormonogenic hypothyroidism with goiter, SLC5A5-related, dog",MONDO,disease,DISEASE_3269
3270,3270,3270,3270,3270,3270,3270,3270,MONDO:0019797,acrodysostosis,MONDO,disease,DISEASE_3270
3271,3271,3271,3271,3271,3271,3271,3271,MONDO:0021063,malignant colon neoplasm,MONDO,disease,DISEASE_3271
3272,3272,3272,3272,3272,3272,3272,3272,MONDO:0017160,behavioral variant of frontotemporal dementia,MONDO,disease,DISEASE_3272
3273,3273,3273,3273,3273,3273,3273,3273,MONDO:0008063,"nasal alar collapse, bilateral",MONDO,disease,DISEASE_3273
3274,3274,3274,3274,3274,3274,3274,3274,MONDO:1010066,"microcephaly, non-human animal",MONDO,disease,DISEASE_3274
3275,3275,3275,3275,3275,3275,3275,3275,MONDO:0016003,ehrlichiosis,MONDO,disease,DISEASE_3275
3276,3276,3276,3276,3276,3276,3276,3276,MONDO:0001431,toxic or nutritional optic neuropathy,MONDO,disease,DISEASE_3276
3277,3277,3277,3277,3277,3277,3277,3277,MONDO:0003911,ciliary body mixed cell melanoma,MONDO,disease,DISEASE_3277
3278,3278,3278,3278,3278,3278,3278,3278,MONDO:0017766,disorder of manganese transport,MONDO,disease,DISEASE_3278
3279,3279,3279,3279,3279,3279,3279,3279,MONDO:0004660,lung carcinoma in situ,MONDO,disease,DISEASE_3279
3280,3280,3280,3280,3280,3280,3280,3280,MONDO:0014919,sessile serrated polyposis cancer syndrome,MONDO,disease,DISEASE_3280
3281,3281,3281,3281,3281,3281,3281,3281,MONDO:0017298,acute zonal occult outer retinopathy,MONDO,disease,DISEASE_3281
3282,3282,3282,3282,3282,3282,3282,3282,MONDO:0859376,"hydrocephalus, congenital, 5, susceptibility to",MONDO,disease,DISEASE_3282
3283,3283,3283,3283,3283,3283,3283,3283,MONDO:0859175_MONDO:0013163,nephronophthisis-like nephropathy,MONDO_grouped,disease,DISEASE_3283
3284,3284,3284,3284,3284,3284,3284,3284,MONDO:0024335_MONDO:0001895,retrobulbar neuritis,MONDO_grouped,disease,DISEASE_3284
3285,3285,3285,3285,3285,3285,3285,3285,MONDO:0008410,Scheuermann disease,MONDO,disease,DISEASE_3285
3286,3286,3286,3286,3286,3286,3286,3286,MONDO:0002435,oculomotor nerve neoplasm,MONDO,disease,DISEASE_3286
3287,3287,3287,3287,3287,3287,3287,3287,MONDO:0010785,maternally-inherited diabetes and deafness,MONDO,disease,DISEASE_3287
3288,3288,3288,3288,3288,3288,3288,3288,MONDO:0037872,bordetellosis,MONDO,disease,DISEASE_3288
3289,3289,3289,3289,3289,3289,3289,3289,MONDO:1010617,"congenital hypothyroidism, DUOX2-related, pig",MONDO,disease,DISEASE_3289
3290,3290,3290,3290,3290,3290,3290,3290,MONDO:0000314_MONDO:0100329,primary bacterial infectious disease,MONDO_grouped,disease,DISEASE_3290
3291,3291,3291,3291,3291,3291,3291,3291,MONDO:0859747,grade I lymphomatoid granulomatosis,MONDO,disease,DISEASE_3291
3292,3292,3292,3292,3292,3292,3292,3292,MONDO:0006951_MONDO:0001630_MONDO:0001985_MONDO:0002088_MONDO:0004583,retinal vein occlusion,MONDO_grouped,disease,DISEASE_3292
3293,3293,3293,3293,3293,3293,3293,3293,MONDO:0021351,neoplasm of neck,MONDO,disease,DISEASE_3293
3294,3294,3294,3294,3294,3294,3294,3294,MONDO:0007591,obsolete facial hypertrichosis,MONDO,disease,DISEASE_3294
3295,3295,3295,3295,3295,3295,3295,3295,MONDO:0001464_MONDO:0002139,sigmoid colon cancer,MONDO_grouped,disease,DISEASE_3295
3296,3296,3296,3296,3296,3296,3296,3296,MONDO:0012114,"Ehlers-Danlos syndrome, Beasley-Cohen type",MONDO,disease,DISEASE_3296
3297,3297,3297,3297,3297,3297,3297,3297,MONDO:0044768,vagus nerve paraganglioma,MONDO,disease,DISEASE_3297
3298,3298,3298,3298,3298,3298,3298,3298,MONDO:0018130,brain dopamine-serotonin vesicular transport disease,MONDO,disease,DISEASE_3298
3299,3299,3299,3299,3299,3299,3299,3299,MONDO:0004475,thymus clear cell carcinoma,MONDO,disease,DISEASE_3299
3300,3300,3300,3300,3300,3300,3300,3300,MONDO:0010163,Tyrosinosis,MONDO,disease,DISEASE_3300
3301,3301,3301,3301,3301,3301,3301,3301,MONDO:0023557,infective vaginitis,MONDO,disease,DISEASE_3301
3302,3302,3302,3302,3302,3302,3302,3302,MONDO:1011618,"Waardenburg syndrome, golden hamster",MONDO,disease,DISEASE_3302
3303,3303,3303,3303,3303,3303,3303,3303,MONDO:0009497,Kifafa seizure disorder,MONDO,disease,DISEASE_3303
3304,3304,3304,3304,3304,3304,3304,3304,MONDO:0013317,torsade-de-pointes syndrome with short coupling interval,MONDO,disease,DISEASE_3304
3305,3305,3305,3305,3305,3305,3305,3305,MONDO:0022553,BD syndrome,MONDO,disease,DISEASE_3305
3306,3306,3306,3306,3306,3306,3306,3306,MONDO:0000005,"alopecia, isolated",MONDO,disease,DISEASE_3306
3307,3307,3307,3307,3307,3307,3307,3307,MONDO:0003901,cerebellar hemangioblastoma,MONDO,disease,DISEASE_3307
3308,3308,3308,3308,3308,3308,3308,3308,MONDO:0019920,paternal uniparental disomy of chromosome 5,MONDO,disease,DISEASE_3308
3309,3309,3309,3309,3309,3309,3309,3309,MONDO:0008359,radio-renal syndrome,MONDO,disease,DISEASE_3309
3310,3310,3310,3310,3310,3310,3310,3310,MONDO:0017792,7p22.1 microduplication syndrome,MONDO,disease,DISEASE_3310
3311,3311,3311,3311,3311,3311,3311,3311,MONDO:0005844,chalazion,MONDO,disease,DISEASE_3311
3312,3312,3312,3312,3312,3312,3312,3312,MONDO:0001378,urachus cancer,MONDO,disease,DISEASE_3312
3313,3313,3313,3313,3313,3313,3313,3313,MONDO:0008963,Chediak-Higashi syndrome,MONDO,disease,DISEASE_3313
3314,3314,3314,3314,3314,3314,3314,3314,MONDO:0003164,cauda equina neoplasm,MONDO,disease,DISEASE_3314
3315,3315,3315,3315,3315,3315,3315,3315,MONDO:0014559,progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome,MONDO,disease,DISEASE_3315
3316,3316,3316,3316,3316,3316,3316,3316,MONDO:0006574,lipomatosis,MONDO,disease,DISEASE_3316
3317,3317,3317,3317,3317,3317,3317,3317,MONDO:0010795,oncocytic neoplasm,MONDO,disease,DISEASE_3317
3318,3318,3318,3318,3318,3318,3318,3318,MONDO:1011772,"hoof wall separation syndrome, non-human animal",MONDO,disease,DISEASE_3318
3319,3319,3319,3319,3319,3319,3319,3319,MONDO:0003428_MONDO:0002404_MONDO:0003948,brain hemangioma,MONDO_grouped,disease,DISEASE_3319
3320,3320,3320,3320,3320,3320,3320,3320,MONDO:1011943,"pituitary dwarfism, non-human animal",MONDO,disease,DISEASE_3320
3321,3321,3321,3321,3321,3321,3321,3321,MONDO:0958268,non-syndromic congenital bronchial atresia,MONDO,disease,DISEASE_3321
3322,3322,3322,3322,3322,3322,3322,3322,MONDO:0012301,"mitochondrial DNA depletion syndrome, myopathic form",MONDO,disease,DISEASE_3322
3323,3323,3323,3323,3323,3323,3323,3323,MONDO:0016444,primary anetoderma,MONDO,disease,DISEASE_3323
3324,3324,3324,3324,3324,3324,3324,3324,MONDO:0001815,extrapyramidal and movement disease,MONDO,disease,DISEASE_3324
3325,3325,3325,3325,3325,3325,3325,3325,MONDO:0009300_MONDO:0013588_MONDO:0014504_MONDO:0013972_MONDO:0014126_MONDO:0033047_MONDO:0017312,Perrault syndrome,MONDO_grouped,disease,DISEASE_3325
3326,3326,3326,3326,3326,3326,3326,3326,MONDO:0012392,2-methylbutyryl-CoA dehydrogenase deficiency,MONDO,disease,DISEASE_3326
3327,3327,3327,3327,3327,3327,3327,3327,MONDO:0022653,cardiomyopathy due to anthracyclines,MONDO,disease,DISEASE_3327
3328,3328,3328,3328,3328,3328,3328,3328,MONDO:0024343,pityriasis simplex,MONDO,disease,DISEASE_3328
3329,3329,3329,3329,3329,3329,3329,3329,MONDO:0010713,"properdin deficiency, X-linked",MONDO,disease,DISEASE_3329
3330,3330,3330,3330,3330,3330,3330,3330,MONDO:0022798,Cohen Lockood Wyborney syndrome,MONDO,disease,DISEASE_3330
3331,3331,3331,3331,3331,3331,3331,3331,MONDO:0005870,necatoriasis,MONDO,disease,DISEASE_3331
3332,3332,3332,3332,3332,3332,3332,3332,MONDO:0014344_MONDO:0013988_MONDO:0060663_MONDO:0014000_MONDO:0032913_MONDO:0013463_MONDO:0859532_MONDO:0000119,"congenital heart defects, multiple types",MONDO_grouped,disease,DISEASE_3332
3333,3333,3333,3333,3333,3333,3333,3333,MONDO:0009679,arthrogryposis due to muscular dystrophy,MONDO,disease,DISEASE_3333
3334,3334,3334,3334,3334,3334,3334,3334,MONDO:0007147,obstructive sleep apnea syndrome,MONDO,disease,DISEASE_3334
3335,3335,3335,3335,3335,3335,3335,3335,MONDO:1012536,"atypical thrombasthenia, horse",MONDO,disease,DISEASE_3335
3336,3336,3336,3336,3336,3336,3336,3336,MONDO:0004283,vulvar clear cell hidradenocarcinoma,MONDO,disease,DISEASE_3336
3337,3337,3337,3337,3337,3337,3337,3337,MONDO:0006247,histiocytic and dendritic cell neoplasm,MONDO,disease,DISEASE_3337
3338,3338,3338,3338,3338,3338,3338,3338,MONDO:0018757,supratip dysplasia,MONDO,disease,DISEASE_3338
3339,3339,3339,3339,3339,3339,3339,3339,MONDO:0859149_MONDO:0007788_MONDO:0005347_MONDO:1011537,hypertriglyceridemia,MONDO_grouped,disease,DISEASE_3339
3340,3340,3340,3340,3340,3340,3340,3340,MONDO:0007576,esophageal cancer,MONDO,disease,DISEASE_3340
3341,3341,3341,3341,3341,3341,3341,3341,MONDO:0018172,malignant sex cord stromal tumor of ovary,MONDO,disease,DISEASE_3341
3342,3342,3342,3342,3342,3342,3342,3342,MONDO:0012212_MONDO:0030500_MONDO:0013897_MONDO:0012427_MONDO:0018954,Loeys-Dietz syndrome,MONDO_grouped,disease,DISEASE_3342
3343,3343,3343,3343,3343,3343,3343,3343,MONDO:0013877,mitochondrial pyruvate carrier deficiency,MONDO,disease,DISEASE_3343
3344,3344,3344,3344,3344,3344,3344,3344,MONDO:0032900,neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements,MONDO,disease,DISEASE_3344
3345,3345,3345,3345,3345,3345,3345,3345,MONDO:0025485,feline acquired immunodeficiency syndrome,MONDO,disease,DISEASE_3345
3346,3346,3346,3346,3346,3346,3346,3346,MONDO:0024283,Demodex folliculitis,MONDO,disease,DISEASE_3346
3347,3347,3347,3347,3347,3347,3347,3347,MONDO:0004177,benign urethral neoplasm,MONDO,disease,DISEASE_3347
3348,3348,3348,3348,3348,3348,3348,3348,MONDO:0957465,multifocal tuberculosis,MONDO,disease,DISEASE_3348
3349,3349,3349,3349,3349,3349,3349,3349,MONDO:0020583,chromosome 17 disorder,MONDO,disease,DISEASE_3349
3350,3350,3350,3350,3350,3350,3350,3350,MONDO:0015006,"epidermolysis bullosa simplex 6, generalized, with scarring and hair loss",MONDO,disease,DISEASE_3350
3351,3351,3351,3351,3351,3351,3351,3351,MONDO:0032798,"ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features",MONDO,disease,DISEASE_3351
3352,3352,3352,3352,3352,3352,3352,3352,MONDO:1012588_MONDO:1012589,"oculocutaneous albinism, TYR-related, Japanese raccoon dog",MONDO_grouped,disease,DISEASE_3352
3353,3353,3353,3353,3353,3353,3353,3353,MONDO:0003157,disappearing bone disease,MONDO,disease,DISEASE_3353
3354,3354,3354,3354,3354,3354,3354,3354,MONDO:0956981_MONDO:0956994_MONDO:0956995,"astrocytoma, IDH-mutant, grade",MONDO_grouped,disease,DISEASE_3354
3355,3355,3355,3355,3355,3355,3355,3355,MONDO:0008270_MONDO:0017525_MONDO:0017526,polydactyly of a triphalangeal thumb,MONDO_grouped,disease,DISEASE_3355
3356,3356,3356,3356,3356,3356,3356,3356,MONDO:0016227,hereditary episodic ataxia,MONDO,disease,DISEASE_3356
3357,3357,3357,3357,3357,3357,3357,3357,MONDO:0006239,head and neck paraganglioma,MONDO,disease,DISEASE_3357
3358,3358,3358,3358,3358,3358,3358,3358,MONDO:0014833,heart and brain malformation syndrome,MONDO,disease,DISEASE_3358
3359,3359,3359,3359,3359,3359,3359,3359,MONDO:0014710,autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency,MONDO,disease,DISEASE_3359
3360,3360,3360,3360,3360,3360,3360,3360,MONDO:0020944_MONDO:0100504,fungal infection of eye,MONDO_grouped,disease,DISEASE_3360
3361,3361,3361,3361,3361,3361,3361,3361,MONDO:0100131,pediatric acute respiratory distress syndrome,MONDO,disease,DISEASE_3361
3362,3362,3362,3362,3362,3362,3362,3362,MONDO:0001103,giardiasis,MONDO,disease,DISEASE_3362
3363,3363,3363,3363,3363,3363,3363,3363,MONDO:0001127,tibialis tendinitis,MONDO,disease,DISEASE_3363
3364,3364,3364,3364,3364,3364,3364,3364,MONDO:0002713,epidural spinal canal neoplasm,MONDO,disease,DISEASE_3364
3365,3365,3365,3365,3365,3365,3365,3365,MONDO:0002487,breast granular cell tumor,MONDO,disease,DISEASE_3365
3366,3366,3366,3366,3366,3366,3366,3366,MONDO:0002582_MONDO:0004644,subacute leukemia,MONDO_grouped,disease,DISEASE_3366
3367,3367,3367,3367,3367,3367,3367,3367,MONDO:0100178,"dermatitis, atopic, susceptibility to",MONDO,disease,DISEASE_3367
3368,3368,3368,3368,3368,3368,3368,3368,MONDO:0003273,sternum cancer,MONDO,disease,DISEASE_3368
3369,3369,3369,3369,3369,3369,3369,3369,MONDO:0020529,ACTH-independent Cushing syndrome,MONDO,disease,DISEASE_3369
3370,3370,3370,3370,3370,3370,3370,3370,MONDO:0013309,chromosome 2p12-p11.2 deletion syndrome,MONDO,disease,DISEASE_3370
3371,3371,3371,3371,3371,3371,3371,3371,MONDO:0003759,childhood ovarian yolk sac tumor,MONDO,disease,DISEASE_3371
3372,3372,3372,3372,3372,3372,3372,3372,MONDO:0005120,Drosophila C virus infection,MONDO,disease,DISEASE_3372
3373,3373,3373,3373,3373,3373,3373,3373,MONDO:0007368,familial benign copper deficiency,MONDO,disease,DISEASE_3373
3374,3374,3374,3374,3374,3374,3374,3374,MONDO:0009093,dermatoleukodystrophy,MONDO,disease,DISEASE_3374
3375,3375,3375,3375,3375,3375,3375,3375,MONDO:0013227,congenital plasminogen activator inhibitor type 1 deficiency,MONDO,disease,DISEASE_3375
3376,3376,3376,3376,3376,3376,3376,3376,MONDO:0043112,lachiewicz sibley syndrome,MONDO,disease,DISEASE_3376
3377,3377,3377,3377,3377,3377,3377,3377,MONDO:0017804,autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome,MONDO,disease,DISEASE_3377
3378,3378,3378,3378,3378,3378,3378,3378,MONDO:0006286,major salivary gland mucoepidermoid carcinoma,MONDO,disease,DISEASE_3378
3379,3379,3379,3379,3379,3379,3379,3379,MONDO:0007570,erythema palmare hereditarium,MONDO,disease,DISEASE_3379
3380,3380,3380,3380,3380,3380,3380,3380,MONDO:0009724,nail-patella-like renal disease,MONDO,disease,DISEASE_3380
3381,3381,3381,3381,3381,3381,3381,3381,MONDO:0007564,pilomatrixoma,MONDO,disease,DISEASE_3381
3382,3382,3382,3382,3382,3382,3382,3382,MONDO:1010874_MONDO:1010875_MONDO:1010897_MONDO:1010902,"Niemann-Pick disease, NPC1-related, domestic cat",MONDO_grouped,disease,DISEASE_3382
3383,3383,3383,3383,3383,3383,3383,3383,MONDO:0043137,isolated microcephaly,MONDO,disease,DISEASE_3383
3384,3384,3384,3384,3384,3384,3384,3384,MONDO:0011435,"microcephaly 2, primary, autosomal recessive, with or without cortical malformations",MONDO,disease,DISEASE_3384
3385,3385,3385,3385,3385,3385,3385,3385,MONDO:0008215,adult-onset autosomal dominant demyelinating leukodystrophy,MONDO,disease,DISEASE_3385
3386,3386,3386,3386,3386,3386,3386,3386,MONDO:0022820,congenital articular rigidity,MONDO,disease,DISEASE_3386
3387,3387,3387,3387,3387,3387,3387,3387,MONDO:0060778,adult Fanconi syndrome,MONDO,disease,DISEASE_3387
3388,3388,3388,3388,3388,3388,3388,3388,MONDO:0001036,hypopyon,MONDO,disease,DISEASE_3388
3389,3389,3389,3389,3389,3389,3389,3389,MONDO:0009913,"prune belly syndrome with pulmonic stenosis, intellectual disability, and deafness",MONDO,disease,DISEASE_3389
3390,3390,3390,3390,3390,3390,3390,3390,MONDO:0000928,eyelid melanoma,MONDO,disease,DISEASE_3390
3391,3391,3391,3391,3391,3391,3391,3391,MONDO:0010058_MONDO:0008408,"scapuloperoneal spinal muscular atrophy, autosomal recessive",MONDO_grouped,disease,DISEASE_3391
3392,3392,3392,3392,3392,3392,3392,3392,MONDO:0009359,multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome,MONDO,disease,DISEASE_3392
3393,3393,3393,3393,3393,3393,3393,3393,MONDO:0008541,spermatic cord torsion,MONDO,disease,DISEASE_3393
3394,3394,3394,3394,3394,3394,3394,3394,MONDO:0006176,cribriform carcinoma,MONDO,disease,DISEASE_3394
3395,3395,3395,3395,3395,3395,3395,3395,MONDO:0011173_MONDO:0008554_MONDO:0013794_MONDO:0005029,thrombocythemia,MONDO_grouped,disease,DISEASE_3395
3396,3396,3396,3396,3396,3396,3396,3396,MONDO:0005624,atrophic thyroiditis,MONDO,disease,DISEASE_3396
3397,3397,3397,3397,3397,3397,3397,3397,MONDO:0011562_MONDO:0011764_MONDO:0008200,autosomal dominant Parkinson disease,MONDO_grouped,disease,DISEASE_3397
3398,3398,3398,3398,3398,3398,3398,3398,MONDO:0011848,headache associated with sexual activity,MONDO,disease,DISEASE_3398
3399,3399,3399,3399,3399,3399,3399,3399,MONDO:0004393,mixed astrocytoma-ependymoma,MONDO,disease,DISEASE_3399
3400,3400,3400,3400,3400,3400,3400,3400,MONDO:0030906,Trichomonas tenax infectious disease,MONDO,disease,DISEASE_3400
3401,3401,3401,3401,3401,3401,3401,3401,MONDO:0019278,hair anomaly,MONDO,disease,DISEASE_3401
3402,3402,3402,3402,3402,3402,3402,3402,MONDO:0016424,progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome,MONDO,disease,DISEASE_3402
3403,3403,3403,3403,3403,3403,3403,3403,MONDO:1011234,"microphthalmia, Campbell's desert hamster",MONDO,disease,DISEASE_3403
3404,3404,3404,3404,3404,3404,3404,3404,MONDO:1011795,"masticatory muscle myositis, non-human animal",MONDO,disease,DISEASE_3404
3405,3405,3405,3405,3405,3405,3405,3405,MONDO:0019922,paternal uniparental disomy of chromosome 7,MONDO,disease,DISEASE_3405
3406,3406,3406,3406,3406,3406,3406,3406,MONDO:1011443,"Alzheimer disease, non-human animal",MONDO,disease,DISEASE_3406
3407,3407,3407,3407,3407,3407,3407,3407,MONDO:1012441,"familial episodic spinocerebellar ataxia, sheep",MONDO,disease,DISEASE_3407
3408,3408,3408,3408,3408,3408,3408,3408,MONDO:0008595,"trichoepitheliomas, multiple desmoplastic",MONDO,disease,DISEASE_3408
3409,3409,3409,3409,3409,3409,3409,3409,MONDO:0009902,cutaneous porphyria,MONDO,disease,DISEASE_3409
3410,3410,3410,3410,3410,3410,3410,3410,MONDO:0044903,myelofibrosis,MONDO,disease,DISEASE_3410
3411,3411,3411,3411,3411,3411,3411,3411,MONDO:0005595,laryngeal squamous cell carcinoma,MONDO,disease,DISEASE_3411
3412,3412,3412,3412,3412,3412,3412,3412,MONDO:0018124,Oncogenic osteomalacia,MONDO,disease,DISEASE_3412
3413,3413,3413,3413,3413,3413,3413,3413,MONDO:0003268,mixed glioma,MONDO,disease,DISEASE_3413
3414,3414,3414,3414,3414,3414,3414,3414,MONDO:0014948,"short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay",MONDO,disease,DISEASE_3414
3415,3415,3415,3415,3415,3415,3415,3415,MONDO:0013321,forsythe-wakeling syndrome,MONDO,disease,DISEASE_3415
3416,3416,3416,3416,3416,3416,3416,3416,MONDO:0006572_MONDO:0043923_MONDO:0016770,lichen planus,MONDO_grouped,disease,DISEASE_3416
3417,3417,3417,3417,3417,3417,3417,3417,MONDO:0015723,trisomy 12p,MONDO,disease,DISEASE_3417
3418,3418,3418,3418,3418,3418,3418,3418,MONDO:1012475,"recurrent uveitis, horse",MONDO,disease,DISEASE_3418
3419,3419,3419,3419,3419,3419,3419,3419,MONDO:0043156,nephrotic syndrome ocular anomalies,MONDO,disease,DISEASE_3419
3420,3420,3420,3420,3420,3420,3420,3420,MONDO:0022805,colonic malakoplakia,MONDO,disease,DISEASE_3420
3421,3421,3421,3421,3421,3421,3421,3421,MONDO:0008908_MONDO:0011257_MONDO:0013968_MONDO:0012783_MONDO:0014271_MONDO:0012211_MONDO:0013049_MONDO:0012637_MONDO:0012052_MONDO:0008907_MONDO:0012556_MONDO:0011629_MONDO:0011964_MONDO:0018273_MONDO:0018349_MONDO:0100588,MGAT2-congenital disorder of glycosylation,MONDO_grouped,disease,DISEASE_3421
3422,3422,3422,3422,3422,3422,3422,3422,MONDO:0015706,mosaic trisomy 1,MONDO,disease,DISEASE_3422
3423,3423,3423,3423,3423,3423,3423,3423,MONDO:0018192,paratesticular adenocarcinoma,MONDO,disease,DISEASE_3423
3424,3424,3424,3424,3424,3424,3424,3424,MONDO:0006162,colorectal neuroendocrine tumor G1,MONDO,disease,DISEASE_3424
3425,3425,3425,3425,3425,3425,3425,3425,MONDO:1011784,"premature senesence, non-human animal",MONDO,disease,DISEASE_3425
3426,3426,3426,3426,3426,3426,3426,3426,MONDO:0002905,mutism,MONDO,disease,DISEASE_3426
3427,3427,3427,3427,3427,3427,3427,3427,MONDO:0022998,distal arthrogryposis Moore weaver type,MONDO,disease,DISEASE_3427
3428,3428,3428,3428,3428,3428,3428,3428,MONDO:0044982,drug pseudoallergy,MONDO,disease,DISEASE_3428
3429,3429,3429,3429,3429,3429,3429,3429,MONDO:0800148,autoinflammatory syndrome due to TBK1 deficiency,MONDO,disease,DISEASE_3429
3430,3430,3430,3430,3430,3430,3430,3430,MONDO:0014375_MONDO:0013184,congenital diarrhea 7 with exudative enteropathy,MONDO_grouped,disease,DISEASE_3430
3431,3431,3431,3431,3431,3431,3431,3431,MONDO:1010057,"congenital hypothyroidism, non-human animal",MONDO,disease,DISEASE_3431
3432,3432,3432,3432,3432,3432,3432,3432,MONDO:0005900,parotitis,MONDO,disease,DISEASE_3432
3433,3433,3433,3433,3433,3433,3433,3433,MONDO:0859203,"rhizomelic dysplasia, Ain-Naz type",MONDO,disease,DISEASE_3433
3434,3434,3434,3434,3434,3434,3434,3434,MONDO:0003811,ovarian seromucinous tumor,MONDO,disease,DISEASE_3434
3435,3435,3435,3435,3435,3435,3435,3435,MONDO:0859301,neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects,MONDO,disease,DISEASE_3435
3436,3436,3436,3436,3436,3436,3436,3436,MONDO:0002300,dermis tumor,MONDO,disease,DISEASE_3436
3437,3437,3437,3437,3437,3437,3437,3437,MONDO:0008052,myopathy with storage of glycoproteins and Glycosaminoglycans,MONDO,disease,DISEASE_3437
3438,3438,3438,3438,3438,3438,3438,3438,MONDO:0008734,"adrenocortical carcinoma, hereditary",MONDO,disease,DISEASE_3438
3439,3439,3439,3439,3439,3439,3439,3439,MONDO:0035337,Duane retraction syndrome with congenital deafness,MONDO,disease,DISEASE_3439
3440,3440,3440,3440,3440,3440,3440,3440,MONDO:0016938,partial trisomy of chromosome 20,MONDO,disease,DISEASE_3440
3441,3441,3441,3441,3441,3441,3441,3441,MONDO:0023757,meralgia paresthetica,MONDO,disease,DISEASE_3441
3442,3442,3442,3442,3442,3442,3442,3442,MONDO:1012089,"gastric dilatation volvulus syndrome, domestic guinea pig",MONDO,disease,DISEASE_3442
3443,3443,3443,3443,3443,3443,3443,3443,MONDO:0005215_MONDO:0002205,vulvar carcinoma,MONDO_grouped,disease,DISEASE_3443
3444,3444,3444,3444,3444,3444,3444,3444,MONDO:0018881,myelodysplastic syndrome,MONDO,disease,DISEASE_3444
3445,3445,3445,3445,3445,3445,3445,3445,MONDO:0043775,respiratory paralysis,MONDO,disease,DISEASE_3445
3446,3446,3446,3446,3446,3446,3446,3446,MONDO:0004320,adult infiltrating astrocytic neoplasm,MONDO,disease,DISEASE_3446
3447,3447,3447,3447,3447,3447,3447,3447,MONDO:0024263,neonatal aspiration syndrome,MONDO,disease,DISEASE_3447
3448,3448,3448,3448,3448,3448,3448,3448,MONDO:0009120,"diverticulosis of bowel, hernia, and retinal detachment",MONDO,disease,DISEASE_3448
3449,3449,3449,3449,3449,3449,3449,3449,MONDO:0021354,tumor of adipose tissue,MONDO,disease,DISEASE_3449
3450,3450,3450,3450,3450,3450,3450,3450,MONDO:0100249,"46,XX testicular disorder of sex development",MONDO,disease,DISEASE_3450
3451,3451,3451,3451,3451,3451,3451,3451,MONDO:0003212,nasal cavity carcinoma,MONDO,disease,DISEASE_3451
3452,3452,3452,3452,3452,3452,3452,3452,MONDO:0859170,retinal dystrophy and microvillus inclusion disease,MONDO,disease,DISEASE_3452
3453,3453,3453,3453,3453,3453,3453,3453,MONDO:0010243,X-linked immunoneurologic disorder,MONDO,disease,DISEASE_3453
3454,3454,3454,3454,3454,3454,3454,3454,MONDO:0008039,tropical spastic paraparesis,MONDO,disease,DISEASE_3454
3455,3455,3455,3455,3455,3455,3455,3455,MONDO:1011884,"acral mutilation syndrome, non-human animal",MONDO,disease,DISEASE_3455
3456,3456,3456,3456,3456,3456,3456,3456,MONDO:0014748,progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome,MONDO,disease,DISEASE_3456
3457,3457,3457,3457,3457,3457,3457,3457,MONDO:1010729,"leukocyte adhesion deficiency, ITGB2-related, cattle",MONDO,disease,DISEASE_3457
3458,3458,3458,3458,3458,3458,3458,3458,MONDO:0056797,neurodevelopmental disorder with midbrain and hindbrain malformations,MONDO,disease,DISEASE_3458
3459,3459,3459,3459,3459,3459,3459,3459,MONDO:0971034,thyroid gland cribriform morular carcinoma,MONDO,disease,DISEASE_3459
3460,3460,3460,3460,3460,3460,3460,3460,MONDO:0011199,"nephropathy, progressive tubulointerstitial, with cholestatic liver disease",MONDO,disease,DISEASE_3460
3461,3461,3461,3461,3461,3461,3461,3461,MONDO:0019143,angiostrongyliasis,MONDO,disease,DISEASE_3461
3462,3462,3462,3462,3462,3462,3462,3462,MONDO:0002014,"autosomal recessive Ehlers-Danlos syndrome, vascular type",MONDO,disease,DISEASE_3462
3463,3463,3463,3463,3463,3463,3463,3463,MONDO:0006826,kwashiorkor,MONDO,disease,DISEASE_3463
3464,3464,3464,3464,3464,3464,3464,3464,MONDO:0024582,male reproductive system neoplasm,MONDO,disease,DISEASE_3464
3465,3465,3465,3465,3465,3465,3465,3465,MONDO:0012068,"brachial palsy, familial congenital",MONDO,disease,DISEASE_3465
3466,3466,3466,3466,3466,3466,3466,3466,MONDO:0008677,obsolete widow's peak,MONDO,disease,DISEASE_3466
3467,3467,3467,3467,3467,3467,3467,3467,MONDO:0011352,"neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and enamel hypoplasia",MONDO,disease,DISEASE_3467
3468,3468,3468,3468,3468,3468,3468,3468,MONDO:1012108,"hypertrophic neuropathy, dog",MONDO,disease,DISEASE_3468
3469,3469,3469,3469,3469,3469,3469,3469,MONDO:0008597_MONDO:0019176,"obsolete trichorhinophalangeal syndrome,",MONDO_grouped,disease,DISEASE_3469
3470,3470,3470,3470,3470,3470,3470,3470,MONDO:0850301,pemphigoid,MONDO,disease,DISEASE_3470
3471,3471,3471,3471,3471,3471,3471,3471,MONDO:1011989,"blindness with enlarged globe, non-human animal",MONDO,disease,DISEASE_3471
3472,3472,3472,3472,3472,3472,3472,3472,MONDO:0024171,radio-digito-facial dysplasia,MONDO,disease,DISEASE_3472
3473,3473,3473,3473,3473,3473,3473,3473,MONDO:0018127,16q24.1 microdeletion syndrome,MONDO,disease,DISEASE_3473
3474,3474,3474,3474,3474,3474,3474,3474,MONDO:0025385,bluetongue,MONDO,disease,DISEASE_3474
3475,3475,3475,3475,3475,3475,3475,3475,MONDO:0859592_MONDO:0956996_MONDO:0956997,IDH-mutant and 1p/19q-codeleted oligodendroglioma,MONDO_grouped,disease,DISEASE_3475
3476,3476,3476,3476,3476,3476,3476,3476,MONDO:0001733,occlusion of tributary of retinal vein,MONDO,disease,DISEASE_3476
3477,3477,3477,3477,3477,3477,3477,3477,MONDO:1010582,"familial goiter, water buffalo",MONDO,disease,DISEASE_3477
3478,3478,3478,3478,3478,3478,3478,3478,MONDO:1011240,"microphthalmia, Eastern wapiti",MONDO,disease,DISEASE_3478
3479,3479,3479,3479,3479,3479,3479,3479,MONDO:0004635,postcricoid region cancer,MONDO,disease,DISEASE_3479
3480,3480,3480,3480,3480,3480,3480,3480,MONDO:0858926,"developmental delay, hypotrophy, and dysmorphic features without moebius syndrome",MONDO,disease,DISEASE_3480
3481,3481,3481,3481,3481,3481,3481,3481,MONDO:0800128,combined immunodeficiency due to POLE2 deficiency,MONDO,disease,DISEASE_3481
3482,3482,3482,3482,3482,3482,3482,3482,MONDO:1012338,"reduced glutathione deficiency, goat",MONDO,disease,DISEASE_3482
3483,3483,3483,3483,3483,3483,3483,3483,MONDO:0700198,porcine lymphoma,MONDO,disease,DISEASE_3483
3484,3484,3484,3484,3484,3484,3484,3484,MONDO:0018343,periodic paralysis with later-onset distal motor neuropathy,MONDO,disease,DISEASE_3484
3485,3485,3485,3485,3485,3485,3485,3485,MONDO:0030538,"dystonia 34, myoclonic",MONDO,disease,DISEASE_3485
3486,3486,3486,3486,3486,3486,3486,3486,MONDO:0800298_MONDO:0800364_MONDO:0800365,"peroxisome biogenesis disorder, complementation group",MONDO_grouped,disease,DISEASE_3486
3487,3487,3487,3487,3487,3487,3487,3487,MONDO:0015766,cholera,MONDO,disease,DISEASE_3487
3488,3488,3488,3488,3488,3488,3488,3488,MONDO:0010517,"ciliary dyskinesia, primary, 36, X-linked",MONDO,disease,DISEASE_3488
3489,3489,3489,3489,3489,3489,3489,3489,MONDO:1012202_MONDO:1012203_MONDO:1012204_MONDO:1012205,"osteodystrophy, dog",MONDO_grouped,disease,DISEASE_3489
3490,3490,3490,3490,3490,3490,3490,3490,MONDO:0000378,malignant Sertoli cell tumor,MONDO,disease,DISEASE_3490
3491,3491,3491,3491,3491,3491,3491,3491,MONDO:1012850,"dilated cardiomyopathy, DMD-related, rabbit",MONDO,disease,DISEASE_3491
3492,3492,3492,3492,3492,3492,3492,3492,MONDO:0010299,hypoxanthine guanine phosphoribosyltransferase partial deficiency,MONDO,disease,DISEASE_3492
3493,3493,3493,3493,3493,3493,3493,3493,MONDO:0019303,premature aging syndrome,MONDO,disease,DISEASE_3493
3494,3494,3494,3494,3494,3494,3494,3494,MONDO:0001899,rheumatic congestive heart failure,MONDO,disease,DISEASE_3494
3495,3495,3495,3495,3495,3495,3495,3495,MONDO:1012263,"tapetal degeneration, dog",MONDO,disease,DISEASE_3495
3496,3496,3496,3496,3496,3496,3496,3496,MONDO:0018447,chondromyxoid fibroma,MONDO,disease,DISEASE_3496
3497,3497,3497,3497,3497,3497,3497,3497,MONDO:0100080,cardioectodermal syndrome,MONDO,disease,DISEASE_3497
3498,3498,3498,3498,3498,3498,3498,3498,MONDO:0006614,subcorneal pustular dermatosis,MONDO,disease,DISEASE_3498
3499,3499,3499,3499,3499,3499,3499,3499,MONDO:0859531,"neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures",MONDO,disease,DISEASE_3499
3500,3500,3500,3500,3500,3500,3500,3500,MONDO:0958129,COQ7-related distal hereditary motor neuropathy,MONDO,disease,DISEASE_3500
3501,3501,3501,3501,3501,3501,3501,3501,MONDO:0010815,spondyloepiphyseal dysplasia tarda with characteristic facies,MONDO,disease,DISEASE_3501
3502,3502,3502,3502,3502,3502,3502,3502,MONDO:0008807,"obsolete apnea, central sleep",MONDO,disease,DISEASE_3502
3503,3503,3503,3503,3503,3503,3503,3503,MONDO:1011347,"post-COVID-19 disorder, non-human animal",MONDO,disease,DISEASE_3503
3504,3504,3504,3504,3504,3504,3504,3504,MONDO:1011974,"aniridia with cataract, non-human animal",MONDO,disease,DISEASE_3504
3505,3505,3505,3505,3505,3505,3505,3505,MONDO:0008830,aspartylglucosaminuria,MONDO,disease,DISEASE_3505
3506,3506,3506,3506,3506,3506,3506,3506,MONDO:0100052,acetazolamide-responsive hereditary episodic ataxia,MONDO,disease,DISEASE_3506
3507,3507,3507,3507,3507,3507,3507,3507,MONDO:0033980,RELA fusion-positive ependymoma,MONDO,disease,DISEASE_3507
3508,3508,3508,3508,3508,3508,3508,3508,MONDO:0008665,ptosis-vocal cord paralysis syndrome,MONDO,disease,DISEASE_3508
3509,3509,3509,3509,3509,3509,3509,3509,MONDO:0006783,hemopneumothorax,MONDO,disease,DISEASE_3509
3510,3510,3510,3510,3510,3510,3510,3510,MONDO:0008334_MONDO:0013554_MONDO:0011387_MONDO:0011434_MONDO:0011542_MONDO:0011573_MONDO:0011926_MONDO:0012542_MONDO:0012896_MONDO:0012959_MONDO:0013057,"psoriasis 1, susceptibility to",MONDO_grouped,disease,DISEASE_3510
3511,3511,3511,3511,3511,3511,3511,3511,MONDO:0010034,obsolete anosmia for butyl mercaptan,MONDO,disease,DISEASE_3511
3512,3512,3512,3512,3512,3512,3512,3512,MONDO:0700225,hereditary gallbladder disorder,MONDO,disease,DISEASE_3512
3513,3513,3513,3513,3513,3513,3513,3513,MONDO:0014787,severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome,MONDO,disease,DISEASE_3513
3514,3514,3514,3514,3514,3514,3514,3514,MONDO:0859519,neurodevelopmental disorder with absent speech and movement and behavioral abnormalities,MONDO,disease,DISEASE_3514
3515,3515,3515,3515,3515,3515,3515,3515,MONDO:0004449,intraductal breast myoepitheliosis,MONDO,disease,DISEASE_3515
3516,3516,3516,3516,3516,3516,3516,3516,MONDO:0015781,facial dysmorphism-shawl scrotum-joint laxity syndrome,MONDO,disease,DISEASE_3516
3517,3517,3517,3517,3517,3517,3517,3517,MONDO:0007251,campomelic dysplasia,MONDO,disease,DISEASE_3517
3518,3518,3518,3518,3518,3518,3518,3518,MONDO:0005831,lymph node tuberculosis,MONDO,disease,DISEASE_3518
3519,3519,3519,3519,3519,3519,3519,3519,MONDO:0017793,marfanoid habitus-inguinal hernia-advanced bone age syndrome,MONDO,disease,DISEASE_3519
3520,3520,3520,3520,3520,3520,3520,3520,MONDO:0013458,hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome,MONDO,disease,DISEASE_3520
3521,3521,3521,3521,3521,3521,3521,3521,MONDO:0003047,thymic large cell neuroendocrine carcinoma,MONDO,disease,DISEASE_3521
3522,3522,3522,3522,3522,3522,3522,3522,MONDO:0021392_MONDO:0021400_MONDO:0021416,polyp of large intestine,MONDO_grouped,disease,DISEASE_3522
3523,3523,3523,3523,3523,3523,3523,3523,MONDO:0004017,pineal region immature teratoma,MONDO,disease,DISEASE_3523
3524,3524,3524,3524,3524,3524,3524,3524,MONDO:0018475,PRKAR1B-related neurodegenerative dementia with intermediate filaments,MONDO,disease,DISEASE_3524
3525,3525,3525,3525,3525,3525,3525,3525,MONDO:0859369,"joint contractures, osteochondromas, and B-cell lymphoma",MONDO,disease,DISEASE_3525
3526,3526,3526,3526,3526,3526,3526,3526,MONDO:0004928_MONDO:0001082,lymph node disorder,MONDO_grouped,disease,DISEASE_3526
3527,3527,3527,3527,3527,3527,3527,3527,MONDO:0015075,thyroid gland carcinoma,MONDO,disease,DISEASE_3527
3528,3528,3528,3528,3528,3528,3528,3528,MONDO:0024469,chondrogenic neoplasm,MONDO,disease,DISEASE_3528
3529,3529,3529,3529,3529,3529,3529,3529,MONDO:0004332,lung hilum cancer,MONDO,disease,DISEASE_3529
3530,3530,3530,3530,3530,3530,3530,3530,MONDO:0100251,familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome,MONDO,disease,DISEASE_3530
3531,3531,3531,3531,3531,3531,3531,3531,MONDO:0008926,COFS syndrome,MONDO,disease,DISEASE_3531
3532,3532,3532,3532,3532,3532,3532,3532,MONDO:0005497_MONDO:0002614,bone development disease,MONDO_grouped,disease,DISEASE_3532
3533,3533,3533,3533,3533,3533,3533,3533,MONDO:0026722,Mullegama-Klein-Martinez syndrome,MONDO,disease,DISEASE_3533
3534,3534,3534,3534,3534,3534,3534,3534,MONDO:0016952,partial duplication of the long arm of chromosome 1,MONDO,disease,DISEASE_3534
3535,3535,3535,3535,3535,3535,3535,3535,MONDO:0015758,primary cutaneous T-cell lymphoma,MONDO,disease,DISEASE_3535
3536,3536,3536,3536,3536,3536,3536,3536,MONDO:0015270,butyrylcholinesterase deficiency,MONDO,disease,DISEASE_3536
3537,3537,3537,3537,3537,3537,3537,3537,MONDO:0100184,GTP cyclohydrolase I deficiency,MONDO,disease,DISEASE_3537
3538,3538,3538,3538,3538,3538,3538,3538,MONDO:1012564,"growth and respiratory lethal syndrome, cattle",MONDO,disease,DISEASE_3538
3539,3539,3539,3539,3539,3539,3539,3539,MONDO:0015401,maxillary arteriovenous malformation,MONDO,disease,DISEASE_3539
3540,3540,3540,3540,3540,3540,3540,3540,MONDO:0030482_MONDO:0033614_MONDO:0031019_MONDO:0032906_MONDO:0957309_MONDO:0030512_MONDO:0030673_MONDO:0957958_MONDO:0957274_MONDO:0032905_MONDO:0975796_MONDO:0957221_MONDO:0971149_MONDO:0975746,"spastic paraplegia 84, autosomal recessive",MONDO_grouped,disease,DISEASE_3540
3541,3541,3541,3541,3541,3541,3541,3541,MONDO:0800485,AKT3-related overgrowth spectrum,MONDO,disease,DISEASE_3541
3542,3542,3542,3542,3542,3542,3542,3542,MONDO:0011337_MONDO:0011336_MONDO:0012146_MONDO:0013135_MONDO:0009974_MONDO:0015541_MONDO:0015544_MONDO:0015542_MONDO:0033557,familial hemophagocytic lymphohistiocytosis,MONDO_grouped,disease,DISEASE_3542
3543,3543,3543,3543,3543,3543,3543,3543,MONDO:0600002_MONDO:0600003,hemorrhagic fever,MONDO_grouped,disease,DISEASE_3543
3544,3544,3544,3544,3544,3544,3544,3544,MONDO:1012446,"non-specific digestive disorder, rabbit",MONDO,disease,DISEASE_3544
3545,3545,3545,3545,3545,3545,3545,3545,MONDO:0007068,adenylosuccinate lyase deficiency,MONDO,disease,DISEASE_3545
3546,3546,3546,3546,3546,3546,3546,3546,MONDO:0032818,neurodevelopmental disorder with cerebellar hypoplasia and spasticity,MONDO,disease,DISEASE_3546
3547,3547,3547,3547,3547,3547,3547,3547,MONDO:0002197,minor vestibular glands adenoma,MONDO,disease,DISEASE_3547
3548,3548,3548,3548,3548,3548,3548,3548,MONDO:0008861,3-methylcrotonyl-CoA carboxylase 1 deficiency,MONDO,disease,DISEASE_3548
3549,3549,3549,3549,3549,3549,3549,3549,MONDO:0005749_MONDO:0004806,eosinophilic pneumonia,MONDO_grouped,disease,DISEASE_3549
3550,3550,3550,3550,3550,3550,3550,3550,MONDO:0019887,distal trisomy 16q,MONDO,disease,DISEASE_3550
3551,3551,3551,3551,3551,3551,3551,3551,MONDO:0013131_MONDO:0008265_MONDO:0008263_MONDO:0014860_MONDO:0033004_MONDO:0971178_MONDO:0031062_MONDO:0033281_MONDO:0020642_MONDO:1011057_MONDO:0011483_MONDO:1011049_MONDO:1011050_MONDO:1011051_MONDO:1011053_MONDO:1011055_MONDO:1011056_MONDO:1011060_MONDO:1011061,polycystic kidney disease,MONDO_grouped,disease,DISEASE_3551
3552,3552,3552,3552,3552,3552,3552,3552,MONDO:0004559,malignant glandular tumor of peripheral nerve sheath,MONDO,disease,DISEASE_3552
3553,3553,3553,3553,3553,3553,3553,3553,MONDO:0005271,allergic disease,MONDO,disease,DISEASE_3553
3554,3554,3554,3554,3554,3554,3554,3554,MONDO:0002847,skeletal muscle cancer,MONDO,disease,DISEASE_3554
3555,3555,3555,3555,3555,3555,3555,3555,MONDO:1011963,"proportionate dwarfism with inflammatory lesions, non-human animal",MONDO,disease,DISEASE_3555
3556,3556,3556,3556,3556,3556,3556,3556,MONDO:0014096,microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome,MONDO,disease,DISEASE_3556
3557,3557,3557,3557,3557,3557,3557,3557,MONDO:0043129,merlob grunebaum reisner syndrome,MONDO,disease,DISEASE_3557
3558,3558,3558,3558,3558,3558,3558,3558,MONDO:0014725,spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome,MONDO,disease,DISEASE_3558
3559,3559,3559,3559,3559,3559,3559,3559,MONDO:1012809,"hypertrophic cardiomyopathy, MYH7-related, domestic cat",MONDO,disease,DISEASE_3559
3560,3560,3560,3560,3560,3560,3560,3560,MONDO:0008777,gelatinous drop-like corneal dystrophy,MONDO,disease,DISEASE_3560
3561,3561,3561,3561,3561,3561,3561,3561,MONDO:1010831,"tetradysmelia, cattle",MONDO,disease,DISEASE_3561
3562,3562,3562,3562,3562,3562,3562,3562,MONDO:0012740,"chromosome 22q11.2 deletion syndrome, distal",MONDO,disease,DISEASE_3562
3563,3563,3563,3563,3563,3563,3563,3563,MONDO:1012131,"immunoglobulin G deficiency, chicken",MONDO,disease,DISEASE_3563
3564,3564,3564,3564,3564,3564,3564,3564,MONDO:0005988,toxocariasis,MONDO,disease,DISEASE_3564
3565,3565,3565,3565,3565,3565,3565,3565,MONDO:0700176_MONDO:0700185,feline lymphoma,MONDO_grouped,disease,DISEASE_3565
3566,3566,3566,3566,3566,3566,3566,3566,MONDO:0009965,Perlman syndrome,MONDO,disease,DISEASE_3566
3567,3567,3567,3567,3567,3567,3567,3567,MONDO:0003341,subungual glomus tumor,MONDO,disease,DISEASE_3567
3568,3568,3568,3568,3568,3568,3568,3568,MONDO:0019735,polymyalgia rheumatica,MONDO,disease,DISEASE_3568
3569,3569,3569,3569,3569,3569,3569,3569,MONDO:0800175,cardiogenic shock,MONDO,disease,DISEASE_3569
3570,3570,3570,3570,3570,3570,3570,3570,MONDO:0021657,ovarian sex cord-stromal tumor,MONDO,disease,DISEASE_3570
3571,3571,3571,3571,3571,3571,3571,3571,MONDO:0019384,encephalitis lethargica,MONDO,disease,DISEASE_3571
3572,3572,3572,3572,3572,3572,3572,3572,MONDO:0044316,"thrombocytopenia, anemia, and myelofibrosis",MONDO,disease,DISEASE_3572
3573,3573,3573,3573,3573,3573,3573,3573,MONDO:0043110,jones hersh yusk syndrome,MONDO,disease,DISEASE_3573
3574,3574,3574,3574,3574,3574,3574,3574,MONDO:0001024,pneumonic plague,MONDO,disease,DISEASE_3574
3575,3575,3575,3575,3575,3575,3575,3575,MONDO:0007819,solitary median maxillary central incisor syndrome,MONDO,disease,DISEASE_3575
3576,3576,3576,3576,3576,3576,3576,3576,MONDO:0011479,postural orthostatic tachycardia syndrome,MONDO,disease,DISEASE_3576
3577,3577,3577,3577,3577,3577,3577,3577,MONDO:0005365_MONDO:0020677,hearing loss disorder,MONDO_grouped,disease,DISEASE_3577
3578,3578,3578,3578,3578,3578,3578,3578,MONDO:0004469,pseudovascular skin squamous cell carcinoma,MONDO,disease,DISEASE_3578
3579,3579,3579,3579,3579,3579,3579,3579,MONDO:0014527,progeroid features-hepatocellular carcinoma predisposition syndrome,MONDO,disease,DISEASE_3579
3580,3580,3580,3580,3580,3580,3580,3580,MONDO:0029144,extraoral halitosis due to methanethiol oxidase deficiency,MONDO,disease,DISEASE_3580
3581,3581,3581,3581,3581,3581,3581,3581,MONDO:0004960,monoclonal gammopathy,MONDO,disease,DISEASE_3581
3582,3582,3582,3582,3582,3582,3582,3582,MONDO:0019867,mosaic trisomy 8,MONDO,disease,DISEASE_3582
3583,3583,3583,3583,3583,3583,3583,3583,MONDO:0008992,Juberg-Hayward syndrome,MONDO,disease,DISEASE_3583
3584,3584,3584,3584,3584,3584,3584,3584,MONDO:0020804,basal cell carcinoma,MONDO,disease,DISEASE_3584
3585,3585,3585,3585,3585,3585,3585,3585,MONDO:0013670,"myopia, high, with cataract and vitreoretinal degeneration",MONDO,disease,DISEASE_3585
3586,3586,3586,3586,3586,3586,3586,3586,MONDO:0001523,luxation of globe,MONDO,disease,DISEASE_3586
3587,3587,3587,3587,3587,3587,3587,3587,MONDO:0009361,autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius,MONDO,disease,DISEASE_3587
3588,3588,3588,3588,3588,3588,3588,3588,MONDO:0022897,craniosynostosis exostoses nevus epibulbar dermoid,MONDO,disease,DISEASE_3588
3589,3589,3589,3589,3589,3589,3589,3589,MONDO:0008012,Monophalangy of great toe,MONDO,disease,DISEASE_3589
3590,3590,3590,3590,3590,3590,3590,3590,MONDO:0004970,adenocarcinoma,MONDO,disease,DISEASE_3590
3591,3591,3591,3591,3591,3591,3591,3591,MONDO:0018193,testicular teratoma,MONDO,disease,DISEASE_3591
3592,3592,3592,3592,3592,3592,3592,3592,MONDO:0003367_MONDO:0003351,gastric leiomyosarcoma,MONDO_grouped,disease,DISEASE_3592
3593,3593,3593,3593,3593,3593,3593,3593,MONDO:1012055,"cyclic neutropenia, dog",MONDO,disease,DISEASE_3593
3594,3594,3594,3594,3594,3594,3594,3594,MONDO:1010237,"polymicrogyria, non-human animal",MONDO,disease,DISEASE_3594
3595,3595,3595,3595,3595,3595,3595,3595,MONDO:0011703,spongiform encephalopathy with neuropsychiatric features,MONDO,disease,DISEASE_3595
3596,3596,3596,3596,3596,3596,3596,3596,MONDO:0008814,hyperargininemia,MONDO,disease,DISEASE_3596
3597,3597,3597,3597,3597,3597,3597,3597,MONDO:1012544,"neuropathy and feather color dilution, Northern goshawk",MONDO,disease,DISEASE_3597
3598,3598,3598,3598,3598,3598,3598,3598,MONDO:0006178,dedifferentiated solitary fibrous tumor,MONDO,disease,DISEASE_3598
3599,3599,3599,3599,3599,3599,3599,3599,MONDO:0957428,B-lymphoblastic leukemia/lymphoma with t(17;19),MONDO,disease,DISEASE_3599
3600,3600,3600,3600,3600,3600,3600,3600,MONDO:0037003,malignant phyllodes tumor,MONDO,disease,DISEASE_3600
3601,3601,3601,3601,3601,3601,3601,3601,MONDO:0700139,canine neoplasm,MONDO,disease,DISEASE_3601
3602,3602,3602,3602,3602,3602,3602,3602,MONDO:0016505_MONDO:0006174,aldosterone-producing adrenal cortex adenoma,MONDO_grouped,disease,DISEASE_3602
3603,3603,3603,3603,3603,3603,3603,3603,MONDO:0009912,prolactin deficiency with obesity and enlarged testes,MONDO,disease,DISEASE_3603
3604,3604,3604,3604,3604,3604,3604,3604,MONDO:0958034_MONDO:0958022,"lipodystrophy, familial partial,",MONDO_grouped,disease,DISEASE_3604
3605,3605,3605,3605,3605,3605,3605,3605,MONDO:0005379_MONDO:0024614,neurotic disorder,MONDO_grouped,disease,DISEASE_3605
3606,3606,3606,3606,3606,3606,3606,3606,MONDO:0002744,fallopian tube mucinous adenocarcinoma,MONDO,disease,DISEASE_3606
3607,3607,3607,3607,3607,3607,3607,3607,MONDO:0016189,qualitative or quantitative defects of filamin C,MONDO,disease,DISEASE_3607
3608,3608,3608,3608,3608,3608,3608,3608,MONDO:1011700,"trapped neutrophil syndrome, non-human animal",MONDO,disease,DISEASE_3608
3609,3609,3609,3609,3609,3609,3609,3609,MONDO:0000492,chronic venous insufficiency,MONDO,disease,DISEASE_3609
3610,3610,3610,3610,3610,3610,3610,3610,MONDO:0800389,monochloroacetic acid poisoning,MONDO,disease,DISEASE_3610
3611,3611,3611,3611,3611,3611,3611,3611,MONDO:0004375,end stage renal failure,MONDO,disease,DISEASE_3611
3612,3612,3612,3612,3612,3612,3612,3612,MONDO:1040031,dyneinopathy,MONDO,disease,DISEASE_3612
3613,3613,3613,3613,3613,3613,3613,3613,MONDO:1012120,"hypothyroidism and dwarfism, Sumatran tiger",MONDO,disease,DISEASE_3613
3614,3614,3614,3614,3614,3614,3614,3614,MONDO:0008866,"bifid nose, autosomal recessive",MONDO,disease,DISEASE_3614
3615,3615,3615,3615,3615,3615,3615,3615,MONDO:0010640,"Leber optic atrophy, susceptibility to",MONDO,disease,DISEASE_3615
3616,3616,3616,3616,3616,3616,3616,3616,MONDO:1011403_MONDO:1011400_MONDO:1011675_MONDO:1011676,"hyperadrenocorticism, non-human animal",MONDO_grouped,disease,DISEASE_3616
3617,3617,3617,3617,3617,3617,3617,3617,MONDO:0008258,platelet signal processing defect,MONDO,disease,DISEASE_3617
3618,3618,3618,3618,3618,3618,3618,3618,MONDO:0013587,glycogen storage disease due to lactate dehydrogenase H-subunit deficiency,MONDO,disease,DISEASE_3618
3619,3619,3619,3619,3619,3619,3619,3619,MONDO:0000965,liver lipoma,MONDO,disease,DISEASE_3619
3620,3620,3620,3620,3620,3620,3620,3620,MONDO:0002708,retinitis,MONDO,disease,DISEASE_3620
3621,3621,3621,3621,3621,3621,3621,3621,MONDO:0012120,pyruvate dehydrogenase phosphatase deficiency,MONDO,disease,DISEASE_3621
3622,3622,3622,3622,3622,3622,3622,3622,MONDO:0007409,cryptomicrotia-brachydactyly-excess fingertip arch syndrome,MONDO,disease,DISEASE_3622
3623,3623,3623,3623,3623,3623,3623,3623,MONDO:0968989_MONDO:0970960_MONDO:0970961_MONDO:0970963,non-saccular limited dorsal myeloschisis,MONDO_grouped,disease,DISEASE_3623
3624,3624,3624,3624,3624,3624,3624,3624,MONDO:0023134,febrile ulceronecrotic Mucha-Habermann disease,MONDO,disease,DISEASE_3624
3625,3625,3625,3625,3625,3625,3625,3625,MONDO:0012325,Nguyen syndrome,MONDO,disease,DISEASE_3625
3626,3626,3626,3626,3626,3626,3626,3626,MONDO:0019627,isolated congenital alacrima,MONDO,disease,DISEASE_3626
3627,3627,3627,3627,3627,3627,3627,3627,MONDO:0001651,scrotum squamous cell carcinoma,MONDO,disease,DISEASE_3627
3628,3628,3628,3628,3628,3628,3628,3628,MONDO:0006637,acute kidney tubular necrosis,MONDO,disease,DISEASE_3628
3629,3629,3629,3629,3629,3629,3629,3629,MONDO:0006317,neurothekeoma,MONDO,disease,DISEASE_3629
3630,3630,3630,3630,3630,3630,3630,3630,MONDO:0004230,adenomatoid tumor,MONDO,disease,DISEASE_3630
3631,3631,3631,3631,3631,3631,3631,3631,MONDO:0006119,breast mucosa-associated lymphoid tissue lymphoma,MONDO,disease,DISEASE_3631
3632,3632,3632,3632,3632,3632,3632,3632,MONDO:0007556,"epidermolysis bullosa simplex 2F, with mottled pigmentation",MONDO,disease,DISEASE_3632
3633,3633,3633,3633,3633,3633,3633,3633,MONDO:0100222,A20 haploinsufficiency,MONDO,disease,DISEASE_3633
3634,3634,3634,3634,3634,3634,3634,3634,MONDO:0007921,yellow nail syndrome,MONDO,disease,DISEASE_3634
3635,3635,3635,3635,3635,3635,3635,3635,MONDO:0022496,arthrogryposis IUGR thoracic dystrophy,MONDO,disease,DISEASE_3635
3636,3636,3636,3636,3636,3636,3636,3636,MONDO:0009246,Friedreich ataxia and congenital glaucoma,MONDO,disease,DISEASE_3636
3637,3637,3637,3637,3637,3637,3637,3637,MONDO:0022975,diaphragmatic agenesis radial aplasia omphalocele,MONDO,disease,DISEASE_3637
3638,3638,3638,3638,3638,3638,3638,3638,MONDO:1011269,"early onset cataract HSF4-related, dog",MONDO,disease,DISEASE_3638
3639,3639,3639,3639,3639,3639,3639,3639,MONDO:0010993,Harrod syndrome,MONDO,disease,DISEASE_3639
3640,3640,3640,3640,3640,3640,3640,3640,MONDO:0040699,necrotizing scleritis,MONDO,disease,DISEASE_3640
3641,3641,3641,3641,3641,3641,3641,3641,MONDO:0035403,serous cystadenoma of childhood,MONDO,disease,DISEASE_3641
3642,3642,3642,3642,3642,3642,3642,3642,MONDO:0017762_MONDO:0017764,disorder of copper metabolism,MONDO_grouped,disease,DISEASE_3642
3643,3643,3643,3643,3643,3643,3643,3643,MONDO:0016700_MONDO:0003690,anaplastic ependymoma,MONDO_grouped,disease,DISEASE_3643
3644,3644,3644,3644,3644,3644,3644,3644,MONDO:0009564,Marden-Walker syndrome,MONDO,disease,DISEASE_3644
3645,3645,3645,3645,3645,3645,3645,3645,MONDO:0007449,dermo-odonto dysplasia,MONDO,disease,DISEASE_3645
3646,3646,3646,3646,3646,3646,3646,3646,MONDO:1012370,"degenerative neuromuscular disease, cattle",MONDO,disease,DISEASE_3646
3647,3647,3647,3647,3647,3647,3647,3647,MONDO:0008366,red cell permeability defect,MONDO,disease,DISEASE_3647
3648,3648,3648,3648,3648,3648,3648,3648,MONDO:0001471,histoplasmosis meningitis,MONDO,disease,DISEASE_3648
3649,3649,3649,3649,3649,3649,3649,3649,MONDO:0014799_MONDO:0030465_MONDO:0007283_MONDO:0007287_MONDO:0012665_MONDO:0007286_MONDO:0007282_MONDO:0032735_MONDO:0011015_MONDO:0013744_MONDO:0007279_MONDO:0014565_MONDO:0013859_MONDO:0014673_MONDO:0012395_MONDO:0012489_MONDO:0012260_MONDO:0010544_MONDO:0013484_MONDO:0005129_MONDO:0045050_MONDO:0011587_MONDO:0011808_MONDO:0012175,cataract,MONDO_grouped,disease,DISEASE_3649
3650,3650,3650,3650,3650,3650,3650,3650,MONDO:0044339_MONDO:0044753,lumbar disk degenerative disorder,MONDO_grouped,disease,DISEASE_3650
3651,3651,3651,3651,3651,3651,3651,3651,MONDO:0003718,occlusion precerebral artery,MONDO,disease,DISEASE_3651
3652,3652,3652,3652,3652,3652,3652,3652,MONDO:0024235,Brenner tumor,MONDO,disease,DISEASE_3652
3653,3653,3653,3653,3653,3653,3653,3653,MONDO:0019191,IgG4-related dacryoadenitis and sialadenitis,MONDO,disease,DISEASE_3653
3654,3654,3654,3654,3654,3654,3654,3654,MONDO:0006693,cerebral arterial disease,MONDO,disease,DISEASE_3654
3655,3655,3655,3655,3655,3655,3655,3655,MONDO:0013090,chromosome 19q13.11 deletion syndrome,MONDO,disease,DISEASE_3655
3656,3656,3656,3656,3656,3656,3656,3656,MONDO:0024462_MONDO:0007966,susceptibility to familial cutaneous melanoma,MONDO_grouped,disease,DISEASE_3656
3657,3657,3657,3657,3657,3657,3657,3657,MONDO:0008226_MONDO:0012051,"periodontitis, aggressive",MONDO_grouped,disease,DISEASE_3657
3658,3658,3658,3658,3658,3658,3658,3658,MONDO:0016374,cranial neuralgia,MONDO,disease,DISEASE_3658
3659,3659,3659,3659,3659,3659,3659,3659,MONDO:0007329,"cirrhosis, familial",MONDO,disease,DISEASE_3659
3660,3660,3660,3660,3660,3660,3660,3660,MONDO:0013334,cocoon syndrome,MONDO,disease,DISEASE_3660
3661,3661,3661,3661,3661,3661,3661,3661,MONDO:0100137,telomere syndrome,MONDO,disease,DISEASE_3661
3662,3662,3662,3662,3662,3662,3662,3662,MONDO:1011709,"ear necrosis syndrome, non-human animal",MONDO,disease,DISEASE_3662
3663,3663,3663,3663,3663,3663,3663,3663,MONDO:0700106,"immune system disorder, non-human animal",MONDO,disease,DISEASE_3663
3664,3664,3664,3664,3664,3664,3664,3664,MONDO:0006028,cecum adenocarcinoma,MONDO,disease,DISEASE_3664
3665,3665,3665,3665,3665,3665,3665,3665,MONDO:0002255,hypertrophic elongation of cervix,MONDO,disease,DISEASE_3665
3666,3666,3666,3666,3666,3666,3666,3666,MONDO:0005440,embryonal carcinoma,MONDO,disease,DISEASE_3666
3667,3667,3667,3667,3667,3667,3667,3667,MONDO:0003363,malignant dermis tumor,MONDO,disease,DISEASE_3667
3668,3668,3668,3668,3668,3668,3668,3668,MONDO:0011171,odonto-tricho-ungual-digito-palmar syndrome,MONDO,disease,DISEASE_3668
3669,3669,3669,3669,3669,3669,3669,3669,MONDO:0017630,X-linked complicated spastic paraplegia type 1,MONDO,disease,DISEASE_3669
3670,3670,3670,3670,3670,3670,3670,3670,MONDO:0005086_MONDO:0002395_MONDO:0005206_MONDO:0006053,renal cell carcinoma,MONDO_grouped,disease,DISEASE_3670
3671,3671,3671,3671,3671,3671,3671,3671,MONDO:0958162,B acute lymphoblastic leukemia with DUX4 rearrangement,MONDO,disease,DISEASE_3671
3672,3672,3672,3672,3672,3672,3672,3672,MONDO:1012908,"cryopyrin-associated periodic syndrome, NLRP3-related, pig",MONDO,disease,DISEASE_3672
3673,3673,3673,3673,3673,3673,3673,3673,MONDO:0003059_MONDO:0002887_MONDO:0002886,bile duct cancer,MONDO_grouped,disease,DISEASE_3673
3674,3674,3674,3674,3674,3674,3674,3674,MONDO:0004547,reticular pattern testicular yolk sac tumor,MONDO,disease,DISEASE_3674
3675,3675,3675,3675,3675,3675,3675,3675,MONDO:0016311,Bockenheimer syndrome,MONDO,disease,DISEASE_3675
3676,3676,3676,3676,3676,3676,3676,3676,MONDO:1012309,"degenerative myeloencephalopathy, horse",MONDO,disease,DISEASE_3676
3677,3677,3677,3677,3677,3677,3677,3677,MONDO:0850097,autoimmune limbic encephalitis,MONDO,disease,DISEASE_3677
3678,3678,3678,3678,3678,3678,3678,3678,MONDO:0007191,Behcet disease,MONDO,disease,DISEASE_3678
3679,3679,3679,3679,3679,3679,3679,3679,MONDO:0015905,syndromic dyslipidemia,MONDO,disease,DISEASE_3679
3680,3680,3680,3680,3680,3680,3680,3680,MONDO:0000590_MONDO:0000586_MONDO:0000603_MONDO:0000569,autoimmune disorder of peripheral nervous system,MONDO_grouped,disease,DISEASE_3680
3681,3681,3681,3681,3681,3681,3681,3681,MONDO:0013595,hyperbiliverdinemia,MONDO,disease,DISEASE_3681
3682,3682,3682,3682,3682,3682,3682,3682,MONDO:0006619_MONDO:0006528,viral exanthem,MONDO_grouped,disease,DISEASE_3682
3683,3683,3683,3683,3683,3683,3683,3683,MONDO:0100258,phytanoyl-CoA hydroxylase deficiency,MONDO,disease,DISEASE_3683
3684,3684,3684,3684,3684,3684,3684,3684,MONDO:0033544,Tolchin-Le Caignec syndrome,MONDO,disease,DISEASE_3684
3685,3685,3685,3685,3685,3685,3685,3685,MONDO:0017759,disorder of catecholamine synthesis,MONDO,disease,DISEASE_3685
3686,3686,3686,3686,3686,3686,3686,3686,MONDO:1010443,"cardiomyopathy, cattle",MONDO,disease,DISEASE_3686
3687,3687,3687,3687,3687,3687,3687,3687,MONDO:0023659_MONDO:0014942_MONDO:0014328_MONDO:0100079_MONDO:0032678_MONDO:0014593_MONDO:0014150_MONDO:0033361_MONDO:0033363_MONDO:0030727_MONDO:0014505_MONDO:0957780_MONDO:0013389_MONDO:0032858_MONDO:0859314_MONDO:0031021_MONDO:0012812_MONDO:0014868_MONDO:0032663_MONDO:0020631_MONDO:0054845_MONDO:0025353_MONDO:0013387_MONDO:0013388_MONDO:0033372_MONDO:0032813_MONDO:0014607_MONDO:0010632_MONDO:0033371_MONDO:0033368_MONDO:0013801_MONDO:0014533_MONDO:0958331_MONDO:0032710_MONDO:0014933_MONDO:0032598_MONDO:0030957_MONDO:0020632_MONDO:0014859_MONDO:0033373_MONDO:0030856_MONDO:0032808_MONDO:0031052_MONDO:0014392_MONDO:0958330_MONDO:0014371_MONDO:0014377_MONDO:0015002_MONDO:0033369_MONDO:0859327_MONDO:0033374_MONDO:0014916_MONDO:0014895_MONDO:0014625_MONDO:0010246_MONDO:0957248_MONDO:0029138_MONDO:0859325_MONDO:0014598_MONDO:0030268_MONDO:0032918_MONDO:0012245_MONDO:0014917_MONDO:0030881_MONDO:0031055_MONDO:0010396_MONDO:0970945_MONDO:0033370_MONDO:0032725_MONDO:0014199_MONDO:0014921_MONDO:0968946_MONDO:0032895_MONDO:0015025_MONDO:0033365_MONDO:0020630_MONDO:0014595_MONDO:0014201_MONDO:0014133_MONDO:0034106_MONDO:0032752_MONDO:0032822_MONDO:0032812_MONDO:0010472_MONDO:0015000_MONDO:0013989_MONDO:0030072_MONDO:0030059_MONDO:0957812_MONDO:0030472_MONDO:0014949_MONDO:0014647_MONDO:0010375_MONDO:0030473_MONDO:0033367_MONDO:0013056_MONDO:0030054_MONDO:0033362_MONDO:0030695_MONDO:0030453_MONDO:0014719_MONDO:0032768_MONDO:0032657_MONDO:0013277_MONDO:0014003_MONDO:0033366_MONDO:0014360_MONDO:0014718_MONDO:0033364_MONDO:0014947_MONDO:0014477_MONDO:0032880_MONDO:0100062,developmental and epileptic encephalopathy,MONDO_grouped,disease,DISEASE_3687
3688,3688,3688,3688,3688,3688,3688,3688,MONDO:0009766,oculocerebral hypopigmentation syndrome of Preus,MONDO,disease,DISEASE_3688
3689,3689,3689,3689,3689,3689,3689,3689,MONDO:0060592,Sweeney-Cox syndrome,MONDO,disease,DISEASE_3689
3690,3690,3690,3690,3690,3690,3690,3690,MONDO:0007078_MONDO:0012911_MONDO:0012912_MONDO:0008749_MONDO:0011301_MONDO:0019992,pseudohypoparathyroidism,MONDO_grouped,disease,DISEASE_3690
3691,3691,3691,3691,3691,3691,3691,3691,MONDO:0010535,Bazex-Dupre-Christol syndrome,MONDO,disease,DISEASE_3691
3692,3692,3692,3692,3692,3692,3692,3692,MONDO:0001777_MONDO:0001838,acute gonococcal cystitis,MONDO_grouped,disease,DISEASE_3692
3693,3693,3693,3693,3693,3693,3693,3693,MONDO:0005943,Rhabditida infectious disease,MONDO,disease,DISEASE_3693
3694,3694,3694,3694,3694,3694,3694,3694,MONDO:0018163_MONDO:0013051_MONDO:0030337_MONDO:0009052_MONDO:0958335_MONDO:0013754_MONDO:0027462_MONDO:0027451_MONDO:0019572_MONDO:0019573,autosomal recessive cutis laxa,MONDO_grouped,disease,DISEASE_3694
3695,3695,3695,3695,3695,3695,3695,3695,MONDO:0017550,"humero-radial synostosis, unilateral",MONDO,disease,DISEASE_3695
3696,3696,3696,3696,3696,3696,3696,3696,MONDO:0030878,Kaya-Barakat-Masson syndrome,MONDO,disease,DISEASE_3696
3697,3697,3697,3697,3697,3697,3697,3697,MONDO:0015195,atresia of urethra,MONDO,disease,DISEASE_3697
3698,3698,3698,3698,3698,3698,3698,3698,MONDO:0017245,intralobar congenital pulmonary sequestration,MONDO,disease,DISEASE_3698
3699,3699,3699,3699,3699,3699,3699,3699,MONDO:0019115,obesity due to melanocortin 4 receptor deficiency,MONDO,disease,DISEASE_3699
3700,3700,3700,3700,3700,3700,3700,3700,MONDO:0008111,oculodentodigital dysplasia,MONDO,disease,DISEASE_3700
3701,3701,3701,3701,3701,3701,3701,3701,MONDO:0005962,skeletal tuberculosis,MONDO,disease,DISEASE_3701
3702,3702,3702,3702,3702,3702,3702,3702,MONDO:0019406,craniofacial conodysplasia,MONDO,disease,DISEASE_3702
3703,3703,3703,3703,3703,3703,3703,3703,MONDO:0007055_MONDO:0019695,Acromicric dysplasia,MONDO_grouped,disease,DISEASE_3703
3704,3704,3704,3704,3704,3704,3704,3704,MONDO:0002270_MONDO:0001507_MONDO:0002842_MONDO:0004640,viral gastritis,MONDO_grouped,disease,DISEASE_3704
3705,3705,3705,3705,3705,3705,3705,3705,MONDO:0003766_MONDO:0003081,thalamic cancer,MONDO_grouped,disease,DISEASE_3705
3706,3706,3706,3706,3706,3706,3706,3706,MONDO:1011863_MONDO:1012292,"subacute necrotising encephalopathy of Leigh, non-human animal",MONDO_grouped,disease,DISEASE_3706
3707,3707,3707,3707,3707,3707,3707,3707,MONDO:0002329,testicular disorder,MONDO,disease,DISEASE_3707
3708,3708,3708,3708,3708,3708,3708,3708,MONDO:0005716,contagious pleuropneumonia,MONDO,disease,DISEASE_3708
3709,3709,3709,3709,3709,3709,3709,3709,MONDO:0004815,osteosclerotic plasma cell myeloma,MONDO,disease,DISEASE_3709
3710,3710,3710,3710,3710,3710,3710,3710,MONDO:0700190,chicken bursal lymphoma,MONDO,disease,DISEASE_3710
3711,3711,3711,3711,3711,3711,3711,3711,MONDO:1012229,"progressive spinal myelopathy, cattle",MONDO,disease,DISEASE_3711
3712,3712,3712,3712,3712,3712,3712,3712,MONDO:0017816_MONDO:0017817_MONDO:0800127,primary systemic amyloidosis,MONDO_grouped,disease,DISEASE_3712
3713,3713,3713,3713,3713,3713,3713,3713,MONDO:1012180,"myoclonus epilepsy of Lafora, Eurasian elk",MONDO,disease,DISEASE_3713
3714,3714,3714,3714,3714,3714,3714,3714,MONDO:1010548_MONDO:1010549,"diprosopus, cattle",MONDO_grouped,disease,DISEASE_3714
3715,3715,3715,3715,3715,3715,3715,3715,MONDO:1040043_MONDO:1040049_MONDO:1040048_MONDO:1040044_MONDO:1040047_MONDO:1040042_MONDO:0700236_MONDO:0700237_MONDO:1040045,BBS1-related ciliopathy,MONDO_grouped,disease,DISEASE_3715
3716,3716,3716,3716,3716,3716,3716,3716,MONDO:0001983_MONDO:0002449,peripheral degeneration of cornea,MONDO_grouped,disease,DISEASE_3716
3717,3717,3717,3717,3717,3717,3717,3717,MONDO:0000638,benign glioma,MONDO,disease,DISEASE_3717
3718,3718,3718,3718,3718,3718,3718,3718,MONDO:0008205_MONDO:0017472_MONDO:0017473,patella aplasia/hypoplasia,MONDO_grouped,disease,DISEASE_3718
3719,3719,3719,3719,3719,3719,3719,3719,MONDO:1011587,"porphyria, domestic cat",MONDO,disease,DISEASE_3719
3720,3720,3720,3720,3720,3720,3720,3720,MONDO:0010462,syndromic X-linked intellectual disability Chudley-Schwartz type,MONDO,disease,DISEASE_3720
3721,3721,3721,3721,3721,3721,3721,3721,MONDO:0008917,heart defects-limb shortening syndrome,MONDO,disease,DISEASE_3721
3722,3722,3722,3722,3722,3722,3722,3722,MONDO:1012415,"sebaceous adenitis, dog",MONDO,disease,DISEASE_3722
3723,3723,3723,3723,3723,3723,3723,3723,MONDO:0012535,"holoprosencephaly, recurrent infections, and monocytosis",MONDO,disease,DISEASE_3723
3724,3724,3724,3724,3724,3724,3724,3724,MONDO:0007962,megalodactyly,MONDO,disease,DISEASE_3724
3725,3725,3725,3725,3725,3725,3725,3725,MONDO:0009403,hypertelorism and tetralogy of fallot,MONDO,disease,DISEASE_3725
3726,3726,3726,3726,3726,3726,3726,3726,MONDO:0015703,T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta,MONDO,disease,DISEASE_3726
3727,3727,3727,3727,3727,3727,3727,3727,MONDO:0009113,hemolytic anemia due to diphosphoglycerate mutase deficiency,MONDO,disease,DISEASE_3727
3728,3728,3728,3728,3728,3728,3728,3728,MONDO:0012190,"epidermolysis bullosa simplex 7, with nephropathy and deafness",MONDO,disease,DISEASE_3728
3729,3729,3729,3729,3729,3729,3729,3729,MONDO:0003387,urethra clear cell adenocarcinoma,MONDO,disease,DISEASE_3729
3730,3730,3730,3730,3730,3730,3730,3730,MONDO:0014878_MONDO:0011089_MONDO:0024266_MONDO:0011827_MONDO:1010464_MONDO:1010465_MONDO:1010467_MONDO:1010468_MONDO:1010469,patent ductus arteriosus,MONDO_grouped,disease,DISEASE_3730
3731,3731,3731,3731,3731,3731,3731,3731,MONDO:0018865_MONDO:0044663,striate palmoplantar keratoderma,MONDO_grouped,disease,DISEASE_3731
3732,3732,3732,3732,3732,3732,3732,3732,MONDO:0020554,Heiner syndrome,MONDO,disease,DISEASE_3732
3733,3733,3733,3733,3733,3733,3733,3733,MONDO:0011836,thyroid Hurthle cell carcinoma,MONDO,disease,DISEASE_3733
3734,3734,3734,3734,3734,3734,3734,3734,MONDO:0017375,congenital enterovirus infection,MONDO,disease,DISEASE_3734
3735,3735,3735,3735,3735,3735,3735,3735,MONDO:0001411,synostosis,MONDO,disease,DISEASE_3735
3736,3736,3736,3736,3736,3736,3736,3736,MONDO:0042485,infective arthritis,MONDO,disease,DISEASE_3736
3737,3737,3737,3737,3737,3737,3737,3737,MONDO:0012517,Gaucher disease due to saposin C deficiency,MONDO,disease,DISEASE_3737
3738,3738,3738,3738,3738,3738,3738,3738,MONDO:0005904,pericarditis,MONDO,disease,DISEASE_3738
3739,3739,3739,3739,3739,3739,3739,3739,MONDO:0006044,nephrosclerosis,MONDO,disease,DISEASE_3739
3740,3740,3740,3740,3740,3740,3740,3740,MONDO:0958091,cleft palate-congenital heart defect-intellectual disability syndrome,MONDO,disease,DISEASE_3740
3741,3741,3741,3741,3741,3741,3741,3741,MONDO:0009826,PA polymorphism of alpha-2-globulin,MONDO,disease,DISEASE_3741
3742,3742,3742,3742,3742,3742,3742,3742,MONDO:0100544,age-related clonal hematopoiesis,MONDO,disease,DISEASE_3742
3743,3743,3743,3743,3743,3743,3743,3743,MONDO:1010282,"azoospermia, non-human animal",MONDO,disease,DISEASE_3743
3744,3744,3744,3744,3744,3744,3744,3744,MONDO:0020739_MONDO:0014851_MONDO:0000212,"hypercalcemia, infantile",MONDO_grouped,disease,DISEASE_3744
3745,3745,3745,3745,3745,3745,3745,3745,MONDO:0006003,uterine corpus cancer,MONDO,disease,DISEASE_3745
3746,3746,3746,3746,3746,3746,3746,3746,MONDO:0017953,hereditary periodic fever syndrome,MONDO,disease,DISEASE_3746
3747,3747,3747,3747,3747,3747,3747,3747,MONDO:1011042_MONDO:1012592_MONDO:1012595_MONDO:1012597_MONDO:1012598_MONDO:1012794,"oculocutaneous albinism, OCA2-related, dog",MONDO_grouped,disease,DISEASE_3747
3748,3748,3748,3748,3748,3748,3748,3748,MONDO:0022608,brittle bone syndrome lethal type,MONDO,disease,DISEASE_3748
3749,3749,3749,3749,3749,3749,3749,3749,MONDO:0015681,childhood disintegrative disorder,MONDO,disease,DISEASE_3749
3750,3750,3750,3750,3750,3750,3750,3750,MONDO:0002433,malignant cranial nerve neoplasm,MONDO,disease,DISEASE_3750
3751,3751,3751,3751,3751,3751,3751,3751,MONDO:0100416,"acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation",MONDO,disease,DISEASE_3751
3752,3752,3752,3752,3752,3752,3752,3752,MONDO:0005126,tuberculoid leprosy,MONDO,disease,DISEASE_3752
3753,3753,3753,3753,3753,3753,3753,3753,MONDO:0015228,pentasomy X,MONDO,disease,DISEASE_3753
3754,3754,3754,3754,3754,3754,3754,3754,MONDO:0003476,clear cell ependymoma,MONDO,disease,DISEASE_3754
3755,3755,3755,3755,3755,3755,3755,3755,MONDO:1012469_MONDO:1012470_MONDO:1012471,"pentalogy of Fallot, dog",MONDO_grouped,disease,DISEASE_3755
3756,3756,3756,3756,3756,3756,3756,3756,MONDO:0015199,aniridia - intellectual disability syndrome,MONDO,disease,DISEASE_3756
3757,3757,3757,3757,3757,3757,3757,3757,MONDO:1010043,"cystic fibrosis, non-human animal",MONDO,disease,DISEASE_3757
3758,3758,3758,3758,3758,3758,3758,3758,MONDO:0000167,Huntington disease and related disorders,MONDO,disease,DISEASE_3758
3759,3759,3759,3759,3759,3759,3759,3759,MONDO:1010632,"factor VII deficiency, dog",MONDO,disease,DISEASE_3759
3760,3760,3760,3760,3760,3760,3760,3760,MONDO:0060677,chromosome 1p35 deletion syndrome,MONDO,disease,DISEASE_3760
3761,3761,3761,3761,3761,3761,3761,3761,MONDO:0008203,Passovoy factor defect,MONDO,disease,DISEASE_3761
3762,3762,3762,3762,3762,3762,3762,3762,MONDO:1011152,"anodontia, domestic cat",MONDO,disease,DISEASE_3762
3763,3763,3763,3763,3763,3763,3763,3763,MONDO:0006394_MONDO:0006396,rectal tubular adenoma,MONDO_grouped,disease,DISEASE_3763
3764,3764,3764,3764,3764,3764,3764,3764,MONDO:0001660,proliferative diabetic retinopathy,MONDO,disease,DISEASE_3764
3765,3765,3765,3765,3765,3765,3765,3765,MONDO:0014209,early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome,MONDO,disease,DISEASE_3765
3766,3766,3766,3766,3766,3766,3766,3766,MONDO:0009717,Schwartz-Jampel syndrome,MONDO,disease,DISEASE_3766
3767,3767,3767,3767,3767,3767,3767,3767,MONDO:0007209,Weismann-Netter syndrome,MONDO,disease,DISEASE_3767
3768,3768,3768,3768,3768,3768,3768,3768,MONDO:0019220_MONDO:0019250,inborn disorder of cobalamin metabolism and transport,MONDO_grouped,disease,DISEASE_3768
3769,3769,3769,3769,3769,3769,3769,3769,MONDO:0020297,Noonan syndrome and Noonan-related syndrome,MONDO,disease,DISEASE_3769
3770,3770,3770,3770,3770,3770,3770,3770,MONDO:0022817,congenital amputation,MONDO,disease,DISEASE_3770
3771,3771,3771,3771,3771,3771,3771,3771,MONDO:0019020,PANDAS,MONDO,disease,DISEASE_3771
3772,3772,3772,3772,3772,3772,3772,3772,MONDO:0000620,breast benign neoplasm,MONDO,disease,DISEASE_3772
3773,3773,3773,3773,3773,3773,3773,3773,MONDO:0019530_MONDO:0000722_MONDO:0011348_MONDO:0017424,non-syndromic syndactyly,MONDO_grouped,disease,DISEASE_3773
3774,3774,3774,3774,3774,3774,3774,3774,MONDO:1010856,"Krabbe disease, domestic cat",MONDO,disease,DISEASE_3774
3775,3775,3775,3775,3775,3775,3775,3775,MONDO:0008092,hereditary neutrophilia,MONDO,disease,DISEASE_3775
3776,3776,3776,3776,3776,3776,3776,3776,MONDO:0060491,neurodevelopmental disorder with involuntary movements,MONDO,disease,DISEASE_3776
3777,3777,3777,3777,3777,3777,3777,3777,MONDO:0014148,estrogen resistance syndrome,MONDO,disease,DISEASE_3777
3778,3778,3778,3778,3778,3778,3778,3778,MONDO:0007274,carpal displacement,MONDO,disease,DISEASE_3778
3779,3779,3779,3779,3779,3779,3779,3779,MONDO:0014831,progeroid and marfanoid aspect-lipodystrophy syndrome,MONDO,disease,DISEASE_3779
3780,3780,3780,3780,3780,3780,3780,3780,MONDO:0009380,Dubin-Johnson syndrome,MONDO,disease,DISEASE_3780
3781,3781,3781,3781,3781,3781,3781,3781,MONDO:0005475_MONDO:0100431,migraine with aura,MONDO_grouped,disease,DISEASE_3781
3782,3782,3782,3782,3782,3782,3782,3782,MONDO:0021041,pleural solitary fibrous tumor,MONDO,disease,DISEASE_3782
3783,3783,3783,3783,3783,3783,3783,3783,MONDO:0019219,inborn disorder of neurotransmitter metabolism and transport,MONDO,disease,DISEASE_3783
3784,3784,3784,3784,3784,3784,3784,3784,MONDO:0859005,preaxial digit brachydactyly-webbed fingers,MONDO,disease,DISEASE_3784
3785,3785,3785,3785,3785,3785,3785,3785,MONDO:0021370,neoplasm of minor salivary gland,MONDO,disease,DISEASE_3785
3786,3786,3786,3786,3786,3786,3786,3786,MONDO:0010123,obsolete absent thumb-short stature-immunodeficiency syndrome,MONDO,disease,DISEASE_3786
3787,3787,3787,3787,3787,3787,3787,3787,MONDO:0023188,Freiberg disease,MONDO,disease,DISEASE_3787
3788,3788,3788,3788,3788,3788,3788,3788,MONDO:0018963,hereditary methemoglobinemia,MONDO,disease,DISEASE_3788
3789,3789,3789,3789,3789,3789,3789,3789,MONDO:0024305,acquired hyperprolactinemia,MONDO,disease,DISEASE_3789
3790,3790,3790,3790,3790,3790,3790,3790,MONDO:1012608,"fasting unconjugated hyperbilirubinemia, Bolivian squirrel monkey",MONDO,disease,DISEASE_3790
3791,3791,3791,3791,3791,3791,3791,3791,MONDO:1012678,"Waardenburg syndrome, MITF-related, pig",MONDO,disease,DISEASE_3791
3792,3792,3792,3792,3792,3792,3792,3792,MONDO:0014720_MONDO:0020250_MONDO:0016646,autosomal dominant optic atrophy plus syndrome,MONDO_grouped,disease,DISEASE_3792
3793,3793,3793,3793,3793,3793,3793,3793,MONDO:0850107,postinfectious cerebellitis,MONDO,disease,DISEASE_3793
3794,3794,3794,3794,3794,3794,3794,3794,MONDO:1011410,"vitamin-K-dependent blood coagulation factors deficiency, non-human animal",MONDO,disease,DISEASE_3794
3795,3795,3795,3795,3795,3795,3795,3795,MONDO:0019956,encephalitis,MONDO,disease,DISEASE_3795
3796,3796,3796,3796,3796,3796,3796,3796,MONDO:0700207,constitutional delay of growth and puberty,MONDO,disease,DISEASE_3796
3797,3797,3797,3797,3797,3797,3797,3797,MONDO:0021290,carcinoma in situ of appendix,MONDO,disease,DISEASE_3797
3798,3798,3798,3798,3798,3798,3798,3798,MONDO:0002955,vulva basal cell carcinoma,MONDO,disease,DISEASE_3798
3799,3799,3799,3799,3799,3799,3799,3799,MONDO:0001054_MONDO:0001722,double pterygium,MONDO_grouped,disease,DISEASE_3799
3800,3800,3800,3800,3800,3800,3800,3800,MONDO:0006478,undifferentiated pancreatic carcinoma,MONDO,disease,DISEASE_3800
3801,3801,3801,3801,3801,3801,3801,3801,MONDO:0021460,benign neoplasm of salivary gland,MONDO,disease,DISEASE_3801
3802,3802,3802,3802,3802,3802,3802,3802,MONDO:1011352,"radiation-induced disorder, non-human animal",MONDO,disease,DISEASE_3802
3803,3803,3803,3803,3803,3803,3803,3803,MONDO:0006683_MONDO:0006682_MONDO:0004569,brachial plexus neuropathy,MONDO_grouped,disease,DISEASE_3803
3804,3804,3804,3804,3804,3804,3804,3804,MONDO:0020674,vascular insufficiency disorder,MONDO,disease,DISEASE_3804
3805,3805,3805,3805,3805,3805,3805,3805,MONDO:1011956,"growth-hormone-receptor deficiency dwarfism, non-human animal",MONDO,disease,DISEASE_3805
3806,3806,3806,3806,3806,3806,3806,3806,MONDO:0007747,isolated hyperchlorhidrosis,MONDO,disease,DISEASE_3806
3807,3807,3807,3807,3807,3807,3807,3807,MONDO:0006167,combined lung carcinoma,MONDO,disease,DISEASE_3807
3808,3808,3808,3808,3808,3808,3808,3808,MONDO:0021088_MONDO:0004373,papillary meningioma,MONDO_grouped,disease,DISEASE_3808
3809,3809,3809,3809,3809,3809,3809,3809,MONDO:0013318,early repolarization associated with ventricular fibrillation,MONDO,disease,DISEASE_3809
3810,3810,3810,3810,3810,3810,3810,3810,MONDO:0016139,qualitative or quantitative protein defects in neuromuscular diseases,MONDO,disease,DISEASE_3810
3811,3811,3811,3811,3811,3811,3811,3811,MONDO:0001649,fungal esophagitis,MONDO,disease,DISEASE_3811
3812,3812,3812,3812,3812,3812,3812,3812,MONDO:1011920,"yellow-semen syndrome, non-human animal",MONDO,disease,DISEASE_3812
3813,3813,3813,3813,3813,3813,3813,3813,MONDO:0001233_MONDO:0006881,orbital tenonitis,MONDO_grouped,disease,DISEASE_3813
3814,3814,3814,3814,3814,3814,3814,3814,MONDO:0043287,superior vena cava syndrome,MONDO,disease,DISEASE_3814
3815,3815,3815,3815,3815,3815,3815,3815,MONDO:0800404,PCARE-related retinopathy,MONDO,disease,DISEASE_3815
3816,3816,3816,3816,3816,3816,3816,3816,MONDO:1010285,"atrophic rhinitis, non-human animal",MONDO,disease,DISEASE_3816
3817,3817,3817,3817,3817,3817,3817,3817,MONDO:0007558,self-limited childhood occipital epilepsy,MONDO,disease,DISEASE_3817
3818,3818,3818,3818,3818,3818,3818,3818,MONDO:0004792,cancer of isthmus of fallopian tube,MONDO,disease,DISEASE_3818
3819,3819,3819,3819,3819,3819,3819,3819,MONDO:1010233_MONDO:1011843,"hydrocephalus, non-human animal",MONDO_grouped,disease,DISEASE_3819
3820,3820,3820,3820,3820,3820,3820,3820,MONDO:0957386,"neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities",MONDO,disease,DISEASE_3820
3821,3821,3821,3821,3821,3821,3821,3821,MONDO:0005110,idiopathic cardiomyopathy,MONDO,disease,DISEASE_3821
3822,3822,3822,3822,3822,3822,3822,3822,MONDO:0007925,myelodysplastic syndrome associated with isolated del(5q),MONDO,disease,DISEASE_3822
3823,3823,3823,3823,3823,3823,3823,3823,MONDO:0004593,Bartholin duct cyst,MONDO,disease,DISEASE_3823
3824,3824,3824,3824,3824,3824,3824,3824,MONDO:0006145_MONDO:0004997_MONDO:0000977_MONDO:0006146,chondroid chordoma,MONDO_grouped,disease,DISEASE_3824
3825,3825,3825,3825,3825,3825,3825,3825,MONDO:0001038,perforated corneal ulcer,MONDO,disease,DISEASE_3825
3826,3826,3826,3826,3826,3826,3826,3826,MONDO:0004294,gestational ovarian choriocarcinoma,MONDO,disease,DISEASE_3826
3827,3827,3827,3827,3827,3827,3827,3827,MONDO:0015863,polyembryoma,MONDO,disease,DISEASE_3827
3828,3828,3828,3828,3828,3828,3828,3828,MONDO:0971064,orofacial clefting-cardiac anomalies-facial dysmorphism syndrome,MONDO,disease,DISEASE_3828
3829,3829,3829,3829,3829,3829,3829,3829,MONDO:0957430,childhood-onset schizophrenia,MONDO,disease,DISEASE_3829
3830,3830,3830,3830,3830,3830,3830,3830,MONDO:0017712,combined pancreatic lipase-colipase deficiency,MONDO,disease,DISEASE_3830
3831,3831,3831,3831,3831,3831,3831,3831,MONDO:0005752,epidural abscess,MONDO,disease,DISEASE_3831
3832,3832,3832,3832,3832,3832,3832,3832,MONDO:0022402,agyria-pachygyria type 1,MONDO,disease,DISEASE_3832
3833,3833,3833,3833,3833,3833,3833,3833,MONDO:0100307,adult Refsum disease due to PEX7 defect,MONDO,disease,DISEASE_3833
3834,3834,3834,3834,3834,3834,3834,3834,MONDO:0011517,pseudohyperaldosteronism type 2,MONDO,disease,DISEASE_3834
3835,3835,3835,3835,3835,3835,3835,3835,MONDO:0975877,neurodevelopmental disorder with variable familial hypercholanemia,MONDO,disease,DISEASE_3835
3836,3836,3836,3836,3836,3836,3836,3836,MONDO:0044919,malignant renal pelvis neoplasm,MONDO,disease,DISEASE_3836
3837,3837,3837,3837,3837,3837,3837,3837,MONDO:0800491,early-infantile DEE,MONDO,disease,DISEASE_3837
3838,3838,3838,3838,3838,3838,3838,3838,MONDO:0003889,"infiltrating bladder urothelial carcinoma, clear cell variant",MONDO,disease,DISEASE_3838
3839,3839,3839,3839,3839,3839,3839,3839,MONDO:0005822_MONDO:0040923_MONDO:0040922,latent syphilis,MONDO_grouped,disease,DISEASE_3839
3840,3840,3840,3840,3840,3840,3840,3840,MONDO:0001181,secondary corneal edema,MONDO,disease,DISEASE_3840
3841,3841,3841,3841,3841,3841,3841,3841,MONDO:1012509,"degenerative suspensory ligament desmitis, horse",MONDO,disease,DISEASE_3841
3842,3842,3842,3842,3842,3842,3842,3842,MONDO:0016989,Fuchs heterochromic iridocyclitis,MONDO,disease,DISEASE_3842
3843,3843,3843,3843,3843,3843,3843,3843,MONDO:0022196,chronic erosive gastritis,MONDO,disease,DISEASE_3843
3844,3844,3844,3844,3844,3844,3844,3844,MONDO:1011181_MONDO:1011154_MONDO:1011179_MONDO:1011180_MONDO:1011182,"osteopetrosis, cattle",MONDO_grouped,disease,DISEASE_3844
3845,3845,3845,3845,3845,3845,3845,3845,MONDO:0007342,clubfoot,MONDO,disease,DISEASE_3845
3846,3846,3846,3846,3846,3846,3846,3846,MONDO:0015413,median cleft of the upper lip and maxilla,MONDO,disease,DISEASE_3846
3847,3847,3847,3847,3847,3847,3847,3847,MONDO:0800187,"immunodeficiency 83, susceptibility to viral infections",MONDO,disease,DISEASE_3847
3848,3848,3848,3848,3848,3848,3848,3848,MONDO:0016477,Beckwith-Wiedemann syndrome due to 11p15 microdeletion,MONDO,disease,DISEASE_3848
3849,3849,3849,3849,3849,3849,3849,3849,MONDO:1010030,pediatric high-grade glioma,MONDO,disease,DISEASE_3849
3850,3850,3850,3850,3850,3850,3850,3850,MONDO:0100018_MONDO:0100037,adult onset pityriasis rubra pilaris,MONDO_grouped,disease,DISEASE_3850
3851,3851,3851,3851,3851,3851,3851,3851,MONDO:0012784,autosomal recessive ataxia due to ubiquinone deficiency,MONDO,disease,DISEASE_3851
3852,3852,3852,3852,3852,3852,3852,3852,MONDO:0019895,distal monosomy 4q,MONDO,disease,DISEASE_3852
3853,3853,3853,3853,3853,3853,3853,3853,MONDO:0009935,"pulmonary hypertension, primary, autosomal recessive",MONDO,disease,DISEASE_3853
3854,3854,3854,3854,3854,3854,3854,3854,MONDO:0011065,Hunter-McAlpine craniosynostosis,MONDO,disease,DISEASE_3854
3855,3855,3855,3855,3855,3855,3855,3855,MONDO:0014082,cryptosporidiosis-chronic cholangitis-liver disease syndrome,MONDO,disease,DISEASE_3855
3856,3856,3856,3856,3856,3856,3856,3856,MONDO:0035313,lymphoplasmacytic inflammatory pseudotumor of the liver,MONDO,disease,DISEASE_3856
3857,3857,3857,3857,3857,3857,3857,3857,MONDO:0971069,Phelan-McDermid syndrome due to SHANK3 mutation,MONDO,disease,DISEASE_3857
3858,3858,3858,3858,3858,3858,3858,3858,MONDO:0003563,diffuse pulmonary fibrosis,MONDO,disease,DISEASE_3858
3859,3859,3859,3859,3859,3859,3859,3859,MONDO:0000640,central nervous system primitive neuroectodermal neoplasm,MONDO,disease,DISEASE_3859
3860,3860,3860,3860,3860,3860,3860,3860,MONDO:0014226_MONDO:0005807,idiopathic CD4 lymphocytopenia,MONDO_grouped,disease,DISEASE_3860
3861,3861,3861,3861,3861,3861,3861,3861,MONDO:0009674,"muscular dystrophy, adult-onset, with leukoencephalopathy",MONDO,disease,DISEASE_3861
3862,3862,3862,3862,3862,3862,3862,3862,MONDO:0009904,Gitelman syndrome,MONDO,disease,DISEASE_3862
3863,3863,3863,3863,3863,3863,3863,3863,MONDO:0005570,hematologic disorder,MONDO,disease,DISEASE_3863
3864,3864,3864,3864,3864,3864,3864,3864,MONDO:0015005,"epilepsy, early-onset, vitamin B6-dependent",MONDO,disease,DISEASE_3864
3865,3865,3865,3865,3865,3865,3865,3865,MONDO:0017471_MONDO:0017469_MONDO:0017470_MONDO:0017468_MONDO:0017563,congenital patella dislocation,MONDO_grouped,disease,DISEASE_3865
3866,3866,3866,3866,3866,3866,3866,3866,MONDO:0007713,clonic hemifacial spasm,MONDO,disease,DISEASE_3866
3867,3867,3867,3867,3867,3867,3867,3867,MONDO:0018114,obsolete isolated brachycephaly,MONDO,disease,DISEASE_3867
3868,3868,3868,3868,3868,3868,3868,3868,MONDO:0000262,otomycosis,MONDO,disease,DISEASE_3868
3869,3869,3869,3869,3869,3869,3869,3869,MONDO:0000744_MONDO:0000749,lung abscess,MONDO_grouped,disease,DISEASE_3869
3870,3870,3870,3870,3870,3870,3870,3870,MONDO:0002727,olfactory nerve disorder,MONDO,disease,DISEASE_3870
3871,3871,3871,3871,3871,3871,3871,3871,MONDO:0009282,multiple acyl-CoA dehydrogenase deficiency,MONDO,disease,DISEASE_3871
3872,3872,3872,3872,3872,3872,3872,3872,MONDO:0011182,trimethylaminuria,MONDO,disease,DISEASE_3872
3873,3873,3873,3873,3873,3873,3873,3873,MONDO:0007668,globulin anomaly involving beta (2A)-globulin,MONDO,disease,DISEASE_3873
3874,3874,3874,3874,3874,3874,3874,3874,MONDO:0022471,childhood aortic valve stenosis,MONDO,disease,DISEASE_3874
3875,3875,3875,3875,3875,3875,3875,3875,MONDO:0005232,large cell carcinoma,MONDO,disease,DISEASE_3875
3876,3876,3876,3876,3876,3876,3876,3876,MONDO:0007354,coloboma of optic nerve,MONDO,disease,DISEASE_3876
3877,3877,3877,3877,3877,3877,3877,3877,MONDO:0008354,purpura simplex,MONDO,disease,DISEASE_3877
3878,3878,3878,3878,3878,3878,3878,3878,MONDO:1011243,"congenital nystagmus, dog",MONDO,disease,DISEASE_3878
3879,3879,3879,3879,3879,3879,3879,3879,MONDO:0009332,congenital hematological disorder,MONDO,disease,DISEASE_3879
3880,3880,3880,3880,3880,3880,3880,3880,MONDO:0957003,hereditary neuro-ophthalmological disease,MONDO,disease,DISEASE_3880
3881,3881,3881,3881,3881,3881,3881,3881,MONDO:0044981,pseudoallergy,MONDO,disease,DISEASE_3881
3882,3882,3882,3882,3882,3882,3882,3882,MONDO:0003770_MONDO:0004256_MONDO:0004317_MONDO:0004396_MONDO:0004498,thoracic spinal canal and spinal cord meningioma,MONDO_grouped,disease,DISEASE_3882
3883,3883,3883,3883,3883,3883,3883,3883,MONDO:0018738,benign metanephric tumor,MONDO,disease,DISEASE_3883
3884,3884,3884,3884,3884,3884,3884,3884,MONDO:0021093_MONDO:0013573_MONDO:0013323_MONDO:0013719_MONDO:0009032,cranioectodermal dysplasia,MONDO_grouped,disease,DISEASE_3884
3885,3885,3885,3885,3885,3885,3885,3885,MONDO:0004231,spindle cell variant squamous cell breast carcinoma,MONDO,disease,DISEASE_3885
3886,3886,3886,3886,3886,3886,3886,3886,MONDO:0043468,acne keloid,MONDO,disease,DISEASE_3886
3887,3887,3887,3887,3887,3887,3887,3887,MONDO:0002427,cerebellar disorder,MONDO,disease,DISEASE_3887
3888,3888,3888,3888,3888,3888,3888,3888,MONDO:0010686,N syndrome,MONDO,disease,DISEASE_3888
3889,3889,3889,3889,3889,3889,3889,3889,MONDO:0019371_MONDO:0016158,narcolepsy without cataplexy,MONDO_grouped,disease,DISEASE_3889
3890,3890,3890,3890,3890,3890,3890,3890,MONDO:0008467,Czeizel-Losonci syndrome,MONDO,disease,DISEASE_3890
3891,3891,3891,3891,3891,3891,3891,3891,MONDO:0002972,posterior mediastinum cancer,MONDO,disease,DISEASE_3891
3892,3892,3892,3892,3892,3892,3892,3892,MONDO:1011302,"branchial arch disease, non-human animal",MONDO,disease,DISEASE_3892
3893,3893,3893,3893,3893,3893,3893,3893,MONDO:0002156_MONDO:0002158,fallopian tube disorder,MONDO_grouped,disease,DISEASE_3893
3894,3894,3894,3894,3894,3894,3894,3894,MONDO:0006990,suppurative uveitis,MONDO,disease,DISEASE_3894
3895,3895,3895,3895,3895,3895,3895,3895,MONDO:0021678_MONDO:0021679,gram-negative bacterial infections,MONDO_grouped,disease,DISEASE_3895
3896,3896,3896,3896,3896,3896,3896,3896,MONDO:0004500,lung superior sulcus carcinoma,MONDO,disease,DISEASE_3896
3897,3897,3897,3897,3897,3897,3897,3897,MONDO:0004637,aryepiglottic fold cancer,MONDO,disease,DISEASE_3897
3898,3898,3898,3898,3898,3898,3898,3898,MONDO:0005119,anthrax infection,MONDO,disease,DISEASE_3898
3899,3899,3899,3899,3899,3899,3899,3899,MONDO:0017993,cerebral sinovenous thrombosis,MONDO,disease,DISEASE_3899
3900,3900,3900,3900,3900,3900,3900,3900,MONDO:1012308,"self-mutilation syndrome, horse",MONDO,disease,DISEASE_3900
3901,3901,3901,3901,3901,3901,3901,3901,MONDO:1012468,"pentalogy of Fallot, Amur tiger",MONDO,disease,DISEASE_3901
3902,3902,3902,3902,3902,3902,3902,3902,MONDO:0015260,diphyllobothriasis,MONDO,disease,DISEASE_3902
3903,3903,3903,3903,3903,3903,3903,3903,MONDO:1010164,"Wilson disease, non-human animal",MONDO,disease,DISEASE_3903
3904,3904,3904,3904,3904,3904,3904,3904,MONDO:0006880,oral leukoedema,MONDO,disease,DISEASE_3904
3905,3905,3905,3905,3905,3905,3905,3905,MONDO:0003466_MONDO:0003469,spindle cell synovial sarcoma,MONDO_grouped,disease,DISEASE_3905
3906,3906,3906,3906,3906,3906,3906,3906,MONDO:0027772,lung colloid adenocarcinoma,MONDO,disease,DISEASE_3906
3907,3907,3907,3907,3907,3907,3907,3907,MONDO:0010728,SCARF syndrome,MONDO,disease,DISEASE_3907
3908,3908,3908,3908,3908,3908,3908,3908,MONDO:0024520_MONDO:0014319_MONDO:0030822_MONDO:0024519,renal hypodysplasia/aplasia,MONDO_grouped,disease,DISEASE_3908
3909,3909,3909,3909,3909,3909,3909,3909,MONDO:0013331,"factor 5 and Factor VIII, combined deficiency of, 2",MONDO,disease,DISEASE_3909
3910,3910,3910,3910,3910,3910,3910,3910,MONDO:0002259,gonadal disorder,MONDO,disease,DISEASE_3910
3911,3911,3911,3911,3911,3911,3911,3911,MONDO:0001549,hemolytic-uremic syndrome,MONDO,disease,DISEASE_3911
3912,3912,3912,3912,3912,3912,3912,3912,MONDO:0020495,PEHO-like syndrome,MONDO,disease,DISEASE_3912
3913,3913,3913,3913,3913,3913,3913,3913,MONDO:0000070_MONDO:0010282_MONDO:0011941_MONDO:0012606_MONDO:0013045,"Mycobacterium tuberculosis, susceptibility",MONDO_grouped,disease,DISEASE_3913
3914,3914,3914,3914,3914,3914,3914,3914,MONDO:0003724,non-proliferative fibrocystic change of the breast,MONDO,disease,DISEASE_3914
3915,3915,3915,3915,3915,3915,3915,3915,MONDO:0008204,"obsolete patella aplasia, coxa vara, and tarsal synostosis",MONDO,disease,DISEASE_3915
3916,3916,3916,3916,3916,3916,3916,3916,MONDO:0016860,familial adenomatous polyposis due to 5q22.2 microdeletion,MONDO,disease,DISEASE_3916
3917,3917,3917,3917,3917,3917,3917,3917,MONDO:0009731,nephrosis-deafness-urinary tract-digital malformations syndrome,MONDO,disease,DISEASE_3917
3918,3918,3918,3918,3918,3918,3918,3918,MONDO:0013789,DDOST-congenital disorder of glycosylation,MONDO,disease,DISEASE_3918
3919,3919,3919,3919,3919,3919,3919,3919,MONDO:0037742,endometrioid stromal and related neoplasms,MONDO,disease,DISEASE_3919
3920,3920,3920,3920,3920,3920,3920,3920,MONDO:0003050,lung large cell carcinoma,MONDO,disease,DISEASE_3920
3921,3921,3921,3921,3921,3921,3921,3921,MONDO:0011359,acromelic frontonasal dysostosis,MONDO,disease,DISEASE_3921
3922,3922,3922,3922,3922,3922,3922,3922,MONDO:0009015,corneal dystrophy-perceptive deafness syndrome,MONDO,disease,DISEASE_3922
3923,3923,3923,3923,3923,3923,3923,3923,MONDO:0017805,intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome,MONDO,disease,DISEASE_3923
3924,3924,3924,3924,3924,3924,3924,3924,MONDO:0004321,endometrial mixed adenocarcinoma,MONDO,disease,DISEASE_3924
3925,3925,3925,3925,3925,3925,3925,3925,MONDO:0009224,fetal iodine syndrome,MONDO,disease,DISEASE_3925
3926,3926,3926,3926,3926,3926,3926,3926,MONDO:0009427,obsolete infantile hypophosphatasia,MONDO,disease,DISEASE_3926
3927,3927,3927,3927,3927,3927,3927,3927,MONDO:0009429,"hypophosphatemia, renal, with intracerebral calcifications",MONDO,disease,DISEASE_3927
3928,3928,3928,3928,3928,3928,3928,3928,MONDO:0010908,loose anagen syndrome,MONDO,disease,DISEASE_3928
3929,3929,3929,3929,3929,3929,3929,3929,MONDO:0021501,benign neoplasm of small intestine,MONDO,disease,DISEASE_3929
3930,3930,3930,3930,3930,3930,3930,3930,MONDO:0019092,infantile apnea,MONDO,disease,DISEASE_3930
3931,3931,3931,3931,3931,3931,3931,3931,MONDO:0019156,angioosteohypotrophic syndrome,MONDO,disease,DISEASE_3931
3932,3932,3932,3932,3932,3932,3932,3932,MONDO:0100506,Cockayne spectrum with or without cerebrooculofacioskeletal syndrome,MONDO,disease,DISEASE_3932
3933,3933,3933,3933,3933,3933,3933,3933,MONDO:0011432,"blepharophimosis - intellectual disability syndrome, Verloes type",MONDO,disease,DISEASE_3933
3934,3934,3934,3934,3934,3934,3934,3934,MONDO:0015491,immune complex mediated vasculitis,MONDO,disease,DISEASE_3934
3935,3935,3935,3935,3935,3935,3935,3935,MONDO:0012154_MONDO:0032941_MONDO:0012227_MONDO:0001384_MONDO:0012228_MONDO:0012229_MONDO:0012230_MONDO:0012469_MONDO:1011263,myopia,MONDO_grouped,disease,DISEASE_3935
3936,3936,3936,3936,3936,3936,3936,3936,MONDO:0007337,cleft palate-lateral synechia syndrome,MONDO,disease,DISEASE_3936
3937,3937,3937,3937,3937,3937,3937,3937,MONDO:0005478,torsades de pointes,MONDO,disease,DISEASE_3937
3938,3938,3938,3938,3938,3938,3938,3938,MONDO:0012594,complement factor I deficiency,MONDO,disease,DISEASE_3938
3939,3939,3939,3939,3939,3939,3939,3939,MONDO:0021455,benign neoplasm of neck,MONDO,disease,DISEASE_3939
3940,3940,3940,3940,3940,3940,3940,3940,MONDO:0008896,"campomelia, Cumming type",MONDO,disease,DISEASE_3940
3941,3941,3941,3941,3941,3941,3941,3941,MONDO:0017600,hairy cell leukemia variant,MONDO,disease,DISEASE_3941
3942,3942,3942,3942,3942,3942,3942,3942,MONDO:0011778,"multiple epiphyseal dysplasia, Al-Gazali type",MONDO,disease,DISEASE_3942
3943,3943,3943,3943,3943,3943,3943,3943,MONDO:0019757,alobar holoprosencephaly,MONDO,disease,DISEASE_3943
3944,3944,3944,3944,3944,3944,3944,3944,MONDO:0005130,celiac disease,MONDO,disease,DISEASE_3944
3945,3945,3945,3945,3945,3945,3945,3945,MONDO:0014667_MONDO:0014668_MONDO:0011451_MONDO:0014051,"cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency",MONDO_grouped,disease,DISEASE_3945
3946,3946,3946,3946,3946,3946,3946,3946,MONDO:0020663,malignant spindle cell neoplasm,MONDO,disease,DISEASE_3946
3947,3947,3947,3947,3947,3947,3947,3947,MONDO:0012657,Mungan syndrome,MONDO,disease,DISEASE_3947
3948,3948,3948,3948,3948,3948,3948,3948,MONDO:0012650,Cernunnos-XLF deficiency,MONDO,disease,DISEASE_3948
3949,3949,3949,3949,3949,3949,3949,3949,MONDO:0700280,post-treatment Lyme disease syndrome,MONDO,disease,DISEASE_3949
3950,3950,3950,3950,3950,3950,3950,3950,MONDO:1010716,"acute intermittent porphyria, domestic cat",MONDO,disease,DISEASE_3950
3951,3951,3951,3951,3951,3951,3951,3951,MONDO:1012874_MONDO:1012896,"deafness, OSBPL2-related, pig",MONDO_grouped,disease,DISEASE_3951
3952,3952,3952,3952,3952,3952,3952,3952,MONDO:0004478,pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma,MONDO,disease,DISEASE_3952
3953,3953,3953,3953,3953,3953,3953,3953,MONDO:0019755,developmental defect during embryogenesis,MONDO,disease,DISEASE_3953
3954,3954,3954,3954,3954,3954,3954,3954,MONDO:0019193_MONDO:0012104_MONDO:0027766_MONDO:0020089,acquired generalized lipodystrophy,MONDO_grouped,disease,DISEASE_3954
3955,3955,3955,3955,3955,3955,3955,3955,MONDO:0037252,thecoma,MONDO,disease,DISEASE_3955
3956,3956,3956,3956,3956,3956,3956,3956,MONDO:0016359,limited systemic sclerosis,MONDO,disease,DISEASE_3956
3957,3957,3957,3957,3957,3957,3957,3957,MONDO:0035375,multisystem inflammatory syndrome in children and adults,MONDO,disease,DISEASE_3957
3958,3958,3958,3958,3958,3958,3958,3958,MONDO:0019916,maternal uniparental disomy of chromosome 16,MONDO,disease,DISEASE_3958
3959,3959,3959,3959,3959,3959,3959,3959,MONDO:0001956,capillary leak syndrome,MONDO,disease,DISEASE_3959
3960,3960,3960,3960,3960,3960,3960,3960,MONDO:0010954,"Wiskott-Aldrich syndrome, autosomal dominant form",MONDO,disease,DISEASE_3960
3961,3961,3961,3961,3961,3961,3961,3961,MONDO:0001495,hematocele of tunica vaginalis testis,MONDO,disease,DISEASE_3961
3962,3962,3962,3962,3962,3962,3962,3962,MONDO:0016947,partial duplication of the short arm of chromosome 10,MONDO,disease,DISEASE_3962
3963,3963,3963,3963,3963,3963,3963,3963,MONDO:0006638,acute retinal necrosis syndrome,MONDO,disease,DISEASE_3963
3964,3964,3964,3964,3964,3964,3964,3964,MONDO:0001232,orbital osteomyelitis,MONDO,disease,DISEASE_3964
3965,3965,3965,3965,3965,3965,3965,3965,MONDO:0024504,enterochromaffin cell serotonin-producing pancreatic neuroendocrine tumor,MONDO,disease,DISEASE_3965
3966,3966,3966,3966,3966,3966,3966,3966,MONDO:0011322,"Oroacral syndrome, Verloes-Koulischer type",MONDO,disease,DISEASE_3966
3967,3967,3967,3967,3967,3967,3967,3967,MONDO:0004796_MONDO:0024891,infectious meningitis,MONDO_grouped,disease,DISEASE_3967
3968,3968,3968,3968,3968,3968,3968,3968,MONDO:0017180,10q22.3q23.3 microduplication syndrome,MONDO,disease,DISEASE_3968
3969,3969,3969,3969,3969,3969,3969,3969,MONDO:0002636,accessory nerve disorder,MONDO,disease,DISEASE_3969
3970,3970,3970,3970,3970,3970,3970,3970,MONDO:0009922,Pseudouridinuria and mental defect,MONDO,disease,DISEASE_3970
3971,3971,3971,3971,3971,3971,3971,3971,MONDO:0013375,"Klippel-Feil syndrome 3, autosomal dominant",MONDO,disease,DISEASE_3971
3972,3972,3972,3972,3972,3972,3972,3972,MONDO:0005373_MONDO:0042972,meningococcal infection,MONDO_grouped,disease,DISEASE_3972
3973,3973,3973,3973,3973,3973,3973,3973,MONDO:1012615,"mesangiocapillary glomerulonephritis, type I, sheep",MONDO,disease,DISEASE_3973
3974,3974,3974,3974,3974,3974,3974,3974,MONDO:0100094,cannabinoid hyperemesis syndrome,MONDO,disease,DISEASE_3974
3975,3975,3975,3975,3975,3975,3975,3975,MONDO:0013791,"thrombophilia due to protein S deficiency, autosomal recessive",MONDO,disease,DISEASE_3975
3976,3976,3976,3976,3976,3976,3976,3976,MONDO:0100126,P5CS deficiency,MONDO,disease,DISEASE_3976
3977,3977,3977,3977,3977,3977,3977,3977,MONDO:0003170,gliofibroma,MONDO,disease,DISEASE_3977
3978,3978,3978,3978,3978,3978,3978,3978,MONDO:0044138,hyalitis,MONDO,disease,DISEASE_3978
3979,3979,3979,3979,3979,3979,3979,3979,MONDO:0019012,Carpenter syndrome,MONDO,disease,DISEASE_3979
3980,3980,3980,3980,3980,3980,3980,3980,MONDO:0030963,Li-Campeau syndrome,MONDO,disease,DISEASE_3980
3981,3981,3981,3981,3981,3981,3981,3981,MONDO:0100212,IFAP syndrome,MONDO,disease,DISEASE_3981
3982,3982,3982,3982,3982,3982,3982,3982,MONDO:0018710,megalencephaly-severe kyphoscoliosis-overgrowth syndrome,MONDO,disease,DISEASE_3982
3983,3983,3983,3983,3983,3983,3983,3983,MONDO:0100295,"Alzheimer disease, susceptibility to, mitochondrial",MONDO,disease,DISEASE_3983
3984,3984,3984,3984,3984,3984,3984,3984,MONDO:0022573_MONDO:0022574,biliary atresia intrahepatic non syndromic form,MONDO_grouped,disease,DISEASE_3984
3985,3985,3985,3985,3985,3985,3985,3985,MONDO:0030539,"central hypoventilation syndrome, congenital, 3",MONDO,disease,DISEASE_3985
3986,3986,3986,3986,3986,3986,3986,3986,MONDO:0011202,RHYNS syndrome,MONDO,disease,DISEASE_3986
3987,3987,3987,3987,3987,3987,3987,3987,MONDO:0019527,undifferentiated connective tissue syndrome,MONDO,disease,DISEASE_3987
3988,3988,3988,3988,3988,3988,3988,3988,MONDO:0009763,obesity-hypoventilation syndrome,MONDO,disease,DISEASE_3988
3989,3989,3989,3989,3989,3989,3989,3989,MONDO:0016031,facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome,MONDO,disease,DISEASE_3989
3990,3990,3990,3990,3990,3990,3990,3990,MONDO:0001856,splenic artery aneurysm,MONDO,disease,DISEASE_3990
3991,3991,3991,3991,3991,3991,3991,3991,MONDO:1011307,"chromosomal disorder, non-human animal",MONDO,disease,DISEASE_3991
3992,3992,3992,3992,3992,3992,3992,3992,MONDO:0859355_MONDO:0018252,inflammatory poikiloderma with hair abnormalities and acral keratoses,MONDO_grouped,disease,DISEASE_3992
3993,3993,3993,3993,3993,3993,3993,3993,MONDO:0009243,Fraser-like syndrome,MONDO,disease,DISEASE_3993
3994,3994,3994,3994,3994,3994,3994,3994,MONDO:0007998,microspherophakia-metaphyseal dysplasia syndrome,MONDO,disease,DISEASE_3994
3995,3995,3995,3995,3995,3995,3995,3995,MONDO:0054867,paraomphalocele,MONDO,disease,DISEASE_3995
3996,3996,3996,3996,3996,3996,3996,3996,MONDO:1011214_MONDO:1011213_MONDO:1011216,"coloboma, dog",MONDO_grouped,disease,DISEASE_3996
3997,3997,3997,3997,3997,3997,3997,3997,MONDO:0002235,eyelid neoplasm,MONDO,disease,DISEASE_3997
3998,3998,3998,3998,3998,3998,3998,3998,MONDO:0009109,lysinuric protein intolerance,MONDO,disease,DISEASE_3998
3999,3999,3999,3999,3999,3999,3999,3999,MONDO:0019431,primitive portal vein thrombosis,MONDO,disease,DISEASE_3999
4000,4000,4000,4000,4000,4000,4000,4000,MONDO:0009925,autosomal recessive inherited pseudoxanthoma elasticum,MONDO,disease,DISEASE_4000
4001,4001,4001,4001,4001,4001,4001,4001,MONDO:0004632,obsolete Hodgkin's granuloma,MONDO,disease,DISEASE_4001
4002,4002,4002,4002,4002,4002,4002,4002,MONDO:0016554,neonatal iodine exposure,MONDO,disease,DISEASE_4002
4003,4003,4003,4003,4003,4003,4003,4003,MONDO:0011929,chromosome 1p36 deletion syndrome,MONDO,disease,DISEASE_4003
4004,4004,4004,4004,4004,4004,4004,4004,MONDO:0009204,lethal faciocardiomelic dysplasia,MONDO,disease,DISEASE_4004
4005,4005,4005,4005,4005,4005,4005,4005,MONDO:0011430,pulverulent cataract,MONDO,disease,DISEASE_4005
4006,4006,4006,4006,4006,4006,4006,4006,MONDO:0007664_MONDO:0008328_MONDO:0011311_MONDO:0012357_MONDO:0012515_MONDO:0013134_MONDO:0012646_MONDO:0007665_MONDO:0012101_MONDO:0012102_MONDO:0012645_MONDO:0800210,"glaucoma 1, open angle",MONDO_grouped,disease,DISEASE_4006
4007,4007,4007,4007,4007,4007,4007,4007,MONDO:0003314,endometrioid stromal and related neoplasms of the vagina,MONDO,disease,DISEASE_4007
4008,4008,4008,4008,4008,4008,4008,4008,MONDO:0015342,acute transverse myelitis,MONDO,disease,DISEASE_4008
4009,4009,4009,4009,4009,4009,4009,4009,MONDO:0700105,"difference of sexual differentiation, non-human animal",MONDO,disease,DISEASE_4009
4010,4010,4010,4010,4010,4010,4010,4010,MONDO:0016747,primary melanoma of the central nervous system,MONDO,disease,DISEASE_4010
4011,4011,4011,4011,4011,4011,4011,4011,MONDO:0010253,"migraine, familial typical, susceptibility to, 2",MONDO,disease,DISEASE_4011
4012,4012,4012,4012,4012,4012,4012,4012,MONDO:0003519,malignant syringoma,MONDO,disease,DISEASE_4012
4013,4013,4013,4013,4013,4013,4013,4013,MONDO:0003040_MONDO:0003398,retrograde amnesia,MONDO_grouped,disease,DISEASE_4013
4014,4014,4014,4014,4014,4014,4014,4014,MONDO:0010763_MONDO:0010767,"spermatogenic failure, Y-linked",MONDO_grouped,disease,DISEASE_4014
4015,4015,4015,4015,4015,4015,4015,4015,MONDO:0004371,spinal multifocal clear cell meningioma,MONDO,disease,DISEASE_4015
4016,4016,4016,4016,4016,4016,4016,4016,MONDO:0021064_MONDO:0006291,jugulotympanic paraganglioma,MONDO_grouped,disease,DISEASE_4016
4017,4017,4017,4017,4017,4017,4017,4017,MONDO:0011825,"streptococcus, group A, severity of infection by",MONDO,disease,DISEASE_4017
4018,4018,4018,4018,4018,4018,4018,4018,MONDO:0100281_MONDO:0012491,"macroglobulinemia, Waldenstrom",MONDO_grouped,disease,DISEASE_4018
4019,4019,4019,4019,4019,4019,4019,4019,MONDO:0002102,cheilitis,MONDO,disease,DISEASE_4019
4020,4020,4020,4020,4020,4020,4020,4020,MONDO:0014241,"leukemia, acute lymphoblastic, susceptibility to, 3",MONDO,disease,DISEASE_4020
4021,4021,4021,4021,4021,4021,4021,4021,MONDO:0008999,Cohen syndrome,MONDO,disease,DISEASE_4021
4022,4022,4022,4022,4022,4022,4022,4022,MONDO:0020716_MONDO:0010135_MONDO:0010133_MONDO:0010137_MONDO:0011792_MONDO:0010136,thyroid dyshormonogenesis,MONDO_grouped,disease,DISEASE_4022
4023,4023,4023,4023,4023,4023,4023,4023,MONDO:0020675,ischemic bowel disorder,MONDO,disease,DISEASE_4023
4024,4024,4024,4024,4024,4024,4024,4024,MONDO:0018931,"mucolipidosis type III, alpha/beta",MONDO,disease,DISEASE_4024
4025,4025,4025,4025,4025,4025,4025,4025,MONDO:0019970,Sinding-Larsen-Johansson disease,MONDO,disease,DISEASE_4025
4026,4026,4026,4026,4026,4026,4026,4026,MONDO:0100542,clonal hematopoiesis,MONDO,disease,DISEASE_4026
4027,4027,4027,4027,4027,4027,4027,4027,MONDO:0012967,hemolytic anemia due to adenylate kinase deficiency,MONDO,disease,DISEASE_4027
4028,4028,4028,4028,4028,4028,4028,4028,MONDO:0020112,vitamin B12- and folate-independent constitutional megaloblastic anemia,MONDO,disease,DISEASE_4028
4029,4029,4029,4029,4029,4029,4029,4029,MONDO:0016822,myalgia-eosinophilia syndrome associated with tryptophan,MONDO,disease,DISEASE_4029
4030,4030,4030,4030,4030,4030,4030,4030,MONDO:0009821,lethal osteosclerotic bone dysplasia,MONDO,disease,DISEASE_4030
4031,4031,4031,4031,4031,4031,4031,4031,MONDO:1012449,"squamous cell carcinoma of the digit, dog",MONDO,disease,DISEASE_4031
4032,4032,4032,4032,4032,4032,4032,4032,MONDO:1011842,"granule cell type cerebellar hypoplasia, non-human animal",MONDO,disease,DISEASE_4032
4033,4033,4033,4033,4033,4033,4033,4033,MONDO:0005555,cycloplegia,MONDO,disease,DISEASE_4033
4034,4034,4034,4034,4034,4034,4034,4034,MONDO:0011776,CINCA syndrome,MONDO,disease,DISEASE_4034
4035,4035,4035,4035,4035,4035,4035,4035,MONDO:0015126,polyendocrinopathy,MONDO,disease,DISEASE_4035
4036,4036,4036,4036,4036,4036,4036,4036,MONDO:0006908,pituitary apoplexy,MONDO,disease,DISEASE_4036
4037,4037,4037,4037,4037,4037,4037,4037,MONDO:0019113,benign paroxysmal torticollis of infancy,MONDO,disease,DISEASE_4037
4038,4038,4038,4038,4038,4038,4038,4038,MONDO:0004430,penis mixed squamous cell carcinoma,MONDO,disease,DISEASE_4038
4039,4039,4039,4039,4039,4039,4039,4039,MONDO:0011533,temtamy preaxial brachydactyly syndrome,MONDO,disease,DISEASE_4039
4040,4040,4040,4040,4040,4040,4040,4040,MONDO:0021470,benign neoplasm of pancreas,MONDO,disease,DISEASE_4040
4041,4041,4041,4041,4041,4041,4041,4041,MONDO:0021379,neoplasm of epicardium,MONDO,disease,DISEASE_4041
4042,4042,4042,4042,4042,4042,4042,4042,MONDO:0015314,primary laryngeal lymphangioma,MONDO,disease,DISEASE_4042
4043,4043,4043,4043,4043,4043,4043,4043,MONDO:0045019,lactation disease,MONDO,disease,DISEASE_4043
4044,4044,4044,4044,4044,4044,4044,4044,MONDO:0003894,mediastinal melanocytic neurilemmoma,MONDO,disease,DISEASE_4044
4045,4045,4045,4045,4045,4045,4045,4045,MONDO:1010306,"osteochondrodysplasia, non-human animal",MONDO,disease,DISEASE_4045
4046,4046,4046,4046,4046,4046,4046,4046,MONDO:0056817,rectal adenosquamous carcinoma,MONDO,disease,DISEASE_4046
4047,4047,4047,4047,4047,4047,4047,4047,MONDO:0017755,inborn disorder of bilirubin metabolism,MONDO,disease,DISEASE_4047
4048,4048,4048,4048,4048,4048,4048,4048,MONDO:1012768,"cancer, TP53-related, crab-eating macaque",MONDO,disease,DISEASE_4048
4049,4049,4049,4049,4049,4049,4049,4049,MONDO:0008884,oculoosteocutaneous syndrome,MONDO,disease,DISEASE_4049
4050,4050,4050,4050,4050,4050,4050,4050,MONDO:0017694,"glycogen storage disease due to acid maltase deficiency, infantile onset",MONDO,disease,DISEASE_4050
4051,4051,4051,4051,4051,4051,4051,4051,MONDO:1010000,pythiosis,MONDO,disease,DISEASE_4051
4052,4052,4052,4052,4052,4052,4052,4052,MONDO:0030801,monosomy 7 myelodysplasia and leukemia syndrome 2,MONDO,disease,DISEASE_4052
4053,4053,4053,4053,4053,4053,4053,4053,MONDO:1010281,"testicular regression syndrome, non-human animal",MONDO,disease,DISEASE_4053
4054,4054,4054,4054,4054,4054,4054,4054,MONDO:0007826,"incisors, shovel-shaped",MONDO,disease,DISEASE_4054
4055,4055,4055,4055,4055,4055,4055,4055,MONDO:0011208,malignant atrophic papulosis,MONDO,disease,DISEASE_4055
4056,4056,4056,4056,4056,4056,4056,4056,MONDO:0043576,endarteritis,MONDO,disease,DISEASE_4056
4057,4057,4057,4057,4057,4057,4057,4057,MONDO:0003609,seminal vesicle cystadenoma,MONDO,disease,DISEASE_4057
4058,4058,4058,4058,4058,4058,4058,4058,MONDO:0007186,gastroesophageal reflux disease,MONDO,disease,DISEASE_4058
4059,4059,4059,4059,4059,4059,4059,4059,MONDO:0000893,mixed mucinous and nonmucinous bronchioloalveolar adenocarcinoma,MONDO,disease,DISEASE_4059
4060,4060,4060,4060,4060,4060,4060,4060,MONDO:0018240,TRPV4-related bone disorder,MONDO,disease,DISEASE_4060
4061,4061,4061,4061,4061,4061,4061,4061,MONDO:0006552,folliculitis,MONDO,disease,DISEASE_4061
4062,4062,4062,4062,4062,4062,4062,4062,MONDO:0024620,meningitis caused by poliovirus,MONDO,disease,DISEASE_4062
4063,4063,4063,4063,4063,4063,4063,4063,MONDO:1010613,"hyperaldosteronism, domestic cat",MONDO,disease,DISEASE_4063
4064,4064,4064,4064,4064,4064,4064,4064,MONDO:1011486,"complement component 2 deficiency, domestic guinea pig",MONDO,disease,DISEASE_4064
4065,4065,4065,4065,4065,4065,4065,4065,MONDO:0013251,Birbeck granule deficiency,MONDO,disease,DISEASE_4065
4066,4066,4066,4066,4066,4066,4066,4066,MONDO:0003532,breast papillary carcinoma,MONDO,disease,DISEASE_4066
4067,4067,4067,4067,4067,4067,4067,4067,MONDO:0016307_MONDO:0016308_MONDO:0016309_MONDO:0016310,"Niemann-Pick disease type C, severe early infantile neurologic onset",MONDO_grouped,disease,DISEASE_4067
4068,4068,4068,4068,4068,4068,4068,4068,MONDO:0014622,isolated focal non-epidermolytic palmoplantar keratoderma,MONDO,disease,DISEASE_4068
4069,4069,4069,4069,4069,4069,4069,4069,MONDO:0001136,chylocele of tunica vaginalis,MONDO,disease,DISEASE_4069
4070,4070,4070,4070,4070,4070,4070,4070,MONDO:0009446,ichthyosis-intellectual disability-dwarfism-renal impairment syndrome,MONDO,disease,DISEASE_4070
4071,4071,4071,4071,4071,4071,4071,4071,MONDO:0700205,"ehrlichiosis, non-human animal",MONDO,disease,DISEASE_4071
4072,4072,4072,4072,4072,4072,4072,4072,MONDO:0016029,esthesioneuroblastoma,MONDO,disease,DISEASE_4072
4073,4073,4073,4073,4073,4073,4073,4073,MONDO:0006183,disseminated peritoneal leiomyomatosis,MONDO,disease,DISEASE_4073
4074,4074,4074,4074,4074,4074,4074,4074,MONDO:0012593,brain-lung-thyroid syndrome,MONDO,disease,DISEASE_4074
4075,4075,4075,4075,4075,4075,4075,4075,MONDO:0000678,simultanagnosia,MONDO,disease,DISEASE_4075
4076,4076,4076,4076,4076,4076,4076,4076,MONDO:0007503,ear without helix,MONDO,disease,DISEASE_4076
4077,4077,4077,4077,4077,4077,4077,4077,MONDO:0018010_MONDO:0020122_MONDO:0600023,juvenile idiopathic inflammatory myopathy,MONDO_grouped,disease,DISEASE_4077
4078,4078,4078,4078,4078,4078,4078,4078,MONDO:0010069,spondylocostal dysostosis-anal and genitourinary malformations syndrome,MONDO,disease,DISEASE_4078
4079,4079,4079,4079,4079,4079,4079,4079,MONDO:0032586,"diarrhea 10, protein-losing enteropathy type",MONDO,disease,DISEASE_4079
4080,4080,4080,4080,4080,4080,4080,4080,MONDO:0034820,cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome,MONDO,disease,DISEASE_4080
4081,4081,4081,4081,4081,4081,4081,4081,MONDO:0100008,food protein-induced enterocolitis syndrome,MONDO,disease,DISEASE_4081
4082,4082,4082,4082,4082,4082,4082,4082,MONDO:0006209,fibroblastic neoplasm,MONDO,disease,DISEASE_4082
4083,4083,4083,4083,4083,4083,4083,4083,MONDO:0019670_MONDO:0019671,ulnar hemimelia,MONDO_grouped,disease,DISEASE_4083
4084,4084,4084,4084,4084,4084,4084,4084,MONDO:1010294,"rheumatoid arthritis, non-human animal",MONDO,disease,DISEASE_4084
4085,4085,4085,4085,4085,4085,4085,4085,MONDO:0001778,dermoid cyst of skin,MONDO,disease,DISEASE_4085
4086,4086,4086,4086,4086,4086,4086,4086,MONDO:0022942,deafness mesenteric diverticula of small bowel neuropathy,MONDO,disease,DISEASE_4086
4087,4087,4087,4087,4087,4087,4087,4087,MONDO:0016088,hypoxanthine-guanine phosphoribosyltransferase deficiency,MONDO,disease,DISEASE_4087
4088,4088,4088,4088,4088,4088,4088,4088,MONDO:0009172,enterocolitis,MONDO,disease,DISEASE_4088
4089,4089,4089,4089,4089,4089,4089,4089,MONDO:0002247,factor X deficiency,MONDO,disease,DISEASE_4089
4090,4090,4090,4090,4090,4090,4090,4090,MONDO:1011166_MONDO:1011167_MONDO:1011168,"osteochondritis dissecans, snow leopard",MONDO_grouped,disease,DISEASE_4090
4091,4091,4091,4091,4091,4091,4091,4091,MONDO:0042726,"macrogyria, pseudobulbar palsy and intellectual disability",MONDO,disease,DISEASE_4091
4092,4092,4092,4092,4092,4092,4092,4092,MONDO:0014556,"congenital contractures of the limbs and face, hypotonia, and developmental delay",MONDO,disease,DISEASE_4092
4093,4093,4093,4093,4093,4093,4093,4093,MONDO:0023050,ectrodactyly cardiopathy dysmorphism,MONDO,disease,DISEASE_4093
4094,4094,4094,4094,4094,4094,4094,4094,MONDO:0008721,medium chain acyl-CoA dehydrogenase deficiency,MONDO,disease,DISEASE_4094
4095,4095,4095,4095,4095,4095,4095,4095,MONDO:0859161,"onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome",MONDO,disease,DISEASE_4095
4096,4096,4096,4096,4096,4096,4096,4096,MONDO:0006416,small intestinal Burkitt lymphoma,MONDO,disease,DISEASE_4096
4097,4097,4097,4097,4097,4097,4097,4097,MONDO:0013353,"intellectual disability, anterior maxillary protrusion, and strabismus",MONDO,disease,DISEASE_4097
4098,4098,4098,4098,4098,4098,4098,4098,MONDO:0020405,straddling and/or overriding mitral valve,MONDO,disease,DISEASE_4098
4099,4099,4099,4099,4099,4099,4099,4099,MONDO:0008794,"anhidrosis, familial generalized, with abnormal or absent sweat glands",MONDO,disease,DISEASE_4099
4100,4100,4100,4100,4100,4100,4100,4100,MONDO:0044873,childhood myelodysplastic syndrome,MONDO,disease,DISEASE_4100
4101,4101,4101,4101,4101,4101,4101,4101,MONDO:0014751,palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome,MONDO,disease,DISEASE_4101
4102,4102,4102,4102,4102,4102,4102,4102,MONDO:0006467,thyroid gland squamous cell carcinoma,MONDO,disease,DISEASE_4102
4103,4103,4103,4103,4103,4103,4103,4103,MONDO:0019190,juvenile polyposis of infancy,MONDO,disease,DISEASE_4103
4104,4104,4104,4104,4104,4104,4104,4104,MONDO:0012208_MONDO:0019306,congenital reticular ichthyosiform erythroderma,MONDO_grouped,disease,DISEASE_4104
4105,4105,4105,4105,4105,4105,4105,4105,MONDO:0004144,fibrous meningioma,MONDO,disease,DISEASE_4105
4106,4106,4106,4106,4106,4106,4106,4106,MONDO:1011665,"anal furunculosis, non-human animal",MONDO,disease,DISEASE_4106
4107,4107,4107,4107,4107,4107,4107,4107,MONDO:0044748,anaplasmosis in cattle,MONDO,disease,DISEASE_4107
4108,4108,4108,4108,4108,4108,4108,4108,MONDO:0011044,"ectrodactyly of lower limbs, congenital heart defect, and micrognathia",MONDO,disease,DISEASE_4108
4109,4109,4109,4109,4109,4109,4109,4109,MONDO:0025270,"toxoplasmosis, non-human animal",MONDO,disease,DISEASE_4109
4110,4110,4110,4110,4110,4110,4110,4110,MONDO:0850415,rhabdomyolysis-myalgia syndrome,MONDO,disease,DISEASE_4110
4111,4111,4111,4111,4111,4111,4111,4111,MONDO:0017599,splenic diffuse red pulp small B-cell lymphoma,MONDO,disease,DISEASE_4111
4112,4112,4112,4112,4112,4112,4112,4112,MONDO:0010233,"heterotopia, periventricular, X-linked dominant",MONDO,disease,DISEASE_4112
4113,4113,4113,4113,4113,4113,4113,4113,MONDO:0043975,autonomic dysreflexia,MONDO,disease,DISEASE_4113
4114,4114,4114,4114,4114,4114,4114,4114,MONDO:0100556,PRRT2-associated paroxysmal movement disorder,MONDO,disease,DISEASE_4114
4115,4115,4115,4115,4115,4115,4115,4115,MONDO:0004274,mixed epithelial/mesenchymal metaplastic breast carcinoma,MONDO,disease,DISEASE_4115
4116,4116,4116,4116,4116,4116,4116,4116,MONDO:0000474_MONDO:0001322,pericardium disorder,MONDO_grouped,disease,DISEASE_4116
4117,4117,4117,4117,4117,4117,4117,4117,MONDO:0033618,Vissers-Bodmer syndrome,MONDO,disease,DISEASE_4117
4118,4118,4118,4118,4118,4118,4118,4118,MONDO:0008297,variegate porphyria,MONDO,disease,DISEASE_4118
4119,4119,4119,4119,4119,4119,4119,4119,MONDO:0019475,subcutaneous panniculitis-like T-cell lymphoma,MONDO,disease,DISEASE_4119
4120,4120,4120,4120,4120,4120,4120,4120,MONDO:0005077,pertussis,MONDO,disease,DISEASE_4120
4121,4121,4121,4121,4121,4121,4121,4121,MONDO:0018671_MONDO:0018992,IgG4-related kidney disease,MONDO_grouped,disease,DISEASE_4121
4122,4122,4122,4122,4122,4122,4122,4122,MONDO:0000335,parenchymatous neurosyphilis,MONDO,disease,DISEASE_4122
4123,4123,4123,4123,4123,4123,4123,4123,MONDO:0010714,Pelizeaus-Merzbacher spectrum disorder,MONDO,disease,DISEASE_4123
4124,4124,4124,4124,4124,4124,4124,4124,MONDO:0016344,hydranencephaly,MONDO,disease,DISEASE_4124
4125,4125,4125,4125,4125,4125,4125,4125,MONDO:0018334,chronic hiccup,MONDO,disease,DISEASE_4125
4126,4126,4126,4126,4126,4126,4126,4126,MONDO:0014816,split-foot malformation-mesoaxial polydactyly syndrome,MONDO,disease,DISEASE_4126
4127,4127,4127,4127,4127,4127,4127,4127,MONDO:0008508,"symphalangism, C. S. Lewis type",MONDO,disease,DISEASE_4127
4128,4128,4128,4128,4128,4128,4128,4128,MONDO:1012306_MONDO:1012307,"cutaneous papillomatosis, horse",MONDO_grouped,disease,DISEASE_4128
4129,4129,4129,4129,4129,4129,4129,4129,MONDO:0032738,"gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy",MONDO,disease,DISEASE_4129
4130,4130,4130,4130,4130,4130,4130,4130,MONDO:0850289,human betaherpesvirus 5 infectious disease,MONDO,disease,DISEASE_4130
4131,4131,4131,4131,4131,4131,4131,4131,MONDO:0008396,"oculodental syndrome, Rutherfurd type",MONDO,disease,DISEASE_4131
4132,4132,4132,4132,4132,4132,4132,4132,MONDO:0032791_MONDO:0007617_MONDO:0032702_MONDO:0025699_MONDO:0032912_MONDO:0054831_MONDO:0014838_MONDO:0033492_MONDO:0015452,Coffin-Siris syndrome,MONDO_grouped,disease,DISEASE_4132
4133,4133,4133,4133,4133,4133,4133,4133,MONDO:0007986,metatropic dysplasia,MONDO,disease,DISEASE_4133
4134,4134,4134,4134,4134,4134,4134,4134,MONDO:0001543,lesion of sciatic nerve,MONDO,disease,DISEASE_4134
4135,4135,4135,4135,4135,4135,4135,4135,MONDO:0000413,infancy electroclinical syndrome,MONDO,disease,DISEASE_4135
4136,4136,4136,4136,4136,4136,4136,4136,MONDO:0800477,SETD2-related neurodevelopmental disorder without or with macrocephaly/overgrowth,MONDO,disease,DISEASE_4136
4137,4137,4137,4137,4137,4137,4137,4137,MONDO:0850090,fibrosis-neurodegeneration-cerebral angiomatosis syndrome,MONDO,disease,DISEASE_4137
4138,4138,4138,4138,4138,4138,4138,4138,MONDO:1011892,"spinal intradural arachnoid cyst, non-human animal",MONDO,disease,DISEASE_4138
4139,4139,4139,4139,4139,4139,4139,4139,MONDO:0005176,benign insulitis,MONDO,disease,DISEASE_4139
4140,4140,4140,4140,4140,4140,4140,4140,MONDO:0009573,megaepiphyseal dwarfism,MONDO,disease,DISEASE_4140
4141,4141,4141,4141,4141,4141,4141,4141,MONDO:0016360,marcothrombocytopenia with mitral valve insufficiency,MONDO,disease,DISEASE_4141
4142,4142,4142,4142,4142,4142,4142,4142,MONDO:0016379,erosive pustular dermatosis of the scalp,MONDO,disease,DISEASE_4142
4143,4143,4143,4143,4143,4143,4143,4143,MONDO:0022888,craniostenosis cataract,MONDO,disease,DISEASE_4143
4144,4144,4144,4144,4144,4144,4144,4144,MONDO:0007405,Crouzon syndrome,MONDO,disease,DISEASE_4144
4145,4145,4145,4145,4145,4145,4145,4145,MONDO:0006953,Rh isoimmunization,MONDO,disease,DISEASE_4145
4146,4146,4146,4146,4146,4146,4146,4146,MONDO:0004497_MONDO:0002897_MONDO:0002896,tertiary syphilis,MONDO_grouped,disease,DISEASE_4146
4147,4147,4147,4147,4147,4147,4147,4147,MONDO:0016499,autoimmune autonomic ganglionopathy,MONDO,disease,DISEASE_4147
4148,4148,4148,4148,4148,4148,4148,4148,MONDO:0018087,viral hemorrhagic fever,MONDO,disease,DISEASE_4148
4149,4149,4149,4149,4149,4149,4149,4149,MONDO:1010019,"arrhythmogenic right ventricular cardiomyopathy, non-human animal",MONDO,disease,DISEASE_4149
4150,4150,4150,4150,4150,4150,4150,4150,MONDO:0016151,qualitative or quantitative defects of perlecan,MONDO,disease,DISEASE_4150
4151,4151,4151,4151,4151,4151,4151,4151,MONDO:0014263,8q24.3 microdeletion syndrome,MONDO,disease,DISEASE_4151
4152,4152,4152,4152,4152,4152,4152,4152,MONDO:0850070,CADINS disease,MONDO,disease,DISEASE_4152
4153,4153,4153,4153,4153,4153,4153,4153,MONDO:0700051,liver abscess (disease),MONDO,disease,DISEASE_4153
4154,4154,4154,4154,4154,4154,4154,4154,MONDO:0859289_MONDO:0021189,intestinal dysmotility syndrome,MONDO_grouped,disease,DISEASE_4154
4155,4155,4155,4155,4155,4155,4155,4155,MONDO:0015494,isolated dystonia,MONDO,disease,DISEASE_4155
4156,4156,4156,4156,4156,4156,4156,4156,MONDO:0018424,inherited lipoic acid biosynthesis defect,MONDO,disease,DISEASE_4156
4157,4157,4157,4157,4157,4157,4157,4157,MONDO:1010244,"L-2-hydroxyglutaricacidemia, non-human animal",MONDO,disease,DISEASE_4157
4158,4158,4158,4158,4158,4158,4158,4158,MONDO:0850618,injection anthrax,MONDO,disease,DISEASE_4158
4159,4159,4159,4159,4159,4159,4159,4159,MONDO:0008751,corticosterone methyloxidase type 1 deficiency,MONDO,disease,DISEASE_4159
4160,4160,4160,4160,4160,4160,4160,4160,MONDO:0017933,hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation,MONDO,disease,DISEASE_4160
4161,4161,4161,4161,4161,4161,4161,4161,MONDO:0021068,ovarian neoplasm,MONDO,disease,DISEASE_4161
4162,4162,4162,4162,4162,4162,4162,4162,MONDO:0014160,TCR-alpha-beta-positive T-cell deficiency,MONDO,disease,DISEASE_4162
4163,4163,4163,4163,4163,4163,4163,4163,MONDO:0958017_MONDO:0030726_MONDO:0032899_MONDO:0042490_MONDO:0957809_MONDO:0013139,"neutropenia, severe congenital, 11, autosomal dominant",MONDO_grouped,disease,DISEASE_4163
4164,4164,4164,4164,4164,4164,4164,4164,MONDO:0007144,"aortic arch interruption, facial palsy, and retinal coloboma",MONDO,disease,DISEASE_4164
4165,4165,4165,4165,4165,4165,4165,4165,MONDO:0971062,developmental delay-language impairment-dopa responsive dystonia-parkinsonism syndrome due to a NR4A2 point mutation,MONDO,disease,DISEASE_4165
4166,4166,4166,4166,4166,4166,4166,4166,MONDO:0002967,dermatophytosis of scalp or beard,MONDO,disease,DISEASE_4166
4167,4167,4167,4167,4167,4167,4167,4167,MONDO:0005606_MONDO:0024660,tubular adenocarcinoma,MONDO_grouped,disease,DISEASE_4167
4168,4168,4168,4168,4168,4168,4168,4168,MONDO:0100467_MONDO:0013817_MONDO:0012266_MONDO:0012264_MONDO:0012265,preeclampsia/eclampsia,MONDO_grouped,disease,DISEASE_4168
4169,4169,4169,4169,4169,4169,4169,4169,MONDO:0859324,"developmental delay, language impairment, and ocular abnormalities",MONDO,disease,DISEASE_4169
4170,4170,4170,4170,4170,4170,4170,4170,MONDO:0060688,"hyperthyroxinemia, euthyroid, caused by generalized 5-prime-deiodinase deficiency",MONDO,disease,DISEASE_4170
4171,4171,4171,4171,4171,4171,4171,4171,MONDO:0007430,dens evaginatus,MONDO,disease,DISEASE_4171
4172,4172,4172,4172,4172,4172,4172,4172,MONDO:0011049,Fine-Lubinsky syndrome,MONDO,disease,DISEASE_4172
4173,4173,4173,4173,4173,4173,4173,4173,MONDO:1012973_MONDO:1011940_MONDO:1011991_MONDO:1011656,"skeletal dysplasia, non-human animal",MONDO_grouped,disease,DISEASE_4173
4174,4174,4174,4174,4174,4174,4174,4174,MONDO:0018064,trigonocephaly-broad thumbs syndrome,MONDO,disease,DISEASE_4174
4175,4175,4175,4175,4175,4175,4175,4175,MONDO:0001881,toxic shock syndrome,MONDO,disease,DISEASE_4175
4176,4176,4176,4176,4176,4176,4176,4176,MONDO:0010716,X-linked lethal multiple pterygium syndrome,MONDO,disease,DISEASE_4176
4177,4177,4177,4177,4177,4177,4177,4177,MONDO:0859194,Boudin-Mortier syndrome,MONDO,disease,DISEASE_4177
4178,4178,4178,4178,4178,4178,4178,4178,MONDO:0011462,pyogenic arthritis-pyoderma gangrenosum-acne syndrome,MONDO,disease,DISEASE_4178
4179,4179,4179,4179,4179,4179,4179,4179,MONDO:0023226,gershinibaruch Leibo syndrome,MONDO,disease,DISEASE_4179
4180,4180,4180,4180,4180,4180,4180,4180,MONDO:0006845_MONDO:0006758,male genital tuberculosis,MONDO_grouped,disease,DISEASE_4180
4181,4181,4181,4181,4181,4181,4181,4181,MONDO:0010748,torticollis-keloids-cryptorchidism-renal dysplasia syndrome,MONDO,disease,DISEASE_4181
4182,4182,4182,4182,4182,4182,4182,4182,MONDO:1010236,"syringomyelia, non-human animal",MONDO,disease,DISEASE_4182
4183,4183,4183,4183,4183,4183,4183,4183,MONDO:0007918,"microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability",MONDO,disease,DISEASE_4183
4184,4184,4184,4184,4184,4184,4184,4184,MONDO:0016460,polyvalvular heart disease syndrome,MONDO,disease,DISEASE_4184
4185,4185,4185,4185,4185,4185,4185,4185,MONDO:0021175,herpetic vulvovaginitis,MONDO,disease,DISEASE_4185
4186,4186,4186,4186,4186,4186,4186,4186,MONDO:0019555,panniculitis and localized lipodystrophy,MONDO,disease,DISEASE_4186
4187,4187,4187,4187,4187,4187,4187,4187,MONDO:0018233,otopalatodigital syndrome spectrum disorder,MONDO,disease,DISEASE_4187
4188,4188,4188,4188,4188,4188,4188,4188,MONDO:0012006,craniosynostosis with ocular abnormalities and hallucal defects,MONDO,disease,DISEASE_4188
4189,4189,4189,4189,4189,4189,4189,4189,MONDO:0009830,parkinsonian-pyramidal syndrome,MONDO,disease,DISEASE_4189
4190,4190,4190,4190,4190,4190,4190,4190,MONDO:0009211,congenital factor VII deficiency,MONDO,disease,DISEASE_4190
4191,4191,4191,4191,4191,4191,4191,4191,MONDO:1010741,"autoimmune lymphoproliferative syndrome, domestic cat",MONDO,disease,DISEASE_4191
4192,4192,4192,4192,4192,4192,4192,4192,MONDO:1012899,"hydrallantois, SLC12A1-related, cattle",MONDO,disease,DISEASE_4192
4193,4193,4193,4193,4193,4193,4193,4193,MONDO:1040026,metastatic malignant neoplasm in the brain,MONDO,disease,DISEASE_4193
4194,4194,4194,4194,4194,4194,4194,4194,MONDO:0002735,anal canal adenocarcinoma,MONDO,disease,DISEASE_4194
4195,4195,4195,4195,4195,4195,4195,4195,MONDO:0016464_MONDO:0012520,insulin-resistance syndrome,MONDO_grouped,disease,DISEASE_4195
4196,4196,4196,4196,4196,4196,4196,4196,MONDO:0005806,hypopharynx cancer,MONDO,disease,DISEASE_4196
4197,4197,4197,4197,4197,4197,4197,4197,MONDO:0007773,hyperproglucagonemia,MONDO,disease,DISEASE_4197
4198,4198,4198,4198,4198,4198,4198,4198,MONDO:0957544_MONDO:0014312_MONDO:0011234_MONDO:0957543_MONDO:0013845_MONDO:0000107,auriculocondylar syndrome,MONDO_grouped,disease,DISEASE_4198
4199,4199,4199,4199,4199,4199,4199,4199,MONDO:0016654,ring chromosome 5,MONDO,disease,DISEASE_4199
4200,4200,4200,4200,4200,4200,4200,4200,MONDO:0007181,axial osteomalacia,MONDO,disease,DISEASE_4200
4201,4201,4201,4201,4201,4201,4201,4201,MONDO:1010580,"familial goiter, golden hamster",MONDO,disease,DISEASE_4201
4202,4202,4202,4202,4202,4202,4202,4202,MONDO:0020257,supranuclear oculomotor palsy,MONDO,disease,DISEASE_4202
4203,4203,4203,4203,4203,4203,4203,4203,MONDO:0002307_MONDO:0002306,blepharoconjunctivitis,MONDO_grouped,disease,DISEASE_4203
4204,4204,4204,4204,4204,4204,4204,4204,MONDO:1012660,"mucolipidosis, GNPTAB-related, domestic cat",MONDO,disease,DISEASE_4204
4205,4205,4205,4205,4205,4205,4205,4205,MONDO:0002496,submucosal invasive colon adenocarcinoma,MONDO,disease,DISEASE_4205
4206,4206,4206,4206,4206,4206,4206,4206,MONDO:0022733,choreoacanthocytosis amyotrophic,MONDO,disease,DISEASE_4206
4207,4207,4207,4207,4207,4207,4207,4207,MONDO:0003068,postauricular lymphadenitis,MONDO,disease,DISEASE_4207
4208,4208,4208,4208,4208,4208,4208,4208,MONDO:0008578,"toe, rotated fifth",MONDO,disease,DISEASE_4208
4209,4209,4209,4209,4209,4209,4209,4209,MONDO:1012530,"cavitating leukodystrophy, dog",MONDO,disease,DISEASE_4209
4210,4210,4210,4210,4210,4210,4210,4210,MONDO:0007107,"anal sphincter myopathy, internal",MONDO,disease,DISEASE_4210
4211,4211,4211,4211,4211,4211,4211,4211,MONDO:0009773_MONDO:0017134,odonto-onycho-dermal dysplasia,MONDO_grouped,disease,DISEASE_4211
4212,4212,4212,4212,4212,4212,4212,4212,MONDO:1012900,"xanthinuria, XDH-related, dog",MONDO,disease,DISEASE_4212
4213,4213,4213,4213,4213,4213,4213,4213,MONDO:0033261,"hearing loss, autosomal dominant 34, with or without inflammation",MONDO,disease,DISEASE_4213
4214,4214,4214,4214,4214,4214,4214,4214,MONDO:1011548_MONDO:1011549,"junctionalis epidermolysis bullosa, dog",MONDO_grouped,disease,DISEASE_4214
4215,4215,4215,4215,4215,4215,4215,4215,MONDO:0045048,toxemia of pregnancy,MONDO,disease,DISEASE_4215
4216,4216,4216,4216,4216,4216,4216,4216,MONDO:0019819,double-orifice mitral valve,MONDO,disease,DISEASE_4216
4217,4217,4217,4217,4217,4217,4217,4217,MONDO:0011539_MONDO:0014513_MONDO:0014326_MONDO:0012237_MONDO:0009725_MONDO:0012538_MONDO:0014138_MONDO:0018958,nemaline myopathy,MONDO_grouped,disease,DISEASE_4217
4218,4218,4218,4218,4218,4218,4218,4218,MONDO:0800039,MELAS syndrome caused by mutation in MTND5,MONDO,disease,DISEASE_4218
4219,4219,4219,4219,4219,4219,4219,4219,MONDO:0957997,"diabetes, deafness, developmental delay, and short stature syndrome",MONDO,disease,DISEASE_4219
4220,4220,4220,4220,4220,4220,4220,4220,MONDO:0004532,auditory system cancer,MONDO,disease,DISEASE_4220
4221,4221,4221,4221,4221,4221,4221,4221,MONDO:0024388,Clostridium infectious disease,MONDO,disease,DISEASE_4221
4222,4222,4222,4222,4222,4222,4222,4222,MONDO:0002332_MONDO:0005966,splenic disorder,MONDO_grouped,disease,DISEASE_4222
4223,4223,4223,4223,4223,4223,4223,4223,MONDO:0001396,abnormal threshold of rods,MONDO,disease,DISEASE_4223
4224,4224,4224,4224,4224,4224,4224,4224,MONDO:0021762,acrocoxomesomelic dysplasia,MONDO,disease,DISEASE_4224
4225,4225,4225,4225,4225,4225,4225,4225,MONDO:1012206,"paroxysm, chicken",MONDO,disease,DISEASE_4225
4226,4226,4226,4226,4226,4226,4226,4226,MONDO:0019942,distal arthrogryposis,MONDO,disease,DISEASE_4226
4227,4227,4227,4227,4227,4227,4227,4227,MONDO:0017618,congenital sucrase-isomaltase deficiency with starch intolerance,MONDO,disease,DISEASE_4227
4228,4228,4228,4228,4228,4228,4228,4228,MONDO:1012713,"benign familial juvenile epilepsy, LGI2-related, dog",MONDO,disease,DISEASE_4228
4229,4229,4229,4229,4229,4229,4229,4229,MONDO:0024298,vitamin deficiency disorder,MONDO,disease,DISEASE_4229
4230,4230,4230,4230,4230,4230,4230,4230,MONDO:0016096,malignant non-dysgerminomatous germ cell tumor of ovary,MONDO,disease,DISEASE_4230
4231,4231,4231,4231,4231,4231,4231,4231,MONDO:0027696,voriconazole toxicity,MONDO,disease,DISEASE_4231
4232,4232,4232,4232,4232,4232,4232,4232,MONDO:0015848,obsolete septate vagina,MONDO,disease,DISEASE_4232
4233,4233,4233,4233,4233,4233,4233,4233,MONDO:0018092,Vogt-Koyanagi-Harada disease,MONDO,disease,DISEASE_4233
4234,4234,4234,4234,4234,4234,4234,4234,MONDO:0021130,disorder of sphingolipid biosynthesis,MONDO,disease,DISEASE_4234
4235,4235,4235,4235,4235,4235,4235,4235,MONDO:0019112,cancer-associated retinopathy,MONDO,disease,DISEASE_4235
4236,4236,4236,4236,4236,4236,4236,4236,MONDO:0006344,ovarian yolk sac tumor,MONDO,disease,DISEASE_4236
4237,4237,4237,4237,4237,4237,4237,4237,MONDO:0044739,Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome,MONDO,disease,DISEASE_4237
4238,4238,4238,4238,4238,4238,4238,4238,MONDO:0014925_MONDO:0024556_MONDO:0014924_MONDO:0054776_MONDO:0020310,"epilepsy, familial focal, with variable foci",MONDO_grouped,disease,DISEASE_4238
4239,4239,4239,4239,4239,4239,4239,4239,MONDO:0850286,exercise-induced bronchoconstriction,MONDO,disease,DISEASE_4239
4240,4240,4240,4240,4240,4240,4240,4240,MONDO:0021157,gonococcal cervicitis,MONDO,disease,DISEASE_4240
4241,4241,4241,4241,4241,4241,4241,4241,MONDO:0018956,idiopathic bronchiectasis,MONDO,disease,DISEASE_4241
4242,4242,4242,4242,4242,4242,4242,4242,MONDO:0008256,platelet membrane fluidity,MONDO,disease,DISEASE_4242
4243,4243,4243,4243,4243,4243,4243,4243,MONDO:1012305,"hypocatalasia, dog",MONDO,disease,DISEASE_4243
4244,4244,4244,4244,4244,4244,4244,4244,MONDO:8000023,type 3 autoimmune lymphoproliferative syndrome,MONDO,disease,DISEASE_4244
4245,4245,4245,4245,4245,4245,4245,4245,MONDO:0005663,Barre-Lieou syndrome,MONDO,disease,DISEASE_4245
4246,4246,4246,4246,4246,4246,4246,4246,MONDO:0002051_MONDO:0000653,integumentary system disorder,MONDO_grouped,disease,DISEASE_4246
4247,4247,4247,4247,4247,4247,4247,4247,MONDO:0019672,fibular hemimelia,MONDO,disease,DISEASE_4247
4248,4248,4248,4248,4248,4248,4248,4248,MONDO:0019083,Leigh syndrome with cardiomyopathy,MONDO,disease,DISEASE_4248
4249,4249,4249,4249,4249,4249,4249,4249,MONDO:0016416,diphallia,MONDO,disease,DISEASE_4249
4250,4250,4250,4250,4250,4250,4250,4250,MONDO:0016824,infantile myofibromatosis,MONDO,disease,DISEASE_4250
4251,4251,4251,4251,4251,4251,4251,4251,MONDO:0700114,"vector-borne disease, non-human animal",MONDO,disease,DISEASE_4251
4252,4252,4252,4252,4252,4252,4252,4252,MONDO:0016749,tumor of cranial and spinal nerves,MONDO,disease,DISEASE_4252
4253,4253,4253,4253,4253,4253,4253,4253,MONDO:0008735,adrenocortical unresponsiveness to ACTH with postreceptor defect,MONDO,disease,DISEASE_4253
4254,4254,4254,4254,4254,4254,4254,4254,MONDO:0017404,distal Xq28 microduplication syndrome,MONDO,disease,DISEASE_4254
4255,4255,4255,4255,4255,4255,4255,4255,MONDO:0019311,wooly hair nevus,MONDO,disease,DISEASE_4255
4256,4256,4256,4256,4256,4256,4256,4256,MONDO:1011965,"disproportionate short-limbed chondrodysplasia, non-human animal",MONDO,disease,DISEASE_4256
4257,4257,4257,4257,4257,4257,4257,4257,MONDO:1010996,"spinal muscular atrophy, domestic cat",MONDO,disease,DISEASE_4257
4258,4258,4258,4258,4258,4258,4258,4258,MONDO:0004687,severe nonproliferative diabetic retinopathy,MONDO,disease,DISEASE_4258
4259,4259,4259,4259,4259,4259,4259,4259,MONDO:0000839,obsolete congenital abnormality,MONDO,disease,DISEASE_4259
4260,4260,4260,4260,4260,4260,4260,4260,MONDO:0005786,Hepadnaviridae infectious disease,MONDO,disease,DISEASE_4260
4261,4261,4261,4261,4261,4261,4261,4261,MONDO:0022934,Davis Lafer syndrome,MONDO,disease,DISEASE_4261
4262,4262,4262,4262,4262,4262,4262,4262,MONDO:0006521,acneiform dermatitis,MONDO,disease,DISEASE_4262
4263,4263,4263,4263,4263,4263,4263,4263,MONDO:0016601,adult-onset citrullinemia type I,MONDO,disease,DISEASE_4263
4264,4264,4264,4264,4264,4264,4264,4264,MONDO:0019716,overgrowth syndrome,MONDO,disease,DISEASE_4264
4265,4265,4265,4265,4265,4265,4265,4265,MONDO:0100100,SELENON-related myopathy,MONDO,disease,DISEASE_4265
4266,4266,4266,4266,4266,4266,4266,4266,MONDO:0014562,neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome,MONDO,disease,DISEASE_4266
4267,4267,4267,4267,4267,4267,4267,4267,MONDO:0018330,mucinous adenocarcinoma of the appendix,MONDO,disease,DISEASE_4267
4268,4268,4268,4268,4268,4268,4268,4268,MONDO:0968959,isolated arhinencephaly,MONDO,disease,DISEASE_4268
4269,4269,4269,4269,4269,4269,4269,4269,MONDO:0018741,paracetamol poisoning,MONDO,disease,DISEASE_4269
4270,4270,4270,4270,4270,4270,4270,4270,MONDO:0002328,intracranial hemangioma,MONDO,disease,DISEASE_4270
4271,4271,4271,4271,4271,4271,4271,4271,MONDO:1011436,"histiocytosis, non-human animal",MONDO,disease,DISEASE_4271
4272,4272,4272,4272,4272,4272,4272,4272,MONDO:0018173,acute opioid poisoning,MONDO,disease,DISEASE_4272
4273,4273,4273,4273,4273,4273,4273,4273,MONDO:0014793,microcephaly-congenital cataract-psoriasiform dermatitis syndrome,MONDO,disease,DISEASE_4273
4274,4274,4274,4274,4274,4274,4274,4274,MONDO:0000650,peritoneal benign neoplasm,MONDO,disease,DISEASE_4274
4275,4275,4275,4275,4275,4275,4275,4275,MONDO:0006137,cervical intraepithelial neoplasia grade 2/3,MONDO,disease,DISEASE_4275
4276,4276,4276,4276,4276,4276,4276,4276,MONDO:0016856,Mowat-Wilson syndrome due to a ZEB2 point mutation,MONDO,disease,DISEASE_4276
4277,4277,4277,4277,4277,4277,4277,4277,MONDO:0018617,baroreflex failure,MONDO,disease,DISEASE_4277
4278,4278,4278,4278,4278,4278,4278,4278,MONDO:0004406,adult central nervous system mixed germ cell tumor,MONDO,disease,DISEASE_4278
4279,4279,4279,4279,4279,4279,4279,4279,MONDO:0700151,canine glioma,MONDO,disease,DISEASE_4279
4280,4280,4280,4280,4280,4280,4280,4280,MONDO:0100049_MONDO:0011607_MONDO:0012898_MONDO:0013020_MONDO:0013639,"narcolepsy, susceptibility to",MONDO_grouped,disease,DISEASE_4280
4281,4281,4281,4281,4281,4281,4281,4281,MONDO:0009067_MONDO:0019745_MONDO:0019746,cystinuria,MONDO_grouped,disease,DISEASE_4281
4282,4282,4282,4282,4282,4282,4282,4282,MONDO:0016112_MONDO:0017931,hereditary inclusion-body myopathy,MONDO_grouped,disease,DISEASE_4282
4283,4283,4283,4283,4283,4283,4283,4283,MONDO:0018900,corticosteroid-sensitive aseptic abscess syndrome,MONDO,disease,DISEASE_4283
4284,4284,4284,4284,4284,4284,4284,4284,MONDO:0011782,angioid streaks,MONDO,disease,DISEASE_4284
4285,4285,4285,4285,4285,4285,4285,4285,MONDO:0100430,fibrotic liver disease,MONDO,disease,DISEASE_4285
4286,4286,4286,4286,4286,4286,4286,4286,MONDO:0022603,brachydactyly tibial hypoplasia,MONDO,disease,DISEASE_4286
4287,4287,4287,4287,4287,4287,4287,4287,MONDO:0011919_MONDO:0013303_MONDO:0012027_MONDO:0012028_MONDO:0012263_MONDO:0800274,"autoimmune disease, susceptibility to",MONDO_grouped,disease,DISEASE_4287
4288,4288,4288,4288,4288,4288,4288,4288,MONDO:0002619_MONDO:0003720_MONDO:0003728_MONDO:0003742_MONDO:0004435,bone fibrosarcoma,MONDO_grouped,disease,DISEASE_4288
4289,4289,4289,4289,4289,4289,4289,4289,MONDO:0016345,non-familial restrictive cardiomyopathy,MONDO,disease,DISEASE_4289
4290,4290,4290,4290,4290,4290,4290,4290,MONDO:0012907,blindness - scoliosis - arachnodactyly syndrome,MONDO,disease,DISEASE_4290
4291,4291,4291,4291,4291,4291,4291,4291,MONDO:0005814_MONDO:0005020_MONDO:0000916_MONDO:0001678,intestinal cancer,MONDO_grouped,disease,DISEASE_4291
4292,4292,4292,4292,4292,4292,4292,4292,MONDO:0005392,scoliosis,MONDO,disease,DISEASE_4292
4293,4293,4293,4293,4293,4293,4293,4293,MONDO:0001023,prolymphocytic leukemia,MONDO,disease,DISEASE_4293
4294,4294,4294,4294,4294,4294,4294,4294,MONDO:0003615,nerve compression syndrome,MONDO,disease,DISEASE_4294
4295,4295,4295,4295,4295,4295,4295,4295,MONDO:1010470,"persistent truncus arteriosus, alpaca",MONDO,disease,DISEASE_4295
4296,4296,4296,4296,4296,4296,4296,4296,MONDO:0001813,squamous blepharitis,MONDO,disease,DISEASE_4296
4297,4297,4297,4297,4297,4297,4297,4297,MONDO:0011009,"muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers",MONDO,disease,DISEASE_4297
4298,4298,4298,4298,4298,4298,4298,4298,MONDO:0100228,LAMA2-related muscular dystrophy,MONDO,disease,DISEASE_4298
4299,4299,4299,4299,4299,4299,4299,4299,MONDO:1010631,"Chediak-Higashi syndrome, cattle",MONDO,disease,DISEASE_4299
4300,4300,4300,4300,4300,4300,4300,4300,MONDO:0003988,sternum lymphoma,MONDO,disease,DISEASE_4300
4301,4301,4301,4301,4301,4301,4301,4301,MONDO:1012939,"perinatal mortality syndrome, GCK-related, cattle",MONDO,disease,DISEASE_4301
4302,4302,4302,4302,4302,4302,4302,4302,MONDO:1010943_MONDO:1010944_MONDO:1010945,"mycosis fungoides, dog",MONDO_grouped,disease,DISEASE_4302
4303,4303,4303,4303,4303,4303,4303,4303,MONDO:0005242,empyema,MONDO,disease,DISEASE_4303
4304,4304,4304,4304,4304,4304,4304,4304,MONDO:0007071,"adrenocortical hypofunction, chronic primary congenital",MONDO,disease,DISEASE_4304
4305,4305,4305,4305,4305,4305,4305,4305,MONDO:0020044_MONDO:0020046,autosomal recessive metabolic cerebellar ataxia,MONDO_grouped,disease,DISEASE_4305
4306,4306,4306,4306,4306,4306,4306,4306,MONDO:0032925,"respiratory papillomatosis, juvenile recurrent, congenital",MONDO,disease,DISEASE_4306
4307,4307,4307,4307,4307,4307,4307,4307,MONDO:0007132,anonychia-ectrodactyly,MONDO,disease,DISEASE_4307
4308,4308,4308,4308,4308,4308,4308,4308,MONDO:0008348,pulmonary nodular lymphoid hyperplasia,MONDO,disease,DISEASE_4308
4309,4309,4309,4309,4309,4309,4309,4309,MONDO:0001954,thrombophlebitis migrans,MONDO,disease,DISEASE_4309
4310,4310,4310,4310,4310,4310,4310,4310,MONDO:0858958,high-grade astrocytoma with piloid features,MONDO,disease,DISEASE_4310
4311,4311,4311,4311,4311,4311,4311,4311,MONDO:0002076,pneumothorax,MONDO,disease,DISEASE_4311
4312,4312,4312,4312,4312,4312,4312,4312,MONDO:0004984,basal-like breast carcinoma,MONDO,disease,DISEASE_4312
4313,4313,4313,4313,4313,4313,4313,4313,MONDO:0004849,pulmonary emphysema,MONDO,disease,DISEASE_4313
4314,4314,4314,4314,4314,4314,4314,4314,MONDO:0024432,nerve plexus disorder,MONDO,disease,DISEASE_4314
4315,4315,4315,4315,4315,4315,4315,4315,MONDO:0016669,sickle cell-hemoglobin c disease syndrome,MONDO,disease,DISEASE_4315
4316,4316,4316,4316,4316,4316,4316,4316,MONDO:0020649,warty carcinoma of the penis,MONDO,disease,DISEASE_4316
4317,4317,4317,4317,4317,4317,4317,4317,MONDO:0003695_MONDO:0006045_MONDO:0003922_MONDO:0004222,ovarian clear cell adenofibroma,MONDO_grouped,disease,DISEASE_4317
4318,4318,4318,4318,4318,4318,4318,4318,MONDO:0006800,ideomotor apraxia,MONDO,disease,DISEASE_4318
4319,4319,4319,4319,4319,4319,4319,4319,MONDO:0011514,tricuspid atresia,MONDO,disease,DISEASE_4319
4320,4320,4320,4320,4320,4320,4320,4320,MONDO:0017201,Spasmus nutans,MONDO,disease,DISEASE_4320
4321,4321,4321,4321,4321,4321,4321,4321,MONDO:0008592,tricho-dento-osseous syndrome,MONDO,disease,DISEASE_4321
4322,4322,4322,4322,4322,4322,4322,4322,MONDO:0021131,frontal lobe ependymal tumor,MONDO,disease,DISEASE_4322
4323,4323,4323,4323,4323,4323,4323,4323,MONDO:0011150,acroosteolysis-keloid-like lesions-premature aging syndrome,MONDO,disease,DISEASE_4323
4324,4324,4324,4324,4324,4324,4324,4324,MONDO:1011156,"Marfan syndrome, cattle",MONDO,disease,DISEASE_4324
4325,4325,4325,4325,4325,4325,4325,4325,MONDO:0004182,stage IVb bladder cancer,MONDO,disease,DISEASE_4325
4326,4326,4326,4326,4326,4326,4326,4326,MONDO:0024291,vascular malformation,MONDO,disease,DISEASE_4326
4327,4327,4327,4327,4327,4327,4327,4327,MONDO:1011994,"fluoroquinolone-induced retinal degeneration, non-human animal",MONDO,disease,DISEASE_4327
4328,4328,4328,4328,4328,4328,4328,4328,MONDO:0100548,SERAC1-related neurological disorder,MONDO,disease,DISEASE_4328
4329,4329,4329,4329,4329,4329,4329,4329,MONDO:0011340_MONDO:0019804_MONDO:0015395,congenital tracheal stenosis,MONDO_grouped,disease,DISEASE_4329
4330,4330,4330,4330,4330,4330,4330,4330,MONDO:0025389,"brucellosis, bovine",MONDO,disease,DISEASE_4330
4331,4331,4331,4331,4331,4331,4331,4331,MONDO:0020459,unstable hemoglobin disease,MONDO,disease,DISEASE_4331
4332,4332,4332,4332,4332,4332,4332,4332,MONDO:0035161,progressive dementia with neuroserpin inclusion bodies,MONDO,disease,DISEASE_4332
4333,4333,4333,4333,4333,4333,4333,4333,MONDO:0009605,methemoglobinemia type 4,MONDO,disease,DISEASE_4333
4334,4334,4334,4334,4334,4334,4334,4334,MONDO:1012515,"pectinate ligament dysplasia, dog",MONDO,disease,DISEASE_4334
4335,4335,4335,4335,4335,4335,4335,4335,MONDO:0005638,agnosia,MONDO,disease,DISEASE_4335
4336,4336,4336,4336,4336,4336,4336,4336,MONDO:0100405,"acute myeloid leukemia, Non-KMT2A MLLT10 rearrangement positive",MONDO,disease,DISEASE_4336
4337,4337,4337,4337,4337,4337,4337,4337,MONDO:0011998,autosomal dominant slowed nerve conduction velocity,MONDO,disease,DISEASE_4337
4338,4338,4338,4338,4338,4338,4338,4338,MONDO:1040019,Enterococcus infectious disease,MONDO,disease,DISEASE_4338
4339,4339,4339,4339,4339,4339,4339,4339,MONDO:0002853,rectum rhabdomyosarcoma,MONDO,disease,DISEASE_4339
4340,4340,4340,4340,4340,4340,4340,4340,MONDO:0004488,cervical atypical polypoid adenomyoma,MONDO,disease,DISEASE_4340
4341,4341,4341,4341,4341,4341,4341,4341,MONDO:0018823,X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome,MONDO,disease,DISEASE_4341
4342,4342,4342,4342,4342,4342,4342,4342,MONDO:0002846_MONDO:0003052,granulomatous gastritis,MONDO_grouped,disease,DISEASE_4342
4343,4343,4343,4343,4343,4343,4343,4343,MONDO:0004067,gallbladder mucinous adenocarcinoma,MONDO,disease,DISEASE_4343
4344,4344,4344,4344,4344,4344,4344,4344,MONDO:0010063,corneal-cerebellar syndrome,MONDO,disease,DISEASE_4344
4345,4345,4345,4345,4345,4345,4345,4345,MONDO:1011691,"platelet function defect, non-human animal",MONDO,disease,DISEASE_4345
4346,4346,4346,4346,4346,4346,4346,4346,MONDO:0020407,complete atrioventricular canal-ventricle hypoplasia syndrome,MONDO,disease,DISEASE_4346
4347,4347,4347,4347,4347,4347,4347,4347,MONDO:0020746,"contractures, pterygia, and variable skeletal fusions syndrome 1B",MONDO,disease,DISEASE_4347
4348,4348,4348,4348,4348,4348,4348,4348,MONDO:0958075,intramedullary non-dysraphic spinal cord lipoma,MONDO,disease,DISEASE_4348
4349,4349,4349,4349,4349,4349,4349,4349,MONDO:0000463,Ochoa syndrome,MONDO,disease,DISEASE_4349
4350,4350,4350,4350,4350,4350,4350,4350,MONDO:0023696,Marinesco-Sjogren-like syndrome,MONDO,disease,DISEASE_4350
4351,4351,4351,4351,4351,4351,4351,4351,MONDO:1011331_MONDO:1011404,"metabolic disease, non-human animal",MONDO_grouped,disease,DISEASE_4351
4352,4352,4352,4352,4352,4352,4352,4352,MONDO:0012496,Koolen-de Vries syndrome,MONDO,disease,DISEASE_4352
4353,4353,4353,4353,4353,4353,4353,4353,MONDO:0010061,autosomal recessive cerebellar ataxia-blindness-deafness syndrome,MONDO,disease,DISEASE_4353
4354,4354,4354,4354,4354,4354,4354,4354,MONDO:0044627,acute macular neuroretinopathy,MONDO,disease,DISEASE_4354
4355,4355,4355,4355,4355,4355,4355,4355,MONDO:0013851,autosomal dominant aplasia and myelodysplasia,MONDO,disease,DISEASE_4355
4356,4356,4356,4356,4356,4356,4356,4356,MONDO:1012674_MONDO:1012721_MONDO:1012922,"centronuclear myopathy, HACD1-related, dog",MONDO_grouped,disease,DISEASE_4356
4357,4357,4357,4357,4357,4357,4357,4357,MONDO:0016923,partial duplication of chromosome 3,MONDO,disease,DISEASE_4357
4358,4358,4358,4358,4358,4358,4358,4358,MONDO:0004699_MONDO:0006231,gastrointestinal lymphoma,MONDO_grouped,disease,DISEASE_4358
4359,4359,4359,4359,4359,4359,4359,4359,MONDO:1010861,"lysosomal storage disease, domestic cat",MONDO,disease,DISEASE_4359
4360,4360,4360,4360,4360,4360,4360,4360,MONDO:1011726,"immunoglobulin A deficiency, non-human animal",MONDO,disease,DISEASE_4360
4361,4361,4361,4361,4361,4361,4361,4361,MONDO:0007347,obsolete Coxsackievirus B3 susceptibility,MONDO,disease,DISEASE_4361
4362,4362,4362,4362,4362,4362,4362,4362,MONDO:0010378_MONDO:0015354,X-linked hereditary sensory and autonomic neuropathy with hearing loss,MONDO_grouped,disease,DISEASE_4362
4363,4363,4363,4363,4363,4363,4363,4363,MONDO:1010926_MONDO:1012684,"congenital muscular dystonia, ATP2A1-related, cattle",MONDO_grouped,disease,DISEASE_4363
4364,4364,4364,4364,4364,4364,4364,4364,MONDO:0000673,integrative agnosia,MONDO,disease,DISEASE_4364
4365,4365,4365,4365,4365,4365,4365,4365,MONDO:0002626,spinal accessory nerve neoplasm,MONDO,disease,DISEASE_4365
4366,4366,4366,4366,4366,4366,4366,4366,MONDO:0024659,colorectal Kaposi sarcoma,MONDO,disease,DISEASE_4366
4367,4367,4367,4367,4367,4367,4367,4367,MONDO:0001290,allergic cutaneous vasculitis,MONDO,disease,DISEASE_4367
4368,4368,4368,4368,4368,4368,4368,4368,MONDO:0009312,lipodystrophy due to peptidic growth factors deficiency,MONDO,disease,DISEASE_4368
4369,4369,4369,4369,4369,4369,4369,4369,MONDO:0004494,"testicular yolk sac tumor, hepatoid pattern",MONDO,disease,DISEASE_4369
4370,4370,4370,4370,4370,4370,4370,4370,MONDO:0010854,Toriello-Lacassie-Droste syndrome,MONDO,disease,DISEASE_4370
4371,4371,4371,4371,4371,4371,4371,4371,MONDO:0009546,macrosomia adiposa congenita,MONDO,disease,DISEASE_4371
4372,4372,4372,4372,4372,4372,4372,4372,MONDO:0021250,tonsil neoplasm,MONDO,disease,DISEASE_4372
4373,4373,4373,4373,4373,4373,4373,4373,MONDO:0009323,Halothane hepatitis,MONDO,disease,DISEASE_4373
4374,4374,4374,4374,4374,4374,4374,4374,MONDO:0000328_MONDO:1010719,hyperphosphatemia,MONDO_grouped,disease,DISEASE_4374
4375,4375,4375,4375,4375,4375,4375,4375,MONDO:0024279_MONDO:0005001,chronic endometritis,MONDO_grouped,disease,DISEASE_4375
4376,4376,4376,4376,4376,4376,4376,4376,MONDO:1012547,"vitreous degeneration, dog",MONDO,disease,DISEASE_4376
4377,4377,4377,4377,4377,4377,4377,4377,MONDO:0007399,TWIST1-related craniosynostosis,MONDO,disease,DISEASE_4377
4378,4378,4378,4378,4378,4378,4378,4378,MONDO:0001401,female breast nipple and areola cancer,MONDO,disease,DISEASE_4378
4379,4379,4379,4379,4379,4379,4379,4379,MONDO:0021207_MONDO:0000708,Crohn jejunitis,MONDO_grouped,disease,DISEASE_4379
4380,4380,4380,4380,4380,4380,4380,4380,MONDO:0018435,acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2),MONDO,disease,DISEASE_4380
4381,4381,4381,4381,4381,4381,4381,4381,MONDO:0004341,colloid carcinoma of the pancreas,MONDO,disease,DISEASE_4381
4382,4382,4382,4382,4382,4382,4382,4382,MONDO:0008591,tremor-nystagmus-duodenal ulcer syndrome,MONDO,disease,DISEASE_4382
4383,4383,4383,4383,4383,4383,4383,4383,MONDO:0005961,sinusitis,MONDO,disease,DISEASE_4383
4384,4384,4384,4384,4384,4384,4384,4384,MONDO:1012374,"blindness with enlarged globe, chicken",MONDO,disease,DISEASE_4384
4385,4385,4385,4385,4385,4385,4385,4385,MONDO:0018630,hereditary nonpolyposis colon cancer,MONDO,disease,DISEASE_4385
4386,4386,4386,4386,4386,4386,4386,4386,MONDO:1012081_MONDO:1012082,"tetragametic chimerism, bighorn sheep",MONDO_grouped,disease,DISEASE_4386
4387,4387,4387,4387,4387,4387,4387,4387,MONDO:0021237,adrenal medulla neoplasm,MONDO,disease,DISEASE_4387
4388,4388,4388,4388,4388,4388,4388,4388,MONDO:0001695,senile ectropion,MONDO,disease,DISEASE_4388
4389,4389,4389,4389,4389,4389,4389,4389,MONDO:0001656,megaesophagus,MONDO,disease,DISEASE_4389
4390,4390,4390,4390,4390,4390,4390,4390,MONDO:0002860,testis rhabdomyosarcoma,MONDO,disease,DISEASE_4390
4391,4391,4391,4391,4391,4391,4391,4391,MONDO:0024379,"circadian rhythm sleep disorder, irregular sleep wake type",MONDO,disease,DISEASE_4391
4392,4392,4392,4392,4392,4392,4392,4392,MONDO:0018148,vasoproliferative tumor of retina,MONDO,disease,DISEASE_4392
4393,4393,4393,4393,4393,4393,4393,4393,MONDO:0006912,pneumatosis cystoides intestinalis,MONDO,disease,DISEASE_4393
4394,4394,4394,4394,4394,4394,4394,4394,MONDO:0002105,toxic megacolon,MONDO,disease,DISEASE_4394
4395,4395,4395,4395,4395,4395,4395,4395,MONDO:0001567,nephrocalcinosis,MONDO,disease,DISEASE_4395
4396,4396,4396,4396,4396,4396,4396,4396,MONDO:0007739,Huntington disease,MONDO,disease,DISEASE_4396
4397,4397,4397,4397,4397,4397,4397,4397,MONDO:0015566,2q24 microdeletion syndrome,MONDO,disease,DISEASE_4397
4398,4398,4398,4398,4398,4398,4398,4398,MONDO:0022316,hair defect with photosensitivity and intellectual disability syndrome,MONDO,disease,DISEASE_4398
4399,4399,4399,4399,4399,4399,4399,4399,MONDO:0011577,"myopathy, proximal, and ophthalmoplegia",MONDO,disease,DISEASE_4399
4400,4400,4400,4400,4400,4400,4400,4400,MONDO:0008637,bifid uvula,MONDO,disease,DISEASE_4400
4401,4401,4401,4401,4401,4401,4401,4401,MONDO:0014532,autosomal dominant mitochondrial myopathy with exercise intolerance,MONDO,disease,DISEASE_4401
4402,4402,4402,4402,4402,4402,4402,4402,MONDO:0006382,poorly differentiated thyroid gland carcinoma,MONDO,disease,DISEASE_4402
4403,4403,4403,4403,4403,4403,4403,4403,MONDO:0300000,SSR3-CDG,MONDO,disease,DISEASE_4403
4404,4404,4404,4404,4404,4404,4404,4404,MONDO:0100515,mirror movements 1 and/or agenesis of the corpus callosum,MONDO,disease,DISEASE_4404
4405,4405,4405,4405,4405,4405,4405,4405,MONDO:0011236,hyperinsulinism due to glucokinase deficiency,MONDO,disease,DISEASE_4405
4406,4406,4406,4406,4406,4406,4406,4406,MONDO:0016556,transient congenital hypothyroidism due to neonatal factor,MONDO,disease,DISEASE_4406
4407,4407,4407,4407,4407,4407,4407,4407,MONDO:0971133,isolated segmental infantile hemangioma,MONDO,disease,DISEASE_4407
4408,4408,4408,4408,4408,4408,4408,4408,MONDO:0007697,hand clasping pattern,MONDO,disease,DISEASE_4408
4409,4409,4409,4409,4409,4409,4409,4409,MONDO:0010242,"fetal akinesia syndrome, X-linked",MONDO,disease,DISEASE_4409
4410,4410,4410,4410,4410,4410,4410,4410,MONDO:0019364,pseudotyphus of California,MONDO,disease,DISEASE_4410
4411,4411,4411,4411,4411,4411,4411,4411,MONDO:0017286,tempi syndrome,MONDO,disease,DISEASE_4411
4412,4412,4412,4412,4412,4412,4412,4412,MONDO:0015795,undifferentiated embryonal sarcoma of the liver,MONDO,disease,DISEASE_4412
4413,4413,4413,4413,4413,4413,4413,4413,MONDO:0002345,cervicitis,MONDO,disease,DISEASE_4413
4414,4414,4414,4414,4414,4414,4414,4414,MONDO:0000402,small cell carcinoma,MONDO,disease,DISEASE_4414
4415,4415,4415,4415,4415,4415,4415,4415,MONDO:0013583,occipital pachygyria and polymicrogyria,MONDO,disease,DISEASE_4415
4416,4416,4416,4416,4416,4416,4416,4416,MONDO:0043003,familial acanthosis nigricans,MONDO,disease,DISEASE_4416
4417,4417,4417,4417,4417,4417,4417,4417,MONDO:0043069,Zerres Rietschel Majewski syndrome,MONDO,disease,DISEASE_4417
4418,4418,4418,4418,4418,4418,4418,4418,MONDO:1012812,"leukodystrophy, TSEN54-related, dog",MONDO,disease,DISEASE_4418
4419,4419,4419,4419,4419,4419,4419,4419,MONDO:0017782,developmental and speech delay due to SOX5 deficiency,MONDO,disease,DISEASE_4419
4420,4420,4420,4420,4420,4420,4420,4420,MONDO:1010566,"diabetes insipidus, Japanese quail",MONDO,disease,DISEASE_4420
4421,4421,4421,4421,4421,4421,4421,4421,MONDO:0007351_MONDO:0020356,coloboma of macula,MONDO_grouped,disease,DISEASE_4421
4422,4422,4422,4422,4422,4422,4422,4422,MONDO:0016025,obsolete myoclonic-astatic epilepsy,MONDO,disease,DISEASE_4422
4423,4423,4423,4423,4423,4423,4423,4423,MONDO:0005775,G6PD deficiency,MONDO,disease,DISEASE_4423
4424,4424,4424,4424,4424,4424,4424,4424,MONDO:1010106,"multiple acyl-coa dehydrogenase deficiency, non-human animal",MONDO,disease,DISEASE_4424
4425,4425,4425,4425,4425,4425,4425,4425,MONDO:0037740,"malignant central nervous system mesenchymal, non-meningothelial neoplasm",MONDO,disease,DISEASE_4425
4426,4426,4426,4426,4426,4426,4426,4426,MONDO:0021240,tongue neoplasm,MONDO,disease,DISEASE_4426
4427,4427,4427,4427,4427,4427,4427,4427,MONDO:0009013,"convulsive disorder, familial, with prenatal or early onset",MONDO,disease,DISEASE_4427
4428,4428,4428,4428,4428,4428,4428,4428,MONDO:0030703,autoimmune vasculitis,MONDO,disease,DISEASE_4428
4429,4429,4429,4429,4429,4429,4429,4429,MONDO:0010663,"intellectual disability-hypotonic facies syndrome, X-linked, 1",MONDO,disease,DISEASE_4429
4430,4430,4430,4430,4430,4430,4430,4430,MONDO:0017569,de Barsy syndrome,MONDO,disease,DISEASE_4430
4431,4431,4431,4431,4431,4431,4431,4431,MONDO:0018554,pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis,MONDO,disease,DISEASE_4431
4432,4432,4432,4432,4432,4432,4432,4432,MONDO:0005109,HIV infectious disease,MONDO,disease,DISEASE_4432
4433,4433,4433,4433,4433,4433,4433,4433,MONDO:0003624,acinic cell breast carcinoma,MONDO,disease,DISEASE_4433
4434,4434,4434,4434,4434,4434,4434,4434,MONDO:0001178,pseudopterygium,MONDO,disease,DISEASE_4434
4435,4435,4435,4435,4435,4435,4435,4435,MONDO:0026767,"immunodeficiency 74, COVID-19-related, X-linked",MONDO,disease,DISEASE_4435
4436,4436,4436,4436,4436,4436,4436,4436,MONDO:0005118,human granulocytic ehrlichiosis,MONDO,disease,DISEASE_4436
4437,4437,4437,4437,4437,4437,4437,4437,MONDO:0018918,carcinoma of gallbladder and extrahepatic biliary tract,MONDO,disease,DISEASE_4437
4438,4438,4438,4438,4438,4438,4438,4438,MONDO:0004252,small intestinal L-cell glucagon-like peptide producing tumor,MONDO,disease,DISEASE_4438
4439,4439,4439,4439,4439,4439,4439,4439,MONDO:0002908_MONDO:0005557_MONDO:0037871_MONDO:0019226,glucose metabolism disease,MONDO_grouped,disease,DISEASE_4439
4440,4440,4440,4440,4440,4440,4440,4440,MONDO:0043237,glossodynia,MONDO,disease,DISEASE_4440
4441,4441,4441,4441,4441,4441,4441,4441,MONDO:0003218,adenocarcinoma in situ,MONDO,disease,DISEASE_4441
4442,4442,4442,4442,4442,4442,4442,4442,MONDO:0009986,"retinopathy, pigmentary, and intellectual disability",MONDO,disease,DISEASE_4442
4443,4443,4443,4443,4443,4443,4443,4443,MONDO:1012364_MONDO:1012365,"Laron dwarfism, pig",MONDO_grouped,disease,DISEASE_4443
4444,4444,4444,4444,4444,4444,4444,4444,MONDO:0019028,amoebiasis due to Entamoeba histolytica,MONDO,disease,DISEASE_4444
4445,4445,4445,4445,4445,4445,4445,4445,MONDO:0012883,acute promyelocytic leukemia,MONDO,disease,DISEASE_4445
4446,4446,4446,4446,4446,4446,4446,4446,MONDO:0968978,aplasia cutis-enamel dysplasia syndrome,MONDO,disease,DISEASE_4446
4447,4447,4447,4447,4447,4447,4447,4447,MONDO:0001809,adhesions of uterus,MONDO,disease,DISEASE_4447
4448,4448,4448,4448,4448,4448,4448,4448,MONDO:0004261,periductal breast myoepitheliosis,MONDO,disease,DISEASE_4448
4449,4449,4449,4449,4449,4449,4449,4449,MONDO:0018932,cirrhotic cardiomyopathy,MONDO,disease,DISEASE_4449
4450,4450,4450,4450,4450,4450,4450,4450,MONDO:0971036,thyroid gland mucinous carcinoma,MONDO,disease,DISEASE_4450
4451,4451,4451,4451,4451,4451,4451,4451,MONDO:0018565,congenital urachal anomaly,MONDO,disease,DISEASE_4451
4452,4452,4452,4452,4452,4452,4452,4452,MONDO:0018759,childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome,MONDO,disease,DISEASE_4452
4453,4453,4453,4453,4453,4453,4453,4453,MONDO:0004367,petroclival meningioma,MONDO,disease,DISEASE_4453
4454,4454,4454,4454,4454,4454,4454,4454,MONDO:0005565,blastoma,MONDO,disease,DISEASE_4454
4455,4455,4455,4455,4455,4455,4455,4455,MONDO:1010275,"cryptorchidism, non-human animal",MONDO,disease,DISEASE_4455
4456,4456,4456,4456,4456,4456,4456,4456,MONDO:1011909,"renal disease, non-human animal",MONDO,disease,DISEASE_4456
4457,4457,4457,4457,4457,4457,4457,4457,MONDO:0021160_MONDO:0021161_MONDO:0004852_MONDO:0020971,gonococcal cystitis,MONDO_grouped,disease,DISEASE_4457
4458,4458,4458,4458,4458,4458,4458,4458,MONDO:0008661_MONDO:1010125,vitiligo,MONDO_grouped,disease,DISEASE_4458
4459,4459,4459,4459,4459,4459,4459,4459,MONDO:0024312,cancer of short bone of upper limb,MONDO,disease,DISEASE_4459
4460,4460,4460,4460,4460,4460,4460,4460,MONDO:0010548_MONDO:0010529_MONDO:0010534,"spinocerebellar ataxia, X-linked",MONDO_grouped,disease,DISEASE_4460
4461,4461,4461,4461,4461,4461,4461,4461,MONDO:0006224,gastric hamartomatous polyp,MONDO,disease,DISEASE_4461
4462,4462,4462,4462,4462,4462,4462,4462,MONDO:0021943,tuberculoma,MONDO,disease,DISEASE_4462
4463,4463,4463,4463,4463,4463,4463,4463,MONDO:0045063,major salivary gland adenoid cystic carcinoma,MONDO,disease,DISEASE_4463
4464,4464,4464,4464,4464,4464,4464,4464,MONDO:0022647,cardiomelic syndrome stratton Koehler type,MONDO,disease,DISEASE_4464
4465,4465,4465,4465,4465,4465,4465,4465,MONDO:0014471,mitochondrial proton-transporting ATP synthase complex deficiency,MONDO,disease,DISEASE_4465
4466,4466,4466,4466,4466,4466,4466,4466,MONDO:0021630,lipoma of face,MONDO,disease,DISEASE_4466
4467,4467,4467,4467,4467,4467,4467,4467,MONDO:0000888,gastrointestinal mucositis,MONDO,disease,DISEASE_4467
4468,4468,4468,4468,4468,4468,4468,4468,MONDO:1010850,"glycogen storage disease, GAA-related, dog",MONDO,disease,DISEASE_4468
4469,4469,4469,4469,4469,4469,4469,4469,MONDO:0008606,Say-field-Coldwell syndrome,MONDO,disease,DISEASE_4469
4470,4470,4470,4470,4470,4470,4470,4470,MONDO:0015069,neuroendocrine tumor of the anal canal,MONDO,disease,DISEASE_4470
4471,4471,4471,4471,4471,4471,4471,4471,MONDO:0024487,nail infection,MONDO,disease,DISEASE_4471
4472,4472,4472,4472,4472,4472,4472,4472,MONDO:0005742,emphysematous cholecystitis,MONDO,disease,DISEASE_4472
4473,4473,4473,4473,4473,4473,4473,4473,MONDO:0002703,appendix mucinous cystadenocarcinoma,MONDO,disease,DISEASE_4473
4474,4474,4474,4474,4474,4474,4474,4474,MONDO:0019337,autoimmune bullous skin disease,MONDO,disease,DISEASE_4474
4475,4475,4475,4475,4475,4475,4475,4475,MONDO:0009297_MONDO:0019741,familial renal glucosuria,MONDO_grouped,disease,DISEASE_4475
4476,4476,4476,4476,4476,4476,4476,4476,MONDO:0008521,tarsal-carpal coalition syndrome,MONDO,disease,DISEASE_4476
4477,4477,4477,4477,4477,4477,4477,4477,MONDO:0012638,microphthalmia-brain atrophy syndrome,MONDO,disease,DISEASE_4477
4478,4478,4478,4478,4478,4478,4478,4478,MONDO:0016733,ganglioglioma,MONDO,disease,DISEASE_4478
4479,4479,4479,4479,4479,4479,4479,4479,MONDO:0018534,squamous cell carcinoma of liver and intrahepatic biliary tract,MONDO,disease,DISEASE_4479
4480,4480,4480,4480,4480,4480,4480,4480,MONDO:0019780,anotia,MONDO,disease,DISEASE_4480
4481,4481,4481,4481,4481,4481,4481,4481,MONDO:0005960,silicosis,MONDO,disease,DISEASE_4481
4482,4482,4482,4482,4482,4482,4482,4482,MONDO:0004076_MONDO:0006442,tendon sheath lipoma,MONDO_grouped,disease,DISEASE_4482
4483,4483,4483,4483,4483,4483,4483,4483,MONDO:0007011,uveoparotid fever,MONDO,disease,DISEASE_4483
4484,4484,4484,4484,4484,4484,4484,4484,MONDO:1011999,"pectinate ligament dysplasia, non-human animal",MONDO,disease,DISEASE_4484
4485,4485,4485,4485,4485,4485,4485,4485,MONDO:0004319,hypercalcemic type ovarian small cell carcinoma,MONDO,disease,DISEASE_4485
4486,4486,4486,4486,4486,4486,4486,4486,MONDO:0100190,gastric intestinal metaplasia,MONDO,disease,DISEASE_4486
4487,4487,4487,4487,4487,4487,4487,4487,MONDO:0016544,IgG4-related mesenteritis,MONDO,disease,DISEASE_4487
4488,4488,4488,4488,4488,4488,4488,4488,MONDO:0001794,Pthirus pubis infestation,MONDO,disease,DISEASE_4488
4489,4489,4489,4489,4489,4489,4489,4489,MONDO:0016908,partial monosomy of the long arm of chromosome 9,MONDO,disease,DISEASE_4489
4490,4490,4490,4490,4490,4490,4490,4490,MONDO:0009220,"visceral steatosis, congenital",MONDO,disease,DISEASE_4490
4491,4491,4491,4491,4491,4491,4491,4491,MONDO:0008193,"paralysis agitans, juvenile, of Hunt",MONDO,disease,DISEASE_4491
4492,4492,4492,4492,4492,4492,4492,4492,MONDO:0013047,glycogen storage disease due to lactate dehydrogenase M-subunit deficiency,MONDO,disease,DISEASE_4492
4493,4493,4493,4493,4493,4493,4493,4493,MONDO:0021472,benign neoplasm of scrotum,MONDO,disease,DISEASE_4493
4494,4494,4494,4494,4494,4494,4494,4494,MONDO:0030982,sulfide quinone oxidoreductase deficiency,MONDO,disease,DISEASE_4494
4495,4495,4495,4495,4495,4495,4495,4495,MONDO:0018544,adrenoleukodystrophy,MONDO,disease,DISEASE_4495
4496,4496,4496,4496,4496,4496,4496,4496,MONDO:0008264,autosomal dominant medullary cystic kidney disease with or without hyperuricemia,MONDO,disease,DISEASE_4496
4497,4497,4497,4497,4497,4497,4497,4497,MONDO:0859199,developmental delay with or without intellectual impairment or behavioral abnormalities,MONDO,disease,DISEASE_4497
4498,4498,4498,4498,4498,4498,4498,4498,MONDO:0009772,oculorenocerebellar syndrome,MONDO,disease,DISEASE_4498
4499,4499,4499,4499,4499,4499,4499,4499,MONDO:0025303,anaplasmosis,MONDO,disease,DISEASE_4499
4500,4500,4500,4500,4500,4500,4500,4500,MONDO:0700241_MONDO:1040037_MONDO:0700242,IMPG2-related recessive retinopathy,MONDO_grouped,disease,DISEASE_4500
4501,4501,4501,4501,4501,4501,4501,4501,MONDO:0016237,diffuse neonatal hemangiomatosis,MONDO,disease,DISEASE_4501
4502,4502,4502,4502,4502,4502,4502,4502,MONDO:0000108_MONDO:0013723_MONDO:0013724,"bacteremia, susceptibility",MONDO_grouped,disease,DISEASE_4502
4503,4503,4503,4503,4503,4503,4503,4503,MONDO:0011444,Duane retraction syndrome 2,MONDO,disease,DISEASE_4503
4504,4504,4504,4504,4504,4504,4504,4504,MONDO:0006754,esophageal diverticulosis,MONDO,disease,DISEASE_4504
4505,4505,4505,4505,4505,4505,4505,4505,MONDO:0001034,marginal corneal ulcer,MONDO,disease,DISEASE_4505
4506,4506,4506,4506,4506,4506,4506,4506,MONDO:0007745,Gilbert syndrome,MONDO,disease,DISEASE_4506
4507,4507,4507,4507,4507,4507,4507,4507,MONDO:0034127,IgA pemphigus,MONDO,disease,DISEASE_4507
4508,4508,4508,4508,4508,4508,4508,4508,MONDO:0002878_MONDO:0016260,uterine corpus adenosarcoma,MONDO_grouped,disease,DISEASE_4508
4509,4509,4509,4509,4509,4509,4509,4509,MONDO:0015646,orgasm-induced seizures,MONDO,disease,DISEASE_4509
4510,4510,4510,4510,4510,4510,4510,4510,MONDO:1010612,"pheochromocytoma, domestic cat",MONDO,disease,DISEASE_4510
4511,4511,4511,4511,4511,4511,4511,4511,MONDO:0100070,neuroendocrine disorder,MONDO,disease,DISEASE_4511
4512,4512,4512,4512,4512,4512,4512,4512,MONDO:0001639,deficiency anemia,MONDO,disease,DISEASE_4512
4513,4513,4513,4513,4513,4513,4513,4513,MONDO:0003420,bile duct cystadenoma,MONDO,disease,DISEASE_4513
4514,4514,4514,4514,4514,4514,4514,4514,MONDO:0009254,fucosidosis,MONDO,disease,DISEASE_4514
4515,4515,4515,4515,4515,4515,4515,4515,MONDO:0011735_MONDO:0011971_MONDO:0010626_MONDO:0011528_MONDO:0011985_MONDO:0003947,hyper-IgM syndrome,MONDO_grouped,disease,DISEASE_4515
4516,4516,4516,4516,4516,4516,4516,4516,MONDO:1010095,"citrullinemia, non-human animal",MONDO,disease,DISEASE_4516
4517,4517,4517,4517,4517,4517,4517,4517,MONDO:0019829,congenital anomaly of superior vena cava,MONDO,disease,DISEASE_4517
4518,4518,4518,4518,4518,4518,4518,4518,MONDO:0009615,methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency,MONDO,disease,DISEASE_4518
4519,4519,4519,4519,4519,4519,4519,4519,MONDO:0018338,activated PI3K-delta syndrome,MONDO,disease,DISEASE_4519
4520,4520,4520,4520,4520,4520,4520,4520,MONDO:0012095,intellectual disability-brachydactyly-Pierre Robin syndrome,MONDO,disease,DISEASE_4520
4521,4521,4521,4521,4521,4521,4521,4521,MONDO:0004903_MONDO:0003085_MONDO:0001465_MONDO:0004794_MONDO:0033821,deep keratitis,MONDO_grouped,disease,DISEASE_4521
4522,4522,4522,4522,4522,4522,4522,4522,MONDO:1011520,"hemophilia A, crab-eating macaque",MONDO,disease,DISEASE_4522
4523,4523,4523,4523,4523,4523,4523,4523,MONDO:0006974,small cell sarcoma,MONDO,disease,DISEASE_4523
4524,4524,4524,4524,4524,4524,4524,4524,MONDO:0800131,"hyper-IgE recurrent infection syndrome 4A, autosomal dominant",MONDO,disease,DISEASE_4524
4525,4525,4525,4525,4525,4525,4525,4525,MONDO:0004522_MONDO:0005195,infectious peritonitis,MONDO_grouped,disease,DISEASE_4525
4526,4526,4526,4526,4526,4526,4526,4526,MONDO:0004661,trachea carcinoma in situ,MONDO,disease,DISEASE_4526
4527,4527,4527,4527,4527,4527,4527,4527,MONDO:0016351,anti-HLA hyperimmunization,MONDO,disease,DISEASE_4527
4528,4528,4528,4528,4528,4528,4528,4528,MONDO:0003404,adult yolk sac tumor,MONDO,disease,DISEASE_4528
4529,4529,4529,4529,4529,4529,4529,4529,MONDO:0005978,theileriasis,MONDO,disease,DISEASE_4529
4530,4530,4530,4530,4530,4530,4530,4530,MONDO:1012062,"hyperosmolar nonketotic diabetes mellitus, domestic cat",MONDO,disease,DISEASE_4530
4531,4531,4531,4531,4531,4531,4531,4531,MONDO:0100508,salivary gland type cancer of the breast,MONDO,disease,DISEASE_4531
4532,4532,4532,4532,4532,4532,4532,4532,MONDO:0100280,Waldenstrom macroglobulinemia,MONDO,disease,DISEASE_4532
4533,4533,4533,4533,4533,4533,4533,4533,MONDO:0010199,white forelock with malformations,MONDO,disease,DISEASE_4533
4534,4534,4534,4534,4534,4534,4534,4534,MONDO:0006952,retinopathy of prematurity,MONDO,disease,DISEASE_4534
4535,4535,4535,4535,4535,4535,4535,4535,MONDO:0015438,ring chromosome 22,MONDO,disease,DISEASE_4535
4536,4536,4536,4536,4536,4536,4536,4536,MONDO:0859165,"neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities",MONDO,disease,DISEASE_4536
4537,4537,4537,4537,4537,4537,4537,4537,MONDO:0008260,Kindler syndrome,MONDO,disease,DISEASE_4537
4538,4538,4538,4538,4538,4538,4538,4538,MONDO:0007929,obsolete Epstein syndrome,MONDO,disease,DISEASE_4538
4539,4539,4539,4539,4539,4539,4539,4539,MONDO:0006378,pleural epithelioid mesothelioma,MONDO,disease,DISEASE_4539
4540,4540,4540,4540,4540,4540,4540,4540,MONDO:0001462,descending colon cancer,MONDO,disease,DISEASE_4540
4541,4541,4541,4541,4541,4541,4541,4541,MONDO:0019175,primary lymphedema,MONDO,disease,DISEASE_4541
4542,4542,4542,4542,4542,4542,4542,4542,MONDO:0001892,spinal cord lymphoma,MONDO,disease,DISEASE_4542
4543,4543,4543,4543,4543,4543,4543,4543,MONDO:0002167,rectum malignant melanoma,MONDO,disease,DISEASE_4543
4544,4544,4544,4544,4544,4544,4544,4544,MONDO:0800441,"NKX2.5-related congenital, conduction and myopathic heart disease",MONDO,disease,DISEASE_4544
4545,4545,4545,4545,4545,4545,4545,4545,MONDO:0008569_MONDO:0010131,"thyroid hormone resistance, generalized, autosomal dominant",MONDO_grouped,disease,DISEASE_4545
4546,4546,4546,4546,4546,4546,4546,4546,MONDO:1012961,"cancer, TP53-related, dog",MONDO,disease,DISEASE_4546
4547,4547,4547,4547,4547,4547,4547,4547,MONDO:0001327,pelvic muscle wasting,MONDO,disease,DISEASE_4547
4548,4548,4548,4548,4548,4548,4548,4548,MONDO:0004292,supraglottis verrucous carcinoma,MONDO,disease,DISEASE_4548
4549,4549,4549,4549,4549,4549,4549,4549,MONDO:1012384,"forelimb-girdle muscular anomaly, cattle",MONDO,disease,DISEASE_4549
4550,4550,4550,4550,4550,4550,4550,4550,MONDO:0018189,autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome,MONDO,disease,DISEASE_4550
4551,4551,4551,4551,4551,4551,4551,4551,MONDO:0004729,dyskinesia of esophagus,MONDO,disease,DISEASE_4551
4552,4552,4552,4552,4552,4552,4552,4552,MONDO:0005345_MONDO:1011091_MONDO:1011092_MONDO:1011093_MONDO:1011094_MONDO:1011095,hypospadias,MONDO_grouped,disease,DISEASE_4552
4553,4553,4553,4553,4553,4553,4553,4553,MONDO:0011422_MONDO:0008368_MONDO:0018440_MONDO:0017829,autosomal recessive proximal renal tubular acidosis,MONDO_grouped,disease,DISEASE_4553
4554,4554,4554,4554,4554,4554,4554,4554,MONDO:0013271,frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome,MONDO,disease,DISEASE_4554
4555,4555,4555,4555,4555,4555,4555,4555,MONDO:0002412_MONDO:0017703,disorder of glycogen metabolism,MONDO_grouped,disease,DISEASE_4555
4556,4556,4556,4556,4556,4556,4556,4556,MONDO:0007192,"beta-amino acids, renal transport of",MONDO,disease,DISEASE_4556
4557,4557,4557,4557,4557,4557,4557,4557,MONDO:0015230,anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome,MONDO,disease,DISEASE_4557
4558,4558,4558,4558,4558,4558,4558,4558,MONDO:0015632,FASTKD2-related infantile mitochondrial encephalomyopathy,MONDO,disease,DISEASE_4558
4559,4559,4559,4559,4559,4559,4559,4559,MONDO:0010532,infantile-onset X-linked spinal muscular atrophy,MONDO,disease,DISEASE_4559
4560,4560,4560,4560,4560,4560,4560,4560,MONDO:0005967,splenic tuberculosis,MONDO,disease,DISEASE_4560
4561,4561,4561,4561,4561,4561,4561,4561,MONDO:0800030_MONDO:0030669,gastrointestinal defects and immunodeficiency syndrome,MONDO_grouped,disease,DISEASE_4561
4562,4562,4562,4562,4562,4562,4562,4562,MONDO:0850126,testicular sex cord-stromal benign neoplasm,MONDO,disease,DISEASE_4562
4563,4563,4563,4563,4563,4563,4563,4563,MONDO:0012648,isobutyryl-CoA dehydrogenase deficiency,MONDO,disease,DISEASE_4563
4564,4564,4564,4564,4564,4564,4564,4564,MONDO:0032848,"immunodeficiency 65, susceptibility to viral infections",MONDO,disease,DISEASE_4564
4565,4565,4565,4565,4565,4565,4565,4565,MONDO:0020462,tarsal kink syndrome,MONDO,disease,DISEASE_4565
4566,4566,4566,4566,4566,4566,4566,4566,MONDO:0011922,nonimmune chronic idiopathic neutropenia of adults,MONDO,disease,DISEASE_4566
4567,4567,4567,4567,4567,4567,4567,4567,MONDO:0003963,diffuse infiltrative lymphocytosis syndrome,MONDO,disease,DISEASE_4567
4568,4568,4568,4568,4568,4568,4568,4568,MONDO:0043294,linear scleroderma,MONDO,disease,DISEASE_4568
4569,4569,4569,4569,4569,4569,4569,4569,MONDO:0011343,"follicular atrophoderma, perioral pigmented, with milia and epidermoid cysts",MONDO,disease,DISEASE_4569
4570,4570,4570,4570,4570,4570,4570,4570,MONDO:0017344,Epstein-Barr virus-associated carcinoma,MONDO,disease,DISEASE_4570
4571,4571,4571,4571,4571,4571,4571,4571,MONDO:1012572,"cancer, pig",MONDO,disease,DISEASE_4571
4572,4572,4572,4572,4572,4572,4572,4572,MONDO:0010340_MONDO:0010343,"Asperger syndrome, X-linked, susceptibility to",MONDO_grouped,disease,DISEASE_4572
4573,4573,4573,4573,4573,4573,4573,4573,MONDO:1012706,"arachnomelia syndrome, MOCS1-related, cattle",MONDO,disease,DISEASE_4573
4574,4574,4574,4574,4574,4574,4574,4574,MONDO:0005312,pouchitis,MONDO,disease,DISEASE_4574
4575,4575,4575,4575,4575,4575,4575,4575,MONDO:0004259,endocervical carcinoma,MONDO,disease,DISEASE_4575
4576,4576,4576,4576,4576,4576,4576,4576,MONDO:0006544,erythema infectiosum,MONDO,disease,DISEASE_4576
4577,4577,4577,4577,4577,4577,4577,4577,MONDO:0009839,progressive supranuclear palsy-parkinsonism syndrome,MONDO,disease,DISEASE_4577
4578,4578,4578,4578,4578,4578,4578,4578,MONDO:0017886,MIT family translocation renal cell carcinoma,MONDO,disease,DISEASE_4578
4579,4579,4579,4579,4579,4579,4579,4579,MONDO:0011838,Bothnia retinal dystrophy,MONDO,disease,DISEASE_4579
4580,4580,4580,4580,4580,4580,4580,4580,MONDO:0012001,"mandibulofacial dysostosis with ptosis, autosomal dominant",MONDO,disease,DISEASE_4580
4581,4581,4581,4581,4581,4581,4581,4581,MONDO:0016598,autosomal recessive secondary polycythemia not associated with VHL gene,MONDO,disease,DISEASE_4581
4582,4582,4582,4582,4582,4582,4582,4582,MONDO:1010021,"tetralogy of fallot, non-human animal",MONDO,disease,DISEASE_4582
4583,4583,4583,4583,4583,4583,4583,4583,MONDO:1010124,"autoimmune lymphoproliferative syndrome, non-human animal",MONDO,disease,DISEASE_4583
4584,4584,4584,4584,4584,4584,4584,4584,MONDO:1010973_MONDO:1010974_MONDO:1010975_MONDO:1012221,"hepatic encephalopathy, dog",MONDO_grouped,disease,DISEASE_4584
4585,4585,4585,4585,4585,4585,4585,4585,MONDO:0019074,bilateral acute depigmentation of the iris,MONDO,disease,DISEASE_4585
4586,4586,4586,4586,4586,4586,4586,4586,MONDO:0030871,vertebral hypersegmentation and orofacial anomalies,MONDO,disease,DISEASE_4586
4587,4587,4587,4587,4587,4587,4587,4587,MONDO:0003400,childhood endodermal sinus tumor,MONDO,disease,DISEASE_4587
4588,4588,4588,4588,4588,4588,4588,4588,MONDO:0013497,Okt4 epitope deficiency,MONDO,disease,DISEASE_4588
4589,4589,4589,4589,4589,4589,4589,4589,MONDO:0018160,hereditary retinoblastoma,MONDO,disease,DISEASE_4589
4590,4590,4590,4590,4590,4590,4590,4590,MONDO:0010645,oculocerebrorenal syndrome,MONDO,disease,DISEASE_4590
4591,4591,4591,4591,4591,4591,4591,4591,MONDO:0100283,overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes,MONDO,disease,DISEASE_4591
4592,4592,4592,4592,4592,4592,4592,4592,MONDO:0003199,anal carcinoma,MONDO,disease,DISEASE_4592
4593,4593,4593,4593,4593,4593,4593,4593,MONDO:0017026_MONDO:0017015_MONDO:0017014_MONDO:0017019,interstitial lung disease specific to adulthood,MONDO_grouped,disease,DISEASE_4593
4594,4594,4594,4594,4594,4594,4594,4594,MONDO:0003787,childhood testicular mixed germ cell cancer,MONDO,disease,DISEASE_4594
4595,4595,4595,4595,4595,4595,4595,4595,MONDO:0019152,Oguchi disease,MONDO,disease,DISEASE_4595
4596,4596,4596,4596,4596,4596,4596,4596,MONDO:0958343,PAPASH syndrome,MONDO,disease,DISEASE_4596
4597,4597,4597,4597,4597,4597,4597,4597,MONDO:0032943,neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies,MONDO,disease,DISEASE_4597
4598,4598,4598,4598,4598,4598,4598,4598,MONDO:0004633,"Hodgkin's lymphoma, mixed cellularity",MONDO,disease,DISEASE_4598
4599,4599,4599,4599,4599,4599,4599,4599,MONDO:1012859,"hypertrophic cardiomyopathy, ALMS1-related, domestic cat",MONDO,disease,DISEASE_4599
4600,4600,4600,4600,4600,4600,4600,4600,MONDO:0008500,"striae distensae, familial",MONDO,disease,DISEASE_4600
4601,4601,4601,4601,4601,4601,4601,4601,MONDO:0018364,malignant epithelial tumor of ovary,MONDO,disease,DISEASE_4601
4602,4602,4602,4602,4602,4602,4602,4602,MONDO:1011609,"vitamin-K-dependent blood coagulation factors deficiency, domestic cat",MONDO,disease,DISEASE_4602
4603,4603,4603,4603,4603,4603,4603,4603,MONDO:0957477,MYT1L-related developmental delay-intellectual disability-obesity syndrome,MONDO,disease,DISEASE_4603
4604,4604,4604,4604,4604,4604,4604,4604,MONDO:0018256,acute myeloid leukemia with t(8;16)(p11;p13) translocation,MONDO,disease,DISEASE_4604
4605,4605,4605,4605,4605,4605,4605,4605,MONDO:0008924,congenital cataract-ichthyosis syndrome,MONDO,disease,DISEASE_4605
4606,4606,4606,4606,4606,4606,4606,4606,MONDO:0033948,acquired angioedema with C1Inh deficiency,MONDO,disease,DISEASE_4606
4607,4607,4607,4607,4607,4607,4607,4607,MONDO:0035740,acquired factor XI deficiency,MONDO,disease,DISEASE_4607
4608,4608,4608,4608,4608,4608,4608,4608,MONDO:0003181,lung adenoid cystic carcinoma,MONDO,disease,DISEASE_4608
4609,4609,4609,4609,4609,4609,4609,4609,MONDO:0700017,chromosome 10 disorder,MONDO,disease,DISEASE_4609
4610,4610,4610,4610,4610,4610,4610,4610,MONDO:0004671,penis carcinoma in situ,MONDO,disease,DISEASE_4610
4611,4611,4611,4611,4611,4611,4611,4611,MONDO:0010276,"radioulnar synostosis, radial ray abnormalities, and severe malformations in the male",MONDO,disease,DISEASE_4611
4612,4612,4612,4612,4612,4612,4612,4612,MONDO:0011243,grange syndrome,MONDO,disease,DISEASE_4612
4613,4613,4613,4613,4613,4613,4613,4613,MONDO:0006851,meconium aspiration syndrome,MONDO,disease,DISEASE_4613
4614,4614,4614,4614,4614,4614,4614,4614,MONDO:0024634_MONDO:0000956_MONDO:0024635,large intestine disorder,MONDO_grouped,disease,DISEASE_4614
4615,4615,4615,4615,4615,4615,4615,4615,MONDO:0010188,familial isolated deficiency of vitamin E,MONDO,disease,DISEASE_4615
4616,4616,4616,4616,4616,4616,4616,4616,MONDO:0850008,anterior segment developmental abnormality with extraocular manifestations,MONDO,disease,DISEASE_4616
4617,4617,4617,4617,4617,4617,4617,4617,MONDO:0008269_MONDO:0017524,polydactyly of a biphalangeal thumb,MONDO_grouped,disease,DISEASE_4617
4618,4618,4618,4618,4618,4618,4618,4618,MONDO:0022823,congenital contractures,MONDO,disease,DISEASE_4618
4619,4619,4619,4619,4619,4619,4619,4619,MONDO:0017323,hypocalcemic rickets,MONDO,disease,DISEASE_4619
4620,4620,4620,4620,4620,4620,4620,4620,MONDO:1010435,"atrial septal defect, domestic cat",MONDO,disease,DISEASE_4620
4621,4621,4621,4621,4621,4621,4621,4621,MONDO:0001650,acute cystitis,MONDO,disease,DISEASE_4621
4622,4622,4622,4622,4622,4622,4622,4622,MONDO:0010292,Uruguay Faciocardiomusculoskeletal syndrome,MONDO,disease,DISEASE_4622
4623,4623,4623,4623,4623,4623,4623,4623,MONDO:0024251,Minamata disease,MONDO,disease,DISEASE_4623
4624,4624,4624,4624,4624,4624,4624,4624,MONDO:1011829,"progressive ataxia with degenerative thoracic myelopathy, non-human animal",MONDO,disease,DISEASE_4624
4625,4625,4625,4625,4625,4625,4625,4625,MONDO:0016380,acquired hypertrichosis lanuginosa,MONDO,disease,DISEASE_4625
4626,4626,4626,4626,4626,4626,4626,4626,MONDO:0007860,focal palmoplantar and gingival keratoderma,MONDO,disease,DISEASE_4626
4627,4627,4627,4627,4627,4627,4627,4627,MONDO:1010849,"glycogen storage disease II, Japanese quail",MONDO,disease,DISEASE_4627
4628,4628,4628,4628,4628,4628,4628,4628,MONDO:0017909,inherited glutathione synthetase deficiency,MONDO,disease,DISEASE_4628
4629,4629,4629,4629,4629,4629,4629,4629,MONDO:1010329,"Leber congenital amaurosis, non-human animal",MONDO,disease,DISEASE_4629
4630,4630,4630,4630,4630,4630,4630,4630,MONDO:0001876,renal artery atheroma,MONDO,disease,DISEASE_4630
4631,4631,4631,4631,4631,4631,4631,4631,MONDO:0022598,brachydactyly absence of distal phalanges,MONDO,disease,DISEASE_4631
4632,4632,4632,4632,4632,4632,4632,4632,MONDO:0004322,non-gestational ovarian choriocarcinoma,MONDO,disease,DISEASE_4632
4633,4633,4633,4633,4633,4633,4633,4633,MONDO:0032759_MONDO:0032870,intellectual developmental disorder with short stature and variable skeletal anomalies,MONDO_grouped,disease,DISEASE_4633
4634,4634,4634,4634,4634,4634,4634,4634,MONDO:1012546,"cytochrome B-related exercise intolerance, sheep",MONDO,disease,DISEASE_4634
4635,4635,4635,4635,4635,4635,4635,4635,MONDO:0007861,isolated cloverleaf skull syndrome,MONDO,disease,DISEASE_4635
4636,4636,4636,4636,4636,4636,4636,4636,MONDO:0006002,urogenital tuberculosis,MONDO,disease,DISEASE_4636
4637,4637,4637,4637,4637,4637,4637,4637,MONDO:0000481,cervical dystonia,MONDO,disease,DISEASE_4637
4638,4638,4638,4638,4638,4638,4638,4638,MONDO:1012607,"glycogen storage disease IV, horse",MONDO,disease,DISEASE_4638
4639,4639,4639,4639,4639,4639,4639,4639,MONDO:0006603,reactive cutaneous fibrous lesion,MONDO,disease,DISEASE_4639
4640,4640,4640,4640,4640,4640,4640,4640,MONDO:1011755,"sebaceous adenitis, non-human animal",MONDO,disease,DISEASE_4640
4641,4641,4641,4641,4641,4641,4641,4641,MONDO:0004918,central corneal ulcer,MONDO,disease,DISEASE_4641
4642,4642,4642,4642,4642,4642,4642,4642,MONDO:1010923_MONDO:1010924_MONDO:1010925,"muscular dystrophy, Duchenne type, dog",MONDO_grouped,disease,DISEASE_4642
4643,4643,4643,4643,4643,4643,4643,4643,MONDO:0043224,multi-infarct dementia,MONDO,disease,DISEASE_4643
4644,4644,4644,4644,4644,4644,4644,4644,MONDO:0006781,Helicobacter pylori infectious disease,MONDO,disease,DISEASE_4644
4645,4645,4645,4645,4645,4645,4645,4645,MONDO:0042962,Slti-Salem syndrome,MONDO,disease,DISEASE_4645
4646,4646,4646,4646,4646,4646,4646,4646,MONDO:0001538,retinal ischemia,MONDO,disease,DISEASE_4646
4647,4647,4647,4647,4647,4647,4647,4647,MONDO:1012881,"microcephaly, MFSD2A-related, sheep",MONDO,disease,DISEASE_4647
4648,4648,4648,4648,4648,4648,4648,4648,MONDO:0958273,cleft palate-congenital heart defect-intellectual disability syndrome due to MEIS2 mutation,MONDO,disease,DISEASE_4648
4649,4649,4649,4649,4649,4649,4649,4649,MONDO:0008145,Ollier disease,MONDO,disease,DISEASE_4649
4650,4650,4650,4650,4650,4650,4650,4650,MONDO:1011287,"night blindness, dog",MONDO,disease,DISEASE_4650
4651,4651,4651,4651,4651,4651,4651,4651,MONDO:0010353,"deafness-intellectual disability, Martin-Probst type syndrome",MONDO,disease,DISEASE_4651
4652,4652,4652,4652,4652,4652,4652,4652,MONDO:0012749,"mesomelic dysplasia, camera type",MONDO,disease,DISEASE_4652
4653,4653,4653,4653,4653,4653,4653,4653,MONDO:0008529,"T-cell Subgroups, non-HLA-linked",MONDO,disease,DISEASE_4653
4654,4654,4654,4654,4654,4654,4654,4654,MONDO:0012391,neuronal ceroid lipofuscinosis 8 northern epilepsy variant,MONDO,disease,DISEASE_4654
4655,4655,4655,4655,4655,4655,4655,4655,MONDO:0022948,Deal Barratt Dillon syndrome,MONDO,disease,DISEASE_4655
4656,4656,4656,4656,4656,4656,4656,4656,MONDO:0024389_MONDO:0006929,anaerobic bacteria infectious disease,MONDO_grouped,disease,DISEASE_4656
4657,4657,4657,4657,4657,4657,4657,4657,MONDO:0800179,periprosthetic joint infection,MONDO,disease,DISEASE_4657
4658,4658,4658,4658,4658,4658,4658,4658,MONDO:0009820,osteoporosis-pseudoglioma syndrome,MONDO,disease,DISEASE_4658
4659,4659,4659,4659,4659,4659,4659,4659,MONDO:0700133,"adenoma, non-human",MONDO,disease,DISEASE_4659
4660,4660,4660,4660,4660,4660,4660,4660,MONDO:0001576,telangiectasis,MONDO,disease,DISEASE_4660
4661,4661,4661,4661,4661,4661,4661,4661,MONDO:0044657,MME-related autosomal dominant Charcot Marie Tooth disease type 2,MONDO,disease,DISEASE_4661
4662,4662,4662,4662,4662,4662,4662,4662,MONDO:0032883,intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures,MONDO,disease,DISEASE_4662
4663,4663,4663,4663,4663,4663,4663,4663,MONDO:0017930,mixed sclerosing bone dystrophy with extra-skeletal manifestations,MONDO,disease,DISEASE_4663
4664,4664,4664,4664,4664,4664,4664,4664,MONDO:0006324,normal breast-like subtype of breast carcinoma,MONDO,disease,DISEASE_4664
4665,4665,4665,4665,4665,4665,4665,4665,MONDO:0008281,"polyposis, intestinal, scattered and discrete",MONDO,disease,DISEASE_4665
4666,4666,4666,4666,4666,4666,4666,4666,MONDO:0003424_MONDO:0003935,oncocytic adenoma,MONDO_grouped,disease,DISEASE_4666
4667,4667,4667,4667,4667,4667,4667,4667,MONDO:1011983,"tapetal degeneration, non-human animal",MONDO,disease,DISEASE_4667
4668,4668,4668,4668,4668,4668,4668,4668,MONDO:0003741,juvenile type testicular granulosa cell tumor,MONDO,disease,DISEASE_4668
4669,4669,4669,4669,4669,4669,4669,4669,MONDO:0018000,hereditary thrombocytosis with transverse limb defect,MONDO,disease,DISEASE_4669
4670,4670,4670,4670,4670,4670,4670,4670,MONDO:0009523,Lichtenstein syndrome,MONDO,disease,DISEASE_4670
4671,4671,4671,4671,4671,4671,4671,4671,MONDO:0032745,developmental delay with variable intellectual impairment and behavioral abnormalities,MONDO,disease,DISEASE_4671
4672,4672,4672,4672,4672,4672,4672,4672,MONDO:1011695,"thrombopathia, non-human animal",MONDO,disease,DISEASE_4672
4673,4673,4673,4673,4673,4673,4673,4673,MONDO:0008346_MONDO:0020553,pulmonary hemosiderosis,MONDO_grouped,disease,DISEASE_4673
4674,4674,4674,4674,4674,4674,4674,4674,MONDO:0003820,mature ovarian teratoma,MONDO,disease,DISEASE_4674
4675,4675,4675,4675,4675,4675,4675,4675,MONDO:1012019,"atrial septal defect and atrial fibrillation, horse",MONDO,disease,DISEASE_4675
4676,4676,4676,4676,4676,4676,4676,4676,MONDO:0016883,partial deletion of the short arm of chromosome 1,MONDO,disease,DISEASE_4676
4677,4677,4677,4677,4677,4677,4677,4677,MONDO:0015197,aneurysm of sinus of Valsalva,MONDO,disease,DISEASE_4677
4678,4678,4678,4678,4678,4678,4678,4678,MONDO:1011075,"urolithiasis, Siberian chipmunk",MONDO,disease,DISEASE_4678
4679,4679,4679,4679,4679,4679,4679,4679,MONDO:1012734,"Waardenburg syndrome, EDNRB-related, sheep",MONDO,disease,DISEASE_4679
4680,4680,4680,4680,4680,4680,4680,4680,MONDO:0019649,idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis,MONDO,disease,DISEASE_4680
4681,4681,4681,4681,4681,4681,4681,4681,MONDO:0009862,dihydropteridine reductase deficiency,MONDO,disease,DISEASE_4681
4682,4682,4682,4682,4682,4682,4682,4682,MONDO:1010816,"polydactyly, guanaco",MONDO,disease,DISEASE_4682
4683,4683,4683,4683,4683,4683,4683,4683,MONDO:0005950_MONDO:8000004,Salmonella gastroenteritis,MONDO_grouped,disease,DISEASE_4683
4684,4684,4684,4684,4684,4684,4684,4684,MONDO:0008216,pelvic lipomatosis with crossed renal ectopia,MONDO,disease,DISEASE_4684
4685,4685,4685,4685,4685,4685,4685,4685,MONDO:0010710,Pierre Robin syndrome-faciodigital anomaly syndrome,MONDO,disease,DISEASE_4685
4686,4686,4686,4686,4686,4686,4686,4686,MONDO:0010104,non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome,MONDO,disease,DISEASE_4686
4687,4687,4687,4687,4687,4687,4687,4687,MONDO:0700018,chromosome 11 disorder,MONDO,disease,DISEASE_4687
4688,4688,4688,4688,4688,4688,4688,4688,MONDO:0958085,digenic hemochromatosis,MONDO,disease,DISEASE_4688
4689,4689,4689,4689,4689,4689,4689,4689,MONDO:0014633_MONDO:0015346_MONDO:0005754_MONDO:0019487,epilepsy with myoclonic atonic seizures,MONDO_grouped,disease,DISEASE_4689
4690,4690,4690,4690,4690,4690,4690,4690,MONDO:0020698,inborn error of biotin metabolism,MONDO,disease,DISEASE_4690
4691,4691,4691,4691,4691,4691,4691,4691,MONDO:0012944,"chromosome 17P13.3, telomeric, duplication syndrome",MONDO,disease,DISEASE_4691
4692,4692,4692,4692,4692,4692,4692,4692,MONDO:0006032_MONDO:0004118,cystitis,MONDO_grouped,disease,DISEASE_4692
4693,4693,4693,4693,4693,4693,4693,4693,MONDO:0800422,"cirrhosis, noncryptogenic, susceptibility to",MONDO,disease,DISEASE_4693
4694,4694,4694,4694,4694,4694,4694,4694,MONDO:0008604,triphalangeal thumb with double phalanges,MONDO,disease,DISEASE_4694
4695,4695,4695,4695,4695,4695,4695,4695,MONDO:0024307,prothrombin deficiency,MONDO,disease,DISEASE_4695
4696,4696,4696,4696,4696,4696,4696,4696,MONDO:0005461,endometrium adenocarcinoma,MONDO,disease,DISEASE_4696
4697,4697,4697,4697,4697,4697,4697,4697,MONDO:0017386_MONDO:0004233_MONDO:0004513,pleomorphic rhabdomyosarcoma,MONDO_grouped,disease,DISEASE_4697
4698,4698,4698,4698,4698,4698,4698,4698,MONDO:0004333,pancreatic ACTH-producing neuroendocrine tumor,MONDO,disease,DISEASE_4698
4699,4699,4699,4699,4699,4699,4699,4699,MONDO:0012369_MONDO:0012835_MONDO:0010433_MONDO:0011138_MONDO:0011520_MONDO:0011560_MONDO:0012036_MONDO:0012361_MONDO:0012403_MONDO:0012404_MONDO:0012584_MONDO:0012834_MONDO:0012836_MONDO:0012884_MONDO:0013152,"systemic lupus erythematosus, susceptibility to",MONDO_grouped,disease,DISEASE_4699
4700,4700,4700,4700,4700,4700,4700,4700,MONDO:0007772_MONDO:0013777_MONDO:0013778_MONDO:0013782_MONDO:0013781_MONDO:0019162_MONDO:0019161_MONDO:0018638_MONDO:0019643,pseudohypoaldosteronism,MONDO_grouped,disease,DISEASE_4700
4701,4701,4701,4701,4701,4701,4701,4701,MONDO:0008386_MONDO:0011233_MONDO:0011097_MONDO:0019187,Axenfeld-Rieger syndrome,MONDO_grouped,disease,DISEASE_4701
4702,4702,4702,4702,4702,4702,4702,4702,MONDO:0033667,Delpire-McNeill syndrome,MONDO,disease,DISEASE_4702
4703,4703,4703,4703,4703,4703,4703,4703,MONDO:1010118_MONDO:1011756,"systemic lupus erythematosus, non-human animal",MONDO_grouped,disease,DISEASE_4703
4704,4704,4704,4704,4704,4704,4704,4704,MONDO:0017981,syngnathia-cleft palate syndrome,MONDO,disease,DISEASE_4704
4705,4705,4705,4705,4705,4705,4705,4705,MONDO:0021159_MONDO:0001575_MONDO:0001837,gonococcal salpingitis,MONDO_grouped,disease,DISEASE_4705
4706,4706,4706,4706,4706,4706,4706,4706,MONDO:0044311,"brachycephaly, trichomegaly, and developmental delay",MONDO,disease,DISEASE_4706
4707,4707,4707,4707,4707,4707,4707,4707,MONDO:0021079,childhood neoplasm,MONDO,disease,DISEASE_4707
4708,4708,4708,4708,4708,4708,4708,4708,MONDO:0007096,amenorrhea-galactorrhea syndrome,MONDO,disease,DISEASE_4708
4709,4709,4709,4709,4709,4709,4709,4709,MONDO:0043579,enteritis,MONDO,disease,DISEASE_4709
4710,4710,4710,4710,4710,4710,4710,4710,MONDO:1010196_MONDO:1010201,"congenital myopathy, non-human animal",MONDO_grouped,disease,DISEASE_4710
4711,4711,4711,4711,4711,4711,4711,4711,MONDO:0100480,autoimmune primary adrenal insufficiency,MONDO,disease,DISEASE_4711
4712,4712,4712,4712,4712,4712,4712,4712,MONDO:0010648_MONDO:0007440_MONDO:0012685_MONDO:0000694_MONDO:0012881_MONDO:0012319_MONDO:0012642_MONDO:0012686_MONDO:0012877_MONDO:0012882,major affective disorder,MONDO_grouped,disease,DISEASE_4712
4713,4713,4713,4713,4713,4713,4713,4713,MONDO:0021248,nervous system neoplasm,MONDO,disease,DISEASE_4713
4714,4714,4714,4714,4714,4714,4714,4714,MONDO:0009390,hyperlysinuria with hyperammonemia,MONDO,disease,DISEASE_4714
4715,4715,4715,4715,4715,4715,4715,4715,MONDO:0003645_MONDO:0001974_MONDO:0001975_MONDO:0003644_MONDO:0021281,cavernous hemangioma of face,MONDO_grouped,disease,DISEASE_4715
4716,4716,4716,4716,4716,4716,4716,4716,MONDO:0008881,kyphomelic dysplasia,MONDO,disease,DISEASE_4716
4717,4717,4717,4717,4717,4717,4717,4717,MONDO:0006596,photoallergic dermatitis,MONDO,disease,DISEASE_4717
4718,4718,4718,4718,4718,4718,4718,4718,MONDO:0000087_MONDO:1011003,polymicrogyria,MONDO_grouped,disease,DISEASE_4718
4719,4719,4719,4719,4719,4719,4719,4719,MONDO:0971095,6q25.1 microdeletion syndrome,MONDO,disease,DISEASE_4719
4720,4720,4720,4720,4720,4720,4720,4720,MONDO:0011184,childhood apraxia of speech,MONDO,disease,DISEASE_4720
4721,4721,4721,4721,4721,4721,4721,4721,MONDO:0012482,"West Nile virus, susceptibility to",MONDO,disease,DISEASE_4721
4722,4722,4722,4722,4722,4722,4722,4722,MONDO:0014974,"sudden cardiac failure, alcohol-induced",MONDO,disease,DISEASE_4722
4723,4723,4723,4723,4723,4723,4723,4723,MONDO:0005583,non-human animal disease,MONDO,disease,DISEASE_4723
4724,4724,4724,4724,4724,4724,4724,4724,MONDO:0957481,idiopathic pregnancy-associated osteoporosis,MONDO,disease,DISEASE_4724
4725,4725,4725,4725,4725,4725,4725,4725,MONDO:0015471,benign focal seizures of adolescence,MONDO,disease,DISEASE_4725
4726,4726,4726,4726,4726,4726,4726,4726,MONDO:0004221,uterine corpus perivascular epithelioid cell tumor,MONDO,disease,DISEASE_4726
4727,4727,4727,4727,4727,4727,4727,4727,MONDO:0018632,11q22.2q22.3 microdeletion syndrome,MONDO,disease,DISEASE_4727
4728,4728,4728,4728,4728,4728,4728,4728,MONDO:0850013,twin anemia-polycythemia sequence,MONDO,disease,DISEASE_4728
4729,4729,4729,4729,4729,4729,4729,4729,MONDO:0004682,retromolar area cancer,MONDO,disease,DISEASE_4729
4730,4730,4730,4730,4730,4730,4730,4730,MONDO:0011004,lissencephaly type 3-metacarpal bone dysplasia syndrome,MONDO,disease,DISEASE_4730
4731,4731,4731,4731,4731,4731,4731,4731,MONDO:0009157_MONDO:0009525_MONDO:0008464_MONDO:0010736_MONDO:0011535_MONDO:0016576_MONDO:0011709,split hand-foot malformation,MONDO_grouped,disease,DISEASE_4731
4732,4732,4732,4732,4732,4732,4732,4732,MONDO:0002761,cervical verrucous carcinoma,MONDO,disease,DISEASE_4732
4733,4733,4733,4733,4733,4733,4733,4733,MONDO:0005462,primitive neuroectodermal tumor,MONDO,disease,DISEASE_4733
4734,4734,4734,4734,4734,4734,4734,4734,MONDO:0015592_MONDO:0017179_MONDO:0018003,limbic encephalitis with LGI1 antibodies,MONDO_grouped,disease,DISEASE_4734
4735,4735,4735,4735,4735,4735,4735,4735,MONDO:0006713,corneal neovascularization,MONDO,disease,DISEASE_4735
4736,4736,4736,4736,4736,4736,4736,4736,MONDO:0010642,Lesch-Nyhan phenotype with normal HGPRT,MONDO,disease,DISEASE_4736
4737,4737,4737,4737,4737,4737,4737,4737,MONDO:0013313,ectodermal dysplasia-cutaneous syndactyly syndrome,MONDO,disease,DISEASE_4737
4738,4738,4738,4738,4738,4738,4738,4738,MONDO:0850345,lung pleomorphic carcinoma,MONDO,disease,DISEASE_4738
4739,4739,4739,4739,4739,4739,4739,4739,MONDO:1012912,"complex skeletal dysplasia, LTBP3-related, domestic cat",MONDO,disease,DISEASE_4739
4740,4740,4740,4740,4740,4740,4740,4740,MONDO:0009628,obsolete microcolon,MONDO,disease,DISEASE_4740
4741,4741,4741,4741,4741,4741,4741,4741,MONDO:0009800_MONDO:0017194,"Blount disease, adolescent",MONDO_grouped,disease,DISEASE_4741
4742,4742,4742,4742,4742,4742,4742,4742,MONDO:0015324,cataract-intellectual disability-anal atresia-urinary defects syndrome,MONDO,disease,DISEASE_4742
4743,4743,4743,4743,4743,4743,4743,4743,MONDO:1011235,"microphthalmia, Nile tilapia",MONDO,disease,DISEASE_4743
4744,4744,4744,4744,4744,4744,4744,4744,MONDO:0002683,adult choroid plexus neoplasm,MONDO,disease,DISEASE_4744
4745,4745,4745,4745,4745,4745,4745,4745,MONDO:0006055,sex cord-stromal tumor,MONDO,disease,DISEASE_4745
4746,4746,4746,4746,4746,4746,4746,4746,MONDO:0003147,space motion sickness,MONDO,disease,DISEASE_4746
4747,4747,4747,4747,4747,4747,4747,4747,MONDO:0006038,indeterminate colitis,MONDO,disease,DISEASE_4747
4748,4748,4748,4748,4748,4748,4748,4748,MONDO:0007984,metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome,MONDO,disease,DISEASE_4748
4749,4749,4749,4749,4749,4749,4749,4749,MONDO:0010455,"X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia",MONDO,disease,DISEASE_4749
4750,4750,4750,4750,4750,4750,4750,4750,MONDO:0030491,immunodeficiency 91 and hyperinflammation,MONDO,disease,DISEASE_4750
4751,4751,4751,4751,4751,4751,4751,4751,MONDO:0001637,cicatricial entropion,MONDO,disease,DISEASE_4751
4752,4752,4752,4752,4752,4752,4752,4752,MONDO:0015307,Madras motor neuron disease,MONDO,disease,DISEASE_4752
4753,4753,4753,4753,4753,4753,4753,4753,MONDO:0016455,virus-associated trichodysplasia spinulosa,MONDO,disease,DISEASE_4753
4754,4754,4754,4754,4754,4754,4754,4754,MONDO:0019235,inborn disorder of phenylalanine and tyrosine metabolism,MONDO,disease,DISEASE_4754
4755,4755,4755,4755,4755,4755,4755,4755,MONDO:0017768,reflex epilepsy,MONDO,disease,DISEASE_4755
4756,4756,4756,4756,4756,4756,4756,4756,MONDO:0011677,Megarbane syndrome,MONDO,disease,DISEASE_4756
4757,4757,4757,4757,4757,4757,4757,4757,MONDO:0850338,"spinal ependymoma, MYCN-amplified",MONDO,disease,DISEASE_4757
4758,4758,4758,4758,4758,4758,4758,4758,MONDO:1010744,"atopic dermatitis, domestic cat",MONDO,disease,DISEASE_4758
4759,4759,4759,4759,4759,4759,4759,4759,MONDO:0022826,congenital cystic eye multiple ocular and intracranial anomalies,MONDO,disease,DISEASE_4759
4760,4760,4760,4760,4760,4760,4760,4760,MONDO:0018971,isolated oxycephaly,MONDO,disease,DISEASE_4760
4761,4761,4761,4761,4761,4761,4761,4761,MONDO:1011817,"anal sac gland carcinoma, non-human animal",MONDO,disease,DISEASE_4761
4762,4762,4762,4762,4762,4762,4762,4762,MONDO:0019015,omphalocele,MONDO,disease,DISEASE_4762
4763,4763,4763,4763,4763,4763,4763,4763,MONDO:0015059,progressive non-fluent aphasia,MONDO,disease,DISEASE_4763
4764,4764,4764,4764,4764,4764,4764,4764,MONDO:1011422,"severe combined immunodeficiency disease, non-human animal",MONDO,disease,DISEASE_4764
4765,4765,4765,4765,4765,4765,4765,4765,MONDO:0035511,ricin poisoning,MONDO,disease,DISEASE_4765
4766,4766,4766,4766,4766,4766,4766,4766,MONDO:0019621,chronic pneumonitis of infancy,MONDO,disease,DISEASE_4766
4767,4767,4767,4767,4767,4767,4767,4767,MONDO:0056814,hormone-resistant prostate carcinoma,MONDO,disease,DISEASE_4767
4768,4768,4768,4768,4768,4768,4768,4768,MONDO:0011500,Becker nevus syndrome,MONDO,disease,DISEASE_4768
4769,4769,4769,4769,4769,4769,4769,4769,MONDO:0017314,"Ehlers-Danlos syndrome, vascular type",MONDO,disease,DISEASE_4769
4770,4770,4770,4770,4770,4770,4770,4770,MONDO:0971105,neonatal renal venous thrombosis,MONDO,disease,DISEASE_4770
4771,4771,4771,4771,4771,4771,4771,4771,MONDO:0001017,epididymal adenocarcinoma,MONDO,disease,DISEASE_4771
4772,4772,4772,4772,4772,4772,4772,4772,MONDO:0700153,canine lung adenocarcinoma,MONDO,disease,DISEASE_4772
4773,4773,4773,4773,4773,4773,4773,4773,MONDO:0012316,Majeed syndrome,MONDO,disease,DISEASE_4773
4774,4774,4774,4774,4774,4774,4774,4774,MONDO:0044622,EMILIN-1-related connective tissue disease,MONDO,disease,DISEASE_4774
4775,4775,4775,4775,4775,4775,4775,4775,MONDO:0021085,gastric neoplasm,MONDO,disease,DISEASE_4775
4776,4776,4776,4776,4776,4776,4776,4776,MONDO:0011967,"heterotopia, periventricular, associated with chromosome 5P anomalies",MONDO,disease,DISEASE_4776
4777,4777,4777,4777,4777,4777,4777,4777,MONDO:0017587,onychomatricoma,MONDO,disease,DISEASE_4777
4778,4778,4778,4778,4778,4778,4778,4778,MONDO:0015463,craniodigital syndrome-intellectual disability syndrome,MONDO,disease,DISEASE_4778
4779,4779,4779,4779,4779,4779,4779,4779,MONDO:0004106,"testicular yolk sac tumor, macrocystic pattern",MONDO,disease,DISEASE_4779
4780,4780,4780,4780,4780,4780,4780,4780,MONDO:0041535,mesenteric lymphadenitis due to Yersinia infection,MONDO,disease,DISEASE_4780
4781,4781,4781,4781,4781,4781,4781,4781,MONDO:0043096,holoacardius amorphus,MONDO,disease,DISEASE_4781
4782,4782,4782,4782,4782,4782,4782,4782,MONDO:0019418,X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome,MONDO,disease,DISEASE_4782
4783,4783,4783,4783,4783,4783,4783,4783,MONDO:0001149,microcephaly,MONDO,disease,DISEASE_4783
4784,4784,4784,4784,4784,4784,4784,4784,MONDO:0005321,Fuchs' endothelial dystrophy,MONDO,disease,DISEASE_4784
4785,4785,4785,4785,4785,4785,4785,4785,MONDO:1012927_MONDO:1012951,"Alzheimer disease, APP-related, crab-eating macaque",MONDO_grouped,disease,DISEASE_4785
4786,4786,4786,4786,4786,4786,4786,4786,MONDO:0005259,Asperger syndrome,MONDO,disease,DISEASE_4786
4787,4787,4787,4787,4787,4787,4787,4787,MONDO:0002648,mammary Paget disease,MONDO,disease,DISEASE_4787
4788,4788,4788,4788,4788,4788,4788,4788,MONDO:0015519,congenital or early infantile CACH syndrome,MONDO,disease,DISEASE_4788
4789,4789,4789,4789,4789,4789,4789,4789,MONDO:0003054,benign meningioma,MONDO,disease,DISEASE_4789
4790,4790,4790,4790,4790,4790,4790,4790,MONDO:0002912,brainstem cancer,MONDO,disease,DISEASE_4790
4791,4791,4791,4791,4791,4791,4791,4791,MONDO:0003175,salivary gland adenoid cystic carcinoma,MONDO,disease,DISEASE_4791
4792,4792,4792,4792,4792,4792,4792,4792,MONDO:0006687,burning mouth syndrome,MONDO,disease,DISEASE_4792
4793,4793,4793,4793,4793,4793,4793,4793,MONDO:0016018,diabetic embryopathy,MONDO,disease,DISEASE_4793
4794,4794,4794,4794,4794,4794,4794,4794,MONDO:0024863,small size posterior uveal melanoma,MONDO,disease,DISEASE_4794
4795,4795,4795,4795,4795,4795,4795,4795,MONDO:0958193_MONDO:0958178_MONDO:0957400,"cataracts, hearing impairment, nephrotic syndrome, and enterocolitis",MONDO_grouped,disease,DISEASE_4795
4796,4796,4796,4796,4796,4796,4796,4796,MONDO:0003249,pineal gland cancer,MONDO,disease,DISEASE_4796
4797,4797,4797,4797,4797,4797,4797,4797,MONDO:1011728,"immunoglobulin G2 deficiency, non-human animal",MONDO,disease,DISEASE_4797
4798,4798,4798,4798,4798,4798,4798,4798,MONDO:0002125,status epilepticus,MONDO,disease,DISEASE_4798
4799,4799,4799,4799,4799,4799,4799,4799,MONDO:0005438,metastatic malignant neoplasm in the lymph nodes,MONDO,disease,DISEASE_4799
4800,4800,4800,4800,4800,4800,4800,4800,MONDO:0018784,pediatric multiple sclerosis,MONDO,disease,DISEASE_4800
4801,4801,4801,4801,4801,4801,4801,4801,MONDO:0022800,type 2 collagenopathy,MONDO,disease,DISEASE_4801
4802,4802,4802,4802,4802,4802,4802,4802,MONDO:0000299_MONDO:0004755,thelaziasis,MONDO_grouped,disease,DISEASE_4802
4803,4803,4803,4803,4803,4803,4803,4803,MONDO:0016933,partial trisomy/tetrasomy of the short arm of chromosome 12,MONDO,disease,DISEASE_4803
4804,4804,4804,4804,4804,4804,4804,4804,MONDO:1010077,"Pelger-Huet anomaly, non-human animal",MONDO,disease,DISEASE_4804
4805,4805,4805,4805,4805,4805,4805,4805,MONDO:0002913,cerebellar neoplasm,MONDO,disease,DISEASE_4805
4806,4806,4806,4806,4806,4806,4806,4806,MONDO:1010105,"pyruvate dehydrogenase deficiency, non-human animal",MONDO,disease,DISEASE_4806
4807,4807,4807,4807,4807,4807,4807,4807,MONDO:0007206,"bone pain, periodic",MONDO,disease,DISEASE_4807
4808,4808,4808,4808,4808,4808,4808,4808,MONDO:0700166,canine transmissible venereal tumor,MONDO,disease,DISEASE_4808
4809,4809,4809,4809,4809,4809,4809,4809,MONDO:0033613,neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities,MONDO,disease,DISEASE_4809
4810,4810,4810,4810,4810,4810,4810,4810,MONDO:0045037,hyalohyphomycosis,MONDO,disease,DISEASE_4810
4811,4811,4811,4811,4811,4811,4811,4811,MONDO:0015786,Prader-Willi syndrome due to imprinting mutation,MONDO,disease,DISEASE_4811
4812,4812,4812,4812,4812,4812,4812,4812,MONDO:0032901,Catifa syndrome,MONDO,disease,DISEASE_4812
4813,4813,4813,4813,4813,4813,4813,4813,MONDO:0004446,olfactory groove meningioma,MONDO,disease,DISEASE_4813
4814,4814,4814,4814,4814,4814,4814,4814,MONDO:0020734,obsolete erythrocyte AMP deaminase deficiency,MONDO,disease,DISEASE_4814
4815,4815,4815,4815,4815,4815,4815,4815,MONDO:0011918,anxiety,MONDO,disease,DISEASE_4815
4816,4816,4816,4816,4816,4816,4816,4816,MONDO:0002373,benign mesothelioma,MONDO,disease,DISEASE_4816
4817,4817,4817,4817,4817,4817,4817,4817,MONDO:1012911,"neuromuscular channelopathy, KCNG1-related, cattle",MONDO,disease,DISEASE_4817
4818,4818,4818,4818,4818,4818,4818,4818,MONDO:1011333,"mouth disorder, non-human animal",MONDO,disease,DISEASE_4818
4819,4819,4819,4819,4819,4819,4819,4819,MONDO:1010324,"microphthalmia, non-human animal",MONDO,disease,DISEASE_4819
4820,4820,4820,4820,4820,4820,4820,4820,MONDO:1012025,"respiratory distress syndrome, pig",MONDO,disease,DISEASE_4820
4821,4821,4821,4821,4821,4821,4821,4821,MONDO:0021053,carotid body paraganglioma,MONDO,disease,DISEASE_4821
4822,4822,4822,4822,4822,4822,4822,4822,MONDO:0043653,herpes labialis,MONDO,disease,DISEASE_4822
4823,4823,4823,4823,4823,4823,4823,4823,MONDO:0009699,action myoclonus-renal failure syndrome,MONDO,disease,DISEASE_4823
4824,4824,4824,4824,4824,4824,4824,4824,MONDO:0000380_MONDO:0005289_MONDO:0001743_MONDO:0001758,paranasal sinus carcinoma,MONDO_grouped,disease,DISEASE_4824
4825,4825,4825,4825,4825,4825,4825,4825,MONDO:0009568,mast syndrome,MONDO,disease,DISEASE_4825
4826,4826,4826,4826,4826,4826,4826,4826,MONDO:0004780,strictly posterior acute myocardial infarction,MONDO,disease,DISEASE_4826
4827,4827,4827,4827,4827,4827,4827,4827,MONDO:0030880_MONDO:0012074_MONDO:0016584,mandibuloacral dysplasia progeroid syndrome,MONDO_grouped,disease,DISEASE_4827
4828,4828,4828,4828,4828,4828,4828,4828,MONDO:0015357_MONDO:0016000,secondary hypoparathyroidism due to impaired parathormon secretion,MONDO_grouped,disease,DISEASE_4828
4829,4829,4829,4829,4829,4829,4829,4829,MONDO:0017788,contractures - webbed neck - micrognathia - hypoplastic nipples syndrome,MONDO,disease,DISEASE_4829
4830,4830,4830,4830,4830,4830,4830,4830,MONDO:0800299,"myopathy, congenital, with excess of muscle spindles",MONDO,disease,DISEASE_4830
4831,4831,4831,4831,4831,4831,4831,4831,MONDO:1011938,"arthrogryposis and palatoschisis syndrome, non-human animal",MONDO,disease,DISEASE_4831
4832,4832,4832,4832,4832,4832,4832,4832,MONDO:0035432,POMGNT2-related limb-girdle muscular dystrophy R24,MONDO,disease,DISEASE_4832
4833,4833,4833,4833,4833,4833,4833,4833,MONDO:0008188,"papillomatosis, confluent and reticulated",MONDO,disease,DISEASE_4833
4834,4834,4834,4834,4834,4834,4834,4834,MONDO:0017574,chronic intestinal pseudoobstruction,MONDO,disease,DISEASE_4834
4835,4835,4835,4835,4835,4835,4835,4835,MONDO:0007344,"cluster headache, familial",MONDO,disease,DISEASE_4835
4836,4836,4836,4836,4836,4836,4836,4836,MONDO:0010463,"X-linked dominant chondrodysplasia, Chassaing-Lacombe type",MONDO,disease,DISEASE_4836
4837,4837,4837,4837,4837,4837,4837,4837,MONDO:0017863,digitalis poisoning,MONDO,disease,DISEASE_4837
4838,4838,4838,4838,4838,4838,4838,4838,MONDO:0020535,house allergic alveolitis,MONDO,disease,DISEASE_4838
4839,4839,4839,4839,4839,4839,4839,4839,MONDO:0019820,univentricular cardiopathy,MONDO,disease,DISEASE_4839
4840,4840,4840,4840,4840,4840,4840,4840,MONDO:0019401,sporadic idiopathic steroid-resistant nephrotic syndrome,MONDO,disease,DISEASE_4840
4841,4841,4841,4841,4841,4841,4841,4841,MONDO:0001927,pulmonary valve insufficiency,MONDO,disease,DISEASE_4841
4842,4842,4842,4842,4842,4842,4842,4842,MONDO:0032775,neurodevelopmental disorder with seizures and speech and walking impairment,MONDO,disease,DISEASE_4842
4843,4843,4843,4843,4843,4843,4843,4843,MONDO:1011606,"vestibular disease, dog",MONDO,disease,DISEASE_4843
4844,4844,4844,4844,4844,4844,4844,4844,MONDO:0010750,ulnar hypoplasia-split foot syndrome,MONDO,disease,DISEASE_4844
4845,4845,4845,4845,4845,4845,4845,4845,MONDO:0016376,confetti-like macular atrophy,MONDO,disease,DISEASE_4845
4846,4846,4846,4846,4846,4846,4846,4846,MONDO:0004845,aphthous stomatitis,MONDO,disease,DISEASE_4846
4847,4847,4847,4847,4847,4847,4847,4847,MONDO:0001226,acute contagious conjunctivitis,MONDO,disease,DISEASE_4847
4848,4848,4848,4848,4848,4848,4848,4848,MONDO:0000955,ileum cancer,MONDO,disease,DISEASE_4848
4849,4849,4849,4849,4849,4849,4849,4849,MONDO:0000615,progesterone-receptor positive breast cancer,MONDO,disease,DISEASE_4849
4850,4850,4850,4850,4850,4850,4850,4850,MONDO:0005964,sphenoid sinusitis,MONDO,disease,DISEASE_4850
4851,4851,4851,4851,4851,4851,4851,4851,MONDO:0005499_MONDO:0002542,brain glioma,MONDO_grouped,disease,DISEASE_4851
4852,4852,4852,4852,4852,4852,4852,4852,MONDO:0021275,papilloma of eyelid,MONDO,disease,DISEASE_4852
4853,4853,4853,4853,4853,4853,4853,4853,MONDO:0700102_MONDO:0700100,"lymphoma, non-human animal",MONDO_grouped,disease,DISEASE_4853
4854,4854,4854,4854,4854,4854,4854,4854,MONDO:0008315_MONDO:0003105,prostate cancer,MONDO_grouped,disease,DISEASE_4854
4855,4855,4855,4855,4855,4855,4855,4855,MONDO:0006919,potassium deficiency,MONDO,disease,DISEASE_4855
4856,4856,4856,4856,4856,4856,4856,4856,MONDO:0003617,chronic salpingitis,MONDO,disease,DISEASE_4856
4857,4857,4857,4857,4857,4857,4857,4857,MONDO:0003256,neurohypophysis granular cell tumor,MONDO,disease,DISEASE_4857
4858,4858,4858,4858,4858,4858,4858,4858,MONDO:0005772,geotrichosis,MONDO,disease,DISEASE_4858
4859,4859,4859,4859,4859,4859,4859,4859,MONDO:0958099,idiopathic subglottic stenosis,MONDO,disease,DISEASE_4859
4860,4860,4860,4860,4860,4860,4860,4860,MONDO:0022613,bruyn scheltens syndrome,MONDO,disease,DISEASE_4860
4861,4861,4861,4861,4861,4861,4861,4861,MONDO:0009496,Kniest-like dysplasia with pursed lips and ectopia lentis,MONDO,disease,DISEASE_4861
4862,4862,4862,4862,4862,4862,4862,4862,MONDO:0006742,endemic goiter,MONDO,disease,DISEASE_4862
4863,4863,4863,4863,4863,4863,4863,4863,MONDO:0968945,"neurodevelopmental disorder with language impairment, autism, and attention deficit-hyperactivity disorder",MONDO,disease,DISEASE_4863
4864,4864,4864,4864,4864,4864,4864,4864,MONDO:1012171,"muscle contracture and chondrodysplasia, cattle",MONDO,disease,DISEASE_4864
4865,4865,4865,4865,4865,4865,4865,4865,MONDO:0858956,diffuse leptomeningeal glioneuronal tumor,MONDO,disease,DISEASE_4865
4866,4866,4866,4866,4866,4866,4866,4866,MONDO:0100132,intrahepatic bile duct adenosquamous carcinoma,MONDO,disease,DISEASE_4866
4867,4867,4867,4867,4867,4867,4867,4867,MONDO:0019752,pediatric Castleman disease,MONDO,disease,DISEASE_4867
4868,4868,4868,4868,4868,4868,4868,4868,MONDO:0004846,placental abruption,MONDO,disease,DISEASE_4868
4869,4869,4869,4869,4869,4869,4869,4869,MONDO:0019016,maternally-inherited progressive external ophthalmoplegia,MONDO,disease,DISEASE_4869
4870,4870,4870,4870,4870,4870,4870,4870,MONDO:1012076,"facial digital syndrome, cattle",MONDO,disease,DISEASE_4870
4871,4871,4871,4871,4871,4871,4871,4871,MONDO:0019230,inborn disorder of ornithine or proline metabolism,MONDO,disease,DISEASE_4871
4872,4872,4872,4872,4872,4872,4872,4872,MONDO:0020201,obsolete conjunctival telangiectasia,MONDO,disease,DISEASE_4872
4873,4873,4873,4873,4873,4873,4873,4873,MONDO:0019268,epidermal disease,MONDO,disease,DISEASE_4873
4874,4874,4874,4874,4874,4874,4874,4874,MONDO:0006823,Klinefelter syndrome,MONDO,disease,DISEASE_4874
4875,4875,4875,4875,4875,4875,4875,4875,MONDO:0004907,alopecia,MONDO,disease,DISEASE_4875
4876,4876,4876,4876,4876,4876,4876,4876,MONDO:0017004,partial monosomy of the short arm of chromosome X,MONDO,disease,DISEASE_4876
4877,4877,4877,4877,4877,4877,4877,4877,MONDO:1010854,"Krabbe disease, Rhesus monkey",MONDO,disease,DISEASE_4877
4878,4878,4878,4878,4878,4878,4878,4878,MONDO:1012001,"bilateral corneal stromal loss, non-human animal",MONDO,disease,DISEASE_4878
4879,4879,4879,4879,4879,4879,4879,4879,MONDO:0006993,systolic heart failure,MONDO,disease,DISEASE_4879
4880,4880,4880,4880,4880,4880,4880,4880,MONDO:0030813,immunodeficiency 101 (varicella zoster virus-specific),MONDO,disease,DISEASE_4880
4881,4881,4881,4881,4881,4881,4881,4881,MONDO:0005724,cryptococcosis,MONDO,disease,DISEASE_4881
4882,4882,4882,4882,4882,4882,4882,4882,MONDO:0008222,Andersen-Tawil syndrome,MONDO,disease,DISEASE_4882
4883,4883,4883,4883,4883,4883,4883,4883,MONDO:0003171,pineal gland astrocytoma,MONDO,disease,DISEASE_4883
4884,4884,4884,4884,4884,4884,4884,4884,MONDO:0002408,hereditary hyperbilirubinemia,MONDO,disease,DISEASE_4884
4885,4885,4885,4885,4885,4885,4885,4885,MONDO:0002203,constipation disorder,MONDO,disease,DISEASE_4885
4886,4886,4886,4886,4886,4886,4886,4886,MONDO:0011592_MONDO:0011151_MONDO:0007589_MONDO:0014652_MONDO:0033123_MONDO:0013218_MONDO:0019516,exudative vitreoretinopathy,MONDO_grouped,disease,DISEASE_4886
4887,4887,4887,4887,4887,4887,4887,4887,MONDO:1010088,anti-SAE dermatomyositis,MONDO,disease,DISEASE_4887
4888,4888,4888,4888,4888,4888,4888,4888,MONDO:1011425,"Ehlers-Danlos syndrome, non-human animal",MONDO,disease,DISEASE_4888
4889,4889,4889,4889,4889,4889,4889,4889,MONDO:1011244,"retinal degeneration, crab-eating macaque",MONDO,disease,DISEASE_4889
4890,4890,4890,4890,4890,4890,4890,4890,MONDO:0001230,acute orbital inflammation,MONDO,disease,DISEASE_4890
4891,4891,4891,4891,4891,4891,4891,4891,MONDO:0005763_MONDO:0043479_MONDO:0025371_MONDO:0005944,Flaviviridae infectious disease,MONDO_grouped,disease,DISEASE_4891
4892,4892,4892,4892,4892,4892,4892,4892,MONDO:0002143,vaginal yolk sac tumor,MONDO,disease,DISEASE_4892
4893,4893,4893,4893,4893,4893,4893,4893,MONDO:0008796,aniridia-renal agenesis-psychomotor retardation syndrome,MONDO,disease,DISEASE_4893
4894,4894,4894,4894,4894,4894,4894,4894,MONDO:0003305,cellular neurofibroma,MONDO,disease,DISEASE_4894
4895,4895,4895,4895,4895,4895,4895,4895,MONDO:0016942,partial trisomy/tetrasomy of the short arm of chromosome 5,MONDO,disease,DISEASE_4895
4896,4896,4896,4896,4896,4896,4896,4896,MONDO:0019908,ring chromosome 15,MONDO,disease,DISEASE_4896
4897,4897,4897,4897,4897,4897,4897,4897,MONDO:0700247,RAB18 deficiency,MONDO,disease,DISEASE_4897
4898,4898,4898,4898,4898,4898,4898,4898,MONDO:0012549,"autosomal recessive ataxia, Beauce type",MONDO,disease,DISEASE_4898
4899,4899,4899,4899,4899,4899,4899,4899,MONDO:0013099,"combined pituitary hormone deficiencies, genetic form",MONDO,disease,DISEASE_4899
4900,4900,4900,4900,4900,4900,4900,4900,MONDO:0016187,qualitative or quantitative defects of desmin,MONDO,disease,DISEASE_4900
4901,4901,4901,4901,4901,4901,4901,4901,MONDO:0006562,obsolete incontinentia pigmenti achromians,MONDO,disease,DISEASE_4901
4902,4902,4902,4902,4902,4902,4902,4902,MONDO:0000628,central nervous system organ benign neoplasm,MONDO,disease,DISEASE_4902
4903,4903,4903,4903,4903,4903,4903,4903,MONDO:0005670,blackwater fever,MONDO,disease,DISEASE_4903
4904,4904,4904,4904,4904,4904,4904,4904,MONDO:0002462_MONDO:1011043_MONDO:0001645_MONDO:1011044_MONDO:1012093,glomerulonephritis,MONDO_grouped,disease,DISEASE_4904
4905,4905,4905,4905,4905,4905,4905,4905,MONDO:0019537,hemoglobin D disease,MONDO,disease,DISEASE_4905
4906,4906,4906,4906,4906,4906,4906,4906,MONDO:0859167,hypokalemic tubulopathy and deafness,MONDO,disease,DISEASE_4906
4907,4907,4907,4907,4907,4907,4907,4907,MONDO:0004871,perianal hematoma,MONDO,disease,DISEASE_4907
4908,4908,4908,4908,4908,4908,4908,4908,MONDO:0005288,intestinal polyp,MONDO,disease,DISEASE_4908
4909,4909,4909,4909,4909,4909,4909,4909,MONDO:0000930,nodular malignant melanoma,MONDO,disease,DISEASE_4909
4910,4910,4910,4910,4910,4910,4910,4910,MONDO:0012467_MONDO:0010091_MONDO:0015526,cold-induced sweating syndrome,MONDO_grouped,disease,DISEASE_4910
4911,4911,4911,4911,4911,4911,4911,4911,MONDO:0013679_MONDO:0010016_MONDO:0017838,sclerosteosis,MONDO_grouped,disease,DISEASE_4911
4912,4912,4912,4912,4912,4912,4912,4912,MONDO:0013140_MONDO:0011880_MONDO:0014230_MONDO:0013503_MONDO:0007257_MONDO:0014642,"candidiasis, familial",MONDO_grouped,disease,DISEASE_4912
4913,4913,4913,4913,4913,4913,4913,4913,MONDO:0015627,multiple epiphyseal dysplasia due to collagen 9 anomaly,MONDO,disease,DISEASE_4913
4914,4914,4914,4914,4914,4914,4914,4914,MONDO:0021812,adnexal spiradenoma/cylindroma of a sweat gland,MONDO,disease,DISEASE_4914
4915,4915,4915,4915,4915,4915,4915,4915,MONDO:0010026,SHORT syndrome,MONDO,disease,DISEASE_4915
4916,4916,4916,4916,4916,4916,4916,4916,MONDO:0017170,idiopathic recurrent stupor,MONDO,disease,DISEASE_4916
4917,4917,4917,4917,4917,4917,4917,4917,MONDO:0022323,2-hydroxyethyl methacrylate sensitization,MONDO,disease,DISEASE_4917
4918,4918,4918,4918,4918,4918,4918,4918,MONDO:1011826,"dysplastic gangliocytoma of the cerebellum, non-human animal",MONDO,disease,DISEASE_4918
4919,4919,4919,4919,4919,4919,4919,4919,MONDO:0021299,carcinoma in situ of extrahepatic bile duct,MONDO,disease,DISEASE_4919
4920,4920,4920,4920,4920,4920,4920,4920,MONDO:0008350,pulmonic stenosis and deafness,MONDO,disease,DISEASE_4920
4921,4921,4921,4921,4921,4921,4921,4921,MONDO:0100162,IKBKG-related immunodeficiency with or without ectodermal dysplasia,MONDO,disease,DISEASE_4921
4922,4922,4922,4922,4922,4922,4922,4922,MONDO:0010711,TARP syndrome,MONDO,disease,DISEASE_4922
4923,4923,4923,4923,4923,4923,4923,4923,MONDO:0009397,neonatal severe primary hyperparathyroidism,MONDO,disease,DISEASE_4923
4924,4924,4924,4924,4924,4924,4924,4924,MONDO:0850010,congenital optic disk excavation,MONDO,disease,DISEASE_4924
4925,4925,4925,4925,4925,4925,4925,4925,MONDO:0004618,diplegia of upper limb,MONDO,disease,DISEASE_4925
4926,4926,4926,4926,4926,4926,4926,4926,MONDO:0021244,submandibular gland neoplasm,MONDO,disease,DISEASE_4926
4927,4927,4927,4927,4927,4927,4927,4927,MONDO:0019006,familial idiopathic steroid-resistant nephrotic syndrome,MONDO,disease,DISEASE_4927
4928,4928,4928,4928,4928,4928,4928,4928,MONDO:0002333,splenic abscess,MONDO,disease,DISEASE_4928
4929,4929,4929,4929,4929,4929,4929,4929,MONDO:0009315,congenital factor XII deficiency,MONDO,disease,DISEASE_4929
4930,4930,4930,4930,4930,4930,4930,4930,MONDO:0018658,19p13.3 microduplication syndrome,MONDO,disease,DISEASE_4930
4931,4931,4931,4931,4931,4931,4931,4931,MONDO:0022887,craniofrontonasal syndrome Teebi type,MONDO,disease,DISEASE_4931
4932,4932,4932,4932,4932,4932,4932,4932,MONDO:0850071,developmental delay-immunodeficiency-leukoencephalopathy-hypohomocysteinemia syndrome,MONDO,disease,DISEASE_4932
4933,4933,4933,4933,4933,4933,4933,4933,MONDO:0017895,familial papillary or follicular thyroid carcinoma,MONDO,disease,DISEASE_4933
4934,4934,4934,4934,4934,4934,4934,4934,MONDO:1011595_MONDO:1011594,"rickets, pig",MONDO_grouped,disease,DISEASE_4934
4935,4935,4935,4935,4935,4935,4935,4935,MONDO:0002552,vascular myelopathy,MONDO,disease,DISEASE_4935
4936,4936,4936,4936,4936,4936,4936,4936,MONDO:0006662,aseptic meningitis,MONDO,disease,DISEASE_4936
4937,4937,4937,4937,4937,4937,4937,4937,MONDO:0100262_MONDO:0100259_MONDO:0100272_MONDO:0100266_MONDO:0100263_MONDO:0100260_MONDO:0100264_MONDO:0100271_MONDO:0100269_MONDO:0100261_MONDO:0100267_MONDO:0100270_MONDO:0100268_MONDO:0100279,peroxisome biogenesis disorder due to PEX5 defect,MONDO_grouped,disease,DISEASE_4937
4938,4938,4938,4938,4938,4938,4938,4938,MONDO:0008046,autosomal dominant myoglobinuria,MONDO,disease,DISEASE_4938
4939,4939,4939,4939,4939,4939,4939,4939,MONDO:0014168,severe combined immunodeficiency due to CORO1A deficiency,MONDO,disease,DISEASE_4939
4940,4940,4940,4940,4940,4940,4940,4940,MONDO:1012729,"porcine stress syndrome, DMD-related, pig",MONDO,disease,DISEASE_4940
4941,4941,4941,4941,4941,4941,4941,4941,MONDO:0700253,paraneoplastic hematological syndrome,MONDO,disease,DISEASE_4941
4942,4942,4942,4942,4942,4942,4942,4942,MONDO:0002688,duodenal obstruction,MONDO,disease,DISEASE_4942
4943,4943,4943,4943,4943,4943,4943,4943,MONDO:0009951,"radiculoneuropathy, fatal neonatal",MONDO,disease,DISEASE_4943
4944,4944,4944,4944,4944,4944,4944,4944,MONDO:0012335,obesity due to pro-opiomelanocortin deficiency,MONDO,disease,DISEASE_4944
4945,4945,4945,4945,4945,4945,4945,4945,MONDO:0005750,ephemeral fever,MONDO,disease,DISEASE_4945
4946,4946,4946,4946,4946,4946,4946,4946,MONDO:0009635_MONDO:1010546,microvillus inclusion disease,MONDO_grouped,disease,DISEASE_4946
4947,4947,4947,4947,4947,4947,4947,4947,MONDO:0016323,chronic respiratory distress with surfactant metabolism deficiency,MONDO,disease,DISEASE_4947
4948,4948,4948,4948,4948,4948,4948,4948,MONDO:0012892,"bone fragility with contractures, arterial rupture, and deafness",MONDO,disease,DISEASE_4948
4949,4949,4949,4949,4949,4949,4949,4949,MONDO:0021639_MONDO:0021640,grade II glioma,MONDO_grouped,disease,DISEASE_4949
4950,4950,4950,4950,4950,4950,4950,4950,MONDO:0010304_MONDO:0800250,"Graves disease, susceptibility to, X-linked",MONDO_grouped,disease,DISEASE_4950
4951,4951,4951,4951,4951,4951,4951,4951,MONDO:0005848,miliary tuberculosis,MONDO,disease,DISEASE_4951
4952,4952,4952,4952,4952,4952,4952,4952,MONDO:0016193,qualitative or quantitative defects of alpha-actin,MONDO,disease,DISEASE_4952
4953,4953,4953,4953,4953,4953,4953,4953,MONDO:1011964,"idiopathic congenital chondrodystrophy, non-human animal",MONDO,disease,DISEASE_4953
4954,4954,4954,4954,4954,4954,4954,4954,MONDO:0015099_MONDO:0017092_MONDO:0017093,unilateral hemispheric polymicrogyria,MONDO_grouped,disease,DISEASE_4954
4955,4955,4955,4955,4955,4955,4955,4955,MONDO:1012436,"lacrimal fistula, cattle",MONDO,disease,DISEASE_4955
4956,4956,4956,4956,4956,4956,4956,4956,MONDO:0015204,microlissencephaly,MONDO,disease,DISEASE_4956
4957,4957,4957,4957,4957,4957,4957,4957,MONDO:0001186,depersonalization disorder,MONDO,disease,DISEASE_4957
4958,4958,4958,4958,4958,4958,4958,4958,MONDO:0025113,poultry disease,MONDO,disease,DISEASE_4958
4959,4959,4959,4959,4959,4959,4959,4959,MONDO:0008317,proteolytic capacity of plasma,MONDO,disease,DISEASE_4959
4960,4960,4960,4960,4960,4960,4960,4960,MONDO:0008486,steatocystoma multiplex-natal teeth syndrome,MONDO,disease,DISEASE_4960
4961,4961,4961,4961,4961,4961,4961,4961,MONDO:0024417,perceptual disorders,MONDO,disease,DISEASE_4961
4962,4962,4962,4962,4962,4962,4962,4962,MONDO:0957284,"nemaline myopathy 5C, autosomal dominant",MONDO,disease,DISEASE_4962
4963,4963,4963,4963,4963,4963,4963,4963,MONDO:0001529,pancytopenia,MONDO,disease,DISEASE_4963
4964,4964,4964,4964,4964,4964,4964,4964,MONDO:1010739,"severe combined immunodeficiency disease, pig",MONDO,disease,DISEASE_4964
4965,4965,4965,4965,4965,4965,4965,4965,MONDO:0001546,hypermobility of coccyx,MONDO,disease,DISEASE_4965
4966,4966,4966,4966,4966,4966,4966,4966,MONDO:1012129,"immunoglobulin A deficiency, gray wolf",MONDO,disease,DISEASE_4966
4967,4967,4967,4967,4967,4967,4967,4967,MONDO:0006801,ileal neoplasm,MONDO,disease,DISEASE_4967
4968,4968,4968,4968,4968,4968,4968,4968,MONDO:0019383,acute disseminated encephalomyelitis,MONDO,disease,DISEASE_4968
4969,4969,4969,4969,4969,4969,4969,4969,MONDO:0015451,univentricular heart,MONDO,disease,DISEASE_4969
4970,4970,4970,4970,4970,4970,4970,4970,MONDO:0022960,dermatocardioskeletal syndrome boronne type,MONDO,disease,DISEASE_4970
4971,4971,4971,4971,4971,4971,4971,4971,MONDO:0005798,HIV-associated nephropathy,MONDO,disease,DISEASE_4971
4972,4972,4972,4972,4972,4972,4972,4972,MONDO:0003737,malignant testicular Leydig cell tumor,MONDO,disease,DISEASE_4972
4973,4973,4973,4973,4973,4973,4973,4973,MONDO:0010370_MONDO:0012555_MONDO:0013864_MONDO:0007387_MONDO:0957921_MONDO:0010471_MONDO:0016033,Cornelia de Lange syndrome,MONDO_grouped,disease,DISEASE_4973
4974,4974,4974,4974,4974,4974,4974,4974,MONDO:0859233_MONDO:0009183_MONDO:0012807,"epidermolysis bullosa, junctional 6, with pyloric atresia",MONDO_grouped,disease,DISEASE_4974
4975,4975,4975,4975,4975,4975,4975,4975,MONDO:0017416,postpoliomyelitis syndrome,MONDO,disease,DISEASE_4975
4976,4976,4976,4976,4976,4976,4976,4976,MONDO:0800155,inborn disorder of glycine and serine metabolism,MONDO,disease,DISEASE_4976
4977,4977,4977,4977,4977,4977,4977,4977,MONDO:0004749,myocardium cancer,MONDO,disease,DISEASE_4977
4978,4978,4978,4978,4978,4978,4978,4978,MONDO:1011806,"immune-mediated myositis, non-human animal",MONDO,disease,DISEASE_4978
4979,4979,4979,4979,4979,4979,4979,4979,MONDO:0021018,autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6),MONDO,disease,DISEASE_4979
4980,4980,4980,4980,4980,4980,4980,4980,MONDO:0009856,Peters plus syndrome,MONDO,disease,DISEASE_4980
4981,4981,4981,4981,4981,4981,4981,4981,MONDO:0006989,suppurative periapical periodontitis,MONDO,disease,DISEASE_4981
4982,4982,4982,4982,4982,4982,4982,4982,MONDO:0008935,cerebellar ataxia-hypogonadism syndrome,MONDO,disease,DISEASE_4982
4983,4983,4983,4983,4983,4983,4983,4983,MONDO:0044001,"hearing loss, mixed conductive-sensorineural",MONDO,disease,DISEASE_4983
4984,4984,4984,4984,4984,4984,4984,4984,MONDO:0005905,periodic limb movement disorder,MONDO,disease,DISEASE_4984
4985,4985,4985,4985,4985,4985,4985,4985,MONDO:0036218,lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster,MONDO,disease,DISEASE_4985
4986,4986,4986,4986,4986,4986,4986,4986,MONDO:0021184,deltaretrovirus infections,MONDO,disease,DISEASE_4986
4987,4987,4987,4987,4987,4987,4987,4987,MONDO:0016127_MONDO:0004471,bacterial myositis,MONDO_grouped,disease,DISEASE_4987
4988,4988,4988,4988,4988,4988,4988,4988,MONDO:1011462,"Alzheimer disease, domestic cat",MONDO,disease,DISEASE_4988
4989,4989,4989,4989,4989,4989,4989,4989,MONDO:0009841,PEHO syndrome,MONDO,disease,DISEASE_4989
4990,4990,4990,4990,4990,4990,4990,4990,MONDO:0012126,familial avascular necrosis of femoral head,MONDO,disease,DISEASE_4990
4991,4991,4991,4991,4991,4991,4991,4991,MONDO:0005973,Strongylida infectious disease,MONDO,disease,DISEASE_4991
4992,4992,4992,4992,4992,4992,4992,4992,MONDO:0041755,twin reversal arterial perfusion syndrome,MONDO,disease,DISEASE_4992
4993,4993,4993,4993,4993,4993,4993,4993,MONDO:0005253,high output heart failure,MONDO,disease,DISEASE_4993
4994,4994,4994,4994,4994,4994,4994,4994,MONDO:1010024,"atrial fibrillation, non-human animal",MONDO,disease,DISEASE_4994
4995,4995,4995,4995,4995,4995,4995,4995,MONDO:0018879,lichen planopilaris,MONDO,disease,DISEASE_4995
4996,4996,4996,4996,4996,4996,4996,4996,MONDO:0010339,"epilepsy, X-linked 1, with variable learning disabilities and behavior disorders",MONDO,disease,DISEASE_4996
4997,4997,4997,4997,4997,4997,4997,4997,MONDO:0850058,chronic neurovisceral acid sphingomyelinase deficiency,MONDO,disease,DISEASE_4997
4998,4998,4998,4998,4998,4998,4998,4998,MONDO:0018694,isolated tracheo-esophageal fistula,MONDO,disease,DISEASE_4998
4999,4999,4999,4999,4999,4999,4999,4999,MONDO:0006430,splenic mantle cell lymphoma,MONDO,disease,DISEASE_4999
5000,5000,5000,5000,5000,5000,5000,5000,MONDO:0009145,SchC6pf-Schulz-Passarge syndrome,MONDO,disease,DISEASE_5000
5001,5001,5001,5001,5001,5001,5001,5001,MONDO:0022712,oculo digital syndrome,MONDO,disease,DISEASE_5001
5002,5002,5002,5002,5002,5002,5002,5002,MONDO:0015084,FRAXF syndrome,MONDO,disease,DISEASE_5002
5003,5003,5003,5003,5003,5003,5003,5003,MONDO:0014098_MONDO:0011448_MONDO:0014431,CIDEC-related familial partial lipodystrophy,MONDO_grouped,disease,DISEASE_5003
5004,5004,5004,5004,5004,5004,5004,5004,MONDO:0003073,trilateral retinoblastoma,MONDO,disease,DISEASE_5004
5005,5005,5005,5005,5005,5005,5005,5005,MONDO:1010845_MONDO:1010846_MONDO:1010848_MONDO:1010878,"GM1 gangliosidosis, GLB1-related, dog",MONDO_grouped,disease,DISEASE_5005
5006,5006,5006,5006,5006,5006,5006,5006,MONDO:0000332,sennetsu fever,MONDO,disease,DISEASE_5006
5007,5007,5007,5007,5007,5007,5007,5007,MONDO:1010678,"AA amyloidosis, island gray fox",MONDO,disease,DISEASE_5007
5008,5008,5008,5008,5008,5008,5008,5008,MONDO:0009248,fructose and galactose intolerance,MONDO,disease,DISEASE_5008
5009,5009,5009,5009,5009,5009,5009,5009,MONDO:0013881,"epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome",MONDO,disease,DISEASE_5009
5010,5010,5010,5010,5010,5010,5010,5010,MONDO:0010441,CK syndrome,MONDO,disease,DISEASE_5010
5011,5011,5011,5011,5011,5011,5011,5011,MONDO:0016491,hemoglobin E-beta-thalassemia syndrome,MONDO,disease,DISEASE_5011
5012,5012,5012,5012,5012,5012,5012,5012,MONDO:0004588,night blindness,MONDO,disease,DISEASE_5012
5013,5013,5013,5013,5013,5013,5013,5013,MONDO:0002478,mixed germ cell-sex cord-stromal tumor,MONDO,disease,DISEASE_5013
5014,5014,5014,5014,5014,5014,5014,5014,MONDO:0018762,non-acquired combined pituitary hormone deficiency,MONDO,disease,DISEASE_5014
5015,5015,5015,5015,5015,5015,5015,5015,MONDO:0000630,immune system organ benign neoplasm,MONDO,disease,DISEASE_5015
5016,5016,5016,5016,5016,5016,5016,5016,MONDO:0004001,compartment syndrome,MONDO,disease,DISEASE_5016
5017,5017,5017,5017,5017,5017,5017,5017,MONDO:0018516,epithelial tumor of anal canal,MONDO,disease,DISEASE_5017
5018,5018,5018,5018,5018,5018,5018,5018,MONDO:0000595,sexual and gender identity disorders,MONDO,disease,DISEASE_5018
5019,5019,5019,5019,5019,5019,5019,5019,MONDO:0007838,Jacobsen syndrome,MONDO,disease,DISEASE_5019
5020,5020,5020,5020,5020,5020,5020,5020,MONDO:1010883_MONDO:1010884_MONDO:1012687_MONDO:1012688_MONDO:1012690,"GM2 gangliosidosis, HEXB-related dog",MONDO_grouped,disease,DISEASE_5020
5021,5021,5021,5021,5021,5021,5021,5021,MONDO:0007020,Wernicke encephalopathy,MONDO,disease,DISEASE_5021
5022,5022,5022,5022,5022,5022,5022,5022,MONDO:0013614,hypertelorism-preauricular sinus-punctual pits-deafness syndrome,MONDO,disease,DISEASE_5022
5023,5023,5023,5023,5023,5023,5023,5023,MONDO:0006284,major salivary gland carcinoma,MONDO,disease,DISEASE_5023
5024,5024,5024,5024,5024,5024,5024,5024,MONDO:0018346,ferro-cerebro-cutaneous syndrome,MONDO,disease,DISEASE_5024
5025,5025,5025,5025,5025,5025,5025,5025,MONDO:0035592,congenital infiltrating lipomatosis of the face,MONDO,disease,DISEASE_5025
5026,5026,5026,5026,5026,5026,5026,5026,MONDO:0008181,"palmaris longus muscle, absence of",MONDO,disease,DISEASE_5026
5027,5027,5027,5027,5027,5027,5027,5027,MONDO:1010234,"olivopontocerebellar atrophy, non-human animal",MONDO,disease,DISEASE_5027
5028,5028,5028,5028,5028,5028,5028,5028,MONDO:0006234,grade III prostatic intraepithelial neoplasia,MONDO,disease,DISEASE_5028
5029,5029,5029,5029,5029,5029,5029,5029,MONDO:0957912,organophosphate-induced delayed polyneuropathy,MONDO,disease,DISEASE_5029
5030,5030,5030,5030,5030,5030,5030,5030,MONDO:1011556,"medium-chain acyl-CoA dehydrogenase deficiency, dog",MONDO,disease,DISEASE_5030
5031,5031,5031,5031,5031,5031,5031,5031,MONDO:0024481,skin appendage disorder,MONDO,disease,DISEASE_5031
5032,5032,5032,5032,5032,5032,5032,5032,MONDO:0016672,hereditary persistence of fetal hemoglobin-sickle cell disease syndrome,MONDO,disease,DISEASE_5032
5033,5033,5033,5033,5033,5033,5033,5033,MONDO:0017732_MONDO:0017733,"alpha-mannosidosis, infantile form",MONDO_grouped,disease,DISEASE_5033
5034,5034,5034,5034,5034,5034,5034,5034,MONDO:0005087,respiratory system disorder,MONDO,disease,DISEASE_5034
5035,5035,5035,5035,5035,5035,5035,5035,MONDO:1012766_MONDO:1012943,"dwarfism, GON4L-related, cattle",MONDO_grouped,disease,DISEASE_5035
5036,5036,5036,5036,5036,5036,5036,5036,MONDO:0021562,omphalitis,MONDO,disease,DISEASE_5036
5037,5037,5037,5037,5037,5037,5037,5037,MONDO:0012221_MONDO:0012222_MONDO:0017779_MONDO:0019264,alpha-N-acetylgalactosaminidase deficiency,MONDO_grouped,disease,DISEASE_5037
5038,5038,5038,5038,5038,5038,5038,5038,MONDO:0024892,soft tissue amyloid neoplasm,MONDO,disease,DISEASE_5038
5039,5039,5039,5039,5039,5039,5039,5039,MONDO:0031322,triopia,MONDO,disease,DISEASE_5039
5040,5040,5040,5040,5040,5040,5040,5040,MONDO:0016893,partial deletion of the short arm of chromosome 11,MONDO,disease,DISEASE_5040
5041,5041,5041,5041,5041,5041,5041,5041,MONDO:0000182,congenital myasthenic syndrome with tubular aggregates,MONDO,disease,DISEASE_5041
5042,5042,5042,5042,5042,5042,5042,5042,MONDO:0001075,steatorrhea,MONDO,disease,DISEASE_5042
5043,5043,5043,5043,5043,5043,5043,5043,MONDO:0700271,CHEK2-related cancer predisposition,MONDO,disease,DISEASE_5043
5044,5044,5044,5044,5044,5044,5044,5044,MONDO:0019178,auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome,MONDO,disease,DISEASE_5044
5045,5045,5045,5045,5045,5045,5045,5045,MONDO:0001884,abducens nerve neoplasm,MONDO,disease,DISEASE_5045
5046,5046,5046,5046,5046,5046,5046,5046,MONDO:0010964_MONDO:0007561_MONDO:0010844_MONDO:0009189_MONDO:0054680_MONDO:0011765_MONDO:0013591_MONDO:0011109_MONDO:0016648,"epiphyseal dysplasia, multiple",MONDO_grouped,disease,DISEASE_5046
5047,5047,5047,5047,5047,5047,5047,5047,MONDO:0009743,"neurologic disease, infantile multisystem, with osseous fragility",MONDO,disease,DISEASE_5047
5048,5048,5048,5048,5048,5048,5048,5048,MONDO:0011511,"clavicular hypoplasia, zygomatic arch hypoplasia, and micrognathia",MONDO,disease,DISEASE_5048
5049,5049,5049,5049,5049,5049,5049,5049,MONDO:0005159_MONDO:0005082_MONDO:0002854_MONDO:0002450_MONDO:0000996_MONDO:0002452_MONDO:0003368_MONDO:0004124_MONDO:0006390,prostate carcinoma,MONDO_grouped,disease,DISEASE_5049
5050,5050,5050,5050,5050,5050,5050,5050,MONDO:1011532_MONDO:1011533,"hyperadrenocorticism, domestic ferret",MONDO_grouped,disease,DISEASE_5050
5051,5051,5051,5051,5051,5051,5051,5051,MONDO:0005276,dental caries,MONDO,disease,DISEASE_5051
5052,5052,5052,5052,5052,5052,5052,5052,MONDO:0019409,idiopathic juvenile osteoporosis,MONDO,disease,DISEASE_5052
5053,5053,5053,5053,5053,5053,5053,5053,MONDO:0008309,primary release disorder of platelets,MONDO,disease,DISEASE_5053
5054,5054,5054,5054,5054,5054,5054,5054,MONDO:1012631,"XX difference of sexual development, common carp",MONDO,disease,DISEASE_5054
5055,5055,5055,5055,5055,5055,5055,5055,MONDO:0018143,"pyruvate carboxylase deficiency, benign type",MONDO,disease,DISEASE_5055
5056,5056,5056,5056,5056,5056,5056,5056,MONDO:0006762,freemartinism,MONDO,disease,DISEASE_5056
5057,5057,5057,5057,5057,5057,5057,5057,MONDO:0012047,"alopecia universalis congenita, 10Y gonadal dysgenesis, and laryngomalacia",MONDO,disease,DISEASE_5057
5058,5058,5058,5058,5058,5058,5058,5058,MONDO:0016129_MONDO:0002840_MONDO:0018439,eosinophilic gastroenteritis,MONDO_grouped,disease,DISEASE_5058
5059,5059,5059,5059,5059,5059,5059,5059,MONDO:0000706_MONDO:0000707,chemical colitis,MONDO_grouped,disease,DISEASE_5059
5060,5060,5060,5060,5060,5060,5060,5060,MONDO:0018980,"acrofacial dysostosis, Kennedy-Teebi type",MONDO,disease,DISEASE_5060
5061,5061,5061,5061,5061,5061,5061,5061,MONDO:0008833_MONDO:0014174_MONDO:0017417,renal-hepatic-pancreatic dysplasia,MONDO_grouped,disease,DISEASE_5061
5062,5062,5062,5062,5062,5062,5062,5062,MONDO:0015898,adrenogenital syndrome,MONDO,disease,DISEASE_5062
5063,5063,5063,5063,5063,5063,5063,5063,MONDO:0002806,bronchogenic carcinoma,MONDO,disease,DISEASE_5063
5064,5064,5064,5064,5064,5064,5064,5064,MONDO:1010438,"cardiomyopathy, salmonids",MONDO,disease,DISEASE_5064
5065,5065,5065,5065,5065,5065,5065,5065,MONDO:0975795,Kariminejad neurodevelopmental syndrome,MONDO,disease,DISEASE_5065
5066,5066,5066,5066,5066,5066,5066,5066,MONDO:0023119,familial myelofibrosis,MONDO,disease,DISEASE_5066
5067,5067,5067,5067,5067,5067,5067,5067,MONDO:0002482,nipple neoplasm,MONDO,disease,DISEASE_5067
5068,5068,5068,5068,5068,5068,5068,5068,MONDO:0005890,osteitis fibrosa,MONDO,disease,DISEASE_5068
5069,5069,5069,5069,5069,5069,5069,5069,MONDO:0007808,ichthyosis hystrix of Curth-Macklin,MONDO,disease,DISEASE_5069
5070,5070,5070,5070,5070,5070,5070,5070,MONDO:0009053,ALDH18A1-related de Barsy syndrome,MONDO,disease,DISEASE_5070
5071,5071,5071,5071,5071,5071,5071,5071,MONDO:0003093,mucoepidermoid esophageal carcinoma,MONDO,disease,DISEASE_5071
5072,5072,5072,5072,5072,5072,5072,5072,MONDO:0015584,febrile infection-related epilepsy syndrome,MONDO,disease,DISEASE_5072
5073,5073,5073,5073,5073,5073,5073,5073,MONDO:0009333,mullerian derivatives-lymphangiectasia-polydactyly syndrome,MONDO,disease,DISEASE_5073
5074,5074,5074,5074,5074,5074,5074,5074,MONDO:0017347,plasmablastic lymphoma,MONDO,disease,DISEASE_5074
5075,5075,5075,5075,5075,5075,5075,5075,MONDO:0020435,"atrial septal defect, coronary sinus type",MONDO,disease,DISEASE_5075
5076,5076,5076,5076,5076,5076,5076,5076,MONDO:0005011_MONDO:0005535,Crohn disease,MONDO_grouped,disease,DISEASE_5076
5077,5077,5077,5077,5077,5077,5077,5077,MONDO:0003915,cortical thymoma,MONDO,disease,DISEASE_5077
5078,5078,5078,5078,5078,5078,5078,5078,MONDO:0044633,idiopathic pleuroparenchymal fibroelastosis,MONDO,disease,DISEASE_5078
5079,5079,5079,5079,5079,5079,5079,5079,MONDO:1011469,"amyloidosis, domestic goose",MONDO,disease,DISEASE_5079
5080,5080,5080,5080,5080,5080,5080,5080,MONDO:0012275,fetal valproate syndrome,MONDO,disease,DISEASE_5080
5081,5081,5081,5081,5081,5081,5081,5081,MONDO:0017583,mirror polydactyly-vertebral segmentation-limbs defects syndrome,MONDO,disease,DISEASE_5081
5082,5082,5082,5082,5082,5082,5082,5082,MONDO:0003927,posterior uveal melanoma,MONDO,disease,DISEASE_5082
5083,5083,5083,5083,5083,5083,5083,5083,MONDO:0000663,anosognosia,MONDO,disease,DISEASE_5083
5084,5084,5084,5084,5084,5084,5084,5084,MONDO:0003255,mediastinal granular cell myoblastoma,MONDO,disease,DISEASE_5084
5085,5085,5085,5085,5085,5085,5085,5085,MONDO:0006179_MONDO:0044785,desmoplastic ameloblastoma,MONDO_grouped,disease,DISEASE_5085
5086,5086,5086,5086,5086,5086,5086,5086,MONDO:0008710,RAB23-related Carpenter syndrome,MONDO,disease,DISEASE_5086
5087,5087,5087,5087,5087,5087,5087,5087,MONDO:0012511,preterm premature rupture of the membranes,MONDO,disease,DISEASE_5087
5088,5088,5088,5088,5088,5088,5088,5088,MONDO:0018129_MONDO:0011811,autosomal recessive cerebellar ataxia with late-onset spasticity,MONDO_grouped,disease,DISEASE_5088
5089,5089,5089,5089,5089,5089,5089,5089,MONDO:0007202,blepharoptosis-myopia-ectopia lentis syndrome,MONDO,disease,DISEASE_5089
5090,5090,5090,5090,5090,5090,5090,5090,MONDO:0010066,familial isolated congenital asplenia,MONDO,disease,DISEASE_5090
5091,5091,5091,5091,5091,5091,5091,5091,MONDO:0011816,lathosterolosis,MONDO,disease,DISEASE_5091
5092,5092,5092,5092,5092,5092,5092,5092,MONDO:0005592,smooth surface dental caries,MONDO,disease,DISEASE_5092
5093,5093,5093,5093,5093,5093,5093,5093,MONDO:0024521_MONDO:0014950_MONDO:0014187_MONDO:0014514_MONDO:0013418_MONDO:0007568_MONDO:0012730_MONDO:0030731_MONDO:0024559_MONDO:0007031_MONDO:0011770_MONDO:0012343_MONDO:0012751_MONDO:0013716_MONDO:1012381,"aortic aneurysm, familial abdominal",MONDO_grouped,disease,DISEASE_5093
5094,5094,5094,5094,5094,5094,5094,5094,MONDO:0015771,mosaic trisomy 7,MONDO,disease,DISEASE_5094
5095,5095,5095,5095,5095,5095,5095,5095,MONDO:0008138,syndromic orbital border hypoplasia,MONDO,disease,DISEASE_5095
5096,5096,5096,5096,5096,5096,5096,5096,MONDO:0001924,dystrophies primarily involving the retinal pigment epithelium,MONDO,disease,DISEASE_5096
5097,5097,5097,5097,5097,5097,5097,5097,MONDO:0019669,hypochondrogenesis,MONDO,disease,DISEASE_5097
5098,5098,5098,5098,5098,5098,5098,5098,MONDO:0007994,micromelic bone dysplasia with cloverleaf skull,MONDO,disease,DISEASE_5098
5099,5099,5099,5099,5099,5099,5099,5099,MONDO:0018428,9q31.1q31.3 microdeletion syndrome,MONDO,disease,DISEASE_5099
5100,5100,5100,5100,5100,5100,5100,5100,MONDO:0006656,aortitis,MONDO,disease,DISEASE_5100
5101,5101,5101,5101,5101,5101,5101,5101,MONDO:1012887,"skeletal-cardio-enteric dysplasia, MAP2K2-related, cattle",MONDO,disease,DISEASE_5101
5102,5102,5102,5102,5102,5102,5102,5102,MONDO:0012166,autosomal dominant sensory ataxia 1,MONDO,disease,DISEASE_5102
5103,5103,5103,5103,5103,5103,5103,5103,MONDO:0002751,bladder adenocarcinoma,MONDO,disease,DISEASE_5103
5104,5104,5104,5104,5104,5104,5104,5104,MONDO:0850144,germ cell benign neoplasm,MONDO,disease,DISEASE_5104
5105,5105,5105,5105,5105,5105,5105,5105,MONDO:1012525,"Meckel-like hepatorenal fibrocystic dysplasia syndrome, sheep",MONDO,disease,DISEASE_5105
5106,5106,5106,5106,5106,5106,5106,5106,MONDO:0012271,mesoaxial synostotic syndactyly with phalangeal reduction,MONDO,disease,DISEASE_5106
5107,5107,5107,5107,5107,5107,5107,5107,MONDO:0011450_MONDO:0013253_MONDO:0957530_MONDO:0012933_MONDO:0100526_MONDO:0013669,"breast-ovarian cancer, familial, susceptibility to",MONDO_grouped,disease,DISEASE_5107
5108,5108,5108,5108,5108,5108,5108,5108,MONDO:0008453_MONDO:0014121_MONDO:0008026_MONDO:0018190,"adult-onset proximal spinal muscular atrophy, autosomal dominant",MONDO_grouped,disease,DISEASE_5108
5109,5109,5109,5109,5109,5109,5109,5109,MONDO:0008938,early-onset cerebellar ataxia with retained tendon reflexes,MONDO,disease,DISEASE_5109
5110,5110,5110,5110,5110,5110,5110,5110,MONDO:0001109,petrositis,MONDO,disease,DISEASE_5110
5111,5111,5111,5111,5111,5111,5111,5111,MONDO:0002021,gingival disorder,MONDO,disease,DISEASE_5111
5112,5112,5112,5112,5112,5112,5112,5112,MONDO:1012319,"high-frequency tremor, macaques",MONDO,disease,DISEASE_5112
5113,5113,5113,5113,5113,5113,5113,5113,MONDO:0007090,"amastia, bilateral, with ureteral triplication and dysmorphism",MONDO,disease,DISEASE_5113
5114,5114,5114,5114,5114,5114,5114,5114,MONDO:0017082,basal encephalocele,MONDO,disease,DISEASE_5114
5115,5115,5115,5115,5115,5115,5115,5115,MONDO:0011438_MONDO:0100486,acne,MONDO_grouped,disease,DISEASE_5115
5116,5116,5116,5116,5116,5116,5116,5116,MONDO:0020550,gestational choriocarcinoma,MONDO,disease,DISEASE_5116
5117,5117,5117,5117,5117,5117,5117,5117,MONDO:0006507,hereditary hemochromatosis,MONDO,disease,DISEASE_5117
5118,5118,5118,5118,5118,5118,5118,5118,MONDO:0020412,congenital patent ductus arteriosus aneurysm,MONDO,disease,DISEASE_5118
5119,5119,5119,5119,5119,5119,5119,5119,MONDO:0956987,EZB-MYC+ diffuse large B-cell lymphoma,MONDO,disease,DISEASE_5119
5120,5120,5120,5120,5120,5120,5120,5120,MONDO:0035759,factor V atlanta bleeding disorder,MONDO,disease,DISEASE_5120
5121,5121,5121,5121,5121,5121,5121,5121,MONDO:0015103,pulmonary valve agenesis-tetralogy of fallot-absence of ductus arteriosus syndrome,MONDO,disease,DISEASE_5121
5122,5122,5122,5122,5122,5122,5122,5122,MONDO:0015396,congenital laryngeal cyst,MONDO,disease,DISEASE_5122
5123,5123,5123,5123,5123,5123,5123,5123,MONDO:0011885_MONDO:0800337,tubulointerstitial nephritis and uveitis syndrome,MONDO_grouped,disease,DISEASE_5123
5124,5124,5124,5124,5124,5124,5124,5124,MONDO:0007456,"diarrhea, glucose-stimulated secretory, with common variable immunodeficiency",MONDO,disease,DISEASE_5124
5125,5125,5125,5125,5125,5125,5125,5125,MONDO:0001757,frontal sinus neoplasm,MONDO,disease,DISEASE_5125
5126,5126,5126,5126,5126,5126,5126,5126,MONDO:0018006,adult-onset distal myopathy due to VCP mutation,MONDO,disease,DISEASE_5126
5127,5127,5127,5127,5127,5127,5127,5127,MONDO:0700148,canine transitional cell carcinoma,MONDO,disease,DISEASE_5127
5128,5128,5128,5128,5128,5128,5128,5128,MONDO:0850295,acquired laryngomalacia,MONDO,disease,DISEASE_5128
5129,5129,5129,5129,5129,5129,5129,5129,MONDO:0001355,ocular siderosis,MONDO,disease,DISEASE_5129
5130,5130,5130,5130,5130,5130,5130,5130,MONDO:0003671,septal myocardial infarction,MONDO,disease,DISEASE_5130
5131,5131,5131,5131,5131,5131,5131,5131,MONDO:0013031,"chromosome 5Q14.3 deletion syndrome, distal",MONDO,disease,DISEASE_5131
5132,5132,5132,5132,5132,5132,5132,5132,MONDO:0016839,distal 17p13.3 microdeletion syndrome,MONDO,disease,DISEASE_5132
5133,5133,5133,5133,5133,5133,5133,5133,MONDO:0100157_MONDO:0100156_MONDO:0009853,Imerslund-Grasbeck syndrome,MONDO_grouped,disease,DISEASE_5133
5134,5134,5134,5134,5134,5134,5134,5134,MONDO:0016625,acquired deficiency anemia,MONDO,disease,DISEASE_5134
5135,5135,5135,5135,5135,5135,5135,5135,MONDO:1011484,"beta-mannosidosis, springbok",MONDO,disease,DISEASE_5135
5136,5136,5136,5136,5136,5136,5136,5136,MONDO:0000728,ptosis,MONDO,disease,DISEASE_5136
5137,5137,5137,5137,5137,5137,5137,5137,MONDO:0008339,antecubital pterygium syndrome,MONDO,disease,DISEASE_5137
5138,5138,5138,5138,5138,5138,5138,5138,MONDO:0024655_MONDO:0002133,rheumatic pericarditis,MONDO_grouped,disease,DISEASE_5138
5139,5139,5139,5139,5139,5139,5139,5139,MONDO:0011911,craniolenticulosutural dysplasia,MONDO,disease,DISEASE_5139
5140,5140,5140,5140,5140,5140,5140,5140,MONDO:0017834,secondary hypereosinophilic syndrome,MONDO,disease,DISEASE_5140
5141,5141,5141,5141,5141,5141,5141,5141,MONDO:0014629,autoimmune interstitial lung disease-arthritis syndrome,MONDO,disease,DISEASE_5141
5142,5142,5142,5142,5142,5142,5142,5142,MONDO:1011538,"hypertriglyceridemia, domestic cat",MONDO,disease,DISEASE_5142
5143,5143,5143,5143,5143,5143,5143,5143,MONDO:0009814,osteopenia-intellectual disability-sparse hair syndrome,MONDO,disease,DISEASE_5143
5144,5144,5144,5144,5144,5144,5144,5144,MONDO:0009087,"deafness, neural, congenital moderate",MONDO,disease,DISEASE_5144
5145,5145,5145,5145,5145,5145,5145,5145,MONDO:0017636,hemiparkinsonism-hemiatrophy syndrome,MONDO,disease,DISEASE_5145
5146,5146,5146,5146,5146,5146,5146,5146,MONDO:0003446,papillary hidradenoma,MONDO,disease,DISEASE_5146
5147,5147,5147,5147,5147,5147,5147,5147,MONDO:0043904,"leishmaniasis, diffuse cutaneous",MONDO,disease,DISEASE_5147
5148,5148,5148,5148,5148,5148,5148,5148,MONDO:0009405,cervical hypertrichosis-peripheral neuropathy syndrome,MONDO,disease,DISEASE_5148
5149,5149,5149,5149,5149,5149,5149,5149,MONDO:0000368,extrapulmonary tuberculosis,MONDO,disease,DISEASE_5149
5150,5150,5150,5150,5150,5150,5150,5150,MONDO:0032805,"hypopigmentation, organomegaly, and delayed myelination and development",MONDO,disease,DISEASE_5150
5151,5151,5151,5151,5151,5151,5151,5151,MONDO:0040728,Campylobacter fetus infectious disease,MONDO,disease,DISEASE_5151
5152,5152,5152,5152,5152,5152,5152,5152,MONDO:0008989,citrulline transport defect,MONDO,disease,DISEASE_5152
5153,5153,5153,5153,5153,5153,5153,5153,MONDO:0003320,blastema predominant kidney Wilms tumor,MONDO,disease,DISEASE_5153
5154,5154,5154,5154,5154,5154,5154,5154,MONDO:0009802,"osteodysplasty, precocious, of Danks, Mayne, and Kozlowski",MONDO,disease,DISEASE_5154
5155,5155,5155,5155,5155,5155,5155,5155,MONDO:0032685,"infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development",MONDO,disease,DISEASE_5155
5156,5156,5156,5156,5156,5156,5156,5156,MONDO:0003535,fallopian tube papillary adenocarcinoma,MONDO,disease,DISEASE_5156
5157,5157,5157,5157,5157,5157,5157,5157,MONDO:0041182,polymorphic light eruption,MONDO,disease,DISEASE_5157
5158,5158,5158,5158,5158,5158,5158,5158,MONDO:0700146,canine prostate carcinoma,MONDO,disease,DISEASE_5158
5159,5159,5159,5159,5159,5159,5159,5159,MONDO:0008097,linear nevus sebaceous syndrome,MONDO,disease,DISEASE_5159
5160,5160,5160,5160,5160,5160,5160,5160,MONDO:1012742_MONDO:1012764,"primary open angle glaucoma, ADAMTS10-related, dog",MONDO_grouped,disease,DISEASE_5160
5161,5161,5161,5161,5161,5161,5161,5161,MONDO:1040001,TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations,MONDO,disease,DISEASE_5161
5162,5162,5162,5162,5162,5162,5162,5162,MONDO:0800401,CERKL-related retinopathy,MONDO,disease,DISEASE_5162
5163,5163,5163,5163,5163,5163,5163,5163,MONDO:0006930,pseudobulbar palsy,MONDO,disease,DISEASE_5163
5164,5164,5164,5164,5164,5164,5164,5164,MONDO:0009163,"encephalomalacia, multilocular",MONDO,disease,DISEASE_5164
5165,5165,5165,5165,5165,5165,5165,5165,MONDO:0004451,sarcomatous intrahepatic cholangiocarcinoma,MONDO,disease,DISEASE_5165
5166,5166,5166,5166,5166,5166,5166,5166,MONDO:0004448,frontal sinus inverted papilloma,MONDO,disease,DISEASE_5166
5167,5167,5167,5167,5167,5167,5167,5167,MONDO:0018159,atypical hemolytic-uremic syndrome with DGKE deficiency,MONDO,disease,DISEASE_5167
5168,5168,5168,5168,5168,5168,5168,5168,MONDO:0017105,glioependymal/ependymal cyst,MONDO,disease,DISEASE_5168
5169,5169,5169,5169,5169,5169,5169,5169,MONDO:0019287,ectodermal dysplasia syndrome,MONDO,disease,DISEASE_5169
5170,5170,5170,5170,5170,5170,5170,5170,MONDO:0016219,dysmorphism-pectus carinatum-joint laxity syndrome,MONDO,disease,DISEASE_5170
5171,5171,5171,5171,5171,5171,5171,5171,MONDO:0032830,snijders blok-fisher syndrome,MONDO,disease,DISEASE_5171
5172,5172,5172,5172,5172,5172,5172,5172,MONDO:0005629,Acanthamoeba keratitis,MONDO,disease,DISEASE_5172
5173,5173,5173,5173,5173,5173,5173,5173,MONDO:0010122,congenital thrombotic thrombocytopenic purpura,MONDO,disease,DISEASE_5173
5174,5174,5174,5174,5174,5174,5174,5174,MONDO:0010090,Summitt syndrome,MONDO,disease,DISEASE_5174
5175,5175,5175,5175,5175,5175,5175,5175,MONDO:0014492,wooly hair-palmoplantar keratoderma syndrome,MONDO,disease,DISEASE_5175
5176,5176,5176,5176,5176,5176,5176,5176,MONDO:0015259,brachydactyly-mesomelia-intellectual disability-heart defects syndrome,MONDO,disease,DISEASE_5176
5177,5177,5177,5177,5177,5177,5177,5177,MONDO:0002341,granulomatous angiitis,MONDO,disease,DISEASE_5177
5178,5178,5178,5178,5178,5178,5178,5178,MONDO:0004394,maxillary sinus squamous cell carcinoma,MONDO,disease,DISEASE_5178
5179,5179,5179,5179,5179,5179,5179,5179,MONDO:0005700,chickenpox,MONDO,disease,DISEASE_5179
5180,5180,5180,5180,5180,5180,5180,5180,MONDO:0004140,intermediate malignant teratoma,MONDO,disease,DISEASE_5180
5181,5181,5181,5181,5181,5181,5181,5181,MONDO:0002495,colon signet ring cell adenocarcinoma,MONDO,disease,DISEASE_5181
5182,5182,5182,5182,5182,5182,5182,5182,MONDO:0008982,central areolar choroidal dystrophy,MONDO,disease,DISEASE_5182
5183,5183,5183,5183,5183,5183,5183,5183,MONDO:0044624,pediatric collagenous gastritis,MONDO,disease,DISEASE_5183
5184,5184,5184,5184,5184,5184,5184,5184,MONDO:0001917_MONDO:0002240,chronic perichondritis of pinna,MONDO_grouped,disease,DISEASE_5184
5185,5185,5185,5185,5185,5185,5185,5185,MONDO:0022417,alopecia congenita keratosis palmoplantaris,MONDO,disease,DISEASE_5185
5186,5186,5186,5186,5186,5186,5186,5186,MONDO:0020813,benign testicular sertoli cell tumor,MONDO,disease,DISEASE_5186
5187,5187,5187,5187,5187,5187,5187,5187,MONDO:0022983,Dieterich disease,MONDO,disease,DISEASE_5187
5188,5188,5188,5188,5188,5188,5188,5188,MONDO:1010269,"hypospadias, non-human animal",MONDO,disease,DISEASE_5188
5189,5189,5189,5189,5189,5189,5189,5189,MONDO:1011802,"congenital merosin-deficient muscular dystrophy, non-human animal",MONDO,disease,DISEASE_5189
5190,5190,5190,5190,5190,5190,5190,5190,MONDO:0018821,X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability,MONDO,disease,DISEASE_5190
5191,5191,5191,5191,5191,5191,5191,5191,MONDO:0011275_MONDO:0008717,"acromesomelic dysplasia 1, Maroteaux type",MONDO_grouped,disease,DISEASE_5191
5192,5192,5192,5192,5192,5192,5192,5192,MONDO:0005073_MONDO:0044794,melanocytic nevus,MONDO_grouped,disease,DISEASE_5192
5193,5193,5193,5193,5193,5193,5193,5193,MONDO:0041825,bacterial meningitis caused by gram-negative bacteria,MONDO,disease,DISEASE_5193
5194,5194,5194,5194,5194,5194,5194,5194,MONDO:0016255,uterine corpus mixed epithelial and mesenchymal neoplasm,MONDO,disease,DISEASE_5194
5195,5195,5195,5195,5195,5195,5195,5195,MONDO:0011213,Pierpont syndrome,MONDO,disease,DISEASE_5195
5196,5196,5196,5196,5196,5196,5196,5196,MONDO:0800377,"ACTH-independent adrenal Cushing syndrome, somatic",MONDO,disease,DISEASE_5196
5197,5197,5197,5197,5197,5197,5197,5197,MONDO:1012978,"ichthyosis, dog",MONDO,disease,DISEASE_5197
5198,5198,5198,5198,5198,5198,5198,5198,MONDO:0016875,partial deletion of chromosome 10,MONDO,disease,DISEASE_5198
5199,5199,5199,5199,5199,5199,5199,5199,MONDO:1011284,"retinopathy, RDH5-related, domestic cat",MONDO,disease,DISEASE_5199
5200,5200,5200,5200,5200,5200,5200,5200,MONDO:0008760,beta-ketothiolase deficiency,MONDO,disease,DISEASE_5200
5201,5201,5201,5201,5201,5201,5201,5201,MONDO:0003619_MONDO:0001173,salpingitis,MONDO_grouped,disease,DISEASE_5201
5202,5202,5202,5202,5202,5202,5202,5202,MONDO:0009533,Dahlberg-Borer-Newcomer syndrome,MONDO,disease,DISEASE_5202
5203,5203,5203,5203,5203,5203,5203,5203,MONDO:0859761,SLC12A2-related autosomal recessive neonatal-developmental delay-intellectual disability-feeding difficulty-sensorineural deafness syndrome,MONDO,disease,DISEASE_5203
5204,5204,5204,5204,5204,5204,5204,5204,MONDO:0001671,mucocele of appendix,MONDO,disease,DISEASE_5204
5205,5205,5205,5205,5205,5205,5205,5205,MONDO:0005888,ornithosis,MONDO,disease,DISEASE_5205
5206,5206,5206,5206,5206,5206,5206,5206,MONDO:0030025,"neurodevelopmental disorder with hypotonia, microcephaly, and seizures",MONDO,disease,DISEASE_5206
5207,5207,5207,5207,5207,5207,5207,5207,MONDO:0019266,SAPHO syndrome,MONDO,disease,DISEASE_5207
5208,5208,5208,5208,5208,5208,5208,5208,MONDO:0019597,"obsolete 46,XY disorder of sex development due to isolated 17,20-lyase deficiency",MONDO,disease,DISEASE_5208
5209,5209,5209,5209,5209,5209,5209,5209,MONDO:0019713,non-syndromic limb reduction defect,MONDO,disease,DISEASE_5209
5210,5210,5210,5210,5210,5210,5210,5210,MONDO:0014056_MONDO:0007964_MONDO:0007963_MONDO:0012183_MONDO:0013759_MONDO:0013133_MONDO:0011954_MONDO:0012842_MONDO:0013510,"melanoma, cutaneous malignant, susceptibility to",MONDO_grouped,disease,DISEASE_5210
5211,5211,5211,5211,5211,5211,5211,5211,MONDO:0025457,"pulmonary adenomatosis, ovine",MONDO,disease,DISEASE_5211
5212,5212,5212,5212,5212,5212,5212,5212,MONDO:0005196,obsolete teratozoospermia,MONDO,disease,DISEASE_5212
5213,5213,5213,5213,5213,5213,5213,5213,MONDO:0017860,methanol poisoning,MONDO,disease,DISEASE_5213
5214,5214,5214,5214,5214,5214,5214,5214,MONDO:0859243,"neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities",MONDO,disease,DISEASE_5214
5215,5215,5215,5215,5215,5215,5215,5215,MONDO:0016647,obsolete autosomal recessive Stickler syndrome,MONDO,disease,DISEASE_5215
5216,5216,5216,5216,5216,5216,5216,5216,MONDO:0010333,corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome,MONDO,disease,DISEASE_5216
5217,5217,5217,5217,5217,5217,5217,5217,MONDO:0015820,primary cutaneous B-cell lymphoma,MONDO,disease,DISEASE_5217
5218,5218,5218,5218,5218,5218,5218,5218,MONDO:1011875,"progressive ataxia with head tremor and seizures, non-human animal",MONDO,disease,DISEASE_5218
5219,5219,5219,5219,5219,5219,5219,5219,MONDO:0014236_MONDO:0020681_MONDO:0011142,"Ehlers-Danlos syndrome, musculocontractural",MONDO_grouped,disease,DISEASE_5219
5220,5220,5220,5220,5220,5220,5220,5220,MONDO:0011590,anisomastia,MONDO,disease,DISEASE_5220
5221,5221,5221,5221,5221,5221,5221,5221,MONDO:1010232,"hydranencephaly, non-human animal",MONDO,disease,DISEASE_5221
5222,5222,5222,5222,5222,5222,5222,5222,MONDO:0007084,familial focal alopecia,MONDO,disease,DISEASE_5222
5223,5223,5223,5223,5223,5223,5223,5223,MONDO:0006604,rosacea,MONDO,disease,DISEASE_5223
5224,5224,5224,5224,5224,5224,5224,5224,MONDO:0008906,obsolete carbimazole sensitivity,MONDO,disease,DISEASE_5224
5225,5225,5225,5225,5225,5225,5225,5225,MONDO:0011078,"anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis",MONDO,disease,DISEASE_5225
5226,5226,5226,5226,5226,5226,5226,5226,MONDO:0020599,acquired coagulation factor deficiency,MONDO,disease,DISEASE_5226
5227,5227,5227,5227,5227,5227,5227,5227,MONDO:0007892,Lenz-Majewski hyperostotic dwarfism,MONDO,disease,DISEASE_5227
5228,5228,5228,5228,5228,5228,5228,5228,MONDO:0859287,"neurodevelopmental disorder with microcephaly, hypotonia, and absent language",MONDO,disease,DISEASE_5228
5229,5229,5229,5229,5229,5229,5229,5229,MONDO:0008461,splenomegaly syndrome with splenic Germinal center hypoplasia and reduced circulating T helper cells,MONDO,disease,DISEASE_5229
5230,5230,5230,5230,5230,5230,5230,5230,MONDO:1012008,"alloxan-diabetes, dog",MONDO,disease,DISEASE_5230
5231,5231,5231,5231,5231,5231,5231,5231,MONDO:0003486,basaloid squamous cell carcinoma,MONDO,disease,DISEASE_5231
5232,5232,5232,5232,5232,5232,5232,5232,MONDO:0010718,absent radius-anogenital anomalies syndrome,MONDO,disease,DISEASE_5232
5233,5233,5233,5233,5233,5233,5233,5233,MONDO:0020478,Leber plus disease,MONDO,disease,DISEASE_5233
5234,5234,5234,5234,5234,5234,5234,5234,MONDO:0850306,latent autoimmune diabetes in adults,MONDO,disease,DISEASE_5234
5235,5235,5235,5235,5235,5235,5235,5235,MONDO:0018319,familial episodic pain syndrome,MONDO,disease,DISEASE_5235
5236,5236,5236,5236,5236,5236,5236,5236,MONDO:0002514,hepatobiliary neoplasm,MONDO,disease,DISEASE_5236
5237,5237,5237,5237,5237,5237,5237,5237,MONDO:0003710,ovarian mixed germ cell neoplasm,MONDO,disease,DISEASE_5237
5238,5238,5238,5238,5238,5238,5238,5238,MONDO:0060629,"neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive",MONDO,disease,DISEASE_5238
5239,5239,5239,5239,5239,5239,5239,5239,MONDO:0002074,Behcet syndrome arthropathy,MONDO,disease,DISEASE_5239
5240,5240,5240,5240,5240,5240,5240,5240,MONDO:1010715,"multiple acyl-CoA dehydrogenase deficiency, horse",MONDO,disease,DISEASE_5240
5241,5241,5241,5241,5241,5241,5241,5241,MONDO:0016841,20p12.3 microdeletion syndrome,MONDO,disease,DISEASE_5241
5242,5242,5242,5242,5242,5242,5242,5242,MONDO:0011841,biotin-responsive basal ganglia disease,MONDO,disease,DISEASE_5242
5243,5243,5243,5243,5243,5243,5243,5243,MONDO:0010108,testicular germ cell tumor,MONDO,disease,DISEASE_5243
5244,5244,5244,5244,5244,5244,5244,5244,MONDO:0025376,African horse sickness,MONDO,disease,DISEASE_5244
5245,5245,5245,5245,5245,5245,5245,5245,MONDO:1030000,hyperinsulinemic hypoglycemia with polycystic kidney disease,MONDO,disease,DISEASE_5245
5246,5246,5246,5246,5246,5246,5246,5246,MONDO:0000482,focal hand dystonia,MONDO,disease,DISEASE_5246
5247,5247,5247,5247,5247,5247,5247,5247,MONDO:0004678,dermatophytosis,MONDO,disease,DISEASE_5247
5248,5248,5248,5248,5248,5248,5248,5248,MONDO:0006769,gastroparesis,MONDO,disease,DISEASE_5248
5249,5249,5249,5249,5249,5249,5249,5249,MONDO:0019605_MONDO:0019991,immunotactoid or fibrillary glomerulopathy,MONDO_grouped,disease,DISEASE_5249
5250,5250,5250,5250,5250,5250,5250,5250,MONDO:0011738,bilateral frontoparietal polymicrogyria,MONDO,disease,DISEASE_5250
5251,5251,5251,5251,5251,5251,5251,5251,MONDO:0019438_MONDO:0018613_MONDO:0019732,AL amyloidosis,MONDO_grouped,disease,DISEASE_5251
5252,5252,5252,5252,5252,5252,5252,5252,MONDO:0002712,epidural spinal canal angiolipoma,MONDO,disease,DISEASE_5252
5253,5253,5253,5253,5253,5253,5253,5253,MONDO:0016571,macrocephaly-short stature-paraplegia syndrome,MONDO,disease,DISEASE_5253
5254,5254,5254,5254,5254,5254,5254,5254,MONDO:0006166,columnar cell hyperplasia of the breast,MONDO,disease,DISEASE_5254
5255,5255,5255,5255,5255,5255,5255,5255,MONDO:0023106,Fairbank disease,MONDO,disease,DISEASE_5255
5256,5256,5256,5256,5256,5256,5256,5256,MONDO:0100022,neonatal/infantile epilepsy syndrome,MONDO,disease,DISEASE_5256
5257,5257,5257,5257,5257,5257,5257,5257,MONDO:0004090,vulvar basaloid squamous cell carcinoma,MONDO,disease,DISEASE_5257
5258,5258,5258,5258,5258,5258,5258,5258,MONDO:0006499,hamartoma,MONDO,disease,DISEASE_5258
5259,5259,5259,5259,5259,5259,5259,5259,MONDO:0020386_MONDO:0018498,double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis,MONDO_grouped,disease,DISEASE_5259
5260,5260,5260,5260,5260,5260,5260,5260,MONDO:0004733,pyriform sinus cancer,MONDO,disease,DISEASE_5260
5261,5261,5261,5261,5261,5261,5261,5261,MONDO:0100171_MONDO:0100182_MONDO:0100232_MONDO:0011084_MONDO:0100231,"psoriasis, susceptibility to",MONDO_grouped,disease,DISEASE_5261
5262,5262,5262,5262,5262,5262,5262,5262,MONDO:0007258,"canine teeth, absence of upper permanent",MONDO,disease,DISEASE_5262
5263,5263,5263,5263,5263,5263,5263,5263,MONDO:1010028,"cerebral amyloid angiopathy, non-human animal",MONDO,disease,DISEASE_5263
5264,5264,5264,5264,5264,5264,5264,5264,MONDO:0035562,acquired human prion disease,MONDO,disease,DISEASE_5264
5265,5265,5265,5265,5265,5265,5265,5265,MONDO:1011009,"Horner syndrome, dog",MONDO,disease,DISEASE_5265
5266,5266,5266,5266,5266,5266,5266,5266,MONDO:0014057,"maple syrup urine disease, mild variant",MONDO,disease,DISEASE_5266
5267,5267,5267,5267,5267,5267,5267,5267,MONDO:0021205,disorder of ear,MONDO,disease,DISEASE_5267
5268,5268,5268,5268,5268,5268,5268,5268,MONDO:0000644,cervical benign neoplasm,MONDO,disease,DISEASE_5268
5269,5269,5269,5269,5269,5269,5269,5269,MONDO:0016903,partial deletion of the long arm of chromosome 4,MONDO,disease,DISEASE_5269
5270,5270,5270,5270,5270,5270,5270,5270,MONDO:0001475,neutropenia,MONDO,disease,DISEASE_5270
5271,5271,5271,5271,5271,5271,5271,5271,MONDO:0800181,OPA1-related optic atrophy with or without extraocular features,MONDO,disease,DISEASE_5271
5272,5272,5272,5272,5272,5272,5272,5272,MONDO:0020292,congenital anomaly of the great arteries,MONDO,disease,DISEASE_5272
5273,5273,5273,5273,5273,5273,5273,5273,MONDO:0975848,Morimoto-Ryu-Malicdan neuromuscular syndrome,MONDO,disease,DISEASE_5273
5274,5274,5274,5274,5274,5274,5274,5274,MONDO:0012045_MONDO:0011300_MONDO:0008053_MONDO:0012388,"myopia 5, autosomal dominant",MONDO_grouped,disease,DISEASE_5274
5275,5275,5275,5275,5275,5275,5275,5275,MONDO:0007263,cardiac rhythm disease,MONDO,disease,DISEASE_5275
5276,5276,5276,5276,5276,5276,5276,5276,MONDO:0002257,ankylosis,MONDO,disease,DISEASE_5276
5277,5277,5277,5277,5277,5277,5277,5277,MONDO:0023571,Kozlowski Rafinski Klicharska syndrome,MONDO,disease,DISEASE_5277
5278,5278,5278,5278,5278,5278,5278,5278,MONDO:0016668,sickle cell-beta-thalassemia disease syndrome,MONDO,disease,DISEASE_5278
5279,5279,5279,5279,5279,5279,5279,5279,MONDO:1012087_MONDO:1012088,"alpha fucosidosis, dog",MONDO_grouped,disease,DISEASE_5279
5280,5280,5280,5280,5280,5280,5280,5280,MONDO:0005049,obsolete intracranial hemorrhage,MONDO,disease,DISEASE_5280
5281,5281,5281,5281,5281,5281,5281,5281,MONDO:0004988_MONDO:0005590_MONDO:0002058_MONDO:0004270,breast adenocarcinoma,MONDO_grouped,disease,DISEASE_5281
5282,5282,5282,5282,5282,5282,5282,5282,MONDO:1012489,"hypotrichosis with short life expectancy, domestic cat",MONDO,disease,DISEASE_5282
5283,5283,5283,5283,5283,5283,5283,5283,MONDO:0001930_MONDO:0001931_MONDO:0043994,acute cholangitis,MONDO_grouped,disease,DISEASE_5283
5284,5284,5284,5284,5284,5284,5284,5284,MONDO:0015774,thoraco-abdominal enteric duplication,MONDO,disease,DISEASE_5284
5285,5285,5285,5285,5285,5285,5285,5285,MONDO:0002050_MONDO:0001098,depressive disorder,MONDO_grouped,disease,DISEASE_5285
5286,5286,5286,5286,5286,5286,5286,5286,MONDO:0001882,bacteriuria,MONDO,disease,DISEASE_5286
5287,5287,5287,5287,5287,5287,5287,5287,MONDO:0850059,hereditary persistence of fetal hemoglobin-intellectual disability syndrome,MONDO,disease,DISEASE_5287
5288,5288,5288,5288,5288,5288,5288,5288,MONDO:0018438,eosinophilic gastrointestinal disease,MONDO,disease,DISEASE_5288
5289,5289,5289,5289,5289,5289,5289,5289,MONDO:0004117,ampulla of vater small cell neuroendocrine carcinoma,MONDO,disease,DISEASE_5289
5290,5290,5290,5290,5290,5290,5290,5290,MONDO:0016662,idiopathic recurrent pericarditis,MONDO,disease,DISEASE_5290
5291,5291,5291,5291,5291,5291,5291,5291,MONDO:0009083,conductive deafness-malformed external ear syndrome,MONDO,disease,DISEASE_5291
5292,5292,5292,5292,5292,5292,5292,5292,MONDO:0007167_MONDO:0007168_MONDO:0009727_MONDO:0000389,atelosteogenesis,MONDO_grouped,disease,DISEASE_5292
5293,5293,5293,5293,5293,5293,5293,5293,MONDO:0850073_MONDO:0015338_MONDO:0850072_MONDO:0850074_MONDO:0850075_MONDO:0850076_MONDO:0850077_MONDO:0850078_MONDO:0850079_MONDO:0850080_MONDO:0850081_MONDO:0850082_MONDO:0850083,non-syndromic unicoronal craniosynostosis,MONDO_grouped,disease,DISEASE_5293
5294,5294,5294,5294,5294,5294,5294,5294,MONDO:0011863,prostate cancer aggressiveness quantitative trait locus on chromosome 19,MONDO,disease,DISEASE_5294
5295,5295,5295,5295,5295,5295,5295,5295,MONDO:0000986,pleurisy,MONDO,disease,DISEASE_5295
5296,5296,5296,5296,5296,5296,5296,5296,MONDO:0013178,congenital muscular dystrophy due to LMNA mutation,MONDO,disease,DISEASE_5296
5297,5297,5297,5297,5297,5297,5297,5297,MONDO:0007972,Meniere disease,MONDO,disease,DISEASE_5297
5298,5298,5298,5298,5298,5298,5298,5298,MONDO:0023206,functional pancreatic neuroendocrine tumor,MONDO,disease,DISEASE_5298
5299,5299,5299,5299,5299,5299,5299,5299,MONDO:0011344,"parotitis, juvenile recurrent",MONDO,disease,DISEASE_5299
5300,5300,5300,5300,5300,5300,5300,5300,MONDO:0018142,"pyruvate carboxylase deficiency, severe neonatal type",MONDO,disease,DISEASE_5300
5301,5301,5301,5301,5301,5301,5301,5301,MONDO:0012495,"spondyloepimetaphyseal dysplasia, Genevieve type",MONDO,disease,DISEASE_5301
5302,5302,5302,5302,5302,5302,5302,5302,MONDO:0006582,mongolian spot,MONDO,disease,DISEASE_5302
5303,5303,5303,5303,5303,5303,5303,5303,MONDO:0019111,familial thrombocytosis,MONDO,disease,DISEASE_5303
5304,5304,5304,5304,5304,5304,5304,5304,MONDO:0054581_MONDO:0054582_MONDO:0007142,Townes-Brocks syndrome,MONDO_grouped,disease,DISEASE_5304
5305,5305,5305,5305,5305,5305,5305,5305,MONDO:0005393,gout,MONDO,disease,DISEASE_5305
5306,5306,5306,5306,5306,5306,5306,5306,MONDO:0023628,levator syndrome,MONDO,disease,DISEASE_5306
5307,5307,5307,5307,5307,5307,5307,5307,MONDO:0001443,tympanosclerosis,MONDO,disease,DISEASE_5307
5308,5308,5308,5308,5308,5308,5308,5308,MONDO:0003236,atypical polypoid adenomyoma,MONDO,disease,DISEASE_5308
5309,5309,5309,5309,5309,5309,5309,5309,MONDO:0858957,multinodular and vacuolating neuronal tumor,MONDO,disease,DISEASE_5309
5310,5310,5310,5310,5310,5310,5310,5310,MONDO:0009803,congenital osteogenesis imperfecta-microcephaly-cataracts syndrome,MONDO,disease,DISEASE_5310
5311,5311,5311,5311,5311,5311,5311,5311,MONDO:0004427,supraglottis neoplasm,MONDO,disease,DISEASE_5311
5312,5312,5312,5312,5312,5312,5312,5312,MONDO:0004142,lung combined large cell neuroendocrine carcinoma,MONDO,disease,DISEASE_5312
5313,5313,5313,5313,5313,5313,5313,5313,MONDO:0010576,X-linked mixed hearing loss with perilymphatic gusher,MONDO,disease,DISEASE_5313
5314,5314,5314,5314,5314,5314,5314,5314,MONDO:0030976,oculomotor-abducens synkinesis,MONDO,disease,DISEASE_5314
5315,5315,5315,5315,5315,5315,5315,5315,MONDO:0800442,MYH-6 related congenital heart defects,MONDO,disease,DISEASE_5315
5316,5316,5316,5316,5316,5316,5316,5316,MONDO:0007252,Gordon syndrome,MONDO,disease,DISEASE_5316
5317,5317,5317,5317,5317,5317,5317,5317,MONDO:0007983_MONDO:0000138,Schmid metaphyseal chondrodysplasia,MONDO_grouped,disease,DISEASE_5317
5318,5318,5318,5318,5318,5318,5318,5318,MONDO:0003349_MONDO:0003287,central nervous system leiomyosarcoma,MONDO_grouped,disease,DISEASE_5318
5319,5319,5319,5319,5319,5319,5319,5319,MONDO:0007402,"creatine phosphokinase, elevated serum",MONDO,disease,DISEASE_5319
5320,5320,5320,5320,5320,5320,5320,5320,MONDO:0005210,uterine corpus sarcoma,MONDO,disease,DISEASE_5320
5321,5321,5321,5321,5321,5321,5321,5321,MONDO:0100113,hearing loss with skin disease,MONDO,disease,DISEASE_5321
5322,5322,5322,5322,5322,5322,5322,5322,MONDO:0025082,"helminthiasis, animal",MONDO,disease,DISEASE_5322
5323,5323,5323,5323,5323,5323,5323,5323,MONDO:1011472,"amyloidosis, golden hamster",MONDO,disease,DISEASE_5323
5324,5324,5324,5324,5324,5324,5324,5324,MONDO:1010018,"persistent truncus arteriosus, non-human animal",MONDO,disease,DISEASE_5324
5325,5325,5325,5325,5325,5325,5325,5325,MONDO:0017925,T-cell immunodeficiency with epidermodysplasia verruciformis,MONDO,disease,DISEASE_5325
5326,5326,5326,5326,5326,5326,5326,5326,MONDO:0009729,nephropathy - deafness - hyperparathyroidism syndrome,MONDO,disease,DISEASE_5326
5327,5327,5327,5327,5327,5327,5327,5327,MONDO:0001445,obsolete neurogenic bladder,MONDO,disease,DISEASE_5327
5328,5328,5328,5328,5328,5328,5328,5328,MONDO:0001634,bladder leiomyoma,MONDO,disease,DISEASE_5328
5329,5329,5329,5329,5329,5329,5329,5329,MONDO:0003141,cerebellopontine angle embryonal tumor,MONDO,disease,DISEASE_5329
5330,5330,5330,5330,5330,5330,5330,5330,MONDO:1010060,"pheochromocytoma, non-human animal",MONDO,disease,DISEASE_5330
5331,5331,5331,5331,5331,5331,5331,5331,MONDO:0005335,colorectal neoplasm,MONDO,disease,DISEASE_5331
5332,5332,5332,5332,5332,5332,5332,5332,MONDO:0043291,Rokitansky-Aschoff sinuses of the gallbladder,MONDO,disease,DISEASE_5332
5333,5333,5333,5333,5333,5333,5333,5333,MONDO:0021496,benign neoplasm of lip,MONDO,disease,DISEASE_5333
5334,5334,5334,5334,5334,5334,5334,5334,MONDO:1010976,"Huntington disease, Rhesus monkey",MONDO,disease,DISEASE_5334
5335,5335,5335,5335,5335,5335,5335,5335,MONDO:0002190,vulvar syringoma,MONDO,disease,DISEASE_5335
5336,5336,5336,5336,5336,5336,5336,5336,MONDO:0021752,Achard-Thiers syndrome,MONDO,disease,DISEASE_5336
5337,5337,5337,5337,5337,5337,5337,5337,MONDO:0019656,sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis,MONDO,disease,DISEASE_5337
5338,5338,5338,5338,5338,5338,5338,5338,MONDO:0006723,denture stomatitis,MONDO,disease,DISEASE_5338
5339,5339,5339,5339,5339,5339,5339,5339,MONDO:0015558,isolated bone marrow mastocytosis,MONDO,disease,DISEASE_5339
5340,5340,5340,5340,5340,5340,5340,5340,MONDO:0021171,"Timothy syndrome, classic type",MONDO,disease,DISEASE_5340
5341,5341,5341,5341,5341,5341,5341,5341,MONDO:0005616,pulmonary mucoepidermoid carcinoma,MONDO,disease,DISEASE_5341
5342,5342,5342,5342,5342,5342,5342,5342,MONDO:0014534,lissencephaly 6 with microcephaly,MONDO,disease,DISEASE_5342
5343,5343,5343,5343,5343,5343,5343,5343,MONDO:0015569,congenital nasal pyriform aperture stenosis with holoprosencephaly,MONDO,disease,DISEASE_5343
5344,5344,5344,5344,5344,5344,5344,5344,MONDO:0004445,bladder papillary clear cell adenocarcinoma,MONDO,disease,DISEASE_5344
5345,5345,5345,5345,5345,5345,5345,5345,MONDO:0011045,MMEP syndrome,MONDO,disease,DISEASE_5345
5346,5346,5346,5346,5346,5346,5346,5346,MONDO:0016550_MONDO:0016551,"congenital primary megaureter, obstructed form",MONDO_grouped,disease,DISEASE_5346
5347,5347,5347,5347,5347,5347,5347,5347,MONDO:0024797,adult brain stem neoplasm,MONDO,disease,DISEASE_5347
5348,5348,5348,5348,5348,5348,5348,5348,MONDO:1012372,"progressive ataxia with head tremor and seizures, dog",MONDO,disease,DISEASE_5348
5349,5349,5349,5349,5349,5349,5349,5349,MONDO:0004631,tongue cancer,MONDO,disease,DISEASE_5349
5350,5350,5350,5350,5350,5350,5350,5350,MONDO:0004953,invasive ductal breast carcinoma,MONDO,disease,DISEASE_5350
5351,5351,5351,5351,5351,5351,5351,5351,MONDO:0016948,partial duplication of the short arm of chromosome 11,MONDO,disease,DISEASE_5351
5352,5352,5352,5352,5352,5352,5352,5352,MONDO:0009090,"hearing loss, sensorineural, autosomal-mitochondrial type",MONDO,disease,DISEASE_5352
5353,5353,5353,5353,5353,5353,5353,5353,MONDO:0009692,primary myelofibrosis,MONDO,disease,DISEASE_5353
5354,5354,5354,5354,5354,5354,5354,5354,MONDO:0003808,mediastinal extraskeletal osteosarcoma,MONDO,disease,DISEASE_5354
5355,5355,5355,5355,5355,5355,5355,5355,MONDO:0021309,malignant neoplasm of endocervix,MONDO,disease,DISEASE_5355
5356,5356,5356,5356,5356,5356,5356,5356,MONDO:0019635,idiopathic achalasia,MONDO,disease,DISEASE_5356
5357,5357,5357,5357,5357,5357,5357,5357,MONDO:0023091,esophageal atresia coloboma talipes,MONDO,disease,DISEASE_5357
5358,5358,5358,5358,5358,5358,5358,5358,MONDO:0007553,epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase,MONDO,disease,DISEASE_5358
5359,5359,5359,5359,5359,5359,5359,5359,MONDO:0002638,glossopharyngeal nerve neoplasm,MONDO,disease,DISEASE_5359
5360,5360,5360,5360,5360,5360,5360,5360,MONDO:0017393,blepharophimosis - intellectual disability syndrome,MONDO,disease,DISEASE_5360
5361,5361,5361,5361,5361,5361,5361,5361,MONDO:0002528,synovium neoplasm,MONDO,disease,DISEASE_5361
5362,5362,5362,5362,5362,5362,5362,5362,MONDO:0008189,"papillomatosis, florid, of nipple",MONDO,disease,DISEASE_5362
5363,5363,5363,5363,5363,5363,5363,5363,MONDO:1011440,"gastrointestinal stromal tumour, non-human animal",MONDO,disease,DISEASE_5363
5364,5364,5364,5364,5364,5364,5364,5364,MONDO:0014609,cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome,MONDO,disease,DISEASE_5364
5365,5365,5365,5365,5365,5365,5365,5365,MONDO:0021086,gingival neoplasm,MONDO,disease,DISEASE_5365
5366,5366,5366,5366,5366,5366,5366,5366,MONDO:1010647,"hypereosinophilic syndrome, dog",MONDO,disease,DISEASE_5366
5367,5367,5367,5367,5367,5367,5367,5367,MONDO:0005007,colon mucinous adenocarcinoma,MONDO,disease,DISEASE_5367
5368,5368,5368,5368,5368,5368,5368,5368,MONDO:0015086,cloverleaf skull-asphyxiating thoracic dysplasia syndrome,MONDO,disease,DISEASE_5368
5369,5369,5369,5369,5369,5369,5369,5369,MONDO:0016764,isolated anophthalmia-microphthalmia syndrome,MONDO,disease,DISEASE_5369
5370,5370,5370,5370,5370,5370,5370,5370,MONDO:0001798_MONDO:1040027,hypermobility syndrome,MONDO_grouped,disease,DISEASE_5370
5371,5371,5371,5371,5371,5371,5371,5371,MONDO:0007519,Edinburgh malformation syndrome,MONDO,disease,DISEASE_5371
5372,5372,5372,5372,5372,5372,5372,5372,MONDO:0024326,pleural adenomatoid tumor,MONDO,disease,DISEASE_5372
5373,5373,5373,5373,5373,5373,5373,5373,MONDO:0043836,"tuberculosis, spinal",MONDO,disease,DISEASE_5373
5374,5374,5374,5374,5374,5374,5374,5374,MONDO:0017649,hemidystonia-hemiatrophy syndrome,MONDO,disease,DISEASE_5374
5375,5375,5375,5375,5375,5375,5375,5375,MONDO:1010852,"glycogen storage disease, GAA-related, cattle",MONDO,disease,DISEASE_5375
5376,5376,5376,5376,5376,5376,5376,5376,MONDO:0001452,pseudoretinitis pigmentosa,MONDO,disease,DISEASE_5376
5377,5377,5377,5377,5377,5377,5377,5377,MONDO:1010344,"Peters anomaly, non-human animal",MONDO,disease,DISEASE_5377
5378,5378,5378,5378,5378,5378,5378,5378,MONDO:0004095,B-cell neoplasm,MONDO,disease,DISEASE_5378
5379,5379,5379,5379,5379,5379,5379,5379,MONDO:0002132,skull cancer,MONDO,disease,DISEASE_5379
5380,5380,5380,5380,5380,5380,5380,5380,MONDO:0054835,classic dopamine transporter deficiency syndrome,MONDO,disease,DISEASE_5380
5381,5381,5381,5381,5381,5381,5381,5381,MONDO:0015164,acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent,MONDO,disease,DISEASE_5381
5382,5382,5382,5382,5382,5382,5382,5382,MONDO:0018181,staphylococcal scalded skin syndrome,MONDO,disease,DISEASE_5382
5383,5383,5383,5383,5383,5383,5383,5383,MONDO:0010392,glycogen storage disease due to phosphoglycerate kinase 1 deficiency,MONDO,disease,DISEASE_5383
5384,5384,5384,5384,5384,5384,5384,5384,MONDO:0001842_MONDO:0003704,uterine corpus dissecting leiomyoma,MONDO_grouped,disease,DISEASE_5384
5385,5385,5385,5385,5385,5385,5385,5385,MONDO:0850421,acute hemorrhagic pancreatitis,MONDO,disease,DISEASE_5385
5386,5386,5386,5386,5386,5386,5386,5386,MONDO:0004715,liver carcinoma in situ,MONDO,disease,DISEASE_5386
5387,5387,5387,5387,5387,5387,5387,5387,MONDO:0018839,acquired schizencephaly,MONDO,disease,DISEASE_5387
5388,5388,5388,5388,5388,5388,5388,5388,MONDO:0018553,urachal diverticulum,MONDO,disease,DISEASE_5388
5389,5389,5389,5389,5389,5389,5389,5389,MONDO:0021050_MONDO:0003434_MONDO:0020653,vaginal neoplasm,MONDO_grouped,disease,DISEASE_5389
5390,5390,5390,5390,5390,5390,5390,5390,MONDO:1010407,"epilepsy, golden hamster",MONDO,disease,DISEASE_5390
5391,5391,5391,5391,5391,5391,5391,5391,MONDO:0007393,cranioacrofacial syndrome,MONDO,disease,DISEASE_5391
5392,5392,5392,5392,5392,5392,5392,5392,MONDO:0010759,Wildervanck syndrome,MONDO,disease,DISEASE_5392
5393,5393,5393,5393,5393,5393,5393,5393,MONDO:0019429,"X-linked neurodegenerative syndrome, Hamel type",MONDO,disease,DISEASE_5393
5394,5394,5394,5394,5394,5394,5394,5394,MONDO:0011962,endometrial cancer,MONDO,disease,DISEASE_5394
5395,5395,5395,5395,5395,5395,5395,5395,MONDO:0014608_MONDO:0012516_MONDO:0015483_MONDO:0009559_MONDO:1010521,mandibulofacial dysostosis with alopecia,MONDO_grouped,disease,DISEASE_5395
5396,5396,5396,5396,5396,5396,5396,5396,MONDO:0005204,primary antiphospholipid syndrome,MONDO,disease,DISEASE_5396
5397,5397,5397,5397,5397,5397,5397,5397,MONDO:0100034,cerebral folate deficiency,MONDO,disease,DISEASE_5397
5398,5398,5398,5398,5398,5398,5398,5398,MONDO:1011701,"combined deficiency of factors IX and XII, non-human animal",MONDO,disease,DISEASE_5398
5399,5399,5399,5399,5399,5399,5399,5399,MONDO:0004663,colon carcinoma in situ,MONDO,disease,DISEASE_5399
5400,5400,5400,5400,5400,5400,5400,5400,MONDO:0001646_MONDO:0001151,benign secondary hypertension,MONDO_grouped,disease,DISEASE_5400
5401,5401,5401,5401,5401,5401,5401,5401,MONDO:0012046,"congenital corneal opacities, cornea guttata, and corectopia",MONDO,disease,DISEASE_5401
5402,5402,5402,5402,5402,5402,5402,5402,MONDO:0019153,brain malformation-congenital heart disease-postaxial polydactyly syndrome,MONDO,disease,DISEASE_5402
5403,5403,5403,5403,5403,5403,5403,5403,MONDO:0004883,hereditary choroidal atrophy,MONDO,disease,DISEASE_5403
5404,5404,5404,5404,5404,5404,5404,5404,MONDO:0024648_MONDO:0003557_MONDO:0003858,optic tract meningioma,MONDO_grouped,disease,DISEASE_5404
5405,5405,5405,5405,5405,5405,5405,5405,MONDO:0002068,female breast lower-inner quadrant cancer,MONDO,disease,DISEASE_5405
5406,5406,5406,5406,5406,5406,5406,5406,MONDO:0007243,Burkitt lymphoma,MONDO,disease,DISEASE_5406
5407,5407,5407,5407,5407,5407,5407,5407,MONDO:0016420,familial flecked retinopathy,MONDO,disease,DISEASE_5407
5408,5408,5408,5408,5408,5408,5408,5408,MONDO:0025085,"hepatitis, viral, animal",MONDO,disease,DISEASE_5408
5409,5409,5409,5409,5409,5409,5409,5409,MONDO:0013539,hypotonia-failure to thrive-microcephaly syndrome,MONDO,disease,DISEASE_5409
5410,5410,5410,5410,5410,5410,5410,5410,MONDO:0004813,tuberculous pneumothorax,MONDO,disease,DISEASE_5410
5411,5411,5411,5411,5411,5411,5411,5411,MONDO:0009530,lipoid proteinosis,MONDO,disease,DISEASE_5411
5412,5412,5412,5412,5412,5412,5412,5412,MONDO:0500000,episodic angioedema with eosinophilia,MONDO,disease,DISEASE_5412
5413,5413,5413,5413,5413,5413,5413,5413,MONDO:0008245,piebald trait-neurologic defects syndrome,MONDO,disease,DISEASE_5413
5414,5414,5414,5414,5414,5414,5414,5414,MONDO:0018542,severe congenital neutropenia,MONDO,disease,DISEASE_5414
5415,5415,5415,5415,5415,5415,5415,5415,MONDO:0004575,choline deficiency disease,MONDO,disease,DISEASE_5415
5416,5416,5416,5416,5416,5416,5416,5416,MONDO:0019336,Gardner syndrome,MONDO,disease,DISEASE_5416
5417,5417,5417,5417,5417,5417,5417,5417,MONDO:1012359,"progressive rod-cone degeneration, dog",MONDO,disease,DISEASE_5417
5418,5418,5418,5418,5418,5418,5418,5418,MONDO:0015734,rectal duplication,MONDO,disease,DISEASE_5418
5419,5419,5419,5419,5419,5419,5419,5419,MONDO:0018835,nodular regenerative hyperplasia of the liver,MONDO,disease,DISEASE_5419
5420,5420,5420,5420,5420,5420,5420,5420,MONDO:0800195,achalasia-alacrima syndrome,MONDO,disease,DISEASE_5420
5421,5421,5421,5421,5421,5421,5421,5421,MONDO:0009511,"Larsen-like syndrome, B3GAT3 type",MONDO,disease,DISEASE_5421
5422,5422,5422,5422,5422,5422,5422,5422,MONDO:0017571,Proteus-like syndrome,MONDO,disease,DISEASE_5422
5423,5423,5423,5423,5423,5423,5423,5423,MONDO:0044995,parasympathetic nervous system disorder,MONDO,disease,DISEASE_5423
5424,5424,5424,5424,5424,5424,5424,5424,MONDO:0010406,chromosome Xp11.22 duplication syndrome,MONDO,disease,DISEASE_5424
5425,5425,5425,5425,5425,5425,5425,5425,MONDO:0044648,kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome,MONDO,disease,DISEASE_5425
5426,5426,5426,5426,5426,5426,5426,5426,MONDO:0013571,acatalasia,MONDO,disease,DISEASE_5426
5427,5427,5427,5427,5427,5427,5427,5427,MONDO:0032650_MONDO:0957985_MONDO:0859241_MONDO:0031006,"neurodegeneration, childhood-onset, with cerebellar atrophy",MONDO_grouped,disease,DISEASE_5427
5428,5428,5428,5428,5428,5428,5428,5428,MONDO:0013954,Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency,MONDO,disease,DISEASE_5428
5429,5429,5429,5429,5429,5429,5429,5429,MONDO:0024415,hemorrhagic duodenitis,MONDO,disease,DISEASE_5429
5430,5430,5430,5430,5430,5430,5430,5430,MONDO:0008428,septooptic dysplasia,MONDO,disease,DISEASE_5430
5431,5431,5431,5431,5431,5431,5431,5431,MONDO:0024246,syringofibroadenoma,MONDO,disease,DISEASE_5431
5432,5432,5432,5432,5432,5432,5432,5432,MONDO:0003493,thymus squamous cell carcinoma,MONDO,disease,DISEASE_5432
5433,5433,5433,5433,5433,5433,5433,5433,MONDO:0015751,craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome,MONDO,disease,DISEASE_5433
5434,5434,5434,5434,5434,5434,5434,5434,MONDO:0700023,chromosome 16 disorder,MONDO,disease,DISEASE_5434
5435,5435,5435,5435,5435,5435,5435,5435,MONDO:0006982,subacute thyroiditis,MONDO,disease,DISEASE_5435
5436,5436,5436,5436,5436,5436,5436,5436,MONDO:0017921,hearing loss-familial salivary gland insensitivity to aldosterone syndrome,MONDO,disease,DISEASE_5436
5437,5437,5437,5437,5437,5437,5437,5437,MONDO:1011039_MONDO:1011040,"oculocutaneous albinism, SLC45A2-related, dog",MONDO_grouped,disease,DISEASE_5437
5438,5438,5438,5438,5438,5438,5438,5438,MONDO:0957427,B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2),MONDO,disease,DISEASE_5438
5439,5439,5439,5439,5439,5439,5439,5439,MONDO:0800096,abnormal mineralization disorder,MONDO,disease,DISEASE_5439
5440,5440,5440,5440,5440,5440,5440,5440,MONDO:0002275,generalized atherosclerosis,MONDO,disease,DISEASE_5440
5441,5441,5441,5441,5441,5441,5441,5441,MONDO:0018026,tetraploidy syndrome,MONDO,disease,DISEASE_5441
5442,5442,5442,5442,5442,5442,5442,5442,MONDO:0005995,trichostrongylosis,MONDO,disease,DISEASE_5442
5443,5443,5443,5443,5443,5443,5443,5443,MONDO:0006502,acute respiratory distress syndrome,MONDO,disease,DISEASE_5443
5444,5444,5444,5444,5444,5444,5444,5444,MONDO:0005833_MONDO:0044986_MONDO:0000612,lymphatic system disorder,MONDO_grouped,disease,DISEASE_5444
5445,5445,5445,5445,5445,5445,5445,5445,MONDO:0006980,struma ovarii,MONDO,disease,DISEASE_5445
5446,5446,5446,5446,5446,5446,5446,5446,MONDO:0024567_MONDO:0014777_MONDO:0014823_MONDO:0014176,"hypotonia, infantile, with psychomotor retardation and characteristic facies",MONDO_grouped,disease,DISEASE_5446
5447,5447,5447,5447,5447,5447,5447,5447,MONDO:0700003,obstetric disorder,MONDO,disease,DISEASE_5447
5448,5448,5448,5448,5448,5448,5448,5448,MONDO:0044211,idiopathic urticaria,MONDO,disease,DISEASE_5448
5449,5449,5449,5449,5449,5449,5449,5449,MONDO:0001655,dissociated nystagmus,MONDO,disease,DISEASE_5449
5450,5450,5450,5450,5450,5450,5450,5450,MONDO:0009985,retinohepatoendocrinologic syndrome,MONDO,disease,DISEASE_5450
5451,5451,5451,5451,5451,5451,5451,5451,MONDO:0016541,acquired secondary polycythemia,MONDO,disease,DISEASE_5451
5452,5452,5452,5452,5452,5452,5452,5452,MONDO:0017894_MONDO:0018437,acute myeloid leukemia with CEBPA somatic mutations,MONDO_grouped,disease,DISEASE_5452
5453,5453,5453,5453,5453,5453,5453,5453,MONDO:0004225,monoclonal gammopathy of uncertain significance,MONDO,disease,DISEASE_5453
5454,5454,5454,5454,5454,5454,5454,5454,MONDO:0006802,inappropriate ADH syndrome,MONDO,disease,DISEASE_5454
5455,5455,5455,5455,5455,5455,5455,5455,MONDO:0020858_MONDO:0032869,mitochondrial complex 5 (ATP synthase) deficiency nuclear,MONDO_grouped,disease,DISEASE_5455
5456,5456,5456,5456,5456,5456,5456,5456,MONDO:0002747,endometrial mucinous adenocarcinoma,MONDO,disease,DISEASE_5456
5457,5457,5457,5457,5457,5457,5457,5457,MONDO:0032707,turnpenny-fry syndrome,MONDO,disease,DISEASE_5457
5458,5458,5458,5458,5458,5458,5458,5458,MONDO:0003008,hereditary renal cell carcinoma,MONDO,disease,DISEASE_5458
5459,5459,5459,5459,5459,5459,5459,5459,MONDO:1011782,"hepatocellular fibrinogen storage disease, non-human animal",MONDO,disease,DISEASE_5459
5460,5460,5460,5460,5460,5460,5460,5460,MONDO:0007742,5-hydroxytryptamine oxygenase regulator,MONDO,disease,DISEASE_5460
5461,5461,5461,5461,5461,5461,5461,5461,MONDO:0018623,postpartum psychosis,MONDO,disease,DISEASE_5461
5462,5462,5462,5462,5462,5462,5462,5462,MONDO:0006677,bile reflux,MONDO,disease,DISEASE_5462
5463,5463,5463,5463,5463,5463,5463,5463,MONDO:0019444_MONDO:0005996,trichinellosis,MONDO_grouped,disease,DISEASE_5463
5464,5464,5464,5464,5464,5464,5464,5464,MONDO:0010109,tetraamelia with ectodermal dysplasia and lacrimal duct abnormalities,MONDO,disease,DISEASE_5464
5465,5465,5465,5465,5465,5465,5465,5465,MONDO:0018698,hereditary neuroendocrine tumor of small intestine,MONDO,disease,DISEASE_5465
5466,5466,5466,5466,5466,5466,5466,5466,MONDO:0956993,posterior fossa group B ependymoma,MONDO,disease,DISEASE_5466
5467,5467,5467,5467,5467,5467,5467,5467,MONDO:1012930,"familial acute respiratory distress syndrome, ANLN-related, dog",MONDO,disease,DISEASE_5467
5468,5468,5468,5468,5468,5468,5468,5468,MONDO:0017012,partial duplication of the short arm of chromosome 1,MONDO,disease,DISEASE_5468
5469,5469,5469,5469,5469,5469,5469,5469,MONDO:0018502,hereditary gastric cancer,MONDO,disease,DISEASE_5469
5470,5470,5470,5470,5470,5470,5470,5470,MONDO:0027666,codeine toxicity,MONDO,disease,DISEASE_5470
5471,5471,5471,5471,5471,5471,5471,5471,MONDO:0004384,maxillary sinus inverted papilloma,MONDO,disease,DISEASE_5471
5472,5472,5472,5472,5472,5472,5472,5472,MONDO:0016457,ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome,MONDO,disease,DISEASE_5472
5473,5473,5473,5473,5473,5473,5473,5473,MONDO:0850201,hereditary alpha tryptasemia syndrome,MONDO,disease,DISEASE_5473
5474,5474,5474,5474,5474,5474,5474,5474,MONDO:0033856,LAMA5-related multisystemic syndrome,MONDO,disease,DISEASE_5474
5475,5475,5475,5475,5475,5475,5475,5475,MONDO:0008229,"peroneal nerve, accessory deep",MONDO,disease,DISEASE_5475
5476,5476,5476,5476,5476,5476,5476,5476,MONDO:0014731,seizures-scoliosis-macrocephaly syndrome,MONDO,disease,DISEASE_5476
5477,5477,5477,5477,5477,5477,5477,5477,MONDO:0006164_MONDO:0006156,colorectal sessile serrated adenoma/polyp,MONDO_grouped,disease,DISEASE_5477
5478,5478,5478,5478,5478,5478,5478,5478,MONDO:0021117,lung neoplasm,MONDO,disease,DISEASE_5478
5479,5479,5479,5479,5479,5479,5479,5479,MONDO:0003389,epithelial-myoepithelial carcinoma,MONDO,disease,DISEASE_5479
5480,5480,5480,5480,5480,5480,5480,5480,MONDO:0018015_MONDO:0003366,intermittent hydrarthrosis,MONDO_grouped,disease,DISEASE_5480
5481,5481,5481,5481,5481,5481,5481,5481,MONDO:0971119,proteoglycan-related bone disorder,MONDO,disease,DISEASE_5481
5482,5482,5482,5482,5482,5482,5482,5482,MONDO:0800114,follicular bronchiolits,MONDO,disease,DISEASE_5482
5483,5483,5483,5483,5483,5483,5483,5483,MONDO:0019288,skin pigmentation disorder,MONDO,disease,DISEASE_5483
5484,5484,5484,5484,5484,5484,5484,5484,MONDO:1011716,"hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome, non-human animal",MONDO,disease,DISEASE_5484
5485,5485,5485,5485,5485,5485,5485,5485,MONDO:0005356,coronary vasospasm,MONDO,disease,DISEASE_5485
5486,5486,5486,5486,5486,5486,5486,5486,MONDO:0007025,chancre,MONDO,disease,DISEASE_5486
5487,5487,5487,5487,5487,5487,5487,5487,MONDO:0018715,congenital hemangioma,MONDO,disease,DISEASE_5487
5488,5488,5488,5488,5488,5488,5488,5488,MONDO:0018825,PYCR2-related microcephaly-progressive leukoencephalopathy,MONDO,disease,DISEASE_5488
5489,5489,5489,5489,5489,5489,5489,5489,MONDO:0032596,"myasthenic syndrome, congenital, 23, presynaptic",MONDO,disease,DISEASE_5489
5490,5490,5490,5490,5490,5490,5490,5490,MONDO:1010817,"polydactyly, llama",MONDO,disease,DISEASE_5490
5491,5491,5491,5491,5491,5491,5491,5491,MONDO:1010214,"non-hodgkin lymphoma, non-human animal",MONDO,disease,DISEASE_5491
5492,5492,5492,5492,5492,5492,5492,5492,MONDO:0016594,superficial siderosis,MONDO,disease,DISEASE_5492
5493,5493,5493,5493,5493,5493,5493,5493,MONDO:0043544,nosocomial infection,MONDO,disease,DISEASE_5493
5494,5494,5494,5494,5494,5494,5494,5494,MONDO:0013204_MONDO:0012425_MONDO:0014228_MONDO:0007637_MONDO:0013203_MONDO:0013206_MONDO:0013205_MONDO:0013207,"corneal dystrophy, Fuchs endothelial",MONDO_grouped,disease,DISEASE_5494
5495,5495,5495,5495,5495,5495,5495,5495,MONDO:0005104,aJCC grade 1 sarcoma,MONDO,disease,DISEASE_5495
5496,5496,5496,5496,5496,5496,5496,5496,MONDO:1012165,"micromelia, Japanese quail",MONDO,disease,DISEASE_5496
5497,5497,5497,5497,5497,5497,5497,5497,MONDO:0010675,"muscular dystrophy, cardiac type",MONDO,disease,DISEASE_5497
5498,5498,5498,5498,5498,5498,5498,5498,MONDO:0002013,lymphangioma,MONDO,disease,DISEASE_5498
5499,5499,5499,5499,5499,5499,5499,5499,MONDO:0032936,"myopathy, congenital, with respiratory insufficiency and bone fractures",MONDO,disease,DISEASE_5499
5500,5500,5500,5500,5500,5500,5500,5500,MONDO:0800453_MONDO:0010826,juvenile absence epilepsy,MONDO_grouped,disease,DISEASE_5500
5501,5501,5501,5501,5501,5501,5501,5501,MONDO:0020500,Marburg hemorrhagic fever,MONDO,disease,DISEASE_5501
5502,5502,5502,5502,5502,5502,5502,5502,MONDO:0019496,neuroendocrine neoplasm,MONDO,disease,DISEASE_5502
5503,5503,5503,5503,5503,5503,5503,5503,MONDO:0001503,primary eye hypotony,MONDO,disease,DISEASE_5503
5504,5504,5504,5504,5504,5504,5504,5504,MONDO:0020418,dysphagia lusoria,MONDO,disease,DISEASE_5504
5505,5505,5505,5505,5505,5505,5505,5505,MONDO:0000232,Flinders island spotted fever,MONDO,disease,DISEASE_5505
5506,5506,5506,5506,5506,5506,5506,5506,MONDO:0002356,pancreas disorder,MONDO,disease,DISEASE_5506
5507,5507,5507,5507,5507,5507,5507,5507,MONDO:0968979,neurodevelopmental disorder with hypotonia and seizures,MONDO,disease,DISEASE_5507
5508,5508,5508,5508,5508,5508,5508,5508,MONDO:0700270,ATM-related cancer predisposition,MONDO,disease,DISEASE_5508
5509,5509,5509,5509,5509,5509,5509,5509,MONDO:0018639,caudal regression-sirenomelia spectrum,MONDO,disease,DISEASE_5509
5510,5510,5510,5510,5510,5510,5510,5510,MONDO:0004573,ariboflavinosis,MONDO,disease,DISEASE_5510
5511,5511,5511,5511,5511,5511,5511,5511,MONDO:0025003,goat disease,MONDO,disease,DISEASE_5511
5512,5512,5512,5512,5512,5512,5512,5512,MONDO:0957955,"immunodeficiency 114, folate-responsive",MONDO,disease,DISEASE_5512
5513,5513,5513,5513,5513,5513,5513,5513,MONDO:0006287,malignancy in giant cell tumor of bone,MONDO,disease,DISEASE_5513
5514,5514,5514,5514,5514,5514,5514,5514,MONDO:0012996,AGAT deficiency,MONDO,disease,DISEASE_5514
5515,5515,5515,5515,5515,5515,5515,5515,MONDO:0008620_MONDO:0023599,upper limb mesomelic dysplasia,MONDO_grouped,disease,DISEASE_5515
5516,5516,5516,5516,5516,5516,5516,5516,MONDO:0001228,conjunctival folliculosis,MONDO,disease,DISEASE_5516
5517,5517,5517,5517,5517,5517,5517,5517,MONDO:0044273,"obsolete hypertension, diastolic, resistance to",MONDO,disease,DISEASE_5517
5518,5518,5518,5518,5518,5518,5518,5518,MONDO:0008524,"syringomas, multiple",MONDO,disease,DISEASE_5518
5519,5519,5519,5519,5519,5519,5519,5519,MONDO:1012335,"bone spavin, red deer",MONDO,disease,DISEASE_5519
5520,5520,5520,5520,5520,5520,5520,5520,MONDO:0015073,"gallbladder neuroendocrine tumor, grade 1/2",MONDO,disease,DISEASE_5520
5521,5521,5521,5521,5521,5521,5521,5521,MONDO:0015477,pinnae fistula or cyst,MONDO,disease,DISEASE_5521
5522,5522,5522,5522,5522,5522,5522,5522,MONDO:0056820,nasal cavity and paranasal sinus neoplasm,MONDO,disease,DISEASE_5522
5523,5523,5523,5523,5523,5523,5523,5523,MONDO:0100255,adenosine kinase deficiency,MONDO,disease,DISEASE_5523
5524,5524,5524,5524,5524,5524,5524,5524,MONDO:0025484,simian acquired immunodeficiency syndrome,MONDO,disease,DISEASE_5524
5525,5525,5525,5525,5525,5525,5525,5525,MONDO:0003330,urinary tract obstruction,MONDO,disease,DISEASE_5525
5526,5526,5526,5526,5526,5526,5526,5526,MONDO:0002181,exostosis,MONDO,disease,DISEASE_5526
5527,5527,5527,5527,5527,5527,5527,5527,MONDO:0800413,"antisocial behavior, susceptibility to",MONDO,disease,DISEASE_5527
5528,5528,5528,5528,5528,5528,5528,5528,MONDO:0006828,nasal cavity and paranasal sinus lethal midline granuloma,MONDO,disease,DISEASE_5528
5529,5529,5529,5529,5529,5529,5529,5529,MONDO:0009298,GOMBO syndrome,MONDO,disease,DISEASE_5529
5530,5530,5530,5530,5530,5530,5530,5530,MONDO:0011054,autosomal recessive amelia,MONDO,disease,DISEASE_5530
5531,5531,5531,5531,5531,5531,5531,5531,MONDO:0007630,North Carolina macular dystrophy,MONDO,disease,DISEASE_5531
5532,5532,5532,5532,5532,5532,5532,5532,MONDO:0006576,Ludwig's angina,MONDO,disease,DISEASE_5532
5533,5533,5533,5533,5533,5533,5533,5533,MONDO:0002365_MONDO:0003411,kidney hemangiopericytoma,MONDO_grouped,disease,DISEASE_5533
5534,5534,5534,5534,5534,5534,5534,5534,MONDO:0021210,trachea neoplasm,MONDO,disease,DISEASE_5534
5535,5535,5535,5535,5535,5535,5535,5535,MONDO:1011864,"polymicrogyria and asymmetrical ventricular dilation, non-human animal",MONDO,disease,DISEASE_5535
5536,5536,5536,5536,5536,5536,5536,5536,MONDO:0054749,obsolete body mass index quantitative trait locus 19,MONDO,disease,DISEASE_5536
5537,5537,5537,5537,5537,5537,5537,5537,MONDO:0004240,posterior urethra cancer,MONDO,disease,DISEASE_5537
5538,5538,5538,5538,5538,5538,5538,5538,MONDO:0007685,granulosis rubra nasi,MONDO,disease,DISEASE_5538
5539,5539,5539,5539,5539,5539,5539,5539,MONDO:0001635,bladder squamous papilloma,MONDO,disease,DISEASE_5539
5540,5540,5540,5540,5540,5540,5540,5540,MONDO:0003987,lung lymphoma,MONDO,disease,DISEASE_5540
5541,5541,5541,5541,5541,5541,5541,5541,MONDO:0021334,immunoproliferative disorder,MONDO,disease,DISEASE_5541
5542,5542,5542,5542,5542,5542,5542,5542,MONDO:0018170,idiopathic nephrotic syndrome,MONDO,disease,DISEASE_5542
5543,5543,5543,5543,5543,5543,5543,5543,MONDO:0000940,trypanosomiasis,MONDO,disease,DISEASE_5543
5544,5544,5544,5544,5544,5544,5544,5544,MONDO:0015165,acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor,MONDO,disease,DISEASE_5544
5545,5545,5545,5545,5545,5545,5545,5545,MONDO:0001670,tooth resorption,MONDO,disease,DISEASE_5545
5546,5546,5546,5546,5546,5546,5546,5546,MONDO:1010748,"Ehlers-Danlos syndrome, dermatosparaxis type, ADAMTS2-related, cattle",MONDO,disease,DISEASE_5546
5547,5547,5547,5547,5547,5547,5547,5547,MONDO:0045008,cholesterol metabolism disease,MONDO,disease,DISEASE_5547
5548,5548,5548,5548,5548,5548,5548,5548,MONDO:0013461,inosine triphosphatase deficiency,MONDO,disease,DISEASE_5548
5549,5549,5549,5549,5549,5549,5549,5549,MONDO:0015479,submucosal cleft palate,MONDO,disease,DISEASE_5549
5550,5550,5550,5550,5550,5550,5550,5550,MONDO:0006257,jejunal neuroendocrine tumor G1,MONDO,disease,DISEASE_5550
5551,5551,5551,5551,5551,5551,5551,5551,MONDO:0006400,salivary gland acinic cell carcinoma,MONDO,disease,DISEASE_5551
5552,5552,5552,5552,5552,5552,5552,5552,MONDO:0007072,ADULT syndrome,MONDO,disease,DISEASE_5552
5553,5553,5553,5553,5553,5553,5553,5553,MONDO:0003272,mixed epithelial stromal tumor,MONDO,disease,DISEASE_5553
5554,5554,5554,5554,5554,5554,5554,5554,MONDO:1012172,"shivers, horse",MONDO,disease,DISEASE_5554
5555,5555,5555,5555,5555,5555,5555,5555,MONDO:0008466,Karsch-Neugebauer syndrome,MONDO,disease,DISEASE_5555
5556,5556,5556,5556,5556,5556,5556,5556,MONDO:0001966_MONDO:0001817,chronic closed-angle glaucoma,MONDO_grouped,disease,DISEASE_5556
5557,5557,5557,5557,5557,5557,5557,5557,MONDO:0018736,kaposiform lymphangiomatosis,MONDO,disease,DISEASE_5557
5558,5558,5558,5558,5558,5558,5558,5558,MONDO:1011627,"myoclonus epilepsy of Lafora, non-human animal",MONDO,disease,DISEASE_5558
5559,5559,5559,5559,5559,5559,5559,5559,MONDO:0004922,developmental coordination disorder,MONDO,disease,DISEASE_5559
5560,5560,5560,5560,5560,5560,5560,5560,MONDO:0018547,acute tricyclic antidepressant poisoning,MONDO,disease,DISEASE_5560
5561,5561,5561,5561,5561,5561,5561,5561,MONDO:0003554,adenosquamous colon carcinoma,MONDO,disease,DISEASE_5561
5562,5562,5562,5562,5562,5562,5562,5562,MONDO:0021291,carcinoma in situ of fundus of stomach,MONDO,disease,DISEASE_5562
5563,5563,5563,5563,5563,5563,5563,5563,MONDO:0016498_MONDO:0016500,acute pure sensory neuropathy,MONDO_grouped,disease,DISEASE_5563
5564,5564,5564,5564,5564,5564,5564,5564,MONDO:0009193,"epithelial squamous dysplasia, keratinizing desquamative, of urinary tract",MONDO,disease,DISEASE_5564
5565,5565,5565,5565,5565,5565,5565,5565,MONDO:0010911_MONDO:0003430_MONDO:0006238_MONDO:0006388,prolactin-producing pituitary gland adenoma,MONDO_grouped,disease,DISEASE_5565
5566,5566,5566,5566,5566,5566,5566,5566,MONDO:0018749,hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome,MONDO,disease,DISEASE_5566
5567,5567,5567,5567,5567,5567,5567,5567,MONDO:0007271,familial cutaneous collagenoma,MONDO,disease,DISEASE_5567
5568,5568,5568,5568,5568,5568,5568,5568,MONDO:0001905,bicipital tenosynovitis,MONDO,disease,DISEASE_5568
5569,5569,5569,5569,5569,5569,5569,5569,MONDO:0004405,Barrett adenocarcinoma,MONDO,disease,DISEASE_5569
5570,5570,5570,5570,5570,5570,5570,5570,MONDO:0971177,immunodeficiency 123 with HPV-related verrucosis,MONDO,disease,DISEASE_5570
5571,5571,5571,5571,5571,5571,5571,5571,MONDO:0043510_MONDO:0005621_MONDO:0800482,brain injury,MONDO_grouped,disease,DISEASE_5571
5572,5572,5572,5572,5572,5572,5572,5572,MONDO:0005252,heart failure,MONDO,disease,DISEASE_5572
5573,5573,5573,5573,5573,5573,5573,5573,MONDO:0010404_MONDO:0010547_MONDO:0016612,X-linked non progressive cerebellar ataxia,MONDO_grouped,disease,DISEASE_5573
5574,5574,5574,5574,5574,5574,5574,5574,MONDO:0000231,Far eastern spotted fever,MONDO,disease,DISEASE_5574
5575,5575,5575,5575,5575,5575,5575,5575,MONDO:0043280,Wallerian degeneration,MONDO,disease,DISEASE_5575
5576,5576,5576,5576,5576,5576,5576,5576,MONDO:0017932,muscular hypertrophy-hepatomegaly-polyhydramnios syndrome,MONDO,disease,DISEASE_5576
5577,5577,5577,5577,5577,5577,5577,5577,MONDO:0018974,paraneoplastic pemphigus,MONDO,disease,DISEASE_5577
5578,5578,5578,5578,5578,5578,5578,5578,MONDO:0016702,oligoastrocytoma,MONDO,disease,DISEASE_5578
5579,5579,5579,5579,5579,5579,5579,5579,MONDO:0002274,monoclonal paraproteinemia disease,MONDO,disease,DISEASE_5579
5580,5580,5580,5580,5580,5580,5580,5580,MONDO:0010930,anophthalmia plus syndrome,MONDO,disease,DISEASE_5580
5581,5581,5581,5581,5581,5581,5581,5581,MONDO:0008540,extensor tendons of finger anomalies,MONDO,disease,DISEASE_5581
5582,5582,5582,5582,5582,5582,5582,5582,MONDO:0020422,aortopulmonary coronary arterial course,MONDO,disease,DISEASE_5582
5583,5583,5583,5583,5583,5583,5583,5583,MONDO:0800314,"xeroderma pigmentosum, type G/Cockayne syndrome",MONDO,disease,DISEASE_5583
5584,5584,5584,5584,5584,5584,5584,5584,MONDO:0700257_MONDO:0700258_MONDO:0700259_MONDO:0700263,RNASEH2B-related type 1 interferonopathy,MONDO_grouped,disease,DISEASE_5584
5585,5585,5585,5585,5585,5585,5585,5585,MONDO:0013714,mannose-binding lectin deficiency,MONDO,disease,DISEASE_5585
5586,5586,5586,5586,5586,5586,5586,5586,MONDO:0006009_MONDO:0020067,viral encephalitis,MONDO_grouped,disease,DISEASE_5586
5587,5587,5587,5587,5587,5587,5587,5587,MONDO:0006313,nabothian cyst,MONDO,disease,DISEASE_5587
5588,5588,5588,5588,5588,5588,5588,5588,MONDO:1012931,"chondrodysplasia, EVC2-related, cattle",MONDO,disease,DISEASE_5588
5589,5589,5589,5589,5589,5589,5589,5589,MONDO:0008374_MONDO:0012507_MONDO:0012398_MONDO:0019118_MONDO:1012242,retinal cone dystrophy,MONDO_grouped,disease,DISEASE_5589
5590,5590,5590,5590,5590,5590,5590,5590,MONDO:0013426,aneurysm-osteoarthritis syndrome,MONDO,disease,DISEASE_5590
5591,5591,5591,5591,5591,5591,5591,5591,MONDO:0000971,chest wall lipoma,MONDO,disease,DISEASE_5591
5592,5592,5592,5592,5592,5592,5592,5592,MONDO:0008336,"pterygium colli, isolated",MONDO,disease,DISEASE_5592
5593,5593,5593,5593,5593,5593,5593,5593,MONDO:0005405,childhood onset asthma,MONDO,disease,DISEASE_5593
5594,5594,5594,5594,5594,5594,5594,5594,MONDO:0009861_MONDO:1010724,phenylketonuria,MONDO_grouped,disease,DISEASE_5594
5595,5595,5595,5595,5595,5595,5595,5595,MONDO:1010754,"X-linked hypohidrotic ectodermal dysplasia, EDA-related, dog",MONDO,disease,DISEASE_5595
5596,5596,5596,5596,5596,5596,5596,5596,MONDO:0015010,atypical glycine encephalopathy,MONDO,disease,DISEASE_5596
5597,5597,5597,5597,5597,5597,5597,5597,MONDO:1010051,"diabetes insipidus, non-human animal",MONDO,disease,DISEASE_5597
5598,5598,5598,5598,5598,5598,5598,5598,MONDO:0045030,non-infectious diarrheal disease,MONDO,disease,DISEASE_5598
5599,5599,5599,5599,5599,5599,5599,5599,MONDO:0008593,trichomegaly,MONDO,disease,DISEASE_5599
5600,5600,5600,5600,5600,5600,5600,5600,MONDO:0011092,ribbing disease,MONDO,disease,DISEASE_5600
5601,5601,5601,5601,5601,5601,5601,5601,MONDO:0016222,spindle cell hemangioma,MONDO,disease,DISEASE_5601
5602,5602,5602,5602,5602,5602,5602,5602,MONDO:0019891,monosomy 22,MONDO,disease,DISEASE_5602
5603,5603,5603,5603,5603,5603,5603,5603,MONDO:0033816,thygeson superficial punctate keratopathy,MONDO,disease,DISEASE_5603
5604,5604,5604,5604,5604,5604,5604,5604,MONDO:0850287,aspirin-induced respiratory disease,MONDO,disease,DISEASE_5604
5605,5605,5605,5605,5605,5605,5605,5605,MONDO:0006402,salivary gland basal cell adenocarcinoma,MONDO,disease,DISEASE_5605
5606,5606,5606,5606,5606,5606,5606,5606,MONDO:0005231_MONDO:0005366_MONDO:0005354_MONDO:0100371_MONDO:0100370,hepatitis C virus infection,MONDO_grouped,disease,DISEASE_5606
5607,5607,5607,5607,5607,5607,5607,5607,MONDO:0025135,"tuberculosis, avian",MONDO,disease,DISEASE_5607
5608,5608,5608,5608,5608,5608,5608,5608,MONDO:0002550,hypoglossal nerve neoplasm,MONDO,disease,DISEASE_5608
5609,5609,5609,5609,5609,5609,5609,5609,MONDO:0003310,Monckeberg arteriosclerosis,MONDO,disease,DISEASE_5609
5610,5610,5610,5610,5610,5610,5610,5610,MONDO:0014551,short stature with nonspecific skeletal abnormalities,MONDO,disease,DISEASE_5610
5611,5611,5611,5611,5611,5611,5611,5611,MONDO:0003145,supratentorial primitive neuroectodermal tumor,MONDO,disease,DISEASE_5611
5612,5612,5612,5612,5612,5612,5612,5612,MONDO:0011141,"megaloblastic anemia, folate-responsive",MONDO,disease,DISEASE_5612
5613,5613,5613,5613,5613,5613,5613,5613,MONDO:0032698,neurodevelopmental disorder with central and peripheral motor dysfunction,MONDO,disease,DISEASE_5613
5614,5614,5614,5614,5614,5614,5614,5614,MONDO:0001718,scleritis,MONDO,disease,DISEASE_5614
5615,5615,5615,5615,5615,5615,5615,5615,MONDO:0022171,chromhidrosis,MONDO,disease,DISEASE_5615
5616,5616,5616,5616,5616,5616,5616,5616,MONDO:0971001,immunodeficiency 121 with autoinflammation,MONDO,disease,DISEASE_5616
5617,5617,5617,5617,5617,5617,5617,5617,MONDO:0015160,multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome,MONDO,disease,DISEASE_5617
5618,5618,5618,5618,5618,5618,5618,5618,MONDO:1012763_MONDO:1012787_MONDO:1012788_MONDO:1012802_MONDO:1012803,"neuroaxonal dystrophy, TECPR2-related, dog",MONDO_grouped,disease,DISEASE_5618
5619,5619,5619,5619,5619,5619,5619,5619,MONDO:0007816,obsolete immune suppression,MONDO,disease,DISEASE_5619
5620,5620,5620,5620,5620,5620,5620,5620,MONDO:0016342_MONDO:0017401_MONDO:0017402_MONDO:0017403,familial isolated arrhythmogenic right ventricular dysplasia,MONDO_grouped,disease,DISEASE_5620
5621,5621,5621,5621,5621,5621,5621,5621,MONDO:0043494,arteritis,MONDO,disease,DISEASE_5621
5622,5622,5622,5622,5622,5622,5622,5622,MONDO:0018145,congenital retinal arteriovenous communication,MONDO,disease,DISEASE_5622
5623,5623,5623,5623,5623,5623,5623,5623,MONDO:0010112,"thalamic degeneration, symmetric infantile",MONDO,disease,DISEASE_5623
5624,5624,5624,5624,5624,5624,5624,5624,MONDO:1012237,"renal insufficiency, dog",MONDO,disease,DISEASE_5624
5625,5625,5625,5625,5625,5625,5625,5625,MONDO:0004176_MONDO:0004306,childhood extraosseous osteosarcoma,MONDO_grouped,disease,DISEASE_5625
5626,5626,5626,5626,5626,5626,5626,5626,MONDO:0045001,cardiac ventricle disorder,MONDO,disease,DISEASE_5626
5627,5627,5627,5627,5627,5627,5627,5627,MONDO:0007277,cataract-aberrant oral frenula-growth delay syndrome,MONDO,disease,DISEASE_5627
5628,5628,5628,5628,5628,5628,5628,5628,MONDO:0005299,brain ischemia,MONDO,disease,DISEASE_5628
5629,5629,5629,5629,5629,5629,5629,5629,MONDO:0004304,mixed cell type adenoma of parathyroid,MONDO,disease,DISEASE_5629
5630,5630,5630,5630,5630,5630,5630,5630,MONDO:0020395,valvar pulmonary stenosis,MONDO,disease,DISEASE_5630
5631,5631,5631,5631,5631,5631,5631,5631,MONDO:0700195,rous sarcoma,MONDO,disease,DISEASE_5631
5632,5632,5632,5632,5632,5632,5632,5632,MONDO:0009056_MONDO:0010573,cutis verticis gyrata and intellectual disability,MONDO_grouped,disease,DISEASE_5632
5633,5633,5633,5633,5633,5633,5633,5633,MONDO:0032784,neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements,MONDO,disease,DISEASE_5633
5634,5634,5634,5634,5634,5634,5634,5634,MONDO:0007952,maxillofacial dysostosis,MONDO,disease,DISEASE_5634
5635,5635,5635,5635,5635,5635,5635,5635,MONDO:1011731,"multiple autoimmune diseases syndrome, non-human animal",MONDO,disease,DISEASE_5635
5636,5636,5636,5636,5636,5636,5636,5636,MONDO:0002052_MONDO:0005832,lymphadenitis,MONDO_grouped,disease,DISEASE_5636
5637,5637,5637,5637,5637,5637,5637,5637,MONDO:0008383_MONDO:1011153_MONDO:0043267_MONDO:0004586_MONDO:0008384,rheumatoid arthritis,MONDO_grouped,disease,DISEASE_5637
5638,5638,5638,5638,5638,5638,5638,5638,MONDO:0006281,lung signet ring cell carcinoma,MONDO,disease,DISEASE_5638
5639,5639,5639,5639,5639,5639,5639,5639,MONDO:1011833_MONDO:1011899,"cerebellar Purkinje cell degeneration, non-human animal",MONDO_grouped,disease,DISEASE_5639
5640,5640,5640,5640,5640,5640,5640,5640,MONDO:0016650,paternal uniparental disomy of chromosome 1,MONDO,disease,DISEASE_5640
5641,5641,5641,5641,5641,5641,5641,5641,MONDO:0022863,corneal crystals myopathy neuropathy,MONDO,disease,DISEASE_5641
5642,5642,5642,5642,5642,5642,5642,5642,MONDO:0100192_MONDO:0001106,liver failure,MONDO_grouped,disease,DISEASE_5642
5643,5643,5643,5643,5643,5643,5643,5643,MONDO:0003884,lipoma of the rectum,MONDO,disease,DISEASE_5643
5644,5644,5644,5644,5644,5644,5644,5644,MONDO:0006813,intradermal nevus,MONDO,disease,DISEASE_5644
5645,5645,5645,5645,5645,5645,5645,5645,MONDO:0003478,childhood ependymoma,MONDO,disease,DISEASE_5645
5646,5646,5646,5646,5646,5646,5646,5646,MONDO:0018211,Balint syndrome,MONDO,disease,DISEASE_5646
5647,5647,5647,5647,5647,5647,5647,5647,MONDO:0971125,torpedo maculopathy,MONDO,disease,DISEASE_5647
5648,5648,5648,5648,5648,5648,5648,5648,MONDO:0008411,ulnar-mammary syndrome,MONDO,disease,DISEASE_5648
5649,5649,5649,5649,5649,5649,5649,5649,MONDO:0005792,herpes simplex virus gingivostomatitis,MONDO,disease,DISEASE_5649
5650,5650,5650,5650,5650,5650,5650,5650,MONDO:0005308,ciliopathy,MONDO,disease,DISEASE_5650
5651,5651,5651,5651,5651,5651,5651,5651,MONDO:0008572,"tibia, hypoplasia or aplasia of, with polydactyly",MONDO,disease,DISEASE_5651
5652,5652,5652,5652,5652,5652,5652,5652,MONDO:0004251,small intestine neoplasm,MONDO,disease,DISEASE_5652
5653,5653,5653,5653,5653,5653,5653,5653,MONDO:0005519,renal pelvis carcinoma,MONDO,disease,DISEASE_5653
5654,5654,5654,5654,5654,5654,5654,5654,MONDO:0010692,nuclear ribonucleic acid,MONDO,disease,DISEASE_5654
5655,5655,5655,5655,5655,5655,5655,5655,MONDO:0020801,rectal medullary carcinoma,MONDO,disease,DISEASE_5655
5656,5656,5656,5656,5656,5656,5656,5656,MONDO:0001417,tracheal lymphoma,MONDO,disease,DISEASE_5656
5657,5657,5657,5657,5657,5657,5657,5657,MONDO:0016993,generalized peeling skin syndrome type C,MONDO,disease,DISEASE_5657
5658,5658,5658,5658,5658,5658,5658,5658,MONDO:0001871_MONDO:0003135,acute diffuse glomerulonephritis,MONDO_grouped,disease,DISEASE_5658
5659,5659,5659,5659,5659,5659,5659,5659,MONDO:0023597,laryngeal papillomatosis,MONDO,disease,DISEASE_5659
5660,5660,5660,5660,5660,5660,5660,5660,MONDO:0006530,cholesteatoma,MONDO,disease,DISEASE_5660
5661,5661,5661,5661,5661,5661,5661,5661,MONDO:0015528,congenital epulis,MONDO,disease,DISEASE_5661
5662,5662,5662,5662,5662,5662,5662,5662,MONDO:0003089,extrahepatic bile duct mucoepidermoid carcinoma,MONDO,disease,DISEASE_5662
5663,5663,5663,5663,5663,5663,5663,5663,MONDO:0018023,hemoglobin M disease,MONDO,disease,DISEASE_5663
5664,5664,5664,5664,5664,5664,5664,5664,MONDO:0001065,supine hypotensive syndrome,MONDO,disease,DISEASE_5664
5665,5665,5665,5665,5665,5665,5665,5665,MONDO:0700065,trisomy,MONDO,disease,DISEASE_5665
5666,5666,5666,5666,5666,5666,5666,5666,MONDO:0001430,deep corneal vascularisation,MONDO,disease,DISEASE_5666
5667,5667,5667,5667,5667,5667,5667,5667,MONDO:0100462,"short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans",MONDO,disease,DISEASE_5667
5668,5668,5668,5668,5668,5668,5668,5668,MONDO:0007024_MONDO:0042370,Yersinia pseudotuberculosis infectious disease,MONDO_grouped,disease,DISEASE_5668
5669,5669,5669,5669,5669,5669,5669,5669,MONDO:0011617,"arthropathy, erosive",MONDO,disease,DISEASE_5669
5670,5670,5670,5670,5670,5670,5670,5670,MONDO:0005381_MONDO:0800486,bone disorder,MONDO_grouped,disease,DISEASE_5670
5671,5671,5671,5671,5671,5671,5671,5671,MONDO:0008590_MONDO:0013888_MONDO:0011201_MONDO:0014756_MONDO:0030027_MONDO:0012671,"tremor, hereditary essential",MONDO_grouped,disease,DISEASE_5671
5672,5672,5672,5672,5672,5672,5672,5672,MONDO:0010475,X-linked central congenital hypothyroidism with late-onset testicular enlargement,MONDO,disease,DISEASE_5672
5673,5673,5673,5673,5673,5673,5673,5673,MONDO:0002444,melancholia,MONDO,disease,DISEASE_5673
5674,5674,5674,5674,5674,5674,5674,5674,MONDO:0005778,haemonchiasis,MONDO,disease,DISEASE_5674
5675,5675,5675,5675,5675,5675,5675,5675,MONDO:1040051,IMPDH1-related retinopathy,MONDO,disease,DISEASE_5675
5676,5676,5676,5676,5676,5676,5676,5676,MONDO:0009846,pentosuria,MONDO,disease,DISEASE_5676
5677,5677,5677,5677,5677,5677,5677,5677,MONDO:0009462,"inosine phosphorylase deficiency, immune defect due to",MONDO,disease,DISEASE_5677
5678,5678,5678,5678,5678,5678,5678,5678,MONDO:0020812,"exposure, dental pulp",MONDO,disease,DISEASE_5678
5679,5679,5679,5679,5679,5679,5679,5679,MONDO:0016866,partial deletion of chromosome 1,MONDO,disease,DISEASE_5679
5680,5680,5680,5680,5680,5680,5680,5680,MONDO:0011120,"neural tube defects, folate-sensitive",MONDO,disease,DISEASE_5680
5681,5681,5681,5681,5681,5681,5681,5681,MONDO:0016534,infundibulo-neurohypophysitis,MONDO,disease,DISEASE_5681
5682,5682,5682,5682,5682,5682,5682,5682,MONDO:0006260,kidney medullary carcinoma,MONDO,disease,DISEASE_5682
5683,5683,5683,5683,5683,5683,5683,5683,MONDO:1010038,"gingival hypertrophy, non-human animal",MONDO,disease,DISEASE_5683
5684,5684,5684,5684,5684,5684,5684,5684,MONDO:0016932,partial duplication of chromosome 11,MONDO,disease,DISEASE_5684
5685,5685,5685,5685,5685,5685,5685,5685,MONDO:1010672,"Bernard-Soulier syndrome, GP9-related, dog",MONDO,disease,DISEASE_5685
5686,5686,5686,5686,5686,5686,5686,5686,MONDO:0021605,benign eyelid neoplasm,MONDO,disease,DISEASE_5686
5687,5687,5687,5687,5687,5687,5687,5687,MONDO:0016458,8q12 microduplication syndrome,MONDO,disease,DISEASE_5687
5688,5688,5688,5688,5688,5688,5688,5688,MONDO:0018911_MONDO:0012348_MONDO:0014674_MONDO:0014589_MONDO:0007452_MONDO:0012513_MONDO:0011668_MONDO:0007453_MONDO:0013242_MONDO:0011667_MONDO:0013240_MONDO:0010894_MONDO:0012818,maturity-onset diabetes of the young,MONDO_grouped,disease,DISEASE_5688
5689,5689,5689,5689,5689,5689,5689,5689,MONDO:0019898,distal monosomy 14q,MONDO,disease,DISEASE_5689
5690,5690,5690,5690,5690,5690,5690,5690,MONDO:0010704_MONDO:0010571_MONDO:0019027,otopalatodigital syndrome,MONDO_grouped,disease,DISEASE_5690
5691,5691,5691,5691,5691,5691,5691,5691,MONDO:0001008,blepharophimosis,MONDO,disease,DISEASE_5691
5692,5692,5692,5692,5692,5692,5692,5692,MONDO:0005302,"attention deficit hyperactivity disorder, inattentive type",MONDO,disease,DISEASE_5692
5693,5693,5693,5693,5693,5693,5693,5693,MONDO:0025087,classical swine fever,MONDO,disease,DISEASE_5693
5694,5694,5694,5694,5694,5694,5694,5694,MONDO:0020214_MONDO:0020212,posterior corneal dystrophy,MONDO_grouped,disease,DISEASE_5694
5695,5695,5695,5695,5695,5695,5695,5695,MONDO:0020391,pulmonary artery coming from the aorta,MONDO,disease,DISEASE_5695
5696,5696,5696,5696,5696,5696,5696,5696,MONDO:0026730,Basilicata-Akhtar syndrome,MONDO,disease,DISEASE_5696
5697,5697,5697,5697,5697,5697,5697,5697,MONDO:0008102,"sick sinus syndrome 2, autosomal dominant",MONDO,disease,DISEASE_5697
5698,5698,5698,5698,5698,5698,5698,5698,MONDO:0018281,congenital muscular dystrophy with hyperlaxity,MONDO,disease,DISEASE_5698
5699,5699,5699,5699,5699,5699,5699,5699,MONDO:0001617,transient global amnesia,MONDO,disease,DISEASE_5699
5700,5700,5700,5700,5700,5700,5700,5700,MONDO:0015839,septate uterus,MONDO,disease,DISEASE_5700
5701,5701,5701,5701,5701,5701,5701,5701,MONDO:0019276_MONDO:0006541,inherited epidermolysis bullosa,MONDO_grouped,disease,DISEASE_5701
5702,5702,5702,5702,5702,5702,5702,5702,MONDO:0017285,penoscrotal transposition,MONDO,disease,DISEASE_5702
5703,5703,5703,5703,5703,5703,5703,5703,MONDO:0013118,Nijmegen breakage syndrome-like disorder,MONDO,disease,DISEASE_5703
5704,5704,5704,5704,5704,5704,5704,5704,MONDO:0016418,"multiple system atrophy, cerebellar type",MONDO,disease,DISEASE_5704
5705,5705,5705,5705,5705,5705,5705,5705,MONDO:0020571,relapsing epidemic typhus,MONDO,disease,DISEASE_5705
5706,5706,5706,5706,5706,5706,5706,5706,MONDO:0002405,hepatic vascular disorder,MONDO,disease,DISEASE_5706
5707,5707,5707,5707,5707,5707,5707,5707,MONDO:0015760,T-cell non-Hodgkin lymphoma,MONDO,disease,DISEASE_5707
5708,5708,5708,5708,5708,5708,5708,5708,MONDO:0010180_MONDO:0015826,autosomal recessive spondylocostal dysostosis,MONDO_grouped,disease,DISEASE_5708
5709,5709,5709,5709,5709,5709,5709,5709,MONDO:1012741,"Chiari-like malformation, dog",MONDO,disease,DISEASE_5709
5710,5710,5710,5710,5710,5710,5710,5710,MONDO:0008158,dacryocystitis-osteopoikilosis syndrome,MONDO,disease,DISEASE_5710
5711,5711,5711,5711,5711,5711,5711,5711,MONDO:0011308,GRACILE syndrome,MONDO,disease,DISEASE_5711
5712,5712,5712,5712,5712,5712,5712,5712,MONDO:0800204,calvarial doughnut lesions with bone fragility and spondylometaphyseal dysplasia,MONDO,disease,DISEASE_5712
5713,5713,5713,5713,5713,5713,5713,5713,MONDO:0001074,chronic tic disorder,MONDO,disease,DISEASE_5713
5714,5714,5714,5714,5714,5714,5714,5714,MONDO:0800291,"crossed polydactyly, type I",MONDO,disease,DISEASE_5714
5715,5715,5715,5715,5715,5715,5715,5715,MONDO:0014403,short stature due to GHSR deficiency,MONDO,disease,DISEASE_5715
5716,5716,5716,5716,5716,5716,5716,5716,MONDO:0018678,polyclonal hyperviscosity syndrome,MONDO,disease,DISEASE_5716
5717,5717,5717,5717,5717,5717,5717,5717,MONDO:0015600,"X-linked intellectual disability, Cilliers type",MONDO,disease,DISEASE_5717
5718,5718,5718,5718,5718,5718,5718,5718,MONDO:0004386,uterine corpus atypical polypoid adenomyoma,MONDO,disease,DISEASE_5718
5719,5719,5719,5719,5719,5719,5719,5719,MONDO:0016562,progressive supranuclear palsy-pure akinesia with gait freezing syndrome,MONDO,disease,DISEASE_5719
5720,5720,5720,5720,5720,5720,5720,5720,MONDO:0100006,secondary mast cell activation syndrome,MONDO,disease,DISEASE_5720
5721,5721,5721,5721,5721,5721,5721,5721,MONDO:0024338,mucinous neoplasm,MONDO,disease,DISEASE_5721
5722,5722,5722,5722,5722,5722,5722,5722,MONDO:0035777,parenteral nutrition-associated cholestasis,MONDO,disease,DISEASE_5722
5723,5723,5723,5723,5723,5723,5723,5723,MONDO:1012782,"progressive retinal atrophy, Whippet, dog",MONDO,disease,DISEASE_5723
5724,5724,5724,5724,5724,5724,5724,5724,MONDO:0016439,elastoderma,MONDO,disease,DISEASE_5724
5725,5725,5725,5725,5725,5725,5725,5725,MONDO:0020475,dermotrichic syndrome,MONDO,disease,DISEASE_5725
5726,5726,5726,5726,5726,5726,5726,5726,MONDO:0001301,rumination disorder,MONDO,disease,DISEASE_5726
5727,5727,5727,5727,5727,5727,5727,5727,MONDO:0008725_MONDO:0017972_MONDO:0017973,congenital lipoid adrenal hyperplasia due to STAR deficency,MONDO_grouped,disease,DISEASE_5727
5728,5728,5728,5728,5728,5728,5728,5728,MONDO:0001035,hypopyon ulcer,MONDO,disease,DISEASE_5728
5729,5729,5729,5729,5729,5729,5729,5729,MONDO:0021487,benign neoplasm of choroid,MONDO,disease,DISEASE_5729
5730,5730,5730,5730,5730,5730,5730,5730,MONDO:0015807,myopic macular degeneration,MONDO,disease,DISEASE_5730
5731,5731,5731,5731,5731,5731,5731,5731,MONDO:1010225,"cystic hygroma, non-human animal",MONDO,disease,DISEASE_5731
5732,5732,5732,5732,5732,5732,5732,5732,MONDO:0015813,primary cutaneous marginal zone B-cell lymphoma,MONDO,disease,DISEASE_5732
5733,5733,5733,5733,5733,5733,5733,5733,MONDO:0021521,benign neoplasm of mediastinum,MONDO,disease,DISEASE_5733
5734,5734,5734,5734,5734,5734,5734,5734,MONDO:0030970,"immunodeficiency 106, susceptibility to viral infections",MONDO,disease,DISEASE_5734
5735,5735,5735,5735,5735,5735,5735,5735,MONDO:0004866,eustachian tube disorder,MONDO,disease,DISEASE_5735
5736,5736,5736,5736,5736,5736,5736,5736,MONDO:0002787,adamantinous craniopharyngioma,MONDO,disease,DISEASE_5736
5737,5737,5737,5737,5737,5737,5737,5737,MONDO:0017364,POEMS syndrome,MONDO,disease,DISEASE_5737
5738,5738,5738,5738,5738,5738,5738,5738,MONDO:0001365,necrosis of ear ossicle,MONDO,disease,DISEASE_5738
5739,5739,5739,5739,5739,5739,5739,5739,MONDO:0100199,diffuse gastric and lobular breast cancer syndrome with or without cleft lip and/or palate,MONDO,disease,DISEASE_5739
5740,5740,5740,5740,5740,5740,5740,5740,MONDO:0005561_MONDO:0003803,aortic disorder,MONDO_grouped,disease,DISEASE_5740
5741,5741,5741,5741,5741,5741,5741,5741,MONDO:0017758,disorder of vitamin and non-protein cofactor absorption and transport,MONDO,disease,DISEASE_5741
5742,5742,5742,5742,5742,5742,5742,5742,MONDO:0016407,oligomeganephronia,MONDO,disease,DISEASE_5742
5743,5743,5743,5743,5743,5743,5743,5743,MONDO:0012161,susceptibility to respiratory infections associated with CD8alpha chain mutation,MONDO,disease,DISEASE_5743
5744,5744,5744,5744,5744,5744,5744,5744,MONDO:0100188,combined ApoA-I and ApoC-III deficiency,MONDO,disease,DISEASE_5744
5745,5745,5745,5745,5745,5745,5745,5745,MONDO:0007857,keratosis palmaris et plantaris-clinodactyly syndrome,MONDO,disease,DISEASE_5745
5746,5746,5746,5746,5746,5746,5746,5746,MONDO:0003984,internal auditory canal lipoma,MONDO,disease,DISEASE_5746
5747,5747,5747,5747,5747,5747,5747,5747,MONDO:0008780,"amyotrophic lateral sclerosis type 2, juvenile",MONDO,disease,DISEASE_5747
5748,5748,5748,5748,5748,5748,5748,5748,MONDO:0002775,anovulation,MONDO,disease,DISEASE_5748
5749,5749,5749,5749,5749,5749,5749,5749,MONDO:0021163,kidney neoplasm,MONDO,disease,DISEASE_5749
5750,5750,5750,5750,5750,5750,5750,5750,MONDO:0022781,cleft lip palate-tetraphocomelia,MONDO,disease,DISEASE_5750
5751,5751,5751,5751,5751,5751,5751,5751,MONDO:0002681,choroid plexus cancer,MONDO,disease,DISEASE_5751
5752,5752,5752,5752,5752,5752,5752,5752,MONDO:0014579_MONDO:0012433_MONDO:0011756_MONDO:0014712_MONDO:0011755_MONDO:0012225_MONDO:0013326_MONDO:0009962_MONDO:0017842,Senior-Loken syndrome,MONDO_grouped,disease,DISEASE_5752
5753,5753,5753,5753,5753,5753,5753,5753,MONDO:1011674,"hyperosmolar nonketotic diabetes mellitus, non-human animal",MONDO,disease,DISEASE_5753
5754,5754,5754,5754,5754,5754,5754,5754,MONDO:0004021,mediastinal malignant lymphoma,MONDO,disease,DISEASE_5754
5755,5755,5755,5755,5755,5755,5755,5755,MONDO:0011021,"neuronal intestinal dysplasia, type B",MONDO,disease,DISEASE_5755
5756,5756,5756,5756,5756,5756,5756,5756,MONDO:0800344,brachydactyly-syndactyly-oligodactyly syndrome,MONDO,disease,DISEASE_5756
5757,5757,5757,5757,5757,5757,5757,5757,MONDO:0013678,EDICT syndrome,MONDO,disease,DISEASE_5757
5758,5758,5758,5758,5758,5758,5758,5758,MONDO:0022633,camptodactyly joint contractures and facial skeletal dysplasia,MONDO,disease,DISEASE_5758
5759,5759,5759,5759,5759,5759,5759,5759,MONDO:0000379,malignant Sertoli-Leydig cell tumor,MONDO,disease,DISEASE_5759
5760,5760,5760,5760,5760,5760,5760,5760,MONDO:1012230,"protein C deficiency, horse",MONDO,disease,DISEASE_5760
5761,5761,5761,5761,5761,5761,5761,5761,MONDO:0005224_MONDO:0020320,acute myeloblastic leukemia without maturation,MONDO_grouped,disease,DISEASE_5761
5762,5762,5762,5762,5762,5762,5762,5762,MONDO:0002267,obstructive lung disease,MONDO,disease,DISEASE_5762
5763,5763,5763,5763,5763,5763,5763,5763,MONDO:0006403,salivary gland carcinoma ex pleomorphic adenoma,MONDO,disease,DISEASE_5763
5764,5764,5764,5764,5764,5764,5764,5764,MONDO:0007489,dysplasia epiphysealis hemimelica,MONDO,disease,DISEASE_5764
5765,5765,5765,5765,5765,5765,5765,5765,MONDO:0971068,Phelan-McDermid syndrome due to 22q13.3 deletion,MONDO,disease,DISEASE_5765
5766,5766,5766,5766,5766,5766,5766,5766,MONDO:0001928,suppurative cholangitis,MONDO,disease,DISEASE_5766
5767,5767,5767,5767,5767,5767,5767,5767,MONDO:0019075,Bosley-Salih-Alorainy syndrome,MONDO,disease,DISEASE_5767
5768,5768,5768,5768,5768,5768,5768,5768,MONDO:0009848,dissecting cellulitis of the scalp,MONDO,disease,DISEASE_5768
5769,5769,5769,5769,5769,5769,5769,5769,MONDO:0007481,Leri-Weill dyschondrosteosis,MONDO,disease,DISEASE_5769
5770,5770,5770,5770,5770,5770,5770,5770,MONDO:0100148,X-linked complex neurodevelopmental disorder,MONDO,disease,DISEASE_5770
5771,5771,5771,5771,5771,5771,5771,5771,MONDO:0000440,metabolic acidosis,MONDO,disease,DISEASE_5771
5772,5772,5772,5772,5772,5772,5772,5772,MONDO:0957111_MONDO:0957112_MONDO:0957113_MONDO:0957114_MONDO:0957115,neurological muscular channelopathy due to a genetic sodium channel defect,MONDO_grouped,disease,DISEASE_5772
5773,5773,5773,5773,5773,5773,5773,5773,MONDO:1011206,"periodontitis, Rhesus monkey",MONDO,disease,DISEASE_5773
5774,5774,5774,5774,5774,5774,5774,5774,MONDO:0014881,transketolase deficiency,MONDO,disease,DISEASE_5774
5775,5775,5775,5775,5775,5775,5775,5775,MONDO:0007392,coxoauricular syndrome,MONDO,disease,DISEASE_5775
5776,5776,5776,5776,5776,5776,5776,5776,MONDO:0020800,demyelinating disease of central nervous system,MONDO,disease,DISEASE_5776
5777,5777,5777,5777,5777,5777,5777,5777,MONDO:0024238,cerebral degeneration,MONDO,disease,DISEASE_5777
5778,5778,5778,5778,5778,5778,5778,5778,MONDO:0007477,3-M syndrome,MONDO,disease,DISEASE_5778
5779,5779,5779,5779,5779,5779,5779,5779,MONDO:0800380,"17-alpha-hydroxylase/17,20-lyase deficiency, combined partial",MONDO,disease,DISEASE_5779
5780,5780,5780,5780,5780,5780,5780,5780,MONDO:0016988,hyperinsulinism due to HNF4A deficiency,MONDO,disease,DISEASE_5780
5781,5781,5781,5781,5781,5781,5781,5781,MONDO:0008727,congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency,MONDO,disease,DISEASE_5781
5782,5782,5782,5782,5782,5782,5782,5782,MONDO:0000746,obsolete inguinal hernia,MONDO,disease,DISEASE_5782
5783,5783,5783,5783,5783,5783,5783,5783,MONDO:0020703,erythroid neoplasm,MONDO,disease,DISEASE_5783
5784,5784,5784,5784,5784,5784,5784,5784,MONDO:0060690,phenytoin toxicity,MONDO,disease,DISEASE_5784
5785,5785,5785,5785,5785,5785,5785,5785,MONDO:0968986,chaotic conus spinal cord lipoma,MONDO,disease,DISEASE_5785
5786,5786,5786,5786,5786,5786,5786,5786,MONDO:0008720,congenital isolated adrenocorticotropic hormone deficiency,MONDO,disease,DISEASE_5786
5787,5787,5787,5787,5787,5787,5787,5787,MONDO:0008071,autosomal dominant progressive nephropathy with hypertension,MONDO,disease,DISEASE_5787
5788,5788,5788,5788,5788,5788,5788,5788,MONDO:0011732,familial digital arthropathy-brachydactyly,MONDO,disease,DISEASE_5788
5789,5789,5789,5789,5789,5789,5789,5789,MONDO:0002334,hematopoietic and lymphoid system neoplasm,MONDO,disease,DISEASE_5789
5790,5790,5790,5790,5790,5790,5790,5790,MONDO:0004289,glottis verrucous carcinoma,MONDO,disease,DISEASE_5790
5791,5791,5791,5791,5791,5791,5791,5791,MONDO:0002694,cavernous sinus thrombosis,MONDO,disease,DISEASE_5791
5792,5792,5792,5792,5792,5792,5792,5792,MONDO:0010173,Mayer-Rokitansky-Kuster-Hauser syndrome type 1,MONDO,disease,DISEASE_5792
5793,5793,5793,5793,5793,5793,5793,5793,MONDO:0002730,childhood kidney neoplasm,MONDO,disease,DISEASE_5793
5794,5794,5794,5794,5794,5794,5794,5794,MONDO:0006513,estrogen-receptor negative breast cancer,MONDO,disease,DISEASE_5794
5795,5795,5795,5795,5795,5795,5795,5795,MONDO:0005875,Newcastle disease,MONDO,disease,DISEASE_5795
5796,5796,5796,5796,5796,5796,5796,5796,MONDO:0004910,mitral valve prolapse,MONDO,disease,DISEASE_5796
5797,5797,5797,5797,5797,5797,5797,5797,MONDO:0100187,opioid-induced constipation,MONDO,disease,DISEASE_5797
5798,5798,5798,5798,5798,5798,5798,5798,MONDO:1012751_MONDO:1012752,"chondrodysplasia, COL2A1-related, pig",MONDO_grouped,disease,DISEASE_5798
5799,5799,5799,5799,5799,5799,5799,5799,MONDO:0100221,IFAP syndrome 2,MONDO,disease,DISEASE_5799
5800,5800,5800,5800,5800,5800,5800,5800,MONDO:1012013,"arthritis deformans, pig",MONDO,disease,DISEASE_5800
5801,5801,5801,5801,5801,5801,5801,5801,MONDO:0019170_MONDO:0018593_MONDO:0018592_MONDO:0018594_MONDO:0018596,polyarteritis nodosa,MONDO_grouped,disease,DISEASE_5801
5802,5802,5802,5802,5802,5802,5802,5802,MONDO:0044781,nephrotic syndrome of childhood - steroid sensitive,MONDO,disease,DISEASE_5802
5803,5803,5803,5803,5803,5803,5803,5803,MONDO:0004093,esophageal basaloid carcinoma,MONDO,disease,DISEASE_5803
5804,5804,5804,5804,5804,5804,5804,5804,MONDO:0004557,congenital fibrosarcoma,MONDO,disease,DISEASE_5804
5805,5805,5805,5805,5805,5805,5805,5805,MONDO:1040038,TTLL5-related retinopathy,MONDO,disease,DISEASE_5805
5806,5806,5806,5806,5806,5806,5806,5806,MONDO:0001271,lens subluxation,MONDO,disease,DISEASE_5806
5807,5807,5807,5807,5807,5807,5807,5807,MONDO:0044098,ovarian ectopic pregnancy,MONDO,disease,DISEASE_5807
5808,5808,5808,5808,5808,5808,5808,5808,MONDO:0017492_MONDO:0017493,"fibular hemimelia, unilateral",MONDO_grouped,disease,DISEASE_5808
5809,5809,5809,5809,5809,5809,5809,5809,MONDO:0019613_MONDO:0017822_MONDO:0003603,non-functioning pituitary adenoma,MONDO_grouped,disease,DISEASE_5809
5810,5810,5810,5810,5810,5810,5810,5810,MONDO:0011956_MONDO:0030004_MONDO:0011824_MONDO:0011627_MONDO:0012801_MONDO:0013265_MONDO:0013258_MONDO:0012261_MONDO:0012533_MONDO:0012566_MONDO:0012567_MONDO:0012578_MONDO:0012600_MONDO:0012601_MONDO:0014041_MONDO:0800275_MONDO:0800287_MONDO:0800416_MONDO:0800417,"autism, susceptibility to",MONDO_grouped,disease,DISEASE_5810
5811,5811,5811,5811,5811,5811,5811,5811,MONDO:0001967,gonadal dysgenesis,MONDO,disease,DISEASE_5811
5812,5812,5812,5812,5812,5812,5812,5812,MONDO:0035410_MONDO:0035411,isolated congenital aglossia,MONDO_grouped,disease,DISEASE_5812
5813,5813,5813,5813,5813,5813,5813,5813,MONDO:0007400,Jackson-Weiss syndrome,MONDO,disease,DISEASE_5813
5814,5814,5814,5814,5814,5814,5814,5814,MONDO:0700174,horse transitional cell carcinoma,MONDO,disease,DISEASE_5814
5815,5815,5815,5815,5815,5815,5815,5815,MONDO:0018022,hemoglobin Lepore-beta-thalassemia syndrome,MONDO,disease,DISEASE_5815
5816,5816,5816,5816,5816,5816,5816,5816,MONDO:0020439,patent foramen ovale,MONDO,disease,DISEASE_5816
5817,5817,5817,5817,5817,5817,5817,5817,MONDO:0021578,sternal neoplasm,MONDO,disease,DISEASE_5817
5818,5818,5818,5818,5818,5818,5818,5818,MONDO:0011775_MONDO:0014902_MONDO:0008067,"nasopharyngeal carcinoma, susceptibility to",MONDO_grouped,disease,DISEASE_5818
5819,5819,5819,5819,5819,5819,5819,5819,MONDO:0016226,specific language disorder,MONDO,disease,DISEASE_5819
5820,5820,5820,5820,5820,5820,5820,5820,MONDO:0006357,parotid gland carcinoma ex pleomorphic adenoma,MONDO,disease,DISEASE_5820
5821,5821,5821,5821,5821,5821,5821,5821,MONDO:0001205,hypersecretion glaucoma,MONDO,disease,DISEASE_5821
5822,5822,5822,5822,5822,5822,5822,5822,MONDO:0003095,laryngeal mucoepidermoid carcinoma,MONDO,disease,DISEASE_5822
5823,5823,5823,5823,5823,5823,5823,5823,MONDO:0012503,thiopurine S-methyltransferase deficiency,MONDO,disease,DISEASE_5823
5824,5824,5824,5824,5824,5824,5824,5824,MONDO:0021932,infection by Trypanosoma gambiense,MONDO,disease,DISEASE_5824
5825,5825,5825,5825,5825,5825,5825,5825,MONDO:1012417,"persistent right aortic arch with subclavian artery and ligamentum arteriosum, dog",MONDO,disease,DISEASE_5825
5826,5826,5826,5826,5826,5826,5826,5826,MONDO:1011559,"methemoglobinemia, domestic cat",MONDO,disease,DISEASE_5826
5827,5827,5827,5827,5827,5827,5827,5827,MONDO:0003636,vulvar sebaceous carcinoma,MONDO,disease,DISEASE_5827
5828,5828,5828,5828,5828,5828,5828,5828,MONDO:0021437,lipoma of stomach,MONDO,disease,DISEASE_5828
5829,5829,5829,5829,5829,5829,5829,5829,MONDO:0015448,mitochondrial complex III deficiency,MONDO,disease,DISEASE_5829
5830,5830,5830,5830,5830,5830,5830,5830,MONDO:0016097,symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers,MONDO,disease,DISEASE_5830
5831,5831,5831,5831,5831,5831,5831,5831,MONDO:0000310,Alkhurma hemorrhagic fever,MONDO,disease,DISEASE_5831
5832,5832,5832,5832,5832,5832,5832,5832,MONDO:1012357,"hypochondroplastic dwarfism, dog",MONDO,disease,DISEASE_5832
5833,5833,5833,5833,5833,5833,5833,5833,MONDO:0007129_MONDO:0859339_MONDO:0014901_MONDO:0011477_MONDO:0014999_MONDO:0007881_MONDO:0014749_MONDO:0011265_MONDO:0012583,"tooth agenesis, selective",MONDO_grouped,disease,DISEASE_5833
5834,5834,5834,5834,5834,5834,5834,5834,MONDO:1012497,"Lundehund syndrome, dog",MONDO,disease,DISEASE_5834
5835,5835,5835,5835,5835,5835,5835,5835,MONDO:0001944,mixed malaria,MONDO,disease,DISEASE_5835
5836,5836,5836,5836,5836,5836,5836,5836,MONDO:1010638,"factor XI deficiency, cattle",MONDO,disease,DISEASE_5836
5837,5837,5837,5837,5837,5837,5837,5837,MONDO:1012277_MONDO:1012278_MONDO:1012281_MONDO:1012282,"tremor, ducks",MONDO_grouped,disease,DISEASE_5837
5838,5838,5838,5838,5838,5838,5838,5838,MONDO:0012579,autoimmune pulmonary alveolar proteinosis,MONDO,disease,DISEASE_5838
5839,5839,5839,5839,5839,5839,5839,5839,MONDO:0001709,hypercalcemic sarcoidosis,MONDO,disease,DISEASE_5839
5840,5840,5840,5840,5840,5840,5840,5840,MONDO:0010858,macrocephaly-spastic paraplegia-dysmorphism syndrome,MONDO,disease,DISEASE_5840
5841,5841,5841,5841,5841,5841,5841,5841,MONDO:0006969,sialadenitis,MONDO,disease,DISEASE_5841
5842,5842,5842,5842,5842,5842,5842,5842,MONDO:1011774,"digital dermatitis, non-human animal",MONDO,disease,DISEASE_5842
5843,5843,5843,5843,5843,5843,5843,5843,MONDO:0009302,XY type gonadal dysgenesis-associated anomalies syndrome,MONDO,disease,DISEASE_5843
5844,5844,5844,5844,5844,5844,5844,5844,MONDO:0023200,Fryns Fabry Remans syndrome,MONDO,disease,DISEASE_5844
5845,5845,5845,5845,5845,5845,5845,5845,MONDO:0005127,lepromatous leprosy,MONDO,disease,DISEASE_5845
5846,5846,5846,5846,5846,5846,5846,5846,MONDO:0700019,chromosome 12 disorder,MONDO,disease,DISEASE_5846
5847,5847,5847,5847,5847,5847,5847,5847,MONDO:1010223,"prostate cancer, non-human animal",MONDO,disease,DISEASE_5847
5848,5848,5848,5848,5848,5848,5848,5848,MONDO:0010879,CODAS syndrome,MONDO,disease,DISEASE_5848
5849,5849,5849,5849,5849,5849,5849,5849,MONDO:0010961,obesity due to prohormone convertase I deficiency,MONDO,disease,DISEASE_5849
5850,5850,5850,5850,5850,5850,5850,5850,MONDO:0015571,deletion 5q35,MONDO,disease,DISEASE_5850
5851,5851,5851,5851,5851,5851,5851,5851,MONDO:0019125,relapsing polychondritis,MONDO,disease,DISEASE_5851
5852,5852,5852,5852,5852,5852,5852,5852,MONDO:0018360,neonatal lupus erythematosus,MONDO,disease,DISEASE_5852
5853,5853,5853,5853,5853,5853,5853,5853,MONDO:0004030,ureter transitional cell carcinoma,MONDO,disease,DISEASE_5853
5854,5854,5854,5854,5854,5854,5854,5854,MONDO:0004482,fibroosseous pseudotumor of the digits,MONDO,disease,DISEASE_5854
5855,5855,5855,5855,5855,5855,5855,5855,MONDO:0957432,neonatal compartment syndrome,MONDO,disease,DISEASE_5855
5856,5856,5856,5856,5856,5856,5856,5856,MONDO:0013226,combined immunodeficiency with faciooculoskeletal anomalies,MONDO,disease,DISEASE_5856
5857,5857,5857,5857,5857,5857,5857,5857,MONDO:0004502,parapharyngeal meningioma,MONDO,disease,DISEASE_5857
5858,5858,5858,5858,5858,5858,5858,5858,MONDO:0007976,mesomelic dwarfism of hypoplastic tibia and radius type,MONDO,disease,DISEASE_5858
5859,5859,5859,5859,5859,5859,5859,5859,MONDO:0001971,farmer's lung disease,MONDO,disease,DISEASE_5859
5860,5860,5860,5860,5860,5860,5860,5860,MONDO:0016263,primitive neuroectodermal tumor of the corpus uteri,MONDO,disease,DISEASE_5860
5861,5861,5861,5861,5861,5861,5861,5861,MONDO:0008418,"scleroderma, familial progressive",MONDO,disease,DISEASE_5861
5862,5862,5862,5862,5862,5862,5862,5862,MONDO:0037256,serous neoplasm,MONDO,disease,DISEASE_5862
5863,5863,5863,5863,5863,5863,5863,5863,MONDO:0018510,small intestine neuroendocrine neoplasm,MONDO,disease,DISEASE_5863
5864,5864,5864,5864,5864,5864,5864,5864,MONDO:1011350,"premature aging syndrome, non-human animal",MONDO,disease,DISEASE_5864
5865,5865,5865,5865,5865,5865,5865,5865,MONDO:0006095,atypical carcinoid tumor,MONDO,disease,DISEASE_5865
5866,5866,5866,5866,5866,5866,5866,5866,MONDO:0004829,Krukenberg carcinoma,MONDO,disease,DISEASE_5866
5867,5867,5867,5867,5867,5867,5867,5867,MONDO:0009102,diaminopentanuria,MONDO,disease,DISEASE_5867
5868,5868,5868,5868,5868,5868,5868,5868,MONDO:0010719,radiation sensitivity of natural killer activity,MONDO,disease,DISEASE_5868
5869,5869,5869,5869,5869,5869,5869,5869,MONDO:0003669,testicular seminoma,MONDO,disease,DISEASE_5869
5870,5870,5870,5870,5870,5870,5870,5870,MONDO:0041903,gonococcal infection of joint,MONDO,disease,DISEASE_5870
5871,5871,5871,5871,5871,5871,5871,5871,MONDO:0018357,neonatal antiphospholipid syndrome,MONDO,disease,DISEASE_5871
5872,5872,5872,5872,5872,5872,5872,5872,MONDO:0009900,polysyndactyly-cardiac malformation syndrome,MONDO,disease,DISEASE_5872
5873,5873,5873,5873,5873,5873,5873,5873,MONDO:0006933,pulmonary plasma cell granuloma,MONDO,disease,DISEASE_5873
5874,5874,5874,5874,5874,5874,5874,5874,MONDO:0004546,lumbar plexus neoplasm,MONDO,disease,DISEASE_5874
5875,5875,5875,5875,5875,5875,5875,5875,MONDO:0045014,tetrahydrobiopterin metabolic process disease,MONDO,disease,DISEASE_5875
5876,5876,5876,5876,5876,5876,5876,5876,MONDO:0001091,lipoma of colon,MONDO,disease,DISEASE_5876
5877,5877,5877,5877,5877,5877,5877,5877,MONDO:0004286,pancreatic intraductal papillary-mucinous neoplasm,MONDO,disease,DISEASE_5877
5878,5878,5878,5878,5878,5878,5878,5878,MONDO:0015380_MONDO:0040700,facial dermoid cyst,MONDO_grouped,disease,DISEASE_5878
5879,5879,5879,5879,5879,5879,5879,5879,MONDO:0002202,outlet dysfunction constipation,MONDO,disease,DISEASE_5879
5880,5880,5880,5880,5880,5880,5880,5880,MONDO:0013127_MONDO:0013717_MONDO:0013441_MONDO:0008831_MONDO:0012644,asphyxiating thoracic dystrophy,MONDO_grouped,disease,DISEASE_5880
5881,5881,5881,5881,5881,5881,5881,5881,MONDO:0023230,Ghose-Sachdev-Kumar syndrome,MONDO,disease,DISEASE_5881
5882,5882,5882,5882,5882,5882,5882,5882,MONDO:0004057,micropapillary variant infiltrating bladder urothelial carcinoma,MONDO,disease,DISEASE_5882
5883,5883,5883,5883,5883,5883,5883,5883,MONDO:0024294_MONDO:0024295,skin disorder caused by infection,MONDO_grouped,disease,DISEASE_5883
5884,5884,5884,5884,5884,5884,5884,5884,MONDO:0001000,mixed mineral dust pneumoconiosis,MONDO,disease,DISEASE_5884
5885,5885,5885,5885,5885,5885,5885,5885,MONDO:0010604_MONDO:0010602_MONDO:0015719_MONDO:0018660_MONDO:0015715_MONDO:1011519_MONDO:1011521_MONDO:1011523_MONDO:1011524_MONDO:1011525,hemophilia,MONDO_grouped,disease,DISEASE_5885
5886,5886,5886,5886,5886,5886,5886,5886,MONDO:0010100,Tay-Sachs disease,MONDO,disease,DISEASE_5886
5887,5887,5887,5887,5887,5887,5887,5887,MONDO:0024321,disorder of GPI anchor biosynthesis,MONDO,disease,DISEASE_5887
5888,5888,5888,5888,5888,5888,5888,5888,MONDO:0020247,congenital vitreoretinal dysplasia,MONDO,disease,DISEASE_5888
5889,5889,5889,5889,5889,5889,5889,5889,MONDO:0012908,complement component 6 deficiency,MONDO,disease,DISEASE_5889
5890,5890,5890,5890,5890,5890,5890,5890,MONDO:0017601,diffuse large B-cell lymphoma with chronic inflammation,MONDO,disease,DISEASE_5890
5891,5891,5891,5891,5891,5891,5891,5891,MONDO:0019200_MONDO:0013469_MONDO:0010259_MONDO:0008377_MONDO:0013395_MONDO:0013052_MONDO:0011137_MONDO:0010320_MONDO:0012477_MONDO:0012943_MONDO:0013468_MONDO:0054708_MONDO:0012625_MONDO:0011272_MONDO:0012813_MONDO:0014345_MONDO:0014093_MONDO:0008379_MONDO:0012523_MONDO:0859308_MONDO:0008378_MONDO:0014871_MONDO:0044314_MONDO:0013429_MONDO:0036482_MONDO:0032834_MONDO:0030071_MONDO:0013175_MONDO:0012363_MONDO:0013402_MONDO:0014323_MONDO:0014692_MONDO:0013314_MONDO:0032577_MONDO:0032940_MONDO:0013414_MONDO:0014929_MONDO:0010945_MONDO:0859367_MONDO:0010818_MONDO:0013437_MONDO:0013315_MONDO:0010806_MONDO:0013425_MONDO:0013405_MONDO:0010828_MONDO:0013516_MONDO:0013413_MONDO:0011935_MONDO:0013436_MONDO:0044320_MONDO:0015013_MONDO:0013610_MONDO:0014400_MONDO:0012796_MONDO:0013407_MONDO:0010761_MONDO:0957314_MONDO:0032604_MONDO:0013611_MONDO:0012463_MONDO:0012367_MONDO:0032689_MONDO:0013447_MONDO:0010827_MONDO:0013263_MONDO:0014687_MONDO:0011075_MONDO:0012024_MONDO:0014618_MONDO:0013312_MONDO:0030797_MONDO:0013328_MONDO:0000910_MONDO:0010227_MONDO:0011974_MONDO:0011630_MONDO:0014653_MONDO:0013274_MONDO:0014256_MONDO:0010723_MONDO:0030619_MONDO:0033563_MONDO:0013780_MONDO:1011259_MONDO:0010374_MONDO:0011259_MONDO:0800348_MONDO:0800352_MONDO:0800359_MONDO:0975840_MONDO:1011258,retinitis pigmentosa,MONDO_grouped,disease,DISEASE_5891
5892,5892,5892,5892,5892,5892,5892,5892,MONDO:0017833,primary hypereosinophilic syndrome,MONDO,disease,DISEASE_5892
5893,5893,5893,5893,5893,5893,5893,5893,MONDO:0000973,external ear lipoma,MONDO,disease,DISEASE_5893
5894,5894,5894,5894,5894,5894,5894,5894,MONDO:0056805,benign peripheral nerve granular cell tumor,MONDO,disease,DISEASE_5894
5895,5895,5895,5895,5895,5895,5895,5895,MONDO:0006898,periarthritis,MONDO,disease,DISEASE_5895
5896,5896,5896,5896,5896,5896,5896,5896,MONDO:0001564,binocular vision disease,MONDO,disease,DISEASE_5896
5897,5897,5897,5897,5897,5897,5897,5897,MONDO:0700099,"adenocarcinoma, non-human animal",MONDO,disease,DISEASE_5897
5898,5898,5898,5898,5898,5898,5898,5898,MONDO:0020959,Mansonella ozzardi infection,MONDO,disease,DISEASE_5898
5899,5899,5899,5899,5899,5899,5899,5899,MONDO:0009346,histidinuria due to a renal tubular defect,MONDO,disease,DISEASE_5899
5900,5900,5900,5900,5900,5900,5900,5900,MONDO:0004972_MONDO:0003422,adenoma,MONDO_grouped,disease,DISEASE_5900
5901,5901,5901,5901,5901,5901,5901,5901,MONDO:0008684,Wolf-Hirschhorn syndrome,MONDO,disease,DISEASE_5901
5902,5902,5902,5902,5902,5902,5902,5902,MONDO:0009487,keratoconus and congenital hip dysplasia,MONDO,disease,DISEASE_5902
5903,5903,5903,5903,5903,5903,5903,5903,MONDO:0014081,severe combined immunodeficiency due to CARD11 deficiency,MONDO,disease,DISEASE_5903
5904,5904,5904,5904,5904,5904,5904,5904,MONDO:1010547,"diprosopus, domestic cat",MONDO,disease,DISEASE_5904
5905,5905,5905,5905,5905,5905,5905,5905,MONDO:0018259,didymosis aplasticosebacea,MONDO,disease,DISEASE_5905
5906,5906,5906,5906,5906,5906,5906,5906,MONDO:0018667,pleural empyema,MONDO,disease,DISEASE_5906
5907,5907,5907,5907,5907,5907,5907,5907,MONDO:0005009,congestive heart failure,MONDO,disease,DISEASE_5907
5908,5908,5908,5908,5908,5908,5908,5908,MONDO:0014251,"melioidosis, susceptibility to",MONDO,disease,DISEASE_5908
5909,5909,5909,5909,5909,5909,5909,5909,MONDO:0013214_MONDO:0859180,"bile acid malabsorption, primary",MONDO_grouped,disease,DISEASE_5909
5910,5910,5910,5910,5910,5910,5910,5910,MONDO:0100470,reactive airway disease,MONDO,disease,DISEASE_5910
5911,5911,5911,5911,5911,5911,5911,5911,MONDO:0016898,partial monosomy of the short arm of chromosome 20,MONDO,disease,DISEASE_5911
5912,5912,5912,5912,5912,5912,5912,5912,MONDO:0010746,"thumbs, congenital Clasped",MONDO,disease,DISEASE_5912
5913,5913,5913,5913,5913,5913,5913,5913,MONDO:0008393,Rubinstein-Taybi syndrome due to CREBBP mutations,MONDO,disease,DISEASE_5913
5914,5914,5914,5914,5914,5914,5914,5914,MONDO:0000950,asthenopia,MONDO,disease,DISEASE_5914
5915,5915,5915,5915,5915,5915,5915,5915,MONDO:0957811,"Alport syndrome 3b, autosomal recessive",MONDO,disease,DISEASE_5915
5916,5916,5916,5916,5916,5916,5916,5916,MONDO:1011477_MONDO:1011478,"autoimmune hemolytic anemia, dog",MONDO_grouped,disease,DISEASE_5916
5917,5917,5917,5917,5917,5917,5917,5917,MONDO:0011916_MONDO:0011569_MONDO:0010877_MONDO:0010699_MONDO:0013959_MONDO:0007308_MONDO:0007309_MONDO:0014736_MONDO:0014836_MONDO:0012096_MONDO:0011085_MONDO:0010551_MONDO:0011633_MONDO:0014012_MONDO:0007307_MONDO:0013212_MONDO:0010550_MONDO:0013338_MONDO:0010949_MONDO:0011894_MONDO:0011534_MONDO:0030433_MONDO:0011527_MONDO:0014467_MONDO:0011890_MONDO:0013644_MONDO:0011475_MONDO:0011066_MONDO:0014208_MONDO:0011901_MONDO:0007311_MONDO:0011902_MONDO:0011113_MONDO:0032728_MONDO:0011903_MONDO:0010689_MONDO:0014117_MONDO:0012250_MONDO:0054833_MONDO:0008961_MONDO:0011687_MONDO:0012640_MONDO:0013753_MONDO:0012014_MONDO:0012231_MONDO:0011889_MONDO:0014511_MONDO:0011570_MONDO:0014726_MONDO:0011091_MONDO:0014154_MONDO:0007790_MONDO:0014733_MONDO:0011675_MONDO:0030458_MONDO:0014566_MONDO:0010995_MONDO:0014866_MONDO:0014735_MONDO:0014665_MONDO:0019011_MONDO:0018993_MONDO:0015626_MONDO:0018995_MONDO:0018994_MONDO:0016454_MONDO:0007310_MONDO:0007312_MONDO:0044640,Charcot-Marie-Tooth disease axonal,MONDO_grouped,disease,DISEASE_5917
5918,5918,5918,5918,5918,5918,5918,5918,MONDO:0021541_MONDO:0003194_MONDO:0003154_MONDO:0021542,hemangioma of retina,MONDO_grouped,disease,DISEASE_5918
5919,5919,5919,5919,5919,5919,5919,5919,MONDO:0005371_MONDO:0004049,mood disorder,MONDO_grouped,disease,DISEASE_5919
5920,5920,5920,5920,5920,5920,5920,5920,MONDO:0008404,scalp-ear-nipple syndrome,MONDO,disease,DISEASE_5920
5921,5921,5921,5921,5921,5921,5921,5921,MONDO:0000634,thoracic benign neoplasm,MONDO,disease,DISEASE_5921
5922,5922,5922,5922,5922,5922,5922,5922,MONDO:0004101,multicentric papillary thyroid carcinoma,MONDO,disease,DISEASE_5922
5923,5923,5923,5923,5923,5923,5923,5923,MONDO:1010314,"Van den Ende-Gupta syndrome, non-human animal",MONDO,disease,DISEASE_5923
5924,5924,5924,5924,5924,5924,5924,5924,MONDO:0002864,anus rhabdomyosarcoma,MONDO,disease,DISEASE_5924
5925,5925,5925,5925,5925,5925,5925,5925,MONDO:0013740,lethal occipital encephalocele-skeletal dysplasia syndrome,MONDO,disease,DISEASE_5925
5926,5926,5926,5926,5926,5926,5926,5926,MONDO:0018183,staphylococcal necrotizing pneumonia,MONDO,disease,DISEASE_5926
5927,5927,5927,5927,5927,5927,5927,5927,MONDO:1010648,"hypereosinophilic syndrome, domestic cat",MONDO,disease,DISEASE_5927
5928,5928,5928,5928,5928,5928,5928,5928,MONDO:1012418,"anal furunculosis, dog",MONDO,disease,DISEASE_5928
5929,5929,5929,5929,5929,5929,5929,5929,MONDO:1010116,sudden unexpected infant death,MONDO,disease,DISEASE_5929
5930,5930,5930,5930,5930,5930,5930,5930,MONDO:0001622,mechanical lagophthalmos,MONDO,disease,DISEASE_5930
5931,5931,5931,5931,5931,5931,5931,5931,MONDO:0001875,epicondylitis,MONDO,disease,DISEASE_5931
5932,5932,5932,5932,5932,5932,5932,5932,MONDO:1010601_MONDO:1010602_MONDO:1010603_MONDO:1010605_MONDO:1010606_MONDO:1010604,"congenital hypothyroidism, chicken",MONDO_grouped,disease,DISEASE_5932
5933,5933,5933,5933,5933,5933,5933,5933,MONDO:0859210,chromosome 16q12 duplication syndrome,MONDO,disease,DISEASE_5933
5934,5934,5934,5934,5934,5934,5934,5934,MONDO:1010967,"Dandy-Walker syndrome, sheep",MONDO,disease,DISEASE_5934
5935,5935,5935,5935,5935,5935,5935,5935,MONDO:0043683,Leriche syndrome,MONDO,disease,DISEASE_5935
5936,5936,5936,5936,5936,5936,5936,5936,MONDO:0012217_MONDO:0009806_MONDO:0017195,Bruck syndrome,MONDO_grouped,disease,DISEASE_5936
5937,5937,5937,5937,5937,5937,5937,5937,MONDO:0014896,congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome,MONDO,disease,DISEASE_5937
5938,5938,5938,5938,5938,5938,5938,5938,MONDO:0002991,adenocarcinofibroma,MONDO,disease,DISEASE_5938
5939,5939,5939,5939,5939,5939,5939,5939,MONDO:0005817,Kluver-Bucy syndrome,MONDO,disease,DISEASE_5939
5940,5940,5940,5940,5940,5940,5940,5940,MONDO:1011805,"exercise induced metabolic myopathy, non-human animal",MONDO,disease,DISEASE_5940
5941,5941,5941,5941,5941,5941,5941,5941,MONDO:0003582,hereditary breast ovarian cancer syndrome,MONDO,disease,DISEASE_5941
5942,5942,5942,5942,5942,5942,5942,5942,MONDO:0032772_MONDO:0032651,"brain abnormalities, neurodegeneration, and dysosteosclerosis",MONDO_grouped,disease,DISEASE_5942
5943,5943,5943,5943,5943,5943,5943,5943,MONDO:1010979_MONDO:1010980_MONDO:1010981,"hydranencephaly, dog",MONDO_grouped,disease,DISEASE_5943
5944,5944,5944,5944,5944,5944,5944,5944,MONDO:1012605,"glycogen storage disease IV, dog",MONDO,disease,DISEASE_5944
5945,5945,5945,5945,5945,5945,5945,5945,MONDO:0015579,Hb Bart's hydrops fetalis,MONDO,disease,DISEASE_5945
5946,5946,5946,5946,5946,5946,5946,5946,MONDO:0005391,restless legs syndrome,MONDO,disease,DISEASE_5946
5947,5947,5947,5947,5947,5947,5947,5947,MONDO:0007443,congenital unilateral hypoplasia of depressor anguli oris,MONDO,disease,DISEASE_5947
5948,5948,5948,5948,5948,5948,5948,5948,MONDO:0015688,"myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2",MONDO,disease,DISEASE_5948
5949,5949,5949,5949,5949,5949,5949,5949,MONDO:0009365_MONDO:0013585_MONDO:0006037,hydrolethalus syndrome,MONDO_grouped,disease,DISEASE_5949
5950,5950,5950,5950,5950,5950,5950,5950,MONDO:0007836,IVIC syndrome,MONDO,disease,DISEASE_5950
5951,5951,5951,5951,5951,5951,5951,5951,MONDO:0002756,solitary plasmacytoma of chest wall,MONDO,disease,DISEASE_5951
5952,5952,5952,5952,5952,5952,5952,5952,MONDO:0971035,thyroid gland mixed medullary and follicular cell-derived carcinoma,MONDO,disease,DISEASE_5952
5953,5953,5953,5953,5953,5953,5953,5953,MONDO:1011995,"gyrate atrophy of choroid and retina, non-human animal",MONDO,disease,DISEASE_5953
5954,5954,5954,5954,5954,5954,5954,5954,MONDO:0800290,Li-fraumeni-like syndrome,MONDO,disease,DISEASE_5954
5955,5955,5955,5955,5955,5955,5955,5955,MONDO:0019169,pyruvate dehydrogenase deficiency,MONDO,disease,DISEASE_5955
5956,5956,5956,5956,5956,5956,5956,5956,MONDO:0016688,fibrillary astrocytoma,MONDO,disease,DISEASE_5956
5957,5957,5957,5957,5957,5957,5957,5957,MONDO:0004549,cork-handlers' disease,MONDO,disease,DISEASE_5957
5958,5958,5958,5958,5958,5958,5958,5958,MONDO:0005471,neurally mediated hypotension,MONDO,disease,DISEASE_5958
5959,5959,5959,5959,5959,5959,5959,5959,MONDO:0006268,liver diffuse large B-cell lymphoma,MONDO,disease,DISEASE_5959
5960,5960,5960,5960,5960,5960,5960,5960,MONDO:0042977_MONDO:0011114_MONDO:0012800,"trichoepithelioma, multiple familial",MONDO_grouped,disease,DISEASE_5960
5961,5961,5961,5961,5961,5961,5961,5961,MONDO:0008696,acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome,MONDO,disease,DISEASE_5961
5962,5962,5962,5962,5962,5962,5962,5962,MONDO:0001765,polyneuropathy in collagen vascular disease,MONDO,disease,DISEASE_5962
5963,5963,5963,5963,5963,5963,5963,5963,MONDO:0008545,"thalassemia, beta+, silent allele",MONDO,disease,DISEASE_5963
5964,5964,5964,5964,5964,5964,5964,5964,MONDO:0859749,grade III lymphomatoid granulomatosis,MONDO,disease,DISEASE_5964
5965,5965,5965,5965,5965,5965,5965,5965,MONDO:0019722,glomerular disorder,MONDO,disease,DISEASE_5965
5966,5966,5966,5966,5966,5966,5966,5966,MONDO:1011317,"endocrine system disorder, non-human animal",MONDO,disease,DISEASE_5966
5967,5967,5967,5967,5967,5967,5967,5967,MONDO:0700170,equine neoplasm,MONDO,disease,DISEASE_5967
5968,5968,5968,5968,5968,5968,5968,5968,MONDO:0005847,middle lobe syndrome,MONDO,disease,DISEASE_5968
5969,5969,5969,5969,5969,5969,5969,5969,MONDO:0013316,occult macular dystrophy,MONDO,disease,DISEASE_5969
5970,5970,5970,5970,5970,5970,5970,5970,MONDO:0011739_MONDO:0013235_MONDO:0013236_MONDO:0032867_MONDO:0013685,"pancreatic cancer, susceptibility to",MONDO_grouped,disease,DISEASE_5970
5971,5971,5971,5971,5971,5971,5971,5971,MONDO:0037253,ovarian thecoma,MONDO,disease,DISEASE_5971
5972,5972,5972,5972,5972,5972,5972,5972,MONDO:0008973,"chondrodysplasia punctata, Toriello type",MONDO,disease,DISEASE_5972
5973,5973,5973,5973,5973,5973,5973,5973,MONDO:0002246,perichondritis of auricle,MONDO,disease,DISEASE_5973
5974,5974,5974,5974,5974,5974,5974,5974,MONDO:1010977_MONDO:1010978,"Huntington disease, pig",MONDO_grouped,disease,DISEASE_5974
5975,5975,5975,5975,5975,5975,5975,5975,MONDO:0021009,salivary gland mucoepidermoid carcinoma,MONDO,disease,DISEASE_5975
5976,5976,5976,5976,5976,5976,5976,5976,MONDO:0024645,retroperitoneal neoplasm,MONDO,disease,DISEASE_5976
5977,5977,5977,5977,5977,5977,5977,5977,MONDO:0045059,cribriform carcinoma of breast,MONDO,disease,DISEASE_5977
5978,5978,5978,5978,5978,5978,5978,5978,MONDO:0019634,familial nasal acilia,MONDO,disease,DISEASE_5978
5979,5979,5979,5979,5979,5979,5979,5979,MONDO:0043985,central nervous system lupus,MONDO,disease,DISEASE_5979
5980,5980,5980,5980,5980,5980,5980,5980,MONDO:0036045,euthyroid dysprealbuminemic hyperthyroxinemia,MONDO,disease,DISEASE_5980
5981,5981,5981,5981,5981,5981,5981,5981,MONDO:1012017,"atopy, dog",MONDO,disease,DISEASE_5981
5982,5982,5982,5982,5982,5982,5982,5982,MONDO:0009159,"Ehlers-Danlos syndrome, cardiac valvular type",MONDO,disease,DISEASE_5982
5983,5983,5983,5983,5983,5983,5983,5983,MONDO:0002173_MONDO:0004466,neuroma,MONDO_grouped,disease,DISEASE_5983
5984,5984,5984,5984,5984,5984,5984,5984,MONDO:0006065,lactose intolerance adult type,MONDO,disease,DISEASE_5984
5985,5985,5985,5985,5985,5985,5985,5985,MONDO:0009958,adult Refsum disease,MONDO,disease,DISEASE_5985
5986,5986,5986,5986,5986,5986,5986,5986,MONDO:0010523,X-linked reticulate pigmentary disorder,MONDO,disease,DISEASE_5986
5987,5987,5987,5987,5987,5987,5987,5987,MONDO:0013024,chronic thromboembolic pulmonary hypertension,MONDO,disease,DISEASE_5987
5988,5988,5988,5988,5988,5988,5988,5988,MONDO:0004764,fibular collateral ligament bursitis,MONDO,disease,DISEASE_5988
5989,5989,5989,5989,5989,5989,5989,5989,MONDO:0008284,polyposis of gastric fundus without polyposis coli,MONDO,disease,DISEASE_5989
5990,5990,5990,5990,5990,5990,5990,5990,MONDO:0800129,"autoinflammatory disease, X-linked",MONDO,disease,DISEASE_5990
5991,5991,5991,5991,5991,5991,5991,5991,MONDO:0957832,craniometadiaphyseal osteosclerosis with hip dysplasia,MONDO,disease,DISEASE_5991
5992,5992,5992,5992,5992,5992,5992,5992,MONDO:0000995_MONDO:0023121,familial periodic paralysis,MONDO_grouped,disease,DISEASE_5992
5993,5993,5993,5993,5993,5993,5993,5993,MONDO:0042601,Samson-Gardner syndrome,MONDO,disease,DISEASE_5993
5994,5994,5994,5994,5994,5994,5994,5994,MONDO:0030840_MONDO:0010159_MONDO:0030841_MONDO:0030843_MONDO:0031219,mismatch repair cancer syndrome,MONDO_grouped,disease,DISEASE_5994
5995,5995,5995,5995,5995,5995,5995,5995,MONDO:0013730,graft versus host disease,MONDO,disease,DISEASE_5995
5996,5996,5996,5996,5996,5996,5996,5996,MONDO:0021726,abdominal cystic lymphangioma,MONDO,disease,DISEASE_5996
5997,5997,5997,5997,5997,5997,5997,5997,MONDO:0005745,Enoplea infectious disease,MONDO,disease,DISEASE_5997
5998,5998,5998,5998,5998,5998,5998,5998,MONDO:1010063_MONDO:1011739_MONDO:1012977,"congenital adrenal hypoplasia, non-human animal",MONDO_grouped,disease,DISEASE_5998
5999,5999,5999,5999,5999,5999,5999,5999,MONDO:0016742,mixed germ cell tumor of central nervous system,MONDO,disease,DISEASE_5999
6000,6000,6000,6000,6000,6000,6000,6000,MONDO:0001594,Achilles bursitis,MONDO,disease,DISEASE_6000
6001,6001,6001,6001,6001,6001,6001,6001,MONDO:0015661,dextrocardia,MONDO,disease,DISEASE_6001
6002,6002,6002,6002,6002,6002,6002,6002,MONDO:0015772,trisomy 8q,MONDO,disease,DISEASE_6002
6003,6003,6003,6003,6003,6003,6003,6003,MONDO:0024653,skull neoplasm,MONDO,disease,DISEASE_6003
6004,6004,6004,6004,6004,6004,6004,6004,MONDO:0030929_MONDO:0030928,"microcephaly 27, primary, autosomal dominant",MONDO_grouped,disease,DISEASE_6004
6005,6005,6005,6005,6005,6005,6005,6005,MONDO:0032631_MONDO:0032632_MONDO:0032611_MONDO:0032612_MONDO:0032622_MONDO:0032621_MONDO:0032910_MONDO:0032606_MONDO:0032619_MONDO:0032620_MONDO:0026720_MONDO:0032618_MONDO:0032617_MONDO:0026721_MONDO:0032613_MONDO:0032608_MONDO:0032609_MONDO:0032616_MONDO:0030997_MONDO:0032615_MONDO:0032610_MONDO:0032624_MONDO:0033560_MONDO:0032623_MONDO:0032625_MONDO:0032626_MONDO:0032636_MONDO:0032630_MONDO:0030902_MONDO:0032629_MONDO:0032635_MONDO:0032627_MONDO:0032633_MONDO:0032634_MONDO:0032628,"mitochondrial complex 1 deficiency, nuclear",MONDO_grouped,disease,DISEASE_6005
6006,6006,6006,6006,6006,6006,6006,6006,MONDO:0042493,gastric non-hodgkin lymphoma,MONDO,disease,DISEASE_6006
6007,6007,6007,6007,6007,6007,6007,6007,MONDO:8000006_MONDO:0030374_MONDO:0023880,WHIM syndrome,MONDO_grouped,disease,DISEASE_6007
6008,6008,6008,6008,6008,6008,6008,6008,MONDO:0013059_MONDO:0030361_MONDO:0030362_MONDO:0012471_MONDO:0009165_MONDO:0012472_MONDO:0014367_MONDO:0014007_MONDO:0012429_MONDO:0018866,Aicardi-Goutieres syndrome,MONDO_grouped,disease,DISEASE_6008
6009,6009,6009,6009,6009,6009,6009,6009,MONDO:0011745,"duodenojejunal atresia with volvulus, absent dorsal mesentery, and absent superior mesenteric artery",MONDO,disease,DISEASE_6009
6010,6010,6010,6010,6010,6010,6010,6010,MONDO:0957495,"hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature",MONDO,disease,DISEASE_6010
6011,6011,6011,6011,6011,6011,6011,6011,MONDO:0021697,chlamydia infectious disease,MONDO,disease,DISEASE_6011
6012,6012,6012,6012,6012,6012,6012,6012,MONDO:0100541,GATA5-related congenital heart defects,MONDO,disease,DISEASE_6012
6013,6013,6013,6013,6013,6013,6013,6013,MONDO:0003796_MONDO:0003997,rectum Kaposi sarcoma,MONDO_grouped,disease,DISEASE_6013
6014,6014,6014,6014,6014,6014,6014,6014,MONDO:0002119,ossifying fibroma,MONDO,disease,DISEASE_6014
6015,6015,6015,6015,6015,6015,6015,6015,MONDO:1011238_MONDO:1011237_MONDO:1011239_MONDO:1011241_MONDO:1011242,"microphthalmia, dog",MONDO_grouped,disease,DISEASE_6015
6016,6016,6016,6016,6016,6016,6016,6016,MONDO:0008573,"tibial torsion, bilateral medial",MONDO,disease,DISEASE_6016
6017,6017,6017,6017,6017,6017,6017,6017,MONDO:0024429,Alice in Wonderland syndrome,MONDO,disease,DISEASE_6017
6018,6018,6018,6018,6018,6018,6018,6018,MONDO:0004468,anal canal Paget disease,MONDO,disease,DISEASE_6018
6019,6019,6019,6019,6019,6019,6019,6019,MONDO:0021380,neoplasm of myocardium,MONDO,disease,DISEASE_6019
6020,6020,6020,6020,6020,6020,6020,6020,MONDO:0021292,carcinoma in situ of gastric body,MONDO,disease,DISEASE_6020
6021,6021,6021,6021,6021,6021,6021,6021,MONDO:0017827,malignant peripheral nerve sheath tumor,MONDO,disease,DISEASE_6021
6022,6022,6022,6022,6022,6022,6022,6022,MONDO:0013646,chromosome 8q21.11 deletion syndrome,MONDO,disease,DISEASE_6022
6023,6023,6023,6023,6023,6023,6023,6023,MONDO:0013922_MONDO:0013871_MONDO:0014350_MONDO:0014991_MONDO:0014767_MONDO:0958328_MONDO:0013443_MONDO:0011715_MONDO:0008869_MONDO:0013358_MONDO:0019342,Seckel syndrome,MONDO_grouped,disease,DISEASE_6023
6024,6024,6024,6024,6024,6024,6024,6024,MONDO:1012434_MONDO:1012435,"congenital hydranencephaly and cerebellar hypoplasia, water buffalo",MONDO_grouped,disease,DISEASE_6024
6025,6025,6025,6025,6025,6025,6025,6025,MONDO:0013675_MONDO:0014611_MONDO:0014132_MONDO:0957382_MONDO:0011582_MONDO:0054785_MONDO:0033282_MONDO:0971174_MONDO:0975806,multiple mitochondrial dysfunctions syndrome,MONDO_grouped,disease,DISEASE_6025
6026,6026,6026,6026,6026,6026,6026,6026,MONDO:0016713,central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor,MONDO,disease,DISEASE_6026
6027,6027,6027,6027,6027,6027,6027,6027,MONDO:0006297,maxillary sinus adenoid cystic carcinoma,MONDO,disease,DISEASE_6027
6028,6028,6028,6028,6028,6028,6028,6028,MONDO:0032873,retinitis pigmentosa 87 with choroidal involvement,MONDO,disease,DISEASE_6028
6029,6029,6029,6029,6029,6029,6029,6029,MONDO:0007811,ichthyosis-cheek-eyebrow syndrome,MONDO,disease,DISEASE_6029
6030,6030,6030,6030,6030,6030,6030,6030,MONDO:0019985,drug-related renal tubular dysgenesis,MONDO,disease,DISEASE_6030
6031,6031,6031,6031,6031,6031,6031,6031,MONDO:0700024,chromosome 19 disorder,MONDO,disease,DISEASE_6031
6032,6032,6032,6032,6032,6032,6032,6032,MONDO:0009609,methylcobalamin deficiency type cblG,MONDO,disease,DISEASE_6032
6033,6033,6033,6033,6033,6033,6033,6033,MONDO:0013941,metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria,MONDO,disease,DISEASE_6033
6034,6034,6034,6034,6034,6034,6034,6034,MONDO:0007548,transient bullous dermolysis of the newborn,MONDO,disease,DISEASE_6034
6035,6035,6035,6035,6035,6035,6035,6035,MONDO:0010390,ocular albinism with late-onset sensorineural deafness,MONDO,disease,DISEASE_6035
6036,6036,6036,6036,6036,6036,6036,6036,MONDO:0023646,lipodermatosclerosis,MONDO,disease,DISEASE_6036
6037,6037,6037,6037,6037,6037,6037,6037,MONDO:0016894,partial deletion of the short arm of chromosome 16,MONDO,disease,DISEASE_6037
6038,6038,6038,6038,6038,6038,6038,6038,MONDO:0020764,Brown-Pearce carcinoma,MONDO,disease,DISEASE_6038
6039,6039,6039,6039,6039,6039,6039,6039,MONDO:1012185,"necrotising myelopathy, dog",MONDO,disease,DISEASE_6039
6040,6040,6040,6040,6040,6040,6040,6040,MONDO:0700159,canine acanthomatous epulis,MONDO,disease,DISEASE_6040
6041,6041,6041,6041,6041,6041,6041,6041,MONDO:0002183,enthesopathy,MONDO,disease,DISEASE_6041
6042,6042,6042,6042,6042,6042,6042,6042,MONDO:0002629,bone osteosarcoma,MONDO,disease,DISEASE_6042
6043,6043,6043,6043,6043,6043,6043,6043,MONDO:0021498,benign neoplasm of placenta,MONDO,disease,DISEASE_6043
6044,6044,6044,6044,6044,6044,6044,6044,MONDO:0044764,benign choroid plexus neoplasm,MONDO,disease,DISEASE_6044
6045,6045,6045,6045,6045,6045,6045,6045,MONDO:0022611,Brunoni syndrome,MONDO,disease,DISEASE_6045
6046,6046,6046,6046,6046,6046,6046,6046,MONDO:0024247,benign eccrine neoplasm,MONDO,disease,DISEASE_6046
6047,6047,6047,6047,6047,6047,6047,6047,MONDO:0001182,idiopathic corneal edema,MONDO,disease,DISEASE_6047
6048,6048,6048,6048,6048,6048,6048,6048,MONDO:0017116_MONDO:0017117,congenital communicating hydrocephalus,MONDO_grouped,disease,DISEASE_6048
6049,6049,6049,6049,6049,6049,6049,6049,MONDO:0958238,"hyperemesis gravidarum, susceptibility to",MONDO,disease,DISEASE_6049
6050,6050,6050,6050,6050,6050,6050,6050,MONDO:0019440_MONDO:0017810_MONDO:0018590,wild type ABeta2M amyloidosis,MONDO_grouped,disease,DISEASE_6050
6051,6051,6051,6051,6051,6051,6051,6051,MONDO:0000412,neonatal period electroclinical syndrome,MONDO,disease,DISEASE_6051
6052,6052,6052,6052,6052,6052,6052,6052,MONDO:0013299,chromosome 6q11-q14 deletion syndrome,MONDO,disease,DISEASE_6052
6053,6053,6053,6053,6053,6053,6053,6053,MONDO:0042496,ergotism,MONDO,disease,DISEASE_6053
6054,6054,6054,6054,6054,6054,6054,6054,MONDO:0007330,congenital pseudoarthrosis of clavicle,MONDO,disease,DISEASE_6054
6055,6055,6055,6055,6055,6055,6055,6055,MONDO:0006796,hypertensive encephalopathy,MONDO,disease,DISEASE_6055
6056,6056,6056,6056,6056,6056,6056,6056,MONDO:1012051,"Collie eye anomaly, dog",MONDO,disease,DISEASE_6056
6057,6057,6057,6057,6057,6057,6057,6057,MONDO:1010449,"dilated cardiomyopathy, domestic cat",MONDO,disease,DISEASE_6057
6058,6058,6058,6058,6058,6058,6058,6058,MONDO:0001300_MONDO:0001292,autonomic neuropathy,MONDO_grouped,disease,DISEASE_6058
6059,6059,6059,6059,6059,6059,6059,6059,MONDO:0012005,"growth failure, microcephaly, intellectual disability, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy",MONDO,disease,DISEASE_6059
6060,6060,6060,6060,6060,6060,6060,6060,MONDO:0019067,idiopathic steroid-sensitive nephrotic syndrome,MONDO,disease,DISEASE_6060
6061,6061,6061,6061,6061,6061,6061,6061,MONDO:0014624,Brown syndrome,MONDO,disease,DISEASE_6061
6062,6062,6062,6062,6062,6062,6062,6062,MONDO:1011157,"osteoarthritis, domestic guinea pig",MONDO,disease,DISEASE_6062
6063,6063,6063,6063,6063,6063,6063,6063,MONDO:0021241,buccal mucosa neoplasm,MONDO,disease,DISEASE_6063
6064,6064,6064,6064,6064,6064,6064,6064,MONDO:0009720,Keipert syndrome,MONDO,disease,DISEASE_6064
6065,6065,6065,6065,6065,6065,6065,6065,MONDO:0013857,"alar cleft, isolated",MONDO,disease,DISEASE_6065
6066,6066,6066,6066,6066,6066,6066,6066,MONDO:1012704_MONDO:1012705,"oculoskeletal dysplasia, COL9A3-related, dog",MONDO_grouped,disease,DISEASE_6066
6067,6067,6067,6067,6067,6067,6067,6067,MONDO:0005211_MONDO:0006340_MONDO:0003694_MONDO:0004074_MONDO:0004185_MONDO:0006046,ovarian serous adenocarcinoma,MONDO_grouped,disease,DISEASE_6067
6068,6068,6068,6068,6068,6068,6068,6068,MONDO:0859316,"iron overload, susceptibility to",MONDO,disease,DISEASE_6068
6069,6069,6069,6069,6069,6069,6069,6069,MONDO:0007993,microgastria-limb reduction defect syndrome,MONDO,disease,DISEASE_6069
6070,6070,6070,6070,6070,6070,6070,6070,MONDO:0000421,inborn serine deficiency,MONDO,disease,DISEASE_6070
6071,6071,6071,6071,6071,6071,6071,6071,MONDO:0044871,"dystonia, focal, task-specific",MONDO,disease,DISEASE_6071
6072,6072,6072,6072,6072,6072,6072,6072,MONDO:0006615_MONDO:0002206,sweat gland disorder,MONDO_grouped,disease,DISEASE_6072
6073,6073,6073,6073,6073,6073,6073,6073,MONDO:0002910,peroneal neuropathy,MONDO,disease,DISEASE_6073
6074,6074,6074,6074,6074,6074,6074,6074,MONDO:0007768,hyperparathyroidism 2 with jaw tumors,MONDO,disease,DISEASE_6074
6075,6075,6075,6075,6075,6075,6075,6075,MONDO:0019923,Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11,MONDO,disease,DISEASE_6075
6076,6076,6076,6076,6076,6076,6076,6076,MONDO:0019540,diffuse alveolar hemorrhage,MONDO,disease,DISEASE_6076
6077,6077,6077,6077,6077,6077,6077,6077,MONDO:0957442,autosomal recessive ataxia due to PEX16 deficiency,MONDO,disease,DISEASE_6077
6078,6078,6078,6078,6078,6078,6078,6078,MONDO:0015782,dysmorphism-cleft palate-loose skin syndrome,MONDO,disease,DISEASE_6078
6079,6079,6079,6079,6079,6079,6079,6079,MONDO:0003165_MONDO:0003168_MONDO:0006131,cerebellar astrocytoma,MONDO_grouped,disease,DISEASE_6079
6080,6080,6080,6080,6080,6080,6080,6080,MONDO:0000229,Indian tick typhus,MONDO,disease,DISEASE_6080
6081,6081,6081,6081,6081,6081,6081,6081,MONDO:0100471,vitamin D deficiency,MONDO,disease,DISEASE_6081
6082,6082,6082,6082,6082,6082,6082,6082,MONDO:0000969,pleural lipoma,MONDO,disease,DISEASE_6082
6083,6083,6083,6083,6083,6083,6083,6083,MONDO:0975835,bronchiectasis and nasal polyposis,MONDO,disease,DISEASE_6083
6084,6084,6084,6084,6084,6084,6084,6084,MONDO:0020399,congenital hypoplasia of the mitral valve annulus,MONDO,disease,DISEASE_6084
6085,6085,6085,6085,6085,6085,6085,6085,MONDO:0019297,lymphedema,MONDO,disease,DISEASE_6085
6086,6086,6086,6086,6086,6086,6086,6086,MONDO:0017256_MONDO:0017257,idiopathic anterior uveitis,MONDO_grouped,disease,DISEASE_6086
6087,6087,6087,6087,6087,6087,6087,6087,MONDO:0020357_MONDO:0020355_MONDO:0015480_MONDO:0015481,coloboma of eyelid,MONDO_grouped,disease,DISEASE_6087
6088,6088,6088,6088,6088,6088,6088,6088,MONDO:1010249,"ataxia telangiectasia, non-human animal",MONDO,disease,DISEASE_6088
6089,6089,6089,6089,6089,6089,6089,6089,MONDO:0010694,"nystagmus, myoclonic",MONDO,disease,DISEASE_6089
6090,6090,6090,6090,6090,6090,6090,6090,MONDO:0018078,soft tissue sarcoma,MONDO,disease,DISEASE_6090
6091,6091,6091,6091,6091,6091,6091,6091,MONDO:0008872_MONDO:0008871_MONDO:0000060_MONDO:0008873,microcephalic osteodysplastic primordial dwarfism,MONDO_grouped,disease,DISEASE_6091
6092,6092,6092,6092,6092,6092,6092,6092,MONDO:0016314,obsolete rare carcinoma of pancreas,MONDO,disease,DISEASE_6092
6093,6093,6093,6093,6093,6093,6093,6093,MONDO:0100487,TPM4-related platelet disorder,MONDO,disease,DISEASE_6093
6094,6094,6094,6094,6094,6094,6094,6094,MONDO:0019558_MONDO:0004706,discoid lupus erythematosus,MONDO_grouped,disease,DISEASE_6094
6095,6095,6095,6095,6095,6095,6095,6095,MONDO:0004717_MONDO:0018809,peliosis hepatis,MONDO_grouped,disease,DISEASE_6095
6096,6096,6096,6096,6096,6096,6096,6096,MONDO:0700119,distal chromosome 18q deletion syndrome,MONDO,disease,DISEASE_6096
6097,6097,6097,6097,6097,6097,6097,6097,MONDO:1012454,"congenital myopathy with fiber-type disproportion, dog",MONDO,disease,DISEASE_6097
6098,6098,6098,6098,6098,6098,6098,6098,MONDO:0017862,paraquat poisoning,MONDO,disease,DISEASE_6098
6099,6099,6099,6099,6099,6099,6099,6099,MONDO:0024309_MONDO:0013337_MONDO:0011961_MONDO:0009746_MONDO:0012092_MONDO:0013142_MONDO:0008086_MONDO:0013839_MONDO:0014244_MONDO:0018213_MONDO:0019941_MONDO:0800304,"neuropathy, hereditary sensory and autonomic,",MONDO_grouped,disease,DISEASE_6099
6100,6100,6100,6100,6100,6100,6100,6100,MONDO:0004941,eosinophilia-myalgia syndrome,MONDO,disease,DISEASE_6100
6101,6101,6101,6101,6101,6101,6101,6101,MONDO:0043193,richieri-costa guion-almeida cohen syndrome,MONDO,disease,DISEASE_6101
6102,6102,6102,6102,6102,6102,6102,6102,MONDO:0006073,adenomatoid odontogenic tumor,MONDO,disease,DISEASE_6102
6103,6103,6103,6103,6103,6103,6103,6103,MONDO:0971016_MONDO:0971005_MONDO:0971015_MONDO:0971014_MONDO:0971013_MONDO:0008855,MHC class II deficiency,MONDO_grouped,disease,DISEASE_6103
6104,6104,6104,6104,6104,6104,6104,6104,MONDO:0019832,acquired pituitary hormone deficiency,MONDO,disease,DISEASE_6104
6105,6105,6105,6105,6105,6105,6105,6105,MONDO:0044875,coronary microvascular disorder,MONDO,disease,DISEASE_6105
6106,6106,6106,6106,6106,6106,6106,6106,MONDO:0019254,inborn disorder of purine or pyrimidine metabolism,MONDO,disease,DISEASE_6106
6107,6107,6107,6107,6107,6107,6107,6107,MONDO:0015843,uterine hypoplasia,MONDO,disease,DISEASE_6107
6108,6108,6108,6108,6108,6108,6108,6108,MONDO:0014240_MONDO:0030061_MONDO:0032588_MONDO:0014966_MONDO:0020341,periventricular nodular heterotopia,MONDO_grouped,disease,DISEASE_6108
6109,6109,6109,6109,6109,6109,6109,6109,MONDO:0001281_MONDO:0004913,alternating exotropia,MONDO_grouped,disease,DISEASE_6109
6110,6110,6110,6110,6110,6110,6110,6110,MONDO:0017124,noma,MONDO,disease,DISEASE_6110
6111,6111,6111,6111,6111,6111,6111,6111,MONDO:0015233,caudal appendage-deafness syndrome,MONDO,disease,DISEASE_6111
6112,6112,6112,6112,6112,6112,6112,6112,MONDO:0006090,appendix hyperplastic polyp,MONDO,disease,DISEASE_6112
6113,6113,6113,6113,6113,6113,6113,6113,MONDO:0013361,congenital prothrombin deficiency,MONDO,disease,DISEASE_6113
6114,6114,6114,6114,6114,6114,6114,6114,MONDO:0006187,duodenal villous adenoma,MONDO,disease,DISEASE_6114
6115,6115,6115,6115,6115,6115,6115,6115,MONDO:1011710_MONDO:1011711,"bilateral deafness and vestibular dysfunction, non-human animal",MONDO_grouped,disease,DISEASE_6115
6116,6116,6116,6116,6116,6116,6116,6116,MONDO:0006265,laryngeal small cell carcinoma,MONDO,disease,DISEASE_6116
6117,6117,6117,6117,6117,6117,6117,6117,MONDO:0009905,urban-Rogers-Meyer syndrome,MONDO,disease,DISEASE_6117
6118,6118,6118,6118,6118,6118,6118,6118,MONDO:0043123,massa casaer ceulemans syndrome,MONDO,disease,DISEASE_6118
6119,6119,6119,6119,6119,6119,6119,6119,MONDO:0000583,immunoglobulin beta deficiency,MONDO,disease,DISEASE_6119
6120,6120,6120,6120,6120,6120,6120,6120,MONDO:0011642,carnitine acetyltransferase deficiency,MONDO,disease,DISEASE_6120
6121,6121,6121,6121,6121,6121,6121,6121,MONDO:0000552,breast lobular carcinoma,MONDO,disease,DISEASE_6121
6122,6122,6122,6122,6122,6122,6122,6122,MONDO:0014183_MONDO:0030697_MONDO:0014177_MONDO:0012021_MONDO:0013604_MONDO:0012995_MONDO:0013508_MONDO:0009713_MONDO:0014982_MONDO:0014411_MONDO:0012389_MONDO:0012932_MONDO:0013603,"myopia 23, autosomal recessive",MONDO_grouped,disease,DISEASE_6122
6123,6123,6123,6123,6123,6123,6123,6123,MONDO:0958083,conjoined twins,MONDO,disease,DISEASE_6123
6124,6124,6124,6124,6124,6124,6124,6124,MONDO:0008988_MONDO:0016603_MONDO:0015991,citrullinemia,MONDO_grouped,disease,DISEASE_6124
6125,6125,6125,6125,6125,6125,6125,6125,MONDO:0030009_MONDO:0012487_MONDO:0013492_MONDO:0021035,alopecia-intellectual disability syndrome,MONDO_grouped,disease,DISEASE_6125
6126,6126,6126,6126,6126,6126,6126,6126,MONDO:1010337,"myopia, non-human animal",MONDO,disease,DISEASE_6126
6127,6127,6127,6127,6127,6127,6127,6127,MONDO:0013275,hemolytic anemia due to glucophosphate isomerase deficiency,MONDO,disease,DISEASE_6127
6128,6128,6128,6128,6128,6128,6128,6128,MONDO:0018577,pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa,MONDO,disease,DISEASE_6128
6129,6129,6129,6129,6129,6129,6129,6129,MONDO:0017419,non-syndromic amelia,MONDO,disease,DISEASE_6129
6130,6130,6130,6130,6130,6130,6130,6130,MONDO:0024392,anaerobic balanitis,MONDO,disease,DISEASE_6130
6131,6131,6131,6131,6131,6131,6131,6131,MONDO:0003750,childhood central nervous system germ cell tumor,MONDO,disease,DISEASE_6131
6132,6132,6132,6132,6132,6132,6132,6132,MONDO:0006120,C-cell hyperplasia,MONDO,disease,DISEASE_6132
6133,6133,6133,6133,6133,6133,6133,6133,MONDO:0011921,"aural atresia, congenital",MONDO,disease,DISEASE_6133
6134,6134,6134,6134,6134,6134,6134,6134,MONDO:0003144,medulloepithelioma,MONDO,disease,DISEASE_6134
6135,6135,6135,6135,6135,6135,6135,6135,MONDO:0007639,fundus albipunctatus,MONDO,disease,DISEASE_6135
6136,6136,6136,6136,6136,6136,6136,6136,MONDO:0004730,speech disorder,MONDO,disease,DISEASE_6136
6137,6137,6137,6137,6137,6137,6137,6137,MONDO:0016239,cystinosis,MONDO,disease,DISEASE_6137
6138,6138,6138,6138,6138,6138,6138,6138,MONDO:0009952,radioulnar synostosis-developmental delay-hypotonia syndrome,MONDO,disease,DISEASE_6138
6139,6139,6139,6139,6139,6139,6139,6139,MONDO:0008420_MONDO:0021607,seborrheic keratosis,MONDO_grouped,disease,DISEASE_6139
6140,6140,6140,6140,6140,6140,6140,6140,MONDO:0013991,obesity due to congenital leptin deficiency,MONDO,disease,DISEASE_6140
6141,6141,6141,6141,6141,6141,6141,6141,MONDO:0859328,"hypomagnesemia 7, renal, with or without dilated cardiomyopathy",MONDO,disease,DISEASE_6141
6142,6142,6142,6142,6142,6142,6142,6142,MONDO:0033662,"neurodevelopmental disorder with microcephaly, seizures, and brain atrophy",MONDO,disease,DISEASE_6142
6143,6143,6143,6143,6143,6143,6143,6143,MONDO:0010697,"ophthalmoplegia, external, and myopia",MONDO,disease,DISEASE_6143
6144,6144,6144,6144,6144,6144,6144,6144,MONDO:0022985,diffuse cavernous hemangioma of the rectum,MONDO,disease,DISEASE_6144
6145,6145,6145,6145,6145,6145,6145,6145,MONDO:0000764,epithelial-stromal TGFBI dystrophy,MONDO,disease,DISEASE_6145
6146,6146,6146,6146,6146,6146,6146,6146,MONDO:0003487,pseudoglandular squamous cell carcinoma,MONDO,disease,DISEASE_6146
6147,6147,6147,6147,6147,6147,6147,6147,MONDO:0043589,femoral neck fracture,MONDO,disease,DISEASE_6147
6148,6148,6148,6148,6148,6148,6148,6148,MONDO:0015607,partial chromosome Y deletion,MONDO,disease,DISEASE_6148
6149,6149,6149,6149,6149,6149,6149,6149,MONDO:0011244,Marshall-Smith syndrome,MONDO,disease,DISEASE_6149
6150,6150,6150,6150,6150,6150,6150,6150,MONDO:0007730,histiocytic dermatoarthritis,MONDO,disease,DISEASE_6150
6151,6151,6151,6151,6151,6151,6151,6151,MONDO:0009592,metaphyseal acroscyphodysplasia,MONDO,disease,DISEASE_6151
6152,6152,6152,6152,6152,6152,6152,6152,MONDO:0016755_MONDO:0018975_MONDO:0021061_MONDO:1011566_MONDO:0004752,neurofibroma,MONDO_grouped,disease,DISEASE_6152
6153,6153,6153,6153,6153,6153,6153,6153,MONDO:0013005,EAST syndrome,MONDO,disease,DISEASE_6153
6154,6154,6154,6154,6154,6154,6154,6154,MONDO:1040028_MONDO:1040034_MONDO:0700224,PDE6C-related retinopathy,MONDO_grouped,disease,DISEASE_6154
6155,6155,6155,6155,6155,6155,6155,6155,MONDO:0012136,"carnitine palmitoyl transferase II deficiency, neonatal form",MONDO,disease,DISEASE_6155
6156,6156,6156,6156,6156,6156,6156,6156,MONDO:0018848,IgG4-related retroperitoneal fibrosis,MONDO,disease,DISEASE_6156
6157,6157,6157,6157,6157,6157,6157,6157,MONDO:0013176,"Weill-Marchesani 4 syndrome, recessive",MONDO,disease,DISEASE_6157
6158,6158,6158,6158,6158,6158,6158,6158,MONDO:1011981_MONDO:1011982_MONDO:1011986,"rod-cone degeneration, non-human animal",MONDO_grouped,disease,DISEASE_6158
6159,6159,6159,6159,6159,6159,6159,6159,MONDO:0017149,drug- or toxin-induced pulmonary arterial hypertension,MONDO,disease,DISEASE_6159
6160,6160,6160,6160,6160,6160,6160,6160,MONDO:0018168_MONDO:0019033_MONDO:0018167,primary non-essential cutis verticis gyrata,MONDO_grouped,disease,DISEASE_6160
6161,6161,6161,6161,6161,6161,6161,6161,MONDO:0850348,bladder small cell carcinoma,MONDO,disease,DISEASE_6161
6162,6162,6162,6162,6162,6162,6162,6162,MONDO:0018668,scedosporiosis,MONDO,disease,DISEASE_6162
6163,6163,6163,6163,6163,6163,6163,6163,MONDO:1011779,"neonatal hepatitis, non-human animal",MONDO,disease,DISEASE_6163
6164,6164,6164,6164,6164,6164,6164,6164,MONDO:0014708,ring chromosome 14,MONDO,disease,DISEASE_6164
6165,6165,6165,6165,6165,6165,6165,6165,MONDO:0975952,cerebral cavernous malformations 5,MONDO,disease,DISEASE_6165
6166,6166,6166,6166,6166,6166,6166,6166,MONDO:0019756,lobar holoprosencephaly,MONDO,disease,DISEASE_6166
6167,6167,6167,6167,6167,6167,6167,6167,MONDO:0002077,low implantation of placenta,MONDO,disease,DISEASE_6167
6168,6168,6168,6168,6168,6168,6168,6168,MONDO:0001461,tinea corporis,MONDO,disease,DISEASE_6168
6169,6169,6169,6169,6169,6169,6169,6169,MONDO:0024935,foot rot,MONDO,disease,DISEASE_6169
6170,6170,6170,6170,6170,6170,6170,6170,MONDO:0100066,TH-deficient progressive infantile encephalopathy,MONDO,disease,DISEASE_6170
6171,6171,6171,6171,6171,6171,6171,6171,MONDO:0001426,mediastinum neurofibroma,MONDO,disease,DISEASE_6171
6172,6172,6172,6172,6172,6172,6172,6172,MONDO:0017794,Xq12-q13.3 duplication syndrome,MONDO,disease,DISEASE_6172
6173,6173,6173,6173,6173,6173,6173,6173,MONDO:0019233_MONDO:0100277,disorder of peroxisomal beta oxidation,MONDO_grouped,disease,DISEASE_6173
6174,6174,6174,6174,6174,6174,6174,6174,MONDO:0800447,"bleeding disorder, platelet-type, 13, susceptibility to",MONDO,disease,DISEASE_6174
6175,6175,6175,6175,6175,6175,6175,6175,MONDO:0007643,"gamma-A-globulin, defect in assembly of",MONDO,disease,DISEASE_6175
6176,6176,6176,6176,6176,6176,6176,6176,MONDO:0019222,inborn disorder of methionine cycle and sulfur amino acid metabolism,MONDO,disease,DISEASE_6176
6177,6177,6177,6177,6177,6177,6177,6177,MONDO:0009084,conductive deafness-ptosis-skeletal anomalies syndrome,MONDO,disease,DISEASE_6177
6178,6178,6178,6178,6178,6178,6178,6178,MONDO:0004994,cardiomyopathy,MONDO,disease,DISEASE_6178
6179,6179,6179,6179,6179,6179,6179,6179,MONDO:0013038,CLOVES syndrome,MONDO,disease,DISEASE_6179
6180,6180,6180,6180,6180,6180,6180,6180,MONDO:0019334,autosomal recessive hyperinsulinism due to Kir6.2 deficiency,MONDO,disease,DISEASE_6180
6181,6181,6181,6181,6181,6181,6181,6181,MONDO:0017215,calciphylaxis,MONDO,disease,DISEASE_6181
6182,6182,6182,6182,6182,6182,6182,6182,MONDO:0004539,aortic malignant tumor,MONDO,disease,DISEASE_6182
6183,6183,6183,6183,6183,6183,6183,6183,MONDO:0016607,odontohypophosphatasia,MONDO,disease,DISEASE_6183
6184,6184,6184,6184,6184,6184,6184,6184,MONDO:0016940,partial duplication of the short arm of chromosome 3,MONDO,disease,DISEASE_6184
6185,6185,6185,6185,6185,6185,6185,6185,MONDO:0020577,childhood gonadal germ cell tumor,MONDO,disease,DISEASE_6185
6186,6186,6186,6186,6186,6186,6186,6186,MONDO:0021463,benign neoplasm of parathyroid gland,MONDO,disease,DISEASE_6186
6187,6187,6187,6187,6187,6187,6187,6187,MONDO:0017936,benign Samaritan congenital myopathy,MONDO,disease,DISEASE_6187
6188,6188,6188,6188,6188,6188,6188,6188,MONDO:0033561,deeah syndrome,MONDO,disease,DISEASE_6188
6189,6189,6189,6189,6189,6189,6189,6189,MONDO:0010197,"whistling face syndrome, recessive form",MONDO,disease,DISEASE_6189
6190,6190,6190,6190,6190,6190,6190,6190,MONDO:0004285,pancreatic intraductal papillary-mucinous carcinoma,MONDO,disease,DISEASE_6190
6191,6191,6191,6191,6191,6191,6191,6191,MONDO:0002368,papillary serous cystadenocarcinoma,MONDO,disease,DISEASE_6191
6192,6192,6192,6192,6192,6192,6192,6192,MONDO:0008829,chylous ascites,MONDO,disease,DISEASE_6192
6193,6193,6193,6193,6193,6193,6193,6193,MONDO:0013148_MONDO:0013146_MONDO:0013145_MONDO:0012742_MONDO:0012743_MONDO:0014621_MONDO:0011001_MONDO:0012728_MONDO:0013015_MONDO:0015263,Brugada syndrome,MONDO_grouped,disease,DISEASE_6193
6194,6194,6194,6194,6194,6194,6194,6194,MONDO:0016771_MONDO:0016772_MONDO:0016773,annular atrophic lichen planus,MONDO_grouped,disease,DISEASE_6194
6195,6195,6195,6195,6195,6195,6195,6195,MONDO:0015289,infectious epithelial keratitis,MONDO,disease,DISEASE_6195
6196,6196,6196,6196,6196,6196,6196,6196,MONDO:0015736_MONDO:0015737,intermediate nemaline myopathy,MONDO_grouped,disease,DISEASE_6196
6197,6197,6197,6197,6197,6197,6197,6197,MONDO:0003819_MONDO:0003818,childhood teratoma of the ovary,MONDO_grouped,disease,DISEASE_6197
6198,6198,6198,6198,6198,6198,6198,6198,MONDO:0009711,congenital fiber-type disproportion myopathy,MONDO,disease,DISEASE_6198
6199,6199,6199,6199,6199,6199,6199,6199,MONDO:1011880,"neonatal encephalopathy with seizures, non-human animal",MONDO,disease,DISEASE_6199
6200,6200,6200,6200,6200,6200,6200,6200,MONDO:0006555,granulomatous dermatitis,MONDO,disease,DISEASE_6200
6201,6201,6201,6201,6201,6201,6201,6201,MONDO:0008928,cataract-ataxia-deafness syndrome,MONDO,disease,DISEASE_6201
6202,6202,6202,6202,6202,6202,6202,6202,MONDO:0002243,hemorrhagic disease,MONDO,disease,DISEASE_6202
6203,6203,6203,6203,6203,6203,6203,6203,MONDO:0019424,X-linked intellectual disability-acromegaly-hyperactivity syndrome,MONDO,disease,DISEASE_6203
6204,6204,6204,6204,6204,6204,6204,6204,MONDO:0008944_MONDO:0013764_MONDO:0033308_MONDO:0033309_MONDO:0013763_MONDO:0014288_MONDO:0030462_MONDO:0012432_MONDO:0030933_MONDO:0010431_MONDO:0012539_MONDO:0032570_MONDO:0012078_MONDO:0013824_MONDO:0013608_MONDO:0014928_MONDO:0014927_MONDO:0032902_MONDO:0013896_MONDO:0013745_MONDO:0012694_MONDO:0014770_MONDO:0014297_MONDO:0030353_MONDO:0012855_MONDO:0012849_MONDO:0013994_MONDO:0014771_MONDO:0011963_MONDO:0014724_MONDO:0033310_MONDO:0033311_MONDO:0014664_MONDO:0030454_MONDO:0018772_MONDO:0800363_MONDO:0800372_MONDO:0800382_MONDO:0800383,Joubert syndrome,MONDO_grouped,disease,DISEASE_6204
6205,6205,6205,6205,6205,6205,6205,6205,MONDO:0009271,geroderma osteodysplastica,MONDO,disease,DISEASE_6205
6206,6206,6206,6206,6206,6206,6206,6206,MONDO:0001674,diverticulitis of colon,MONDO,disease,DISEASE_6206
6207,6207,6207,6207,6207,6207,6207,6207,MONDO:0004052,rectal cloacogenic carcinoma,MONDO,disease,DISEASE_6207
6208,6208,6208,6208,6208,6208,6208,6208,MONDO:0011884,hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome,MONDO,disease,DISEASE_6208
6209,6209,6209,6209,6209,6209,6209,6209,MONDO:0017754,inborn disorder of porphyrin metabolism,MONDO,disease,DISEASE_6209
6210,6210,6210,6210,6210,6210,6210,6210,MONDO:1010730,"X-linked severe combined immunodeficiency disease, IL2RG-related, golden hamster",MONDO,disease,DISEASE_6210
6211,6211,6211,6211,6211,6211,6211,6211,MONDO:0019393,idiopathic malabsorption due to bile acid synthesis defects,MONDO,disease,DISEASE_6211
6212,6212,6212,6212,6212,6212,6212,6212,MONDO:0002785,skull base neoplasm,MONDO,disease,DISEASE_6212
6213,6213,6213,6213,6213,6213,6213,6213,MONDO:0010152,trichomegaly-retina pigmentary degeneration-dwarfism syndrome,MONDO,disease,DISEASE_6213
6214,6214,6214,6214,6214,6214,6214,6214,MONDO:0002731,cerebral hemisphere cancer,MONDO,disease,DISEASE_6214
6215,6215,6215,6215,6215,6215,6215,6215,MONDO:0020236,obsolete lens position anomaly,MONDO,disease,DISEASE_6215
6216,6216,6216,6216,6216,6216,6216,6216,MONDO:0009350,Holzgreve-Wagner-Rehder syndrome,MONDO,disease,DISEASE_6216
6217,6217,6217,6217,6217,6217,6217,6217,MONDO:0018673,IgG4-related pachymeningitis,MONDO,disease,DISEASE_6217
6218,6218,6218,6218,6218,6218,6218,6218,MONDO:1011947,"muscle contracture and chondrodysplasia, non-human animal",MONDO,disease,DISEASE_6218
6219,6219,6219,6219,6219,6219,6219,6219,MONDO:0022849,congenital stenosis of cervical medullary canal,MONDO,disease,DISEASE_6219
6220,6220,6220,6220,6220,6220,6220,6220,MONDO:0003722,internal auditory canal meningioma,MONDO,disease,DISEASE_6220
6221,6221,6221,6221,6221,6221,6221,6221,MONDO:0020077_MONDO:0006311,myelodysplastic/myeloproliferative disease,MONDO_grouped,disease,DISEASE_6221
6222,6222,6222,6222,6222,6222,6222,6222,MONDO:0008433,small cell lung carcinoma,MONDO,disease,DISEASE_6222
6223,6223,6223,6223,6223,6223,6223,6223,MONDO:0005673,blind loop syndrome,MONDO,disease,DISEASE_6223
6224,6224,6224,6224,6224,6224,6224,6224,MONDO:0014715,primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection,MONDO,disease,DISEASE_6224
6225,6225,6225,6225,6225,6225,6225,6225,MONDO:0002490_MONDO:0004989_MONDO:0000970_MONDO:0003591_MONDO:0003593,breast sarcoma,MONDO_grouped,disease,DISEASE_6225
6226,6226,6226,6226,6226,6226,6226,6226,MONDO:0022968,dextrocardia with situs inversus,MONDO,disease,DISEASE_6226
6227,6227,6227,6227,6227,6227,6227,6227,MONDO:0009057,cyanosis and hepatic disease,MONDO,disease,DISEASE_6227
6228,6228,6228,6228,6228,6228,6228,6228,MONDO:0009292,glycogen storage disease due to glycogen branching enzyme deficiency,MONDO,disease,DISEASE_6228
6229,6229,6229,6229,6229,6229,6229,6229,MONDO:0004150,breast giant fibroadenoma,MONDO,disease,DISEASE_6229
6230,6230,6230,6230,6230,6230,6230,6230,MONDO:1012559,"anal gland disease, domestic cat",MONDO,disease,DISEASE_6230
6231,6231,6231,6231,6231,6231,6231,6231,MONDO:0018489,autoimmune encephalopathy with parasomnia and obstructive sleep apnea,MONDO,disease,DISEASE_6231
6232,6232,6232,6232,6232,6232,6232,6232,MONDO:0022977,diaphragmatic hernia exomphalos corpus callosum agenesis,MONDO,disease,DISEASE_6232
6233,6233,6233,6233,6233,6233,6233,6233,MONDO:0017715,3-hydroxyacyl-CoA dehydrogenase deficiency,MONDO,disease,DISEASE_6233
6234,6234,6234,6234,6234,6234,6234,6234,MONDO:8000013_MONDO:0030397_MONDO:0024193,"portal hypertension, noncirrhotic",MONDO_grouped,disease,DISEASE_6234
6235,6235,6235,6235,6235,6235,6235,6235,MONDO:0006280,lung sclerosing hemangioma,MONDO,disease,DISEASE_6235
6236,6236,6236,6236,6236,6236,6236,6236,MONDO:0800436_MONDO:0859567_MONDO:0031329,"craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development",MONDO_grouped,disease,DISEASE_6236
6237,6237,6237,6237,6237,6237,6237,6237,MONDO:0005051,invasive lobular breast carcinoma,MONDO,disease,DISEASE_6237
6238,6238,6238,6238,6238,6238,6238,6238,MONDO:0008128,"ophthalmoplegia, familial static",MONDO,disease,DISEASE_6238
6239,6239,6239,6239,6239,6239,6239,6239,MONDO:0010932,progressive bifocal chorioretinal atrophy,MONDO,disease,DISEASE_6239
6240,6240,6240,6240,6240,6240,6240,6240,MONDO:0017625_MONDO:0017624,familial primary hypomagnesemia with hypocalcuria,MONDO_grouped,disease,DISEASE_6240
6241,6241,6241,6241,6241,6241,6241,6241,MONDO:0007418,Darwinian tubercle of pinna,MONDO,disease,DISEASE_6241
6242,6242,6242,6242,6242,6242,6242,6242,MONDO:0018080,obsolete rare germ cell tumor,MONDO,disease,DISEASE_6242
6243,6243,6243,6243,6243,6243,6243,6243,MONDO:0056813,hormone-resistant breast carcinoma,MONDO,disease,DISEASE_6243
6244,6244,6244,6244,6244,6244,6244,6244,MONDO:0012698_MONDO:0010192_MONDO:0008671_MONDO:0008670_MONDO:0007862_MONDO:0010841_MONDO:0013202_MONDO:0013201_MONDO:0019517_MONDO:0018094_MONDO:0012144_MONDO:0011697,Waardenburg syndrome,MONDO_grouped,disease,DISEASE_6244
6245,6245,6245,6245,6245,6245,6245,6245,MONDO:0013351,infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly,MONDO,disease,DISEASE_6245
6246,6246,6246,6246,6246,6246,6246,6246,MONDO:0043339,lathyrism,MONDO,disease,DISEASE_6246
6247,6247,6247,6247,6247,6247,6247,6247,MONDO:0015748,hereditary mucosal leukokeratosis,MONDO,disease,DISEASE_6247
6248,6248,6248,6248,6248,6248,6248,6248,MONDO:0859279_MONDO:0011585_MONDO:0011436,"spinal muscular atrophy, distal, autosomal recessive",MONDO_grouped,disease,DISEASE_6248
6249,6249,6249,6249,6249,6249,6249,6249,MONDO:0800028_MONDO:0030625,"dyskinesia with orofacial involvement, autosomal dominant",MONDO_grouped,disease,DISEASE_6249
6250,6250,6250,6250,6250,6250,6250,6250,MONDO:0014242_MONDO:0011070_MONDO:0017813,van Maldergem syndrome,MONDO_grouped,disease,DISEASE_6250
6251,6251,6251,6251,6251,6251,6251,6251,MONDO:0001175,immature cataract,MONDO,disease,DISEASE_6251
6252,6252,6252,6252,6252,6252,6252,6252,MONDO:0004520,intratubular embryonal carcinoma,MONDO,disease,DISEASE_6252
6253,6253,6253,6253,6253,6253,6253,6253,MONDO:0011807_MONDO:0011942_MONDO:0011943_MONDO:0011944,"systemic lupus erythematosus with hemolytic anemia, susceptibility to, 1",MONDO_grouped,disease,DISEASE_6253
6254,6254,6254,6254,6254,6254,6254,6254,MONDO:0859272,neurodevelopmental disorder with speech delay and variable ocular anomalies,MONDO,disease,DISEASE_6254
6255,6255,6255,6255,6255,6255,6255,6255,MONDO:0007490,carpotarsal osteochondromatosis,MONDO,disease,DISEASE_6255
6256,6256,6256,6256,6256,6256,6256,6256,MONDO:0009980,retinal telangiectasia and hypogammaglobulinemia,MONDO,disease,DISEASE_6256
6257,6257,6257,6257,6257,6257,6257,6257,MONDO:0015798,inflammatory myofibroblastic tumor,MONDO,disease,DISEASE_6257
6258,6258,6258,6258,6258,6258,6258,6258,MONDO:0003284_MONDO:0003376,mediastinum leiomyoma,MONDO_grouped,disease,DISEASE_6258
6259,6259,6259,6259,6259,6259,6259,6259,MONDO:0010800,"Wolfram syndrome, mitochondrial form",MONDO,disease,DISEASE_6259
6260,6260,6260,6260,6260,6260,6260,6260,MONDO:0021026,hereditary epidermal appendage anomaly,MONDO,disease,DISEASE_6260
6261,6261,6261,6261,6261,6261,6261,6261,MONDO:0003046,anus neoplasm,MONDO,disease,DISEASE_6261
6262,6262,6262,6262,6262,6262,6262,6262,MONDO:0010382,fragile X-associated tremor/ataxia syndrome,MONDO,disease,DISEASE_6262
6263,6263,6263,6263,6263,6263,6263,6263,MONDO:0012298,"omphalocele, diaphragmatic hernia, and radial ray defects",MONDO,disease,DISEASE_6263
6264,6264,6264,6264,6264,6264,6264,6264,MONDO:1010230_MONDO:1011777,"hepatic encephalopathy, non-human animal",MONDO_grouped,disease,DISEASE_6264
6265,6265,6265,6265,6265,6265,6265,6265,MONDO:0012916,chromosome 2p16.1-p15 deletion syndrome,MONDO,disease,DISEASE_6265
6266,6266,6266,6266,6266,6266,6266,6266,MONDO:0060624,"neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter",MONDO,disease,DISEASE_6266
6267,6267,6267,6267,6267,6267,6267,6267,MONDO:0014205,severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome,MONDO,disease,DISEASE_6267
6268,6268,6268,6268,6268,6268,6268,6268,MONDO:0011207,"xanthomatosis, susceptibility to",MONDO,disease,DISEASE_6268
6269,6269,6269,6269,6269,6269,6269,6269,MONDO:0011179,"leishmaniasis, tegumentary, susceptibility to",MONDO,disease,DISEASE_6269
6270,6270,6270,6270,6270,6270,6270,6270,MONDO:0060713,"deafness, congenital heart defects, and posterior embryotoxon",MONDO,disease,DISEASE_6270
6271,6271,6271,6271,6271,6271,6271,6271,MONDO:0002510,obsolete germ cell and embryonal cancer,MONDO,disease,DISEASE_6271
6272,6272,6272,6272,6272,6272,6272,6272,MONDO:0009499,Krabbe disease,MONDO,disease,DISEASE_6272
6273,6273,6273,6273,6273,6273,6273,6273,MONDO:0030476_MONDO:0032692_MONDO:0032693_MONDO:0033008_MONDO:0033009_MONDO:0033007_MONDO:0032691_MONDO:0030471_MONDO:0033005_MONDO:0009627,Galloway-Mowat syndrome,MONDO_grouped,disease,DISEASE_6273
6274,6274,6274,6274,6274,6274,6274,6274,MONDO:0008357,radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome,MONDO,disease,DISEASE_6274
6275,6275,6275,6275,6275,6275,6275,6275,MONDO:0019402_MONDO:0016486,beta thalassemia,MONDO_grouped,disease,DISEASE_6275
6276,6276,6276,6276,6276,6276,6276,6276,MONDO:0060591,"immunodeficiency, developmental delay, and hypohomocysteinemia",MONDO,disease,DISEASE_6276
6277,6277,6277,6277,6277,6277,6277,6277,MONDO:0850469,EZB diffuse large B-cell lymphoma,MONDO,disease,DISEASE_6277
6278,6278,6278,6278,6278,6278,6278,6278,MONDO:0015250,spinal atrophy-ophthalmoplegia-pyramidal syndrome,MONDO,disease,DISEASE_6278
6279,6279,6279,6279,6279,6279,6279,6279,MONDO:0021045_MONDO:0060765,fibroepithelial neoplasm,MONDO_grouped,disease,DISEASE_6279
6280,6280,6280,6280,6280,6280,6280,6280,MONDO:0000498_MONDO:0000499,arteritic anterior ischemic optic neuropathy,MONDO_grouped,disease,DISEASE_6280
6281,6281,6281,6281,6281,6281,6281,6281,MONDO:0010474_MONDO:0010494_MONDO:0024552_MONDO:0010672,linear skin defects with multiple congenital anomalies,MONDO_grouped,disease,DISEASE_6281
6282,6282,6282,6282,6282,6282,6282,6282,MONDO:0019134,central neurocytoma,MONDO,disease,DISEASE_6282
6283,6283,6283,6283,6283,6283,6283,6283,MONDO:0003729_MONDO:0004051,aleukemic leukemia cutis,MONDO_grouped,disease,DISEASE_6283
6284,6284,6284,6284,6284,6284,6284,6284,MONDO:0018462,Angelman syndrome due to imprinting defect in 15q11-q13,MONDO,disease,DISEASE_6284
6285,6285,6285,6285,6285,6285,6285,6285,MONDO:0043330,Mirizzi syndrome,MONDO,disease,DISEASE_6285
6286,6286,6286,6286,6286,6286,6286,6286,MONDO:0100476,"lipodystrophy, partial, acquired, susceptibility to",MONDO,disease,DISEASE_6286
6287,6287,6287,6287,6287,6287,6287,6287,MONDO:0013771,transient infantile hypertriglyceridemia and hepatosteatosis,MONDO,disease,DISEASE_6287
6288,6288,6288,6288,6288,6288,6288,6288,MONDO:0030967,"deafness, congenital, and adult-onset progressive leukoencephalopathy",MONDO,disease,DISEASE_6288
6289,6289,6289,6289,6289,6289,6289,6289,MONDO:0042956,Saal-Bulas syndrome,MONDO,disease,DISEASE_6289
6290,6290,6290,6290,6290,6290,6290,6290,MONDO:0007506,obsoleted echo virus 11 sensitivity,MONDO,disease,DISEASE_6290
6291,6291,6291,6291,6291,6291,6291,6291,MONDO:0018432_MONDO:0019446_MONDO:0019447_MONDO:0016774,lichen myxedematosus,MONDO_grouped,disease,DISEASE_6291
6292,6292,6292,6292,6292,6292,6292,6292,MONDO:0012927,chromosome 1q41-q42 deletion syndrome,MONDO,disease,DISEASE_6292
6293,6293,6293,6293,6293,6293,6293,6293,MONDO:0007219,Osebold-Remondini syndrome,MONDO,disease,DISEASE_6293
6294,6294,6294,6294,6294,6294,6294,6294,MONDO:0043120,male pseudohermaphroditism due to defective lh molecule,MONDO,disease,DISEASE_6294
6295,6295,6295,6295,6295,6295,6295,6295,MONDO:0008927,colobomatous optic disc-macular atrophy-chorioretinopathy syndrome,MONDO,disease,DISEASE_6295
6296,6296,6296,6296,6296,6296,6296,6296,MONDO:0041093,central retinal vein occlusion with macular edema,MONDO,disease,DISEASE_6296
6297,6297,6297,6297,6297,6297,6297,6297,MONDO:0006844,magnesium deficiency,MONDO,disease,DISEASE_6297
6298,6298,6298,6298,6298,6298,6298,6298,MONDO:0005116,Whipple disease,MONDO,disease,DISEASE_6298
6299,6299,6299,6299,6299,6299,6299,6299,MONDO:0025453,"pneumonia, progressive interstitial, of sheep",MONDO,disease,DISEASE_6299
6300,6300,6300,6300,6300,6300,6300,6300,MONDO:0002505_MONDO:0004071_MONDO:0021633,childhood astrocytic tumor,MONDO_grouped,disease,DISEASE_6300
6301,6301,6301,6301,6301,6301,6301,6301,MONDO:0015044,mu-heavy chain disease,MONDO,disease,DISEASE_6301
6302,6302,6302,6302,6302,6302,6302,6302,MONDO:0016929,partial duplication of chromosome 8,MONDO,disease,DISEASE_6302
6303,6303,6303,6303,6303,6303,6303,6303,MONDO:0004107,splenic manifestation of leukemia,MONDO,disease,DISEASE_6303
6304,6304,6304,6304,6304,6304,6304,6304,MONDO:0015327,developmental anomaly of metabolic origin,MONDO,disease,DISEASE_6304
6305,6305,6305,6305,6305,6305,6305,6305,MONDO:0018973_MONDO:0009979,patterned dystrophy of the retinal pigment epithelium,MONDO_grouped,disease,DISEASE_6305
6306,6306,6306,6306,6306,6306,6306,6306,MONDO:0001768_MONDO:0002511,stenosis of lacrimal passage,MONDO_grouped,disease,DISEASE_6306
6307,6307,6307,6307,6307,6307,6307,6307,MONDO:0044346,echinococcus granulosus infectious disease,MONDO,disease,DISEASE_6307
6308,6308,6308,6308,6308,6308,6308,6308,MONDO:1011428_MONDO:1011426,"epidermolysis bullosa simplex, non-human animal",MONDO_grouped,disease,DISEASE_6308
6309,6309,6309,6309,6309,6309,6309,6309,MONDO:0018485,"glycogen storage disease due to acid maltase deficiency, late-onset",MONDO,disease,DISEASE_6309
6310,6310,6310,6310,6310,6310,6310,6310,MONDO:0021360,tumor of parathyroid gland,MONDO,disease,DISEASE_6310
6311,6311,6311,6311,6311,6311,6311,6311,MONDO:0002861_MONDO:0001387,testis sarcoma,MONDO_grouped,disease,DISEASE_6311
6312,6312,6312,6312,6312,6312,6312,6312,MONDO:0003631,cervical serous adenocarcinoma,MONDO,disease,DISEASE_6312
6313,6313,6313,6313,6313,6313,6313,6313,MONDO:0003012,sarcomatoid renal cell carcinoma,MONDO,disease,DISEASE_6313
6314,6314,6314,6314,6314,6314,6314,6314,MONDO:1012793,"oculocutaneous albinism, HPS5-related, three-spined stickleback",MONDO,disease,DISEASE_6314
6315,6315,6315,6315,6315,6315,6315,6315,MONDO:0001740,cornea squamous cell carcinoma,MONDO,disease,DISEASE_6315
6316,6316,6316,6316,6316,6316,6316,6316,MONDO:0971107,common arterial trunk with aortic dominance,MONDO,disease,DISEASE_6316
6317,6317,6317,6317,6317,6317,6317,6317,MONDO:0060621,"neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy",MONDO,disease,DISEASE_6317
6318,6318,6318,6318,6318,6318,6318,6318,MONDO:0012843_MONDO:0020759_MONDO:1030001_MONDO:0012763,"epilepsy, childhood absence, susceptibility to",MONDO_grouped,disease,DISEASE_6318
6319,6319,6319,6319,6319,6319,6319,6319,MONDO:0006043,metaplastic breast carcinoma,MONDO,disease,DISEASE_6319
6320,6320,6320,6320,6320,6320,6320,6320,MONDO:0009244,"Freesia Flowers, inability to smell",MONDO,disease,DISEASE_6320
6321,6321,6321,6321,6321,6321,6321,6321,MONDO:0850014,twin-reversed arterial perfusion sequence,MONDO,disease,DISEASE_6321
6322,6322,6322,6322,6322,6322,6322,6322,MONDO:0021178,injury,MONDO,disease,DISEASE_6322
6323,6323,6323,6323,6323,6323,6323,6323,MONDO:0000503,lung adenocarcinoma in situ,MONDO,disease,DISEASE_6323
6324,6324,6324,6324,6324,6324,6324,6324,MONDO:1012141,"multiple lipomatosis, dog",MONDO,disease,DISEASE_6324
6325,6325,6325,6325,6325,6325,6325,6325,MONDO:0010460_MONDO:0010500_MONDO:0010270_MONDO:0030908_MONDO:0010501_MONDO:0010461_MONDO:0010409_MONDO:0010574_MONDO:0010402_MONDO:0010398_MONDO:0010664_MONDO:0010277_MONDO:0010658_MONDO:0000508_MONDO:0020119,syndromic X-linked intellectual disability,MONDO_grouped,disease,DISEASE_6325
6326,6326,6326,6326,6326,6326,6326,6326,MONDO:0012223,"hypotrichosis, progressive patterned scalp, with wiry hair, onycholysis, and cleft lip/palate",MONDO,disease,DISEASE_6326
6327,6327,6327,6327,6327,6327,6327,6327,MONDO:1011494,"Ehlers-Danlos syndrome, domestic cat",MONDO,disease,DISEASE_6327
6328,6328,6328,6328,6328,6328,6328,6328,MONDO:0016987,neuroacanthocytosis,MONDO,disease,DISEASE_6328
6329,6329,6329,6329,6329,6329,6329,6329,MONDO:0021745,psychosocial short stature,MONDO,disease,DISEASE_6329
6330,6330,6330,6330,6330,6330,6330,6330,MONDO:0015298,pellucid marginal degeneration,MONDO,disease,DISEASE_6330
6331,6331,6331,6331,6331,6331,6331,6331,MONDO:0007719_MONDO:0009103_MONDO:0012431,diaphragmatic hernia,MONDO_grouped,disease,DISEASE_6331
6332,6332,6332,6332,6332,6332,6332,6332,MONDO:0005026_MONDO:0006192_MONDO:0003463_MONDO:0006335_MONDO:0003879_MONDO:0004019_MONDO:0004136_MONDO:0004214,endometrioid adenocarcinoma,MONDO_grouped,disease,DISEASE_6332
6333,6333,6333,6333,6333,6333,6333,6333,MONDO:0018748,linear IgA Dermatosis,MONDO,disease,DISEASE_6333
6334,6334,6334,6334,6334,6334,6334,6334,MONDO:1011640,"atrial septal defect and atrial fibrillation, non-human animal",MONDO,disease,DISEASE_6334
6335,6335,6335,6335,6335,6335,6335,6335,MONDO:0011823,developmental malformations-deafness-dystonia syndrome,MONDO,disease,DISEASE_6335
6336,6336,6336,6336,6336,6336,6336,6336,MONDO:0001293,subglottis cancer,MONDO,disease,DISEASE_6336
6337,6337,6337,6337,6337,6337,6337,6337,MONDO:0005062_MONDO:0004638_MONDO:0006842,lymphoma,MONDO_grouped,disease,DISEASE_6337
6338,6338,6338,6338,6338,6338,6338,6338,MONDO:0020686,acute tonsillitis,MONDO,disease,DISEASE_6338
6339,6339,6339,6339,6339,6339,6339,6339,MONDO:0020807,ovarian sertoli-stromal cell tumor,MONDO,disease,DISEASE_6339
6340,6340,6340,6340,6340,6340,6340,6340,MONDO:1010240,"Horner syndrome, non-human animal",MONDO,disease,DISEASE_6340
6341,6341,6341,6341,6341,6341,6341,6341,MONDO:0007338_MONDO:0015092_MONDO:0971092,cleft soft palate,MONDO_grouped,disease,DISEASE_6341
6342,6342,6342,6342,6342,6342,6342,6342,MONDO:0005280,prostatitis,MONDO,disease,DISEASE_6342
6343,6343,6343,6343,6343,6343,6343,6343,MONDO:0010914,"carnitine palmitoyl transferase II deficiency, severe infantile form",MONDO,disease,DISEASE_6343
6344,6344,6344,6344,6344,6344,6344,6344,MONDO:0037105,lung germ cell tumor,MONDO,disease,DISEASE_6344
6345,6345,6345,6345,6345,6345,6345,6345,MONDO:0008401,pleomorphic adenoma,MONDO,disease,DISEASE_6345
6346,6346,6346,6346,6346,6346,6346,6346,MONDO:0018058,tracheal agenesis,MONDO,disease,DISEASE_6346
6347,6347,6347,6347,6347,6347,6347,6347,MONDO:0956965,medulloblastoma SHH activated and TP53 wild-type,MONDO,disease,DISEASE_6347
6348,6348,6348,6348,6348,6348,6348,6348,MONDO:0005922,pleural tuberculosis,MONDO,disease,DISEASE_6348
6349,6349,6349,6349,6349,6349,6349,6349,MONDO:0005515,oral cavity cancer,MONDO,disease,DISEASE_6349
6350,6350,6350,6350,6350,6350,6350,6350,MONDO:0005359,drug-induced liver injury,MONDO,disease,DISEASE_6350
6351,6351,6351,6351,6351,6351,6351,6351,MONDO:0016596,hyperphosphatasia-intellectual disability syndrome,MONDO,disease,DISEASE_6351
6352,6352,6352,6352,6352,6352,6352,6352,MONDO:0800415,"asthma, aspirin-induced, susceptibility to",MONDO,disease,DISEASE_6352
6353,6353,6353,6353,6353,6353,6353,6353,MONDO:0007224,"brachydactyly, type E, with atrial septal defect, type 2",MONDO,disease,DISEASE_6353
6354,6354,6354,6354,6354,6354,6354,6354,MONDO:0958267,non-syndromic bridging bronchus,MONDO,disease,DISEASE_6354
6355,6355,6355,6355,6355,6355,6355,6355,MONDO:0006211,fibrous hamartoma of infancy,MONDO,disease,DISEASE_6355
6356,6356,6356,6356,6356,6356,6356,6356,MONDO:0006161,colorectal juvenile polyp,MONDO,disease,DISEASE_6356
6357,6357,6357,6357,6357,6357,6357,6357,MONDO:1011448,"Fanconi syndrome, non-human animal",MONDO,disease,DISEASE_6357
6358,6358,6358,6358,6358,6358,6358,6358,MONDO:0060774,vaginal fibroepithelial polyp,MONDO,disease,DISEASE_6358
6359,6359,6359,6359,6359,6359,6359,6359,MONDO:0004077,lumbosacral lipoma,MONDO,disease,DISEASE_6359
6360,6360,6360,6360,6360,6360,6360,6360,MONDO:0019370,vulvovaginal gingival syndrome,MONDO,disease,DISEASE_6360
6361,6361,6361,6361,6361,6361,6361,6361,MONDO:0030717,immunodeficiency 97 with autoinflammation,MONDO,disease,DISEASE_6361
6362,6362,6362,6362,6362,6362,6362,6362,MONDO:0009842,Pelger-Huet-like anomaly and episodic fever with abdominal pain,MONDO,disease,DISEASE_6362
6363,6363,6363,6363,6363,6363,6363,6363,MONDO:0021017,synaptopathy,MONDO,disease,DISEASE_6363
6364,6364,6364,6364,6364,6364,6364,6364,MONDO:0015686,primary peritoneal carcinoma,MONDO,disease,DISEASE_6364
6365,6365,6365,6365,6365,6365,6365,6365,MONDO:0009445,ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome,MONDO,disease,DISEASE_6365
6366,6366,6366,6366,6366,6366,6366,6366,MONDO:0006232,giant cell tumor of soft tissue,MONDO,disease,DISEASE_6366
6367,6367,6367,6367,6367,6367,6367,6367,MONDO:0012184,Pierson syndrome,MONDO,disease,DISEASE_6367
6368,6368,6368,6368,6368,6368,6368,6368,MONDO:0009373,seizures-intellectual disability due to hydroxylysinuria syndrome,MONDO,disease,DISEASE_6368
6369,6369,6369,6369,6369,6369,6369,6369,MONDO:0024636,inflammation of heart layer,MONDO,disease,DISEASE_6369
6370,6370,6370,6370,6370,6370,6370,6370,MONDO:0004366,mixed astrocytoma-ependymoma-oligodendroglioma,MONDO,disease,DISEASE_6370
6371,6371,6371,6371,6371,6371,6371,6371,MONDO:0009098,dextrocardia with unusual facies and microphthalmia,MONDO,disease,DISEASE_6371
6372,6372,6372,6372,6372,6372,6372,6372,MONDO:0700172,horse lymphoma,MONDO,disease,DISEASE_6372
6373,6373,6373,6373,6373,6373,6373,6373,MONDO:0007653_MONDO:0019411_MONDO:0019680,genochondromatosis,MONDO_grouped,disease,DISEASE_6373
6374,6374,6374,6374,6374,6374,6374,6374,MONDO:0015185,intestinal polyposis syndrome,MONDO,disease,DISEASE_6374
6375,6375,6375,6375,6375,6375,6375,6375,MONDO:0957560,"hearing loss, noise-induced, susceptibility to",MONDO,disease,DISEASE_6375
6376,6376,6376,6376,6376,6376,6376,6376,MONDO:0005679,bovine virus diarrhea-mucosal disease,MONDO,disease,DISEASE_6376
6377,6377,6377,6377,6377,6377,6377,6377,MONDO:0010312,"radial ray deficiency, X-linked",MONDO,disease,DISEASE_6377
6378,6378,6378,6378,6378,6378,6378,6378,MONDO:0009000,familial reactive perforating collagenosis,MONDO,disease,DISEASE_6378
6379,6379,6379,6379,6379,6379,6379,6379,MONDO:0002610,purpura,MONDO,disease,DISEASE_6379
6380,6380,6380,6380,6380,6380,6380,6380,MONDO:0035344_MONDO:0035345_MONDO:0018477,acute bilirubin encephalopathy,MONDO_grouped,disease,DISEASE_6380
6381,6381,6381,6381,6381,6381,6381,6381,MONDO:0019905,ring chromosome 9,MONDO,disease,DISEASE_6381
6382,6382,6382,6382,6382,6382,6382,6382,MONDO:0008276,generalized juvenile polyposis/juvenile polyposis coli,MONDO,disease,DISEASE_6382
6383,6383,6383,6383,6383,6383,6383,6383,MONDO:0043358,engraftment syndrome,MONDO,disease,DISEASE_6383
6384,6384,6384,6384,6384,6384,6384,6384,MONDO:0971140,well-differentiated papillary mesothelial tumour of the pleura,MONDO,disease,DISEASE_6384
6385,6385,6385,6385,6385,6385,6385,6385,MONDO:0004278,infiltrating bladder urothelial carcinoma sarcomatoid variant,MONDO,disease,DISEASE_6385
6386,6386,6386,6386,6386,6386,6386,6386,MONDO:0100240,inherited thrombophilia,MONDO,disease,DISEASE_6386
6387,6387,6387,6387,6387,6387,6387,6387,MONDO:0020007,absence of the pulmonary artery,MONDO,disease,DISEASE_6387
6388,6388,6388,6388,6388,6388,6388,6388,MONDO:0003494,ovarian squamous cell carcinoma,MONDO,disease,DISEASE_6388
6389,6389,6389,6389,6389,6389,6389,6389,MONDO:0020242_MONDO:0957048,hereditary macular dystrophy,MONDO_grouped,disease,DISEASE_6389
6390,6390,6390,6390,6390,6390,6390,6390,MONDO:0032664_MONDO:0054843_MONDO:0013979_MONDO:0032874_MONDO:0032757_MONDO:0030332_MONDO:0014123_MONDO:0014193_MONDO:0014192_MONDO:0014910_MONDO:0009484_MONDO:0013525_MONDO:0014909_MONDO:0012571_MONDO:0013434_MONDO:0014378_MONDO:0014202_MONDO:0012978_MONDO:0957922_MONDO:0957396_MONDO:0014203_MONDO:0011718_MONDO:0013174_MONDO:0014215_MONDO:0013435_MONDO:0032924_MONDO:0012906_MONDO:0012918_MONDO:0014216_MONDO:0012979_MONDO:0014465_MONDO:0014030_MONDO:0957252_MONDO:0032914_MONDO:0014211_MONDO:0013854_MONDO:0014657_MONDO:0033204_MONDO:0012748_MONDO:0032637_MONDO:0957991_MONDO:0013940_MONDO:0014750_MONDO:0032872_MONDO:0012088_MONDO:0012085_MONDO:0016575_MONDO:1012138_MONDO:0012087_MONDO:0012844_MONDO:1012139_MONDO:1012140,"ciliary dyskinesia, primary",MONDO_grouped,disease,DISEASE_6390
6391,6391,6391,6391,6391,6391,6391,6391,MONDO:0009936,familial primary pulmonary hypoplasia,MONDO,disease,DISEASE_6391
6392,6392,6392,6392,6392,6392,6392,6392,MONDO:0018217,Koolen-de Vries syndrome due to a point mutation,MONDO,disease,DISEASE_6392
6393,6393,6393,6393,6393,6393,6393,6393,MONDO:0008492,stiff skin syndrome,MONDO,disease,DISEASE_6393
6394,6394,6394,6394,6394,6394,6394,6394,MONDO:1012153_MONDO:1012155_MONDO:1012156_MONDO:1012158_MONDO:1012159_MONDO:1012160,"megaesophagus, dog",MONDO_grouped,disease,DISEASE_6394
6395,6395,6395,6395,6395,6395,6395,6395,MONDO:0009949,pyruvate carboxylase deficiency disease,MONDO,disease,DISEASE_6395
6396,6396,6396,6396,6396,6396,6396,6396,MONDO:1010701,"pyruvate kinase deficiency of erythrocyte, dog",MONDO,disease,DISEASE_6396
6397,6397,6397,6397,6397,6397,6397,6397,MONDO:0958001,Alfadhel syndrome,MONDO,disease,DISEASE_6397
6398,6398,6398,6398,6398,6398,6398,6398,MONDO:0011238,"chondrodysplasia punctata, brachytelephalangic, autosomal",MONDO,disease,DISEASE_6398
6399,6399,6399,6399,6399,6399,6399,6399,MONDO:0030475_MONDO:0030070_MONDO:0030474,"heterotaxy, visceral, 11, autosomal, with male infertility",MONDO_grouped,disease,DISEASE_6399
6400,6400,6400,6400,6400,6400,6400,6400,MONDO:0018602,necrotizing soft tissue infection,MONDO,disease,DISEASE_6400
6401,6401,6401,6401,6401,6401,6401,6401,MONDO:1012142,"multiple lipomatosis, pig",MONDO,disease,DISEASE_6401
6402,6402,6402,6402,6402,6402,6402,6402,MONDO:0005945,rhinoscleroma,MONDO,disease,DISEASE_6402
6403,6403,6403,6403,6403,6403,6403,6403,MONDO:1011658,"calvarial hyperostotic syndrome, non-human animal",MONDO,disease,DISEASE_6403
6404,6404,6404,6404,6404,6404,6404,6404,MONDO:0031115,dyskinesia with orofacial involvement,MONDO,disease,DISEASE_6404
6405,6405,6405,6405,6405,6405,6405,6405,MONDO:0859142,Hiatt-Neu-Cooper neurodevelopmental syndrome,MONDO,disease,DISEASE_6405
6406,6406,6406,6406,6406,6406,6406,6406,MONDO:0003036,mucoepidermoid carcinoma,MONDO,disease,DISEASE_6406
6407,6407,6407,6407,6407,6407,6407,6407,MONDO:1010103,"eclampsia, non-human animal",MONDO,disease,DISEASE_6407
6408,6408,6408,6408,6408,6408,6408,6408,MONDO:0011409,"hepatic fibrosis, severe, susceptibility to, due to Schistosoma mansoni infection",MONDO,disease,DISEASE_6408
6409,6409,6409,6409,6409,6409,6409,6409,MONDO:1010675,"anotia, cattle",MONDO,disease,DISEASE_6409
6410,6410,6410,6410,6410,6410,6410,6410,MONDO:0016387,mitochondrial oxidative phosphorylation disorder,MONDO,disease,DISEASE_6410
6411,6411,6411,6411,6411,6411,6411,6411,MONDO:0021446,benign neoplasm of epiglottis,MONDO,disease,DISEASE_6411
6412,6412,6412,6412,6412,6412,6412,6412,MONDO:0056802,synovial bursa disorder,MONDO,disease,DISEASE_6412
6413,6413,6413,6413,6413,6413,6413,6413,MONDO:0030035,"leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome",MONDO,disease,DISEASE_6413
6414,6414,6414,6414,6414,6414,6414,6414,MONDO:0044355,isolated sternocostoclavicular hyperostosis,MONDO,disease,DISEASE_6414
6415,6415,6415,6415,6415,6415,6415,6415,MONDO:0035473,warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome,MONDO,disease,DISEASE_6415
6416,6416,6416,6416,6416,6416,6416,6416,MONDO:0014149,fetal akinesia-cerebral and retinal hemorrhage syndrome,MONDO,disease,DISEASE_6416
6417,6417,6417,6417,6417,6417,6417,6417,MONDO:0968974,large B-cell lymphoma,MONDO,disease,DISEASE_6417
6418,6418,6418,6418,6418,6418,6418,6418,MONDO:0018711,intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome,MONDO,disease,DISEASE_6418
6419,6419,6419,6419,6419,6419,6419,6419,MONDO:0018869,cobblestone lissencephaly,MONDO,disease,DISEASE_6419
6420,6420,6420,6420,6420,6420,6420,6420,MONDO:0011611,"short stature, intellectual disability, callosal agenesis, Heminasal hypoplasia, microphthalmia, and atypical clefting",MONDO,disease,DISEASE_6420
6421,6421,6421,6421,6421,6421,6421,6421,MONDO:0002960,polyradiculopathy,MONDO,disease,DISEASE_6421
6422,6422,6422,6422,6422,6422,6422,6422,MONDO:0018637,familial chylomicronemia syndrome,MONDO,disease,DISEASE_6422
6423,6423,6423,6423,6423,6423,6423,6423,MONDO:0000688,inborn organic aciduria,MONDO,disease,DISEASE_6423
6424,6424,6424,6424,6424,6424,6424,6424,MONDO:0025061,edema disease of swine,MONDO,disease,DISEASE_6424
6425,6425,6425,6425,6425,6425,6425,6425,MONDO:0009198,congenital lethal erythroderma,MONDO,disease,DISEASE_6425
6426,6426,6426,6426,6426,6426,6426,6426,MONDO:1010622,"situs inversus, domestic cat",MONDO,disease,DISEASE_6426
6427,6427,6427,6427,6427,6427,6427,6427,MONDO:0800307,de la Chapelle dysplasia,MONDO,disease,DISEASE_6427
6428,6428,6428,6428,6428,6428,6428,6428,MONDO:0007809,"ichthyosis histrix, Lambert type",MONDO,disease,DISEASE_6428
6429,6429,6429,6429,6429,6429,6429,6429,MONDO:0005290,obsolete rhabdomyolysis,MONDO,disease,DISEASE_6429
6430,6430,6430,6430,6430,6430,6430,6430,MONDO:0013138_MONDO:8000019,"vertigo, benign recurrent",MONDO_grouped,disease,DISEASE_6430
6431,6431,6431,6431,6431,6431,6431,6431,MONDO:0011599,birdshot chorioretinopathy,MONDO,disease,DISEASE_6431
6432,6432,6432,6432,6432,6432,6432,6432,MONDO:0956962,benign teratoma,MONDO,disease,DISEASE_6432
6433,6433,6433,6433,6433,6433,6433,6433,MONDO:0007537,lateral meningocele syndrome,MONDO,disease,DISEASE_6433
6434,6434,6434,6434,6434,6434,6434,6434,MONDO:0015773,fibular dimelia-diplopodia syndrome,MONDO,disease,DISEASE_6434
6435,6435,6435,6435,6435,6435,6435,6435,MONDO:0017604,marginal zone lymphoma,MONDO,disease,DISEASE_6435
6436,6436,6436,6436,6436,6436,6436,6436,MONDO:0035707,blepharophimosis-intellectual disability syndrome/genitopatellar overlap syndrome,MONDO,disease,DISEASE_6436
6437,6437,6437,6437,6437,6437,6437,6437,MONDO:0008007,tooth ankylosis,MONDO,disease,DISEASE_6437
6438,6438,6438,6438,6438,6438,6438,6438,MONDO:0020388_MONDO:0020387,double outlet right ventricle with non-committed subpulmonary ventricular septal defect,MONDO_grouped,disease,DISEASE_6438
6439,6439,6439,6439,6439,6439,6439,6439,MONDO:0015836,Bicervical bicornuate uterus with patent cervix and vagina,MONDO,disease,DISEASE_6439
6440,6440,6440,6440,6440,6440,6440,6440,MONDO:0008443,spastic paraplegia-precocious puberty syndrome,MONDO,disease,DISEASE_6440
6441,6441,6441,6441,6441,6441,6441,6441,MONDO:0005034_MONDO:0004524,thyroid gland follicular carcinoma,MONDO_grouped,disease,DISEASE_6441
6442,6442,6442,6442,6442,6442,6442,6442,MONDO:0009556,malonic aciduria,MONDO,disease,DISEASE_6442
6443,6443,6443,6443,6443,6443,6443,6443,MONDO:0019736,dense deposit disease,MONDO,disease,DISEASE_6443
6444,6444,6444,6444,6444,6444,6444,6444,MONDO:0011750,obsolete insulinoma tumor suppressor gene locus,MONDO,disease,DISEASE_6444
6445,6445,6445,6445,6445,6445,6445,6445,MONDO:0016876,partial deletion of chromosome 11,MONDO,disease,DISEASE_6445
6446,6446,6446,6446,6446,6446,6446,6446,MONDO:0009422,hypohidrosis with abnormal palmar dermal Ridges,MONDO,disease,DISEASE_6446
6447,6447,6447,6447,6447,6447,6447,6447,MONDO:0011110,dyssegmental dysplasia-glaucoma syndrome,MONDO,disease,DISEASE_6447
6448,6448,6448,6448,6448,6448,6448,6448,MONDO:0400000,small intestinal bacterial overgrowth,MONDO,disease,DISEASE_6448
6449,6449,6449,6449,6449,6449,6449,6449,MONDO:0017047,infantile axonal neuropathy,MONDO,disease,DISEASE_6449
6450,6450,6450,6450,6450,6450,6450,6450,MONDO:1012411,"compulsive disorder, dog",MONDO,disease,DISEASE_6450
6451,6451,6451,6451,6451,6451,6451,6451,MONDO:0008985,ciliary dyskinesia with transposition of ciliary microtubules,MONDO,disease,DISEASE_6451
6452,6452,6452,6452,6452,6452,6452,6452,MONDO:0010659,FRAXE intellectual disability,MONDO,disease,DISEASE_6452
6453,6453,6453,6453,6453,6453,6453,6453,MONDO:0014572,Lichtenstein-Knorr syndrome,MONDO,disease,DISEASE_6453
6454,6454,6454,6454,6454,6454,6454,6454,MONDO:0019554,idiopathic localized lipodystrophy,MONDO,disease,DISEASE_6454
6455,6455,6455,6455,6455,6455,6455,6455,MONDO:0013400,"Congenital adrenal insufficiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency",MONDO,disease,DISEASE_6455
6456,6456,6456,6456,6456,6456,6456,6456,MONDO:0001914,scleromalacia perforans,MONDO,disease,DISEASE_6456
6457,6457,6457,6457,6457,6457,6457,6457,MONDO:0018944,gestational trophoblastic neoplasm,MONDO,disease,DISEASE_6457
6458,6458,6458,6458,6458,6458,6458,6458,MONDO:0001542,common peroneal nerve lesion,MONDO,disease,DISEASE_6458
6459,6459,6459,6459,6459,6459,6459,6459,MONDO:0020519,hand-Schuller-Christian disease,MONDO,disease,DISEASE_6459
6460,6460,6460,6460,6460,6460,6460,6460,MONDO:0014023_MONDO:0024607_MONDO:0018278,congenital muscular dystrophy with intellectual disability and severe epilepsy,MONDO_grouped,disease,DISEASE_6460
6461,6461,6461,6461,6461,6461,6461,6461,MONDO:0009500,"kuru, susceptibility to",MONDO,disease,DISEASE_6461
6462,6462,6462,6462,6462,6462,6462,6462,MONDO:0002221_MONDO:0004044,urethral urothelial papilloma,MONDO_grouped,disease,DISEASE_6462
6463,6463,6463,6463,6463,6463,6463,6463,MONDO:0859354_MONDO:0030839_MONDO:0800046_MONDO:0031432,"thyroid hormone metabolism, abnormal",MONDO_grouped,disease,DISEASE_6463
6464,6464,6464,6464,6464,6464,6464,6464,MONDO:0017388,celiac trunk compression syndrome,MONDO,disease,DISEASE_6464
6465,6465,6465,6465,6465,6465,6465,6465,MONDO:0016225,specific learning disability,MONDO,disease,DISEASE_6465
6466,6466,6466,6466,6466,6466,6466,6466,MONDO:0012251,MEDNIK syndrome,MONDO,disease,DISEASE_6466
6467,6467,6467,6467,6467,6467,6467,6467,MONDO:0001566,hypercalcemia disease,MONDO,disease,DISEASE_6467
6468,6468,6468,6468,6468,6468,6468,6468,MONDO:0012233,obsolete Li-Fraumeni syndrome 2,MONDO,disease,DISEASE_6468
6469,6469,6469,6469,6469,6469,6469,6469,MONDO:0859185,neurodevelopmental disorder with hypotonia and dysmorphic facies,MONDO,disease,DISEASE_6469
6470,6470,6470,6470,6470,6470,6470,6470,MONDO:0021953,tuberculous fibrosis of lung,MONDO,disease,DISEASE_6470
6471,6471,6471,6471,6471,6471,6471,6471,MONDO:0975874,"neurodevelopmental disorder with dysmorphic facies, absent speech and ambulation, and brain abnormalities",MONDO,disease,DISEASE_6471
6472,6472,6472,6472,6472,6472,6472,6472,MONDO:0014414,STAT3-related early-onset multisystem autoimmune disease,MONDO,disease,DISEASE_6472
6473,6473,6473,6473,6473,6473,6473,6473,MONDO:0018936_MONDO:0020660,osteoblastoma,MONDO_grouped,disease,DISEASE_6473
6474,6474,6474,6474,6474,6474,6474,6474,MONDO:0019767,hamel cerebro-palato-cardiac syndrome,MONDO,disease,DISEASE_6474
6475,6475,6475,6475,6475,6475,6475,6475,MONDO:0015201_MONDO:0022457,ankyloblepharon filiforme-imperforate anus syndrome,MONDO_grouped,disease,DISEASE_6475
6476,6476,6476,6476,6476,6476,6476,6476,MONDO:0014141_MONDO:0013159_MONDO:0013160_MONDO:0013156_MONDO:0013155_MONDO:0033556,"muscular dystrophy-dystroglycanopathy (congenital with intellectual disability),",MONDO_grouped,disease,DISEASE_6476
6477,6477,6477,6477,6477,6477,6477,6477,MONDO:1010934_MONDO:1012849,"limb-girdle muscular dystrophy, SGCD-related, dog",MONDO_grouped,disease,DISEASE_6477
6478,6478,6478,6478,6478,6478,6478,6478,MONDO:0010385,X-linked lymphoproliferative disease due to XIAP deficiency,MONDO,disease,DISEASE_6478
6479,6479,6479,6479,6479,6479,6479,6479,MONDO:1011254_MONDO:1011264_MONDO:1011272_MONDO:1012685,"rod-cone dysplasia, PDE6A-related, dog",MONDO_grouped,disease,DISEASE_6479
6480,6480,6480,6480,6480,6480,6480,6480,MONDO:0004578,flat retinoschisis,MONDO,disease,DISEASE_6480
6481,6481,6481,6481,6481,6481,6481,6481,MONDO:0000704_MONDO:0002844,lymphocytic colitis,MONDO_grouped,disease,DISEASE_6481
6482,6482,6482,6482,6482,6482,6482,6482,MONDO:0002996,cavernous sinus meningioma,MONDO,disease,DISEASE_6482
6483,6483,6483,6483,6483,6483,6483,6483,MONDO:0010189,"vitiligo, progressive, with intellectual disability and urethral duplication",MONDO,disease,DISEASE_6483
6484,6484,6484,6484,6484,6484,6484,6484,MONDO:0858999,KDM3B-related intellectual disability-facial dysmorphism-short stature syndrome,MONDO,disease,DISEASE_6484
6485,6485,6485,6485,6485,6485,6485,6485,MONDO:0003005,macular retinal edema,MONDO,disease,DISEASE_6485
6486,6486,6486,6486,6486,6486,6486,6486,MONDO:0000030,sleep-related hypermotor epilepsy,MONDO,disease,DISEASE_6486
6487,6487,6487,6487,6487,6487,6487,6487,MONDO:0015256,blepharoptosis-cleft palate-ectrodactyly-dental anomalies syndrome,MONDO,disease,DISEASE_6487
6488,6488,6488,6488,6488,6488,6488,6488,MONDO:0005156,encephalomyelitis,MONDO,disease,DISEASE_6488
6489,6489,6489,6489,6489,6489,6489,6489,MONDO:0100433_MONDO:0018795,ACTB-associated syndromic thrombocytopenia,MONDO_grouped,disease,DISEASE_6489
6490,6490,6490,6490,6490,6490,6490,6490,MONDO:0008731,familial adrenal hypoplasia with absent pituitary luteinizing hormone,MONDO,disease,DISEASE_6490
6491,6491,6491,6491,6491,6491,6491,6491,MONDO:0018572,severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome,MONDO,disease,DISEASE_6491
6492,6492,6492,6492,6492,6492,6492,6492,MONDO:0001257,retinal microaneurysm,MONDO,disease,DISEASE_6492
6493,6493,6493,6493,6493,6493,6493,6493,MONDO:1011336,"nervous system disorder, non-human animal",MONDO,disease,DISEASE_6493
6494,6494,6494,6494,6494,6494,6494,6494,MONDO:0019430,X-linked intellectual disability-ataxia-apraxia syndrome,MONDO,disease,DISEASE_6494
6495,6495,6495,6495,6495,6495,6495,6495,MONDO:0015768,trisomy 5p,MONDO,disease,DISEASE_6495
6496,6496,6496,6496,6496,6496,6496,6496,MONDO:0024569_MONDO:0014571_MONDO:0009786_MONDO:0957978_MONDO:0008133_MONDO:0957935_MONDO:0012543_MONDO:0033549_MONDO:0015011_MONDO:0957824_MONDO:0010698_MONDO:0003608_MONDO:0011536,optic atrophy,MONDO_grouped,disease,DISEASE_6496
6497,6497,6497,6497,6497,6497,6497,6497,MONDO:0015437,ring chromosome 21,MONDO,disease,DISEASE_6497
6498,6498,6498,6498,6498,6498,6498,6498,MONDO:1010202,"myotubular myopathy 1, non-human animal",MONDO,disease,DISEASE_6498
6499,6499,6499,6499,6499,6499,6499,6499,MONDO:0016350,hydrocephalus-blue sclerae-nephropathy syndrome,MONDO,disease,DISEASE_6499
6500,6500,6500,6500,6500,6500,6500,6500,MONDO:0020476,mesial temporal lobe epilepsy with hippocampal sclerosis,MONDO,disease,DISEASE_6500
6501,6501,6501,6501,6501,6501,6501,6501,MONDO:0009983,retinitis pigmentosa-intellectual disability-deafness-hypogenitalism syndrome,MONDO,disease,DISEASE_6501
6502,6502,6502,6502,6502,6502,6502,6502,MONDO:0007386,obsolete human coronavirus sensitivity,MONDO,disease,DISEASE_6502
6503,6503,6503,6503,6503,6503,6503,6503,MONDO:1010773,"pemphigus, domestic cat",MONDO,disease,DISEASE_6503
6504,6504,6504,6504,6504,6504,6504,6504,MONDO:0016560,ptosis-syndactyly-learning difficulties syndrome,MONDO,disease,DISEASE_6504
6505,6505,6505,6505,6505,6505,6505,6505,MONDO:0006579,melanoacanthoma,MONDO,disease,DISEASE_6505
6506,6506,6506,6506,6506,6506,6506,6506,MONDO:0012345,acral peeling skin syndrome,MONDO,disease,DISEASE_6506
6507,6507,6507,6507,6507,6507,6507,6507,MONDO:0002658,iris cancer,MONDO,disease,DISEASE_6507
6508,6508,6508,6508,6508,6508,6508,6508,MONDO:0007896_MONDO:0004600_MONDO:0017893_MONDO:0000875_MONDO:0700193,acute monocytic leukemia,MONDO_grouped,disease,DISEASE_6508
6509,6509,6509,6509,6509,6509,6509,6509,MONDO:0008613,Tuftsin deficiency,MONDO,disease,DISEASE_6509
6510,6510,6510,6510,6510,6510,6510,6510,MONDO:0015333,progeroid syndrome,MONDO,disease,DISEASE_6510
6511,6511,6511,6511,6511,6511,6511,6511,MONDO:1011837_MONDO:1011854,"cerebellar disease, non-human animal",MONDO_grouped,disease,DISEASE_6511
6512,6512,6512,6512,6512,6512,6512,6512,MONDO:0006558,pemphigoid gestationis,MONDO,disease,DISEASE_6512
6513,6513,6513,6513,6513,6513,6513,6513,MONDO:0000266,pulmonary aspergilloma,MONDO,disease,DISEASE_6513
6514,6514,6514,6514,6514,6514,6514,6514,MONDO:1011752,"nasal parakeratosis, non-human animal",MONDO,disease,DISEASE_6514
6515,6515,6515,6515,6515,6515,6515,6515,MONDO:1012599_MONDO:1012744_MONDO:1012745,"autosomal recessive cystinuria, SLC3A1-related, dog",MONDO_grouped,disease,DISEASE_6515
6516,6516,6516,6516,6516,6516,6516,6516,MONDO:0002025,psychiatric disorder,MONDO,disease,DISEASE_6516
6517,6517,6517,6517,6517,6517,6517,6517,MONDO:0007737,humeroradial synostosis,MONDO,disease,DISEASE_6517
6518,6518,6518,6518,6518,6518,6518,6518,MONDO:0004432,mature pericardial teratoma,MONDO,disease,DISEASE_6518
6519,6519,6519,6519,6519,6519,6519,6519,MONDO:0008299,posterior column ataxia,MONDO,disease,DISEASE_6519
6520,6520,6520,6520,6520,6520,6520,6520,MONDO:0010435_MONDO:0010693_MONDO:0010369,"nystagmus 6, congenital, X-linked",MONDO_grouped,disease,DISEASE_6520
6521,6521,6521,6521,6521,6521,6521,6521,MONDO:0015517,common variable immunodeficiency,MONDO,disease,DISEASE_6521
6522,6522,6522,6522,6522,6522,6522,6522,MONDO:1011725,"immunoglobulin 7S deficiency, non-human animal",MONDO,disease,DISEASE_6522
6523,6523,6523,6523,6523,6523,6523,6523,MONDO:0043251,odontoma,MONDO,disease,DISEASE_6523
6524,6524,6524,6524,6524,6524,6524,6524,MONDO:0016967,partial duplication of the long arm of chromosome 17,MONDO,disease,DISEASE_6524
6525,6525,6525,6525,6525,6525,6525,6525,MONDO:0009336,"hemosiderosis, pulmonary, with deficiency of gamma-a globulin",MONDO,disease,DISEASE_6525
6526,6526,6526,6526,6526,6526,6526,6526,MONDO:0011712_MONDO:0007333_MONDO:0019508,van der Woude syndrome,MONDO_grouped,disease,DISEASE_6526
6527,6527,6527,6527,6527,6527,6527,6527,MONDO:0012072_MONDO:0007906,"familial partial lipodystrophy, Kobberling type",MONDO_grouped,disease,DISEASE_6527
6528,6528,6528,6528,6528,6528,6528,6528,MONDO:0859216,"neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis",MONDO,disease,DISEASE_6528
6529,6529,6529,6529,6529,6529,6529,6529,MONDO:0100154_MONDO:0700044,TUBB3-related tubulinopathy,MONDO_grouped,disease,DISEASE_6529
6530,6530,6530,6530,6530,6530,6530,6530,MONDO:0024290,enuresis,MONDO,disease,DISEASE_6530
6531,6531,6531,6531,6531,6531,6531,6531,MONDO:0004948_MONDO:0004963_MONDO:0004947,B-cell chronic lymphocytic leukemia,MONDO_grouped,disease,DISEASE_6531
6532,6532,6532,6532,6532,6532,6532,6532,MONDO:0001376,urinary bladder anterior wall cancer,MONDO,disease,DISEASE_6532
6533,6533,6533,6533,6533,6533,6533,6533,MONDO:0002425,rectosigmoid junction cancer,MONDO,disease,DISEASE_6533
6534,6534,6534,6534,6534,6534,6534,6534,MONDO:0004196,rectal sarcomatoid carcinoma,MONDO,disease,DISEASE_6534
6535,6535,6535,6535,6535,6535,6535,6535,MONDO:0030024,neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities,MONDO,disease,DISEASE_6535
6536,6536,6536,6536,6536,6536,6536,6536,MONDO:0020594,abducens nerve disorder,MONDO,disease,DISEASE_6536
6537,6537,6537,6537,6537,6537,6537,6537,MONDO:0014502,Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency,MONDO,disease,DISEASE_6537
6538,6538,6538,6538,6538,6538,6538,6538,MONDO:0035370,ALPI-related inflammatory bowel disease,MONDO,disease,DISEASE_6538
6539,6539,6539,6539,6539,6539,6539,6539,MONDO:0858944,myxoid glioneuronal tumor,MONDO,disease,DISEASE_6539
6540,6540,6540,6540,6540,6540,6540,6540,MONDO:0013713_MONDO:0800426,"dengue virus, susceptibility to",MONDO_grouped,disease,DISEASE_6540
6541,6541,6541,6541,6541,6541,6541,6541,MONDO:0007945,"mannose 6-phosphate receptor recognition defect, Lebanese type",MONDO,disease,DISEASE_6541
6542,6542,6542,6542,6542,6542,6542,6542,MONDO:0000288,polycystic echinococcosis,MONDO,disease,DISEASE_6542
6543,6543,6543,6543,6543,6543,6543,6543,MONDO:0011970,rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome,MONDO,disease,DISEASE_6543
6544,6544,6544,6544,6544,6544,6544,6544,MONDO:0027667_MONDO:0027687,efavirenz toxicity,MONDO_grouped,disease,DISEASE_6544
6545,6545,6545,6545,6545,6545,6545,6545,MONDO:0018486,visual snow syndrome,MONDO,disease,DISEASE_6545
6546,6546,6546,6546,6546,6546,6546,6546,MONDO:0011176,intestinal hypomagnesemia 1,MONDO,disease,DISEASE_6546
6547,6547,6547,6547,6547,6547,6547,6547,MONDO:0021052,parasympathetic paraganglioma,MONDO,disease,DISEASE_6547
6548,6548,6548,6548,6548,6548,6548,6548,MONDO:0032882,Heyn-Sproul-Jackson syndrome,MONDO,disease,DISEASE_6548
6549,6549,6549,6549,6549,6549,6549,6549,MONDO:0016510,epibulbar lipodermoid-preauricular appendage-polythelia syndrome,MONDO,disease,DISEASE_6549
6550,6550,6550,6550,6550,6550,6550,6550,MONDO:0006140,"cervical mucinous adenocarcinoma, minimal deviation variant",MONDO,disease,DISEASE_6550
6551,6551,6551,6551,6551,6551,6551,6551,MONDO:0017851_MONDO:0019270,erythrokeratodermia variabilis,MONDO_grouped,disease,DISEASE_6551
6552,6552,6552,6552,6552,6552,6552,6552,MONDO:0007241,"bundle branch block, familial isolated complete right",MONDO,disease,DISEASE_6552
6553,6553,6553,6553,6553,6553,6553,6553,MONDO:0022020,Boudhina Yedes Khiari syndrome,MONDO,disease,DISEASE_6553
6554,6554,6554,6554,6554,6554,6554,6554,MONDO:0024302_MONDO:0024303,internal hirudiniasis,MONDO_grouped,disease,DISEASE_6554
6555,6555,6555,6555,6555,6555,6555,6555,MONDO:0005982,tinea infection,MONDO,disease,DISEASE_6555
6556,6556,6556,6556,6556,6556,6556,6556,MONDO:0014573_MONDO:0007204_MONDO:0016085,Cole-Carpenter syndrome,MONDO_grouped,disease,DISEASE_6556
6557,6557,6557,6557,6557,6557,6557,6557,MONDO:0010843_MONDO:0012168_MONDO:0007487_MONDO:0010348_MONDO:0011418_MONDO:0011689_MONDO:0011747_MONDO:0800429_MONDO:0800430,"dyslexia, susceptibility to",MONDO_grouped,disease,DISEASE_6557
6558,6558,6558,6558,6558,6558,6558,6558,MONDO:0044738,Gabriele de Vries syndrome,MONDO,disease,DISEASE_6558
6559,6559,6559,6559,6559,6559,6559,6559,MONDO:0009130,Dyggve-Melchior-Clausen disease,MONDO,disease,DISEASE_6559
6560,6560,6560,6560,6560,6560,6560,6560,MONDO:0001887,Allen-Masters syndrome,MONDO,disease,DISEASE_6560
6561,6561,6561,6561,6561,6561,6561,6561,MONDO:0019195,hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome,MONDO,disease,DISEASE_6561
6562,6562,6562,6562,6562,6562,6562,6562,MONDO:0007956,Pai syndrome,MONDO,disease,DISEASE_6562
6563,6563,6563,6563,6563,6563,6563,6563,MONDO:0020552,placental site trophoblastic tumor,MONDO,disease,DISEASE_6563
6564,6564,6564,6564,6564,6564,6564,6564,MONDO:0022576,bilirubin induced brain injury in the newborn,MONDO,disease,DISEASE_6564
6565,6565,6565,6565,6565,6565,6565,6565,MONDO:0017767,rheumatic fever,MONDO,disease,DISEASE_6565
6566,6566,6566,6566,6566,6566,6566,6566,MONDO:0600010_MONDO:0600011,moderate hypophosphatasia,MONDO_grouped,disease,DISEASE_6566
6567,6567,6567,6567,6567,6567,6567,6567,MONDO:0007673,Glucoglycinuria,MONDO,disease,DISEASE_6567
6568,6568,6568,6568,6568,6568,6568,6568,MONDO:0006688,byssinosis,MONDO,disease,DISEASE_6568
6569,6569,6569,6569,6569,6569,6569,6569,MONDO:0006018,Wissler syndrome,MONDO,disease,DISEASE_6569
6570,6570,6570,6570,6570,6570,6570,6570,MONDO:1012219,"polycystic mononephrosis, dog",MONDO,disease,DISEASE_6570
6571,6571,6571,6571,6571,6571,6571,6571,MONDO:0006767,gastric antral vascular ectasia,MONDO,disease,DISEASE_6571
6572,6572,6572,6572,6572,6572,6572,6572,MONDO:0024359,central sleep apnea due to periodic breathing,MONDO,disease,DISEASE_6572
6573,6573,6573,6573,6573,6573,6573,6573,MONDO:0027029,HHV-6 encephalitis,MONDO,disease,DISEASE_6573
6574,6574,6574,6574,6574,6574,6574,6574,MONDO:0006041,lung carcinoid tumor,MONDO,disease,DISEASE_6574
6575,6575,6575,6575,6575,6575,6575,6575,MONDO:0013122_MONDO:0014998_MONDO:0013121,"glaucoma 3, primary congenital",MONDO_grouped,disease,DISEASE_6575
6576,6576,6576,6576,6576,6576,6576,6576,MONDO:0010720,partial androgen insensitivity syndrome,MONDO,disease,DISEASE_6576
6577,6577,6577,6577,6577,6577,6577,6577,MONDO:0009370_MONDO:0016001_MONDO:1011018_MONDO:1011019,L-2-hydroxyglutaric aciduria,MONDO_grouped,disease,DISEASE_6577
6578,6578,6578,6578,6578,6578,6578,6578,MONDO:0007923,"macrocephaly, benign familial",MONDO,disease,DISEASE_6578
6579,6579,6579,6579,6579,6579,6579,6579,MONDO:0002581_MONDO:0100067,spindle cell rhabdomyosarcoma,MONDO_grouped,disease,DISEASE_6579
6580,6580,6580,6580,6580,6580,6580,6580,MONDO:0001859,algoneurodystrophy,MONDO,disease,DISEASE_6580
6581,6581,6581,6581,6581,6581,6581,6581,MONDO:0004703,bladder carcinoma in situ,MONDO,disease,DISEASE_6581
6582,6582,6582,6582,6582,6582,6582,6582,MONDO:0003110,skin hemangioma,MONDO,disease,DISEASE_6582
6583,6583,6583,6583,6583,6583,6583,6583,MONDO:1011530_MONDO:1011531_MONDO:1012109_MONDO:1011534_MONDO:1012110_MONDO:1012111_MONDO:1012112_MONDO:1012113,"hyperadrenocorticism, dog",MONDO_grouped,disease,DISEASE_6583
6584,6584,6584,6584,6584,6584,6584,6584,MONDO:0020332,systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease,MONDO,disease,DISEASE_6584
6585,6585,6585,6585,6585,6585,6585,6585,MONDO:1010012_MONDO:1010453,"conotruncal heart malformations, non-human animal",MONDO_grouped,disease,DISEASE_6585
6586,6586,6586,6586,6586,6586,6586,6586,MONDO:0054701_MONDO:0027407_MONDO:0012455,Kleefstra syndrome,MONDO_grouped,disease,DISEASE_6586
6587,6587,6587,6587,6587,6587,6587,6587,MONDO:0006827,lateral medullary syndrome,MONDO,disease,DISEASE_6587
6588,6588,6588,6588,6588,6588,6588,6588,MONDO:0024562_MONDO:0859173_MONDO:0001823,sick sinus syndrome,MONDO_grouped,disease,DISEASE_6588
6589,6589,6589,6589,6589,6589,6589,6589,MONDO:0024639,gastric enterochromaffin cell serotonin-producing neuroendocrine tumor,MONDO,disease,DISEASE_6589
6590,6590,6590,6590,6590,6590,6590,6590,MONDO:0859196,"Usmani-Riazuddin syndrome, autosomal recessive",MONDO,disease,DISEASE_6590
6591,6591,6591,6591,6591,6591,6591,6591,MONDO:0016290,Hernández-Aguirre Negrete syndrome,MONDO,disease,DISEASE_6591
6592,6592,6592,6592,6592,6592,6592,6592,MONDO:0001508,patulous eustachian tube,MONDO,disease,DISEASE_6592
6593,6593,6593,6593,6593,6593,6593,6593,MONDO:0700011,chromosome 4 disorder,MONDO,disease,DISEASE_6593
6594,6594,6594,6594,6594,6594,6594,6594,MONDO:0009950,pyruvate kinase deficiency of red cells,MONDO,disease,DISEASE_6594
6595,6595,6595,6595,6595,6595,6595,6595,MONDO:1012974,"hyperbilirubinemia, non-human animal",MONDO,disease,DISEASE_6595
6596,6596,6596,6596,6596,6596,6596,6596,MONDO:0011316,"osteosclerotic chondrodysplasia, lethal, with intracellular inclusions",MONDO,disease,DISEASE_6596
6597,6597,6597,6597,6597,6597,6597,6597,MONDO:0008022,"muscle cramps, familial",MONDO,disease,DISEASE_6597
6598,6598,6598,6598,6598,6598,6598,6598,MONDO:0011059,holoprosencephaly-craniosynostosis syndrome,MONDO,disease,DISEASE_6598
6599,6599,6599,6599,6599,6599,6599,6599,MONDO:1011683,"caprine-like generalized hypoplasia syndrome, non-human animal",MONDO,disease,DISEASE_6599
6600,6600,6600,6600,6600,6600,6600,6600,MONDO:0019611,TSH-secreting pituitary adenoma,MONDO,disease,DISEASE_6600
6601,6601,6601,6601,6601,6601,6601,6601,MONDO:0004799,ulcerative blepharitis,MONDO,disease,DISEASE_6601
6602,6602,6602,6602,6602,6602,6602,6602,MONDO:0002238,ascending colon cancer,MONDO,disease,DISEASE_6602
6603,6603,6603,6603,6603,6603,6603,6603,MONDO:0008877,blue diaper syndrome,MONDO,disease,DISEASE_6603
6604,6604,6604,6604,6604,6604,6604,6604,MONDO:0004014,ethmoid sinus ectopic meningioma,MONDO,disease,DISEASE_6604
6605,6605,6605,6605,6605,6605,6605,6605,MONDO:0017677,focal acral hyperkeratosis,MONDO,disease,DISEASE_6605
6606,6606,6606,6606,6606,6606,6606,6606,MONDO:0016641,limb transversal defect-cardiac anomaly syndrome,MONDO,disease,DISEASE_6606
6607,6607,6607,6607,6607,6607,6607,6607,MONDO:0006509_MONDO:0002533_MONDO:0002512_MONDO:0003462,papillary carcinoma,MONDO_grouped,disease,DISEASE_6607
6608,6608,6608,6608,6608,6608,6608,6608,MONDO:0011381,dominant beta-thalassemia,MONDO,disease,DISEASE_6608
6609,6609,6609,6609,6609,6609,6609,6609,MONDO:0000667_MONDO:0000684,auditory agnosia,MONDO_grouped,disease,DISEASE_6609
6610,6610,6610,6610,6610,6610,6610,6610,MONDO:0002145,disorder of sexual differentiation,MONDO,disease,DISEASE_6610
6611,6611,6611,6611,6611,6611,6611,6611,MONDO:0008525_MONDO:0020509_MONDO:0020508_MONDO:0017987_MONDO:1011001_MONDO:1011002,"syringomyelia, isolated",MONDO_grouped,disease,DISEASE_6611
6612,6612,6612,6612,6612,6612,6612,6612,MONDO:0016438,linear focal dermal elastosis,MONDO,disease,DISEASE_6612
6613,6613,6613,6613,6613,6613,6613,6613,MONDO:0013660,"arthrogryposis, Perthes disease, and upward gaze palsy",MONDO,disease,DISEASE_6613
6614,6614,6614,6614,6614,6614,6614,6614,MONDO:0014558,autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome,MONDO,disease,DISEASE_6614
6615,6615,6615,6615,6615,6615,6615,6615,MONDO:1012775,"cancer, RUNX-related, pig",MONDO,disease,DISEASE_6615
6616,6616,6616,6616,6616,6616,6616,6616,MONDO:0020773,cerebrospinal fluid rhinorrhea,MONDO,disease,DISEASE_6616
6617,6617,6617,6617,6617,6617,6617,6617,MONDO:0008686,isolated familial wooly hair disorder,MONDO,disease,DISEASE_6617
6618,6618,6618,6618,6618,6618,6618,6618,MONDO:0002899,differentiating neuroblastoma,MONDO,disease,DISEASE_6618
6619,6619,6619,6619,6619,6619,6619,6619,MONDO:1010156,"brachydactyly, non-human animal",MONDO,disease,DISEASE_6619
6620,6620,6620,6620,6620,6620,6620,6620,MONDO:0003429_MONDO:0017825_MONDO:0017826,functioning pituitary gland adenoma,MONDO_grouped,disease,DISEASE_6620
6621,6621,6621,6621,6621,6621,6621,6621,MONDO:1012223,"progressive axonopathy, dog",MONDO,disease,DISEASE_6621
6622,6622,6622,6622,6622,6622,6622,6622,MONDO:1010702,"pyruvate kinase deficiency of erythrocyte, domestic cat",MONDO,disease,DISEASE_6622
6623,6623,6623,6623,6623,6623,6623,6623,MONDO:0012550,iris pattern,MONDO,disease,DISEASE_6623
6624,6624,6624,6624,6624,6624,6624,6624,MONDO:0017943,autoerythrocyte sensitization syndrome,MONDO,disease,DISEASE_6624
6625,6625,6625,6625,6625,6625,6625,6625,MONDO:0013352,intellectual disability-severe speech delay-mild dysmorphism syndrome,MONDO,disease,DISEASE_6625
6626,6626,6626,6626,6626,6626,6626,6626,MONDO:1011189_MONDO:1011190,"spinal stenosis, dog",MONDO_grouped,disease,DISEASE_6626
6627,6627,6627,6627,6627,6627,6627,6627,MONDO:0018071,trisomy 18,MONDO,disease,DISEASE_6627
6628,6628,6628,6628,6628,6628,6628,6628,MONDO:0043247,Mallory-Weiss syndrome,MONDO,disease,DISEASE_6628
6629,6629,6629,6629,6629,6629,6629,6629,MONDO:0006946,renal osteodystrophy,MONDO,disease,DISEASE_6629
6630,6630,6630,6630,6630,6630,6630,6630,MONDO:0016965,partial duplication of the long arm of chromosome 15,MONDO,disease,DISEASE_6630
6631,6631,6631,6631,6631,6631,6631,6631,MONDO:0005059,leukemia,MONDO,disease,DISEASE_6631
6632,6632,6632,6632,6632,6632,6632,6632,MONDO:0035774,NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance,MONDO,disease,DISEASE_6632
6633,6633,6633,6633,6633,6633,6633,6633,MONDO:0003908_MONDO:0004503_MONDO:0004511,clivus meningioma,MONDO_grouped,disease,DISEASE_6633
6634,6634,6634,6634,6634,6634,6634,6634,MONDO:0009588,Langer mesomelic dysplasia,MONDO,disease,DISEASE_6634
6635,6635,6635,6635,6635,6635,6635,6635,MONDO:0014628_MONDO:0014204_MONDO:0024538_MONDO:0014004_MONDO:0007247,"basal ganglia calcification, idiopathic",MONDO_grouped,disease,DISEASE_6635
6636,6636,6636,6636,6636,6636,6636,6636,MONDO:0030987,"vertebral, cardiac, tracheoesophageal, renal, and limb defects",MONDO,disease,DISEASE_6636
6637,6637,6637,6637,6637,6637,6637,6637,MONDO:0021459,benign neoplasm of esophagus,MONDO,disease,DISEASE_6637
6638,6638,6638,6638,6638,6638,6638,6638,MONDO:0024276,glandular cell neoplasm,MONDO,disease,DISEASE_6638
6639,6639,6639,6639,6639,6639,6639,6639,MONDO:0025159,"pneumonia of swine, mycoplasmal",MONDO,disease,DISEASE_6639
6640,6640,6640,6640,6640,6640,6640,6640,MONDO:0035437,CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome,MONDO,disease,DISEASE_6640
6641,6641,6641,6641,6641,6641,6641,6641,MONDO:0015757,lymphoid hemopathy,MONDO,disease,DISEASE_6641
6642,6642,6642,6642,6642,6642,6642,6642,MONDO:0017985,congenital radioulnar synostosis,MONDO,disease,DISEASE_6642
6643,6643,6643,6643,6643,6643,6643,6643,MONDO:0024265,Duane syndrome type 1,MONDO,disease,DISEASE_6643
6644,6644,6644,6644,6644,6644,6644,6644,MONDO:0006401,salivary gland adenosquamous carcinoma,MONDO,disease,DISEASE_6644
6645,6645,6645,6645,6645,6645,6645,6645,MONDO:0003092,lacrimal gland mucoepidermoid carcinoma,MONDO,disease,DISEASE_6645
6646,6646,6646,6646,6646,6646,6646,6646,MONDO:1012876_MONDO:1012884,"Parkinson disease, PINK1-related, rhesus monkey",MONDO_grouped,disease,DISEASE_6646
6647,6647,6647,6647,6647,6647,6647,6647,MONDO:0013625_MONDO:0014604_MONDO:0006966_MONDO:0005180_MONDO:0010796_MONDO:0010360_MONDO:0011737_MONDO:0013167,Parkinson disease,MONDO_grouped,disease,DISEASE_6647
6648,6648,6648,6648,6648,6648,6648,6648,MONDO:0021461,benign neoplasm of hypopharynx,MONDO,disease,DISEASE_6648
6649,6649,6649,6649,6649,6649,6649,6649,MONDO:0850371,nonobstructive coronary artery disease,MONDO,disease,DISEASE_6649
6650,6650,6650,6650,6650,6650,6650,6650,MONDO:0021412,polyp of maxillary sinus,MONDO,disease,DISEASE_6650
6651,6651,6651,6651,6651,6651,6651,6651,MONDO:0043106,ichthyosis linearis circumflexa,MONDO,disease,DISEASE_6651
6652,6652,6652,6652,6652,6652,6652,6652,MONDO:1012888,"spinal muscular atrophy, LIX1-related, domestic cat",MONDO,disease,DISEASE_6652
6653,6653,6653,6653,6653,6653,6653,6653,MONDO:0003991,villoglandular endometrial endometrioid adenocarcinoma,MONDO,disease,DISEASE_6653
6654,6654,6654,6654,6654,6654,6654,6654,MONDO:0004429_MONDO:0024663,skin meningioma,MONDO_grouped,disease,DISEASE_6654
6655,6655,6655,6655,6655,6655,6655,6655,MONDO:0019435_MONDO:0018456_MONDO:0023249,rheumatoid factor-positive polyarticular juvenile idiopathic arthritis,MONDO_grouped,disease,DISEASE_6655
6656,6656,6656,6656,6656,6656,6656,6656,MONDO:0001496,male genital organ stricture,MONDO,disease,DISEASE_6656
6657,6657,6657,6657,6657,6657,6657,6657,MONDO:0013341,methylmalonic acidemia due to transcobalamin receptor defect,MONDO,disease,DISEASE_6657
6658,6658,6658,6658,6658,6658,6658,6658,MONDO:0008842,"ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia",MONDO,disease,DISEASE_6658
6659,6659,6659,6659,6659,6659,6659,6659,MONDO:0016818,Mikati-Najjar-Sahli syndrome,MONDO,disease,DISEASE_6659
6660,6660,6660,6660,6660,6660,6660,6660,MONDO:1010932,"congenital myasthenic syndrome, COLQ-related, dog",MONDO,disease,DISEASE_6660
6661,6661,6661,6661,6661,6661,6661,6661,MONDO:0002110,adrenal rest tumor,MONDO,disease,DISEASE_6661
6662,6662,6662,6662,6662,6662,6662,6662,MONDO:0008273,actinic prurigo,MONDO,disease,DISEASE_6662
6663,6663,6663,6663,6663,6663,6663,6663,MONDO:0000429_MONDO:0000426,autosomal genetic disease,MONDO_grouped,disease,DISEASE_6663
6664,6664,6664,6664,6664,6664,6664,6664,MONDO:0005460,swine influenza,MONDO,disease,DISEASE_6664
6665,6665,6665,6665,6665,6665,6665,6665,MONDO:0850053,F12-associated cold autoinflammatory syndrome,MONDO,disease,DISEASE_6665
6666,6666,6666,6666,6666,6666,6666,6666,MONDO:0010124,"thumb, distal hyperextensibility of",MONDO,disease,DISEASE_6666
6667,6667,6667,6667,6667,6667,6667,6667,MONDO:0010732,spastic paraparesis-deafness syndrome,MONDO,disease,DISEASE_6667
6668,6668,6668,6668,6668,6668,6668,6668,MONDO:0001207,neonatal respiratory failure,MONDO,disease,DISEASE_6668
6669,6669,6669,6669,6669,6669,6669,6669,MONDO:0007260,Car factor deficiency,MONDO,disease,DISEASE_6669
6670,6670,6670,6670,6670,6670,6670,6670,MONDO:0016588,infantile mercury poisoning,MONDO,disease,DISEASE_6670
6671,6671,6671,6671,6671,6671,6671,6671,MONDO:0035696,incomplete septal cirrhosis,MONDO,disease,DISEASE_6671
6672,6672,6672,6672,6672,6672,6672,6672,MONDO:0007869,Kyrle disease,MONDO,disease,DISEASE_6672
6673,6673,6673,6673,6673,6673,6673,6673,MONDO:0006460_MONDO:0008565,thyroglossal duct cyst,MONDO_grouped,disease,DISEASE_6673
6674,6674,6674,6674,6674,6674,6674,6674,MONDO:0035312,fibrohistiocytic inflammatory pseudotumor of the liver,MONDO,disease,DISEASE_6674
6675,6675,6675,6675,6675,6675,6675,6675,MONDO:0010380,"cataract, ataxia, short stature, and intellectual disability",MONDO,disease,DISEASE_6675
6676,6676,6676,6676,6676,6676,6676,6676,MONDO:0012504,camptodactyly-tall stature-scoliosis-hearing loss syndrome,MONDO,disease,DISEASE_6676
6677,6677,6677,6677,6677,6677,6677,6677,MONDO:0008806,Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome,MONDO,disease,DISEASE_6677
6678,6678,6678,6678,6678,6678,6678,6678,MONDO:0002630,small cell osteogenic sarcoma,MONDO,disease,DISEASE_6678
6679,6679,6679,6679,6679,6679,6679,6679,MONDO:0006182,digestive system mixed adenoneuroendocrine carcinoma,MONDO,disease,DISEASE_6679
6680,6680,6680,6680,6680,6680,6680,6680,MONDO:0022034,lentivirus infection,MONDO,disease,DISEASE_6680
6681,6681,6681,6681,6681,6681,6681,6681,MONDO:1011045,"nephritis, dog",MONDO,disease,DISEASE_6681
6682,6682,6682,6682,6682,6682,6682,6682,MONDO:0001541_MONDO:0006940,plantar nerve lesion,MONDO_grouped,disease,DISEASE_6682
6683,6683,6683,6683,6683,6683,6683,6683,MONDO:0009866,"phosphoenolpyruvate carboxykinase deficiency, cytosolic",MONDO,disease,DISEASE_6683
6684,6684,6684,6684,6684,6684,6684,6684,MONDO:0017287,IgG4-related disease,MONDO,disease,DISEASE_6684
6685,6685,6685,6685,6685,6685,6685,6685,MONDO:0957981,immunodeficiency 115 with autoinflammation,MONDO,disease,DISEASE_6685
6686,6686,6686,6686,6686,6686,6686,6686,MONDO:1012628,"X-linked progressive retinal atrophy 1, RPGR-related, dog",MONDO,disease,DISEASE_6686
6687,6687,6687,6687,6687,6687,6687,6687,MONDO:0005429,prion disease,MONDO,disease,DISEASE_6687
6688,6688,6688,6688,6688,6688,6688,6688,MONDO:1011917,"idiopathic hypercalciuria, non-human animal",MONDO,disease,DISEASE_6688
6689,6689,6689,6689,6689,6689,6689,6689,MONDO:0021497,benign neoplasm of cerebrum,MONDO,disease,DISEASE_6689
6690,6690,6690,6690,6690,6690,6690,6690,MONDO:0007800,chromosome 18p deletion syndrome,MONDO,disease,DISEASE_6690
6691,6691,6691,6691,6691,6691,6691,6691,MONDO:0002627,chondroblastic osteosarcoma,MONDO,disease,DISEASE_6691
6692,6692,6692,6692,6692,6692,6692,6692,MONDO:0018091,microcephaly-brachydactyly-kyphoscoliosis syndrome,MONDO,disease,DISEASE_6692
6693,6693,6693,6693,6693,6693,6693,6693,MONDO:0003830_MONDO:0003831,type 1 papillary adenoma of the kidney,MONDO_grouped,disease,DISEASE_6693
6694,6694,6694,6694,6694,6694,6694,6694,MONDO:1010242,"Alexander disease, non-human animal",MONDO,disease,DISEASE_6694
6695,6695,6695,6695,6695,6695,6695,6695,MONDO:0014732_MONDO:0958018_MONDO:0012905_MONDO:0054791_MONDO:0014813_MONDO:0032730_MONDO:0009843_MONDO:0033486_MONDO:0054817_MONDO:0012125_MONDO:0014632_MONDO:0025701_MONDO:0030263_MONDO:0012514_MONDO:0033657_MONDO:0014506_MONDO:0859242_MONDO:0014666_MONDO:0054782_MONDO:0859378_MONDO:0012824_MONDO:0975833_MONDO:1012539,hypomyelinating leukodystrophy,MONDO_grouped,disease,DISEASE_6695
6696,6696,6696,6696,6696,6696,6696,6696,MONDO:0042973,familial osteosclerosis,MONDO,disease,DISEASE_6696
6697,6697,6697,6697,6697,6697,6697,6697,MONDO:0024525_MONDO:0013247_MONDO:0014275_MONDO:0030056_MONDO:0001083,Fanconi renotubular syndrome,MONDO_grouped,disease,DISEASE_6697
6698,6698,6698,6698,6698,6698,6698,6698,MONDO:0043982,cubital tunnel syndrome,MONDO,disease,DISEASE_6698
6699,6699,6699,6699,6699,6699,6699,6699,MONDO:0006295,malignant urinary system neoplasm,MONDO,disease,DISEASE_6699
6700,6700,6700,6700,6700,6700,6700,6700,MONDO:0020761,Bowen disease of the skin,MONDO,disease,DISEASE_6700
6701,6701,6701,6701,6701,6701,6701,6701,MONDO:0001953,pyuria,MONDO,disease,DISEASE_6701
6702,6702,6702,6702,6702,6702,6702,6702,MONDO:0013946_MONDO:0012528_MONDO:0013915_MONDO:0013961_MONDO:0013913_MONDO:0030010_MONDO:0013914_MONDO:0030684_MONDO:0012880_MONDO:0009239_MONDO:0007844_MONDO:0013910_MONDO:0030534_MONDO:0014105_MONDO:0012988_MONDO:0009482_MONDO:0009223_MONDO:0007794_MONDO:0014461_MONDO:0014106_MONDO:0014107_MONDO:0014103_MONDO:0013911_MONDO:0013912_MONDO:0014102_MONDO:0010635_MONDO:0013926,hypogonadotropic hypogonadism 15 with or without anosmia,MONDO_grouped,disease,DISEASE_6702
6703,6703,6703,6703,6703,6703,6703,6703,MONDO:0005599,malignant epithelioid mesothelioma,MONDO,disease,DISEASE_6703
6704,6704,6704,6704,6704,6704,6704,6704,MONDO:0005323_MONDO:0021682,bacterial sexually transmitted disease,MONDO_grouped,disease,DISEASE_6704
6705,6705,6705,6705,6705,6705,6705,6705,MONDO:0010428,chromosome Xp11.23-p11.22 duplication syndrome,MONDO,disease,DISEASE_6705
6706,6706,6706,6706,6706,6706,6706,6706,MONDO:0007509_MONDO:0015024_MONDO:0032804,"ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant",MONDO_grouped,disease,DISEASE_6706
6707,6707,6707,6707,6707,6707,6707,6707,MONDO:0011615,East Texas bleeding disorder,MONDO,disease,DISEASE_6707
6708,6708,6708,6708,6708,6708,6708,6708,MONDO:1010578_MONDO:1010579_MONDO:1011605,"diabetes mellitus, cattle",MONDO_grouped,disease,DISEASE_6708
6709,6709,6709,6709,6709,6709,6709,6709,MONDO:0006678,bladder calculus,MONDO,disease,DISEASE_6709
6710,6710,6710,6710,6710,6710,6710,6710,MONDO:1011072,"urolithiasis, Red shanked douc langur",MONDO,disease,DISEASE_6710
6711,6711,6711,6711,6711,6711,6711,6711,MONDO:0009777,Oliver syndrome,MONDO,disease,DISEASE_6711
6712,6712,6712,6712,6712,6712,6712,6712,MONDO:0100180,"diabetes mellitus, ketosis-prone",MONDO,disease,DISEASE_6712
6713,6713,6713,6713,6713,6713,6713,6713,MONDO:0014801,even-plus syndrome,MONDO,disease,DISEASE_6713
6714,6714,6714,6714,6714,6714,6714,6714,MONDO:0014464,progressive encephalopathy with leukodystrophy due to DECR deficiency,MONDO,disease,DISEASE_6714
6715,6715,6715,6715,6715,6715,6715,6715,MONDO:1011659,"gastric dilatation volvulus syndrome, non-human animal",MONDO,disease,DISEASE_6715
6716,6716,6716,6716,6716,6716,6716,6716,MONDO:0044643,congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome,MONDO,disease,DISEASE_6716
6717,6717,6717,6717,6717,6717,6717,6717,MONDO:0017299,acute annular outer retinopathy,MONDO,disease,DISEASE_6717
6718,6718,6718,6718,6718,6718,6718,6718,MONDO:0015713,idiopathic central precocious puberty,MONDO,disease,DISEASE_6718
6719,6719,6719,6719,6719,6719,6719,6719,MONDO:0014355,"cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis",MONDO,disease,DISEASE_6719
6720,6720,6720,6720,6720,6720,6720,6720,MONDO:0002081_MONDO:0000637,musculoskeletal system disorder,MONDO_grouped,disease,DISEASE_6720
6721,6721,6721,6721,6721,6721,6721,6721,MONDO:0007912,lithium transport,MONDO,disease,DISEASE_6721
6722,6722,6722,6722,6722,6722,6722,6722,MONDO:0001011,breast cyst,MONDO,disease,DISEASE_6722
6723,6723,6723,6723,6723,6723,6723,6723,MONDO:0006227_MONDO:0024642,gastric neuroendocrine tumor,MONDO_grouped,disease,DISEASE_6723
6724,6724,6724,6724,6724,6724,6724,6724,MONDO:0971142,diffused pleural mesothelioma,MONDO,disease,DISEASE_6724
6725,6725,6725,6725,6725,6725,6725,6725,MONDO:0016259_MONDO:0016268_MONDO:0016271_MONDO:0016272,carcinosarcoma of the corpus uteri,MONDO_grouped,disease,DISEASE_6725
6726,6726,6726,6726,6726,6726,6726,6726,MONDO:0007505,"earring holes, natural",MONDO,disease,DISEASE_6726
6727,6727,6727,6727,6727,6727,6727,6727,MONDO:0024483_MONDO:0006483,urothelial hyperplasia,MONDO_grouped,disease,DISEASE_6727
6728,6728,6728,6728,6728,6728,6728,6728,MONDO:0030074_MONDO:0016763_MONDO:0008470,spondylometaphyseal dysplasia with corneal dystrophy,MONDO_grouped,disease,DISEASE_6728
6729,6729,6729,6729,6729,6729,6729,6729,MONDO:0015296,cardiac anomalies-heterotaxy syndrome,MONDO,disease,DISEASE_6729
6730,6730,6730,6730,6730,6730,6730,6730,MONDO:0015597,pustulosis palmaris et plantaris,MONDO,disease,DISEASE_6730
6731,6731,6731,6731,6731,6731,6731,6731,MONDO:0021324,malignant neoplasm of abdominal esophagus,MONDO,disease,DISEASE_6731
6732,6732,6732,6732,6732,6732,6732,6732,MONDO:0850152,auditory system benign neoplasm,MONDO,disease,DISEASE_6732
6733,6733,6733,6733,6733,6733,6733,6733,MONDO:0850292,subjective cognitive decline,MONDO,disease,DISEASE_6733
6734,6734,6734,6734,6734,6734,6734,6734,MONDO:0020575,polymorphic ventricular tachycardia,MONDO,disease,DISEASE_6734
6735,6735,6735,6735,6735,6735,6735,6735,MONDO:0025263,"strongyle infections, equine",MONDO,disease,DISEASE_6735
6736,6736,6736,6736,6736,6736,6736,6736,MONDO:0035460,idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunosuppressive therapy,MONDO,disease,DISEASE_6736
6737,6737,6737,6737,6737,6737,6737,6737,MONDO:0012239_MONDO:0008070_MONDO:0800341_MONDO:0859523,"congenital myopathy 4B, autosomal recessive",MONDO_grouped,disease,DISEASE_6737
6738,6738,6738,6738,6738,6738,6738,6738,MONDO:0009583,"blepharophimosis - intellectual disability syndrome, Ohdo type",MONDO,disease,DISEASE_6738
6739,6739,6739,6739,6739,6739,6739,6739,MONDO:0020070,neonatal epilepsy syndrome,MONDO,disease,DISEASE_6739
6740,6740,6740,6740,6740,6740,6740,6740,MONDO:0010426,X-linked endothelial corneal dystrophy,MONDO,disease,DISEASE_6740
6741,6741,6741,6741,6741,6741,6741,6741,MONDO:0007797,hypoparathyroidism-deafness-renal disease syndrome,MONDO,disease,DISEASE_6741
6742,6742,6742,6742,6742,6742,6742,6742,MONDO:0016691_MONDO:0004000_MONDO:0003999_MONDO:0016692,pilocytic astrocytoma,MONDO_grouped,disease,DISEASE_6742
6743,6743,6743,6743,6743,6743,6743,6743,MONDO:1010032,"Jacobsen syndrome, non-human animal",MONDO,disease,DISEASE_6743
6744,6744,6744,6744,6744,6744,6744,6744,MONDO:0035661,TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome,MONDO,disease,DISEASE_6744
6745,6745,6745,6745,6745,6745,6745,6745,MONDO:0043116,Iida Kannari syndrome,MONDO,disease,DISEASE_6745
6746,6746,6746,6746,6746,6746,6746,6746,MONDO:0043085,"chromosome 1, uniparental disomy 1q12 q21",MONDO,disease,DISEASE_6746
6747,6747,6747,6747,6747,6747,6747,6747,MONDO:0003448,benign spiradenoma,MONDO,disease,DISEASE_6747
6748,6748,6748,6748,6748,6748,6748,6748,MONDO:0007137,isolated congenital anosmia,MONDO,disease,DISEASE_6748
6749,6749,6749,6749,6749,6749,6749,6749,MONDO:0007480,dwarfism with stiff joints and ocular abnormalities,MONDO,disease,DISEASE_6749
6750,6750,6750,6750,6750,6750,6750,6750,MONDO:0019882,distal trisomy 8q,MONDO,disease,DISEASE_6750
6751,6751,6751,6751,6751,6751,6751,6751,MONDO:0013760,congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome,MONDO,disease,DISEASE_6751
6752,6752,6752,6752,6752,6752,6752,6752,MONDO:0003197,granular cell carcinoma,MONDO,disease,DISEASE_6752
6753,6753,6753,6753,6753,6753,6753,6753,MONDO:0017212,paraneoplastic uveitis,MONDO,disease,DISEASE_6753
6754,6754,6754,6754,6754,6754,6754,6754,MONDO:0957265,"congenital myopathy 22B, severe fetal",MONDO,disease,DISEASE_6754
6755,6755,6755,6755,6755,6755,6755,6755,MONDO:0000812_MONDO:0045002_MONDO:0037847,vertebral column disorder,MONDO_grouped,disease,DISEASE_6755
6756,6756,6756,6756,6756,6756,6756,6756,MONDO:0022938,deafness goiter stippled epiphyses,MONDO,disease,DISEASE_6756
6757,6757,6757,6757,6757,6757,6757,6757,MONDO:0035027,microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome,MONDO,disease,DISEASE_6757
6758,6758,6758,6758,6758,6758,6758,6758,MONDO:0002489,malignant breast phyllodes tumor,MONDO,disease,DISEASE_6758
6759,6759,6759,6759,6759,6759,6759,6759,MONDO:0016821,shoulder and girdle defects-familial intellectual disability syndrome,MONDO,disease,DISEASE_6759
6760,6760,6760,6760,6760,6760,6760,6760,MONDO:0010337,X-linked intellectual disability-cerebellar hypoplasia syndrome,MONDO,disease,DISEASE_6760
6761,6761,6761,6761,6761,6761,6761,6761,MONDO:0011731,glucose-galactose malabsorption,MONDO,disease,DISEASE_6761
6762,6762,6762,6762,6762,6762,6762,6762,MONDO:0033572,"intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies",MONDO,disease,DISEASE_6762
6763,6763,6763,6763,6763,6763,6763,6763,MONDO:0019813_MONDO:0020289_MONDO:0016582,congenital tricuspid stenosis,MONDO_grouped,disease,DISEASE_6763
6764,6764,6764,6764,6764,6764,6764,6764,MONDO:0021431,squamous cell carcinoma of buccal mucosa,MONDO,disease,DISEASE_6764
6765,6765,6765,6765,6765,6765,6765,6765,MONDO:1010864,"alpha-mannosidosis, domestic cat",MONDO,disease,DISEASE_6765
6766,6766,6766,6766,6766,6766,6766,6766,MONDO:0002503,adult astrocytic tumor,MONDO,disease,DISEASE_6766
6767,6767,6767,6767,6767,6767,6767,6767,MONDO:1011128,"azoospermia, horse",MONDO,disease,DISEASE_6767
6768,6768,6768,6768,6768,6768,6768,6768,MONDO:0000374,bile duct carcinoma in situ,MONDO,disease,DISEASE_6768
6769,6769,6769,6769,6769,6769,6769,6769,MONDO:0017418,chronic intestinal failure,MONDO,disease,DISEASE_6769
6770,6770,6770,6770,6770,6770,6770,6770,MONDO:0005690,Caplan syndrome,MONDO,disease,DISEASE_6770
6771,6771,6771,6771,6771,6771,6771,6771,MONDO:1010459,"hypertrophic cardiomyopathy, domestic cat",MONDO,disease,DISEASE_6771
6772,6772,6772,6772,6772,6772,6772,6772,MONDO:0007184_MONDO:0005339_MONDO:0010410_MONDO:0012899,"alopecia, androgenetic",MONDO_grouped,disease,DISEASE_6772
6773,6773,6773,6773,6773,6773,6773,6773,MONDO:0030837,"neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities",MONDO,disease,DISEASE_6773
6774,6774,6774,6774,6774,6774,6774,6774,MONDO:0019901,non-distal monosomy 20q,MONDO,disease,DISEASE_6774
6775,6775,6775,6775,6775,6775,6775,6775,MONDO:0004035,glomangiomatosis,MONDO,disease,DISEASE_6775
6776,6776,6776,6776,6776,6776,6776,6776,MONDO:0009259,gamma-glutamylcysteine synthetase deficiency,MONDO,disease,DISEASE_6776
6777,6777,6777,6777,6777,6777,6777,6777,MONDO:0700030,complete trisomy 21,MONDO,disease,DISEASE_6777
6778,6778,6778,6778,6778,6778,6778,6778,MONDO:1012275_MONDO:1012276,"tibial dyschondroplasia, chicken",MONDO_grouped,disease,DISEASE_6778
6779,6779,6779,6779,6779,6779,6779,6779,MONDO:0007595,"factor VII and Factor VIII, combined deficiency of",MONDO,disease,DISEASE_6779
6780,6780,6780,6780,6780,6780,6780,6780,MONDO:0003299,colorectal leiomyoma,MONDO,disease,DISEASE_6780
6781,6781,6781,6781,6781,6781,6781,6781,MONDO:0024609,vulvar squamous cell carcinoma,MONDO,disease,DISEASE_6781
6782,6782,6782,6782,6782,6782,6782,6782,MONDO:0002994,pancreatic delta cell neuroendocrine tumor,MONDO,disease,DISEASE_6782
6783,6783,6783,6783,6783,6783,6783,6783,MONDO:0004537,intestinal variant cervical mucinous adenocarcinoma,MONDO,disease,DISEASE_6783
6784,6784,6784,6784,6784,6784,6784,6784,MONDO:0019205,trichodysplasia-amelogenesis imperfecta syndrome,MONDO,disease,DISEASE_6784
6785,6785,6785,6785,6785,6785,6785,6785,MONDO:0007764,"autosomal dominant osteosclerosis, Worth type",MONDO,disease,DISEASE_6785
6786,6786,6786,6786,6786,6786,6786,6786,MONDO:0015529,paroxysmal Hemicrania,MONDO,disease,DISEASE_6786
6787,6787,6787,6787,6787,6787,6787,6787,MONDO:0016442,elastoma,MONDO,disease,DISEASE_6787
6788,6788,6788,6788,6788,6788,6788,6788,MONDO:0020531,long chain acyl-CoA dehydrogenase deficiency,MONDO,disease,DISEASE_6788
6789,6789,6789,6789,6789,6789,6789,6789,MONDO:0002810,pancreatic serous cystic neoplasm,MONDO,disease,DISEASE_6789
6790,6790,6790,6790,6790,6790,6790,6790,MONDO:0009382,"hyperbilirubinemia, shunt, primary",MONDO,disease,DISEASE_6790
6791,6791,6791,6791,6791,6791,6791,6791,MONDO:0957588,"neurodevelopmental disorder with impaired language, behavioral abnormalities, and dysmorphic facies",MONDO,disease,DISEASE_6791
6792,6792,6792,6792,6792,6792,6792,6792,MONDO:0001101,fat necrosis of breast,MONDO,disease,DISEASE_6792
6793,6793,6793,6793,6793,6793,6793,6793,MONDO:0012858,primary CD59 deficiency,MONDO,disease,DISEASE_6793
6794,6794,6794,6794,6794,6794,6794,6794,MONDO:0032680,global developmental delay with or without impaired intellectual development,MONDO,disease,DISEASE_6794
6795,6795,6795,6795,6795,6795,6795,6795,MONDO:1010312,"osteopetrosis with gingival hamartomas, non-human animal",MONDO,disease,DISEASE_6795
6796,6796,6796,6796,6796,6796,6796,6796,MONDO:0017511,"split hand, unilateral",MONDO,disease,DISEASE_6796
6797,6797,6797,6797,6797,6797,6797,6797,MONDO:0016197,qualitative or quantitative defects of selenoprotein N1,MONDO,disease,DISEASE_6797
6798,6798,6798,6798,6798,6798,6798,6798,MONDO:0010511,"vas deferens, congenital bilateral aplasia of, X-linked",MONDO,disease,DISEASE_6798
6799,6799,6799,6799,6799,6799,6799,6799,MONDO:0008422_MONDO:0016828,autosomal dominant sideroblastic anemia,MONDO_grouped,disease,DISEASE_6799
6800,6800,6800,6800,6800,6800,6800,6800,MONDO:0009634,microtia with meatal atresia and conductive deafness,MONDO,disease,DISEASE_6800
6801,6801,6801,6801,6801,6801,6801,6801,MONDO:0010747_MONDO:0010482,X-linked dystonia-parkinsonism,MONDO_grouped,disease,DISEASE_6801
6802,6802,6802,6802,6802,6802,6802,6802,MONDO:0044338,autoimmune primary ovarian failure,MONDO,disease,DISEASE_6802
6803,6803,6803,6803,6803,6803,6803,6803,MONDO:0007520_MONDO:0011428_MONDO:0007516,"ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome",MONDO_grouped,disease,DISEASE_6803
6804,6804,6804,6804,6804,6804,6804,6804,MONDO:0013847,chromosome 16p11.2 duplication syndrome,MONDO,disease,DISEASE_6804
6805,6805,6805,6805,6805,6805,6805,6805,MONDO:0017627,congenital hereditary facial paralysis-variable hearing loss syndrome,MONDO,disease,DISEASE_6805
6806,6806,6806,6806,6806,6806,6806,6806,MONDO:0006270,lobular breast carcinoma in situ,MONDO,disease,DISEASE_6806
6807,6807,6807,6807,6807,6807,6807,6807,MONDO:0018563,adactyly of foot,MONDO,disease,DISEASE_6807
6808,6808,6808,6808,6808,6808,6808,6808,MONDO:0000836,disease of bone structure,MONDO,disease,DISEASE_6808
6809,6809,6809,6809,6809,6809,6809,6809,MONDO:0007601_MONDO:0009572,"familial Mediterranean fever, autosomal dominant",MONDO_grouped,disease,DISEASE_6809
6810,6810,6810,6810,6810,6810,6810,6810,MONDO:1010037,"cleft palate, non-human animal",MONDO,disease,DISEASE_6810
6811,6811,6811,6811,6811,6811,6811,6811,MONDO:0022610,bronchiectasis oligospermia,MONDO,disease,DISEASE_6811
6812,6812,6812,6812,6812,6812,6812,6812,MONDO:0020798_MONDO:0007796,"hypoparathyroidism, familial isolated",MONDO_grouped,disease,DISEASE_6812
6813,6813,6813,6813,6813,6813,6813,6813,MONDO:0018244,obesity due to SIM1 deficiency,MONDO,disease,DISEASE_6813
6814,6814,6814,6814,6814,6814,6814,6814,MONDO:0000343,Barmah forest virus disease,MONDO,disease,DISEASE_6814
6815,6815,6815,6815,6815,6815,6815,6815,MONDO:0014043,microcephalic primordial dwarfism due to ZNF335 deficiency,MONDO,disease,DISEASE_6815
6816,6816,6816,6816,6816,6816,6816,6816,MONDO:0000459,mesenchymal glioblastoma,MONDO,disease,DISEASE_6816
6817,6817,6817,6817,6817,6817,6817,6817,MONDO:0010172,VACTERL with hydrocephalus,MONDO,disease,DISEASE_6817
6818,6818,6818,6818,6818,6818,6818,6818,MONDO:0020768,X-linked deafness,MONDO,disease,DISEASE_6818
6819,6819,6819,6819,6819,6819,6819,6819,MONDO:0019280_MONDO:1010752_MONDO:1010753,hypertrichosis,MONDO_grouped,disease,DISEASE_6819
6820,6820,6820,6820,6820,6820,6820,6820,MONDO:0044913,metastatic malignant neoplasm in the eye,MONDO,disease,DISEASE_6820
6821,6821,6821,6821,6821,6821,6821,6821,MONDO:0019052,inborn errors of metabolism,MONDO,disease,DISEASE_6821
6822,6822,6822,6822,6822,6822,6822,6822,MONDO:0004940,acute female pelvic peritonitis,MONDO,disease,DISEASE_6822
6823,6823,6823,6823,6823,6823,6823,6823,MONDO:1011767,"laminitis, non-human animal",MONDO,disease,DISEASE_6823
6824,6824,6824,6824,6824,6824,6824,6824,MONDO:0016684_MONDO:0016734,anaplastic astrocytoma,MONDO_grouped,disease,DISEASE_6824
6825,6825,6825,6825,6825,6825,6825,6825,MONDO:0011578,familial papillary thyroid carcinoma with renal papillary neoplasia,MONDO,disease,DISEASE_6825
6826,6826,6826,6826,6826,6826,6826,6826,MONDO:0011119,iridogoniodysgenesis,MONDO,disease,DISEASE_6826
6827,6827,6827,6827,6827,6827,6827,6827,MONDO:0032886,Liang-Wang syndrome,MONDO,disease,DISEASE_6827
6828,6828,6828,6828,6828,6828,6828,6828,MONDO:0004135,subacute lymphocytic thyroiditis,MONDO,disease,DISEASE_6828
6829,6829,6829,6829,6829,6829,6829,6829,MONDO:0008893,C syndrome,MONDO,disease,DISEASE_6829
6830,6830,6830,6830,6830,6830,6830,6830,MONDO:0005523,steroid inherited metabolic disorder,MONDO,disease,DISEASE_6830
6831,6831,6831,6831,6831,6831,6831,6831,MONDO:0007628_MONDO:0044203_MONDO:0975805,foveal hypoplasia,MONDO_grouped,disease,DISEASE_6831
6832,6832,6832,6832,6832,6832,6832,6832,MONDO:0032642,"arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development",MONDO,disease,DISEASE_6832
6833,6833,6833,6833,6833,6833,6833,6833,MONDO:0021230,uterine cervix neoplasm,MONDO,disease,DISEASE_6833
6834,6834,6834,6834,6834,6834,6834,6834,MONDO:0023258,glycogen storage disease type 1 due to SLC37A4 mutation,MONDO,disease,DISEASE_6834
6835,6835,6835,6835,6835,6835,6835,6835,MONDO:0017666_MONDO:0018250,diffuse palmoplantar keratoderma,MONDO_grouped,disease,DISEASE_6835
6836,6836,6836,6836,6836,6836,6836,6836,MONDO:0001902,congenital agammaglobulinemia,MONDO,disease,DISEASE_6836
6837,6837,6837,6837,6837,6837,6837,6837,MONDO:0022675,cataract skeletal anomalies,MONDO,disease,DISEASE_6837
6838,6838,6838,6838,6838,6838,6838,6838,MONDO:0002144,obsolete hyperuricemia,MONDO,disease,DISEASE_6838
6839,6839,6839,6839,6839,6839,6839,6839,MONDO:0015436,ring chromosome 20,MONDO,disease,DISEASE_6839
6840,6840,6840,6840,6840,6840,6840,6840,MONDO:0005677,Rickettsia conorii infectious disease,MONDO,disease,DISEASE_6840
6841,6841,6841,6841,6841,6841,6841,6841,MONDO:0016630,isolated delta-storage pool disease,MONDO,disease,DISEASE_6841
6842,6842,6842,6842,6842,6842,6842,6842,MONDO:0009406,hypertrichotic osteochondrodysplasia Cantu type,MONDO,disease,DISEASE_6842
6843,6843,6843,6843,6843,6843,6843,6843,MONDO:1012513_MONDO:1012514,"verrucous epidermal keratinocytic nevi, dog",MONDO_grouped,disease,DISEASE_6843
6844,6844,6844,6844,6844,6844,6844,6844,MONDO:0000501,obsolete Jensen syndrome,MONDO,disease,DISEASE_6844
6845,6845,6845,6845,6845,6845,6845,6845,MONDO:0017901,autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency,MONDO,disease,DISEASE_6845
6846,6846,6846,6846,6846,6846,6846,6846,MONDO:0002621,extraosseous osteosarcoma,MONDO,disease,DISEASE_6846
6847,6847,6847,6847,6847,6847,6847,6847,MONDO:0100491,generalized pustular psoriasis,MONDO,disease,DISEASE_6847
6848,6848,6848,6848,6848,6848,6848,6848,MONDO:0007272,hereditary hypercarotenemia and vitamin A deficiency,MONDO,disease,DISEASE_6848
6849,6849,6849,6849,6849,6849,6849,6849,MONDO:0001582,cicatricial ectropion,MONDO,disease,DISEASE_6849
6850,6850,6850,6850,6850,6850,6850,6850,MONDO:0021276,papilloma of buccal mucosa,MONDO,disease,DISEASE_6850
6851,6851,6851,6851,6851,6851,6851,6851,MONDO:0016939,partial duplication of the short arm of chromosome 2,MONDO,disease,DISEASE_6851
6852,6852,6852,6852,6852,6852,6852,6852,MONDO:0017427,congenital deformities of limbs,MONDO,disease,DISEASE_6852
6853,6853,6853,6853,6853,6853,6853,6853,MONDO:0022949,defective apolipoprotein b-100,MONDO,disease,DISEASE_6853
6854,6854,6854,6854,6854,6854,6854,6854,MONDO:0005545_MONDO:0024313_MONDO:0017592_MONDO:0005970_MONDO:0041879_MONDO:0018180_MONDO:8000001,staphylococcus aureus infection,MONDO_grouped,disease,DISEASE_6854
6855,6855,6855,6855,6855,6855,6855,6855,MONDO:0008694,pseudoprogeria syndrome,MONDO,disease,DISEASE_6855
6856,6856,6856,6856,6856,6856,6856,6856,MONDO:0017329,familial vesicoureteral reflux,MONDO,disease,DISEASE_6856
6857,6857,6857,6857,6857,6857,6857,6857,MONDO:0008099_MONDO:0012498_MONDO:0012497,congenital stationary night blindness autosomal dominant,MONDO_grouped,disease,DISEASE_6857
6858,6858,6858,6858,6858,6858,6858,6858,MONDO:0012909,"skeletal defects, genital hypoplasia, and intellectual disability",MONDO,disease,DISEASE_6858
6859,6859,6859,6859,6859,6859,6859,6859,MONDO:0011050,microcephaly-cardiac defect-lung malsegmentation syndrome,MONDO,disease,DISEASE_6859
6860,6860,6860,6860,6860,6860,6860,6860,MONDO:0015997,ectopia lentis-chorioretinal dystrophy-myopia syndrome,MONDO,disease,DISEASE_6860
6861,6861,6861,6861,6861,6861,6861,6861,MONDO:0009094,dermochondrocorneal dystrophy,MONDO,disease,DISEASE_6861
6862,6862,6862,6862,6862,6862,6862,6862,MONDO:0800388,cardiac glycoside intoxication,MONDO,disease,DISEASE_6862
6863,6863,6863,6863,6863,6863,6863,6863,MONDO:0002888,intraorbital meningioma,MONDO,disease,DISEASE_6863
6864,6864,6864,6864,6864,6864,6864,6864,MONDO:0010787,Kearns-Sayre syndrome,MONDO,disease,DISEASE_6864
6865,6865,6865,6865,6865,6865,6865,6865,MONDO:1010912_MONDO:1010909,"muscular dystrophy, domestic cat",MONDO_grouped,disease,DISEASE_6865
6866,6866,6866,6866,6866,6866,6866,6866,MONDO:0010742,pentalogy of Cantrell,MONDO,disease,DISEASE_6866
6867,6867,6867,6867,6867,6867,6867,6867,MONDO:0020183,neurogenic palpebral tumor,MONDO,disease,DISEASE_6867
6868,6868,6868,6868,6868,6868,6868,6868,MONDO:0002651,anal Paget disease,MONDO,disease,DISEASE_6868
6869,6869,6869,6869,6869,6869,6869,6869,MONDO:1012107,"hyperkinesis, dog",MONDO,disease,DISEASE_6869
6870,6870,6870,6870,6870,6870,6870,6870,MONDO:0025114_MONDO:0024982,"protozoan infections, animal",MONDO_grouped,disease,DISEASE_6870
6871,6871,6871,6871,6871,6871,6871,6871,MONDO:0019889,distal trisomy 22q,MONDO,disease,DISEASE_6871
6872,6872,6872,6872,6872,6872,6872,6872,MONDO:0002258,pharyngitis,MONDO,disease,DISEASE_6872
6873,6873,6873,6873,6873,6873,6873,6873,MONDO:0007297,ADan amyloidosis,MONDO,disease,DISEASE_6873
6874,6874,6874,6874,6874,6874,6874,6874,MONDO:0035475,EPHB4-related lymphatic-related hydrops fetalis,MONDO,disease,DISEASE_6874
6875,6875,6875,6875,6875,6875,6875,6875,MONDO:0000605,hypersensitivity reaction disease,MONDO,disease,DISEASE_6875
6876,6876,6876,6876,6876,6876,6876,6876,MONDO:0017301,pericardial and diaphragmatic defect,MONDO,disease,DISEASE_6876
6877,6877,6877,6877,6877,6877,6877,6877,MONDO:1040050,MKKS-related ciliopathy,MONDO,disease,DISEASE_6877
6878,6878,6878,6878,6878,6878,6878,6878,MONDO:0016759_MONDO:0014349_MONDO:0012438_MONDO:0014874_MONDO:0012683_MONDO:0012890_MONDO:0032643_MONDO:0011866_MONDO:0054844_MONDO:0054669_MONDO:0013993_MONDO:0032831_MONDO:0030438_MONDO:0013438_MONDO:0030259_MONDO:0013990_MONDO:0030260_MONDO:0030258_MONDO:0009166_MONDO:0011948_MONDO:0030261_MONDO:0014370_MONDO:0010190_MONDO:0013853_MONDO:0014351_MONDO:0012891_MONDO:0014485_MONDO:0016396_MONDO:0020135,pontocerebellar hypoplasia,MONDO_grouped,disease,DISEASE_6878
6879,6879,6879,6879,6879,6879,6879,6879,MONDO:0023601_MONDO:0060783,non-classic congenital adrenal hyperplasia,MONDO_grouped,disease,DISEASE_6879
6880,6880,6880,6880,6880,6880,6880,6880,MONDO:0005909,pestivirus infectious disease,MONDO,disease,DISEASE_6880
6881,6881,6881,6881,6881,6881,6881,6881,MONDO:0012374,"brachyphalangy, polydactyly, and tibial aplasia/hypoplasia",MONDO,disease,DISEASE_6881
6882,6882,6882,6882,6882,6882,6882,6882,MONDO:0018793,primary condylar hyperplasia,MONDO,disease,DISEASE_6882
6883,6883,6883,6883,6883,6883,6883,6883,MONDO:1010002,"myoclonus, non-human animal",MONDO,disease,DISEASE_6883
6884,6884,6884,6884,6884,6884,6884,6884,MONDO:0016469,"Ehlers-Danlos syndrome, vascular-like type",MONDO,disease,DISEASE_6884
6885,6885,6885,6885,6885,6885,6885,6885,MONDO:0011404,Caronte,MONDO,disease,DISEASE_6885
6886,6886,6886,6886,6886,6886,6886,6886,MONDO:0021838,Al Gazali Khidr Prem Chandran syndrome,MONDO,disease,DISEASE_6886
6887,6887,6887,6887,6887,6887,6887,6887,MONDO:0010042_MONDO:0011858,spastic diplegia and intellectual disability,MONDO_grouped,disease,DISEASE_6887
6888,6888,6888,6888,6888,6888,6888,6888,MONDO:0008441,spastic paraplegia with associated extrapyramidal signs,MONDO,disease,DISEASE_6888
6889,6889,6889,6889,6889,6889,6889,6889,MONDO:0006375,placental hemangioma,MONDO,disease,DISEASE_6889
6890,6890,6890,6890,6890,6890,6890,6890,MONDO:0010896,pigment dispersion syndrome,MONDO,disease,DISEASE_6890
6891,6891,6891,6891,6891,6891,6891,6891,MONDO:0016113,bulbospinal muscular atrophy,MONDO,disease,DISEASE_6891
6892,6892,6892,6892,6892,6892,6892,6892,MONDO:0015393,nasal ganglioglioma,MONDO,disease,DISEASE_6892
6893,6893,6893,6893,6893,6893,6893,6893,MONDO:0021092,fallopian tube neoplasm,MONDO,disease,DISEASE_6893
6894,6894,6894,6894,6894,6894,6894,6894,MONDO:0700001,shrinking lung syndrome,MONDO,disease,DISEASE_6894
6895,6895,6895,6895,6895,6895,6895,6895,MONDO:0022978,diaphragmatic hernia upper limb defects,MONDO,disease,DISEASE_6895
6896,6896,6896,6896,6896,6896,6896,6896,MONDO:0007432,cerebral arteriopathy with subcortical infarcts and leukoencephalopathy,MONDO,disease,DISEASE_6896
6897,6897,6897,6897,6897,6897,6897,6897,MONDO:0000386,"digestive system neuroendocrine tumor, grade 1/2",MONDO,disease,DISEASE_6897
6898,6898,6898,6898,6898,6898,6898,6898,MONDO:0024568_MONDO:0014659_MONDO:0032844_MONDO:0000023,infantile liver failure syndrome,MONDO_grouped,disease,DISEASE_6898
6899,6899,6899,6899,6899,6899,6899,6899,MONDO:0004530,early invasive cervical adenocarcinoma,MONDO,disease,DISEASE_6899
6900,6900,6900,6900,6900,6900,6900,6900,MONDO:0009438,"hypouricemia, hypercalcinuria, and decreased bone density",MONDO,disease,DISEASE_6900
6901,6901,6901,6901,6901,6901,6901,6901,MONDO:0003124,testicular Leydig cell tumor,MONDO,disease,DISEASE_6901
6902,6902,6902,6902,6902,6902,6902,6902,MONDO:0700126,trisomy 21,MONDO,disease,DISEASE_6902
6903,6903,6903,6903,6903,6903,6903,6903,MONDO:0011839,Newfoundland cone-rod dystrophy,MONDO,disease,DISEASE_6903
6904,6904,6904,6904,6904,6904,6904,6904,MONDO:1010939_MONDO:1010940_MONDO:1010941_MONDO:1010942,"malignant histiocytosis, dog",MONDO_grouped,disease,DISEASE_6904
6905,6905,6905,6905,6905,6905,6905,6905,MONDO:0010155,Dorfman-Chanarin disease,MONDO,disease,DISEASE_6905
6906,6906,6906,6906,6906,6906,6906,6906,MONDO:0007712,oculoauriculovertebral spectrum with radial defects,MONDO,disease,DISEASE_6906
6907,6907,6907,6907,6907,6907,6907,6907,MONDO:1010127,"dermatomyositis, non-human animal",MONDO,disease,DISEASE_6907
6908,6908,6908,6908,6908,6908,6908,6908,MONDO:0007728_MONDO:0013398_MONDO:0013397_MONDO:0024516,"acne inversa, familial",MONDO_grouped,disease,DISEASE_6908
6909,6909,6909,6909,6909,6909,6909,6909,MONDO:0016429,Marburg acute multiple sclerosis,MONDO,disease,DISEASE_6909
6910,6910,6910,6910,6910,6910,6910,6910,MONDO:0004415,lipid-cell variant infiltrating bladder urothelial carcinoma,MONDO,disease,DISEASE_6910
6911,6911,6911,6911,6911,6911,6911,6911,MONDO:0001822,hypolipoproteinemia,MONDO,disease,DISEASE_6911
6912,6912,6912,6912,6912,6912,6912,6912,MONDO:0011361,prostate cancer/brain cancer susceptibility,MONDO,disease,DISEASE_6912
6913,6913,6913,6913,6913,6913,6913,6913,MONDO:0018664,ectopia cordis,MONDO,disease,DISEASE_6913
6914,6914,6914,6914,6914,6914,6914,6914,MONDO:0021144,ovarian clear cell tumor,MONDO,disease,DISEASE_6914
6915,6915,6915,6915,6915,6915,6915,6915,MONDO:1012239,"central retinal degeneration, cheetah",MONDO,disease,DISEASE_6915
6916,6916,6916,6916,6916,6916,6916,6916,MONDO:0010279,terminal osseous dysplasia-pigmentary defects syndrome,MONDO,disease,DISEASE_6916
6917,6917,6917,6917,6917,6917,6917,6917,MONDO:0007498,ear exostoses,MONDO,disease,DISEASE_6917
6918,6918,6918,6918,6918,6918,6918,6918,MONDO:0958302,TFEB-rearranged renal cell carcinoma,MONDO,disease,DISEASE_6918
6919,6919,6919,6919,6919,6919,6919,6919,MONDO:0008235,pheochromocytoma-islet cell tumor syndrome,MONDO,disease,DISEASE_6919
6920,6920,6920,6920,6920,6920,6920,6920,MONDO:0012774,chromosome 15q13.3 microdeletion syndrome,MONDO,disease,DISEASE_6920
6921,6921,6921,6921,6921,6921,6921,6921,MONDO:0016451_MONDO:0016452,idiopathic hypersomnia with long sleep time,MONDO_grouped,disease,DISEASE_6921
6922,6922,6922,6922,6922,6922,6922,6922,MONDO:0023101,facio digito genital syndrome recessive form,MONDO,disease,DISEASE_6922
6923,6923,6923,6923,6923,6923,6923,6923,MONDO:0018511,epithelial tumor of the appendix,MONDO,disease,DISEASE_6923
6924,6924,6924,6924,6924,6924,6924,6924,MONDO:0043083,"coronal synostosis, syndactyly and jejunal atresia",MONDO,disease,DISEASE_6924
6925,6925,6925,6925,6925,6925,6925,6925,MONDO:0004964,"peripheral T-cell lymphoma, not otherwise specified",MONDO,disease,DISEASE_6925
6926,6926,6926,6926,6926,6926,6926,6926,MONDO:0018075,neural tube defect,MONDO,disease,DISEASE_6926
6927,6927,6927,6927,6927,6927,6927,6927,MONDO:1011682,"anal gland disease, non-human animal",MONDO,disease,DISEASE_6927
6928,6928,6928,6928,6928,6928,6928,6928,MONDO:1012310,"neuronal abiotrophy, dog",MONDO,disease,DISEASE_6928
6929,6929,6929,6929,6929,6929,6929,6929,MONDO:0011174,hyperzincemia with functional zinc depletion,MONDO,disease,DISEASE_6929
6930,6930,6930,6930,6930,6930,6930,6930,MONDO:0004247,peptic ulcer disease,MONDO,disease,DISEASE_6930
6931,6931,6931,6931,6931,6931,6931,6931,MONDO:0019068,congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization,MONDO,disease,DISEASE_6931
6932,6932,6932,6932,6932,6932,6932,6932,MONDO:0015045_MONDO:0015046_MONDO:0000659,alpha-heavy chain disease,MONDO_grouped,disease,DISEASE_6932
6933,6933,6933,6933,6933,6933,6933,6933,MONDO:0006748,epilepsia partialis continua,MONDO,disease,DISEASE_6933
6934,6934,6934,6934,6934,6934,6934,6934,MONDO:1011158,"osteoarthritis, sea otter",MONDO,disease,DISEASE_6934
6935,6935,6935,6935,6935,6935,6935,6935,MONDO:1012987,"demyelinating disease, non-human animal",MONDO,disease,DISEASE_6935
6936,6936,6936,6936,6936,6936,6936,6936,MONDO:0001513,pulsating exophthalmos,MONDO,disease,DISEASE_6936
6937,6937,6937,6937,6937,6937,6937,6937,MONDO:0005657_MONDO:0000240,aspergillosis,MONDO_grouped,disease,DISEASE_6937
6938,6938,6938,6938,6938,6938,6938,6938,MONDO:0010154,trigonocephaly-bifid nose-acral anomalies syndrome,MONDO,disease,DISEASE_6938
6939,6939,6939,6939,6939,6939,6939,6939,MONDO:0002562,demyelinating disease,MONDO,disease,DISEASE_6939
6940,6940,6940,6940,6940,6940,6940,6940,MONDO:0017139,oromandibular-limb hypogenesis syndrome,MONDO,disease,DISEASE_6940
6941,6941,6941,6941,6941,6941,6941,6941,MONDO:0001325,penile cancer,MONDO,disease,DISEASE_6941
6942,6942,6942,6942,6942,6942,6942,6942,MONDO:0018261,Nevada syndrome,MONDO,disease,DISEASE_6942
6943,6943,6943,6943,6943,6943,6943,6943,MONDO:0850098,oligoasthenoteratozoospermia,MONDO,disease,DISEASE_6943
6944,6944,6944,6944,6944,6944,6944,6944,MONDO:0020592,disorder of pharynx,MONDO,disease,DISEASE_6944
6945,6945,6945,6945,6945,6945,6945,6945,MONDO:0021388,neoplasm of chest wall,MONDO,disease,DISEASE_6945
6946,6946,6946,6946,6946,6946,6946,6946,MONDO:0001767,stenosis of lacrimal punctum,MONDO,disease,DISEASE_6946
6947,6947,6947,6947,6947,6947,6947,6947,MONDO:0016476,Beckwith-Wiedemann syndrome due to CDKN1C mutation,MONDO,disease,DISEASE_6947
6948,6948,6948,6948,6948,6948,6948,6948,MONDO:0054636,Skraban-Deardorff syndrome,MONDO,disease,DISEASE_6948
6949,6949,6949,6949,6949,6949,6949,6949,MONDO:0007636,frontorhiny,MONDO,disease,DISEASE_6949
6950,6950,6950,6950,6950,6950,6950,6950,MONDO:0021284,carcinoma in situ of ureter,MONDO,disease,DISEASE_6950
6951,6951,6951,6951,6951,6951,6951,6951,MONDO:1012697,"demyelinating disorder, Limousin cattle",MONDO,disease,DISEASE_6951
6952,6952,6952,6952,6952,6952,6952,6952,MONDO:0004369,renal infectious disease,MONDO,disease,DISEASE_6952
6953,6953,6953,6953,6953,6953,6953,6953,MONDO:0010023,combined immunodeficiency due to ZAP70 deficiency,MONDO,disease,DISEASE_6953
6954,6954,6954,6954,6954,6954,6954,6954,MONDO:1030009,persistent atrial fibrillation,MONDO,disease,DISEASE_6954
6955,6955,6955,6955,6955,6955,6955,6955,MONDO:0018688,anti-p200 pemphigoid,MONDO,disease,DISEASE_6955
6956,6956,6956,6956,6956,6956,6956,6956,MONDO:0002525_MONDO:0037858,inherited lipid metabolism disorder,MONDO_grouped,disease,DISEASE_6956
6957,6957,6957,6957,6957,6957,6957,6957,MONDO:0009005,complement component C1r/C1s deficiency,MONDO,disease,DISEASE_6957
6958,6958,6958,6958,6958,6958,6958,6958,MONDO:0009208,faciothoracogenital syndrome,MONDO,disease,DISEASE_6958
6959,6959,6959,6959,6959,6959,6959,6959,MONDO:0022612,Brunsting-Perry syndrome,MONDO,disease,DISEASE_6959
6960,6960,6960,6960,6960,6960,6960,6960,MONDO:0000599,writing disorder,MONDO,disease,DISEASE_6960
6961,6961,6961,6961,6961,6961,6961,6961,MONDO:0016218,Guillain-Barre syndrome,MONDO,disease,DISEASE_6961
6962,6962,6962,6962,6962,6962,6962,6962,MONDO:0006918_MONDO:0006651,posterior uveitis,MONDO_grouped,disease,DISEASE_6962
6963,6963,6963,6963,6963,6963,6963,6963,MONDO:0020434,"atrial septal defect, ostium secundum type",MONDO,disease,DISEASE_6963
6964,6964,6964,6964,6964,6964,6964,6964,MONDO:0001305,laryngostenosis,MONDO,disease,DISEASE_6964
6965,6965,6965,6965,6965,6965,6965,6965,MONDO:0100540,GATA6-related congenital heart disease with or without pancreatic agenesis or neonatal diabetes,MONDO,disease,DISEASE_6965
6966,6966,6966,6966,6966,6966,6966,6966,MONDO:0011626,"acromegaloid features, overgrowth, cleft palate, and hernia",MONDO,disease,DISEASE_6966
6967,6967,6967,6967,6967,6967,6967,6967,MONDO:0007850,autosomal dominant keratitis-ichthyosis-hearing loss syndrome,MONDO,disease,DISEASE_6967
6968,6968,6968,6968,6968,6968,6968,6968,MONDO:0022740,Christian Johnson angenieta syndrome,MONDO,disease,DISEASE_6968
6969,6969,6969,6969,6969,6969,6969,6969,MONDO:1012808,"congenital eye malformation, SIX6-related, dog",MONDO,disease,DISEASE_6969
6970,6970,6970,6970,6970,6970,6970,6970,MONDO:0007557,epidermolysis bullosa with congenital localized absence of skin and deformity of nails,MONDO,disease,DISEASE_6970
6971,6971,6971,6971,6971,6971,6971,6971,MONDO:0017328,non-central nervous system-localized embryonal carcinoma,MONDO,disease,DISEASE_6971
6972,6972,6972,6972,6972,6972,6972,6972,MONDO:0700048,hand-foot syndrome,MONDO,disease,DISEASE_6972
6973,6973,6973,6973,6973,6973,6973,6973,MONDO:0044303,congenital heart defects and ectodermal dysplasia,MONDO,disease,DISEASE_6973
6974,6974,6974,6974,6974,6974,6974,6974,MONDO:0008172_MONDO:0024546_MONDO:0013756,"hypertrophic osteoarthropathy, primary, autosomal dominant",MONDO_grouped,disease,DISEASE_6974
6975,6975,6975,6975,6975,6975,6975,6975,MONDO:0003276_MONDO:0002467_MONDO:0002776,middle ear disorder,MONDO_grouped,disease,DISEASE_6975
6976,6976,6976,6976,6976,6976,6976,6976,MONDO:0001295,idiopathic peripheral autonomic neuropathy,MONDO,disease,DISEASE_6976
6977,6977,6977,6977,6977,6977,6977,6977,MONDO:1012382,"retinal dysplasia and persistent primary vitreous, dog",MONDO,disease,DISEASE_6977
6978,6978,6978,6978,6978,6978,6978,6978,MONDO:1011968,"lethal arthrogryposis syndrome, non-human animal",MONDO,disease,DISEASE_6978
6979,6979,6979,6979,6979,6979,6979,6979,MONDO:0004504,penile urethral cancer,MONDO,disease,DISEASE_6979
6980,6980,6980,6980,6980,6980,6980,6980,MONDO:0011910_MONDO:0018098,obsolete autosomal dominant limb-girdle muscular dystrophy type 1C,MONDO_grouped,disease,DISEASE_6980
6981,6981,6981,6981,6981,6981,6981,6981,MONDO:0003253,vulvar granular cell tumor,MONDO,disease,DISEASE_6981
6982,6982,6982,6982,6982,6982,6982,6982,MONDO:0005408,diabetes mellitus type 2 associated cataract,MONDO,disease,DISEASE_6982
6983,6983,6983,6983,6983,6983,6983,6983,MONDO:0016061,immunodeficiency with factor H anomaly,MONDO,disease,DISEASE_6983
6984,6984,6984,6984,6984,6984,6984,6984,MONDO:0041448,metastasis from malignant tumor of colon,MONDO,disease,DISEASE_6984
6985,6985,6985,6985,6985,6985,6985,6985,MONDO:0017884,papillary renal cell carcinoma,MONDO,disease,DISEASE_6985
6986,6986,6986,6986,6986,6986,6986,6986,MONDO:0957531,neurodevelopmental disorder with microcephaly and movement abnormalities,MONDO,disease,DISEASE_6986
6987,6987,6987,6987,6987,6987,6987,6987,MONDO:0015812,primary cutaneous gamma/delta-positive T-cell lymphoma,MONDO,disease,DISEASE_6987
6988,6988,6988,6988,6988,6988,6988,6988,MONDO:0019583,localized lichen myxedematosus with mixed features of different subtypes,MONDO,disease,DISEASE_6988
6989,6989,6989,6989,6989,6989,6989,6989,MONDO:0004139,normocytic anemia,MONDO,disease,DISEASE_6989
6990,6990,6990,6990,6990,6990,6990,6990,MONDO:0001950,corneal ectasia,MONDO,disease,DISEASE_6990
6991,6991,6991,6991,6991,6991,6991,6991,MONDO:0005725,cyclosporiasis,MONDO,disease,DISEASE_6991
6992,6992,6992,6992,6992,6992,6992,6992,MONDO:0018082_MONDO:0020410_MONDO:0020411,aorto-ventricular tunnel,MONDO_grouped,disease,DISEASE_6992
6993,6993,6993,6993,6993,6993,6993,6993,MONDO:0006824,Krebs 2 carcinoma,MONDO,disease,DISEASE_6993
6994,6994,6994,6994,6994,6994,6994,6994,MONDO:0008799,anophthalmia/microphthalmia-esophageal atresia syndrome,MONDO,disease,DISEASE_6994
6995,6995,6995,6995,6995,6995,6995,6995,MONDO:0032790,neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities,MONDO,disease,DISEASE_6995
6996,6996,6996,6996,6996,6996,6996,6996,MONDO:0016381,hypertrichosis lanuginosa congenita,MONDO,disease,DISEASE_6996
6997,6997,6997,6997,6997,6997,6997,6997,MONDO:0015787_MONDO:0015788,symptomatic form of hemophilia A in female carriers,MONDO_grouped,disease,DISEASE_6997
6998,6998,6998,6998,6998,6998,6998,6998,MONDO:0022799,cold urticaria,MONDO,disease,DISEASE_6998
6999,6999,6999,6999,6999,6999,6999,6999,MONDO:0001793,excessive tearing,MONDO,disease,DISEASE_6999
7000,7000,7000,7000,7000,7000,7000,7000,MONDO:0006920,prediabetes syndrome,MONDO,disease,DISEASE_7000
7001,7001,7001,7001,7001,7001,7001,7001,MONDO:0001211,total internal ophthalmoplegia,MONDO,disease,DISEASE_7001
7002,7002,7002,7002,7002,7002,7002,7002,MONDO:0008096,nevus flammeus of nape of neck,MONDO,disease,DISEASE_7002
7003,7003,7003,7003,7003,7003,7003,7003,MONDO:0044331,obsolete genetic transient congenital hypothyroidism,MONDO,disease,DISEASE_7003
7004,7004,7004,7004,7004,7004,7004,7004,MONDO:0017623,PTEN hamartoma tumor syndrome,MONDO,disease,DISEASE_7004
7005,7005,7005,7005,7005,7005,7005,7005,MONDO:0020567,apnea of prematurity,MONDO,disease,DISEASE_7005
7006,7006,7006,7006,7006,7006,7006,7006,MONDO:0016067,Crandall syndrome,MONDO,disease,DISEASE_7006
7007,7007,7007,7007,7007,7007,7007,7007,MONDO:0004398,mediastinal schwannoma,MONDO,disease,DISEASE_7007
7008,7008,7008,7008,7008,7008,7008,7008,MONDO:0004844,oral mucosa leukoplakia,MONDO,disease,DISEASE_7008
7009,7009,7009,7009,7009,7009,7009,7009,MONDO:0010088,mucosulfatidosis,MONDO,disease,DISEASE_7009
7010,7010,7010,7010,7010,7010,7010,7010,MONDO:0010098,taurodontism,MONDO,disease,DISEASE_7010
7011,7011,7011,7011,7011,7011,7011,7011,MONDO:0003216,ureter adenocarcinoma,MONDO,disease,DISEASE_7011
7012,7012,7012,7012,7012,7012,7012,7012,MONDO:0021500,benign neoplasm of spleen,MONDO,disease,DISEASE_7012
7013,7013,7013,7013,7013,7013,7013,7013,MONDO:0022991,diploid-triploid mosaicism,MONDO,disease,DISEASE_7013
7014,7014,7014,7014,7014,7014,7014,7014,MONDO:0006347,pancreatic large cell neuroendocrine carcinoma,MONDO,disease,DISEASE_7014
7015,7015,7015,7015,7015,7015,7015,7015,MONDO:0008857,Beemer-Ertbruggen syndrome,MONDO,disease,DISEASE_7015
7016,7016,7016,7016,7016,7016,7016,7016,MONDO:0002166_MONDO:0044937_MONDO:0002168,rectum lymphoma,MONDO_grouped,disease,DISEASE_7016
7017,7017,7017,7017,7017,7017,7017,7017,MONDO:0005267_MONDO:0006780,heart disorder,MONDO_grouped,disease,DISEASE_7017
7018,7018,7018,7018,7018,7018,7018,7018,MONDO:0005278,serous adenocarcinoma,MONDO,disease,DISEASE_7018
7019,7019,7019,7019,7019,7019,7019,7019,MONDO:0029135_MONDO:1012426_MONDO:1012427,"muscular dystrophy-dystroglycanopathy (limb-girdle), type C",MONDO_grouped,disease,DISEASE_7019
7020,7020,7020,7020,7020,7020,7020,7020,MONDO:0032842,Siddiqi syndrome,MONDO,disease,DISEASE_7020
7021,7021,7021,7021,7021,7021,7021,7021,MONDO:0018169,morning glory syndrome,MONDO,disease,DISEASE_7021
7022,7022,7022,7022,7022,7022,7022,7022,MONDO:0005829,louping ill,MONDO,disease,DISEASE_7022
7023,7023,7023,7023,7023,7023,7023,7023,MONDO:0800328,"retinitis pigmentosa 94, variable age at onset",MONDO,disease,DISEASE_7023
7024,7024,7024,7024,7024,7024,7024,7024,MONDO:0002938,metatypical basal cell carcinoma,MONDO,disease,DISEASE_7024
7025,7025,7025,7025,7025,7025,7025,7025,MONDO:1012958,"atactic disorder, non-human animal",MONDO,disease,DISEASE_7025
7026,7026,7026,7026,7026,7026,7026,7026,MONDO:0010757,widow's peak syndrome,MONDO,disease,DISEASE_7026
7027,7027,7027,7027,7027,7027,7027,7027,MONDO:0010631_MONDO:1010785,incontinentia pigmenti,MONDO_grouped,disease,DISEASE_7027
7028,7028,7028,7028,7028,7028,7028,7028,MONDO:0006854,mesenchymoma,MONDO,disease,DISEASE_7028
7029,7029,7029,7029,7029,7029,7029,7029,MONDO:0004169,premenstrual tension,MONDO,disease,DISEASE_7029
7030,7030,7030,7030,7030,7030,7030,7030,MONDO:0010420,X-linked erythropoietic protoporphyria,MONDO,disease,DISEASE_7030
7031,7031,7031,7031,7031,7031,7031,7031,MONDO:0017236_MONDO:0001184,rapidly progressive glomerulonephritis,MONDO_grouped,disease,DISEASE_7031
7032,7032,7032,7032,7032,7032,7032,7032,MONDO:0022650,cardiomyopathy diabetes deafness,MONDO,disease,DISEASE_7032
7033,7033,7033,7033,7033,7033,7033,7033,MONDO:0007842,"joint laxity, familial",MONDO,disease,DISEASE_7033
7034,7034,7034,7034,7034,7034,7034,7034,MONDO:0005083_MONDO:0011849,psoriasis,MONDO_grouped,disease,DISEASE_7034
7035,7035,7035,7035,7035,7035,7035,7035,MONDO:0014491_MONDO:0030483_MONDO:0008856_MONDO:0958030_MONDO:0014353_MONDO:0012682_MONDO:0032763_MONDO:0030973_MONDO:0957535_MONDO:0010504_MONDO:0971151_MONDO:0014981_MONDO:0030333_MONDO:0012426_MONDO:0010386_MONDO:0054696_MONDO:0030013_MONDO:0970993_MONDO:0030498_MONDO:0033542_MONDO:0014453_MONDO:0970994_MONDO:0013427_MONDO:0030858_MONDO:0032599_MONDO:0032723_MONDO:0012163_MONDO:0014222_MONDO:0014597_MONDO:0033541_MONDO:0013500_MONDO:0010296_MONDO:0800104_MONDO:0011888_MONDO:0013953_MONDO:0014727_MONDO:0958011_MONDO:0024781_MONDO:0030302_MONDO:0020849_MONDO:0009194_MONDO:0030692_MONDO:0014280_MONDO:0030448_MONDO:0030898_MONDO:0032803_MONDO:0030693_MONDO:0030981_MONDO:0014278_MONDO:0021094_MONDO:0975749_MONDO:0975832_MONDO:0975834,immunodeficiency,MONDO_grouped,disease,DISEASE_7035
7036,7036,7036,7036,7036,7036,7036,7036,MONDO:0009255,galactokinase deficiency,MONDO,disease,DISEASE_7036
7037,7037,7037,7037,7037,7037,7037,7037,MONDO:0020487,Pontiac fever,MONDO,disease,DISEASE_7037
7038,7038,7038,7038,7038,7038,7038,7038,MONDO:0004867_MONDO:0000270,upper respiratory tract disorder,MONDO_grouped,disease,DISEASE_7038
7039,7039,7039,7039,7039,7039,7039,7039,MONDO:0015288,herpes simplex virus keratitis,MONDO,disease,DISEASE_7039
7040,7040,7040,7040,7040,7040,7040,7040,MONDO:0800440_MONDO:0800476,HAND1 related congenital heart defect,MONDO_grouped,disease,DISEASE_7040
7041,7041,7041,7041,7041,7041,7041,7041,MONDO:0859370,"respiratory infections, recurrent, and failure to thrive with or without diarrhea",MONDO,disease,DISEASE_7041
7042,7042,7042,7042,7042,7042,7042,7042,MONDO:0021913,aquagenic pruritus,MONDO,disease,DISEASE_7042
7043,7043,7043,7043,7043,7043,7043,7043,MONDO:0000687,diffuse alopecia areata,MONDO,disease,DISEASE_7043
7044,7044,7044,7044,7044,7044,7044,7044,MONDO:0009122,Dohle bodies and leukemia,MONDO,disease,DISEASE_7044
7045,7045,7045,7045,7045,7045,7045,7045,MONDO:0001407_MONDO:0002567,tracheal cancer,MONDO_grouped,disease,DISEASE_7045
7046,7046,7046,7046,7046,7046,7046,7046,MONDO:0850122,solid adenocarcinoma with mucin production,MONDO,disease,DISEASE_7046
7047,7047,7047,7047,7047,7047,7047,7047,MONDO:0008781_MONDO:0017593,juvenile amyotrophic lateral sclerosis with dementia,MONDO_grouped,disease,DISEASE_7047
7048,7048,7048,7048,7048,7048,7048,7048,MONDO:0800461,COL4A1-related disorder,MONDO,disease,DISEASE_7048
7049,7049,7049,7049,7049,7049,7049,7049,MONDO:0003890,infiltrating bladder urothelial carcinoma,MONDO,disease,DISEASE_7049
7050,7050,7050,7050,7050,7050,7050,7050,MONDO:0800088,lysosomal storage disease with skeletal involvement,MONDO,disease,DISEASE_7050
7051,7051,7051,7051,7051,7051,7051,7051,MONDO:0020127_MONDO:0020249,hereditary peripheral neuropathy,MONDO_grouped,disease,DISEASE_7051
7052,7052,7052,7052,7052,7052,7052,7052,MONDO:0011610,dimethylglycine dehydrogenase deficiency,MONDO,disease,DISEASE_7052
7053,7053,7053,7053,7053,7053,7053,7053,MONDO:0800040,MELAS syndrome caused by mutation in MTND6,MONDO,disease,DISEASE_7053
7054,7054,7054,7054,7054,7054,7054,7054,MONDO:0021112,scrotum cancer,MONDO,disease,DISEASE_7054
7055,7055,7055,7055,7055,7055,7055,7055,MONDO:0000367,taeniasis,MONDO,disease,DISEASE_7055
7056,7056,7056,7056,7056,7056,7056,7056,MONDO:0022430,persistent fetal circulation syndrome,MONDO,disease,DISEASE_7056
7057,7057,7057,7057,7057,7057,7057,7057,MONDO:0009837_MONDO:0002684_MONDO:0003053,choroid plexus papilloma,MONDO_grouped,disease,DISEASE_7057
7058,7058,7058,7058,7058,7058,7058,7058,MONDO:0001282_MONDO:0021576,fallopian tube endometriosis,MONDO_grouped,disease,DISEASE_7058
7059,7059,7059,7059,7059,7059,7059,7059,MONDO:0016425,Hughes-Stovin syndrome,MONDO,disease,DISEASE_7059
7060,7060,7060,7060,7060,7060,7060,7060,MONDO:1011693,"reduced glutathione deficiency due to GCS deficiency, non-human animal",MONDO,disease,DISEASE_7060
7061,7061,7061,7061,7061,7061,7061,7061,MONDO:0008757,alopecia universalis congenita,MONDO,disease,DISEASE_7061
7062,7062,7062,7062,7062,7062,7062,7062,MONDO:0016413,congenital hypothyroidism due to maternal intake of antithyroid drugs,MONDO,disease,DISEASE_7062
7063,7063,7063,7063,7063,7063,7063,7063,MONDO:1012337,"reduced glutathione deficiency, dog",MONDO,disease,DISEASE_7063
7064,7064,7064,7064,7064,7064,7064,7064,MONDO:0017622,congenital sucrase-isomaltase deficiency without sucrose intolerance,MONDO,disease,DISEASE_7064
7065,7065,7065,7065,7065,7065,7065,7065,MONDO:0001085,interstitial nephritis,MONDO,disease,DISEASE_7065
7066,7066,7066,7066,7066,7066,7066,7066,MONDO:0007803,multiple system atrophy,MONDO,disease,DISEASE_7066
7067,7067,7067,7067,7067,7067,7067,7067,MONDO:1012078_MONDO:1012079,"fibrodysplasia ossificans, dog",MONDO_grouped,disease,DISEASE_7067
7068,7068,7068,7068,7068,7068,7068,7068,MONDO:0001463,splenic flexure cancer,MONDO,disease,DISEASE_7068
7069,7069,7069,7069,7069,7069,7069,7069,MONDO:1010665,"Evans syndrome, horse",MONDO,disease,DISEASE_7069
7070,7070,7070,7070,7070,7070,7070,7070,MONDO:0010117_MONDO:0013039_MONDO:0013627,3M syndrome,MONDO_grouped,disease,DISEASE_7070
7071,7071,7071,7071,7071,7071,7071,7071,MONDO:0017186_MONDO:0019265_MONDO:0015625_MONDO:0017187,diazoxide-resistant hyperinsulinism,MONDO_grouped,disease,DISEASE_7071
7072,7072,7072,7072,7072,7072,7072,7072,MONDO:0015819,indolent primary cutaneous B-cell lymphoma,MONDO,disease,DISEASE_7072
7073,7073,7073,7073,7073,7073,7073,7073,MONDO:0004143,psammomatous meningioma,MONDO,disease,DISEASE_7073
7074,7074,7074,7074,7074,7074,7074,7074,MONDO:0017445,acheiria,MONDO,disease,DISEASE_7074
7075,7075,7075,7075,7075,7075,7075,7075,MONDO:0008109,ocular cicatricial pemphigoid,MONDO,disease,DISEASE_7075
7076,7076,7076,7076,7076,7076,7076,7076,MONDO:0010829,CARASIL syndrome,MONDO,disease,DISEASE_7076
7077,7077,7077,7077,7077,7077,7077,7077,MONDO:0100464,acid sphingomyelinase deficiency,MONDO,disease,DISEASE_7077
7078,7078,7078,7078,7078,7078,7078,7078,MONDO:0021935,aspergillus niger infection,MONDO,disease,DISEASE_7078
7079,7079,7079,7079,7079,7079,7079,7079,MONDO:0017381_MONDO:0042971,congenital herpes simplex virus infection,MONDO_grouped,disease,DISEASE_7079
7080,7080,7080,7080,7080,7080,7080,7080,MONDO:0006789,hyperamylasemia,MONDO,disease,DISEASE_7080
7081,7081,7081,7081,7081,7081,7081,7081,MONDO:1010210,"malignant histiocytosis, non-human animal",MONDO,disease,DISEASE_7081
7082,7082,7082,7082,7082,7082,7082,7082,MONDO:0018873,anterior cutaneous nerve entrapment syndrome,MONDO,disease,DISEASE_7082
7083,7083,7083,7083,7083,7083,7083,7083,MONDO:0850100,body integrity dysphoria,MONDO,disease,DISEASE_7083
7084,7084,7084,7084,7084,7084,7084,7084,MONDO:0700156,canine soft tissue sarcoma,MONDO,disease,DISEASE_7084
7085,7085,7085,7085,7085,7085,7085,7085,MONDO:0013110,neurodegenerative syndrome due to cerebral folate transport deficiency,MONDO,disease,DISEASE_7085
7086,7086,7086,7086,7086,7086,7086,7086,MONDO:0015567,cataract-glaucoma syndrome,MONDO,disease,DISEASE_7086
7087,7087,7087,7087,7087,7087,7087,7087,MONDO:0003862,melanotic psammomatous malignant peripheral nerve sheath tumor,MONDO,disease,DISEASE_7087
7088,7088,7088,7088,7088,7088,7088,7088,MONDO:0008186,pancytopenia and occlusive vascular disease,MONDO,disease,DISEASE_7088
7089,7089,7089,7089,7089,7089,7089,7089,MONDO:0007627_MONDO:0009203_MONDO:0013997_MONDO:0013996_MONDO:0018363,focal facial dermal dysplasia,MONDO_grouped,disease,DISEASE_7089
7090,7090,7090,7090,7090,7090,7090,7090,MONDO:0001873,geniculate ganglionitis,MONDO,disease,DISEASE_7090
7091,7091,7091,7091,7091,7091,7091,7091,MONDO:0005743,encephalitozoonosis,MONDO,disease,DISEASE_7091
7092,7092,7092,7092,7092,7092,7092,7092,MONDO:1010315,"periodontitis, non-human animal",MONDO,disease,DISEASE_7092
7093,7093,7093,7093,7093,7093,7093,7093,MONDO:0800130,autoinflammatory syndrome with immunodeficiency,MONDO,disease,DISEASE_7093
7094,7094,7094,7094,7094,7094,7094,7094,MONDO:1010081,"autoimmune thrombocytopenic purpura, non-human animal",MONDO,disease,DISEASE_7094
7095,7095,7095,7095,7095,7095,7095,7095,MONDO:0003303,neurofibroma of gallbladder,MONDO,disease,DISEASE_7095
7096,7096,7096,7096,7096,7096,7096,7096,MONDO:0010977,Brody myopathy,MONDO,disease,DISEASE_7096
7097,7097,7097,7097,7097,7097,7097,7097,MONDO:0015350,17q11.2 microduplication syndrome,MONDO,disease,DISEASE_7097
7098,7098,7098,7098,7098,7098,7098,7098,MONDO:0003443,papillary urothelial neoplasm,MONDO,disease,DISEASE_7098
7099,7099,7099,7099,7099,7099,7099,7099,MONDO:0016561,1q44 microdeletion syndrome,MONDO,disease,DISEASE_7099
7100,7100,7100,7100,7100,7100,7100,7100,MONDO:0005437,testicular dysgenesis syndrome,MONDO,disease,DISEASE_7100
7101,7101,7101,7101,7101,7101,7101,7101,MONDO:0015911,obsolete rare acquired hemolytic anemia,MONDO,disease,DISEASE_7101
7102,7102,7102,7102,7102,7102,7102,7102,MONDO:0957423,immunotherapy induced hypophysitis,MONDO,disease,DISEASE_7102
7103,7103,7103,7103,7103,7103,7103,7103,MONDO:0022945,deafness peripheral neuropathy arterial disease,MONDO,disease,DISEASE_7103
7104,7104,7104,7104,7104,7104,7104,7104,MONDO:0001351,uterine adnexa cancer,MONDO,disease,DISEASE_7104
7105,7105,7105,7105,7105,7105,7105,7105,MONDO:0012428,kyphoscoliosis 1,MONDO,disease,DISEASE_7105
7106,7106,7106,7106,7106,7106,7106,7106,MONDO:1010279,"hymen, imperforate, non-human animal",MONDO,disease,DISEASE_7106
7107,7107,7107,7107,7107,7107,7107,7107,MONDO:0060711,Jaberi-Elahi syndrome,MONDO,disease,DISEASE_7107
7108,7108,7108,7108,7108,7108,7108,7108,MONDO:0035614,sporadic fatal insomnia,MONDO,disease,DISEASE_7108
7109,7109,7109,7109,7109,7109,7109,7109,MONDO:0002532,squamous cell neoplasm,MONDO,disease,DISEASE_7109
7110,7110,7110,7110,7110,7110,7110,7110,MONDO:0015678,"dysplasia of head of femur, Meyer type",MONDO,disease,DISEASE_7110
7111,7111,7111,7111,7111,7111,7111,7111,MONDO:0008019,mullerian aplasia and hyperandrogenism,MONDO,disease,DISEASE_7111
7112,7112,7112,7112,7112,7112,7112,7112,MONDO:0005682,bronchopneumonia,MONDO,disease,DISEASE_7112
7113,7113,7113,7113,7113,7113,7113,7113,MONDO:0850154,tongue carcinoma,MONDO,disease,DISEASE_7113
7114,7114,7114,7114,7114,7114,7114,7114,MONDO:0007059,acrorenal syndrome,MONDO,disease,DISEASE_7114
7115,7115,7115,7115,7115,7115,7115,7115,MONDO:0043170,Pavone Fiumara Rizzo syndrome,MONDO,disease,DISEASE_7115
7116,7116,7116,7116,7116,7116,7116,7116,MONDO:0054551_MONDO:0054550,"avascular necrosis of femoral head, primary",MONDO_grouped,disease,DISEASE_7116
7117,7117,7117,7117,7117,7117,7117,7117,MONDO:0013768_MONDO:0008817,"arterial calcification, generalized, of infancy",MONDO_grouped,disease,DISEASE_7117
7118,7118,7118,7118,7118,7118,7118,7118,MONDO:0006405,salivary gland small cell carcinoma,MONDO,disease,DISEASE_7118
7119,7119,7119,7119,7119,7119,7119,7119,MONDO:0007248,hereditary painful callosities,MONDO,disease,DISEASE_7119
7120,7120,7120,7120,7120,7120,7120,7120,MONDO:0009457_MONDO:0010628,"immunoglobulin d level in plasma, low",MONDO_grouped,disease,DISEASE_7120
7121,7121,7121,7121,7121,7121,7121,7121,MONDO:0002352,larynx cancer,MONDO,disease,DISEASE_7121
7122,7122,7122,7122,7122,7122,7122,7122,MONDO:1010911_MONDO:1010913_MONDO:1010910,"muscular dystrophy, dog",MONDO_grouped,disease,DISEASE_7122
7123,7123,7123,7123,7123,7123,7123,7123,MONDO:0020517,eosinophilic granuloma,MONDO,disease,DISEASE_7123
7124,7124,7124,7124,7124,7124,7124,7124,MONDO:1011305,"cancer or benign tumor, non-human animal",MONDO,disease,DISEASE_7124
7125,7125,7125,7125,7125,7125,7125,7125,MONDO:0033717,congenital cerebellar ataxia due to RNU12 mutation,MONDO,disease,DISEASE_7125
7126,7126,7126,7126,7126,7126,7126,7126,MONDO:1012123,"congenital hypotrichosis with thymic aplasia, domestic cat",MONDO,disease,DISEASE_7126
7127,7127,7127,7127,7127,7127,7127,7127,MONDO:0013866_MONDO:0012588_MONDO:0011144_MONDO:0012188_MONDO:0009744_MONDO:0012414_MONDO:0008767_MONDO:0008769_MONDO:0010830_MONDO:0014147_MONDO:0009745_MONDO:0019260_MONDO:0019262_MONDO:0016295_MONDO:1011570_MONDO:1011571_MONDO:1011578_MONDO:1011577_MONDO:1011568_MONDO:1011573_MONDO:1011574_MONDO:1011575,neuronal ceroid lipofuscinosis,MONDO_grouped,disease,DISEASE_7127
7128,7128,7128,7128,7128,7128,7128,7128,MONDO:0006358,parotid gland squamous cell carcinoma,MONDO,disease,DISEASE_7128
7129,7129,7129,7129,7129,7129,7129,7129,MONDO:0004210,colonic L-cell glucagon-like peptide producing tumor,MONDO,disease,DISEASE_7129
7130,7130,7130,7130,7130,7130,7130,7130,MONDO:0010726,Rett syndrome,MONDO,disease,DISEASE_7130
7131,7131,7131,7131,7131,7131,7131,7131,MONDO:0018895,Plummer-Vinson syndrome,MONDO,disease,DISEASE_7131
7132,7132,7132,7132,7132,7132,7132,7132,MONDO:0016823,mycetoma,MONDO,disease,DISEASE_7132
7133,7133,7133,7133,7133,7133,7133,7133,MONDO:0022618,burning mouth syndrome type 3,MONDO,disease,DISEASE_7133
7134,7134,7134,7134,7134,7134,7134,7134,MONDO:0010138,thyrotoxicosis,MONDO,disease,DISEASE_7134
7135,7135,7135,7135,7135,7135,7135,7135,MONDO:0003733_MONDO:0003731_MONDO:0003732_MONDO:0003734_MONDO:0003875,central nervous system mature teratoma,MONDO_grouped,disease,DISEASE_7135
7136,7136,7136,7136,7136,7136,7136,7136,MONDO:1011458_MONDO:1011998,"glaucoma, primary closed-angle, non-human animal",MONDO_grouped,disease,DISEASE_7136
7137,7137,7137,7137,7137,7137,7137,7137,MONDO:0007546,"myeloproliferative disorder, chronic, with eosinophilia",MONDO,disease,DISEASE_7137
7138,7138,7138,7138,7138,7138,7138,7138,MONDO:0003763,acute stress disorder,MONDO,disease,DISEASE_7138
7139,7139,7139,7139,7139,7139,7139,7139,MONDO:0016677,toxic or drug-related embryofetopathy,MONDO,disease,DISEASE_7139
7140,7140,7140,7140,7140,7140,7140,7140,MONDO:0007825,"incisors, rotation of upper central",MONDO,disease,DISEASE_7140
7141,7141,7141,7141,7141,7141,7141,7141,MONDO:0060702_MONDO:0010076_MONDO:0019666,"spondyloepimetaphyseal dysplasia, di rocco type",MONDO_grouped,disease,DISEASE_7141
7142,7142,7142,7142,7142,7142,7142,7142,MONDO:0008050,MYH7-related skeletal myopathy,MONDO,disease,DISEASE_7142
7143,7143,7143,7143,7143,7143,7143,7143,MONDO:0017266,keratinopathic ichthyosis,MONDO,disease,DISEASE_7143
7144,7144,7144,7144,7144,7144,7144,7144,MONDO:0007760,"hyperlipoproteinemia, type II, and deafness",MONDO,disease,DISEASE_7144
7145,7145,7145,7145,7145,7145,7145,7145,MONDO:0044332,childhood-onset benign chorea with striatal involvement,MONDO,disease,DISEASE_7145
7146,7146,7146,7146,7146,7146,7146,7146,MONDO:0001146,fourth cranial nerve palsy,MONDO,disease,DISEASE_7146
7147,7147,7147,7147,7147,7147,7147,7147,MONDO:0004974_MONDO:0006103_MONDO:0006288_MONDO:0044767,adrenal gland pheochromocytoma,MONDO_grouped,disease,DISEASE_7147
7148,7148,7148,7148,7148,7148,7148,7148,MONDO:0004164,lymphoepithelioma-like acinar prostate adenocarcinoma,MONDO,disease,DISEASE_7148
7149,7149,7149,7149,7149,7149,7149,7149,MONDO:0010483_MONDO:0019769_MONDO:0019766,"X-linked intellectual disability, Cantagrel type",MONDO_grouped,disease,DISEASE_7149
7150,7150,7150,7150,7150,7150,7150,7150,MONDO:0012207,"umbilicus, familial flat",MONDO,disease,DISEASE_7150
7151,7151,7151,7151,7151,7151,7151,7151,MONDO:0006957,root caries,MONDO,disease,DISEASE_7151
7152,7152,7152,7152,7152,7152,7152,7152,MONDO:0100093_MONDO:0100092_MONDO:0013981,"myoclonus, familial",MONDO_grouped,disease,DISEASE_7152
7153,7153,7153,7153,7153,7153,7153,7153,MONDO:0004748,lip disorder,MONDO,disease,DISEASE_7153
7154,7154,7154,7154,7154,7154,7154,7154,MONDO:0011650_MONDO:0800268,"atrioventricular septal defect, susceptibility to",MONDO_grouped,disease,DISEASE_7154
7155,7155,7155,7155,7155,7155,7155,7155,MONDO:0036025,toxicity to dolutegravir,MONDO,disease,DISEASE_7155
7156,7156,7156,7156,7156,7156,7156,7156,MONDO:0015468,craniosynostosis-cataract syndrome,MONDO,disease,DISEASE_7156
7157,7157,7157,7157,7157,7157,7157,7157,MONDO:0001689,hypertrophy of tongue papillae,MONDO,disease,DISEASE_7157
7158,7158,7158,7158,7158,7158,7158,7158,MONDO:0859212,"neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus",MONDO,disease,DISEASE_7158
7159,7159,7159,7159,7159,7159,7159,7159,MONDO:0009037,craniosynostosis with anomalies of the cranial base and digits,MONDO,disease,DISEASE_7159
7160,7160,7160,7160,7160,7160,7160,7160,MONDO:0001472,testicular lymphoma,MONDO,disease,DISEASE_7160
7161,7161,7161,7161,7161,7161,7161,7161,MONDO:0014087_MONDO:0011814_MONDO:0015799,Smith-McCort dysplasia,MONDO_grouped,disease,DISEASE_7161
7162,7162,7162,7162,7162,7162,7162,7162,MONDO:0018468,proton-pump inhibitor-responsive esophageal eosinophilia,MONDO,disease,DISEASE_7162
7163,7163,7163,7163,7163,7163,7163,7163,MONDO:0002749,extracranial neuroblastoma,MONDO,disease,DISEASE_7163
7164,7164,7164,7164,7164,7164,7164,7164,MONDO:0020600,acute pharyngitis,MONDO,disease,DISEASE_7164
7165,7165,7165,7165,7165,7165,7165,7165,MONDO:0000315,commensal bacterial infectious disease,MONDO,disease,DISEASE_7165
7166,7166,7166,7166,7166,7166,7166,7166,MONDO:1012781_MONDO:1012862,"paroxysmal dyskinesia, PIGN-related, dog",MONDO_grouped,disease,DISEASE_7166
7167,7167,7167,7167,7167,7167,7167,7167,MONDO:0007242,butyrylesterase 1,MONDO,disease,DISEASE_7167
7168,7168,7168,7168,7168,7168,7168,7168,MONDO:0004639,perinatal necrotizing enterocolitis,MONDO,disease,DISEASE_7168
7169,7169,7169,7169,7169,7169,7169,7169,MONDO:0004613,acute intestinal ischemia,MONDO,disease,DISEASE_7169
7170,7170,7170,7170,7170,7170,7170,7170,MONDO:0001976,chorea gravidarum,MONDO,disease,DISEASE_7170
7171,7171,7171,7171,7171,7171,7171,7171,MONDO:0004789,cholangitis,MONDO,disease,DISEASE_7171
7172,7172,7172,7172,7172,7172,7172,7172,MONDO:0700179,feline osteosarcoma,MONDO,disease,DISEASE_7172
7173,7173,7173,7173,7173,7173,7173,7173,MONDO:0015457,corpus callosum agenesis-double urinary collecting system syndrome,MONDO,disease,DISEASE_7173
7174,7174,7174,7174,7174,7174,7174,7174,MONDO:0800449,lysosomal acid lipase deficiency,MONDO,disease,DISEASE_7174
7175,7175,7175,7175,7175,7175,7175,7175,MONDO:0001893,spinal cord melanoma,MONDO,disease,DISEASE_7175
7176,7176,7176,7176,7176,7176,7176,7176,MONDO:0006690,carotid artery thrombosis,MONDO,disease,DISEASE_7176
7177,7177,7177,7177,7177,7177,7177,7177,MONDO:1010149,"tricho-dento-osseous-like syndrome, non-human animal",MONDO,disease,DISEASE_7177
7178,7178,7178,7178,7178,7178,7178,7178,MONDO:0022786,cleft palate colobomata radial synostosis deafness,MONDO,disease,DISEASE_7178
7179,7179,7179,7179,7179,7179,7179,7179,MONDO:0020779,cartilage development disorder,MONDO,disease,DISEASE_7179
7180,7180,7180,7180,7180,7180,7180,7180,MONDO:0005620_MONDO:1010508,cerebral amyloid angiopathy,MONDO_grouped,disease,DISEASE_7180
7181,7181,7181,7181,7181,7181,7181,7181,MONDO:0007138_MONDO:0015017_MONDO:0024456_MONDO:0015016_MONDO:0010015_MONDO:0007662_MONDO:0019503,anterior segment dysgenesis,MONDO_grouped,disease,DISEASE_7181
7182,7182,7182,7182,7182,7182,7182,7182,MONDO:0043731,lytic metastatic bone lesion,MONDO,disease,DISEASE_7182
7183,7183,7183,7183,7183,7183,7183,7183,MONDO:0017585,painful orbital and systemic neurofibromas-marfanoid habitus syndrome,MONDO,disease,DISEASE_7183
7184,7184,7184,7184,7184,7184,7184,7184,MONDO:0017929,congenital achiasma,MONDO,disease,DISEASE_7184
7185,7185,7185,7185,7185,7185,7185,7185,MONDO:0007428,deafness-craniofacial syndrome,MONDO,disease,DISEASE_7185
7186,7186,7186,7186,7186,7186,7186,7186,MONDO:0001652,scrotum melanoma,MONDO,disease,DISEASE_7186
7187,7187,7187,7187,7187,7187,7187,7187,MONDO:0012462,autosomal recessive frontotemporal pachygyria,MONDO,disease,DISEASE_7187
7188,7188,7188,7188,7188,7188,7188,7188,MONDO:0019814,straddling or overriding tricuspid valve,MONDO,disease,DISEASE_7188
7189,7189,7189,7189,7189,7189,7189,7189,MONDO:0015752,intellectual disability-cataracts-kyphosis syndrome,MONDO,disease,DISEASE_7189
7190,7190,7190,7190,7190,7190,7190,7190,MONDO:0008247,Robin sequence-oligodactyly syndrome,MONDO,disease,DISEASE_7190
7191,7191,7191,7191,7191,7191,7191,7191,MONDO:0044992,mouth mucosa disorder,MONDO,disease,DISEASE_7191
7192,7192,7192,7192,7192,7192,7192,7192,MONDO:0004213,vulvar non-keratinizing squamous cell carcinoma,MONDO,disease,DISEASE_7192
7193,7193,7193,7193,7193,7193,7193,7193,MONDO:0016985_MONDO:0016984,nevus of Ito,MONDO_grouped,disease,DISEASE_7193
7194,7194,7194,7194,7194,7194,7194,7194,MONDO:0000384,bladder benign neoplasm,MONDO,disease,DISEASE_7194
7195,7195,7195,7195,7195,7195,7195,7195,MONDO:0009077,"deafness, congenital, and familial myoclonic epilepsy",MONDO,disease,DISEASE_7195
7196,7196,7196,7196,7196,7196,7196,7196,MONDO:0010955,ectodermal dysplasia with intellectual disability and syndactyly,MONDO,disease,DISEASE_7196
7197,7197,7197,7197,7197,7197,7197,7197,MONDO:0100152,DKC1-related disorder,MONDO,disease,DISEASE_7197
7198,7198,7198,7198,7198,7198,7198,7198,MONDO:0009908,pterin-4 alpha-carbinolamine dehydratase 1 deficiency,MONDO,disease,DISEASE_7198
7199,7199,7199,7199,7199,7199,7199,7199,MONDO:0020776,chlamydiaceae infections,MONDO,disease,DISEASE_7199
7200,7200,7200,7200,7200,7200,7200,7200,MONDO:0004592,impetigo,MONDO,disease,DISEASE_7200
7201,7201,7201,7201,7201,7201,7201,7201,MONDO:0005656,Ascaridida infectious disease,MONDO,disease,DISEASE_7201
7202,7202,7202,7202,7202,7202,7202,7202,MONDO:0008635,uterine anomalies,MONDO,disease,DISEASE_7202
7203,7203,7203,7203,7203,7203,7203,7203,MONDO:0023182,Franceschini Vardeu Guala syndrome,MONDO,disease,DISEASE_7203
7204,7204,7204,7204,7204,7204,7204,7204,MONDO:0020709,Majocchi granuloma,MONDO,disease,DISEASE_7204
7205,7205,7205,7205,7205,7205,7205,7205,MONDO:1010698,"glycogen storage disease, G6PC1-related, dog",MONDO,disease,DISEASE_7205
7206,7206,7206,7206,7206,7206,7206,7206,MONDO:0003355,ovary leiomyosarcoma,MONDO,disease,DISEASE_7206
7207,7207,7207,7207,7207,7207,7207,7207,MONDO:0016870,partial deletion of chromosome 5,MONDO,disease,DISEASE_7207
7208,7208,7208,7208,7208,7208,7208,7208,MONDO:0019107,Rh deficiency syndrome,MONDO,disease,DISEASE_7208
7209,7209,7209,7209,7209,7209,7209,7209,MONDO:0031045,"arthrogryposis, distal, IIa 11",MONDO,disease,DISEASE_7209
7210,7210,7210,7210,7210,7210,7210,7210,MONDO:0009903,postaxial acrofacial dysostosis,MONDO,disease,DISEASE_7210
7211,7211,7211,7211,7211,7211,7211,7211,MONDO:0011000,guanylate cyclase 2E,MONDO,disease,DISEASE_7211
7212,7212,7212,7212,7212,7212,7212,7212,MONDO:0022656,cardiomyopathy spherocytosis,MONDO,disease,DISEASE_7212
7213,7213,7213,7213,7213,7213,7213,7213,MONDO:0003283,epididymal neoplasm,MONDO,disease,DISEASE_7213
7214,7214,7214,7214,7214,7214,7214,7214,MONDO:0033682,skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome,MONDO,disease,DISEASE_7214
7215,7215,7215,7215,7215,7215,7215,7215,MONDO:0021115,luminal B breast carcinoma,MONDO,disease,DISEASE_7215
7216,7216,7216,7216,7216,7216,7216,7216,MONDO:0003606,adrenal medulla cancer,MONDO,disease,DISEASE_7216
7217,7217,7217,7217,7217,7217,7217,7217,MONDO:0034109,congenital myopathy with reduced type 2 muscle fibers,MONDO,disease,DISEASE_7217
7218,7218,7218,7218,7218,7218,7218,7218,MONDO:0003506,pulmonary artery choriocarcinoma,MONDO,disease,DISEASE_7218
7219,7219,7219,7219,7219,7219,7219,7219,MONDO:0009022,"corpus callosum, agenesis of",MONDO,disease,DISEASE_7219
7220,7220,7220,7220,7220,7220,7220,7220,MONDO:0023704,Martinez Monasterio Pinheiro syndrome,MONDO,disease,DISEASE_7220
7221,7221,7221,7221,7221,7221,7221,7221,MONDO:0010660_MONDO:0010430_MONDO:0010256_MONDO:0010429_MONDO:0010324_MONDO:0010307_MONDO:0010326_MONDO:0010313_MONDO:0010497_MONDO:0010450_MONDO:0010489_MONDO:0010352_MONDO:0010451_MONDO:0010329_MONDO:0049222_MONDO:0010231_MONDO:0010230_MONDO:0010300_MONDO:0010344_MONDO:0010393_MONDO:0010236_MONDO:0010488_MONDO:0010250_MONDO:0010347_MONDO:0010251_MONDO:0010447_MONDO:0010452_MONDO:0010656_MONDO:0010413_MONDO:0010487_MONDO:0010453_MONDO:0010289_MONDO:0010454_MONDO:0010508_MONDO:0010361_MONDO:0030907_MONDO:0010509_MONDO:0010510_MONDO:0010266_MONDO:0010363_MONDO:0010506_MONDO:0010322_MONDO:0010309,"intellectual disability, X-linked",MONDO_grouped,disease,DISEASE_7221
7222,7222,7222,7222,7222,7222,7222,7222,MONDO:0004496_MONDO:0001114,myocarditis,MONDO_grouped,disease,DISEASE_7222
7223,7223,7223,7223,7223,7223,7223,7223,MONDO:0008321,"pruritus, hereditary localized",MONDO,disease,DISEASE_7223
7224,7224,7224,7224,7224,7224,7224,7224,MONDO:0010937,isoproterenol-mediated vasodilatation,MONDO,disease,DISEASE_7224
7225,7225,7225,7225,7225,7225,7225,7225,MONDO:0017626_MONDO:0018101,familial primary hypomagnesemia with normocalcuria,MONDO_grouped,disease,DISEASE_7225
7226,7226,7226,7226,7226,7226,7226,7226,MONDO:1011444,"neuroaxonal dystrophy, non-human animal",MONDO,disease,DISEASE_7226
7227,7227,7227,7227,7227,7227,7227,7227,MONDO:0017607,caudal regression sequence,MONDO,disease,DISEASE_7227
7228,7228,7228,7228,7228,7228,7228,7228,MONDO:0016552_MONDO:0035295,"congenital primary megaureter, nonrefluxing and unobstructed form",MONDO_grouped,disease,DISEASE_7228
7229,7229,7229,7229,7229,7229,7229,7229,MONDO:0017739,disorder of lysosomal-related organelles,MONDO,disease,DISEASE_7229
7230,7230,7230,7230,7230,7230,7230,7230,MONDO:0006428,splenic diffuse large B-cell lymphoma,MONDO,disease,DISEASE_7230
7231,7231,7231,7231,7231,7231,7231,7231,MONDO:0006962_MONDO:0002375,sebaceous adenocarcinoma,MONDO_grouped,disease,DISEASE_7231
7232,7232,7232,7232,7232,7232,7232,7232,MONDO:0013481,chromosome 13q14 deletion syndrome,MONDO,disease,DISEASE_7232
7233,7233,7233,7233,7233,7233,7233,7233,MONDO:0002632,metachronous osteosarcoma of the bone,MONDO,disease,DISEASE_7233
7234,7234,7234,7234,7234,7234,7234,7234,MONDO:1012244,"rod-cone degeneration, domestic guinea pig",MONDO,disease,DISEASE_7234
7235,7235,7235,7235,7235,7235,7235,7235,MONDO:0004226_MONDO:0004254,diffuse intraductal papillomatosis,MONDO_grouped,disease,DISEASE_7235
7236,7236,7236,7236,7236,7236,7236,7236,MONDO:0005938,renal tuberculosis,MONDO,disease,DISEASE_7236
7237,7237,7237,7237,7237,7237,7237,7237,MONDO:0006886,thyroid gland papillary and follicular carcinoma,MONDO,disease,DISEASE_7237
7238,7238,7238,7238,7238,7238,7238,7238,MONDO:0015635,porokeratotic eccrine ostial and dermal duct nevus,MONDO,disease,DISEASE_7238
7239,7239,7239,7239,7239,7239,7239,7239,MONDO:0003070,axillary lymphadenitis,MONDO,disease,DISEASE_7239
7240,7240,7240,7240,7240,7240,7240,7240,MONDO:0017204,toxic maculopathy due to antimalarial drugs,MONDO,disease,DISEASE_7240
7241,7241,7241,7241,7241,7241,7241,7241,MONDO:1010727,"leukocyte adhesion deficiency, ITGB2-related, dog",MONDO,disease,DISEASE_7241
7242,7242,7242,7242,7242,7242,7242,7242,MONDO:0012278_MONDO:0010997_MONDO:0019037_MONDO:0012576,"supranuclear palsy, progressive",MONDO_grouped,disease,DISEASE_7242
7243,7243,7243,7243,7243,7243,7243,7243,MONDO:0003549,adenosquamous bile duct carcinoma,MONDO,disease,DISEASE_7243
7244,7244,7244,7244,7244,7244,7244,7244,MONDO:0000944,cerebral artery occlusion,MONDO,disease,DISEASE_7244
7245,7245,7245,7245,7245,7245,7245,7245,MONDO:1010108,myxedema heart disease,MONDO,disease,DISEASE_7245
7246,7246,7246,7246,7246,7246,7246,7246,MONDO:0010193,Weaver syndrome,MONDO,disease,DISEASE_7246
7247,7247,7247,7247,7247,7247,7247,7247,MONDO:0017425_MONDO:0017426,preaxial polydactyly of fingers,MONDO_grouped,disease,DISEASE_7247
7248,7248,7248,7248,7248,7248,7248,7248,MONDO:0019932,isolated partial vaginal agenesis,MONDO,disease,DISEASE_7248
7249,7249,7249,7249,7249,7249,7249,7249,MONDO:0009885,Scott syndrome,MONDO,disease,DISEASE_7249
7250,7250,7250,7250,7250,7250,7250,7250,MONDO:0045055,glycogen-rich carcinoma,MONDO,disease,DISEASE_7250
7251,7251,7251,7251,7251,7251,7251,7251,MONDO:0000230,Israeli tick typhus,MONDO,disease,DISEASE_7251
7252,7252,7252,7252,7252,7252,7252,7252,MONDO:0009587,mesoaxial hexadactyly and cardiac malformation,MONDO,disease,DISEASE_7252
7253,7253,7253,7253,7253,7253,7253,7253,MONDO:0006546,erythematosquamous dermatosis,MONDO,disease,DISEASE_7253
7254,7254,7254,7254,7254,7254,7254,7254,MONDO:0007304,cervical vertebral Bridge,MONDO,disease,DISEASE_7254
7255,7255,7255,7255,7255,7255,7255,7255,MONDO:0012814,diastasis recti and weakness of the linea alba,MONDO,disease,DISEASE_7255
7256,7256,7256,7256,7256,7256,7256,7256,MONDO:1010082,"Evans syndrome, non-human animal",MONDO,disease,DISEASE_7256
7257,7257,7257,7257,7257,7257,7257,7257,MONDO:0006466,thyroid gland spindle cell tumor with thymus-like differentiation,MONDO,disease,DISEASE_7257
7258,7258,7258,7258,7258,7258,7258,7258,MONDO:0043783,sclerema neonatorum,MONDO,disease,DISEASE_7258
7259,7259,7259,7259,7259,7259,7259,7259,MONDO:0018885,orbital leiomyoma,MONDO,disease,DISEASE_7259
7260,7260,7260,7260,7260,7260,7260,7260,MONDO:0016610,idiopathic eosinophilic myositis,MONDO,disease,DISEASE_7260
7261,7261,7261,7261,7261,7261,7261,7261,MONDO:0850093,obsolete absence epilepsy,MONDO,disease,DISEASE_7261
7262,7262,7262,7262,7262,7262,7262,7262,MONDO:0019577,anonychia-onychodystrophy syndrome,MONDO,disease,DISEASE_7262
7263,7263,7263,7263,7263,7263,7263,7263,MONDO:0021325,malignant neoplasm of thoracic esophagus,MONDO,disease,DISEASE_7263
7264,7264,7264,7264,7264,7264,7264,7264,MONDO:0001684_MONDO:1010607_MONDO:1010608_MONDO:1010609,exocrine pancreatic insufficiency,MONDO_grouped,disease,DISEASE_7264
7265,7265,7265,7265,7265,7265,7265,7265,MONDO:1012626_MONDO:1012627,"progressive degenerative myeloencephalopathy, PNPLA8-related, dog",MONDO_grouped,disease,DISEASE_7265
7266,7266,7266,7266,7266,7266,7266,7266,MONDO:0006404,salivary gland large cell carcinoma,MONDO,disease,DISEASE_7266
7267,7267,7267,7267,7267,7267,7267,7267,MONDO:0035743,factor V amsterdam bleeding disorder,MONDO,disease,DISEASE_7267
7268,7268,7268,7268,7268,7268,7268,7268,MONDO:0007917,lymphedema-cerebral arteriovenous anomaly syndrome,MONDO,disease,DISEASE_7268
7269,7269,7269,7269,7269,7269,7269,7269,MONDO:1012234,"reduced glutathione deficiency due to GCS deficiency, sheep",MONDO,disease,DISEASE_7269
7270,7270,7270,7270,7270,7270,7270,7270,MONDO:1010119,"scleroderma, non-human animal",MONDO,disease,DISEASE_7270
7271,7271,7271,7271,7271,7271,7271,7271,MONDO:0004518,anterior urethra cancer,MONDO,disease,DISEASE_7271
7272,7272,7272,7272,7272,7272,7272,7272,MONDO:0021545,myomatous neoplasm,MONDO,disease,DISEASE_7272
7273,7273,7273,7273,7273,7273,7273,7273,MONDO:0030105_MONDO:0018116_MONDO:1010705,galactosemia,MONDO_grouped,disease,DISEASE_7273
7274,7274,7274,7274,7274,7274,7274,7274,MONDO:0008352,"pupillary membrane, persistence of",MONDO,disease,DISEASE_7274
7275,7275,7275,7275,7275,7275,7275,7275,MONDO:0032920,juvenile arthritis due to defect in LACC1,MONDO,disease,DISEASE_7275
7276,7276,7276,7276,7276,7276,7276,7276,MONDO:0009932,pulmonary bullae causing pneumothorax,MONDO,disease,DISEASE_7276
7277,7277,7277,7277,7277,7277,7277,7277,MONDO:0859305,neurodevelopmental disorder with eye movement abnormalities and ataxia,MONDO,disease,DISEASE_7277
7278,7278,7278,7278,7278,7278,7278,7278,MONDO:0008159_MONDO:0700047,postmenopausal osteoporosis,MONDO_grouped,disease,DISEASE_7278
7279,7279,7279,7279,7279,7279,7279,7279,MONDO:0020477,progeria-associated arthropathy,MONDO,disease,DISEASE_7279
7280,7280,7280,7280,7280,7280,7280,7280,MONDO:0001358,bronchial disorder,MONDO,disease,DISEASE_7280
7281,7281,7281,7281,7281,7281,7281,7281,MONDO:0800313,"xeroderma pigmentosum, type F/Cockayne syndrome",MONDO,disease,DISEASE_7281
7282,7282,7282,7282,7282,7282,7282,7282,MONDO:0001668,internal pathological resorption of tooth,MONDO,disease,DISEASE_7282
7283,7283,7283,7283,7283,7283,7283,7283,MONDO:0018382,epiphysiolysis of the hip,MONDO,disease,DISEASE_7283
7284,7284,7284,7284,7284,7284,7284,7284,MONDO:0006223,gastric diffuse large B-cell lymphoma,MONDO,disease,DISEASE_7284
7285,7285,7285,7285,7285,7285,7285,7285,MONDO:0019806,primary progressive aphasia,MONDO,disease,DISEASE_7285
7286,7286,7286,7286,7286,7286,7286,7286,MONDO:0003083,venous hemangioma,MONDO,disease,DISEASE_7286
7287,7287,7287,7287,7287,7287,7287,7287,MONDO:0009789,"nonarteritic anterior ischemic optic neuropathy, susceptibility to",MONDO,disease,DISEASE_7287
7288,7288,7288,7288,7288,7288,7288,7288,MONDO:0004201,pituitary hypoplasia,MONDO,disease,DISEASE_7288
7289,7289,7289,7289,7289,7289,7289,7289,MONDO:0859273,"liver disease, severe congenital",MONDO,disease,DISEASE_7289
7290,7290,7290,7290,7290,7290,7290,7290,MONDO:0009507,Lambert syndrome,MONDO,disease,DISEASE_7290
7291,7291,7291,7291,7291,7291,7291,7291,MONDO:0007513,ectodermal dysplasia with adrenal cyst,MONDO,disease,DISEASE_7291
7292,7292,7292,7292,7292,7292,7292,7292,MONDO:0006722,dental fluorosis,MONDO,disease,DISEASE_7292
7293,7293,7293,7293,7293,7293,7293,7293,MONDO:0023039,eccrine mucinous carcinoma,MONDO,disease,DISEASE_7293
7294,7294,7294,7294,7294,7294,7294,7294,MONDO:1012527,"ichthyosis fetalis, sheep",MONDO,disease,DISEASE_7294
7295,7295,7295,7295,7295,7295,7295,7295,MONDO:0024954,"larva migrans, visceral",MONDO,disease,DISEASE_7295
7296,7296,7296,7296,7296,7296,7296,7296,MONDO:0006591,panniculitis,MONDO,disease,DISEASE_7296
7297,7297,7297,7297,7297,7297,7297,7297,MONDO:0016540,congenital secondary polycythemia,MONDO,disease,DISEASE_7297
7298,7298,7298,7298,7298,7298,7298,7298,MONDO:0020444,subaortic course of innominate vein,MONDO,disease,DISEASE_7298
7299,7299,7299,7299,7299,7299,7299,7299,MONDO:0015639,benign partial epilepsy with secondarily generalized seizures in infancy,MONDO,disease,DISEASE_7299
7300,7300,7300,7300,7300,7300,7300,7300,MONDO:0023305,heavy metal poisoning,MONDO,disease,DISEASE_7300
7301,7301,7301,7301,7301,7301,7301,7301,MONDO:0002369_MONDO:0003464,cystadenoma,MONDO_grouped,disease,DISEASE_7301
7302,7302,7302,7302,7302,7302,7302,7302,MONDO:0004608,oropharynx cancer,MONDO,disease,DISEASE_7302
7303,7303,7303,7303,7303,7303,7303,7303,MONDO:0021402,polyp of external auditory canal,MONDO,disease,DISEASE_7303
7304,7304,7304,7304,7304,7304,7304,7304,MONDO:0001600,mucocele of salivary gland,MONDO,disease,DISEASE_7304
7305,7305,7305,7305,7305,7305,7305,7305,MONDO:0044342,thoracic disk degenerative disorder,MONDO,disease,DISEASE_7305
7306,7306,7306,7306,7306,7306,7306,7306,MONDO:0020717,autosomal dominant wooly hair,MONDO,disease,DISEASE_7306
7307,7307,7307,7307,7307,7307,7307,7307,MONDO:0019959,glucagonoma,MONDO,disease,DISEASE_7307
7308,7308,7308,7308,7308,7308,7308,7308,MONDO:0019140,acute ackee fruit intoxication,MONDO,disease,DISEASE_7308
7309,7309,7309,7309,7309,7309,7309,7309,MONDO:0043797_MONDO:0037747_MONDO:0005309,spinal cord injury,MONDO_grouped,disease,DISEASE_7309
7310,7310,7310,7310,7310,7310,7310,7310,MONDO:0859254,hepatorenocardiac degenerative fibrosis,MONDO,disease,DISEASE_7310
7311,7311,7311,7311,7311,7311,7311,7311,MONDO:0016969,partial duplication of the long arm of chromosome 19,MONDO,disease,DISEASE_7311
7312,7312,7312,7312,7312,7312,7312,7312,MONDO:0002401,malignant tenosynovial giant cell tumor,MONDO,disease,DISEASE_7312
7313,7313,7313,7313,7313,7313,7313,7313,MONDO:1012039_MONDO:1012421,"cerebellar abiotrophy, domestic cat",MONDO_grouped,disease,DISEASE_7313
7314,7314,7314,7314,7314,7314,7314,7314,MONDO:0012545,neutral lipid storage myopathy,MONDO,disease,DISEASE_7314
7315,7315,7315,7315,7315,7315,7315,7315,MONDO:1012236,"renal dysplasia and bladder aplasia-hypoplasia, sheep",MONDO,disease,DISEASE_7315
7316,7316,7316,7316,7316,7316,7316,7316,MONDO:1010869_MONDO:1010870_MONDO:1010871_MONDO:1010876,"mucopolysaccharidosis, ARSB-related, dog",MONDO_grouped,disease,DISEASE_7316
7317,7317,7317,7317,7317,7317,7317,7317,MONDO:0010695,"occipital hair, white lock of",MONDO,disease,DISEASE_7317
7318,7318,7318,7318,7318,7318,7318,7318,MONDO:0012055,Larsen-like osseous dysplasia-short stature syndrome,MONDO,disease,DISEASE_7318
7319,7319,7319,7319,7319,7319,7319,7319,MONDO:0002999_MONDO:0004452_MONDO:0004383,central nervous system germinoma,MONDO_grouped,disease,DISEASE_7319
7320,7320,7320,7320,7320,7320,7320,7320,MONDO:0004301,fibrosarcomatous osteosarcoma,MONDO,disease,DISEASE_7320
7321,7321,7321,7321,7321,7321,7321,7321,MONDO:0002527,keratoacanthoma,MONDO,disease,DISEASE_7321
7322,7322,7322,7322,7322,7322,7322,7322,MONDO:0003970,gastric fundus carcinoma,MONDO,disease,DISEASE_7322
7323,7323,7323,7323,7323,7323,7323,7323,MONDO:0004684_MONDO:0006345,plantar fibromatosis,MONDO_grouped,disease,DISEASE_7323
7324,7324,7324,7324,7324,7324,7324,7324,MONDO:0800384,cesium poisoning,MONDO,disease,DISEASE_7324
7325,7325,7325,7325,7325,7325,7325,7325,MONDO:0010203,"intellectual disability, Wolff type",MONDO,disease,DISEASE_7325
7326,7326,7326,7326,7326,7326,7326,7326,MONDO:0006738,eccrine acrospiroma,MONDO,disease,DISEASE_7326
7327,7327,7327,7327,7327,7327,7327,7327,MONDO:0016950,partial duplication of the short arm of chromosome 17,MONDO,disease,DISEASE_7327
7328,7328,7328,7328,7328,7328,7328,7328,MONDO:0023171,foix chavany Marie syndrome,MONDO,disease,DISEASE_7328
7329,7329,7329,7329,7329,7329,7329,7329,MONDO:0800432,"obesity, susceptibility to",MONDO,disease,DISEASE_7329
7330,7330,7330,7330,7330,7330,7330,7330,MONDO:0043166,pancreatic lipomatosis duodenal stenosis,MONDO,disease,DISEASE_7330
7331,7331,7331,7331,7331,7331,7331,7331,MONDO:0011605,generalized basaloid follicular hamartoma syndrome,MONDO,disease,DISEASE_7331
7332,7332,7332,7332,7332,7332,7332,7332,MONDO:0018681,neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome,MONDO,disease,DISEASE_7332
7333,7333,7333,7333,7333,7333,7333,7333,MONDO:0100073_MONDO:1040020,methicillin-resistant staphylococcus aureus infectious disease,MONDO_grouped,disease,DISEASE_7333
7334,7334,7334,7334,7334,7334,7334,7334,MONDO:0004523,clear cell squamous cell skin carcinoma,MONDO,disease,DISEASE_7334
7335,7335,7335,7335,7335,7335,7335,7335,MONDO:0004232,large cell keratinizing variant squamous cell breast carcinoma,MONDO,disease,DISEASE_7335
7336,7336,7336,7336,7336,7336,7336,7336,MONDO:0045060,intraductal cribriform breast adenocarcinoma,MONDO,disease,DISEASE_7336
7337,7337,7337,7337,7337,7337,7337,7337,MONDO:0003417,internuclear ophthalmoplegia,MONDO,disease,DISEASE_7337
7338,7338,7338,7338,7338,7338,7338,7338,MONDO:0017726_MONDO:0017724_MONDO:0017725,"Tay-Sachs disease, B variant, adult form",MONDO_grouped,disease,DISEASE_7338
7339,7339,7339,7339,7339,7339,7339,7339,MONDO:0017890,tubulocystic renal cell carcinoma,MONDO,disease,DISEASE_7339
7340,7340,7340,7340,7340,7340,7340,7340,MONDO:0016591,sporadic adult-onset ataxia of unknown etiology,MONDO,disease,DISEASE_7340
7341,7341,7341,7341,7341,7341,7341,7341,MONDO:0100119_MONDO:0800167_MONDO:0800166,Knobloch syndrome,MONDO_grouped,disease,DISEASE_7341
7342,7342,7342,7342,7342,7342,7342,7342,MONDO:0007667,subependymoma,MONDO,disease,DISEASE_7342
7343,7343,7343,7343,7343,7343,7343,7343,MONDO:0012747,glycogen storage disease due to aldolase A deficiency,MONDO,disease,DISEASE_7343
7344,7344,7344,7344,7344,7344,7344,7344,MONDO:0006279,lung sarcomatoid carcinoma,MONDO,disease,DISEASE_7344
7345,7345,7345,7345,7345,7345,7345,7345,MONDO:1011490,"complement component 6 deficiency, rabbit",MONDO,disease,DISEASE_7345
7346,7346,7346,7346,7346,7346,7346,7346,MONDO:0009987,autosomal recessive pericentral pigmentary retinopathy,MONDO,disease,DISEASE_7346
7347,7347,7347,7347,7347,7347,7347,7347,MONDO:0014746,SLC39A8-CDG,MONDO,disease,DISEASE_7347
7348,7348,7348,7348,7348,7348,7348,7348,MONDO:0005999,tuberculous empyema,MONDO,disease,DISEASE_7348
7349,7349,7349,7349,7349,7349,7349,7349,MONDO:0018121,mitochondrial DNA maintenance syndrome,MONDO,disease,DISEASE_7349
7350,7350,7350,7350,7350,7350,7350,7350,MONDO:0011107,congenital hypotrichosis with juvenile macular dystrophy,MONDO,disease,DISEASE_7350
7351,7351,7351,7351,7351,7351,7351,7351,MONDO:0003282_MONDO:0001202,ovarian cyst,MONDO_grouped,disease,DISEASE_7351
7352,7352,7352,7352,7352,7352,7352,7352,MONDO:0011268_MONDO:0009968,"renal tubular acidosis, distal, 3, with or without sensorineural hearing loss",MONDO_grouped,disease,DISEASE_7352
7353,7353,7353,7353,7353,7353,7353,7353,MONDO:0004656,rubella,MONDO,disease,DISEASE_7353
7354,7354,7354,7354,7354,7354,7354,7354,MONDO:0100494,autosomal dominant titinopathy,MONDO,disease,DISEASE_7354
7355,7355,7355,7355,7355,7355,7355,7355,MONDO:0014806_MONDO:0014807_MONDO:0000209,spinal muscular atrophy with congenital bone fractures,MONDO_grouped,disease,DISEASE_7355
7356,7356,7356,7356,7356,7356,7356,7356,MONDO:0001977,ureteral lymphoma,MONDO,disease,DISEASE_7356
7357,7357,7357,7357,7357,7357,7357,7357,MONDO:1012552_MONDO:1012553,"retained placenta, horse",MONDO_grouped,disease,DISEASE_7357
7358,7358,7358,7358,7358,7358,7358,7358,MONDO:0015225,arthrogryposis syndrome,MONDO,disease,DISEASE_7358
7359,7359,7359,7359,7359,7359,7359,7359,MONDO:0044870_MONDO:0044817,acquired torsion dystonia,MONDO_grouped,disease,DISEASE_7359
7360,7360,7360,7360,7360,7360,7360,7360,MONDO:0016885,partial deletion of the short arm of chromosome 3,MONDO,disease,DISEASE_7360
7361,7361,7361,7361,7361,7361,7361,7361,MONDO:0002367,kidney cancer,MONDO,disease,DISEASE_7361
7362,7362,7362,7362,7362,7362,7362,7362,MONDO:0007854,keratolytic winter erythema,MONDO,disease,DISEASE_7362
7363,7363,7363,7363,7363,7363,7363,7363,MONDO:0958116,autosomal recessive combined immunodeficiency due to partial IL6ST deficiency,MONDO,disease,DISEASE_7363
7364,7364,7364,7364,7364,7364,7364,7364,MONDO:0024889,benign mesonephroma,MONDO,disease,DISEASE_7364
7365,7365,7365,7365,7365,7365,7365,7365,MONDO:0019836,congenital anomaly of hepatic vein,MONDO,disease,DISEASE_7365
7366,7366,7366,7366,7366,7366,7366,7366,MONDO:1011633,"progressive ataxia, non-human animal",MONDO,disease,DISEASE_7366
7367,7367,7367,7367,7367,7367,7367,7367,MONDO:0012603_MONDO:0100352_MONDO:0859380_MONDO:0044202,episodic kinesigenic dyskinesia,MONDO_grouped,disease,DISEASE_7367
7368,7368,7368,7368,7368,7368,7368,7368,MONDO:0000598_MONDO:0003039,aphasia,MONDO_grouped,disease,DISEASE_7368
7369,7369,7369,7369,7369,7369,7369,7369,MONDO:0032939_MONDO:0957228,"intellectual developmental disorder, autosomal dominant 63, with macrocephaly",MONDO_grouped,disease,DISEASE_7369
7370,7370,7370,7370,7370,7370,7370,7370,MONDO:0100036,variable-age onset epilepsy syndrome,MONDO,disease,DISEASE_7370
7371,7371,7371,7371,7371,7371,7371,7371,MONDO:0010869,motor neuron disease with dementia and ophthalmoplegia,MONDO,disease,DISEASE_7371
7372,7372,7372,7372,7372,7372,7372,7372,MONDO:0010294,X-linked severe congenital neutropenia,MONDO,disease,DISEASE_7372
7373,7373,7373,7373,7373,7373,7373,7373,MONDO:0006339,ovarian microcystic stromal tumor,MONDO,disease,DISEASE_7373
7374,7374,7374,7374,7374,7374,7374,7374,MONDO:0001804_MONDO:0001774,anterior scleritis,MONDO_grouped,disease,DISEASE_7374
7375,7375,7375,7375,7375,7375,7375,7375,MONDO:0007325,"choreoathetosis, familial inverted",MONDO,disease,DISEASE_7375
7376,7376,7376,7376,7376,7376,7376,7376,MONDO:0022746,chromosome 13p duplication,MONDO,disease,DISEASE_7376
7377,7377,7377,7377,7377,7377,7377,7377,MONDO:0014820,mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type),MONDO,disease,DISEASE_7377
7378,7378,7378,7378,7378,7378,7378,7378,MONDO:0011018,brachyolmia-amelogenesis imperfecta syndrome,MONDO,disease,DISEASE_7378
7379,7379,7379,7379,7379,7379,7379,7379,MONDO:0016095_MONDO:0002881,vaginal rhabdomyosarcoma,MONDO_grouped,disease,DISEASE_7379
7380,7380,7380,7380,7380,7380,7380,7380,MONDO:0022762,chromosome 4 short arm deletion,MONDO,disease,DISEASE_7380
7381,7381,7381,7381,7381,7381,7381,7381,MONDO:0014615_MONDO:0014619_MONDO:0011125_MONDO:0002470,"trichothiodystrophy 2, photosensitive",MONDO_grouped,disease,DISEASE_7381
7382,7382,7382,7382,7382,7382,7382,7382,MONDO:0800421,"cardiomyopathy, familial hypertrophic, 4, susceptibility to",MONDO,disease,DISEASE_7382
7383,7383,7383,7383,7383,7383,7383,7383,MONDO:0009966,NPHP3-related Meckel-like syndrome,MONDO,disease,DISEASE_7383
7384,7384,7384,7384,7384,7384,7384,7384,MONDO:0014886,severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome,MONDO,disease,DISEASE_7384
7385,7385,7385,7385,7385,7385,7385,7385,MONDO:0859573_MONDO:0013815_MONDO:0019698,bent bone dysplasia syndrome,MONDO_grouped,disease,DISEASE_7385
7386,7386,7386,7386,7386,7386,7386,7386,MONDO:0019315_MONDO:0017243,diffuse cutaneous mastocytosis,MONDO_grouped,disease,DISEASE_7386
7387,7387,7387,7387,7387,7387,7387,7387,MONDO:1012963,"centronuclear myopathy, non-human animal",MONDO,disease,DISEASE_7387
7388,7388,7388,7388,7388,7388,7388,7388,MONDO:0003473,spinal cord ependymoma,MONDO,disease,DISEASE_7388
7389,7389,7389,7389,7389,7389,7389,7389,MONDO:0009973,reticular dysgenesis,MONDO,disease,DISEASE_7389
7390,7390,7390,7390,7390,7390,7390,7390,MONDO:0037746,malignant vaginal mixed epithelial and mesenchymal neoplasm,MONDO,disease,DISEASE_7390
7391,7391,7391,7391,7391,7391,7391,7391,MONDO:0009474,"isovaleric acid, inability to smell",MONDO,disease,DISEASE_7391
7392,7392,7392,7392,7392,7392,7392,7392,MONDO:0020064_MONDO:0020110,pulmonary valve agenesis,MONDO_grouped,disease,DISEASE_7392
7393,7393,7393,7393,7393,7393,7393,7393,MONDO:0002832,endometrial transitional cell carcinoma,MONDO,disease,DISEASE_7393
7394,7394,7394,7394,7394,7394,7394,7394,MONDO:0002977_MONDO:0000568,autoimmune disorder of the nervous system,MONDO_grouped,disease,DISEASE_7394
7395,7395,7395,7395,7395,7395,7395,7395,MONDO:0004673,lower lip cancer,MONDO,disease,DISEASE_7395
7396,7396,7396,7396,7396,7396,7396,7396,MONDO:0012870,chromosome 2q31.2 deletion syndrome,MONDO,disease,DISEASE_7396
7397,7397,7397,7397,7397,7397,7397,7397,MONDO:0003198_MONDO:0006421_MONDO:0006422,small intestine adenocarcinoma,MONDO_grouped,disease,DISEASE_7397
7398,7398,7398,7398,7398,7398,7398,7398,MONDO:0012775_MONDO:0014837_MONDO:0008555_MONDO:0010120_MONDO:0030867_MONDO:0014536_MONDO:0010743_MONDO:0957572_MONDO:0957578_MONDO:0002049_MONDO:1010662_MONDO:1010659_MONDO:1010661_MONDO:0008556,thrombocytopenia,MONDO_grouped,disease,DISEASE_7398
7399,7399,7399,7399,7399,7399,7399,7399,MONDO:0100481,active tuberculosis,MONDO,disease,DISEASE_7399
7400,7400,7400,7400,7400,7400,7400,7400,MONDO:0018223,systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood,MONDO,disease,DISEASE_7400
7401,7401,7401,7401,7401,7401,7401,7401,MONDO:0100572,MTOR-related overgrowth spectrum,MONDO,disease,DISEASE_7401
7402,7402,7402,7402,7402,7402,7402,7402,MONDO:1012080,"focal metatarsal fistula, dog",MONDO,disease,DISEASE_7402
7403,7403,7403,7403,7403,7403,7403,7403,MONDO:0010007,microbrachycephaly-ptosis-cleft lip syndrome,MONDO,disease,DISEASE_7403
7404,7404,7404,7404,7404,7404,7404,7404,MONDO:0014419,ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome,MONDO,disease,DISEASE_7404
7405,7405,7405,7405,7405,7405,7405,7405,MONDO:0017324_MONDO:0008660,autosomal recessive hypophosphatemic rickets,MONDO_grouped,disease,DISEASE_7405
7406,7406,7406,7406,7406,7406,7406,7406,MONDO:0016527,glycogen storage disease due to lactate dehydrogenase deficiency,MONDO,disease,DISEASE_7406
7407,7407,7407,7407,7407,7407,7407,7407,MONDO:0034186,autosomal recessive extra-oral halitosis,MONDO,disease,DISEASE_7407
7408,7408,7408,7408,7408,7408,7408,7408,MONDO:0010165,ulna hypoplasia-intellectual disability syndrome,MONDO,disease,DISEASE_7408
7409,7409,7409,7409,7409,7409,7409,7409,MONDO:0014335,diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome,MONDO,disease,DISEASE_7409
7410,7410,7410,7410,7410,7410,7410,7410,MONDO:0007524,"autosomal dominant Ehlers-Danlos syndrome, vascular type",MONDO,disease,DISEASE_7410
7411,7411,7411,7411,7411,7411,7411,7411,MONDO:0009048,curved nail of fourth toe,MONDO,disease,DISEASE_7411
7412,7412,7412,7412,7412,7412,7412,7412,MONDO:0013143,hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency,MONDO,disease,DISEASE_7412
7413,7413,7413,7413,7413,7413,7413,7413,MONDO:0005030,fetal growth restriction,MONDO,disease,DISEASE_7413
7414,7414,7414,7414,7414,7414,7414,7414,MONDO:0024314,parasitemia,MONDO,disease,DISEASE_7414
7415,7415,7415,7415,7415,7415,7415,7415,MONDO:0009167,Bonnemann-Meinecke-Reich syndrome,MONDO,disease,DISEASE_7415
7416,7416,7416,7416,7416,7416,7416,7416,MONDO:1012428,"complement component 4 deficiency, domestic guinea pig",MONDO,disease,DISEASE_7416
7417,7417,7417,7417,7417,7417,7417,7417,MONDO:0010365,"myopathy, congenital, with fiber-type disproportion, X-linked",MONDO,disease,DISEASE_7417
7418,7418,7418,7418,7418,7418,7418,7418,MONDO:0005173,actinic keratosis,MONDO,disease,DISEASE_7418
7419,7419,7419,7419,7419,7419,7419,7419,MONDO:0021310,malignant tumor of neck,MONDO,disease,DISEASE_7419
7420,7420,7420,7420,7420,7420,7420,7420,MONDO:0008209,Char syndrome,MONDO,disease,DISEASE_7420
7421,7421,7421,7421,7421,7421,7421,7421,MONDO:0017408,rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome,MONDO,disease,DISEASE_7421
7422,7422,7422,7422,7422,7422,7422,7422,MONDO:0008277_MONDO:0060766_MONDO:0006314,stomach polyp,MONDO_grouped,disease,DISEASE_7422
7423,7423,7423,7423,7423,7423,7423,7423,MONDO:0006792,hyperglobulinemic purpura,MONDO,disease,DISEASE_7423
7424,7424,7424,7424,7424,7424,7424,7424,MONDO:0004727,vestibule of mouth cancer,MONDO,disease,DISEASE_7424
7425,7425,7425,7425,7425,7425,7425,7425,MONDO:0001925,retinal dystrophy in systemic or cerebroretinal lipidoses,MONDO,disease,DISEASE_7425
7426,7426,7426,7426,7426,7426,7426,7426,MONDO:0007451,"diabetes insipidus, nephrogenic, autosomal",MONDO,disease,DISEASE_7426
7427,7427,7427,7427,7427,7427,7427,7427,MONDO:0035406,furuncular myiasis due to Dermatobia hominis,MONDO,disease,DISEASE_7427
7428,7428,7428,7428,7428,7428,7428,7428,MONDO:0002934,intravascular angioleiomyoma,MONDO,disease,DISEASE_7428
7429,7429,7429,7429,7429,7429,7429,7429,MONDO:0014796_MONDO:0013060_MONDO:0010820_MONDO:0011613_MONDO:0011658,autosomal recessive early-onset Parkinson disease,MONDO_grouped,disease,DISEASE_7429
7430,7430,7430,7430,7430,7430,7430,7430,MONDO:0011024,"dermatitis herpetiformis, familial",MONDO,disease,DISEASE_7430
7431,7431,7431,7431,7431,7431,7431,7431,MONDO:0014723,PMP22-RAI1 contiguous gene duplication syndrome,MONDO,disease,DISEASE_7431
7432,7432,7432,7432,7432,7432,7432,7432,MONDO:0004603,collagenopathy,MONDO,disease,DISEASE_7432
7433,7433,7433,7433,7433,7433,7433,7433,MONDO:0002488,intraductal breast neoplasm,MONDO,disease,DISEASE_7433
7434,7434,7434,7434,7434,7434,7434,7434,MONDO:0002882,colon neuroendocrine neoplasm,MONDO,disease,DISEASE_7434
7435,7435,7435,7435,7435,7435,7435,7435,MONDO:0007511,"ectodermal dysplasia, trichoodontoonychial type",MONDO,disease,DISEASE_7435
7436,7436,7436,7436,7436,7436,7436,7436,MONDO:0020325,anaplastic large cell lymphoma,MONDO,disease,DISEASE_7436
7437,7437,7437,7437,7437,7437,7437,7437,MONDO:0007951,"masticatory muscles, hypertrophy of",MONDO,disease,DISEASE_7437
7438,7438,7438,7438,7438,7438,7438,7438,MONDO:0001663,hole retinal cyst,MONDO,disease,DISEASE_7438
7439,7439,7439,7439,7439,7439,7439,7439,MONDO:0011303_MONDO:0011390_MONDO:0013191_MONDO:0014451_MONDO:0014462_MONDO:0014539_MONDO:0013589_MONDO:0100313_MONDO:0005363_MONDO:0100324,focal segmental glomerulosclerosis,MONDO_grouped,disease,DISEASE_7439
7440,7440,7440,7440,7440,7440,7440,7440,MONDO:0011928,caudal duplication,MONDO,disease,DISEASE_7440
7441,7441,7441,7441,7441,7441,7441,7441,MONDO:0019877,distal trisomy 2q,MONDO,disease,DISEASE_7441
7442,7442,7442,7442,7442,7442,7442,7442,MONDO:0020371,essential iris atrophy,MONDO,disease,DISEASE_7442
7443,7443,7443,7443,7443,7443,7443,7443,MONDO:0009648,peripheral motor neuropathy-dysautonomia syndrome,MONDO,disease,DISEASE_7443
7444,7444,7444,7444,7444,7444,7444,7444,MONDO:0001071,intellectual disability,MONDO,disease,DISEASE_7444
7445,7445,7445,7445,7445,7445,7445,7445,MONDO:1012267,"androgen insensitivity syndrome, pig",MONDO,disease,DISEASE_7445
7446,7446,7446,7446,7446,7446,7446,7446,MONDO:0010561,Coffin-Lowry syndrome,MONDO,disease,DISEASE_7446
7447,7447,7447,7447,7447,7447,7447,7447,MONDO:0015303,macular amyloidosis,MONDO,disease,DISEASE_7447
7448,7448,7448,7448,7448,7448,7448,7448,MONDO:0001764,ethmoidal sinus neoplasm,MONDO,disease,DISEASE_7448
7449,7449,7449,7449,7449,7449,7449,7449,MONDO:0020463,isolated congenital ectropion,MONDO,disease,DISEASE_7449
7450,7450,7450,7450,7450,7450,7450,7450,MONDO:0023286,graphite pneumoconiosis,MONDO,disease,DISEASE_7450
7451,7451,7451,7451,7451,7451,7451,7451,MONDO:1030016,22q-related schwannomatosis,MONDO,disease,DISEASE_7451
7452,7452,7452,7452,7452,7452,7452,7452,MONDO:1011191,"synovial chondromatosis, great horned owl",MONDO,disease,DISEASE_7452
7453,7453,7453,7453,7453,7453,7453,7453,MONDO:0005095_MONDO:0043377,spondyloarthropathy,MONDO_grouped,disease,DISEASE_7453
7454,7454,7454,7454,7454,7454,7454,7454,MONDO:1010444,"cardiomyopathy, goat",MONDO,disease,DISEASE_7454
7455,7455,7455,7455,7455,7455,7455,7455,MONDO:0010502,"intellectual disability, X-linked 99, syndromic, female-restricted",MONDO,disease,DISEASE_7455
7456,7456,7456,7456,7456,7456,7456,7456,MONDO:0013686,"distal myopathy, Tateyama type",MONDO,disease,DISEASE_7456
7457,7457,7457,7457,7457,7457,7457,7457,MONDO:0016844,trisomy 20p,MONDO,disease,DISEASE_7457
7458,7458,7458,7458,7458,7458,7458,7458,MONDO:0018703,isolated splenogonadal fusion,MONDO,disease,DISEASE_7458
7459,7459,7459,7459,7459,7459,7459,7459,MONDO:0005990,tracheitis,MONDO,disease,DISEASE_7459
7460,7460,7460,7460,7460,7460,7460,7460,MONDO:0021097_MONDO:0002061,intraductal breast papilloma,MONDO_grouped,disease,DISEASE_7460
7461,7461,7461,7461,7461,7461,7461,7461,MONDO:0001781,uterine corpus adenomatoid tumor,MONDO,disease,DISEASE_7461
7462,7462,7462,7462,7462,7462,7462,7462,MONDO:0016567,locked-in syndrome,MONDO,disease,DISEASE_7462
7463,7463,7463,7463,7463,7463,7463,7463,MONDO:0019085,vernal keratoconjunctivitis,MONDO,disease,DISEASE_7463
7464,7464,7464,7464,7464,7464,7464,7464,MONDO:0008294,acute intermittent porphyria,MONDO,disease,DISEASE_7464
7465,7465,7465,7465,7465,7465,7465,7465,MONDO:0060779,acquired Fanconi syndrome,MONDO,disease,DISEASE_7465
7466,7466,7466,7466,7466,7466,7466,7466,MONDO:0006455,thymic undifferentiated carcinoma,MONDO,disease,DISEASE_7466
7467,7467,7467,7467,7467,7467,7467,7467,MONDO:0023563,Kotzot-Richter syndrome,MONDO,disease,DISEASE_7467
7468,7468,7468,7468,7468,7468,7468,7468,MONDO:0012530,palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome,MONDO,disease,DISEASE_7468
7469,7469,7469,7469,7469,7469,7469,7469,MONDO:0013802,infantile cerebellar-retinal degeneration,MONDO,disease,DISEASE_7469
7470,7470,7470,7470,7470,7470,7470,7470,MONDO:0011346_MONDO:0010209_MONDO:0000721_MONDO:1011623_MONDO:1011625,xanthinuria,MONDO_grouped,disease,DISEASE_7470
7471,7471,7471,7471,7471,7471,7471,7471,MONDO:0005853,malignant mixed neoplasm,MONDO,disease,DISEASE_7471
7472,7472,7472,7472,7472,7472,7472,7472,MONDO:1011345,"poisoning, non-human animal",MONDO,disease,DISEASE_7472
7473,7473,7473,7473,7473,7473,7473,7473,MONDO:0020584_MONDO:0020725,anemia due to enzyme disorder,MONDO_grouped,disease,DISEASE_7473
7474,7474,7474,7474,7474,7474,7474,7474,MONDO:0011122,obesity disorder,MONDO,disease,DISEASE_7474
7475,7475,7475,7475,7475,7475,7475,7475,MONDO:0001078,tropical sprue,MONDO,disease,DISEASE_7475
7476,7476,7476,7476,7476,7476,7476,7476,MONDO:0001987,senile degeneration of brain,MONDO,disease,DISEASE_7476
7477,7477,7477,7477,7477,7477,7477,7477,MONDO:0010644,"proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis",MONDO,disease,DISEASE_7477
7478,7478,7478,7478,7478,7478,7478,7478,MONDO:0017552_MONDO:0017554_MONDO:0017555,"humero-ulnar synostosis, unilateral",MONDO_grouped,disease,DISEASE_7478
7479,7479,7479,7479,7479,7479,7479,7479,MONDO:0007686,gray platelet syndrome,MONDO,disease,DISEASE_7479
7480,7480,7480,7480,7480,7480,7480,7480,MONDO:0008484,stapes ankylosis with broad thumbs and toes,MONDO,disease,DISEASE_7480
7481,7481,7481,7481,7481,7481,7481,7481,MONDO:0032654,"hyper-IgE recurrent infection syndrome 3, autosomal recessive",MONDO,disease,DISEASE_7481
7482,7482,7482,7482,7482,7482,7482,7482,MONDO:0957790,"immune dysregulation, autoimmunity, and autoinflammation",MONDO,disease,DISEASE_7482
7483,7483,7483,7483,7483,7483,7483,7483,MONDO:0003088,intramuscular hemangioma,MONDO,disease,DISEASE_7483
7484,7484,7484,7484,7484,7484,7484,7484,MONDO:0008439,spastic paraplegia-epilepsy-intellectual disability syndrome,MONDO,disease,DISEASE_7484
7485,7485,7485,7485,7485,7485,7485,7485,MONDO:0009874,Rabson-Mendenhall syndrome,MONDO,disease,DISEASE_7485
7486,7486,7486,7486,7486,7486,7486,7486,MONDO:0008628,ureterocele,MONDO,disease,DISEASE_7486
7487,7487,7487,7487,7487,7487,7487,7487,MONDO:0006853_MONDO:0003041_MONDO:0003042,mesenchymal chondrosarcoma,MONDO_grouped,disease,DISEASE_7487
7488,7488,7488,7488,7488,7488,7488,7488,MONDO:0004765_MONDO:0850283,intrinsic asthma,MONDO_grouped,disease,DISEASE_7488
7489,7489,7489,7489,7489,7489,7489,7489,MONDO:0012672_MONDO:0002155_MONDO:0001751,cholelithiasis,MONDO_grouped,disease,DISEASE_7489
7490,7490,7490,7490,7490,7490,7490,7490,MONDO:0005660,Avulavirus infectious disease,MONDO,disease,DISEASE_7490
7491,7491,7491,7491,7491,7491,7491,7491,MONDO:0009379,Rotor syndrome,MONDO,disease,DISEASE_7491
7492,7492,7492,7492,7492,7492,7492,7492,MONDO:0033181,phenytoin or carbamazepine toxicity,MONDO,disease,DISEASE_7492
7493,7493,7493,7493,7493,7493,7493,7493,MONDO:0019953,mega-cisterna magna,MONDO,disease,DISEASE_7493
7494,7494,7494,7494,7494,7494,7494,7494,MONDO:0002303_MONDO:0006948_MONDO:0002089_MONDO:0001633,central retinal vein occlusion,MONDO_grouped,disease,DISEASE_7494
7495,7495,7495,7495,7495,7495,7495,7495,MONDO:0016440,elastofibroma dorsi,MONDO,disease,DISEASE_7495
7496,7496,7496,7496,7496,7496,7496,7496,MONDO:0006786,hepatic vein thrombosis,MONDO,disease,DISEASE_7496
7497,7497,7497,7497,7497,7497,7497,7497,MONDO:0015234,arachnodactyly-abnormal ossification-intellectual disability syndrome,MONDO,disease,DISEASE_7497
7498,7498,7498,7498,7498,7498,7498,7498,MONDO:0002587,encapsulated thymoma,MONDO,disease,DISEASE_7498
7499,7499,7499,7499,7499,7499,7499,7499,MONDO:0015042,primary plasmacytoma of the bone,MONDO,disease,DISEASE_7499
7500,7500,7500,7500,7500,7500,7500,7500,MONDO:0006417,small intestinal diffuse large B-cell lymphoma,MONDO,disease,DISEASE_7500
7501,7501,7501,7501,7501,7501,7501,7501,MONDO:0100164_MONDO:0016391,permanent neonatal diabetes mellitus,MONDO_grouped,disease,DISEASE_7501
7502,7502,7502,7502,7502,7502,7502,7502,MONDO:0011180,"broad terminal phalanges, familial",MONDO,disease,DISEASE_7502
7503,7503,7503,7503,7503,7503,7503,7503,MONDO:0012255,chromosome 18 pericentric inversion,MONDO,disease,DISEASE_7503
7504,7504,7504,7504,7504,7504,7504,7504,MONDO:0010032,Sjogren-Larsson-like ichthyosis without CNS or eye involvement,MONDO,disease,DISEASE_7504
7505,7505,7505,7505,7505,7505,7505,7505,MONDO:0011241,pseudoacromegaly with severe insulin resistance,MONDO,disease,DISEASE_7505
7506,7506,7506,7506,7506,7506,7506,7506,MONDO:0700279,spastic triplegia,MONDO,disease,DISEASE_7506
7507,7507,7507,7507,7507,7507,7507,7507,MONDO:0018770,Jeune syndrome,MONDO,disease,DISEASE_7507
7508,7508,7508,7508,7508,7508,7508,7508,MONDO:0859578_MONDO:0859577,lacrimoauriculodentodigital syndrome,MONDO_grouped,disease,DISEASE_7508
7509,7509,7509,7509,7509,7509,7509,7509,MONDO:0007899,lichen sclerosus et atrophicus,MONDO,disease,DISEASE_7509
7510,7510,7510,7510,7510,7510,7510,7510,MONDO:0850459,primary cutaneous gamma-delta t-cell lymphoma,MONDO,disease,DISEASE_7510
7511,7511,7511,7511,7511,7511,7511,7511,MONDO:1011928,"laryngeal paralysis, non-human animal",MONDO,disease,DISEASE_7511
7512,7512,7512,7512,7512,7512,7512,7512,MONDO:0020689,AIDS dementia complex,MONDO,disease,DISEASE_7512
7513,7513,7513,7513,7513,7513,7513,7513,MONDO:0001746,optic disk drusen,MONDO,disease,DISEASE_7513
7514,7514,7514,7514,7514,7514,7514,7514,MONDO:0021490,benign neoplasm of sebaceous gland,MONDO,disease,DISEASE_7514
7515,7515,7515,7515,7515,7515,7515,7515,MONDO:0024308,pseudoxanthoma elasticum (inherited or acquired),MONDO,disease,DISEASE_7515
7516,7516,7516,7516,7516,7516,7516,7516,MONDO:0020173,benign tumor of palpebral epidermis,MONDO,disease,DISEASE_7516
7517,7517,7517,7517,7517,7517,7517,7517,MONDO:0002942,sebaceous basal cell carcinoma,MONDO,disease,DISEASE_7517
7518,7518,7518,7518,7518,7518,7518,7518,MONDO:0008818,arterial tortuosity syndrome,MONDO,disease,DISEASE_7518
7519,7519,7519,7519,7519,7519,7519,7519,MONDO:0017340,juvenile nasopharyngeal angiofibroma,MONDO,disease,DISEASE_7519
7520,7520,7520,7520,7520,7520,7520,7520,MONDO:0005246_MONDO:0005178_MONDO:0002933,osteomyelitis,MONDO_grouped,disease,DISEASE_7520
7521,7521,7521,7521,7521,7521,7521,7521,MONDO:0012268,AIDS,MONDO,disease,DISEASE_7521
7522,7522,7522,7522,7522,7522,7522,7522,MONDO:0034145,oculocerebrodental syndrome,MONDO,disease,DISEASE_7522
7523,7523,7523,7523,7523,7523,7523,7523,MONDO:1010298,"osteochondritis dissecans, non-human animal",MONDO,disease,DISEASE_7523
7524,7524,7524,7524,7524,7524,7524,7524,MONDO:0004336,rectal signet ring cell adenocarcinoma,MONDO,disease,DISEASE_7524
7525,7525,7525,7525,7525,7525,7525,7525,MONDO:0019345,shigellosis,MONDO,disease,DISEASE_7525
7526,7526,7526,7526,7526,7526,7526,7526,MONDO:0020347_MONDO:0006702,acute inflammatory demyelinating polyradiculoneuropathy,MONDO_grouped,disease,DISEASE_7526
7527,7527,7527,7527,7527,7527,7527,7527,MONDO:0006201,ethmoid sinus adenoid cystic carcinoma,MONDO,disease,DISEASE_7527
7528,7528,7528,7528,7528,7528,7528,7528,MONDO:0006794,hypersensitivity vasculitis,MONDO,disease,DISEASE_7528
7529,7529,7529,7529,7529,7529,7529,7529,MONDO:0016059,cleft lip/palate-deafness-sacral lipoma syndrome,MONDO,disease,DISEASE_7529
7530,7530,7530,7530,7530,7530,7530,7530,MONDO:0015196,vein of Galen aneurysm,MONDO,disease,DISEASE_7530
7531,7531,7531,7531,7531,7531,7531,7531,MONDO:0004059,dentin sensitivity,MONDO,disease,DISEASE_7531
7532,7532,7532,7532,7532,7532,7532,7532,MONDO:0011326,"citrullinemia, type II, adult-onset",MONDO,disease,DISEASE_7532
7533,7533,7533,7533,7533,7533,7533,7533,MONDO:1012499,"subclinical hypocalcemia, cattle",MONDO,disease,DISEASE_7533
7534,7534,7534,7534,7534,7534,7534,7534,MONDO:0024630,defective phagocytic cell chemotaxis,MONDO,disease,DISEASE_7534
7535,7535,7535,7535,7535,7535,7535,7535,MONDO:0008252,platelet adenylate cyclase activity,MONDO,disease,DISEASE_7535
7536,7536,7536,7536,7536,7536,7536,7536,MONDO:0009472,"acetylation, slow",MONDO,disease,DISEASE_7536
7537,7537,7537,7537,7537,7537,7537,7537,MONDO:0003292_MONDO:0003358,anus leiomyoma,MONDO_grouped,disease,DISEASE_7537
7538,7538,7538,7538,7538,7538,7538,7538,MONDO:0004886,diffuse secondary choroid atrophy,MONDO,disease,DISEASE_7538
7539,7539,7539,7539,7539,7539,7539,7539,MONDO:0044778,nodular lymphocyte predominant Hodgkin lymphoma,MONDO,disease,DISEASE_7539
7540,7540,7540,7540,7540,7540,7540,7540,MONDO:0015261,pseudopelade of Brocq,MONDO,disease,DISEASE_7540
7541,7541,7541,7541,7541,7541,7541,7541,MONDO:0000602,autoimmune disorder of blood,MONDO,disease,DISEASE_7541
7542,7542,7542,7542,7542,7542,7542,7542,MONDO:0100440,"Asperger syndrome, susceptibility to",MONDO,disease,DISEASE_7542
7543,7543,7543,7543,7543,7543,7543,7543,MONDO:0009911,"prolactin deficiency, isolated",MONDO,disease,DISEASE_7543
7544,7544,7544,7544,7544,7544,7544,7544,MONDO:0006447,testicular non-seminomatous germ cell tumor,MONDO,disease,DISEASE_7544
7545,7545,7545,7545,7545,7545,7545,7545,MONDO:0007652,gastric mucosal hypertrophy,MONDO,disease,DISEASE_7545
7546,7546,7546,7546,7546,7546,7546,7546,MONDO:0006365,Peutz-Jeghers polyp,MONDO,disease,DISEASE_7546
7547,7547,7547,7547,7547,7547,7547,7547,MONDO:0030992,"short stature, oligodontia, dysmorphic facies, and motor delay",MONDO,disease,DISEASE_7547
7548,7548,7548,7548,7548,7548,7548,7548,MONDO:0016801,mitochondrial substrate carrier disorder,MONDO,disease,DISEASE_7548
7549,7549,7549,7549,7549,7549,7549,7549,MONDO:0000942,corneal disorder,MONDO,disease,DISEASE_7549
7550,7550,7550,7550,7550,7550,7550,7550,MONDO:0800031,"central hypoventilation syndrome, congenital",MONDO,disease,DISEASE_7550
7551,7551,7551,7551,7551,7551,7551,7551,MONDO:0004160,female stress incontinence,MONDO,disease,DISEASE_7551
7552,7552,7552,7552,7552,7552,7552,7552,MONDO:0008478,"spondylometaphyseal dysplasia, Schmidt type",MONDO,disease,DISEASE_7552
7553,7553,7553,7553,7553,7553,7553,7553,MONDO:0022765,chronic demyelinizing neuropathy with IgM monoclonal,MONDO,disease,DISEASE_7553
7554,7554,7554,7554,7554,7554,7554,7554,MONDO:0005588,chemotherapy-induced oral mucositis,MONDO,disease,DISEASE_7554
7555,7555,7555,7555,7555,7555,7555,7555,MONDO:0010381,Tn polyagglutination syndrome,MONDO,disease,DISEASE_7555
7556,7556,7556,7556,7556,7556,7556,7556,MONDO:0008098,"mesomelic dwarfism, Nievergelt type",MONDO,disease,DISEASE_7556
7557,7557,7557,7557,7557,7557,7557,7557,MONDO:0004269,breast cystic hypersecretory carcinoma,MONDO,disease,DISEASE_7557
7558,7558,7558,7558,7558,7558,7558,7558,MONDO:0021204,chronic otitis media,MONDO,disease,DISEASE_7558
7559,7559,7559,7559,7559,7559,7559,7559,MONDO:1011245_MONDO:1012240_MONDO:1012243_MONDO:1011222,"retinal degeneration, domestic cat",MONDO_grouped,disease,DISEASE_7559
7560,7560,7560,7560,7560,7560,7560,7560,MONDO:1012126,"immunodeficiency disease, domestic cat",MONDO,disease,DISEASE_7560
7561,7561,7561,7561,7561,7561,7561,7561,MONDO:0024416,Neorickettsia infectious disease,MONDO,disease,DISEASE_7561
7562,7562,7562,7562,7562,7562,7562,7562,MONDO:0044660,menstrual cycle-dependent periodic fever,MONDO,disease,DISEASE_7562
7563,7563,7563,7563,7563,7563,7563,7563,MONDO:1010300_MONDO:1010295_MONDO:1011951,"osteopetrosis, non-human animal",MONDO_grouped,disease,DISEASE_7563
7564,7564,7564,7564,7564,7564,7564,7564,MONDO:0010054,spinal muscular atrophy with intellectual disability,MONDO,disease,DISEASE_7564
7565,7565,7565,7565,7565,7565,7565,7565,MONDO:1012494,"autosomal T cell-negative, B cell-negative, NK cell-positive severe combined immunodeficiency disease with sensitivity to ionizing radiation, pig",MONDO,disease,DISEASE_7565
7566,7566,7566,7566,7566,7566,7566,7566,MONDO:0001315,neurocirculatory asthenia,MONDO,disease,DISEASE_7566
7567,7567,7567,7567,7567,7567,7567,7567,MONDO:0019725,pediatric systemic lupus erythematosus,MONDO,disease,DISEASE_7567
7568,7568,7568,7568,7568,7568,7568,7568,MONDO:0018822,global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome,MONDO,disease,DISEASE_7568
7569,7569,7569,7569,7569,7569,7569,7569,MONDO:0005556,lupus nephritis,MONDO,disease,DISEASE_7569
7570,7570,7570,7570,7570,7570,7570,7570,MONDO:0001330,presbyopia,MONDO,disease,DISEASE_7570
7571,7571,7571,7571,7571,7571,7571,7571,MONDO:0001339,portal vein thrombosis,MONDO,disease,DISEASE_7571
7572,7572,7572,7572,7572,7572,7572,7572,MONDO:0700189,chicken neoplasm,MONDO,disease,DISEASE_7572
7573,7573,7573,7573,7573,7573,7573,7573,MONDO:0010907,familial hypertryptophanemia,MONDO,disease,DISEASE_7573
7574,7574,7574,7574,7574,7574,7574,7574,MONDO:0011638_MONDO:0021635,neuroferritinopathy,MONDO_grouped,disease,DISEASE_7574
7575,7575,7575,7575,7575,7575,7575,7575,MONDO:0019526,erythema elevatum diutinum,MONDO,disease,DISEASE_7575
7576,7576,7576,7576,7576,7576,7576,7576,MONDO:1012400_MONDO:1012401,"dilute coat color with neurological defects, dog",MONDO_grouped,disease,DISEASE_7576
7577,7577,7577,7577,7577,7577,7577,7577,MONDO:0009850,"periodontitis, chronic, adult",MONDO,disease,DISEASE_7577
7578,7578,7578,7578,7578,7578,7578,7578,MONDO:0031257,high altitude pulmonary edema,MONDO,disease,DISEASE_7578
7579,7579,7579,7579,7579,7579,7579,7579,MONDO:0022785,cleft palate cardiac defect ectrodactyly,MONDO,disease,DISEASE_7579
7580,7580,7580,7580,7580,7580,7580,7580,MONDO:0100256,CTNNA1-related diffuse gastric and lobular breast cancer syndrome,MONDO,disease,DISEASE_7580
7581,7581,7581,7581,7581,7581,7581,7581,MONDO:0015553_MONDO:0007549_MONDO:1012069,"dystrophic epidermolysis bullosa, nails only",MONDO_grouped,disease,DISEASE_7581
7582,7582,7582,7582,7582,7582,7582,7582,MONDO:0005414,treatment-refractory schizophrenia,MONDO,disease,DISEASE_7582
7583,7583,7583,7583,7583,7583,7583,7583,MONDO:0044337,stromal sarcoma,MONDO,disease,DISEASE_7583
7584,7584,7584,7584,7584,7584,7584,7584,MONDO:0005387_MONDO:0019852_MONDO:0019851,primary ovarian failure,MONDO_grouped,disease,DISEASE_7584
7585,7585,7585,7585,7585,7585,7585,7585,MONDO:0005671,Blastocystis infectious disease,MONDO,disease,DISEASE_7585
7586,7586,7586,7586,7586,7586,7586,7586,MONDO:0009562_MONDO:1011481_MONDO:1011482_MONDO:1011483,beta-mannosidosis,MONDO_grouped,disease,DISEASE_7586
7587,7587,7587,7587,7587,7587,7587,7587,MONDO:0004421,sclerosing breast papilloma,MONDO,disease,DISEASE_7587
7588,7588,7588,7588,7588,7588,7588,7588,MONDO:0000903,myoclonus-dystonia syndrome,MONDO,disease,DISEASE_7588
7589,7589,7589,7589,7589,7589,7589,7589,MONDO:1012937,"Lewy body-like disease, CADPS2-related, yellow-crowned parrot",MONDO,disease,DISEASE_7589
7590,7590,7590,7590,7590,7590,7590,7590,MONDO:0700212,"tuberculosis, non-human animal",MONDO,disease,DISEASE_7590
7591,7591,7591,7591,7591,7591,7591,7591,MONDO:0008175,pacman dysplasia,MONDO,disease,DISEASE_7591
7592,7592,7592,7592,7592,7592,7592,7592,MONDO:0017640,cyanide-induced parkinsonism,MONDO,disease,DISEASE_7592
7593,7593,7593,7593,7593,7593,7593,7593,MONDO:0000961_MONDO:0003944,endobronchial lipoma,MONDO_grouped,disease,DISEASE_7593
7594,7594,7594,7594,7594,7594,7594,7594,MONDO:0011887,"cataract, congenital, with mental impairment and dentate gyrus atrophy",MONDO,disease,DISEASE_7594
7595,7595,7595,7595,7595,7595,7595,7595,MONDO:0009774,cloacal exstrophy,MONDO,disease,DISEASE_7595
7596,7596,7596,7596,7596,7596,7596,7596,MONDO:0003458_MONDO:0004172_MONDO:0016258,uterine corpus adenofibroma,MONDO_grouped,disease,DISEASE_7596
7597,7597,7597,7597,7597,7597,7597,7597,MONDO:0043206,trichostasis spinulosa,MONDO,disease,DISEASE_7597
7598,7598,7598,7598,7598,7598,7598,7598,MONDO:1011431,"Gaucher disease, non-human animal",MONDO,disease,DISEASE_7598
7599,7599,7599,7599,7599,7599,7599,7599,MONDO:0023483_MONDO:0023161_MONDO:0017211,infectious myositis,MONDO_grouped,disease,DISEASE_7599
7600,7600,7600,7600,7600,7600,7600,7600,MONDO:0800125,disseminated visceral giant cell angiitis,MONDO,disease,DISEASE_7600
7601,7601,7601,7601,7601,7601,7601,7601,MONDO:0001945,postencephalitic Parkinson disease,MONDO,disease,DISEASE_7601
7602,7602,7602,7602,7602,7602,7602,7602,MONDO:1010855_MONDO:1010857,"Krabbe disease, dog",MONDO_grouped,disease,DISEASE_7602
7603,7603,7603,7603,7603,7603,7603,7603,MONDO:0003134_MONDO:0001644_MONDO:0003139,proliferative glomerulonephritis,MONDO_grouped,disease,DISEASE_7603
7604,7604,7604,7604,7604,7604,7604,7604,MONDO:0500018,acute fibrinous and organizing pneumonia,MONDO,disease,DISEASE_7604
7605,7605,7605,7605,7605,7605,7605,7605,MONDO:1011585_MONDO:1011586,"pituitary-dependent hyperadrenocorticism, dog",MONDO_grouped,disease,DISEASE_7605
7606,7606,7606,7606,7606,7606,7606,7606,MONDO:0029000,poisoning,MONDO,disease,DISEASE_7606
7607,7607,7607,7607,7607,7607,7607,7607,MONDO:0026045,prurigo nodularis,MONDO,disease,DISEASE_7607
7608,7608,7608,7608,7608,7608,7608,7608,MONDO:0008419_MONDO:0012115_MONDO:0011820_MONDO:0012826_MONDO:0012827,"scoliosis, isolated, susceptibility to",MONDO_grouped,disease,DISEASE_7608
7609,7609,7609,7609,7609,7609,7609,7609,MONDO:0013731_MONDO:0013998,MEGF10-related myopathy,MONDO_grouped,disease,DISEASE_7609
7610,7610,7610,7610,7610,7610,7610,7610,MONDO:0600030,B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1),MONDO,disease,DISEASE_7610
7611,7611,7611,7611,7611,7611,7611,7611,MONDO:0019417,X-linked intellectual disability-precocious puberty-obesity syndrome,MONDO,disease,DISEASE_7611
7612,7612,7612,7612,7612,7612,7612,7612,MONDO:0100560,ligneous conjunctivitis,MONDO,disease,DISEASE_7612
7613,7613,7613,7613,7613,7613,7613,7613,MONDO:0800488,neonatal/infantile-onset self-limited epilepsy syndrome,MONDO,disease,DISEASE_7613
7614,7614,7614,7614,7614,7614,7614,7614,MONDO:0859516,"neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum",MONDO,disease,DISEASE_7614
7615,7615,7615,7615,7615,7615,7615,7615,MONDO:0018889,hyaline body myopathy,MONDO,disease,DISEASE_7615
7616,7616,7616,7616,7616,7616,7616,7616,MONDO:0009235,familial benign flecked retina,MONDO,disease,DISEASE_7616
7617,7617,7617,7617,7617,7617,7617,7617,MONDO:0001647,benign renovascular hypertension,MONDO,disease,DISEASE_7617
7618,7618,7618,7618,7618,7618,7618,7618,MONDO:0021019,X-linked recessive ocular albinism,MONDO,disease,DISEASE_7618
7619,7619,7619,7619,7619,7619,7619,7619,MONDO:0011251,"facial dysmorphism, cleft palate, hearing loss, and camptodactyly",MONDO,disease,DISEASE_7619
7620,7620,7620,7620,7620,7620,7620,7620,MONDO:1012669_MONDO:1012670_MONDO:1012671_MONDO:1012672,"mucopolysaccharidosis IIIB, emu",MONDO_grouped,disease,DISEASE_7620
7621,7621,7621,7621,7621,7621,7621,7621,MONDO:0009752,"neuropathy, painful",MONDO,disease,DISEASE_7621
7622,7622,7622,7622,7622,7622,7622,7622,MONDO:0008187_MONDO:0100081_MONDO:0005383_MONDO:0001942_MONDO:0011924_MONDO:0012384,panic disorder,MONDO_grouped,disease,DISEASE_7622
7623,7623,7623,7623,7623,7623,7623,7623,MONDO:0018280,muscle-eye-brain disease with bilateral multicystic leucodystrophy,MONDO,disease,DISEASE_7623
7624,7624,7624,7624,7624,7624,7624,7624,MONDO:0700217,neonatal sepsis,MONDO,disease,DISEASE_7624
7625,7625,7625,7625,7625,7625,7625,7625,MONDO:0010938,T-B+ severe combined immunodeficiency due to JAK3 deficiency,MONDO,disease,DISEASE_7625
7626,7626,7626,7626,7626,7626,7626,7626,MONDO:0020546,acute graft versus host disease,MONDO,disease,DISEASE_7626
7627,7627,7627,7627,7627,7627,7627,7627,MONDO:0007195,"bifid nose, autosomal dominant",MONDO,disease,DISEASE_7627
7628,7628,7628,7628,7628,7628,7628,7628,MONDO:0017836,erythrokeratoderma en cocardes,MONDO,disease,DISEASE_7628
7629,7629,7629,7629,7629,7629,7629,7629,MONDO:0010432,"thrombophilia, X-linked, due to factor 9 defect",MONDO,disease,DISEASE_7629
7630,7630,7630,7630,7630,7630,7630,7630,MONDO:0700165,canine thyroid gland medullary carcinoma,MONDO,disease,DISEASE_7630
7631,7631,7631,7631,7631,7631,7631,7631,MONDO:0020704_MONDO:0021142,inherited rippling muscle disease,MONDO_grouped,disease,DISEASE_7631
7632,7632,7632,7632,7632,7632,7632,7632,MONDO:0100469,"anosmia, isolated congenital, X-linked",MONDO,disease,DISEASE_7632
7633,7633,7633,7633,7633,7633,7633,7633,MONDO:0020666,Löfgren syndrome,MONDO,disease,DISEASE_7633
7634,7634,7634,7634,7634,7634,7634,7634,MONDO:0015790_MONDO:0004782,central diabetes insipidus,MONDO_grouped,disease,DISEASE_7634
7635,7635,7635,7635,7635,7635,7635,7635,MONDO:0034212,methotrexate toxicity,MONDO,disease,DISEASE_7635
7636,7636,7636,7636,7636,7636,7636,7636,MONDO:0030994,neurodevelopmental disorder with or without autism or seizures,MONDO,disease,DISEASE_7636
7637,7637,7637,7637,7637,7637,7637,7637,MONDO:0001880,median rhomboid glossitis,MONDO,disease,DISEASE_7637
7638,7638,7638,7638,7638,7638,7638,7638,MONDO:1012245_MONDO:1012247,"rod-cone degeneration, domestic cat",MONDO_grouped,disease,DISEASE_7638
7639,7639,7639,7639,7639,7639,7639,7639,MONDO:0011013_MONDO:0014146_MONDO:0018543,autosomal dominant hypocalcemia,MONDO_grouped,disease,DISEASE_7639
7640,7640,7640,7640,7640,7640,7640,7640,MONDO:1010747,"Ehlers-Danlos syndrome, dermatosparaxis type, ADAMTS2-related, domestic cat",MONDO,disease,DISEASE_7640
7641,7641,7641,7641,7641,7641,7641,7641,MONDO:0859008,neurofibromatosis/schwannomatosis,MONDO,disease,DISEASE_7641
7642,7642,7642,7642,7642,7642,7642,7642,MONDO:0971033,intrathyroid thymic carcinoma,MONDO,disease,DISEASE_7642
7643,7643,7643,7643,7643,7643,7643,7643,MONDO:0001453,senile reticular retinal degeneration,MONDO,disease,DISEASE_7643
7644,7644,7644,7644,7644,7644,7644,7644,MONDO:0004316,acantholytic squamous cell skin carcinoma,MONDO,disease,DISEASE_7644
7645,7645,7645,7645,7645,7645,7645,7645,MONDO:0850099_MONDO:0971093,MIR140-related spondyloepiphyseal dysplasia,MONDO_grouped,disease,DISEASE_7645
7646,7646,7646,7646,7646,7646,7646,7646,MONDO:0019811,tricuspid valve agenesis,MONDO,disease,DISEASE_7646
7647,7647,7647,7647,7647,7647,7647,7647,MONDO:0009449,ciliary dyskinesia with defective radial spokes,MONDO,disease,DISEASE_7647
7648,7648,7648,7648,7648,7648,7648,7648,MONDO:0016775,lichen planus pemphigoides,MONDO,disease,DISEASE_7648
7649,7649,7649,7649,7649,7649,7649,7649,MONDO:0010389_MONDO:0017905,X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency,MONDO_grouped,disease,DISEASE_7649
7650,7650,7650,7650,7650,7650,7650,7650,MONDO:0032814,"microangiopathy and leukoencephalopathy, pontine, autosomal dominant",MONDO,disease,DISEASE_7650
7651,7651,7651,7651,7651,7651,7651,7651,MONDO:0025445,Wieacker-Wolff syndrome (spectrum),MONDO,disease,DISEASE_7651
7652,7652,7652,7652,7652,7652,7652,7652,MONDO:0014361,autism spectrum disorder due to AUTS2 deficiency,MONDO,disease,DISEASE_7652
7653,7653,7653,7653,7653,7653,7653,7653,MONDO:0008691,"zinc, elevated plasma",MONDO,disease,DISEASE_7653
7654,7654,7654,7654,7654,7654,7654,7654,MONDO:0968988,saccular spinal dysraphism with a stalk to the dome,MONDO,disease,DISEASE_7654
7655,7655,7655,7655,7655,7655,7655,7655,MONDO:0020979,pilosebaceous hamartoma,MONDO,disease,DISEASE_7655
7656,7656,7656,7656,7656,7656,7656,7656,MONDO:0016194,qualitative or quantitative defects of nebulin,MONDO,disease,DISEASE_7656
7657,7657,7657,7657,7657,7657,7657,7657,MONDO:0002720,sella turcica neoplasm,MONDO,disease,DISEASE_7657
7658,7658,7658,7658,7658,7658,7658,7658,MONDO:0800036,MELAS syndrome caused by mutation in MTTC,MONDO,disease,DISEASE_7658
7659,7659,7659,7659,7659,7659,7659,7659,MONDO:1010208,"myofibrillar myopathy, non-human animal",MONDO,disease,DISEASE_7659
7660,7660,7660,7660,7660,7660,7660,7660,MONDO:0021661,coronary atherosclerosis,MONDO,disease,DISEASE_7660
7661,7661,7661,7661,7661,7661,7661,7661,MONDO:0018920,peripartum cardiomyopathy,MONDO,disease,DISEASE_7661
7662,7662,7662,7662,7662,7662,7662,7662,MONDO:0007155,"arteritis, familial granulomatous, with juvenile polyarthritis",MONDO,disease,DISEASE_7662
7663,7663,7663,7663,7663,7663,7663,7663,MONDO:0007530,electroencephalographic peculiarity: 14 and 6 per sec. positive spike phenomenon,MONDO,disease,DISEASE_7663
7664,7664,7664,7664,7664,7664,7664,7664,MONDO:0043139,microcephaly sparse hair intellectual disability seizures,MONDO,disease,DISEASE_7664
7665,7665,7665,7665,7665,7665,7665,7665,MONDO:0100201,lumbar disk disease,MONDO,disease,DISEASE_7665
7666,7666,7666,7666,7666,7666,7666,7666,MONDO:0005346,gallstones,MONDO,disease,DISEASE_7666
7667,7667,7667,7667,7667,7667,7667,7667,MONDO:0015241,arthrogryposis-like syndrome,MONDO,disease,DISEASE_7667
7668,7668,7668,7668,7668,7668,7668,7668,MONDO:0001279_MONDO:0004312,intraspinal meningioma,MONDO_grouped,disease,DISEASE_7668
7669,7669,7669,7669,7669,7669,7669,7669,MONDO:0043959,pseudolymphoma,MONDO,disease,DISEASE_7669
7670,7670,7670,7670,7670,7670,7670,7670,MONDO:0045015,carbohydrate transport disease,MONDO,disease,DISEASE_7670
7671,7671,7671,7671,7671,7671,7671,7671,MONDO:0015587,rolandic epilepsy-speech dyspraxia syndrome,MONDO,disease,DISEASE_7671
7672,7672,7672,7672,7672,7672,7672,7672,MONDO:0016549,"primary megaureter, adult-onset form",MONDO,disease,DISEASE_7672
7673,7673,7673,7673,7673,7673,7673,7673,MONDO:0100595,furunculosis,MONDO,disease,DISEASE_7673
7674,7674,7674,7674,7674,7674,7674,7674,MONDO:0045069,minor salivary gland carcinoma,MONDO,disease,DISEASE_7674
7675,7675,7675,7675,7675,7675,7675,7675,MONDO:0019973,persistent placoid maculopathy,MONDO,disease,DISEASE_7675
7676,7676,7676,7676,7676,7676,7676,7676,MONDO:0001933,endocrine pancreas disorder,MONDO,disease,DISEASE_7676
7677,7677,7677,7677,7677,7677,7677,7677,MONDO:0007472,basal laminar drusen,MONDO,disease,DISEASE_7677
7678,7678,7678,7678,7678,7678,7678,7678,MONDO:0020650,germ cell tumor of the vulva,MONDO,disease,DISEASE_7678
7679,7679,7679,7679,7679,7679,7679,7679,MONDO:0002563_MONDO:0004236,jejunal somatostatinoma,MONDO_grouped,disease,DISEASE_7679
7680,7680,7680,7680,7680,7680,7680,7680,MONDO:0032666_MONDO:0032644_MONDO:0032614_MONDO:0100045_MONDO:0032667_MONDO:0100043,"epidermodysplasia verruciformis, susceptibility to",MONDO_grouped,disease,DISEASE_7680
7681,7681,7681,7681,7681,7681,7681,7681,MONDO:0006366,Peutz-Jeghers polyp of the stomach,MONDO,disease,DISEASE_7681
7682,7682,7682,7682,7682,7682,7682,7682,MONDO:0008495,platelet storage pool deficiency,MONDO,disease,DISEASE_7682
7683,7683,7683,7683,7683,7683,7683,7683,MONDO:0001204_MONDO:0001188,esophagus sarcoma,MONDO_grouped,disease,DISEASE_7683
7684,7684,7684,7684,7684,7684,7684,7684,MONDO:0020573,inherited disease susceptibility,MONDO,disease,DISEASE_7684
7685,7685,7685,7685,7685,7685,7685,7685,MONDO:0014405,STING-associated vasculopathy with onset in infancy,MONDO,disease,DISEASE_7685
7686,7686,7686,7686,7686,7686,7686,7686,MONDO:0020836,"autism, susceptiblity to",MONDO,disease,DISEASE_7686
7687,7687,7687,7687,7687,7687,7687,7687,MONDO:0017446,apodia,MONDO,disease,DISEASE_7687
7688,7688,7688,7688,7688,7688,7688,7688,MONDO:0700032,complete trisomy 18,MONDO,disease,DISEASE_7688
7689,7689,7689,7689,7689,7689,7689,7689,MONDO:0007416,Balkan nephropathy,MONDO,disease,DISEASE_7689
7690,7690,7690,7690,7690,7690,7690,7690,MONDO:0002817,adrenal gland cancer,MONDO,disease,DISEASE_7690
7691,7691,7691,7691,7691,7691,7691,7691,MONDO:0000283,"Hantavirus hemorrhagic fever with renal syndrome, Seoul virus type",MONDO,disease,DISEASE_7691
7692,7692,7692,7692,7692,7692,7692,7692,MONDO:1012907,"muscular dystrophy-dystroglycanopathy, LARGE1-related, dog",MONDO,disease,DISEASE_7692
7693,7693,7693,7693,7693,7693,7693,7693,MONDO:0100071,cardiocutaneous syndrome,MONDO,disease,DISEASE_7693
7694,7694,7694,7694,7694,7694,7694,7694,MONDO:0003730,aleukemic leukemia,MONDO,disease,DISEASE_7694
7695,7695,7695,7695,7695,7695,7695,7695,MONDO:0001209,common wart,MONDO,disease,DISEASE_7695
7696,7696,7696,7696,7696,7696,7696,7696,MONDO:0016028_MONDO:0035149,erythromelalgia,MONDO_grouped,disease,DISEASE_7696
7697,7697,7697,7697,7697,7697,7697,7697,MONDO:0004579_MONDO:0001435,retinoschisis,MONDO_grouped,disease,DISEASE_7697
7698,7698,7698,7698,7698,7698,7698,7698,MONDO:0015447,differentiated thyroid carcinoma,MONDO,disease,DISEASE_7698
7699,7699,7699,7699,7699,7699,7699,7699,MONDO:0000239,adiaspiromycosis,MONDO,disease,DISEASE_7699
7700,7700,7700,7700,7700,7700,7700,7700,MONDO:0001190_MONDO:0001857_MONDO:0001973,Brucella suis brucellosis,MONDO_grouped,disease,DISEASE_7700
7701,7701,7701,7701,7701,7701,7701,7701,MONDO:0014857,"neurodevelopmental disorder with or without anomalies of the brain, eye, or heart",MONDO,disease,DISEASE_7701
7702,7702,7702,7702,7702,7702,7702,7702,MONDO:0011526,obsolete Sebastian syndrome,MONDO,disease,DISEASE_7702
7703,7703,7703,7703,7703,7703,7703,7703,MONDO:0004007,breast intraductal proliferative lesion,MONDO,disease,DISEASE_7703
7704,7704,7704,7704,7704,7704,7704,7704,MONDO:0013640,familial retinal arterial macroaneurysm,MONDO,disease,DISEASE_7704
7705,7705,7705,7705,7705,7705,7705,7705,MONDO:0019207,DEND syndrome,MONDO,disease,DISEASE_7705
7706,7706,7706,7706,7706,7706,7706,7706,MONDO:0001329,accommodative spasm,MONDO,disease,DISEASE_7706
7707,7707,7707,7707,7707,7707,7707,7707,MONDO:0011353,"atrial septal defect, secundum, with various cardiac and Noncardiac defects",MONDO,disease,DISEASE_7707
7708,7708,7708,7708,7708,7708,7708,7708,MONDO:0004355_MONDO:0001014,childhood leukemia,MONDO_grouped,disease,DISEASE_7708
7709,7709,7709,7709,7709,7709,7709,7709,MONDO:0015638_MONDO:0100025,benign partial epilepsy of infancy with complex partial seizures,MONDO_grouped,disease,DISEASE_7709
7710,7710,7710,7710,7710,7710,7710,7710,MONDO:0003298_MONDO:0003372_MONDO:0003599,vulvar leiomyoma,MONDO_grouped,disease,DISEASE_7710
7711,7711,7711,7711,7711,7711,7711,7711,MONDO:0000531,bronchus mucoepidermoid carcinoma,MONDO,disease,DISEASE_7711
7712,7712,7712,7712,7712,7712,7712,7712,MONDO:0008649,"venular insufficiency, systemic",MONDO,disease,DISEASE_7712
7713,7713,7713,7713,7713,7713,7713,7713,MONDO:0011622,"nephrolithiasis, uric acid, susceptibility to",MONDO,disease,DISEASE_7713
7714,7714,7714,7714,7714,7714,7714,7714,MONDO:0008081,"neurofibromatosis, type IV, of Riccardi",MONDO,disease,DISEASE_7714
7715,7715,7715,7715,7715,7715,7715,7715,MONDO:0001697,reading disorder,MONDO,disease,DISEASE_7715
7716,7716,7716,7716,7716,7716,7716,7716,MONDO:0019182,inherited obesity,MONDO,disease,DISEASE_7716
7717,7717,7717,7717,7717,7717,7717,7717,MONDO:0008462,split lower lip,MONDO,disease,DISEASE_7717
7718,7718,7718,7718,7718,7718,7718,7718,MONDO:0016710,medulloblastoma with extensive nodularity,MONDO,disease,DISEASE_7718
7719,7719,7719,7719,7719,7719,7719,7719,MONDO:1010074,"factor XII deficiency, non-human animal",MONDO,disease,DISEASE_7719
7720,7720,7720,7720,7720,7720,7720,7720,MONDO:0020539,extragonadal non-dysgerminomatous germ cell tumor,MONDO,disease,DISEASE_7720
7721,7721,7721,7721,7721,7721,7721,7721,MONDO:1011283,"syndromic retinal atrophy, BBS7-related, Rhesus monkey",MONDO,disease,DISEASE_7721
7722,7722,7722,7722,7722,7722,7722,7722,MONDO:1012201,"osteochondroma causing progressive posterior paresis, dog",MONDO,disease,DISEASE_7722
7723,7723,7723,7723,7723,7723,7723,7723,MONDO:0008084,"neuropathy, congenital, with arthrogryposis multiplex",MONDO,disease,DISEASE_7723
7724,7724,7724,7724,7724,7724,7724,7724,MONDO:0000975,lipoma of spermatic cord,MONDO,disease,DISEASE_7724
7725,7725,7725,7725,7725,7725,7725,7725,MONDO:1011770,"necrosis of digits, non-human animal",MONDO,disease,DISEASE_7725
7726,7726,7726,7726,7726,7726,7726,7726,MONDO:0015514,hereditary endocrine growth disease,MONDO,disease,DISEASE_7726
7727,7727,7727,7727,7727,7727,7727,7727,MONDO:0022555,Beardwell syndrome,MONDO,disease,DISEASE_7727
7728,7728,7728,7728,7728,7728,7728,7728,MONDO:0002150,hypothalamic disorder,MONDO,disease,DISEASE_7728
7729,7729,7729,7729,7729,7729,7729,7729,MONDO:0060714_MONDO:0060715_MONDO:0100252,"tumoral calcinosis, hyperphosphatemic, familial",MONDO_grouped,disease,DISEASE_7729
7730,7730,7730,7730,7730,7730,7730,7730,MONDO:0016108,autosomal dominant distal myopathy,MONDO,disease,DISEASE_7730
7731,7731,7731,7731,7731,7731,7731,7731,MONDO:1012714_MONDO:1012716,"XY difference of sexual development, dog",MONDO_grouped,disease,DISEASE_7731
7732,7732,7732,7732,7732,7732,7732,7732,MONDO:1011417,"hypertriglyceridemia, non-human animal",MONDO,disease,DISEASE_7732
7733,7733,7733,7733,7733,7733,7733,7733,MONDO:0044796,spindle cell nevus,MONDO,disease,DISEASE_7733
7734,7734,7734,7734,7734,7734,7734,7734,MONDO:0042981_MONDO:0019808,aortic valve stenosis,MONDO_grouped,disease,DISEASE_7734
7735,7735,7735,7735,7735,7735,7735,7735,MONDO:0006545_MONDO:0044719,erythema multiforme,MONDO_grouped,disease,DISEASE_7735
7736,7736,7736,7736,7736,7736,7736,7736,MONDO:0003670,posteroinferior myocardial infarction,MONDO,disease,DISEASE_7736
7737,7737,7737,7737,7737,7737,7737,7737,MONDO:1010737,"periodic fever syndrome, dog",MONDO,disease,DISEASE_7737
7738,7738,7738,7738,7738,7738,7738,7738,MONDO:0017903,autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency,MONDO,disease,DISEASE_7738
7739,7739,7739,7739,7739,7739,7739,7739,MONDO:1011221_MONDO:1011223,"retinal detachment, dog",MONDO_grouped,disease,DISEASE_7739
7740,7740,7740,7740,7740,7740,7740,7740,MONDO:0001849,chronic orbital inflammation,MONDO,disease,DISEASE_7740
7741,7741,7741,7741,7741,7741,7741,7741,MONDO:0009779_MONDO:0008123,autosomal recessive omodysplasia,MONDO_grouped,disease,DISEASE_7741
7742,7742,7742,7742,7742,7742,7742,7742,MONDO:0019543,acquired aneurysmal subarachnoid hemorrhage,MONDO,disease,DISEASE_7742
7743,7743,7743,7743,7743,7743,7743,7743,MONDO:0012574,Potocki-Lupski syndrome,MONDO,disease,DISEASE_7743
7744,7744,7744,7744,7744,7744,7744,7744,MONDO:0023579,Kuster Majewski Hammerstein syndrome,MONDO,disease,DISEASE_7744
7745,7745,7745,7745,7745,7745,7745,7745,MONDO:0003112,malignant gastric germ cell tumor,MONDO,disease,DISEASE_7745
7746,7746,7746,7746,7746,7746,7746,7746,MONDO:0004545_MONDO:0004345,adult malignant schwannoma,MONDO_grouped,disease,DISEASE_7746
7747,7747,7747,7747,7747,7747,7747,7747,MONDO:0017086,primary tethered cord syndrome,MONDO,disease,DISEASE_7747
7748,7748,7748,7748,7748,7748,7748,7748,MONDO:1011885,"episodic falling, non-human animal",MONDO,disease,DISEASE_7748
7749,7749,7749,7749,7749,7749,7749,7749,MONDO:0016740,choriocarcinoma of the central nervous system,MONDO,disease,DISEASE_7749
7750,7750,7750,7750,7750,7750,7750,7750,MONDO:0100358,ectodermal dysplasia WNT10A related,MONDO,disease,DISEASE_7750
7751,7751,7751,7751,7751,7751,7751,7751,MONDO:0005884,opisthorchiasis,MONDO,disease,DISEASE_7751
7752,7752,7752,7752,7752,7752,7752,7752,MONDO:1012254,"spastic syndrome, cattle",MONDO,disease,DISEASE_7752
7753,7753,7753,7753,7753,7753,7753,7753,MONDO:0859336,"muscular dystrophy, congenital, with or without seizures",MONDO,disease,DISEASE_7753
7754,7754,7754,7754,7754,7754,7754,7754,MONDO:0006895,penile neoplasm,MONDO,disease,DISEASE_7754
7755,7755,7755,7755,7755,7755,7755,7755,MONDO:0018258,Angora hair nevus,MONDO,disease,DISEASE_7755
7756,7756,7756,7756,7756,7756,7756,7756,MONDO:0016223,infantile hemangioma of rare localization,MONDO,disease,DISEASE_7756
7757,7757,7757,7757,7757,7757,7757,7757,MONDO:1010075_MONDO:1011408,"hemophilia B, non-human animal",MONDO_grouped,disease,DISEASE_7757
7758,7758,7758,7758,7758,7758,7758,7758,MONDO:0008681,WAGR syndrome,MONDO,disease,DISEASE_7758
7759,7759,7759,7759,7759,7759,7759,7759,MONDO:0018960,congenital primary megaureter,MONDO,disease,DISEASE_7759
7760,7760,7760,7760,7760,7760,7760,7760,MONDO:1012362,"photoreceptor dysplasia, dog",MONDO,disease,DISEASE_7760
7761,7761,7761,7761,7761,7761,7761,7761,MONDO:0006255,intimal sarcoma,MONDO,disease,DISEASE_7761
7762,7762,7762,7762,7762,7762,7762,7762,MONDO:0007941,malocclusion due to protuberant upper front teeth,MONDO,disease,DISEASE_7762
7763,7763,7763,7763,7763,7763,7763,7763,MONDO:0003745_MONDO:0003913_MONDO:0004085_MONDO:0004364,choroid spindle cell melanoma,MONDO_grouped,disease,DISEASE_7763
7764,7764,7764,7764,7764,7764,7764,7764,MONDO:0009620,Say-Barber-Miller syndrome,MONDO,disease,DISEASE_7764
7765,7765,7765,7765,7765,7765,7765,7765,MONDO:0023203,Fuchs atrophia gyrata chorioideae et retinae,MONDO,disease,DISEASE_7765
7766,7766,7766,7766,7766,7766,7766,7766,MONDO:0017880_MONDO:0005991,Rift valley fever,MONDO_grouped,disease,DISEASE_7766
7767,7767,7767,7767,7767,7767,7767,7767,MONDO:0001879,anus cancer,MONDO,disease,DISEASE_7767
7768,7768,7768,7768,7768,7768,7768,7768,MONDO:0030869,spermatogenic failures 50,MONDO,disease,DISEASE_7768
7769,7769,7769,7769,7769,7769,7769,7769,MONDO:0013762,lipoic acid synthetase deficiency,MONDO,disease,DISEASE_7769
7770,7770,7770,7770,7770,7770,7770,7770,MONDO:1011738,"focal metatarsal fistula, non-human animal",MONDO,disease,DISEASE_7770
7771,7771,7771,7771,7771,7771,7771,7771,MONDO:0700149_MONDO:0700140,canine sarcoma,MONDO_grouped,disease,DISEASE_7771
7772,7772,7772,7772,7772,7772,7772,7772,MONDO:0004760,urethral false passage,MONDO,disease,DISEASE_7772
7773,7773,7773,7773,7773,7773,7773,7773,MONDO:0024296,vascular neoplasm,MONDO,disease,DISEASE_7773
7774,7774,7774,7774,7774,7774,7774,7774,MONDO:0017305,syndromic oculocutaneous albinism,MONDO,disease,DISEASE_7774
7775,7775,7775,7775,7775,7775,7775,7775,MONDO:0054697,immunodeficiency 11b with atopic dermatitis,MONDO,disease,DISEASE_7775
7776,7776,7776,7776,7776,7776,7776,7776,MONDO:0004966,gastritis,MONDO,disease,DISEASE_7776
7777,7777,7777,7777,7777,7777,7777,7777,MONDO:0016282,rhabdomyosarcoma of the cervix uteri,MONDO,disease,DISEASE_7777
7778,7778,7778,7778,7778,7778,7778,7778,MONDO:0019359,Rocky mountain spotted fever,MONDO,disease,DISEASE_7778
7779,7779,7779,7779,7779,7779,7779,7779,MONDO:0017906,amyloidosis cutis dyschromia,MONDO,disease,DISEASE_7779
7780,7780,7780,7780,7780,7780,7780,7780,MONDO:0005729,dicrocoeliasis,MONDO,disease,DISEASE_7780
7781,7781,7781,7781,7781,7781,7781,7781,MONDO:0004685,Waldeyer's ring cancer,MONDO,disease,DISEASE_7781
7782,7782,7782,7782,7782,7782,7782,7782,MONDO:0001638,protein-deficiency anemia,MONDO,disease,DISEASE_7782
7783,7783,7783,7783,7783,7783,7783,7783,MONDO:0700135,bovine leukemia,MONDO,disease,DISEASE_7783
7784,7784,7784,7784,7784,7784,7784,7784,MONDO:0957779,neurodevelopmental disorder with language delay and variable cognitive abnormalities,MONDO,disease,DISEASE_7784
7785,7785,7785,7785,7785,7785,7785,7785,MONDO:0002460,lacrimal system cancer,MONDO,disease,DISEASE_7785
7786,7786,7786,7786,7786,7786,7786,7786,MONDO:0010543,Barth syndrome,MONDO,disease,DISEASE_7786
7787,7787,7787,7787,7787,7787,7787,7787,MONDO:0009026,Costello syndrome,MONDO,disease,DISEASE_7787
7788,7788,7788,7788,7788,7788,7788,7788,MONDO:0022538,leukoplakia of gingiva,MONDO,disease,DISEASE_7788
7789,7789,7789,7789,7789,7789,7789,7789,MONDO:1010197,"myositis ossificans, non-human animal",MONDO,disease,DISEASE_7789
7790,7790,7790,7790,7790,7790,7790,7790,MONDO:0005454,lung neuroendocrine neoplasm,MONDO,disease,DISEASE_7790
7791,7791,7791,7791,7791,7791,7791,7791,MONDO:0004977,angioimmunoblastic T-cell lymphoma,MONDO,disease,DISEASE_7791
7792,7792,7792,7792,7792,7792,7792,7792,MONDO:1012512,"naked foal syndrome, horse",MONDO,disease,DISEASE_7792
7793,7793,7793,7793,7793,7793,7793,7793,MONDO:0003214_MONDO:0002804,apocrine adenocarcinoma,MONDO_grouped,disease,DISEASE_7793
7794,7794,7794,7794,7794,7794,7794,7794,MONDO:0016666,unexplained long-lasting fever/inflammatory syndrome,MONDO,disease,DISEASE_7794
7795,7795,7795,7795,7795,7795,7795,7795,MONDO:0008449_MONDO:1010558_MONDO:1010559_MONDO:1010560,spina bifida,MONDO_grouped,disease,DISEASE_7795
7796,7796,7796,7796,7796,7796,7796,7796,MONDO:0004924,chronic canaliculitis,MONDO,disease,DISEASE_7796
7797,7797,7797,7797,7797,7797,7797,7797,MONDO:0014972,"chromosome 19q13.11 deletion syndrome, proximal",MONDO,disease,DISEASE_7797
7798,7798,7798,7798,7798,7798,7798,7798,MONDO:1011178,"osteopetrosis, Japanese quail",MONDO,disease,DISEASE_7798
7799,7799,7799,7799,7799,7799,7799,7799,MONDO:0600026,vanishing lung syndrome,MONDO,disease,DISEASE_7799
7800,7800,7800,7800,7800,7800,7800,7800,MONDO:0011051,"lethal short-limb skeletal dysplasia, Al Gazali type",MONDO,disease,DISEASE_7800
7801,7801,7801,7801,7801,7801,7801,7801,MONDO:0005784,hantavirus hemorrhagic fever with renal syndrome,MONDO,disease,DISEASE_7801
7802,7802,7802,7802,7802,7802,7802,7802,MONDO:0018470,renal agenesis,MONDO,disease,DISEASE_7802
7803,7803,7803,7803,7803,7803,7803,7803,MONDO:0003780,T-cell immunodeficiency,MONDO,disease,DISEASE_7803
7804,7804,7804,7804,7804,7804,7804,7804,MONDO:0006564,irritant dermatitis,MONDO,disease,DISEASE_7804
7805,7805,7805,7805,7805,7805,7805,7805,MONDO:0019369_MONDO:0011441_MONDO:0020572,complex regional pain syndrome,MONDO_grouped,disease,DISEASE_7805
7806,7806,7806,7806,7806,7806,7806,7806,MONDO:0022007,water intoxication,MONDO,disease,DISEASE_7806
7807,7807,7807,7807,7807,7807,7807,7807,MONDO:0007560,reading seizures,MONDO,disease,DISEASE_7807
7808,7808,7808,7808,7808,7808,7808,7808,MONDO:0009505,lactic aciduria due to D-lactic acid,MONDO,disease,DISEASE_7808
7809,7809,7809,7809,7809,7809,7809,7809,MONDO:0016957,partial duplication of the long arm of chromosome 6,MONDO,disease,DISEASE_7809
7810,7810,7810,7810,7810,7810,7810,7810,MONDO:0002973_MONDO:0006749,epithelioid cell melanoma,MONDO_grouped,disease,DISEASE_7810
7811,7811,7811,7811,7811,7811,7811,7811,MONDO:0007497,"ear antitragus, tag at base of",MONDO,disease,DISEASE_7811
7812,7812,7812,7812,7812,7812,7812,7812,MONDO:0004056,bladder papillary urothelial carcinoma,MONDO,disease,DISEASE_7812
7813,7813,7813,7813,7813,7813,7813,7813,MONDO:0005221_MONDO:0003777_MONDO:0003716,renal pelvis urothelial carcinoma,MONDO_grouped,disease,DISEASE_7813
7814,7814,7814,7814,7814,7814,7814,7814,MONDO:0009148,Rosselli-Gulienetti syndrome,MONDO,disease,DISEASE_7814
7815,7815,7815,7815,7815,7815,7815,7815,MONDO:0011624,transaldolase deficiency,MONDO,disease,DISEASE_7815
7816,7816,7816,7816,7816,7816,7816,7816,MONDO:0008230,"peroxidase, salivary",MONDO,disease,DISEASE_7816
7817,7817,7817,7817,7817,7817,7817,7817,MONDO:1012898,"osteopetrosis, SLC4A2-related, cattle",MONDO,disease,DISEASE_7817
7818,7818,7818,7818,7818,7818,7818,7818,MONDO:0002362,serous surface papilloma,MONDO,disease,DISEASE_7818
7819,7819,7819,7819,7819,7819,7819,7819,MONDO:0002851_MONDO:0003034,mediastinum rhabdomyosarcoma,MONDO_grouped,disease,DISEASE_7819
7820,7820,7820,7820,7820,7820,7820,7820,MONDO:0016878,partial deletion of chromosome 16,MONDO,disease,DISEASE_7820
7821,7821,7821,7821,7821,7821,7821,7821,MONDO:0100096,COVID-19,MONDO,disease,DISEASE_7821
7822,7822,7822,7822,7822,7822,7822,7822,MONDO:0971094,cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome due to TAB2 mutation,MONDO,disease,DISEASE_7822
7823,7823,7823,7823,7823,7823,7823,7823,MONDO:0007902,"lichen planus, familial",MONDO,disease,DISEASE_7823
7824,7824,7824,7824,7824,7824,7824,7824,MONDO:0012868,"thrombophilia due to protein S deficiency, autosomal dominant",MONDO,disease,DISEASE_7824
7825,7825,7825,7825,7825,7825,7825,7825,MONDO:0012185_MONDO:0010738_MONDO:0008479,"spondylometaphyseal dysplasia, A4 type",MONDO_grouped,disease,DISEASE_7825
7826,7826,7826,7826,7826,7826,7826,7826,MONDO:0011082,oculoauriculofrontonasal syndrome,MONDO,disease,DISEASE_7826
7827,7827,7827,7827,7827,7827,7827,7827,MONDO:1010833,"Wilson disease, domestic cat",MONDO,disease,DISEASE_7827
7828,7828,7828,7828,7828,7828,7828,7828,MONDO:0007868_MONDO:0044330_MONDO:0013828_MONDO:0013827_MONDO:0021022_MONDO:0017658_MONDO:1011020,hyperekplexia,MONDO_grouped,disease,DISEASE_7828
7829,7829,7829,7829,7829,7829,7829,7829,MONDO:0008308,"priapism, familial idiopathic",MONDO,disease,DISEASE_7829
7830,7830,7830,7830,7830,7830,7830,7830,MONDO:0007987,Kniest dysplasia,MONDO,disease,DISEASE_7830
7831,7831,7831,7831,7831,7831,7831,7831,MONDO:0003454,conjunctival cancer,MONDO,disease,DISEASE_7831
7832,7832,7832,7832,7832,7832,7832,7832,MONDO:0005169,neoplasm of mature T-cells or NK-cells,MONDO,disease,DISEASE_7832
7833,7833,7833,7833,7833,7833,7833,7833,MONDO:0018228,bipartite talus,MONDO,disease,DISEASE_7833
7834,7834,7834,7834,7834,7834,7834,7834,MONDO:0000241,Keshan disease,MONDO,disease,DISEASE_7834
7835,7835,7835,7835,7835,7835,7835,7835,MONDO:0023175,Fontaine farriaux blanckaert syndrome,MONDO,disease,DISEASE_7835
7836,7836,7836,7836,7836,7836,7836,7836,MONDO:0013473,"Hirschsprung disease, cardiac defects, and autonomic dysfunction",MONDO,disease,DISEASE_7836
7837,7837,7837,7837,7837,7837,7837,7837,MONDO:0004591,impetigo herpetiformis,MONDO,disease,DISEASE_7837
7838,7838,7838,7838,7838,7838,7838,7838,MONDO:0850089,Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation,MONDO,disease,DISEASE_7838
7839,7839,7839,7839,7839,7839,7839,7839,MONDO:0017900,autosomal recessive Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency,MONDO,disease,DISEASE_7839
7840,7840,7840,7840,7840,7840,7840,7840,MONDO:0008577,"toe, misshapen",MONDO,disease,DISEASE_7840
7841,7841,7841,7841,7841,7841,7841,7841,MONDO:0011936_MONDO:0008800,microphthalmia with brain and digit anomalies,MONDO_grouped,disease,DISEASE_7841
7842,7842,7842,7842,7842,7842,7842,7842,MONDO:0007536,congenital lobar emphysema,MONDO,disease,DISEASE_7842
7843,7843,7843,7843,7843,7843,7843,7843,MONDO:0019080_MONDO:0800198,alopecia totalis,MONDO_grouped,disease,DISEASE_7843
7844,7844,7844,7844,7844,7844,7844,7844,MONDO:0013055,"Stargardt macular degeneration, absent or hypoplastic corpus callosum, intellectual disability, and dysmorphic features",MONDO,disease,DISEASE_7844
7845,7845,7845,7845,7845,7845,7845,7845,MONDO:0010160_MONDO:0010162_MONDO:0010161_MONDO:0004741,tyrosinemia,MONDO_grouped,disease,DISEASE_7845
7846,7846,7846,7846,7846,7846,7846,7846,MONDO:0008300,Prader-Willi syndrome,MONDO,disease,DISEASE_7846
7847,7847,7847,7847,7847,7847,7847,7847,MONDO:0021296,carcinoma in situ of renal pelvis,MONDO,disease,DISEASE_7847
7848,7848,7848,7848,7848,7848,7848,7848,MONDO:0021907,aplasia cutis autosomal recessive,MONDO,disease,DISEASE_7848
7849,7849,7849,7849,7849,7849,7849,7849,MONDO:0800312,"wooly hair, autosomal recessive 1, with or without hypotrichosis",MONDO,disease,DISEASE_7849
7850,7850,7850,7850,7850,7850,7850,7850,MONDO:0009114,congenital sucrase-isomaltase deficiency,MONDO,disease,DISEASE_7850
7851,7851,7851,7851,7851,7851,7851,7851,MONDO:0020792,dwarfism with tall vertebrae,MONDO,disease,DISEASE_7851
7852,7852,7852,7852,7852,7852,7852,7852,MONDO:0032688,polymicrogyria with or without vascular-type Ehlers-Danlos syndrome,MONDO,disease,DISEASE_7852
7853,7853,7853,7853,7853,7853,7853,7853,MONDO:0017503,"acheiria, bilateral",MONDO,disease,DISEASE_7853
7854,7854,7854,7854,7854,7854,7854,7854,MONDO:0017455,hyperphalangy,MONDO,disease,DISEASE_7854
7855,7855,7855,7855,7855,7855,7855,7855,MONDO:0012324,Frias syndrome,MONDO,disease,DISEASE_7855
7856,7856,7856,7856,7856,7856,7856,7856,MONDO:0010603,hemophilia A with vascular abnormality,MONDO,disease,DISEASE_7856
7857,7857,7857,7857,7857,7857,7857,7857,MONDO:0006873,nutritional deficiency disease,MONDO,disease,DISEASE_7857
7858,7858,7858,7858,7858,7858,7858,7858,MONDO:0021489,benign neoplasm of sweat gland,MONDO,disease,DISEASE_7858
7859,7859,7859,7859,7859,7859,7859,7859,MONDO:0023699,Maroteaux Fonfria syndrome,MONDO,disease,DISEASE_7859
7860,7860,7860,7860,7860,7860,7860,7860,MONDO:0030718_MONDO:0032863_MONDO:0032859_MONDO:0030463_MONDO:0030307_MONDO:0030733_MONDO:0014961_MONDO:0971002_MONDO:0054731_MONDO:0054728_MONDO:0020855_MONDO:0030984_MONDO:0013070_MONDO:0957594_MONDO:0030868_MONDO:0030721_MONDO:0054729_MONDO:0020851_MONDO:0054723_MONDO:0054724_MONDO:0054730_MONDO:0859522_MONDO:0023664_MONDO:0031083_MONDO:0957593_MONDO:0020852_MONDO:0859338_MONDO:0030846_MONDO:0011720_MONDO:0030493_MONDO:0014847_MONDO:0014037_MONDO:0033673_MONDO:0033671_MONDO:0030492_MONDO:0013901_MONDO:0054725_MONDO:0030522_MONDO:0030809_MONDO:0033622_MONDO:0013505_MONDO:0032744_MONDO:0030507_MONDO:0030531_MONDO:0014365_MONDO:0957301_MONDO:0957249_MONDO:0970952_MONDO:0030508_MONDO:0032898_MONDO:0032896_MONDO:0032686_MONDO:0032748_MONDO:0014366_MONDO:0013504_MONDO:0010052_MONDO:0030972_MONDO:0030844_MONDO:0009776_MONDO:0958242_MONDO:0030989_MONDO:0029147_MONDO:0957250_MONDO:0029148_MONDO:0957821_MONDO:0030818_MONDO:0054726_MONDO:0859352_MONDO:0030430_MONDO:0030439_MONDO:0032739_MONDO:0054727_MONDO:0030515_MONDO:0859364_MONDO:0031077_MONDO:0030926_MONDO:0014172_MONDO:0054615_MONDO:0030716_MONDO:0030938_MONDO:0007060_MONDO:0054732_MONDO:0970999_MONDO:0032845_MONDO:0975842_MONDO:0971000_MONDO:0007161_MONDO:0030787_MONDO:0054733_MONDO:0009461_MONDO:0957584_MONDO:0014970_MONDO:0030732_MONDO:0004983_MONDO:0958206_MONDO:0975747_MONDO:0975958,spermatogenic failure,MONDO_grouped,disease,DISEASE_7860
7861,7861,7861,7861,7861,7861,7861,7861,MONDO:0018353,refractory celiac disease,MONDO,disease,DISEASE_7861
7862,7862,7862,7862,7862,7862,7862,7862,MONDO:0005447,testicular cancer,MONDO,disease,DISEASE_7862
7863,7863,7863,7863,7863,7863,7863,7863,MONDO:0012307,"familial scaphocephaly syndrome, McGillivray type",MONDO,disease,DISEASE_7863
7864,7864,7864,7864,7864,7864,7864,7864,MONDO:0031447,"macrothrombocytopenia, isolated",MONDO,disease,DISEASE_7864
7865,7865,7865,7865,7865,7865,7865,7865,MONDO:0800121,cellular interstitial pneumonitis,MONDO,disease,DISEASE_7865
7866,7866,7866,7866,7866,7866,7866,7866,MONDO:0042967,rheumatic disease of mitral valve,MONDO,disease,DISEASE_7866
7867,7867,7867,7867,7867,7867,7867,7867,MONDO:0017193,symptomatic form of Coffin-Lowry syndrome in female carriers,MONDO,disease,DISEASE_7867
7868,7868,7868,7868,7868,7868,7868,7868,MONDO:0000458,proneural glioblastoma,MONDO,disease,DISEASE_7868
7869,7869,7869,7869,7869,7869,7869,7869,MONDO:0100099,retrograde cricopharyngeus dysfunction,MONDO,disease,DISEASE_7869
7870,7870,7870,7870,7870,7870,7870,7870,MONDO:0014058,facial dysmorphism-immunodeficiency-livedo-short stature syndrome,MONDO,disease,DISEASE_7870
7871,7871,7871,7871,7871,7871,7871,7871,MONDO:0043519,burn,MONDO,disease,DISEASE_7871
7872,7872,7872,7872,7872,7872,7872,7872,MONDO:0001762,dentine erosion,MONDO,disease,DISEASE_7872
7873,7873,7873,7873,7873,7873,7873,7873,MONDO:0022513,atrophoderma of Pierini and Pasini,MONDO,disease,DISEASE_7873
7874,7874,7874,7874,7874,7874,7874,7874,MONDO:0100435,Schwartz-Jampel syndrome type 1,MONDO,disease,DISEASE_7874
7875,7875,7875,7875,7875,7875,7875,7875,MONDO:0043143,microphthalmia microtia fetal akinesia,MONDO,disease,DISEASE_7875
7876,7876,7876,7876,7876,7876,7876,7876,MONDO:0000643,vulvar benign neoplasm,MONDO,disease,DISEASE_7876
7877,7877,7877,7877,7877,7877,7877,7877,MONDO:1012354_MONDO:1012355,"polyneuropathy, dog",MONDO_grouped,disease,DISEASE_7877
7878,7878,7878,7878,7878,7878,7878,7878,MONDO:0009139,"dyssegmental dysplasia, Rolland-Desbuquois type",MONDO,disease,DISEASE_7878
7879,7879,7879,7879,7879,7879,7879,7879,MONDO:0012178,"intellectual disability with optic atrophy, facial dysmorphism, microcephaly, and short stature",MONDO,disease,DISEASE_7879
7880,7880,7880,7880,7880,7880,7880,7880,MONDO:0008101,familial supernumerary nipples,MONDO,disease,DISEASE_7880
7881,7881,7881,7881,7881,7881,7881,7881,MONDO:0012499,"Buruli ulcer, susceptibility to",MONDO,disease,DISEASE_7881
7882,7882,7882,7882,7882,7882,7882,7882,MONDO:0023020,dwarfism deafness retinitis pigmentosa,MONDO,disease,DISEASE_7882
7883,7883,7883,7883,7883,7883,7883,7883,MONDO:0004986_MONDO:0003439_MONDO:0004040,urinary bladder carcinoma,MONDO_grouped,disease,DISEASE_7883
7884,7884,7884,7884,7884,7884,7884,7884,MONDO:0004419,lymphoma-like variant infiltrating bladder urothelial carcinoma,MONDO,disease,DISEASE_7884
7885,7885,7885,7885,7885,7885,7885,7885,MONDO:0002742,cervical mucinous adenocarcinoma,MONDO,disease,DISEASE_7885
7886,7886,7886,7886,7886,7886,7886,7886,MONDO:0021187,hyperlipidemia,MONDO,disease,DISEASE_7886
7887,7887,7887,7887,7887,7887,7887,7887,MONDO:0004902,interstitial keratitis,MONDO,disease,DISEASE_7887
7888,7888,7888,7888,7888,7888,7888,7888,MONDO:0004132,anal canal squamous cell carcinoma,MONDO,disease,DISEASE_7888
7889,7889,7889,7889,7889,7889,7889,7889,MONDO:0006601_MONDO:0024349_MONDO:1010760,pityriasis rosea,MONDO_grouped,disease,DISEASE_7889
7890,7890,7890,7890,7890,7890,7890,7890,MONDO:0021543,hemangioma of gingiva,MONDO,disease,DISEASE_7890
7891,7891,7891,7891,7891,7891,7891,7891,MONDO:0006849_MONDO:0000748,mastitis,MONDO_grouped,disease,DISEASE_7891
7892,7892,7892,7892,7892,7892,7892,7892,MONDO:0001397,mononeuropathy,MONDO,disease,DISEASE_7892
7893,7893,7893,7893,7893,7893,7893,7893,MONDO:0025271,"trypanosomiasis, bovine",MONDO,disease,DISEASE_7893
7894,7894,7894,7894,7894,7894,7894,7894,MONDO:0016248,familial ovarian cancer,MONDO,disease,DISEASE_7894
7895,7895,7895,7895,7895,7895,7895,7895,MONDO:0002556,microcystic/reticular schwannoma,MONDO,disease,DISEASE_7895
7896,7896,7896,7896,7896,7896,7896,7896,MONDO:0004650_MONDO:0006104,malignant carotid body paraganglioma,MONDO_grouped,disease,DISEASE_7896
7897,7897,7897,7897,7897,7897,7897,7897,MONDO:0054637_MONDO:0054588_MONDO:0011899,Noonan syndrome-like disorder with loose anagen hair,MONDO_grouped,disease,DISEASE_7897
7898,7898,7898,7898,7898,7898,7898,7898,MONDO:0002852_MONDO:0003601,mediastinum sarcoma,MONDO_grouped,disease,DISEASE_7898
7899,7899,7899,7899,7899,7899,7899,7899,MONDO:0008652,congenital vertical talus,MONDO,disease,DISEASE_7899
7900,7900,7900,7900,7900,7900,7900,7900,MONDO:0011010,Matthew-Wood syndrome,MONDO,disease,DISEASE_7900
7901,7901,7901,7901,7901,7901,7901,7901,MONDO:0015988,multicystic dysplastic kidney,MONDO,disease,DISEASE_7901
7902,7902,7902,7902,7902,7902,7902,7902,MONDO:0018747,acquired epidermolysis bullosa,MONDO,disease,DISEASE_7902
7903,7903,7903,7903,7903,7903,7903,7903,MONDO:0021285,carcinoma in situ of urethra,MONDO,disease,DISEASE_7903
7904,7904,7904,7904,7904,7904,7904,7904,MONDO:0013292,chromosome 4q21 deletion syndrome,MONDO,disease,DISEASE_7904
7905,7905,7905,7905,7905,7905,7905,7905,MONDO:0003652,acute urate nephropathy,MONDO,disease,DISEASE_7905
7906,7906,7906,7906,7906,7906,7906,7906,MONDO:0021834,Akaba Hayasaka syndrome,MONDO,disease,DISEASE_7906
7907,7907,7907,7907,7907,7907,7907,7907,MONDO:0100312,vestibular ataxia,MONDO,disease,DISEASE_7907
7908,7908,7908,7908,7908,7908,7908,7908,MONDO:0007108,anal canal carcinoma,MONDO,disease,DISEASE_7908
7909,7909,7909,7909,7909,7909,7909,7909,MONDO:0005981,tick paralysis,MONDO,disease,DISEASE_7909
7910,7910,7910,7910,7910,7910,7910,7910,MONDO:0002418,ethmoid sinus adenocarcinoma,MONDO,disease,DISEASE_7910
7911,7911,7911,7911,7911,7911,7911,7911,MONDO:0003390,glycogen-rich clear cell breast carcinoma,MONDO,disease,DISEASE_7911
7912,7912,7912,7912,7912,7912,7912,7912,MONDO:0001150,hydrocephalus,MONDO,disease,DISEASE_7912
7913,7913,7913,7913,7913,7913,7913,7913,MONDO:0007512,ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet,MONDO,disease,DISEASE_7913
7914,7914,7914,7914,7914,7914,7914,7914,MONDO:0003275,middle ear cancer,MONDO,disease,DISEASE_7914
7915,7915,7915,7915,7915,7915,7915,7915,MONDO:0012004_MONDO:0006890_MONDO:0004303,parathyroid gland carcinoma,MONDO_grouped,disease,DISEASE_7915
7916,7916,7916,7916,7916,7916,7916,7916,MONDO:0800152,disorder of galactose and fructose metabolism,MONDO,disease,DISEASE_7916
7917,7917,7917,7917,7917,7917,7917,7917,MONDO:0003266,ependymal tumor,MONDO,disease,DISEASE_7917
7918,7918,7918,7918,7918,7918,7918,7918,MONDO:0008537,telecanthus,MONDO,disease,DISEASE_7918
7919,7919,7919,7919,7919,7919,7919,7919,MONDO:0016862,Alagille syndrome due to a JAG1 point mutation,MONDO,disease,DISEASE_7919
7920,7920,7920,7920,7920,7920,7920,7920,MONDO:0010941_MONDO:0010910_MONDO:0000022,nocturnal enuresis,MONDO_grouped,disease,DISEASE_7920
7921,7921,7921,7921,7921,7921,7921,7921,MONDO:0002130,upper limb mononeuronitis,MONDO,disease,DISEASE_7921
7922,7922,7922,7922,7922,7922,7922,7922,MONDO:0007245,"cafe au lait spots, multiple",MONDO,disease,DISEASE_7922
7923,7923,7923,7923,7923,7923,7923,7923,MONDO:1010482_MONDO:1010483_MONDO:1010484_MONDO:1010485,"tetralogy of fallot, dog",MONDO_grouped,disease,DISEASE_7923
7924,7924,7924,7924,7924,7924,7924,7924,MONDO:0019824,non-acquired pituitary hormone deficiency,MONDO,disease,DISEASE_7924
7925,7925,7925,7925,7925,7925,7925,7925,MONDO:0043537,cluster headache syndrome,MONDO,disease,DISEASE_7925
7926,7926,7926,7926,7926,7926,7926,7926,MONDO:0019929,"49,XXXXY syndrome",MONDO,disease,DISEASE_7926
7927,7927,7927,7927,7927,7927,7927,7927,MONDO:0000616,progesterone-receptor negative breast cancer,MONDO,disease,DISEASE_7927
7928,7928,7928,7928,7928,7928,7928,7928,MONDO:0957307,woolly hair-skin fragility syndrome,MONDO,disease,DISEASE_7928
7929,7929,7929,7929,7929,7929,7929,7929,MONDO:0018055,pediatric hepatocellular carcinoma,MONDO,disease,DISEASE_7929
7930,7930,7930,7930,7930,7930,7930,7930,MONDO:0017247,communicating congenital bronchopulmonary-foregut malformation,MONDO,disease,DISEASE_7930
7931,7931,7931,7931,7931,7931,7931,7931,MONDO:0035474,PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis,MONDO,disease,DISEASE_7931
7932,7932,7932,7932,7932,7932,7932,7932,MONDO:0017162,imperforate oropharynx-costo vetebral anomalies syndrome,MONDO,disease,DISEASE_7932
7933,7933,7933,7933,7933,7933,7933,7933,MONDO:0024485,papillary urothelial hyperplasia,MONDO,disease,DISEASE_7933
7934,7934,7934,7934,7934,7934,7934,7934,MONDO:0958182_MONDO:0958188_MONDO:0958187_MONDO:0013343,C1Q deficiency,MONDO_grouped,disease,DISEASE_7934
7935,7935,7935,7935,7935,7935,7935,7935,MONDO:0000259,asymptomatic dengue,MONDO,disease,DISEASE_7935
7936,7936,7936,7936,7936,7936,7936,7936,MONDO:0017949_MONDO:0017947_MONDO:0015033,"ABeta amyloidosis, Arctic type",MONDO_grouped,disease,DISEASE_7936
7937,7937,7937,7937,7937,7937,7937,7937,MONDO:0019105,renal nutcracker syndrome,MONDO,disease,DISEASE_7937
7938,7938,7938,7938,7938,7938,7938,7938,MONDO:0019124,microscopic polyangiitis,MONDO,disease,DISEASE_7938
7939,7939,7939,7939,7939,7939,7939,7939,MONDO:0020425,abnormal number of coronary ostia,MONDO,disease,DISEASE_7939
7940,7940,7940,7940,7940,7940,7940,7940,MONDO:1010697,"citrullinaemia, cattle",MONDO,disease,DISEASE_7940
7941,7941,7941,7941,7941,7941,7941,7941,MONDO:0020651,mixed germ cell tumor of vulva,MONDO,disease,DISEASE_7941
7942,7942,7942,7942,7942,7942,7942,7942,MONDO:0043875,tumor lysis syndrome,MONDO,disease,DISEASE_7942
7943,7943,7943,7943,7943,7943,7943,7943,MONDO:0958239_MONDO:0011589_MONDO:0024549_MONDO:0975809,microphthalmia/coloboma,MONDO_grouped,disease,DISEASE_7943
7944,7944,7944,7944,7944,7944,7944,7944,MONDO:0030073,Mitchell syndrome,MONDO,disease,DISEASE_7944
7945,7945,7945,7945,7945,7945,7945,7945,MONDO:1012193,"thalamic-cerebellar neuropathy, sheep",MONDO,disease,DISEASE_7945
7946,7946,7946,7946,7946,7946,7946,7946,MONDO:0003715,bladder urachal carcinoma,MONDO,disease,DISEASE_7946
7947,7947,7947,7947,7947,7947,7947,7947,MONDO:0009418,hypogonadism with low-grade mental deficiency and microcephaly,MONDO,disease,DISEASE_7947
7948,7948,7948,7948,7948,7948,7948,7948,MONDO:0016020,frontal encephalocele,MONDO,disease,DISEASE_7948
7949,7949,7949,7949,7949,7949,7949,7949,MONDO:0008173_MONDO:0008174_MONDO:0014324_MONDO:0014325_MONDO:0016471,pachyonychia congenita,MONDO_grouped,disease,DISEASE_7949
7950,7950,7950,7950,7950,7950,7950,7950,MONDO:0007174,Lown-Ganong-Levine syndrome,MONDO,disease,DISEASE_7950
7951,7951,7951,7951,7951,7951,7951,7951,MONDO:0019050,inherited hemoglobinopathy,MONDO,disease,DISEASE_7951
7952,7952,7952,7952,7952,7952,7952,7952,MONDO:0016620_MONDO:0006965,primary hypertrophic osteoarthropathy,MONDO_grouped,disease,DISEASE_7952
7953,7953,7953,7953,7953,7953,7953,7953,MONDO:0001572_MONDO:0003295,leiomyoma,MONDO_grouped,disease,DISEASE_7953
7954,7954,7954,7954,7954,7954,7954,7954,MONDO:0006894,patellofemoral pain syndrome,MONDO,disease,DISEASE_7954
7955,7955,7955,7955,7955,7955,7955,7955,MONDO:0017296,"glycerol kinase deficiency, adult form",MONDO,disease,DISEASE_7955
7956,7956,7956,7956,7956,7956,7956,7956,MONDO:0006648,anterior compartment of tibia syndrome,MONDO,disease,DISEASE_7956
7957,7957,7957,7957,7957,7957,7957,7957,MONDO:0016206,idiopathic uveal effusion syndrome,MONDO,disease,DISEASE_7957
7958,7958,7958,7958,7958,7958,7958,7958,MONDO:0005319_MONDO:0005325,humerus fracture,MONDO_grouped,disease,DISEASE_7958
7959,7959,7959,7959,7959,7959,7959,7959,MONDO:0700203_MONDO:0700210,"pestivirus infectious disease, non-human animal",MONDO_grouped,disease,DISEASE_7959
7960,7960,7960,7960,7960,7960,7960,7960,MONDO:0012481_MONDO:0010167,mevalonic aciduria,MONDO_grouped,disease,DISEASE_7960
7961,7961,7961,7961,7961,7961,7961,7961,MONDO:0009895,postaxial polydactyly-dental and vertebral anomalies syndrome,MONDO,disease,DISEASE_7961
7962,7962,7962,7962,7962,7962,7962,7962,MONDO:0007957,mediosternal depigmentation line,MONDO,disease,DISEASE_7962
7963,7963,7963,7963,7963,7963,7963,7963,MONDO:0010712,"panhypopituitarism, X-linked",MONDO,disease,DISEASE_7963
7964,7964,7964,7964,7964,7964,7964,7964,MONDO:0003816,articular cartilage disorder,MONDO,disease,DISEASE_7964
7965,7965,7965,7965,7965,7965,7965,7965,MONDO:1011834_MONDO:1011857_MONDO:1011886,"cerebellar abiotrophy, non-human animal",MONDO_grouped,disease,DISEASE_7965
7966,7966,7966,7966,7966,7966,7966,7966,MONDO:0013046,glycogen storage disease due to muscle beta-enolase deficiency,MONDO,disease,DISEASE_7966
7967,7967,7967,7967,7967,7967,7967,7967,MONDO:1011910,"renal dysplasia and bladder aplasia-hypoplasia, non-human animal",MONDO,disease,DISEASE_7967
7968,7968,7968,7968,7968,7968,7968,7968,MONDO:0019655,sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis,MONDO,disease,DISEASE_7968
7969,7969,7969,7969,7969,7969,7969,7969,MONDO:0003027,thyroid gland angiosarcoma,MONDO,disease,DISEASE_7969
7970,7970,7970,7970,7970,7970,7970,7970,MONDO:0018128,phalangeal microgeodic syndrome,MONDO,disease,DISEASE_7970
7971,7971,7971,7971,7971,7971,7971,7971,MONDO:0859179,neurodevelopmental disorder with dysmorphic facies and thin corpus callosum,MONDO,disease,DISEASE_7971
7972,7972,7972,7972,7972,7972,7972,7972,MONDO:0859187,neurodevelopmental disorder with hypotonia and brain abnormalities,MONDO,disease,DISEASE_7972
7973,7973,7973,7973,7973,7973,7973,7973,MONDO:0700078,triple-positive breast carcinoma,MONDO,disease,DISEASE_7973
7974,7974,7974,7974,7974,7974,7974,7974,MONDO:1010769_MONDO:1010770,"bullous pemphigoid, Rhesus monkey",MONDO_grouped,disease,DISEASE_7974
7975,7975,7975,7975,7975,7975,7975,7975,MONDO:0014940,"neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset",MONDO,disease,DISEASE_7975
7976,7976,7976,7976,7976,7976,7976,7976,MONDO:0000233,Japanese spotted fever,MONDO,disease,DISEASE_7976
7977,7977,7977,7977,7977,7977,7977,7977,MONDO:0010923,proximal myopathy with focal depletion of mitochondria,MONDO,disease,DISEASE_7977
7978,7978,7978,7978,7978,7978,7978,7978,MONDO:0033493_MONDO:0007609_MONDO:0011563_MONDO:0012378_MONDO:0012598_MONDO:0975841,"fibromatosis, gingival",MONDO_grouped,disease,DISEASE_7978
7979,7979,7979,7979,7979,7979,7979,7979,MONDO:0015912,macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss,MONDO,disease,DISEASE_7979
7980,7980,7980,7980,7980,7980,7980,7980,MONDO:0007095,ameloonychohypohidrotic syndrome,MONDO,disease,DISEASE_7980
7981,7981,7981,7981,7981,7981,7981,7981,MONDO:0015299,Asherman syndrome,MONDO,disease,DISEASE_7981
7982,7982,7982,7982,7982,7982,7982,7982,MONDO:1012535,"cardiomyopathy and juvenile mortality, dog",MONDO,disease,DISEASE_7982
7983,7983,7983,7983,7983,7983,7983,7983,MONDO:0011098_MONDO:0700275_MONDO:0012758_MONDO:0012597_MONDO:0012741_MONDO:0013872_MONDO:0011270_MONDO:0012093_MONDO:0012094_MONDO:0012244_MONDO:0012300_MONDO:0012470_MONDO:0012620_MONDO:0012768_MONDO:0012769_MONDO:0012770,"prostate cancer, hereditary",MONDO_grouped,disease,DISEASE_7983
7984,7984,7984,7984,7984,7984,7984,7984,MONDO:0034054,severe combined immunodeficiency due to CD70 deficiency,MONDO,disease,DISEASE_7984
7985,7985,7985,7985,7985,7985,7985,7985,MONDO:1011313,"disorder of development or morphogenesis, non-human animal",MONDO,disease,DISEASE_7985
7986,7986,7986,7986,7986,7986,7986,7986,MONDO:0002969_MONDO:0002970,ciliary body cancer,MONDO_grouped,disease,DISEASE_7986
7987,7987,7987,7987,7987,7987,7987,7987,MONDO:0006243,hepatoid adenocarcinoma,MONDO,disease,DISEASE_7987
7988,7988,7988,7988,7988,7988,7988,7988,MONDO:0005286,palatal neoplasm,MONDO,disease,DISEASE_7988
7989,7989,7989,7989,7989,7989,7989,7989,MONDO:0001841_MONDO:0003782,uterine corpus epithelioid leiomyoma,MONDO_grouped,disease,DISEASE_7989
7990,7990,7990,7990,7990,7990,7990,7990,MONDO:0009388,hyperlysinemia,MONDO,disease,DISEASE_7990
7991,7991,7991,7991,7991,7991,7991,7991,MONDO:0002152,intermittent squint,MONDO,disease,DISEASE_7991
7992,7992,7992,7992,7992,7992,7992,7992,MONDO:0008306_MONDO:0019439,ABri amyloidosis,MONDO_grouped,disease,DISEASE_7992
7993,7993,7993,7993,7993,7993,7993,7993,MONDO:0032890,neuromuscular disease and ocular or auditory anomalies with or without seizures,MONDO,disease,DISEASE_7993
7994,7994,7994,7994,7994,7994,7994,7994,MONDO:0006548,facial dermatosis,MONDO,disease,DISEASE_7994
7995,7995,7995,7995,7995,7995,7995,7995,MONDO:0019108,silent sinus syndrome,MONDO,disease,DISEASE_7995
7996,7996,7996,7996,7996,7996,7996,7996,MONDO:0007486,hereditary benign intraepithelial dyskeratosis,MONDO,disease,DISEASE_7996
7997,7997,7997,7997,7997,7997,7997,7997,MONDO:1012868,"long QT syndrome, KCNQ1-related, rabbit",MONDO,disease,DISEASE_7997
7998,7998,7998,7998,7998,7998,7998,7998,MONDO:0014893,Okur-Chung neurodevelopmental syndrome,MONDO,disease,DISEASE_7998
7999,7999,7999,7999,7999,7999,7999,7999,MONDO:0004365,necrotic uveal melanoma,MONDO,disease,DISEASE_7999
8000,8000,8000,8000,8000,8000,8000,8000,MONDO:0016019,Rasmussen subacute encephalitis,MONDO,disease,DISEASE_8000
8001,8001,8001,8001,8001,8001,8001,8001,MONDO:1011446,"medium-chain acyl-CoA dehydrogenase deficiency, non-human animal",MONDO,disease,DISEASE_8001
8002,8002,8002,8002,8002,8002,8002,8002,MONDO:0005974,strongyloidiasis,MONDO,disease,DISEASE_8002
8003,8003,8003,8003,8003,8003,8003,8003,MONDO:0003664,hemolytic anemia,MONDO,disease,DISEASE_8003
8004,8004,8004,8004,8004,8004,8004,8004,MONDO:0024551,X-linked lymphoproliferative disease due to SH2D1A deficiency,MONDO,disease,DISEASE_8004
8005,8005,8005,8005,8005,8005,8005,8005,MONDO:0003051,non specific chronic endometritis,MONDO,disease,DISEASE_8005
8006,8006,8006,8006,8006,8006,8006,8006,MONDO:0005584_MONDO:0600027,congenital left-sided heart lesions,MONDO_grouped,disease,DISEASE_8006
8007,8007,8007,8007,8007,8007,8007,8007,MONDO:0005491,Chagas cardiomyopathy,MONDO,disease,DISEASE_8007
8008,8008,8008,8008,8008,8008,8008,8008,MONDO:0002237,carbuncle,MONDO,disease,DISEASE_8008
8009,8009,8009,8009,8009,8009,8009,8009,MONDO:0859193,neuroocular syndrome,MONDO,disease,DISEASE_8009
8010,8010,8010,8010,8010,8010,8010,8010,MONDO:0044700,SIN3A-related intellectual disability syndrome due to a point mutation,MONDO,disease,DISEASE_8010
8011,8011,8011,8011,8011,8011,8011,8011,MONDO:0017168,benign epithelial tumor of salivary glands,MONDO,disease,DISEASE_8011
8012,8012,8012,8012,8012,8012,8012,8012,MONDO:0958326,macular dystrophy with or without cone dysfunction,MONDO,disease,DISEASE_8012
8013,8013,8013,8013,8013,8013,8013,8013,MONDO:0007597,"factor VIII and Factor IX, combined deficiency of",MONDO,disease,DISEASE_8013
8014,8014,8014,8014,8014,8014,8014,8014,MONDO:1011096,"alkaptonuria, crab-eating macaque",MONDO,disease,DISEASE_8014
8015,8015,8015,8015,8015,8015,8015,8015,MONDO:0060733,humerofemoral hypoplasia with radiotibial ray deficiency,MONDO,disease,DISEASE_8015
8016,8016,8016,8016,8016,8016,8016,8016,MONDO:0019032,X-linked intellectual disability with isolated growth hormone deficiency,MONDO,disease,DISEASE_8016
8017,8017,8017,8017,8017,8017,8017,8017,MONDO:0020596,mucin-producing carcinoma,MONDO,disease,DISEASE_8017
8018,8018,8018,8018,8018,8018,8018,8018,MONDO:1010629,"Chediak-Higashi syndrome, domestic cat",MONDO,disease,DISEASE_8018
8019,8019,8019,8019,8019,8019,8019,8019,MONDO:1011804,"congenital myopathy with fiber-type disproportion, non-human animal",MONDO,disease,DISEASE_8019
8020,8020,8020,8020,8020,8020,8020,8020,MONDO:0008925,cataract 46 juvenile-onset,MONDO,disease,DISEASE_8020
8021,8021,8021,8021,8021,8021,8021,8021,MONDO:0004664,helminthiasis,MONDO,disease,DISEASE_8021
8022,8022,8022,8022,8022,8022,8022,8022,MONDO:0001506,prostatocystitis,MONDO,disease,DISEASE_8022
8023,8023,8023,8023,8023,8023,8023,8023,MONDO:0017597,T-cell/histiocyte rich large B cell lymphoma,MONDO,disease,DISEASE_8023
8024,8024,8024,8024,8024,8024,8024,8024,MONDO:0025152,non-human ape disease,MONDO,disease,DISEASE_8024
8025,8025,8025,8025,8025,8025,8025,8025,MONDO:0011907,acrocapitofemoral dysplasia,MONDO,disease,DISEASE_8025
8026,8026,8026,8026,8026,8026,8026,8026,MONDO:0018952,argyria,MONDO,disease,DISEASE_8026
8027,8027,8027,8027,8027,8027,8027,8027,MONDO:0012286,"myopathy, autophagic vacuolar, infantile-onset",MONDO,disease,DISEASE_8027
8028,8028,8028,8028,8028,8028,8028,8028,MONDO:0018134,disorder of melanin metabolism,MONDO,disease,DISEASE_8028
8029,8029,8029,8029,8029,8029,8029,8029,MONDO:0009089,deafness-oligodontia syndrome,MONDO,disease,DISEASE_8029
8030,8030,8030,8030,8030,8030,8030,8030,MONDO:0016658,8p23.1 microdeletion syndrome,MONDO,disease,DISEASE_8030
8031,8031,8031,8031,8031,8031,8031,8031,MONDO:0024502,gallbladder neuroendocrine neoplasm,MONDO,disease,DISEASE_8031
8032,8032,8032,8032,8032,8032,8032,8032,MONDO:0011959,sweet syndrome,MONDO,disease,DISEASE_8032
8033,8033,8033,8033,8033,8033,8033,8033,MONDO:0100028_MONDO:0100029,immune epilepsy,MONDO_grouped,disease,DISEASE_8033
8034,8034,8034,8034,8034,8034,8034,8034,MONDO:0007640,Sorsby fundus dystrophy,MONDO,disease,DISEASE_8034
8035,8035,8035,8035,8035,8035,8035,8035,MONDO:0015093,sub-cortical nodular heterotopia,MONDO,disease,DISEASE_8035
8036,8036,8036,8036,8036,8036,8036,8036,MONDO:0019876,8p inverted duplication/deletion syndrome,MONDO,disease,DISEASE_8036
8037,8037,8037,8037,8037,8037,8037,8037,MONDO:0002376,spleen angiosarcoma,MONDO,disease,DISEASE_8037
8038,8038,8038,8038,8038,8038,8038,8038,MONDO:0958229,"bleeding disorder, vascular-type",MONDO,disease,DISEASE_8038
8039,8039,8039,8039,8039,8039,8039,8039,MONDO:0007648,hereditary diffuse gastric adenocarcinoma,MONDO,disease,DISEASE_8039
8040,8040,8040,8040,8040,8040,8040,8040,MONDO:0020516,thymic neuroendocrine carcinoma,MONDO,disease,DISEASE_8040
8041,8041,8041,8041,8041,8041,8041,8041,MONDO:0015291_MONDO:0001395,stromal keratitis,MONDO_grouped,disease,DISEASE_8041
8042,8042,8042,8042,8042,8042,8042,8042,MONDO:1011702,"neonatal pancytopenia, non-human animal",MONDO,disease,DISEASE_8042
8043,8043,8043,8043,8043,8043,8043,8043,MONDO:0018245,2p21 microdeletion syndrome without cystinuria,MONDO,disease,DISEASE_8043
8044,8044,8044,8044,8044,8044,8044,8044,MONDO:0024649_MONDO:0003234_MONDO:0003931,optic tract astrocytoma,MONDO_grouped,disease,DISEASE_8044
8045,8045,8045,8045,8045,8045,8045,8045,MONDO:0010284,Armfield syndrome,MONDO,disease,DISEASE_8045
8046,8046,8046,8046,8046,8046,8046,8046,MONDO:0015445,autosomal dominant coarctation of aorta,MONDO,disease,DISEASE_8046
8047,8047,8047,8047,8047,8047,8047,8047,MONDO:0032607,vertebral anomalies and variable endocrine and T-cell dysfunction,MONDO,disease,DISEASE_8047
8048,8048,8048,8048,8048,8048,8048,8048,MONDO:0004723_MONDO:0003378,liver leiomyoma,MONDO_grouped,disease,DISEASE_8048
8049,8049,8049,8049,8049,8049,8049,8049,MONDO:0014424,obsolete congenital deficiency in alpha-fetoprotein,MONDO,disease,DISEASE_8049
8050,8050,8050,8050,8050,8050,8050,8050,MONDO:0014822,15q14 microdeletion syndrome,MONDO,disease,DISEASE_8050
8051,8051,8051,8051,8051,8051,8051,8051,MONDO:0005425,podoconiosis,MONDO,disease,DISEASE_8051
8052,8052,8052,8052,8052,8052,8052,8052,MONDO:0011378,obsolete CFM1,MONDO,disease,DISEASE_8052
8053,8053,8053,8053,8053,8053,8053,8053,MONDO:0020568,cutaneous myiasis,MONDO,disease,DISEASE_8053
8054,8054,8054,8054,8054,8054,8054,8054,MONDO:0016501,Hermansky-Pudlak syndrome with pulmonary fibrosis,MONDO,disease,DISEASE_8054
8055,8055,8055,8055,8055,8055,8055,8055,MONDO:0044406,arthrogryposis-ectodermal dysplasia-other anomalies syndrome,MONDO,disease,DISEASE_8055
8056,8056,8056,8056,8056,8056,8056,8056,MONDO:0006578,mediastinal lipomatosis,MONDO,disease,DISEASE_8056
8057,8057,8057,8057,8057,8057,8057,8057,MONDO:0010768_MONDO:0002698,gonadoblastoma,MONDO_grouped,disease,DISEASE_8057
8058,8058,8058,8058,8058,8058,8058,8058,MONDO:0007559_MONDO:0012304_MONDO:0012305,photoparoxysmal response,MONDO_grouped,disease,DISEASE_8058
8059,8059,8059,8059,8059,8059,8059,8059,MONDO:0018857,creeping myiasis,MONDO,disease,DISEASE_8059
8060,8060,8060,8060,8060,8060,8060,8060,MONDO:0011073_MONDO:0030088_MONDO:0030087_MONDO:0012480_MONDO:0100165_MONDO:0012522_MONDO:0030089_MONDO:0020525,"diabetes mellitus, transient neonatal",MONDO_grouped,disease,DISEASE_8060
8061,8061,8061,8061,8061,8061,8061,8061,MONDO:1012698,"multifocal symmetrical necrotizing encephalomyelopathy, Simmental cattle",MONDO,disease,DISEASE_8061
8062,8062,8062,8062,8062,8062,8062,8062,MONDO:1012699_MONDO:1012942,"lysosomal storage disease, ARSG related, dog",MONDO_grouped,disease,DISEASE_8062
8063,8063,8063,8063,8063,8063,8063,8063,MONDO:0100237,inherited cutis laxa,MONDO,disease,DISEASE_8063
8064,8064,8064,8064,8064,8064,8064,8064,MONDO:0010215_MONDO:0010210_MONDO:0010211_MONDO:0012531_MONDO:0010212_MONDO:0010216_MONDO:0010213_MONDO:0019600,xeroderma pigmentosum group,MONDO_grouped,disease,DISEASE_8064
8065,8065,8065,8065,8065,8065,8065,8065,MONDO:0004127,lung occult adenocarcinoma,MONDO,disease,DISEASE_8065
8066,8066,8066,8066,8066,8066,8066,8066,MONDO:0006202,extrahepatic bile duct adenosquamous carcinoma,MONDO,disease,DISEASE_8066
8067,8067,8067,8067,8067,8067,8067,8067,MONDO:0011147,chromosome 18q deletion syndrome,MONDO,disease,DISEASE_8067
8068,8068,8068,8068,8068,8068,8068,8068,MONDO:0021845,Aloi Tomasini Isaia syndrome,MONDO,disease,DISEASE_8068
8069,8069,8069,8069,8069,8069,8069,8069,MONDO:0042976,vitamin B deficiency,MONDO,disease,DISEASE_8069
8070,8070,8070,8070,8070,8070,8070,8070,MONDO:1012573,"pyknodysostosis, domestic cat",MONDO,disease,DISEASE_8070
8071,8071,8071,8071,8071,8071,8071,8071,MONDO:0001836,amenorrhea,MONDO,disease,DISEASE_8071
8072,8072,8072,8072,8072,8072,8072,8072,MONDO:0005010,coronary artery disorder,MONDO,disease,DISEASE_8072
8073,8073,8073,8073,8073,8073,8073,8073,MONDO:0007448,familial dermatographia,MONDO,disease,DISEASE_8073
8074,8074,8074,8074,8074,8074,8074,8074,MONDO:0001969,mixed gonadal dysgenesis,MONDO,disease,DISEASE_8074
8075,8075,8075,8075,8075,8075,8075,8075,MONDO:0550003,SEC61B-related polycystic liver disease,MONDO,disease,DISEASE_8075
8076,8076,8076,8076,8076,8076,8076,8076,MONDO:0015140,early-onset autosomal dominant Alzheimer disease,MONDO,disease,DISEASE_8076
8077,8077,8077,8077,8077,8077,8077,8077,MONDO:0020815,dentigerous cyst,MONDO,disease,DISEASE_8077
8078,8078,8078,8078,8078,8078,8078,8078,MONDO:0011507,"diabetes mellitus, congenital autoimmune",MONDO,disease,DISEASE_8078
8079,8079,8079,8079,8079,8079,8079,8079,MONDO:0009707,myopathy with giant abnormal mitochondria,MONDO,disease,DISEASE_8079
8080,8080,8080,8080,8080,8080,8080,8080,MONDO:0020499,Nipah virus disease,MONDO,disease,DISEASE_8080
8081,8081,8081,8081,8081,8081,8081,8081,MONDO:0009357,humeroradial synostosis with craniofacial anomalies,MONDO,disease,DISEASE_8081
8082,8082,8082,8082,8082,8082,8082,8082,MONDO:0002858,ovary rhabdomyosarcoma,MONDO,disease,DISEASE_8082
8083,8083,8083,8083,8083,8083,8083,8083,MONDO:0004045_MONDO:0004350,pediatric intraocular retinoblastoma,MONDO_grouped,disease,DISEASE_8083
8084,8084,8084,8084,8084,8084,8084,8084,MONDO:0060582,auditory neuropathy-optic atrophy syndrome,MONDO,disease,DISEASE_8084
8085,8085,8085,8085,8085,8085,8085,8085,MONDO:0014698,microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome,MONDO,disease,DISEASE_8085
8086,8086,8086,8086,8086,8086,8086,8086,MONDO:0018431,cold-induced sweating syndrome - hyperthermia spectrum,MONDO,disease,DISEASE_8086
8087,8087,8087,8087,8087,8087,8087,8087,MONDO:0017784,Epstein-Barr virus-associated gastric carcinoma,MONDO,disease,DISEASE_8087
8088,8088,8088,8088,8088,8088,8088,8088,MONDO:0001399_MONDO:0002222,ureter leiomyoma,MONDO_grouped,disease,DISEASE_8088
8089,8089,8089,8089,8089,8089,8089,8089,MONDO:0027048,"deafness, Y-linked 2",MONDO,disease,DISEASE_8089
8090,8090,8090,8090,8090,8090,8090,8090,MONDO:0001498,varicocele,MONDO,disease,DISEASE_8090
8091,8091,8091,8091,8091,8091,8091,8091,MONDO:0008801,anosmia for isobutyric acid,MONDO,disease,DISEASE_8091
8092,8092,8092,8092,8092,8092,8092,8092,MONDO:0000342,O'nyong'nyong fever,MONDO,disease,DISEASE_8092
8093,8093,8093,8093,8093,8093,8093,8093,MONDO:0003888,childhood testicular mixed embryonal carcinoma and teratoma,MONDO,disease,DISEASE_8093
8094,8094,8094,8094,8094,8094,8094,8094,MONDO:0018458_MONDO:0007791_MONDO:0007792_MONDO:0010926,familial hypocalciuric hypercalcemia,MONDO_grouped,disease,DISEASE_8094
8095,8095,8095,8095,8095,8095,8095,8095,MONDO:0005876,Nidovirales infectious disease,MONDO,disease,DISEASE_8095
8096,8096,8096,8096,8096,8096,8096,8096,MONDO:0044699,SIN3A-related intellectual disability syndrome,MONDO,disease,DISEASE_8096
8097,8097,8097,8097,8097,8097,8097,8097,MONDO:0016935,partial duplication of chromosome 17,MONDO,disease,DISEASE_8097
8098,8098,8098,8098,8098,8098,8098,8098,MONDO:0015987,scimitar syndrome,MONDO,disease,DISEASE_8098
8099,8099,8099,8099,8099,8099,8099,8099,MONDO:1011276,"retinitis pigmentosa, RP1-related, cattle",MONDO,disease,DISEASE_8099
8100,8100,8100,8100,8100,8100,8100,8100,MONDO:1012882,"Charcot Marie Tooth disease, FGD4-related, cattle",MONDO,disease,DISEASE_8100
8101,8101,8101,8101,8101,8101,8101,8101,MONDO:0021439,benign neoplasm of pituitary gland,MONDO,disease,DISEASE_8101
8102,8102,8102,8102,8102,8102,8102,8102,MONDO:0003391,vulvar alveolar soft part sarcoma,MONDO,disease,DISEASE_8102
8103,8103,8103,8103,8103,8103,8103,8103,MONDO:0004147,noninvasive malignant thymoma,MONDO,disease,DISEASE_8103
8104,8104,8104,8104,8104,8104,8104,8104,MONDO:0021452,benign neoplasm of cornea,MONDO,disease,DISEASE_8104
8105,8105,8105,8105,8105,8105,8105,8105,MONDO:1011798,"forelimb-girdle muscular anomaly, non-human animal",MONDO,disease,DISEASE_8105
8106,8106,8106,8106,8106,8106,8106,8106,MONDO:0700136,bovine protoporphyria,MONDO,disease,DISEASE_8106
8107,8107,8107,8107,8107,8107,8107,8107,MONDO:0008706,Ackerman syndrome,MONDO,disease,DISEASE_8107
8108,8108,8108,8108,8108,8108,8108,8108,MONDO:0005539,small bowel Crohn disease,MONDO,disease,DISEASE_8108
8109,8109,8109,8109,8109,8109,8109,8109,MONDO:0010319_MONDO:0010355_MONDO:0010283_MONDO:0010285_MONDO:0010286_MONDO:0010427_MONDO:0010417,syndromic X-linked intellectual disability Hedera type,MONDO_grouped,disease,DISEASE_8109
8110,8110,8110,8110,8110,8110,8110,8110,MONDO:0000993,prostate squamous cell carcinoma,MONDO,disease,DISEASE_8110
8111,8111,8111,8111,8111,8111,8111,8111,MONDO:0022606,branchial arch disease,MONDO,disease,DISEASE_8111
8112,8112,8112,8112,8112,8112,8112,8112,MONDO:0003087,mucoepidermoid breast carcinoma,MONDO,disease,DISEASE_8112
8113,8113,8113,8113,8113,8113,8113,8113,MONDO:0030999,neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism,MONDO,disease,DISEASE_8113
8114,8114,8114,8114,8114,8114,8114,8114,MONDO:1012909,"dental-skeletal-retinal anomaly, MIA3-related, dog",MONDO,disease,DISEASE_8114
8115,8115,8115,8115,8115,8115,8115,8115,MONDO:0001863,aorta atresia,MONDO,disease,DISEASE_8115
8116,8116,8116,8116,8116,8116,8116,8116,MONDO:0006592,parapsoriasis,MONDO,disease,DISEASE_8116
8117,8117,8117,8117,8117,8117,8117,8117,MONDO:0023558,Kocher-debre-Semelaigne syndrome,MONDO,disease,DISEASE_8117
8118,8118,8118,8118,8118,8118,8118,8118,MONDO:0033658,neurodevelopmental disorder with seizures and brain atrophy,MONDO,disease,DISEASE_8118
8119,8119,8119,8119,8119,8119,8119,8119,MONDO:0007884,"leg ulcers, familial, of juvenile onset",MONDO,disease,DISEASE_8119
8120,8120,8120,8120,8120,8120,8120,8120,MONDO:0016210_MONDO:0001170,alternating hemiplegia,MONDO_grouped,disease,DISEASE_8120
8121,8121,8121,8121,8121,8121,8121,8121,MONDO:0001548,hepatic coma,MONDO,disease,DISEASE_8121
8122,8122,8122,8122,8122,8122,8122,8122,MONDO:0007605,fibrinolytic defect,MONDO,disease,DISEASE_8122
8123,8123,8123,8123,8123,8123,8123,8123,MONDO:0008349,"pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities",MONDO,disease,DISEASE_8123
8124,8124,8124,8124,8124,8124,8124,8124,MONDO:0004716,stomach carcinoma in situ,MONDO,disease,DISEASE_8124
8125,8125,8125,8125,8125,8125,8125,8125,MONDO:0005168,neoplasm of immature B and T cells,MONDO,disease,DISEASE_8125
8126,8126,8126,8126,8126,8126,8126,8126,MONDO:0007057,Acroosteolysis dominant type,MONDO,disease,DISEASE_8126
8127,8127,8127,8127,8127,8127,8127,8127,MONDO:0001810,hypoglossal nerve disorder,MONDO,disease,DISEASE_8127
8128,8128,8128,8128,8128,8128,8128,8128,MONDO:0100163,COVID-19–associated multisystem inflammatory syndrome in children,MONDO,disease,DISEASE_8128
8129,8129,8129,8129,8129,8129,8129,8129,MONDO:1012422,"exfoliative cutaneous lupus erythematosus, dog",MONDO,disease,DISEASE_8129
8130,8130,8130,8130,8130,8130,8130,8130,MONDO:0850198_MONDO:0956966_MONDO:0956967,medulloblastoma non-WNT/non-SHH,MONDO_grouped,disease,DISEASE_8130
8131,8131,8131,8131,8131,8131,8131,8131,MONDO:0004712,herpes simplex dermatitis,MONDO,disease,DISEASE_8131
8132,8132,8132,8132,8132,8132,8132,8132,MONDO:0001699,tinea manuum,MONDO,disease,DISEASE_8132
8133,8133,8133,8133,8133,8133,8133,8133,MONDO:0003674_MONDO:0000990,subendocardial myocardial infarction,MONDO_grouped,disease,DISEASE_8133
8134,8134,8134,8134,8134,8134,8134,8134,MONDO:0958258,Cushing syndrome due to cortisol-producing adrenocortical adenoma,MONDO,disease,DISEASE_8134
8135,8135,8135,8135,8135,8135,8135,8135,MONDO:0017814,primary bone lymphoma,MONDO,disease,DISEASE_8135
8136,8136,8136,8136,8136,8136,8136,8136,MONDO:0009945,pyridoxine-dependent epilepsy,MONDO,disease,DISEASE_8136
8137,8137,8137,8137,8137,8137,8137,8137,MONDO:0030553_MONDO:0012274_MONDO:0009231_MONDO:0008703_MONDO:0019696,acromesomelic dysplasia,MONDO_grouped,disease,DISEASE_8137
8138,8138,8138,8138,8138,8138,8138,8138,MONDO:0018947,centronuclear myopathy,MONDO,disease,DISEASE_8138
8139,8139,8139,8139,8139,8139,8139,8139,MONDO:0043327,cerebrospinal fluid leak,MONDO,disease,DISEASE_8139
8140,8140,8140,8140,8140,8140,8140,8140,MONDO:0018072,persistent truncus arteriosus,MONDO,disease,DISEASE_8140
8141,8141,8141,8141,8141,8141,8141,8141,MONDO:0014094,severe congenital hypochromic anemia with ringed sideroblasts,MONDO,disease,DISEASE_8141
8142,8142,8142,8142,8142,8142,8142,8142,MONDO:0024281,juvenile chronic polyarthritis,MONDO,disease,DISEASE_8142
8143,8143,8143,8143,8143,8143,8143,8143,MONDO:0005525_MONDO:0004932,T-cell leukemia,MONDO_grouped,disease,DISEASE_8143
8144,8144,8144,8144,8144,8144,8144,8144,MONDO:0700045,protothecosis,MONDO,disease,DISEASE_8144
8145,8145,8145,8145,8145,8145,8145,8145,MONDO:0006663,perinatal asphyxia,MONDO,disease,DISEASE_8145
8146,8146,8146,8146,8146,8146,8146,8146,MONDO:0009408,"hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase",MONDO,disease,DISEASE_8146
8147,8147,8147,8147,8147,8147,8147,8147,MONDO:0007441_MONDO:0007442_MONDO:0018849,dentinogenesis imperfecta,MONDO_grouped,disease,DISEASE_8147
8148,8148,8148,8148,8148,8148,8148,8148,MONDO:1010289,"choanal atresia, non-human animal",MONDO,disease,DISEASE_8148
8149,8149,8149,8149,8149,8149,8149,8149,MONDO:1010284,"allergic rhinitis, non-human animal",MONDO,disease,DISEASE_8149
8150,8150,8150,8150,8150,8150,8150,8150,MONDO:0003082,filamentary keratitis,MONDO,disease,DISEASE_8150
8151,8151,8151,8151,8151,8151,8151,8151,MONDO:1010026,"Budd-Chiari syndrome, non-human animal",MONDO,disease,DISEASE_8151
8152,8152,8152,8152,8152,8152,8152,8152,MONDO:0001703,color vision disorder,MONDO,disease,DISEASE_8152
8153,8153,8153,8153,8153,8153,8153,8153,MONDO:0004803,disseminated eosinophilic collagen disease,MONDO,disease,DISEASE_8153
8154,8154,8154,8154,8154,8154,8154,8154,MONDO:0005640,akinetic mutism,MONDO,disease,DISEASE_8154
8155,8155,8155,8155,8155,8155,8155,8155,MONDO:1010241,"giant axonal neuropathy, non-human animal",MONDO,disease,DISEASE_8155
8156,8156,8156,8156,8156,8156,8156,8156,MONDO:0016423_MONDO:0016422_MONDO:0009411_MONDO:0010012_MONDO:0017278_MONDO:1012651,autoimmune polyendocrinopathy,MONDO_grouped,disease,DISEASE_8156
8157,8157,8157,8157,8157,8157,8157,8157,MONDO:0007067,pyruvate kinase hyperactivity,MONDO,disease,DISEASE_8157
8158,8158,8158,8158,8158,8158,8158,8158,MONDO:0002122,neuritis,MONDO,disease,DISEASE_8158
8159,8159,8159,8159,8159,8159,8159,8159,MONDO:1012591_MONDO:1012594_MONDO:1012596,"oculocutaneous albinism, TYR-related, tufted capuchin",MONDO_grouped,disease,DISEASE_8159
8160,8160,8160,8160,8160,8160,8160,8160,MONDO:0021520,benign neoplasm of floor of mouth,MONDO,disease,DISEASE_8160
8161,8161,8161,8161,8161,8161,8161,8161,MONDO:1011503,"Fanconi syndrome, dog",MONDO,disease,DISEASE_8161
8162,8162,8162,8162,8162,8162,8162,8162,MONDO:0100458,MECOM-associated syndrome,MONDO,disease,DISEASE_8162
8163,8163,8163,8163,8163,8163,8163,8163,MONDO:0033641,"cleft palate, proliferative retinopathy, and developmental delay",MONDO,disease,DISEASE_8163
8164,8164,8164,8164,8164,8164,8164,8164,MONDO:0016777,inhalational botulism,MONDO,disease,DISEASE_8164
8165,8165,8165,8165,8165,8165,8165,8165,MONDO:0009749_MONDO:0012411_MONDO:0000128_MONDO:1011013,giant axonal neuropathy,MONDO_grouped,disease,DISEASE_8165
8166,8166,8166,8166,8166,8166,8166,8166,MONDO:0003405,adult central nervous system germ cell tumor,MONDO,disease,DISEASE_8166
8167,8167,8167,8167,8167,8167,8167,8167,MONDO:1011363,"ulcer disease, non-human animal",MONDO,disease,DISEASE_8167
8168,8168,8168,8168,8168,8168,8168,8168,MONDO:0013036,Zechi-Ceide syndrome,MONDO,disease,DISEASE_8168
8169,8169,8169,8169,8169,8169,8169,8169,MONDO:0017523_MONDO:0017527_MONDO:0017528,"polydactyly of a biphalangeal thumb, unilateral",MONDO_grouped,disease,DISEASE_8169
8170,8170,8170,8170,8170,8170,8170,8170,MONDO:0004162,uterine corpus cellular leiomyoma,MONDO,disease,DISEASE_8170
8171,8171,8171,8171,8171,8171,8171,8171,MONDO:0001147,meningocele,MONDO,disease,DISEASE_8171
8172,8172,8172,8172,8172,8172,8172,8172,MONDO:0011269,psoriasis 2,MONDO,disease,DISEASE_8172
8173,8173,8173,8173,8173,8173,8173,8173,MONDO:0018212,familial cervical artery dissection,MONDO,disease,DISEASE_8173
8174,8174,8174,8174,8174,8174,8174,8174,MONDO:0018222,obsolete X-linked intellectual disability due to GRIA3 anomalies,MONDO,disease,DISEASE_8174
8175,8175,8175,8175,8175,8175,8175,8175,MONDO:0015367,Charlie M syndrome,MONDO,disease,DISEASE_8175
8176,8176,8176,8176,8176,8176,8176,8176,MONDO:0021119,non-functioning endocrine neoplasm,MONDO,disease,DISEASE_8176
8177,8177,8177,8177,8177,8177,8177,8177,MONDO:0005216,hypopharyngeal carcinoma,MONDO,disease,DISEASE_8177
8178,8178,8178,8178,8178,8178,8178,8178,MONDO:0015694,malignant melanoma of the mucosa,MONDO,disease,DISEASE_8178
8179,8179,8179,8179,8179,8179,8179,8179,MONDO:0016013,fetal methylmercury syndrome,MONDO,disease,DISEASE_8179
8180,8180,8180,8180,8180,8180,8180,8180,MONDO:0004869_MONDO:0000922,pelvic varices,MONDO_grouped,disease,DISEASE_8180
8181,8181,8181,8181,8181,8181,8181,8181,MONDO:1012483,"exercise-induced pulmonary hemorrhage, horse",MONDO,disease,DISEASE_8181
8182,8182,8182,8182,8182,8182,8182,8182,MONDO:0002865,anus sarcoma,MONDO,disease,DISEASE_8182
8183,8183,8183,8183,8183,8183,8183,8183,MONDO:0018724,X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome,MONDO,disease,DISEASE_8183
8184,8184,8184,8184,8184,8184,8184,8184,MONDO:0800305,myelofibrosis with myeloid metaplasia,MONDO,disease,DISEASE_8184
8185,8185,8185,8185,8185,8185,8185,8185,MONDO:0019094,congenital Epstein-Barr virus infection,MONDO,disease,DISEASE_8185
8186,8186,8186,8186,8186,8186,8186,8186,MONDO:0006626_MONDO:0005266_MONDO:0005016_MONDO:0000960_MONDO:0001299_MONDO:0001583_MONDO:0001687_MONDO:0022972,diabetic neuropathy,MONDO_grouped,disease,DISEASE_8186
8187,8187,8187,8187,8187,8187,8187,8187,MONDO:0005307,obsolete contracture,MONDO,disease,DISEASE_8187
8188,8188,8188,8188,8188,8188,8188,8188,MONDO:1011688_MONDO:1012067,"congenital dyserythropoietic anemia with dyskeratosis and progressive alopecia, non-human animal",MONDO_grouped,disease,DISEASE_8188
8189,8189,8189,8189,8189,8189,8189,8189,MONDO:0019790,neuroleptic malignant syndrome,MONDO,disease,DISEASE_8189
8190,8190,8190,8190,8190,8190,8190,8190,MONDO:0850199,NK cell deficiency,MONDO,disease,DISEASE_8190
8191,8191,8191,8191,8191,8191,8191,8191,MONDO:0011397,"autosomal dominant cerebellar ataxia, deafness and narcolepsy",MONDO,disease,DISEASE_8191
8192,8192,8192,8192,8192,8192,8192,8192,MONDO:0022776,cleft lip and/or palate with mucous cysts of lower,MONDO,disease,DISEASE_8192
8193,8193,8193,8193,8193,8193,8193,8193,MONDO:1012029_MONDO:1012030,"bleeding disorder, pig",MONDO_grouped,disease,DISEASE_8193
8194,8194,8194,8194,8194,8194,8194,8194,MONDO:0001629,Jaccoud syndrome,MONDO,disease,DISEASE_8194
8195,8195,8195,8195,8195,8195,8195,8195,MONDO:0009234,congenital high-molecular-weight kininogen deficiency,MONDO,disease,DISEASE_8195
8196,8196,8196,8196,8196,8196,8196,8196,MONDO:0013507_MONDO:0009309_MONDO:0009310_MONDO:0009308,"granulomatous disease, chronic, autosomal recessive, cytochrome b-positive,",MONDO_grouped,disease,DISEASE_8196
8197,8197,8197,8197,8197,8197,8197,8197,MONDO:0003381_MONDO:0024468_MONDO:0015127,pituitary gland disorder,MONDO_grouped,disease,DISEASE_8197
8198,8198,8198,8198,8198,8198,8198,8198,MONDO:0020073,adolescent-onset epilepsy syndrome,MONDO,disease,DISEASE_8198
8199,8199,8199,8199,8199,8199,8199,8199,MONDO:0007846,KBG syndrome,MONDO,disease,DISEASE_8199
8200,8200,8200,8200,8200,8200,8200,8200,MONDO:0001615_MONDO:0019504,epidemic keratoconjunctivitis,MONDO_grouped,disease,DISEASE_8200
8201,8201,8201,8201,8201,8201,8201,8201,MONDO:0010257_MONDO:0971170_MONDO:0010405,"prostate cancer, hereditary, X-linked",MONDO_grouped,disease,DISEASE_8201
8202,8202,8202,8202,8202,8202,8202,8202,MONDO:0022986,diffuse idiopathic pulmonary neuroendocrine cell hyperplasia,MONDO,disease,DISEASE_8202
8203,8203,8203,8203,8203,8203,8203,8203,MONDO:0019122_MONDO:0017363_MONDO:0015927,idiopathic acute eosinophilic pneumonia,MONDO_grouped,disease,DISEASE_8203
8204,8204,8204,8204,8204,8204,8204,8204,MONDO:0022736,occupational lung disease,MONDO,disease,DISEASE_8204
8205,8205,8205,8205,8205,8205,8205,8205,MONDO:1011853,"neurological syndrome, non-human animal",MONDO,disease,DISEASE_8205
8206,8206,8206,8206,8206,8206,8206,8206,MONDO:0001052,chronic fungal otitis externa,MONDO,disease,DISEASE_8206
8207,8207,8207,8207,8207,8207,8207,8207,MONDO:0060641,neurodevelopmental disorder with or without seizures and gait abnormalities,MONDO,disease,DISEASE_8207
8208,8208,8208,8208,8208,8208,8208,8208,MONDO:0012733,autosomal recessive bestrophinopathy,MONDO,disease,DISEASE_8208
8209,8209,8209,8209,8209,8209,8209,8209,MONDO:0850129,gastroesophageal cancer,MONDO,disease,DISEASE_8209
8210,8210,8210,8210,8210,8210,8210,8210,MONDO:0022802,Collins-Sakati syndrome,MONDO,disease,DISEASE_8210
8211,8211,8211,8211,8211,8211,8211,8211,MONDO:0043127,mehta lewis patton syndrome,MONDO,disease,DISEASE_8211
8212,8212,8212,8212,8212,8212,8212,8212,MONDO:0018494,microcephaly-short stature-intellectual disability-facial dysmorphism syndrome,MONDO,disease,DISEASE_8212
8213,8213,8213,8213,8213,8213,8213,8213,MONDO:0024883,metastatic neoplasm,MONDO,disease,DISEASE_8213
8214,8214,8214,8214,8214,8214,8214,8214,MONDO:1012189,"congenital neuromuscular disease, sheep",MONDO,disease,DISEASE_8214
8215,8215,8215,8215,8215,8215,8215,8215,MONDO:0850009,syndromic microspherophakia,MONDO,disease,DISEASE_8215
8216,8216,8216,8216,8216,8216,8216,8216,MONDO:0001245_MONDO:0002281,microcytic anemia,MONDO_grouped,disease,DISEASE_8216
8217,8217,8217,8217,8217,8217,8217,8217,MONDO:0009524,intellectual disability-spasticity-ectrodactyly syndrome,MONDO,disease,DISEASE_8217
8218,8218,8218,8218,8218,8218,8218,8218,MONDO:1011107_MONDO:1012645,"nephropathy, COL4A4-related, dog",MONDO_grouped,disease,DISEASE_8218
8219,8219,8219,8219,8219,8219,8219,8219,MONDO:0700278_MONDO:0700276_MONDO:0700277,POLR1C-related disorder,MONDO_grouped,disease,DISEASE_8219
8220,8220,8220,8220,8220,8220,8220,8220,MONDO:0008001,"milia, multiple eruptive",MONDO,disease,DISEASE_8220
8221,8221,8221,8221,8221,8221,8221,8221,MONDO:0018257_MONDO:0020510,familial syringomyelia,MONDO_grouped,disease,DISEASE_8221
8222,8222,8222,8222,8222,8222,8222,8222,MONDO:0000469,sinoatrial node disorder,MONDO,disease,DISEASE_8222
8223,8223,8223,8223,8223,8223,8223,8223,MONDO:0007301,cerebrocostomandibular syndrome,MONDO,disease,DISEASE_8223
8224,8224,8224,8224,8224,8224,8224,8224,MONDO:0008644,velocardiofacial syndrome,MONDO,disease,DISEASE_8224
8225,8225,8225,8225,8225,8225,8225,8225,MONDO:1010161,"tibial hemimelia, non-human animal",MONDO,disease,DISEASE_8225
8226,8226,8226,8226,8226,8226,8226,8226,MONDO:1010879_MONDO:1010880_MONDO:1010881_MONDO:1010885_MONDO:1010886_MONDO:1010887_MONDO:1010888_MONDO:1010889_MONDO:1010890_MONDO:1010891_MONDO:1010892_MONDO:1010893_MONDO:1010894_MONDO:1010900_MONDO:1010901_MONDO:1010903_MONDO:1012707,"neuronal ceroid lipofuscinosis, CLN6-related, dog",MONDO_grouped,disease,DISEASE_8226
8227,8227,8227,8227,8227,8227,8227,8227,MONDO:0004834,ischemic fasciitis,MONDO,disease,DISEASE_8227
8228,8228,8228,8228,8228,8228,8228,8228,MONDO:0800394,MERTK-related retinopathy,MONDO,disease,DISEASE_8228
8229,8229,8229,8229,8229,8229,8229,8229,MONDO:0009811,osteoma of middle ear,MONDO,disease,DISEASE_8229
8230,8230,8230,8230,8230,8230,8230,8230,MONDO:0007053_MONDO:0100170_MONDO:0012135_MONDO:0012492_MONDO:0012493_MONDO:0012636_MONDO:0012641_MONDO:0013022_MONDO:0014079,"restless legs syndrome, susceptibility to",MONDO_grouped,disease,DISEASE_8230
8231,8231,8231,8231,8231,8231,8231,8231,MONDO:0016921,partial duplication of chromosome 1,MONDO,disease,DISEASE_8231
8232,8232,8232,8232,8232,8232,8232,8232,MONDO:1010107,"acute intermittent porphyria, non-human animal",MONDO,disease,DISEASE_8232
8233,8233,8233,8233,8233,8233,8233,8233,MONDO:0009784,ophthalmoplegic neuromuscular disorder with abnormal mitochondria,MONDO,disease,DISEASE_8233
8234,8234,8234,8234,8234,8234,8234,8234,MONDO:0003455,bile duct papillary neoplasm,MONDO,disease,DISEASE_8234
8235,8235,8235,8235,8235,8235,8235,8235,MONDO:0000952,cancer of long bone of lower limb,MONDO,disease,DISEASE_8235
8236,8236,8236,8236,8236,8236,8236,8236,MONDO:0005192,exocrine pancreatic carcinoma,MONDO,disease,DISEASE_8236
8237,8237,8237,8237,8237,8237,8237,8237,MONDO:0019242,inborn disorder of branched-chain amino acid metabolism,MONDO,disease,DISEASE_8237
8238,8238,8238,8238,8238,8238,8238,8238,MONDO:0001565,abnormal retinal correspondence,MONDO,disease,DISEASE_8238
8239,8239,8239,8239,8239,8239,8239,8239,MONDO:0016724,papillary tumor of the pineal region,MONDO,disease,DISEASE_8239
8240,8240,8240,8240,8240,8240,8240,8240,MONDO:0010338,X-linked distal spinal muscular atrophy type 3,MONDO,disease,DISEASE_8240
8241,8241,8241,8241,8241,8241,8241,8241,MONDO:0015564,Castleman disease,MONDO,disease,DISEASE_8241
8242,8242,8242,8242,8242,8242,8242,8242,MONDO:0010614,X-linked congenital generalized hypertrichosis,MONDO,disease,DISEASE_8242
8243,8243,8243,8243,8243,8243,8243,8243,MONDO:1011608,"vitamin-K-dependent blood coagulation factors deficiency, dog",MONDO,disease,DISEASE_8243
8244,8244,8244,8244,8244,8244,8244,8244,MONDO:0037737,peritoneal solitary fibrous tumor,MONDO,disease,DISEASE_8244
8245,8245,8245,8245,8245,8245,8245,8245,MONDO:1010783,"ectodermal dysplasia/skin fragility syndrome, dog",MONDO,disease,DISEASE_8245
8246,8246,8246,8246,8246,8246,8246,8246,MONDO:0010371,Aland island eye disease,MONDO,disease,DISEASE_8246
8247,8247,8247,8247,8247,8247,8247,8247,MONDO:0007660,familial ossifying fibroma,MONDO,disease,DISEASE_8247
8248,8248,8248,8248,8248,8248,8248,8248,MONDO:0003646,rectum neuroendocrine neoplasm,MONDO,disease,DISEASE_8248
8249,8249,8249,8249,8249,8249,8249,8249,MONDO:1010078,"polycythemia, non-human animal",MONDO,disease,DISEASE_8249
8250,8250,8250,8250,8250,8250,8250,8250,MONDO:0005101,ulcerative colitis,MONDO,disease,DISEASE_8250
8251,8251,8251,8251,8251,8251,8251,8251,MONDO:0019550,hereditary motor and sensory neuropathy with acrodystrophy,MONDO,disease,DISEASE_8251
8252,8252,8252,8252,8252,8252,8252,8252,MONDO:1010556_MONDO:1010561,"spina bifida, dog",MONDO_grouped,disease,DISEASE_8252
8253,8253,8253,8253,8253,8253,8253,8253,MONDO:0005596,cystadenocarcinoma,MONDO,disease,DISEASE_8253
8254,8254,8254,8254,8254,8254,8254,8254,MONDO:1011921,"pyometra, non-human animal",MONDO,disease,DISEASE_8254
8255,8255,8255,8255,8255,8255,8255,8255,MONDO:0007985,"metatarsus varus, type 1",MONDO,disease,DISEASE_8255
8256,8256,8256,8256,8256,8256,8256,8256,MONDO:0800108,cleft leaflet of tricuspid valve,MONDO,disease,DISEASE_8256
8257,8257,8257,8257,8257,8257,8257,8257,MONDO:0018430,partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome,MONDO,disease,DISEASE_8257
8258,8258,8258,8258,8258,8258,8258,8258,MONDO:0008231,Peyronie disease,MONDO,disease,DISEASE_8258
8259,8259,8259,8259,8259,8259,8259,8259,MONDO:0009581,intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome,MONDO,disease,DISEASE_8259
8260,8260,8260,8260,8260,8260,8260,8260,MONDO:0023093,exertional headache,MONDO,disease,DISEASE_8260
8261,8261,8261,8261,8261,8261,8261,8261,MONDO:0011914,hypotrichosis-lymphedema-telangiectasia syndrome,MONDO,disease,DISEASE_8261
8262,8262,8262,8262,8262,8262,8262,8262,MONDO:0859252,neurodevelopmental disorder with poor growth and skeletal anomalies,MONDO,disease,DISEASE_8262
8263,8263,8263,8263,8263,8263,8263,8263,MONDO:0015461,short rib-polydactyly syndrome,MONDO,disease,DISEASE_8263
8264,8264,8264,8264,8264,8264,8264,8264,MONDO:1010113,"glucocorticoid resistance, non-human animal",MONDO,disease,DISEASE_8264
8265,8265,8265,8265,8265,8265,8265,8265,MONDO:0045022_MONDO:0017736,disorder of organic acid metabolism,MONDO_grouped,disease,DISEASE_8265
8266,8266,8266,8266,8266,8266,8266,8266,MONDO:0858917,cauda equina neuroendocrine tumor,MONDO,disease,DISEASE_8266
8267,8267,8267,8267,8267,8267,8267,8267,MONDO:0008311,progeria-short stature-pigmented nevi syndrome,MONDO,disease,DISEASE_8267
8268,8268,8268,8268,8268,8268,8268,8268,MONDO:1011590_MONDO:1011589_MONDO:1011591_MONDO:1011592_MONDO:1011593,"portosystemic shunt, dog",MONDO_grouped,disease,DISEASE_8268
8269,8269,8269,8269,8269,8269,8269,8269,MONDO:0005956,septicemic plague,MONDO,disease,DISEASE_8269
8270,8270,8270,8270,8270,8270,8270,8270,MONDO:0007837,Johnson neuroectodermal syndrome,MONDO,disease,DISEASE_8270
8271,8271,8271,8271,8271,8271,8271,8271,MONDO:0019214,inborn carbohydrate metabolic disorder,MONDO,disease,DISEASE_8271
8272,8272,8272,8272,8272,8272,8272,8272,MONDO:0010824,disorder of sex development-intellectual disability syndrome,MONDO,disease,DISEASE_8272
8273,8273,8273,8273,8273,8273,8273,8273,MONDO:1012561,"mitochondrial fission encephalopathy, dog",MONDO,disease,DISEASE_8273
8274,8274,8274,8274,8274,8274,8274,8274,MONDO:0015071,middle ear neuroendocrine tumor,MONDO,disease,DISEASE_8274
8275,8275,8275,8275,8275,8275,8275,8275,MONDO:0001537,tuberculous epididymitis,MONDO,disease,DISEASE_8275
8276,8276,8276,8276,8276,8276,8276,8276,MONDO:0100529,Sunflower syndrome,MONDO,disease,DISEASE_8276
8277,8277,8277,8277,8277,8277,8277,8277,MONDO:1011113,"cryptorchidism, Arabian camel",MONDO,disease,DISEASE_8277
8278,8278,8278,8278,8278,8278,8278,8278,MONDO:0019376,West-Nile encephalitis,MONDO,disease,DISEASE_8278
8279,8279,8279,8279,8279,8279,8279,8279,MONDO:0971080,Grisel syndrome,MONDO,disease,DISEASE_8279
8280,8280,8280,8280,8280,8280,8280,8280,MONDO:1010841_MONDO:1012602_MONDO:1012603_MONDO:1012604,"gangliosidosis, domestic cat",MONDO_grouped,disease,DISEASE_8280
8281,8281,8281,8281,8281,8281,8281,8281,MONDO:0100253,Roberts-SC phocomelia syndrome,MONDO,disease,DISEASE_8281
8282,8282,8282,8282,8282,8282,8282,8282,MONDO:0016161,cerebral gigantism-jaw cysts syndrome,MONDO,disease,DISEASE_8282
8283,8283,8283,8283,8283,8283,8283,8283,MONDO:0005369_MONDO:0004993_MONDO:0002928,carcinoid tumor,MONDO_grouped,disease,DISEASE_8283
8284,8284,8284,8284,8284,8284,8284,8284,MONDO:1040016,cerebral artery stenosis,MONDO,disease,DISEASE_8284
8285,8285,8285,8285,8285,8285,8285,8285,MONDO:0016267,undifferentiated carcinoma of the corpus uteri,MONDO,disease,DISEASE_8285
8286,8286,8286,8286,8286,8286,8286,8286,MONDO:0018068,trisomy 13,MONDO,disease,DISEASE_8286
8287,8287,8287,8287,8287,8287,8287,8287,MONDO:0011020,osteoporosis-oculocutaneous hypopigmentation syndrome,MONDO,disease,DISEASE_8287
8288,8288,8288,8288,8288,8288,8288,8288,MONDO:0044101,"pregnancy, cornual",MONDO,disease,DISEASE_8288
8289,8289,8289,8289,8289,8289,8289,8289,MONDO:0019412,dysspondyloenchondromatosis,MONDO,disease,DISEASE_8289
8290,8290,8290,8290,8290,8290,8290,8290,MONDO:0022742,occupational asthma,MONDO,disease,DISEASE_8290
8291,8291,8291,8291,8291,8291,8291,8291,MONDO:0007008,uremia,MONDO,disease,DISEASE_8291
8292,8292,8292,8292,8292,8292,8292,8292,MONDO:0016879,partial deletion of chromosome 17,MONDO,disease,DISEASE_8292
8293,8293,8293,8293,8293,8293,8293,8293,MONDO:0018978,IgG4-related mediastinitis,MONDO,disease,DISEASE_8293
8294,8294,8294,8294,8294,8294,8294,8294,MONDO:0000407,malignant pleural solitary fibrous tumor,MONDO,disease,DISEASE_8294
8295,8295,8295,8295,8295,8295,8295,8295,MONDO:0020730_MONDO:0030883_MONDO:0007275,carpal tunnel syndrome,MONDO_grouped,disease,DISEASE_8295
8296,8296,8296,8296,8296,8296,8296,8296,MONDO:0002936,scrotum basal cell carcinoma,MONDO,disease,DISEASE_8296
8297,8297,8297,8297,8297,8297,8297,8297,MONDO:0013512,hemoglobin H disease,MONDO,disease,DISEASE_8297
8298,8298,8298,8298,8298,8298,8298,8298,MONDO:0020818,secondary dentine,MONDO,disease,DISEASE_8298
8299,8299,8299,8299,8299,8299,8299,8299,MONDO:0956985,lipofibromatosis-like neural tumor,MONDO,disease,DISEASE_8299
8300,8300,8300,8300,8300,8300,8300,8300,MONDO:0001123_MONDO:0001624,chronic sphenoidal sinusitis,MONDO_grouped,disease,DISEASE_8300
8301,8301,8301,8301,8301,8301,8301,8301,MONDO:0012008,Lelis syndrome,MONDO,disease,DISEASE_8301
8302,8302,8302,8302,8302,8302,8302,8302,MONDO:0800443,DEAF1-associated neurodevelopmental disorder,MONDO,disease,DISEASE_8302
8303,8303,8303,8303,8303,8303,8303,8303,MONDO:1010001,"epilepsy, non-human animal",MONDO,disease,DISEASE_8303
8304,8304,8304,8304,8304,8304,8304,8304,MONDO:0004173,adenocarcinoma of skene gland origin,MONDO,disease,DISEASE_8304
8305,8305,8305,8305,8305,8305,8305,8305,MONDO:0008865,Bietti crystalline corneoretinal dystrophy,MONDO,disease,DISEASE_8305
8306,8306,8306,8306,8306,8306,8306,8306,MONDO:0019079_MONDO:0001516,proximal spinal muscular atrophy,MONDO_grouped,disease,DISEASE_8306
8307,8307,8307,8307,8307,8307,8307,8307,MONDO:0020799,basal cell neoplasm,MONDO,disease,DISEASE_8307
8308,8308,8308,8308,8308,8308,8308,8308,MONDO:1011356,"sensory ganglionopathy, non-human animal",MONDO,disease,DISEASE_8308
8309,8309,8309,8309,8309,8309,8309,8309,MONDO:0000874,T-cell childhood lymphoblastic lymphoma,MONDO,disease,DISEASE_8309
8310,8310,8310,8310,8310,8310,8310,8310,MONDO:0017065_MONDO:0017071_MONDO:0017072,lumbosacral spina bifida aperta,MONDO_grouped,disease,DISEASE_8310
8311,8311,8311,8311,8311,8311,8311,8311,MONDO:0008406,obsolete autosomal recessive Emery-Dreifuss muscular dystrophy,MONDO,disease,DISEASE_8311
8312,8312,8312,8312,8312,8312,8312,8312,MONDO:0013727_MONDO:0013728_MONDO:0013729,"pregnancy loss, recurrent, susceptibility to",MONDO_grouped,disease,DISEASE_8312
8313,8313,8313,8313,8313,8313,8313,8313,MONDO:0017331,Pilotto syndrome,MONDO,disease,DISEASE_8313
8314,8314,8314,8314,8314,8314,8314,8314,MONDO:0044201,T+ B+ severe combined immunodeficiency,MONDO,disease,DISEASE_8314
8315,8315,8315,8315,8315,8315,8315,8315,MONDO:0012141,"orofacial cleft 6, susceptibility to",MONDO,disease,DISEASE_8315
8316,8316,8316,8316,8316,8316,8316,8316,MONDO:0014276,combined immunodeficiency due to CD3gamma deficiency,MONDO,disease,DISEASE_8316
8317,8317,8317,8317,8317,8317,8317,8317,MONDO:0014702_MONDO:0018644_MONDO:0015091,autosomal recessive complex spastic paraplegia type 9B,MONDO_grouped,disease,DISEASE_8317
8318,8318,8318,8318,8318,8318,8318,8318,MONDO:1011958_MONDO:1011969,"Laron dwarfism, non-human animal",MONDO_grouped,disease,DISEASE_8318
8319,8319,8319,8319,8319,8319,8319,8319,MONDO:0008792,familial angiolipomatosis,MONDO,disease,DISEASE_8319
8320,8320,8320,8320,8320,8320,8320,8320,MONDO:0009976,retinal degeneration and epilepsy,MONDO,disease,DISEASE_8320
8321,8321,8321,8321,8321,8321,8321,8321,MONDO:0012930,autosomal recessive severe congenital neutropenia due to G6PC3 deficiency,MONDO,disease,DISEASE_8321
8322,8322,8322,8322,8322,8322,8322,8322,MONDO:0002944,external ear carcinoma,MONDO,disease,DISEASE_8322
8323,8323,8323,8323,8323,8323,8323,8323,MONDO:0015677_MONDO:0007197,cardiac diverticulum,MONDO_grouped,disease,DISEASE_8323
8324,8324,8324,8324,8324,8324,8324,8324,MONDO:0002188,vulvar nodular hidradenoma,MONDO,disease,DISEASE_8324
8325,8325,8325,8325,8325,8325,8325,8325,MONDO:0008356,"radial heads, posterior dislocation of",MONDO,disease,DISEASE_8325
8326,8326,8326,8326,8326,8326,8326,8326,MONDO:0033352,"neuropathy, congenital hypomelinating",MONDO,disease,DISEASE_8326
8327,8327,8327,8327,8327,8327,8327,8327,MONDO:0021494,benign neoplasm of parotid gland,MONDO,disease,DISEASE_8327
8328,8328,8328,8328,8328,8328,8328,8328,MONDO:0005902,obsolete peanut allergic reaction,MONDO,disease,DISEASE_8328
8329,8329,8329,8329,8329,8329,8329,8329,MONDO:0012417,"heart-hand syndrome, Slovenian type",MONDO,disease,DISEASE_8329
8330,8330,8330,8330,8330,8330,8330,8330,MONDO:0013310,congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency,MONDO,disease,DISEASE_8330
8331,8331,8331,8331,8331,8331,8331,8331,MONDO:0024615,T-cell and NK-cell neoplasm,MONDO,disease,DISEASE_8331
8332,8332,8332,8332,8332,8332,8332,8332,MONDO:0004693,squamous carcinoma in situ,MONDO,disease,DISEASE_8332
8333,8333,8333,8333,8333,8333,8333,8333,MONDO:1010096,clinically amyopathic dermatomyositis,MONDO,disease,DISEASE_8333
8334,8334,8334,8334,8334,8334,8334,8334,MONDO:0024950_MONDO:0024919,horse disease,MONDO_grouped,disease,DISEASE_8334
8335,8335,8335,8335,8335,8335,8335,8335,MONDO:1012403,"contractural arachnodactyly, cattle",MONDO,disease,DISEASE_8335
8336,8336,8336,8336,8336,8336,8336,8336,MONDO:0011977,8q22.1 microdeletion syndrome,MONDO,disease,DISEASE_8336
8337,8337,8337,8337,8337,8337,8337,8337,MONDO:1012315,"congenital erythropoietic porphyria, zebu cattle",MONDO,disease,DISEASE_8337
8338,8338,8338,8338,8338,8338,8338,8338,MONDO:0044996,cerebral cortex disorder,MONDO,disease,DISEASE_8338
8339,8339,8339,8339,8339,8339,8339,8339,MONDO:0032928,"T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant",MONDO,disease,DISEASE_8339
8340,8340,8340,8340,8340,8340,8340,8340,MONDO:0001940,pleuropneumonia,MONDO,disease,DISEASE_8340
8341,8341,8341,8341,8341,8341,8341,8341,MONDO:0958118,autosomal recessive combined immunodeficiency due to IL6R deficiency,MONDO,disease,DISEASE_8341
8342,8342,8342,8342,8342,8342,8342,8342,MONDO:0018674,IgG4-related submandibular gland disease,MONDO,disease,DISEASE_8342
8343,8343,8343,8343,8343,8343,8343,8343,MONDO:0009967_MONDO:0001909,renal tubular acidosis 3,MONDO_grouped,disease,DISEASE_8343
8344,8344,8344,8344,8344,8344,8344,8344,MONDO:0010902,"spondyloepiphyseal dysplasia, Reardon type",MONDO,disease,DISEASE_8344
8345,8345,8345,8345,8345,8345,8345,8345,MONDO:0045044_MONDO:0045004,ligament disorder,MONDO_grouped,disease,DISEASE_8345
8346,8346,8346,8346,8346,8346,8346,8346,MONDO:0005761,filarial elephantiasis,MONDO,disease,DISEASE_8346
8347,8347,8347,8347,8347,8347,8347,8347,MONDO:0017639,carbon monoxide-induced parkinsonism,MONDO,disease,DISEASE_8347
8348,8348,8348,8348,8348,8348,8348,8348,MONDO:0009688_MONDO:0018325,myasthenia gravis,MONDO_grouped,disease,DISEASE_8348
8349,8349,8349,8349,8349,8349,8349,8349,MONDO:0800102_MONDO:0800405,CNGA3-related retinopathy,MONDO_grouped,disease,DISEASE_8349
8350,8350,8350,8350,8350,8350,8350,8350,MONDO:0012734,SERKAL syndrome,MONDO,disease,DISEASE_8350
8351,8351,8351,8351,8351,8351,8351,8351,MONDO:0035942,B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1),MONDO,disease,DISEASE_8351
8352,8352,8352,8352,8352,8352,8352,8352,MONDO:0001419,trachea squamous cell carcinoma,MONDO,disease,DISEASE_8352
8353,8353,8353,8353,8353,8353,8353,8353,MONDO:1012352,"urticaria pigmentosa, domestic cat",MONDO,disease,DISEASE_8353
8354,8354,8354,8354,8354,8354,8354,8354,MONDO:0008129,"ophthalmoplegia, familial total, with iris transillumination",MONDO,disease,DISEASE_8354
8355,8355,8355,8355,8355,8355,8355,8355,MONDO:0018892,Wyburn-Mason syndrome,MONDO,disease,DISEASE_8355
8356,8356,8356,8356,8356,8356,8356,8356,MONDO:0007876_MONDO:0007877,laryngeal abductor paralysis,MONDO_grouped,disease,DISEASE_8356
8357,8357,8357,8357,8357,8357,8357,8357,MONDO:1011762,"verrucous epidermal keratinocytic nevi, non-human animal",MONDO,disease,DISEASE_8357
8358,8358,8358,8358,8358,8358,8358,8358,MONDO:0004894,cyclotropia,MONDO,disease,DISEASE_8358
8359,8359,8359,8359,8359,8359,8359,8359,MONDO:0030730_MONDO:0030729_MONDO:0030993_MONDO:0031000,Tessadori-van Haaften neurodevelopmental syndrome,MONDO_grouped,disease,DISEASE_8359
8360,8360,8360,8360,8360,8360,8360,8360,MONDO:0022729,chondrodysplasia punctata with steroid sulfatase deficiency,MONDO,disease,DISEASE_8360
8361,8361,8361,8361,8361,8361,8361,8361,MONDO:0850160,B-lymphoblastic leukemia/lymphoma with IL3-IGH,MONDO,disease,DISEASE_8361
8362,8362,8362,8362,8362,8362,8362,8362,MONDO:0001388,glans penis cancer,MONDO,disease,DISEASE_8362
8363,8363,8363,8363,8363,8363,8363,8363,MONDO:0000276,Powassan encephalitis,MONDO,disease,DISEASE_8363
8364,8364,8364,8364,8364,8364,8364,8364,MONDO:0016619_MONDO:0015884,autosomal recessive hypohidrotic ectodermal dysplasia,MONDO_grouped,disease,DISEASE_8364
8365,8365,8365,8365,8365,8365,8365,8365,MONDO:0971131,bilateral diffuse uveal melanocytic proliferation disease,MONDO,disease,DISEASE_8365
8366,8366,8366,8366,8366,8366,8366,8366,MONDO:0100046,"exfoliation syndrome, susceptibility to",MONDO,disease,DISEASE_8366
8367,8367,8367,8367,8367,8367,8367,8367,MONDO:1012190,"neurogenic muscular atrophy, dog",MONDO,disease,DISEASE_8367
8368,8368,8368,8368,8368,8368,8368,8368,MONDO:0000610,marantic endocarditis,MONDO,disease,DISEASE_8368
8369,8369,8369,8369,8369,8369,8369,8369,MONDO:0001710,perforation of bile duct,MONDO,disease,DISEASE_8369
8370,8370,8370,8370,8370,8370,8370,8370,MONDO:0034110,atypical Fanconi syndrome-neonatal hyperinsulinism syndrome,MONDO,disease,DISEASE_8370
8371,8371,8371,8371,8371,8371,8371,8371,MONDO:0044350,"hyperparathyroidism, primary, caused by water clear cell hyperplasia",MONDO,disease,DISEASE_8371
8372,8372,8372,8372,8372,8372,8372,8372,MONDO:0015761,trisomy 10p,MONDO,disease,DISEASE_8372
8373,8373,8373,8373,8373,8373,8373,8373,MONDO:0002702,ovarian cystadenocarcinoma,MONDO,disease,DISEASE_8373
8374,8374,8374,8374,8374,8374,8374,8374,MONDO:0004022,parasagittal meningioma,MONDO,disease,DISEASE_8374
8375,8375,8375,8375,8375,8375,8375,8375,MONDO:0859002,intellectual disability-early-onset cataract-microcephaly syndrome,MONDO,disease,DISEASE_8375
8376,8376,8376,8376,8376,8376,8376,8376,MONDO:0003767,mitral valve disorder,MONDO,disease,DISEASE_8376
8377,8377,8377,8377,8377,8377,8377,8377,MONDO:0015599,atopic keratoconjunctivitis,MONDO,disease,DISEASE_8377
8378,8378,8378,8378,8378,8378,8378,8378,MONDO:0005868,myelophthisic anemia,MONDO,disease,DISEASE_8378
8379,8379,8379,8379,8379,8379,8379,8379,MONDO:0005968_MONDO:0042484,sporotrichosis,MONDO_grouped,disease,DISEASE_8379
8380,8380,8380,8380,8380,8380,8380,8380,MONDO:0003442,bladder papillary urothelial neoplasm,MONDO,disease,DISEASE_8380
8381,8381,8381,8381,8381,8381,8381,8381,MONDO:0004083,Borst-Jadassohn intraepidermal carcinoma,MONDO,disease,DISEASE_8381
8382,8382,8382,8382,8382,8382,8382,8382,MONDO:0004788,cervix squamous papilloma,MONDO,disease,DISEASE_8382
8383,8383,8383,8383,8383,8383,8383,8383,MONDO:0010890,acrocardiofacial syndrome,MONDO,disease,DISEASE_8383
8384,8384,8384,8384,8384,8384,8384,8384,MONDO:0008206,benign paroxysmal tonic upgaze of childhood with ataxia,MONDO,disease,DISEASE_8384
8385,8385,8385,8385,8385,8385,8385,8385,MONDO:1011270,"diabetic cataract, degu",MONDO,disease,DISEASE_8385
8386,8386,8386,8386,8386,8386,8386,8386,MONDO:0018205,distal monosomy 1q,MONDO,disease,DISEASE_8386
8387,8387,8387,8387,8387,8387,8387,8387,MONDO:0002044,spastic ectropion,MONDO,disease,DISEASE_8387
8388,8388,8388,8388,8388,8388,8388,8388,MONDO:0000001,disease,MONDO,disease,DISEASE_8388
8389,8389,8389,8389,8389,8389,8389,8389,MONDO:0004973,adenosquamous lung carcinoma,MONDO,disease,DISEASE_8389
8390,8390,8390,8390,8390,8390,8390,8390,MONDO:0018442,acitretin/etretinate embryopathy,MONDO,disease,DISEASE_8390
8391,8391,8391,8391,8391,8391,8391,8391,MONDO:1010764_MONDO:1010765_MONDO:1010767_MONDO:1010768,"vitiligo, chicken",MONDO_grouped,disease,DISEASE_8391
8392,8392,8392,8392,8392,8392,8392,8392,MONDO:0015762_MONDO:0018804,progressive familial intrahepatic cholestasis,MONDO_grouped,disease,DISEASE_8392
8393,8393,8393,8393,8393,8393,8393,8393,MONDO:0014362,"chromosome 16 inversion, 0.45-Mb",MONDO,disease,DISEASE_8393
8394,8394,8394,8394,8394,8394,8394,8394,MONDO:0007672,glomuvenous malformation,MONDO,disease,DISEASE_8394
8395,8395,8395,8395,8395,8395,8395,8395,MONDO:0001748,maxillary sinus carcinoma,MONDO,disease,DISEASE_8395
8396,8396,8396,8396,8396,8396,8396,8396,MONDO:0011601,neonatal intrahepatic cholestasis due to citrin deficiency,MONDO,disease,DISEASE_8396
8397,8397,8397,8397,8397,8397,8397,8397,MONDO:0011197,hereditary thermosensitive neuropathy,MONDO,disease,DISEASE_8397
8398,8398,8398,8398,8398,8398,8398,8398,MONDO:0012439,Alagille syndrome due to a NOTCH2 point mutation,MONDO,disease,DISEASE_8398
8399,8399,8399,8399,8399,8399,8399,8399,MONDO:0020377_MONDO:0020376_MONDO:0020372_MONDO:0020379_MONDO:0021548_MONDO:0018611,early-onset partial cataract,MONDO_grouped,disease,DISEASE_8399
8400,8400,8400,8400,8400,8400,8400,8400,MONDO:0009956,red skin pigment anomaly of new guinea,MONDO,disease,DISEASE_8400
8401,8401,8401,8401,8401,8401,8401,8401,MONDO:0700002,ATP1A3-associated neurological disorder,MONDO,disease,DISEASE_8401
8402,8402,8402,8402,8402,8402,8402,8402,MONDO:0003425,ophthalmoplegia,MONDO,disease,DISEASE_8402
8403,8403,8403,8403,8403,8403,8403,8403,MONDO:1012166,"mitral valve disease, dog",MONDO,disease,DISEASE_8403
8404,8404,8404,8404,8404,8404,8404,8404,MONDO:0044964,oral cavity mucoepidermoid carcinoma,MONDO,disease,DISEASE_8404
8405,8405,8405,8405,8405,8405,8405,8405,MONDO:0016017,methimazole embryofetopathy,MONDO,disease,DISEASE_8405
8406,8406,8406,8406,8406,8406,8406,8406,MONDO:0037940,inherited auditory system disease,MONDO,disease,DISEASE_8406
8407,8407,8407,8407,8407,8407,8407,8407,MONDO:0850150,kidney cortex disease,MONDO,disease,DISEASE_8407
8408,8408,8408,8408,8408,8408,8408,8408,MONDO:0018983,Tolosa-Hunt syndrome,MONDO,disease,DISEASE_8408
8409,8409,8409,8409,8409,8409,8409,8409,MONDO:1011771,"medial coronoid disease, non-human animal",MONDO,disease,DISEASE_8409
8410,8410,8410,8410,8410,8410,8410,8410,MONDO:0006106,benign smooth muscle neoplasm,MONDO,disease,DISEASE_8410
8411,8411,8411,8411,8411,8411,8411,8411,MONDO:0003086,thymic mucoepidermoid carcinoma,MONDO,disease,DISEASE_8411
8412,8412,8412,8412,8412,8412,8412,8412,MONDO:0003075,bilateral retinoblastoma,MONDO,disease,DISEASE_8412
8413,8413,8413,8413,8413,8413,8413,8413,MONDO:0006249,hyperplastic polyp,MONDO,disease,DISEASE_8413
8414,8414,8414,8414,8414,8414,8414,8414,MONDO:0017750,defect in conserved oligomeric Golgi complex,MONDO,disease,DISEASE_8414
8415,8415,8415,8415,8415,8415,8415,8415,MONDO:0006654,anthracosis,MONDO,disease,DISEASE_8415
8416,8416,8416,8416,8416,8416,8416,8416,MONDO:0020606,sex-linked disease,MONDO,disease,DISEASE_8416
8417,8417,8417,8417,8417,8417,8417,8417,MONDO:0002229,ovarian epithelial tumor,MONDO,disease,DISEASE_8417
8418,8418,8418,8418,8418,8418,8418,8418,MONDO:0018046,thrombocytopenia-Robin sequence syndrome,MONDO,disease,DISEASE_8418
8419,8419,8419,8419,8419,8419,8419,8419,MONDO:0019137,non-24-hour sleep-wake syndrome,MONDO,disease,DISEASE_8419
8420,8420,8420,8420,8420,8420,8420,8420,MONDO:0971032,bladder fermentation syndrome,MONDO,disease,DISEASE_8420
8421,8421,8421,8421,8421,8421,8421,8421,MONDO:0001028,acute pericementitis,MONDO,disease,DISEASE_8421
8422,8422,8422,8422,8422,8422,8422,8422,MONDO:0008835,"asthma, short stature, and elevated IgA",MONDO,disease,DISEASE_8422
8423,8423,8423,8423,8423,8423,8423,8423,MONDO:0000152,thiamine-responsive dysfunction syndrome,MONDO,disease,DISEASE_8423
8424,8424,8424,8424,8424,8424,8424,8424,MONDO:0007885_MONDO:1011550_MONDO:1011551_MONDO:1011552_MONDO:1011553,Legg-Calve-Perthes disease,MONDO_grouped,disease,DISEASE_8424
8425,8425,8425,8425,8425,8425,8425,8425,MONDO:1011438,"nephroma, non-human animal",MONDO,disease,DISEASE_8425
8426,8426,8426,8426,8426,8426,8426,8426,MONDO:0020714,"mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy",MONDO,disease,DISEASE_8426
8427,8427,8427,8427,8427,8427,8427,8427,MONDO:0011619,crumpled helices and small mouth,MONDO,disease,DISEASE_8427
8428,8428,8428,8428,8428,8428,8428,8428,MONDO:0010572,occipital horn syndrome,MONDO,disease,DISEASE_8428
8429,8429,8429,8429,8429,8429,8429,8429,MONDO:0000573,recombinase activating gene 2 deficiency,MONDO,disease,DISEASE_8429
8430,8430,8430,8430,8430,8430,8430,8430,MONDO:0023030,dysmorphism cleft palate loose skin,MONDO,disease,DISEASE_8430
8431,8431,8431,8431,8431,8431,8431,8431,MONDO:0005098,stroke disorder,MONDO,disease,DISEASE_8431
8432,8432,8432,8432,8432,8432,8432,8432,MONDO:0006771,glossitis,MONDO,disease,DISEASE_8432
8433,8433,8433,8433,8433,8433,8433,8433,MONDO:0007500,ear malformation,MONDO,disease,DISEASE_8433
8434,8434,8434,8434,8434,8434,8434,8434,MONDO:0008075_MONDO:0002546_MONDO:0859765_MONDO:1010953,schwannomatosis,MONDO_grouped,disease,DISEASE_8434
8435,8435,8435,8435,8435,8435,8435,8435,MONDO:0001604,lagophthalmos,MONDO,disease,DISEASE_8435
8436,8436,8436,8436,8436,8436,8436,8436,MONDO:0000809,purpura fulminans,MONDO,disease,DISEASE_8436
8437,8437,8437,8437,8437,8437,8437,8437,MONDO:0017735_MONDO:0019809,congenital aortic valve stenosis,MONDO_grouped,disease,DISEASE_8437
8438,8438,8438,8438,8438,8438,8438,8438,MONDO:0031037,famililal cerebral cavernous malformations,MONDO,disease,DISEASE_8438
8439,8439,8439,8439,8439,8439,8439,8439,MONDO:0008285,"polyps, multiple and recurrent inflammatory fibroid, gastrointestinal",MONDO,disease,DISEASE_8439
8440,8440,8440,8440,8440,8440,8440,8440,MONDO:0002268,dyspepsia,MONDO,disease,DISEASE_8440
8441,8441,8441,8441,8441,8441,8441,8441,MONDO:0013863,combined immunodeficiency due to LRBA deficiency,MONDO,disease,DISEASE_8441
8442,8442,8442,8442,8442,8442,8442,8442,MONDO:0009440,"ichthyosiform erythroderma, corneal involvement, and hearing loss",MONDO,disease,DISEASE_8442
8443,8443,8443,8443,8443,8443,8443,8443,MONDO:0024711,malignant mixed epithelial stromal tumor of the kidney,MONDO,disease,DISEASE_8443
8444,8444,8444,8444,8444,8444,8444,8444,MONDO:0009459,"channelopathy-associated congenital insensitivity to pain, autosomal recessive",MONDO,disease,DISEASE_8444
8445,8445,8445,8445,8445,8445,8445,8445,MONDO:0010332,X-linked intellectual disability-cubitus valgus-dysmorphism syndrome,MONDO,disease,DISEASE_8445
8446,8446,8446,8446,8446,8446,8446,8446,MONDO:0003180,cutaneous adenocystic carcinoma,MONDO,disease,DISEASE_8446
8447,8447,8447,8447,8447,8447,8447,8447,MONDO:0019751,autoinflammatory syndrome,MONDO,disease,DISEASE_8447
8448,8448,8448,8448,8448,8448,8448,8448,MONDO:1011449,"immunoglobulin A glomerulonephropathy, non-human animal",MONDO,disease,DISEASE_8448
8449,8449,8449,8449,8449,8449,8449,8449,MONDO:0019121,pneumocystosis,MONDO,disease,DISEASE_8449
8450,8450,8450,8450,8450,8450,8450,8450,MONDO:0005560,brain disorder,MONDO,disease,DISEASE_8450
8451,8451,8451,8451,8451,8451,8451,8451,MONDO:0019333,autosomal recessive hyperinsulinism due to SUR1 deficiency,MONDO,disease,DISEASE_8451
8452,8452,8452,8452,8452,8452,8452,8452,MONDO:0017582_MONDO:0003257_MONDO:0006373_MONDO:0003202_MONDO:0006634_MONDO:0006673_MONDO:0858916,pituitary adenocarcinoma,MONDO_grouped,disease,DISEASE_8452
8453,8453,8453,8453,8453,8453,8453,8453,MONDO:0020757,sporadic hemiplegic migraine,MONDO,disease,DISEASE_8453
8454,8454,8454,8454,8454,8454,8454,8454,MONDO:0005585,chemotherapy-induced hypertension,MONDO,disease,DISEASE_8454
8455,8455,8455,8455,8455,8455,8455,8455,MONDO:0054847_MONDO:0010985_MONDO:0054846_MONDO:0011506_MONDO:0011930_MONDO:0013322_MONDO:0014055_MONDO:0014167_MONDO:0000160,"epilepsy, familial adult myoclonic",MONDO_grouped,disease,DISEASE_8455
8456,8456,8456,8456,8456,8456,8456,8456,MONDO:0019994,maternal uniparental disomy of chromosome 13,MONDO,disease,DISEASE_8456
8457,8457,8457,8457,8457,8457,8457,8457,MONDO:0035447,liver adenomatosis,MONDO,disease,DISEASE_8457
8458,8458,8458,8458,8458,8458,8458,8458,MONDO:0001520,kleptomania,MONDO,disease,DISEASE_8458
8459,8459,8459,8459,8459,8459,8459,8459,MONDO:0016045_MONDO:1012083_MONDO:1012084_MONDO:1012085_MONDO:1012086,tetragametic chimerism,MONDO_grouped,disease,DISEASE_8459
8460,8460,8460,8460,8460,8460,8460,8460,MONDO:0014450_MONDO:0100490,"breasts and/or nipples, aplasia or hypoplasia of",MONDO_grouped,disease,DISEASE_8460
8461,8461,8461,8461,8461,8461,8461,8461,MONDO:0024376,"sleep disorder, initiating and maintaining sleep",MONDO,disease,DISEASE_8461
8462,8462,8462,8462,8462,8462,8462,8462,MONDO:1012972_MONDO:1011321,"hereditary neurological disease, non-human animal",MONDO_grouped,disease,DISEASE_8462
8463,8463,8463,8463,8463,8463,8463,8463,MONDO:0003007,childhood kidney cell carcinoma,MONDO,disease,DISEASE_8463
8464,8464,8464,8464,8464,8464,8464,8464,MONDO:0024381,"circadian rhythm sleep disorder, jet lag type",MONDO,disease,DISEASE_8464
8465,8465,8465,8465,8465,8465,8465,8465,MONDO:0005531,morphine dependence,MONDO,disease,DISEASE_8465
8466,8466,8466,8466,8466,8466,8466,8466,MONDO:1011664,"gluten-sensitive enteropathy, non-human animal",MONDO,disease,DISEASE_8466
8467,8467,8467,8467,8467,8467,8467,8467,MONDO:0019483,methotrexate-associated lymphoproliferative disorders,MONDO,disease,DISEASE_8467
8468,8468,8468,8468,8468,8468,8468,8468,MONDO:0011183,"Paget disease of bone 2, early-onset",MONDO,disease,DISEASE_8468
8469,8469,8469,8469,8469,8469,8469,8469,MONDO:0005050,invasive ductal and lobular carcinoma,MONDO,disease,DISEASE_8469
8470,8470,8470,8470,8470,8470,8470,8470,MONDO:0007991,microcephaly-deafness-intellectual disability syndrome,MONDO,disease,DISEASE_8470
8471,8471,8471,8471,8471,8471,8471,8471,MONDO:0027091,xanthogranulomatous sialadenitis,MONDO,disease,DISEASE_8471
8472,8472,8472,8472,8472,8472,8472,8472,MONDO:0044348_MONDO:0044349,hemoglobinopathy,MONDO_grouped,disease,DISEASE_8472
8473,8473,8473,8473,8473,8473,8473,8473,MONDO:0008742_MONDO:0028226,autosomal dominant severe congenital neutropenia,MONDO_grouped,disease,DISEASE_8473
8474,8474,8474,8474,8474,8474,8474,8474,MONDO:0859143,Radio-Tartaglia syndrome,MONDO,disease,DISEASE_8474
8475,8475,8475,8475,8475,8475,8475,8475,MONDO:0859529,"amyotrophic lateral sclerosis 27, juvenile",MONDO,disease,DISEASE_8475
8476,8476,8476,8476,8476,8476,8476,8476,MONDO:0006566,keratosis,MONDO,disease,DISEASE_8476
8477,8477,8477,8477,8477,8477,8477,8477,MONDO:0011946,diaphanospondylodysostosis,MONDO,disease,DISEASE_8477
8478,8478,8478,8478,8478,8478,8478,8478,MONDO:0958224,"encephalopathy, porphyria-related",MONDO,disease,DISEASE_8478
8479,8479,8479,8479,8479,8479,8479,8479,MONDO:1011424,"complement component 2 deficiency, non-human animal",MONDO,disease,DISEASE_8479
8480,8480,8480,8480,8480,8480,8480,8480,MONDO:0800026,"central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease",MONDO,disease,DISEASE_8480
8481,8481,8481,8481,8481,8481,8481,8481,MONDO:0012554_MONDO:0008955_MONDO:0014696_MONDO:0012553,cerebrooculofacioskeletal syndrome,MONDO_grouped,disease,DISEASE_8481
8482,8482,8482,8482,8482,8482,8482,8482,MONDO:0012586_MONDO:0012011,"coronary artery disease, autosomal dominant",MONDO_grouped,disease,DISEASE_8482
8483,8483,8483,8483,8483,8483,8483,8483,MONDO:0003084,uremic neuropathy,MONDO,disease,DISEASE_8483
8484,8484,8484,8484,8484,8484,8484,8484,MONDO:0859137,"neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia",MONDO,disease,DISEASE_8484
8485,8485,8485,8485,8485,8485,8485,8485,MONDO:0100020,atypical childhood epilepsy with centrotemporal spikes,MONDO,disease,DISEASE_8485
8486,8486,8486,8486,8486,8486,8486,8486,MONDO:0001020,amblyopia,MONDO,disease,DISEASE_8486
8487,8487,8487,8487,8487,8487,8487,8487,MONDO:0002721,necrosis of pituitary,MONDO,disease,DISEASE_8487
8488,8488,8488,8488,8488,8488,8488,8488,MONDO:0008455_MONDO:0010056_MONDO:0009673_MONDO:0009672_MONDO:0009669_MONDO:0850170_MONDO:1010995_MONDO:1010997,"spinal muscular atrophy,",MONDO_grouped,disease,DISEASE_8488
8489,8489,8489,8489,8489,8489,8489,8489,MONDO:0020598,malabsorption syndrome,MONDO,disease,DISEASE_8489
8490,8490,8490,8490,8490,8490,8490,8490,MONDO:0025404,coronaviral enteritis of turkeys,MONDO,disease,DISEASE_8490
8491,8491,8491,8491,8491,8491,8491,8491,MONDO:0958260,dysraphic spinal cord lipoma,MONDO,disease,DISEASE_8491
8492,8492,8492,8492,8492,8492,8492,8492,MONDO:0008843,atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome,MONDO,disease,DISEASE_8492
8493,8493,8493,8493,8493,8493,8493,8493,MONDO:0021358,neoplasm of hypopharynx,MONDO,disease,DISEASE_8493
8494,8494,8494,8494,8494,8494,8494,8494,MONDO:0016478,Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion,MONDO,disease,DISEASE_8494
8495,8495,8495,8495,8495,8495,8495,8495,MONDO:1012269,"tetanic torticollar spasms, turkey",MONDO,disease,DISEASE_8495
8496,8496,8496,8496,8496,8496,8496,8496,MONDO:0008629,"urolithiasis, uric acid, autosomal dominant",MONDO,disease,DISEASE_8496
8497,8497,8497,8497,8497,8497,8497,8497,MONDO:0014455,cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome,MONDO,disease,DISEASE_8497
8498,8498,8498,8498,8498,8498,8498,8498,MONDO:0017230,autosomal semi-dominant severe lipodystrophic laminopathy,MONDO,disease,DISEASE_8498
8499,8499,8499,8499,8499,8499,8499,8499,MONDO:1012654,"XY sex reversal, SRY-related, Western roe deer",MONDO,disease,DISEASE_8499
8500,8500,8500,8500,8500,8500,8500,8500,MONDO:0016014,fetal minoxidil syndrome,MONDO,disease,DISEASE_8500
8501,8501,8501,8501,8501,8501,8501,8501,MONDO:0002440,erythropoietin polycythemia,MONDO,disease,DISEASE_8501
8502,8502,8502,8502,8502,8502,8502,8502,MONDO:0004695,liver lymphoma,MONDO,disease,DISEASE_8502
8503,8503,8503,8503,8503,8503,8503,8503,MONDO:0009718_MONDO:1010100,myxedema,MONDO_grouped,disease,DISEASE_8503
8504,8504,8504,8504,8504,8504,8504,8504,MONDO:0032942,neurodevelopmental disorder with microcephaly and dysmorphic facies,MONDO,disease,DISEASE_8504
8505,8505,8505,8505,8505,8505,8505,8505,MONDO:1010441,"cardiomyopathy, dog",MONDO,disease,DISEASE_8505
8506,8506,8506,8506,8506,8506,8506,8506,MONDO:0010779,mitochondrial non-syndromic sensorineural hearing loss,MONDO,disease,DISEASE_8506
8507,8507,8507,8507,8507,8507,8507,8507,MONDO:0006602,porokeratosis,MONDO,disease,DISEASE_8507
8508,8508,8508,8508,8508,8508,8508,8508,MONDO:0015926_MONDO:0001004,pneumoconiosis,MONDO_grouped,disease,DISEASE_8508
8509,8509,8509,8509,8509,8509,8509,8509,MONDO:0019488_MONDO:0100026,myoclonic epilepsy in non-progressive encephalopathies,MONDO_grouped,disease,DISEASE_8509
8510,8510,8510,8510,8510,8510,8510,8510,MONDO:0018814,non-SCID combined immunodeficiency,MONDO,disease,DISEASE_8510
8511,8511,8511,8511,8511,8511,8511,8511,MONDO:0016615_MONDO:0016616_MONDO:0016617_MONDO:0016618,oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies,MONDO_grouped,disease,DISEASE_8511
8512,8512,8512,8512,8512,8512,8512,8512,MONDO:0003312,ovarian endometrioid stromal and related neoplasms,MONDO,disease,DISEASE_8512
8513,8513,8513,8513,8513,8513,8513,8513,MONDO:0017512,"split hand, bilateral",MONDO,disease,DISEASE_8513
8514,8514,8514,8514,8514,8514,8514,8514,MONDO:0100323,inherited pseudohypoaldosteronism,MONDO,disease,DISEASE_8514
8515,8515,8515,8515,8515,8515,8515,8515,MONDO:0010295,anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome,MONDO,disease,DISEASE_8515
8516,8516,8516,8516,8516,8516,8516,8516,MONDO:0007661,Tourette syndrome,MONDO,disease,DISEASE_8516
8517,8517,8517,8517,8517,8517,8517,8517,MONDO:0002471,bursitis,MONDO,disease,DISEASE_8517
8518,8518,8518,8518,8518,8518,8518,8518,MONDO:0027675,irinotecan toxicity,MONDO,disease,DISEASE_8518
8519,8519,8519,8519,8519,8519,8519,8519,MONDO:0004433,papillary carcinoma of the penis,MONDO,disease,DISEASE_8519
8520,8520,8520,8520,8520,8520,8520,8520,MONDO:0016441,acquired pseudoxanthoma elasticum,MONDO,disease,DISEASE_8520
8521,8521,8521,8521,8521,8521,8521,8521,MONDO:0023551,C1q nephropathy,MONDO,disease,DISEASE_8521
8522,8522,8522,8522,8522,8522,8522,8522,MONDO:0100138,X-linked recessive mitochondrial myopathy,MONDO,disease,DISEASE_8522
8523,8523,8523,8523,8523,8523,8523,8523,MONDO:0013166,GABA aminotransaminase deficiency,MONDO,disease,DISEASE_8523
8524,8524,8524,8524,8524,8524,8524,8524,MONDO:0010769,"hairy ears, Y-linked",MONDO,disease,DISEASE_8524
8525,8525,8525,8525,8525,8525,8525,8525,MONDO:0014285_MONDO:0009135_MONDO:0009134_MONDO:0007109_MONDO:0013355_MONDO:0019403_MONDO:0020337_MONDO:0975829_MONDO:1012538,congenital dyserythropoietic anemia type,MONDO_grouped,disease,DISEASE_8525
8526,8526,8526,8526,8526,8526,8526,8526,MONDO:0100578,FANCM Fanconi-like genomic instability disorder,MONDO,disease,DISEASE_8526
8527,8527,8527,8527,8527,8527,8527,8527,MONDO:0044301,"aortic aneurysm, familial thoracic 11, susceptibility to",MONDO,disease,DISEASE_8527
8528,8528,8528,8528,8528,8528,8528,8528,MONDO:0009671,intellectual disability-myopathy-short stature-endocrine defect syndrome,MONDO,disease,DISEASE_8528
8529,8529,8529,8529,8529,8529,8529,8529,MONDO:0016789,pyruvate metabolism disorder,MONDO,disease,DISEASE_8529
8530,8530,8530,8530,8530,8530,8530,8530,MONDO:0850007,syndromic lacrimal system disorder,MONDO,disease,DISEASE_8530
8531,8531,8531,8531,8531,8531,8531,8531,MONDO:0007726,"hip dysplasia, Beukes type",MONDO,disease,DISEASE_8531
8532,8532,8532,8532,8532,8532,8532,8532,MONDO:0011250_MONDO:0011341,"microcephaly, macrotia, and intellectual disability",MONDO_grouped,disease,DISEASE_8532
8533,8533,8533,8533,8533,8533,8533,8533,MONDO:0800038,MELAS syndrome caused by mutation in MTND1,MONDO,disease,DISEASE_8533
8534,8534,8534,8534,8534,8534,8534,8534,MONDO:0008446,sperm protamine P4,MONDO,disease,DISEASE_8534
8535,8535,8535,8535,8535,8535,8535,8535,MONDO:0004340,mixed ductal-endocrine carcinoma of pancreas,MONDO,disease,DISEASE_8535
8536,8536,8536,8536,8536,8536,8536,8536,MONDO:0019293,skin vascular disease,MONDO,disease,DISEASE_8536
8537,8537,8537,8537,8537,8537,8537,8537,MONDO:0009256,galactorrhea,MONDO,disease,DISEASE_8537
8538,8538,8538,8538,8538,8538,8538,8538,MONDO:0000236,oropharyngeal anthrax,MONDO,disease,DISEASE_8538
8539,8539,8539,8539,8539,8539,8539,8539,MONDO:0002271,colon adenocarcinoma,MONDO,disease,DISEASE_8539
8540,8540,8540,8540,8540,8540,8540,8540,MONDO:0001088,acute inferoposterior infarction,MONDO,disease,DISEASE_8540
8541,8541,8541,8541,8541,8541,8541,8541,MONDO:0003929,vestibular micropapillomatosis,MONDO,disease,DISEASE_8541
8542,8542,8542,8542,8542,8542,8542,8542,MONDO:1010904,"Gaucher disease, GBA1-related, sheep",MONDO,disease,DISEASE_8542
8543,8543,8543,8543,8543,8543,8543,8543,MONDO:1010649,"hypereosinophilic syndrome, horse",MONDO,disease,DISEASE_8543
8544,8544,8544,8544,8544,8544,8544,8544,MONDO:0008426,Shprintzen-Goldberg syndrome,MONDO,disease,DISEASE_8544
8545,8545,8545,8545,8545,8545,8545,8545,MONDO:0010584,"dyskeratosis congenita, X-linked",MONDO,disease,DISEASE_8545
8546,8546,8546,8546,8546,8546,8546,8546,MONDO:0011099,human HOXA1 syndromes,MONDO,disease,DISEASE_8546
8547,8547,8547,8547,8547,8547,8547,8547,MONDO:0045020,glycine metabolism disease,MONDO,disease,DISEASE_8547
8548,8548,8548,8548,8548,8548,8548,8548,MONDO:0002879,uterine body mixed cancer,MONDO,disease,DISEASE_8548
8549,8549,8549,8549,8549,8549,8549,8549,MONDO:0021048,benign mastocytoma,MONDO,disease,DISEASE_8549
8550,8550,8550,8550,8550,8550,8550,8550,MONDO:1012723_MONDO:1012724_MONDO:1012725_MONDO:1012726_MONDO:1012727_MONDO:1012728_MONDO:1012834,"junctional epidermolysis bullosa, LAMA3-related, dog",MONDO_grouped,disease,DISEASE_8550
8551,8551,8551,8551,8551,8551,8551,8551,MONDO:0009687,"myasthenia, congenital, refractory to acetylcholinesterase inhibitors",MONDO,disease,DISEASE_8551
8552,8552,8552,8552,8552,8552,8552,8552,MONDO:0012692,"renal tubular acidosis, distal, with nephrocalcinosis, short stature, intellectual disability, and distinctive facies",MONDO,disease,DISEASE_8552
8553,8553,8553,8553,8553,8553,8553,8553,MONDO:0008048_MONDO:0015705,autosomal dominant centronuclear myopathy,MONDO_grouped,disease,DISEASE_8553
8554,8554,8554,8554,8554,8554,8554,8554,MONDO:0023113,familial colorectal cancer,MONDO,disease,DISEASE_8554
8555,8555,8555,8555,8555,8555,8555,8555,MONDO:1011766,"warts between hooves, non-human animal",MONDO,disease,DISEASE_8555
8556,8556,8556,8556,8556,8556,8556,8556,MONDO:0017373,poliomyelitis,MONDO,disease,DISEASE_8556
8557,8557,8557,8557,8557,8557,8557,8557,MONDO:0060568,Pilarowski-Bjornsson syndrome,MONDO,disease,DISEASE_8557
8558,8558,8558,8558,8558,8558,8558,8558,MONDO:0005470,postprandial hypotension,MONDO,disease,DISEASE_8558
8559,8559,8559,8559,8559,8559,8559,8559,MONDO:0005680,Brill-Zinsser disease,MONDO,disease,DISEASE_8559
8560,8560,8560,8560,8560,8560,8560,8560,MONDO:1010583_MONDO:1010584_MONDO:1010587_MONDO:1010588_MONDO:1010589_MONDO:1010590,"familial goiter, chicken",MONDO_grouped,disease,DISEASE_8560
8561,8561,8561,8561,8561,8561,8561,8561,MONDO:0000227,African tick-bite fever,MONDO,disease,DISEASE_8561
8562,8562,8562,8562,8562,8562,8562,8562,MONDO:0017167,malignant epithelial tumor of salivary glands,MONDO,disease,DISEASE_8562
8563,8563,8563,8563,8563,8563,8563,8563,MONDO:0004937_MONDO:0006798,hypervitaminosis,MONDO_grouped,disease,DISEASE_8563
8564,8564,8564,8564,8564,8564,8564,8564,MONDO:0957426,autosomal recessive hyper-IgE syndrome,MONDO,disease,DISEASE_8564
8565,8565,8565,8565,8565,8565,8565,8565,MONDO:0019091,bronchopulmonary dysplasia,MONDO,disease,DISEASE_8565
8566,8566,8566,8566,8566,8566,8566,8566,MONDO:0023521,Judge Misch wright syndrome,MONDO,disease,DISEASE_8566
8567,8567,8567,8567,8567,8567,8567,8567,MONDO:0007833,"iris pigment layer, cleavage of",MONDO,disease,DISEASE_8567
8568,8568,8568,8568,8568,8568,8568,8568,MONDO:0032677_MONDO:0100472,lissencephaly 9 with complex brainstem malformation,MONDO_grouped,disease,DISEASE_8568
8569,8569,8569,8569,8569,8569,8569,8569,MONDO:0859000,SLC12A2-related developmental delay-intellectual disability-sensorineural deafness syndrome,MONDO,disease,DISEASE_8569
8570,8570,8570,8570,8570,8570,8570,8570,MONDO:0041656,ST-elevation myocardial infarction,MONDO,disease,DISEASE_8570
8571,8571,8571,8571,8571,8571,8571,8571,MONDO:0021078,glandular papilloma,MONDO,disease,DISEASE_8571
8572,8572,8572,8572,8572,8572,8572,8572,MONDO:0032809,"hepatitis, fulminant viral, susceptibility to",MONDO,disease,DISEASE_8572
8573,8573,8573,8573,8573,8573,8573,8573,MONDO:0019198,sympathetic ophthalmia,MONDO,disease,DISEASE_8573
8574,8574,8574,8574,8574,8574,8574,8574,MONDO:0012718,hypotonia with lactic acidemia and hyperammonemia,MONDO,disease,DISEASE_8574
8575,8575,8575,8575,8575,8575,8575,8575,MONDO:0006639_MONDO:0003924_MONDO:0021227_MONDO:0036591_MONDO:0002814_MONDO:0006076_MONDO:0004202_MONDO:0006075,adrenal cortex carcinoma,MONDO_grouped,disease,DISEASE_8575
8576,8576,8576,8576,8576,8576,8576,8576,MONDO:0859239,Chilton-Okur-Chung neurodevelopmental syndrome,MONDO,disease,DISEASE_8576
8577,8577,8577,8577,8577,8577,8577,8577,MONDO:0001563,vestibulocochlear nerve disorder,MONDO,disease,DISEASE_8577
8578,8578,8578,8578,8578,8578,8578,8578,MONDO:0009111,dihydropyrimidinuria,MONDO,disease,DISEASE_8578
8579,8579,8579,8579,8579,8579,8579,8579,MONDO:0043786,serositis,MONDO,disease,DISEASE_8579
8580,8580,8580,8580,8580,8580,8580,8580,MONDO:0004878,female breast upper-outer quadrant cancer,MONDO,disease,DISEASE_8580
8581,8581,8581,8581,8581,8581,8581,8581,MONDO:0030012,Diets-Jongmans syndrome,MONDO,disease,DISEASE_8581
8582,8582,8582,8582,8582,8582,8582,8582,MONDO:0006241,hepatic granuloma,MONDO,disease,DISEASE_8582
8583,8583,8583,8583,8583,8583,8583,8583,MONDO:1010630,"Chediak-Higashi syndrome, killer whale",MONDO,disease,DISEASE_8583
8584,8584,8584,8584,8584,8584,8584,8584,MONDO:1010968_MONDO:1010969_MONDO:1010970_MONDO:1010971_MONDO:1010972,"dysautonomia, dog",MONDO_grouped,disease,DISEASE_8584
8585,8585,8585,8585,8585,8585,8585,8585,MONDO:1012903,"Waardenburg syndrome, SOX10-related, pig",MONDO,disease,DISEASE_8585
8586,8586,8586,8586,8586,8586,8586,8586,MONDO:0005281_MONDO:0005411_MONDO:0012365_MONDO:0012366,gallbladder disorder,MONDO_grouped,disease,DISEASE_8586
8587,8587,8587,8587,8587,8587,8587,8587,MONDO:0011304_MONDO:0011305_MONDO:0859192_MONDO:0020724_MONDO:0000820,cerebral cavernous malformation,MONDO_grouped,disease,DISEASE_8587
8588,8588,8588,8588,8588,8588,8588,8588,MONDO:0010557,choroideremia,MONDO,disease,DISEASE_8588
8589,8589,8589,8589,8589,8589,8589,8589,MONDO:0008902,camptodactyly-ichthyosis syndrome,MONDO,disease,DISEASE_8589
8590,8590,8590,8590,8590,8590,8590,8590,MONDO:0010079,Canavan disease,MONDO,disease,DISEASE_8590
8591,8591,8591,8591,8591,8591,8591,8591,MONDO:0006381,plexiform ameloblastoma,MONDO,disease,DISEASE_8591
8592,8592,8592,8592,8592,8592,8592,8592,MONDO:0006559,hidradenitis suppurativa,MONDO,disease,DISEASE_8592
8593,8593,8593,8593,8593,8593,8593,8593,MONDO:0859224,intellectual disability and myopathy syndrome,MONDO,disease,DISEASE_8593
8594,8594,8594,8594,8594,8594,8594,8594,MONDO:0035737,acquired factor V deficiency,MONDO,disease,DISEASE_8594
8595,8595,8595,8595,8595,8595,8595,8595,MONDO:0020416,Neuhauser anomaly,MONDO,disease,DISEASE_8595
8596,8596,8596,8596,8596,8596,8596,8596,MONDO:0025377,African swine fever,MONDO,disease,DISEASE_8596
8597,8597,8597,8597,8597,8597,8597,8597,MONDO:0010013,schneckenbecken dysplasia,MONDO,disease,DISEASE_8597
8598,8598,8598,8598,8598,8598,8598,8598,MONDO:0019528,inflammatory pseudotumor of the liver,MONDO,disease,DISEASE_8598
8599,8599,8599,8599,8599,8599,8599,8599,MONDO:1012361,"yellow-semen syndrome, turkey",MONDO,disease,DISEASE_8599
8600,8600,8600,8600,8600,8600,8600,8600,MONDO:0010866,infantile osteopetrosis with neuroaxonal dysplasia,MONDO,disease,DISEASE_8600
8601,8601,8601,8601,8601,8601,8601,8601,MONDO:0014186,retinitis pigmentosa with or without situs inversus,MONDO,disease,DISEASE_8601
8602,8602,8602,8602,8602,8602,8602,8602,MONDO:1012251,"congenital lethal spasms, cattle",MONDO,disease,DISEASE_8602
8603,8603,8603,8603,8603,8603,8603,8603,MONDO:0007074,ainhum,MONDO,disease,DISEASE_8603
8604,8604,8604,8604,8604,8604,8604,8604,MONDO:0016709,anaplastic/large cell medulloblastoma,MONDO,disease,DISEASE_8604
8605,8605,8605,8605,8605,8605,8605,8605,MONDO:0002154,trichomoniasis,MONDO,disease,DISEASE_8605
8606,8606,8606,8606,8606,8606,8606,8606,MONDO:0008639,vascular helix of umbilical cord,MONDO,disease,DISEASE_8606
8607,8607,8607,8607,8607,8607,8607,8607,MONDO:0020735_MONDO:0014416,ACTH-independent macronodular adrenal hyperplasia,MONDO_grouped,disease,DISEASE_8607
8608,8608,8608,8608,8608,8608,8608,8608,MONDO:0020667,Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis,MONDO,disease,DISEASE_8608
8609,8609,8609,8609,8609,8609,8609,8609,MONDO:1012518,"immune-mediated myositis, horse",MONDO,disease,DISEASE_8609
8610,8610,8610,8610,8610,8610,8610,8610,MONDO:0005165,benign neoplasm,MONDO,disease,DISEASE_8610
8611,8611,8611,8611,8611,8611,8611,8611,MONDO:0019453,myelodysplastic syndrome with multilineage dysplasia,MONDO,disease,DISEASE_8611
8612,8612,8612,8612,8612,8612,8612,8612,MONDO:0009481,Jumping Frenchmen of Maine,MONDO,disease,DISEASE_8612
8613,8613,8613,8613,8613,8613,8613,8613,MONDO:0023290,grix Blankenship Peterson syndrome,MONDO,disease,DISEASE_8613
8614,8614,8614,8614,8614,8614,8614,8614,MONDO:0012757,"lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome",MONDO,disease,DISEASE_8614
8615,8615,8615,8615,8615,8615,8615,8615,MONDO:1012558,"anal gland disease, dog",MONDO,disease,DISEASE_8615
8616,8616,8616,8616,8616,8616,8616,8616,MONDO:0009696_MONDO:0100577,juvenile myoclonic epilepsy,MONDO_grouped,disease,DISEASE_8616
8617,8617,8617,8617,8617,8617,8617,8617,MONDO:0016071,juvenile hyaline fibromatosis,MONDO,disease,DISEASE_8617
8618,8618,8618,8618,8618,8618,8618,8618,MONDO:0016783,maternal 14q32.2 hypermethylation syndrome,MONDO,disease,DISEASE_8618
8619,8619,8619,8619,8619,8619,8619,8619,MONDO:0020722,nephrolithiasis susceptibility caused by SLC26A1,MONDO,disease,DISEASE_8619
8620,8620,8620,8620,8620,8620,8620,8620,MONDO:0020576,cutaneous vasculitis,MONDO,disease,DISEASE_8620
8621,8621,8621,8621,8621,8621,8621,8621,MONDO:0010801,spondylocamptodactyly syndrome,MONDO,disease,DISEASE_8621
8622,8622,8622,8622,8622,8622,8622,8622,MONDO:0002951,skin adenoid basal cell carcinoma,MONDO,disease,DISEASE_8622
8623,8623,8623,8623,8623,8623,8623,8623,MONDO:0100583,Jeune syndrome - GRK2-related,MONDO,disease,DISEASE_8623
8624,8624,8624,8624,8624,8624,8624,8624,MONDO:0958236_MONDO:0014654_MONDO:0009681_MONDO:0958235_MONDO:0000355,Ullrich congenital muscular dystrophy,MONDO_grouped,disease,DISEASE_8624
8625,8625,8625,8625,8625,8625,8625,8625,MONDO:0001304,benign hypertensive renal disease,MONDO,disease,DISEASE_8625
8626,8626,8626,8626,8626,8626,8626,8626,MONDO:0014755,"skin creases, congenital symmetric circumferential, 2",MONDO,disease,DISEASE_8626
8627,8627,8627,8627,8627,8627,8627,8627,MONDO:0024574,von Willebrand disease (hereditary or acquired),MONDO,disease,DISEASE_8627
8628,8628,8628,8628,8628,8628,8628,8628,MONDO:0003056,lymphoplasmacyte-rich meningioma,MONDO,disease,DISEASE_8628
8629,8629,8629,8629,8629,8629,8629,8629,MONDO:0859365,"neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures",MONDO,disease,DISEASE_8629
8630,8630,8630,8630,8630,8630,8630,8630,MONDO:0100478,brain malformations with or without urinary tract defects,MONDO,disease,DISEASE_8630
8631,8631,8631,8631,8631,8631,8631,8631,MONDO:0010912,"fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement",MONDO,disease,DISEASE_8631
8632,8632,8632,8632,8632,8632,8632,8632,MONDO:0019629,sclerocornea,MONDO,disease,DISEASE_8632
8633,8633,8633,8633,8633,8633,8633,8633,MONDO:0010310,osteopathia striata with cranial sclerosis,MONDO,disease,DISEASE_8633
8634,8634,8634,8634,8634,8634,8634,8634,MONDO:0021994,Berk-Tabatznik syndrome,MONDO,disease,DISEASE_8634
8635,8635,8635,8635,8635,8635,8635,8635,MONDO:0008895,hereditary arterial and articular multiple calcification syndrome,MONDO,disease,DISEASE_8635
8636,8636,8636,8636,8636,8636,8636,8636,MONDO:1010777,"atrichia with papular lesions, Rhesus monkey",MONDO,disease,DISEASE_8636
8637,8637,8637,8637,8637,8637,8637,8637,MONDO:0001731,benign vaginal mixed epithelial and mesenchymal neoplasm,MONDO,disease,DISEASE_8637
8638,8638,8638,8638,8638,8638,8638,8638,MONDO:0004349,retina lymphoma,MONDO,disease,DISEASE_8638
8639,8639,8639,8639,8639,8639,8639,8639,MONDO:0004548,adult type testicular granulosa cell tumor,MONDO,disease,DISEASE_8639
8640,8640,8640,8640,8640,8640,8640,8640,MONDO:0021090,lipid-rich breast carcinoma,MONDO,disease,DISEASE_8640
8641,8641,8641,8641,8641,8641,8641,8641,MONDO:0001250,keratomalacia,MONDO,disease,DISEASE_8641
8642,8642,8642,8642,8642,8642,8642,8642,MONDO:0003219,gastroesophageal junction adenocarcinoma,MONDO,disease,DISEASE_8642
8643,8643,8643,8643,8643,8643,8643,8643,MONDO:0016570,primary pulmonary lymphoma,MONDO,disease,DISEASE_8643
8644,8644,8644,8644,8644,8644,8644,8644,MONDO:0016892,partial deletion of the short arm of chromosome 10,MONDO,disease,DISEASE_8644
8645,8645,8645,8645,8645,8645,8645,8645,MONDO:1011205,"Van den Ende-Gupta syndrome, dog",MONDO,disease,DISEASE_8645
8646,8646,8646,8646,8646,8646,8646,8646,MONDO:0008732,"adrenal hypoplasia, cytomegalic type",MONDO,disease,DISEASE_8646
8647,8647,8647,8647,8647,8647,8647,8647,MONDO:0023098,extrasystoles short stature hyperpigmentation microcephaly,MONDO,disease,DISEASE_8647
8648,8648,8648,8648,8648,8648,8648,8648,MONDO:0021238,cornea neoplasm,MONDO,disease,DISEASE_8648
8649,8649,8649,8649,8649,8649,8649,8649,MONDO:0022461,anophthalmia cleft palate micrognathia,MONDO,disease,DISEASE_8649
8650,8650,8650,8650,8650,8650,8650,8650,MONDO:0008709_MONDO:0019796_MONDO:0000078,acrocephalopolydactyly,MONDO_grouped,disease,DISEASE_8650
8651,8651,8651,8651,8651,8651,8651,8651,MONDO:0009931,pulmonary atresia-intact ventricular septum syndrome,MONDO,disease,DISEASE_8651
8652,8652,8652,8652,8652,8652,8652,8652,MONDO:1010689,"AA amyloidosis, Sumatran tiger",MONDO,disease,DISEASE_8652
8653,8653,8653,8653,8653,8653,8653,8653,MONDO:0004241,Osgood-Schlatter disease,MONDO,disease,DISEASE_8653
8654,8654,8654,8654,8654,8654,8654,8654,MONDO:0000385,benign digestive system neoplasm,MONDO,disease,DISEASE_8654
8655,8655,8655,8655,8655,8655,8655,8655,MONDO:0003616,salpingitis isthmica nodosa,MONDO,disease,DISEASE_8655
8656,8656,8656,8656,8656,8656,8656,8656,MONDO:0017003,partial deletion of chromosome X,MONDO,disease,DISEASE_8656
8657,8657,8657,8657,8657,8657,8657,8657,MONDO:0010533,Arts syndrome,MONDO,disease,DISEASE_8657
8658,8658,8658,8658,8658,8658,8658,8658,MONDO:0021456,benign neoplasm of sternum,MONDO,disease,DISEASE_8658
8659,8659,8659,8659,8659,8659,8659,8659,MONDO:0015559,lymphoadenopathic mastocytosis with eosinophilia,MONDO,disease,DISEASE_8659
8660,8660,8660,8660,8660,8660,8660,8660,MONDO:0014722,Roifman syndrome,MONDO,disease,DISEASE_8660
8661,8661,8661,8661,8661,8661,8661,8661,MONDO:0018077,tularemia,MONDO,disease,DISEASE_8661
8662,8662,8662,8662,8662,8662,8662,8662,MONDO:0016848_MONDO:0008538,juvenile temporal arteritis,MONDO_grouped,disease,DISEASE_8662
8663,8663,8663,8663,8663,8663,8663,8663,MONDO:0014528,chronic atrial and intestinal dysrhythmia,MONDO,disease,DISEASE_8663
8664,8664,8664,8664,8664,8664,8664,8664,MONDO:0016653,2q33.1 microdeletion syndrome,MONDO,disease,DISEASE_8664
8665,8665,8665,8665,8665,8665,8665,8665,MONDO:0021253,gallbladder neoplasm,MONDO,disease,DISEASE_8665
8666,8666,8666,8666,8666,8666,8666,8666,MONDO:1010635,"factor X deficiency, domestic cat",MONDO,disease,DISEASE_8666
8667,8667,8667,8667,8667,8667,8667,8667,MONDO:0010139,isolated thyroid-stimulating hormone deficiency,MONDO,disease,DISEASE_8667
8668,8668,8668,8668,8668,8668,8668,8668,MONDO:0021656,nongerminomatous germ cell tumor,MONDO,disease,DISEASE_8668
8669,8669,8669,8669,8669,8669,8669,8669,MONDO:0019454,myelodysplastic syndrome with excess blasts,MONDO,disease,DISEASE_8669
8670,8670,8670,8670,8670,8670,8670,8670,MONDO:0100121,"SCN4A-related myopathy, autosomal recessive",MONDO,disease,DISEASE_8670
8671,8671,8671,8671,8671,8671,8671,8671,MONDO:0009343,"Hirschsprung disease with ulnar polydactyly, polysyndactyly of big toes, and ventricular septal defect",MONDO,disease,DISEASE_8671
8672,8672,8672,8672,8672,8672,8672,8672,MONDO:0001394,chronic erythremia,MONDO,disease,DISEASE_8672
8673,8673,8673,8673,8673,8673,8673,8673,MONDO:0019145,hereditary thrombophilia due to congenital protein C deficiency,MONDO,disease,DISEASE_8673
8674,8674,8674,8674,8674,8674,8674,8674,MONDO:0001380,bladder dome cancer,MONDO,disease,DISEASE_8674
8675,8675,8675,8675,8675,8675,8675,8675,MONDO:0018531,carcinoma of liver and intrahepatic biliary tract,MONDO,disease,DISEASE_8675
8676,8676,8676,8676,8676,8676,8676,8676,MONDO:0003985,chest wall lymphoma,MONDO,disease,DISEASE_8676
8677,8677,8677,8677,8677,8677,8677,8677,MONDO:0003829,chromophil adenoma of the kidney,MONDO,disease,DISEASE_8677
8678,8678,8678,8678,8678,8678,8678,8678,MONDO:0043197,ruvalcaba churesigaew myhre syndrome,MONDO,disease,DISEASE_8678
8679,8679,8679,8679,8679,8679,8679,8679,MONDO:0002207,vulval Paget disease,MONDO,disease,DISEASE_8679
8680,8680,8680,8680,8680,8680,8680,8680,MONDO:0851100,malignant olfactory nerve neoplasm,MONDO,disease,DISEASE_8680
8681,8681,8681,8681,8681,8681,8681,8681,MONDO:0015439,ring chromosome 4,MONDO,disease,DISEASE_8681
8682,8682,8682,8682,8682,8682,8682,8682,MONDO:0013688,linear and whorled nevoid hypermelanosis,MONDO,disease,DISEASE_8682
8683,8683,8683,8683,8683,8683,8683,8683,MONDO:0003758,childhood testicular germ cell tumor,MONDO,disease,DISEASE_8683
8684,8684,8684,8684,8684,8684,8684,8684,MONDO:0001060,microinvasive gastric cancer,MONDO,disease,DISEASE_8684
8685,8685,8685,8685,8685,8685,8685,8685,MONDO:0006383,"primary cutaneous diffuse large B-cell lymphoma, Leg type",MONDO,disease,DISEASE_8685
8686,8686,8686,8686,8686,8686,8686,8686,MONDO:0006278,lung papilloma,MONDO,disease,DISEASE_8686
8687,8687,8687,8687,8687,8687,8687,8687,MONDO:0011217,desmosterolosis,MONDO,disease,DISEASE_8687
8688,8688,8688,8688,8688,8688,8688,8688,MONDO:1010351_MONDO:1011985,"age-related macular degeneration, non-human animal",MONDO_grouped,disease,DISEASE_8688
8689,8689,8689,8689,8689,8689,8689,8689,MONDO:0020296_MONDO:0016078,congenital arteriovenous fistula,MONDO_grouped,disease,DISEASE_8689
8690,8690,8690,8690,8690,8690,8690,8690,MONDO:0030896,chromosome 13q33-q34 deletion syndrome,MONDO,disease,DISEASE_8690
8691,8691,8691,8691,8691,8691,8691,8691,MONDO:0002175,degeneration of macula and posterior pole,MONDO,disease,DISEASE_8691
8692,8692,8692,8692,8692,8692,8692,8692,MONDO:0000983,exhibitionism,MONDO,disease,DISEASE_8692
8693,8693,8693,8693,8693,8693,8693,8693,MONDO:0018781,KID syndrome,MONDO,disease,DISEASE_8693
8694,8694,8694,8694,8694,8694,8694,8694,MONDO:0020679,conductive hearing loss disorder,MONDO,disease,DISEASE_8694
8695,8695,8695,8695,8695,8695,8695,8695,MONDO:0016686,diffuse astrocytoma,MONDO,disease,DISEASE_8695
8696,8696,8696,8696,8696,8696,8696,8696,MONDO:0006777,hairy tongue,MONDO,disease,DISEASE_8696
8697,8697,8697,8697,8697,8697,8697,8697,MONDO:0017619,congenital sucrase-isomaltase deficiency with minimal starch tolerance,MONDO,disease,DISEASE_8697
8698,8698,8698,8698,8698,8698,8698,8698,MONDO:0010744,thrombocytopenia with elevated serum IgA and renal disease,MONDO,disease,DISEASE_8698
8699,8699,8699,8699,8699,8699,8699,8699,MONDO:0021289,carcinoma in situ of cecum,MONDO,disease,DISEASE_8699
8700,8700,8700,8700,8700,8700,8700,8700,MONDO:0035763,idiopathic non-lupus full-house nephropathy,MONDO,disease,DISEASE_8700
8701,8701,8701,8701,8701,8701,8701,8701,MONDO:0004598,acute cor pulmonale,MONDO,disease,DISEASE_8701
8702,8702,8702,8702,8702,8702,8702,8702,MONDO:0009035_MONDO:0021021_MONDO:0007397_MONDO:0044206,"craniometaphyseal dysplasia, autosomal recessive",MONDO_grouped,disease,DISEASE_8702
8703,8703,8703,8703,8703,8703,8703,8703,MONDO:0020172,palpebral epidermal tumor,MONDO,disease,DISEASE_8703
8704,8704,8704,8704,8704,8704,8704,8704,MONDO:1012303,"masticatory muscle myositis, dog",MONDO,disease,DISEASE_8704
8705,8705,8705,8705,8705,8705,8705,8705,MONDO:0018376_MONDO:0018375,secondary non-traumatic avascular necrosis,MONDO_grouped,disease,DISEASE_8705
8706,8706,8706,8706,8706,8706,8706,8706,MONDO:0005834,lymphogranuloma venereum,MONDO,disease,DISEASE_8706
8707,8707,8707,8707,8707,8707,8707,8707,MONDO:0004517,ureter tuberculosis,MONDO,disease,DISEASE_8707
8708,8708,8708,8708,8708,8708,8708,8708,MONDO:0006389_MONDO:0002574_MONDO:0003033,prostate rhabdomyosarcoma,MONDO_grouped,disease,DISEASE_8708
8709,8709,8709,8709,8709,8709,8709,8709,MONDO:0002898,skin cancer,MONDO,disease,DISEASE_8709
8710,8710,8710,8710,8710,8710,8710,8710,MONDO:1011648,"familial thoracic aortic aneurysm, non-human animal",MONDO,disease,DISEASE_8710
8711,8711,8711,8711,8711,8711,8711,8711,MONDO:0008728,classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency,MONDO,disease,DISEASE_8711
8712,8712,8712,8712,8712,8712,8712,8712,MONDO:0024315,parasitic endophthalmitis,MONDO,disease,DISEASE_8712
8713,8713,8713,8713,8713,8713,8713,8713,MONDO:1011342,"otorhinolaryngologic disease, non-human animal",MONDO,disease,DISEASE_8713
8714,8714,8714,8714,8714,8714,8714,8714,MONDO:0001049,Dressler syndrome,MONDO,disease,DISEASE_8714
8715,8715,8715,8715,8715,8715,8715,8715,MONDO:0005706_MONDO:0005894,coccidioidomycosis,MONDO_grouped,disease,DISEASE_8715
8716,8716,8716,8716,8716,8716,8716,8716,MONDO:0859277,intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects,MONDO,disease,DISEASE_8716
8717,8717,8717,8717,8717,8717,8717,8717,MONDO:0000757,glucocorticoid-induced osteoporosis,MONDO,disease,DISEASE_8717
8718,8718,8718,8718,8718,8718,8718,8718,MONDO:1040014,PPFIA3-related neurodevelopmental disorder,MONDO,disease,DISEASE_8718
8719,8719,8719,8719,8719,8719,8719,8719,MONDO:1011742,"congenital erythropoietic porphyria, non-human animal",MONDO,disease,DISEASE_8719
8720,8720,8720,8720,8720,8720,8720,8720,MONDO:0008036,"myasthenia, limb-girdle, autoimmune",MONDO,disease,DISEASE_8720
8721,8721,8721,8721,8721,8721,8721,8721,MONDO:1012092,"gastric dilatation volvulus syndrome, lesser panda",MONDO,disease,DISEASE_8721
8722,8722,8722,8722,8722,8722,8722,8722,MONDO:0022779,cleft lip palate oligodontia syndactyly pili torti,MONDO,disease,DISEASE_8722
8723,8723,8723,8723,8723,8723,8723,8723,MONDO:0014766,leukodystrophy and acquired microcephaly with or without dystonia;,MONDO,disease,DISEASE_8723
8724,8724,8724,8724,8724,8724,8724,8724,MONDO:0001990,malignant cardiac peripheral nerve sheath neoplasm,MONDO,disease,DISEASE_8724
8725,8725,8725,8725,8725,8725,8725,8725,MONDO:0018988,iridocorneal endothelial syndrome,MONDO,disease,DISEASE_8725
8726,8726,8726,8726,8726,8726,8726,8726,MONDO:0002075,spontaneous tension pneumothorax,MONDO,disease,DISEASE_8726
8727,8727,8727,8727,8727,8727,8727,8727,MONDO:0004554,childhood kidney angiomyolipoma,MONDO,disease,DISEASE_8727
8728,8728,8728,8728,8728,8728,8728,8728,MONDO:0006936,pulmonary valve stenosis,MONDO,disease,DISEASE_8728
8729,8729,8729,8729,8729,8729,8729,8729,MONDO:0005099,subarachnoid hemorrhage,MONDO,disease,DISEASE_8729
8730,8730,8730,8730,8730,8730,8730,8730,MONDO:0000949_MONDO:0001174,conjunctival degeneration,MONDO_grouped,disease,DISEASE_8730
8731,8731,8731,8731,8731,8731,8731,8731,MONDO:0013225_MONDO:0012923_MONDO:0012071_MONDO:0958023_MONDO:0010020_MONDO:0006536,congenital generalized lipodystrophy,MONDO_grouped,disease,DISEASE_8731
8732,8732,8732,8732,8732,8732,8732,8732,MONDO:1010983,"hydrocephalus, yellow-crowned parrot",MONDO,disease,DISEASE_8732
8733,8733,8733,8733,8733,8733,8733,8733,MONDO:0015349,progressive cavitating leukoencephalopathy,MONDO,disease,DISEASE_8733
8734,8734,8734,8734,8734,8734,8734,8734,MONDO:0022804,colobomata unilobar lung heart defect,MONDO,disease,DISEASE_8734
8735,8735,8735,8735,8735,8735,8735,8735,MONDO:0019871,distal trisomy 2p,MONDO,disease,DISEASE_8735
8736,8736,8736,8736,8736,8736,8736,8736,MONDO:0800412,yakut short stature syndrome,MONDO,disease,DISEASE_8736
8737,8737,8737,8737,8737,8737,8737,8737,MONDO:0015699,immunodeficiency due to a classical component pathway complement deficiency,MONDO,disease,DISEASE_8737
8738,8738,8738,8738,8738,8738,8738,8738,MONDO:1012894,"tuberous sclerosis, TSC1-related, pig",MONDO,disease,DISEASE_8738
8739,8739,8739,8739,8739,8739,8739,8739,MONDO:0017769,acquired immunodeficiency,MONDO,disease,DISEASE_8739
8740,8740,8740,8740,8740,8740,8740,8740,MONDO:0014224,developmental delay with autism spectrum disorder and gait instability,MONDO,disease,DISEASE_8740
8741,8741,8741,8741,8741,8741,8741,8741,MONDO:0010850_MONDO:0015416_MONDO:0015417,Tessier number 4 facial cleft,MONDO_grouped,disease,DISEASE_8741
8742,8742,8742,8742,8742,8742,8742,8742,MONDO:0001737,tetanus neonatorum,MONDO,disease,DISEASE_8742
8743,8743,8743,8743,8743,8743,8743,8743,MONDO:0006093,ascending colon neuroendocrine tumor G1,MONDO,disease,DISEASE_8743
8744,8744,8744,8744,8744,8744,8744,8744,MONDO:0007250,camptodactyly of fingers,MONDO,disease,DISEASE_8744
8745,8745,8745,8745,8745,8745,8745,8745,MONDO:0005260,autism,MONDO,disease,DISEASE_8745
8746,8746,8746,8746,8746,8746,8746,8746,MONDO:0010762,"lymphoma, Hodgkin, Y-linked pseudoautosomal",MONDO,disease,DISEASE_8746
8747,8747,8747,8747,8747,8747,8747,8747,MONDO:0017009,partial duplication of the short arm of chromosome X,MONDO,disease,DISEASE_8747
8748,8748,8748,8748,8748,8748,8748,8748,MONDO:0005483,chemotherapy-induced alopecia,MONDO,disease,DISEASE_8748
8749,8749,8749,8749,8749,8749,8749,8749,MONDO:0002468,hyperimmunoglobulin syndrome,MONDO,disease,DISEASE_8749
8750,8750,8750,8750,8750,8750,8750,8750,MONDO:0010594,obsolete inherited genitourinary tract anomalies,MONDO,disease,DISEASE_8750
8751,8751,8751,8751,8751,8751,8751,8751,MONDO:0013224_MONDO:0012252,rhabdoid tumor predisposition syndrome,MONDO_grouped,disease,DISEASE_8751
8752,8752,8752,8752,8752,8752,8752,8752,MONDO:0017490_MONDO:0017491,"tibial hemimelia, unilateral",MONDO_grouped,disease,DISEASE_8752
8753,8753,8753,8753,8753,8753,8753,8753,MONDO:0700194,chicken lymphoma,MONDO,disease,DISEASE_8753
8754,8754,8754,8754,8754,8754,8754,8754,MONDO:0019737,thrombotic microangiopathy,MONDO,disease,DISEASE_8754
8755,8755,8755,8755,8755,8755,8755,8755,MONDO:0019494,primary pediatric heart tumor,MONDO,disease,DISEASE_8755
8756,8756,8756,8756,8756,8756,8756,8756,MONDO:1012492,"neurodegenerative vacuolar storage disease, dog",MONDO,disease,DISEASE_8756
8757,8757,8757,8757,8757,8757,8757,8757,MONDO:0002513,kidney benign neoplasm,MONDO,disease,DISEASE_8757
8758,8758,8758,8758,8758,8758,8758,8758,MONDO:0010646,"macular dystrophy, X-linked",MONDO,disease,DISEASE_8758
8759,8759,8759,8759,8759,8759,8759,8759,MONDO:0032833,"lower urinary tract obstruction, congenital",MONDO,disease,DISEASE_8759
8760,8760,8760,8760,8760,8760,8760,8760,MONDO:1010736,"leukocyte adhesion deficiency, FERMT3-related, dog",MONDO,disease,DISEASE_8760
8761,8761,8761,8761,8761,8761,8761,8761,MONDO:0004163,bladder urachal urothelial carcinoma,MONDO,disease,DISEASE_8761
8762,8762,8762,8762,8762,8762,8762,8762,MONDO:0005434,skin sensitivity to sun,MONDO,disease,DISEASE_8762
8763,8763,8763,8763,8763,8763,8763,8763,MONDO:0011079,"rhizomelic dysplasia, Patterson-Lowry type",MONDO,disease,DISEASE_8763
8764,8764,8764,8764,8764,8764,8764,8764,MONDO:0018709,X-linked intellectual disability-hypotonia-movement disorder syndrome,MONDO,disease,DISEASE_8764
8765,8765,8765,8765,8765,8765,8765,8765,MONDO:0010651,Menkes disease,MONDO,disease,DISEASE_8765
8766,8766,8766,8766,8766,8766,8766,8766,MONDO:0016128_MONDO:0016126_MONDO:0016130,parasitic myositis,MONDO_grouped,disease,DISEASE_8766
8767,8767,8767,8767,8767,8767,8767,8767,MONDO:0024523_MONDO:0013902_MONDO:0032783,aortic valve disease,MONDO_grouped,disease,DISEASE_8767
8768,8768,8768,8768,8768,8768,8768,8768,MONDO:0859302,hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2,MONDO,disease,DISEASE_8768
8769,8769,8769,8769,8769,8769,8769,8769,MONDO:0000683,topographical agnosia,MONDO,disease,DISEASE_8769
8770,8770,8770,8770,8770,8770,8770,8770,MONDO:0020569,intermediate DEND syndrome,MONDO,disease,DISEASE_8770
8771,8771,8771,8771,8771,8771,8771,8771,MONDO:0033564_MONDO:0021575_MONDO:0859521_MONDO:0030523_MONDO:0030490_MONDO:0021573_MONDO:0032810_MONDO:0032696_MONDO:0021574_MONDO:0859330_MONDO:0030925_MONDO:0020837_MONDO:0033565_MONDO:0014769,oocyte maturation defect,MONDO_grouped,disease,DISEASE_8771
8772,8772,8772,8772,8772,8772,8772,8772,MONDO:0009493,Richards-Rundle syndrome,MONDO,disease,DISEASE_8772
8773,8773,8773,8773,8773,8773,8773,8773,MONDO:0035400,seronegative autoimmune hepatitis,MONDO,disease,DISEASE_8773
8774,8774,8774,8774,8774,8774,8774,8774,MONDO:0002008_MONDO:0002006,labyrinthitis,MONDO_grouped,disease,DISEASE_8774
8775,8775,8775,8775,8775,8775,8775,8775,MONDO:0700264,type 1 interferonopathy,MONDO,disease,DISEASE_8775
8776,8776,8776,8776,8776,8776,8776,8776,MONDO:0018333,"multiple acyl-CoA dehydrogenase deficiency, mild type",MONDO,disease,DISEASE_8776
8777,8777,8777,8777,8777,8777,8777,8777,MONDO:1010195_MONDO:1010010_MONDO:1011791,"myopathy, non-human animal",MONDO_grouped,disease,DISEASE_8777
8778,8778,8778,8778,8778,8778,8778,8778,MONDO:0006740,empty sella syndrome,MONDO,disease,DISEASE_8778
8779,8779,8779,8779,8779,8779,8779,8779,MONDO:0022349,congenital absence of septum pellucidum,MONDO,disease,DISEASE_8779
8780,8780,8780,8780,8780,8780,8780,8780,MONDO:0002748,rectum mucinous adenocarcinoma,MONDO,disease,DISEASE_8780
8781,8781,8781,8781,8781,8781,8781,8781,MONDO:0044629,congenital amyoplasia,MONDO,disease,DISEASE_8781
8782,8782,8782,8782,8782,8782,8782,8782,MONDO:0007886_MONDO:0001845_MONDO:0001846,uterine corpus leiomyoma,MONDO_grouped,disease,DISEASE_8782
8783,8783,8783,8783,8783,8783,8783,8783,MONDO:1010128,peritonitis,MONDO,disease,DISEASE_8783
8784,8784,8784,8784,8784,8784,8784,8784,MONDO:0005193,prostate intraepithelial neoplasia,MONDO,disease,DISEASE_8784
8785,8785,8785,8785,8785,8785,8785,8785,MONDO:0007075_MONDO:0011105,"alacrima, congenital, autosomal dominant",MONDO_grouped,disease,DISEASE_8785
8786,8786,8786,8786,8786,8786,8786,8786,MONDO:0041284_MONDO:0006891,primary motor cortex epilepsy,MONDO_grouped,disease,DISEASE_8786
8787,8787,8787,8787,8787,8787,8787,8787,MONDO:0009132,dysautonomia-like disorder,MONDO,disease,DISEASE_8787
8788,8788,8788,8788,8788,8788,8788,8788,MONDO:1030006,Happle-Tinschert syndrome,MONDO,disease,DISEASE_8788
8789,8789,8789,8789,8789,8789,8789,8789,MONDO:0011538,frontoocular syndrome,MONDO,disease,DISEASE_8789
8790,8790,8790,8790,8790,8790,8790,8790,MONDO:0012475,cone dystrophy with supernormal rod response,MONDO,disease,DISEASE_8790
8791,8791,8791,8791,8791,8791,8791,8791,MONDO:0008640_MONDO:0012352,"vasculitis, lymphocytic, nodular",MONDO_grouped,disease,DISEASE_8791
8792,8792,8792,8792,8792,8792,8792,8792,MONDO:0011788,cloverleaf skull-multiple congenital anomalies syndrome,MONDO,disease,DISEASE_8792
8793,8793,8793,8793,8793,8793,8793,8793,MONDO:0002354,benign laryngeal neoplasm,MONDO,disease,DISEASE_8793
8794,8794,8794,8794,8794,8794,8794,8794,MONDO:0020778_MONDO:0020780_MONDO:0014980,cone-rod dystrophy and hearing loss,MONDO_grouped,disease,DISEASE_8794
8795,8795,8795,8795,8795,8795,8795,8795,MONDO:0021203_MONDO:0001234,serous otitis media,MONDO_grouped,disease,DISEASE_8795
8796,8796,8796,8796,8796,8796,8796,8796,MONDO:0008385,rhiny,MONDO,disease,DISEASE_8796
8797,8797,8797,8797,8797,8797,8797,8797,MONDO:0970944,"Leigh syndrome, mitochondrial",MONDO,disease,DISEASE_8797
8798,8798,8798,8798,8798,8798,8798,8798,MONDO:0044275,obsolete carotid intimal medial thickness 1,MONDO,disease,DISEASE_8798
8799,8799,8799,8799,8799,8799,8799,8799,MONDO:0008337,familial pterygium of the conjunctiva,MONDO,disease,DISEASE_8799
8800,8800,8800,8800,8800,8800,8800,8800,MONDO:0003396,epulis,MONDO,disease,DISEASE_8800
8801,8801,8801,8801,8801,8801,8801,8801,MONDO:0006814,iritis,MONDO,disease,DISEASE_8801
8802,8802,8802,8802,8802,8802,8802,8802,MONDO:0020814,miliaria alba,MONDO,disease,DISEASE_8802
8803,8803,8803,8803,8803,8803,8803,8803,MONDO:0002355,glottis carcinoma,MONDO,disease,DISEASE_8803
8804,8804,8804,8804,8804,8804,8804,8804,MONDO:0035472_MONDO:0035499,GJC2-related late-onset primary lymphedema,MONDO_grouped,disease,DISEASE_8804
8805,8805,8805,8805,8805,8805,8805,8805,MONDO:0009017,"corneal degeneration, band-shaped spheroid",MONDO,disease,DISEASE_8805
8806,8806,8806,8806,8806,8806,8806,8806,MONDO:1010466,"patent ductus arteriosus, domestic cat",MONDO,disease,DISEASE_8806
8807,8807,8807,8807,8807,8807,8807,8807,MONDO:0016982_MONDO:0002387_MONDO:0002617_MONDO:0003025_MONDO:0003029,angiosarcoma,MONDO_grouped,disease,DISEASE_8807
8808,8808,8808,8808,8808,8808,8808,8808,MONDO:0011557,"radiation sensitivity/chromosome instability syndrome, autosomal dominant",MONDO,disease,DISEASE_8808
8809,8809,8809,8809,8809,8809,8809,8809,MONDO:0043141,microdontia hypodontia short stature,MONDO,disease,DISEASE_8809
8810,8810,8810,8810,8810,8810,8810,8810,MONDO:0012675,corticosteroid-binding globulin deficiency,MONDO,disease,DISEASE_8810
8811,8811,8811,8811,8811,8811,8811,8811,MONDO:0012802,oculoauricular syndrome,MONDO,disease,DISEASE_8811
8812,8812,8812,8812,8812,8812,8812,8812,MONDO:0008841,ataxia-telangiectasia with generalized skin pigmentation and early death,MONDO,disease,DISEASE_8812
8813,8813,8813,8813,8813,8813,8813,8813,MONDO:0010093,syndesmodysplasic dwarfism,MONDO,disease,DISEASE_8813
8814,8814,8814,8814,8814,8814,8814,8814,MONDO:0001700_MONDO:0015909,megaloblastic anemia,MONDO_grouped,disease,DISEASE_8814
8815,8815,8815,8815,8815,8815,8815,8815,MONDO:0040566,inherited glutathione metabolism disease,MONDO,disease,DISEASE_8815
8816,8816,8816,8816,8816,8816,8816,8816,MONDO:0002935,penis basal cell carcinoma,MONDO,disease,DISEASE_8816
8817,8817,8817,8817,8817,8817,8817,8817,MONDO:1011824,"horn cancer, non-human animal",MONDO,disease,DISEASE_8817
8818,8818,8818,8818,8818,8818,8818,8818,MONDO:0002033,cecum cancer,MONDO,disease,DISEASE_8818
8819,8819,8819,8819,8819,8819,8819,8819,MONDO:0002782,cranial nerve palsy,MONDO,disease,DISEASE_8819
8820,8820,8820,8820,8820,8820,8820,8820,MONDO:0021100,breast neoplasm,MONDO,disease,DISEASE_8820
8821,8821,8821,8821,8821,8821,8821,8821,MONDO:0009761_MONDO:1010963,cystic hygroma,MONDO_grouped,disease,DISEASE_8821
8822,8822,8822,8822,8822,8822,8822,8822,MONDO:0017948,ABetaA21G amyloidosis,MONDO,disease,DISEASE_8822
8823,8823,8823,8823,8823,8823,8823,8823,MONDO:0010851,Lowry-MacLean syndrome,MONDO,disease,DISEASE_8823
8824,8824,8824,8824,8824,8824,8824,8824,MONDO:0015538,indeterminate dendritic cell tumor,MONDO,disease,DISEASE_8824
8825,8825,8825,8825,8825,8825,8825,8825,MONDO:0006298,mediastinal malignant germ cell tumor,MONDO,disease,DISEASE_8825
8826,8826,8826,8826,8826,8826,8826,8826,MONDO:1012586,"oculocutaneous albinism, TYR-related, Japanese ratsnake",MONDO,disease,DISEASE_8826
8827,8827,8827,8827,8827,8827,8827,8827,MONDO:1012174,"myasthenia, Amur tiger",MONDO,disease,DISEASE_8827
8828,8828,8828,8828,8828,8828,8828,8828,MONDO:0016022,early myoclonic encephalopathy,MONDO,disease,DISEASE_8828
8829,8829,8829,8829,8829,8829,8829,8829,MONDO:0019259_MONDO:0016366_MONDO:0019258,classic phenylketonuria,MONDO_grouped,disease,DISEASE_8829
8830,8830,8830,8830,8830,8830,8830,8830,MONDO:0015496,macroglossia,MONDO,disease,DISEASE_8830
8831,8831,8831,8831,8831,8831,8831,8831,MONDO:0958329,Jeffries-Lakhani neurodevelopmental syndrome,MONDO,disease,DISEASE_8831
8832,8832,8832,8832,8832,8832,8832,8832,MONDO:0021739,prurigo,MONDO,disease,DISEASE_8832
8833,8833,8833,8833,8833,8833,8833,8833,MONDO:0014418_MONDO:0009709,"myopathy, centronuclear",MONDO_grouped,disease,DISEASE_8833
8834,8834,8834,8834,8834,8834,8834,8834,MONDO:0100401_MONDO:0100402,"acute myeloid leukemia, del(5q31-q32)",MONDO_grouped,disease,DISEASE_8834
8835,8835,8835,8835,8835,8835,8835,8835,MONDO:0004401,testis refractory cancer,MONDO,disease,DISEASE_8835
8836,8836,8836,8836,8836,8836,8836,8836,MONDO:0017859,colchicine poisoning,MONDO,disease,DISEASE_8836
8837,8837,8837,8837,8837,8837,8837,8837,MONDO:0010126,thymic aplasia with fetal death,MONDO,disease,DISEASE_8837
8838,8838,8838,8838,8838,8838,8838,8838,MONDO:0008939,isolated cerebellar hypoplasia/agenesis,MONDO,disease,DISEASE_8838
8839,8839,8839,8839,8839,8839,8839,8839,MONDO:0008483_MONDO:0012232_MONDO:0013841_MONDO:0013844,"stuttering, familial persistent",MONDO_grouped,disease,DISEASE_8839
8840,8840,8840,8840,8840,8840,8840,8840,MONDO:0020374,cerulean cataract,MONDO,disease,DISEASE_8840
8841,8841,8841,8841,8841,8841,8841,8841,MONDO:0018103,Quinquaud's folliculitis decalvans,MONDO,disease,DISEASE_8841
8842,8842,8842,8842,8842,8842,8842,8842,MONDO:0001041,dentin caries,MONDO,disease,DISEASE_8842
8843,8843,8843,8843,8843,8843,8843,8843,MONDO:0009217,Fanconi-like syndrome,MONDO,disease,DISEASE_8843
8844,8844,8844,8844,8844,8844,8844,8844,MONDO:0012750,lethal arthrogryposis-anterior horn cell disease syndrome,MONDO,disease,DISEASE_8844
8845,8845,8845,8845,8845,8845,8845,8845,MONDO:0004758,scotoma,MONDO,disease,DISEASE_8845
8846,8846,8846,8846,8846,8846,8846,8846,MONDO:0015067,"neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor",MONDO,disease,DISEASE_8846
8847,8847,8847,8847,8847,8847,8847,8847,MONDO:0017178,osteochondritis dissecans,MONDO,disease,DISEASE_8847
8848,8848,8848,8848,8848,8848,8848,8848,MONDO:1010899_MONDO:1011569,"neuronal ceroid lipofuscinosis, Japanese macaque",MONDO_grouped,disease,DISEASE_8848
8849,8849,8849,8849,8849,8849,8849,8849,MONDO:0859307_MONDO:0007340,cleidocranial dysplasia,MONDO_grouped,disease,DISEASE_8849
8850,8850,8850,8850,8850,8850,8850,8850,MONDO:1010718,"dihydropyrimidinase deficiency, domestic cat",MONDO,disease,DISEASE_8850
8851,8851,8851,8851,8851,8851,8851,8851,MONDO:1011140,"choanal atresia, domestic cat",MONDO,disease,DISEASE_8851
8852,8852,8852,8852,8852,8852,8852,8852,MONDO:0004810,acute ethmoiditis,MONDO,disease,DISEASE_8852
8853,8853,8853,8853,8853,8853,8853,8853,MONDO:0013488,"lipodystrophy, partial, acquired, with low complement component c3, with or without glomerulonephritis",MONDO,disease,DISEASE_8853
8854,8854,8854,8854,8854,8854,8854,8854,MONDO:0008477_MONDO:0018255,"spondylometaphyseal dysplasia, Kozlowski type",MONDO_grouped,disease,DISEASE_8854
8855,8855,8855,8855,8855,8855,8855,8855,MONDO:0017770,Robinow-like syndrome,MONDO,disease,DISEASE_8855
8856,8856,8856,8856,8856,8856,8856,8856,MONDO:0004544,chordoid meningioma,MONDO,disease,DISEASE_8856
8857,8857,8857,8857,8857,8857,8857,8857,MONDO:0016800,mitochondrial membrane transport disorder,MONDO,disease,DISEASE_8857
8858,8858,8858,8858,8858,8858,8858,8858,MONDO:0004969,acute quadriplegic myopathy,MONDO,disease,DISEASE_8858
8859,8859,8859,8859,8859,8859,8859,8859,MONDO:0700229,MAK-related retinopathy,MONDO,disease,DISEASE_8859
8860,8860,8860,8860,8860,8860,8860,8860,MONDO:0007214,brachydactyly-preaxial hallux varus syndrome,MONDO,disease,DISEASE_8860
8861,8861,8861,8861,8861,8861,8861,8861,MONDO:0016421,toxic oil syndrome,MONDO,disease,DISEASE_8861
8862,8862,8862,8862,8862,8862,8862,8862,MONDO:1012831,"progressive retinal atrophy, Miniature Schnauzer, dog",MONDO,disease,DISEASE_8862
8863,8863,8863,8863,8863,8863,8863,8863,MONDO:1011672,"hydrallantois, non-human animal",MONDO,disease,DISEASE_8863
8864,8864,8864,8864,8864,8864,8864,8864,MONDO:0019357,congenital narrowing of cervical spinal canal,MONDO,disease,DISEASE_8864
8865,8865,8865,8865,8865,8865,8865,8865,MONDO:0018599,congenital oculomotor nerve palsy,MONDO,disease,DISEASE_8865
8866,8866,8866,8866,8866,8866,8866,8866,MONDO:0005322,ulna fracture,MONDO,disease,DISEASE_8866
8867,8867,8867,8867,8867,8867,8867,8867,MONDO:0000298,dioctophymiasis,MONDO,disease,DISEASE_8867
8868,8868,8868,8868,8868,8868,8868,8868,MONDO:1011517,"glaucoma, Rhesus monkey",MONDO,disease,DISEASE_8868
8869,8869,8869,8869,8869,8869,8869,8869,MONDO:0859190,neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities,MONDO,disease,DISEASE_8869
8870,8870,8870,8870,8870,8870,8870,8870,MONDO:0016851,maternal uniparental disomy of chromosome X,MONDO,disease,DISEASE_8870
8871,8871,8871,8871,8871,8871,8871,8871,MONDO:1010013,"cor triatriatum dexter, non-human animal",MONDO,disease,DISEASE_8871
8872,8872,8872,8872,8872,8872,8872,8872,MONDO:0000514,bone squamous cell carcinoma,MONDO,disease,DISEASE_8872
8873,8873,8873,8873,8873,8873,8873,8873,MONDO:0001360,blind hypotensive eye,MONDO,disease,DISEASE_8873
8874,8874,8874,8874,8874,8874,8874,8874,MONDO:0031007,"spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosis",MONDO,disease,DISEASE_8874
8875,8875,8875,8875,8875,8875,8875,8875,MONDO:0021404,polyp of sphenoidal sinus,MONDO,disease,DISEASE_8875
8876,8876,8876,8876,8876,8876,8876,8876,MONDO:0001556_MONDO:0002127,urethral obstruction,MONDO_grouped,disease,DISEASE_8876
8877,8877,8877,8877,8877,8877,8877,8877,MONDO:0007973,mental and growth retardation with amblyopia,MONDO,disease,DISEASE_8877
8878,8878,8878,8878,8878,8878,8878,8878,MONDO:0019283,nail anomaly,MONDO,disease,DISEASE_8878
8879,8879,8879,8879,8879,8879,8879,8879,MONDO:0009362,growth delay-hydrocephaly-lung hypoplasia syndrome,MONDO,disease,DISEASE_8879
8880,8880,8880,8880,8880,8880,8880,8880,MONDO:0019618,Sheehan syndrome,MONDO,disease,DISEASE_8880
8881,8881,8881,8881,8881,8881,8881,8881,MONDO:0004736_MONDO:0019243_MONDO:0019189_MONDO:0019236_MONDO:0019232_MONDO:0019216_MONDO:0017355,inborn disorder of amino acid metabolism,MONDO_grouped,disease,DISEASE_8881
8882,8882,8882,8882,8882,8882,8882,8882,MONDO:0012833,Crouzon syndrome-acanthosis nigricans syndrome,MONDO,disease,DISEASE_8882
8883,8883,8883,8883,8883,8883,8883,8883,MONDO:0021523,benign neoplasm of pharynx,MONDO,disease,DISEASE_8883
8884,8884,8884,8884,8884,8884,8884,8884,MONDO:1010318,"GAPO syndrome, non-human animal",MONDO,disease,DISEASE_8884
8885,8885,8885,8885,8885,8885,8885,8885,MONDO:0001648,esophageal candidiasis,MONDO,disease,DISEASE_8885
8886,8886,8886,8886,8886,8886,8886,8886,MONDO:0015391,nasopharyngeal teratoma,MONDO,disease,DISEASE_8886
8887,8887,8887,8887,8887,8887,8887,8887,MONDO:1010033,"holoprosencephaly, non-human animal",MONDO,disease,DISEASE_8887
8888,8888,8888,8888,8888,8888,8888,8888,MONDO:0005717,contagious pustular dermatitis,MONDO,disease,DISEASE_8888
8889,8889,8889,8889,8889,8889,8889,8889,MONDO:0003743_MONDO:0003800_MONDO:0003856_MONDO:0004344,heart malignant hemangiopericytoma,MONDO_grouped,disease,DISEASE_8889
8890,8890,8890,8890,8890,8890,8890,8890,MONDO:0010164,"phocomelia, Schinzel type",MONDO,disease,DISEASE_8890
8891,8891,8891,8891,8891,8891,8891,8891,MONDO:0010810,"vitamin D hydroxylation-deficient rickets, type 1B",MONDO,disease,DISEASE_8891
8892,8892,8892,8892,8892,8892,8892,8892,MONDO:0859169,White-Kernohan syndrome,MONDO,disease,DISEASE_8892
8893,8893,8893,8893,8893,8893,8893,8893,MONDO:0002066_MONDO:0002065_MONDO:0004181,breast adenomyoepithelioma,MONDO_grouped,disease,DISEASE_8893
8894,8894,8894,8894,8894,8894,8894,8894,MONDO:0017138,Opitz G/BBB syndrome,MONDO,disease,DISEASE_8894
8895,8895,8895,8895,8895,8895,8895,8895,MONDO:0019544,cocaine intoxication,MONDO,disease,DISEASE_8895
8896,8896,8896,8896,8896,8896,8896,8896,MONDO:0005933,pulmonary blastoma,MONDO,disease,DISEASE_8896
8897,8897,8897,8897,8897,8897,8897,8897,MONDO:0036189,oculogastrointestinal-neurodevelopmental syndrome,MONDO,disease,DISEASE_8897
8898,8898,8898,8898,8898,8898,8898,8898,MONDO:0024524_MONDO:0007483_MONDO:0014169_MONDO:0000736_MONDO:0012993,dyschromatosis universalis hereditaria,MONDO_grouped,disease,DISEASE_8898
8899,8899,8899,8899,8899,8899,8899,8899,MONDO:0002519,anus disorder,MONDO,disease,DISEASE_8899
8900,8900,8900,8900,8900,8900,8900,8900,MONDO:1011746,"facial eczema, non-human animal",MONDO,disease,DISEASE_8900
8901,8901,8901,8901,8901,8901,8901,8901,MONDO:0004726,liver inflammatory myofibroblastic tumor,MONDO,disease,DISEASE_8901
8902,8902,8902,8902,8902,8902,8902,8902,MONDO:0024868,metastatic carcinoma in the adrenal medulla,MONDO,disease,DISEASE_8902
8903,8903,8903,8903,8903,8903,8903,8903,MONDO:0018506,mesenchymal tumor of small intestine,MONDO,disease,DISEASE_8903
8904,8904,8904,8904,8904,8904,8904,8904,MONDO:0016242,hemoglobin C disease,MONDO,disease,DISEASE_8904
8905,8905,8905,8905,8905,8905,8905,8905,MONDO:0014519,"chronic mountain sickness, susceptibility to",MONDO,disease,DISEASE_8905
8906,8906,8906,8906,8906,8906,8906,8906,MONDO:0400006,botryomycosis,MONDO,disease,DISEASE_8906
8907,8907,8907,8907,8907,8907,8907,8907,MONDO:0700175,feline neoplasm,MONDO,disease,DISEASE_8907
8908,8908,8908,8908,8908,8908,8908,8908,MONDO:0012410,Finnish upper limb-onset distal myopathy,MONDO,disease,DISEASE_8908
8909,8909,8909,8909,8909,8909,8909,8909,MONDO:1010522,"frontonasal dysplasia, cattle",MONDO,disease,DISEASE_8909
8910,8910,8910,8910,8910,8910,8910,8910,MONDO:0013043,atypical hemolytic-uremic syndrome with C3 anomaly,MONDO,disease,DISEASE_8910
8911,8911,8911,8911,8911,8911,8911,8911,MONDO:1011949_MONDO:1011970,"occipital dysplasia, non-human animal",MONDO_grouped,disease,DISEASE_8911
8912,8912,8912,8912,8912,8912,8912,8912,MONDO:0016449,mid-dermal elastolysis,MONDO,disease,DISEASE_8912
8913,8913,8913,8913,8913,8913,8913,8913,MONDO:0008614,suppressor of tumorigenicity 3,MONDO,disease,DISEASE_8913
8914,8914,8914,8914,8914,8914,8914,8914,MONDO:0017126,oculo-skeletal-renal syndrome,MONDO,disease,DISEASE_8914
8915,8915,8915,8915,8915,8915,8915,8915,MONDO:1010633,"factor VII deficiency, Asiatic elephant",MONDO,disease,DISEASE_8915
8916,8916,8916,8916,8916,8916,8916,8916,MONDO:0009358,Hutterite cerebroosteonephrodysplasia syndrome,MONDO,disease,DISEASE_8916
8917,8917,8917,8917,8917,8917,8917,8917,MONDO:0019007,vaginal atresia,MONDO,disease,DISEASE_8917
8918,8918,8918,8918,8918,8918,8918,8918,MONDO:0016358,limited cutaneous systemic sclerosis,MONDO,disease,DISEASE_8918
8919,8919,8919,8919,8919,8919,8919,8919,MONDO:0016269,high-grade neuroendocrine carcinoma of the corpus uteri,MONDO,disease,DISEASE_8919
8920,8920,8920,8920,8920,8920,8920,8920,MONDO:0009263,GAPO syndrome,MONDO,disease,DISEASE_8920
8921,8921,8921,8921,8921,8921,8921,8921,MONDO:0023152,fibrocartilaginous embolism,MONDO,disease,DISEASE_8921
8922,8922,8922,8922,8922,8922,8922,8922,MONDO:0008891,riboflavin transporter deficiency,MONDO,disease,DISEASE_8922
8923,8923,8923,8923,8923,8923,8923,8923,MONDO:0007813_MONDO:0007239,superficial epidermolytic ichthyosis,MONDO_grouped,disease,DISEASE_8923
8924,8924,8924,8924,8924,8924,8924,8924,MONDO:0001006,glaucomatous atrophy of optic disk,MONDO,disease,DISEASE_8924
8925,8925,8925,8925,8925,8925,8925,8925,MONDO:0011035,neurofibromatosis-Noonan syndrome,MONDO,disease,DISEASE_8925
8926,8926,8926,8926,8926,8926,8926,8926,MONDO:0011639_MONDO:0010493,Diamond-Blackfan anemia 15 with mandibulofacial dysostosis,MONDO_grouped,disease,DISEASE_8926
8927,8927,8927,8927,8927,8927,8927,8927,MONDO:0005081,preeclampsia,MONDO,disease,DISEASE_8927
8928,8928,8928,8928,8928,8928,8928,8928,MONDO:1011332,"mitochondrial disease, non-human animal",MONDO,disease,DISEASE_8928
8929,8929,8929,8929,8929,8929,8929,8929,MONDO:0013721,complement component 4a deficiency,MONDO,disease,DISEASE_8929
8930,8930,8930,8930,8930,8930,8930,8930,MONDO:0044737,autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction,MONDO,disease,DISEASE_8930
8931,8931,8931,8931,8931,8931,8931,8931,MONDO:0044617,X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome,MONDO,disease,DISEASE_8931
8932,8932,8932,8932,8932,8932,8932,8932,MONDO:0020353,von Hippel anomaly,MONDO,disease,DISEASE_8932
8933,8933,8933,8933,8933,8933,8933,8933,MONDO:0003789,hereditary papillary renal cell carcinoma,MONDO,disease,DISEASE_8933
8934,8934,8934,8934,8934,8934,8934,8934,MONDO:0006233,gonadal teratoma,MONDO,disease,DISEASE_8934
8935,8935,8935,8935,8935,8935,8935,8935,MONDO:1010004,"paroxysmal dyskinesia, non-human animal",MONDO,disease,DISEASE_8935
8936,8936,8936,8936,8936,8936,8936,8936,MONDO:0003579,retinal nerve fiber layer disorder,MONDO,disease,DISEASE_8936
8937,8937,8937,8937,8937,8937,8937,8937,MONDO:0019253,metabolic disease involving other neurotransmitter deficiency,MONDO,disease,DISEASE_8937
8938,8938,8938,8938,8938,8938,8938,8938,MONDO:0024234,Seckel like syndrome majoor-krakauer type,MONDO,disease,DISEASE_8938
8939,8939,8939,8939,8939,8939,8939,8939,MONDO:0013018_MONDO:0000136,"keratosis follicularis spinulosa decalvans, autosomal dominant",MONDO_grouped,disease,DISEASE_8939
8940,8940,8940,8940,8940,8940,8940,8940,MONDO:1011032,"hereditary sensory and autonomic neuropathy, SCN9A-related, dog",MONDO,disease,DISEASE_8940
8941,8941,8941,8941,8941,8941,8941,8941,MONDO:0018204,20q11.2 microduplication syndrome,MONDO,disease,DISEASE_8941
8942,8942,8942,8942,8942,8942,8942,8942,MONDO:0001860,folic acid deficiency anemia,MONDO,disease,DISEASE_8942
8943,8943,8943,8943,8943,8943,8943,8943,MONDO:0800392,GNAT2-related retinopathy,MONDO,disease,DISEASE_8943
8944,8944,8944,8944,8944,8944,8944,8944,MONDO:0002642,trochlear nerve neoplasm,MONDO,disease,DISEASE_8944
8945,8945,8945,8945,8945,8945,8945,8945,MONDO:1012733,"Ehlers-Danlos syndrome with absence of dermatan sulfate proteoglycan, cattle",MONDO,disease,DISEASE_8945
8946,8946,8946,8946,8946,8946,8946,8946,MONDO:0007770,hyperpigmentation of Fuldauer and Kuijpers,MONDO,disease,DISEASE_8946
8947,8947,8947,8947,8947,8947,8947,8947,MONDO:0011382,sickle cell anemia,MONDO,disease,DISEASE_8947
8948,8948,8948,8948,8948,8948,8948,8948,MONDO:0005264,transient ischemic attack,MONDO,disease,DISEASE_8948
8949,8949,8949,8949,8949,8949,8949,8949,MONDO:1012825_MONDO:1012826_MONDO:1012829_MONDO:1012879_MONDO:1012901,"ichthyosis, ABCA12-related, pig",MONDO_grouped,disease,DISEASE_8949
8950,8950,8950,8950,8950,8950,8950,8950,MONDO:0018556,Lambert-Eaton myasthenic syndrome,MONDO,disease,DISEASE_8950
8951,8951,8951,8951,8951,8951,8951,8951,MONDO:0010875,"pachydermodactyly, familial",MONDO,disease,DISEASE_8951
8952,8952,8952,8952,8952,8952,8952,8952,MONDO:0008398,"salivary substance, Clostridium botulinum type",MONDO,disease,DISEASE_8952
8953,8953,8953,8953,8953,8953,8953,8953,MONDO:0700091,ring chromosome disorder,MONDO,disease,DISEASE_8953
8954,8954,8954,8954,8954,8954,8954,8954,MONDO:0020345,obsolete presynaptic congenital myasthenic syndrome,MONDO,disease,DISEASE_8954
8955,8955,8955,8955,8955,8955,8955,8955,MONDO:0032656,"microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum",MONDO,disease,DISEASE_8955
8956,8956,8956,8956,8956,8956,8956,8956,MONDO:0001121_MONDO:0001756_MONDO:0001120_MONDO:0001912,frontal sinusitis,MONDO_grouped,disease,DISEASE_8956
8957,8957,8957,8957,8957,8957,8957,8957,MONDO:1011799,"inherited periodic spasticity, non-human animal",MONDO,disease,DISEASE_8957
8958,8958,8958,8958,8958,8958,8958,8958,MONDO:0020481,myotonia fluctuans,MONDO,disease,DISEASE_8958
8959,8959,8959,8959,8959,8959,8959,8959,MONDO:0015109,congenital anomaly of the mitral subvalvular apparatus,MONDO,disease,DISEASE_8959
8960,8960,8960,8960,8960,8960,8960,8960,MONDO:0018653,Polymerase proofreading-related adenomatous polyposis,MONDO,disease,DISEASE_8960
8961,8961,8961,8961,8961,8961,8961,8961,MONDO:0002385,benign cystic nephroma,MONDO,disease,DISEASE_8961
8962,8962,8962,8962,8962,8962,8962,8962,MONDO:0022432,alves Castelo dos Santos syndrome,MONDO,disease,DISEASE_8962
8963,8963,8963,8963,8963,8963,8963,8963,MONDO:0015725,mosaic trisomy 14,MONDO,disease,DISEASE_8963
8964,8964,8964,8964,8964,8964,8964,8964,MONDO:0005486,tooth agenesis,MONDO,disease,DISEASE_8964
8965,8965,8965,8965,8965,8965,8965,8965,MONDO:0019065,amyloidosis,MONDO,disease,DISEASE_8965
8966,8966,8966,8966,8966,8966,8966,8966,MONDO:0035159,dermoid or epidermoid cyst of the central nervous system,MONDO,disease,DISEASE_8966
8967,8967,8967,8967,8967,8967,8967,8967,MONDO:0016656,7q31 microdeletion syndrome,MONDO,disease,DISEASE_8967
8968,8968,8968,8968,8968,8968,8968,8968,MONDO:0021464,benign neoplasm of cecum,MONDO,disease,DISEASE_8968
8969,8969,8969,8969,8969,8969,8969,8969,MONDO:0008802,"antithrombin, familial hemorrhagic diathesis due to",MONDO,disease,DISEASE_8969
8970,8970,8970,8970,8970,8970,8970,8970,MONDO:0005977,tabes dorsalis,MONDO,disease,DISEASE_8970
8971,8971,8971,8971,8971,8971,8971,8971,MONDO:0010970,"cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies",MONDO,disease,DISEASE_8971
8972,8972,8972,8972,8972,8972,8972,8972,MONDO:0016244,atypical hemolytic-uremic syndrome,MONDO,disease,DISEASE_8972
8973,8973,8973,8973,8973,8973,8973,8973,MONDO:1012738,"hereditary chondrodysplasia, dog",MONDO,disease,DISEASE_8973
8974,8974,8974,8974,8974,8974,8974,8974,MONDO:0013690,Pitt-Hopkins-like syndrome 2,MONDO,disease,DISEASE_8974
8975,8975,8975,8975,8975,8975,8975,8975,MONDO:0025136,"tuberculosis, bovine",MONDO,disease,DISEASE_8975
8976,8976,8976,8976,8976,8976,8976,8976,MONDO:0015947,inherited ichthyosis,MONDO,disease,DISEASE_8976
8977,8977,8977,8977,8977,8977,8977,8977,MONDO:0004165,selective IgD deficiency disease,MONDO,disease,DISEASE_8977
8978,8978,8978,8978,8978,8978,8978,8978,MONDO:0100543,clonal hematopoiesis of indeterminate potential,MONDO,disease,DISEASE_8978
8979,8979,8979,8979,8979,8979,8979,8979,MONDO:0008838,ataxia - deafness - intellectual disability syndrome,MONDO,disease,DISEASE_8979
8980,8980,8980,8980,8980,8980,8980,8980,MONDO:0000539,striated muscle rhabdoid tumor,MONDO,disease,DISEASE_8980
8981,8981,8981,8981,8981,8981,8981,8981,MONDO:0020706,Heberden's node,MONDO,disease,DISEASE_8981
8982,8982,8982,8982,8982,8982,8982,8982,MONDO:0009529,pyruvate dehydrogenase E3 deficiency,MONDO,disease,DISEASE_8982
8983,8983,8983,8983,8983,8983,8983,8983,MONDO:1030008,mitral valve insufficiency,MONDO,disease,DISEASE_8983
8984,8984,8984,8984,8984,8984,8984,8984,MONDO:0002603_MONDO:0006646_MONDO:0006086,angiomyolipoma,MONDO_grouped,disease,DISEASE_8984
8985,8985,8985,8985,8985,8985,8985,8985,MONDO:0012722,Dauwerse-Peters syndrome,MONDO,disease,DISEASE_8985
8986,8986,8986,8986,8986,8986,8986,8986,MONDO:0018929,medial condensing osteitis of the clavicle,MONDO,disease,DISEASE_8986
8987,8987,8987,8987,8987,8987,8987,8987,MONDO:0958000,thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies,MONDO,disease,DISEASE_8987
8988,8988,8988,8988,8988,8988,8988,8988,MONDO:0003996,basal ganglia disorder,MONDO,disease,DISEASE_8988
8989,8989,8989,8989,8989,8989,8989,8989,MONDO:0005828,listeriosis,MONDO,disease,DISEASE_8989
8990,8990,8990,8990,8990,8990,8990,8990,MONDO:0030063,"neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities",MONDO,disease,DISEASE_8990
8991,8991,8991,8991,8991,8991,8991,8991,MONDO:0008132,optic atrophy with demyelinating disease of CNS,MONDO,disease,DISEASE_8991
8992,8992,8992,8992,8992,8992,8992,8992,MONDO:0000410,funisitis,MONDO,disease,DISEASE_8992
8993,8993,8993,8993,8993,8993,8993,8993,MONDO:0012444_MONDO:0013674_MONDO:0024457_MONDO:0054764_MONDO:0054763_MONDO:0014290_MONDO:0010476_MONDO:0958012_MONDO:0018307,neurodegeneration with brain iron accumulation,MONDO_grouped,disease,DISEASE_8993
8994,8994,8994,8994,8994,8994,8994,8994,MONDO:0007975,"meralgia paraesthetica, familial",MONDO,disease,DISEASE_8994
8995,8995,8995,8995,8995,8995,8995,8995,MONDO:0006172,conjunctival nevus,MONDO,disease,DISEASE_8995
8996,8996,8996,8996,8996,8996,8996,8996,MONDO:0007153,"arteries, anomalies of",MONDO,disease,DISEASE_8996
8997,8997,8997,8997,8997,8997,8997,8997,MONDO:1012157,"megaesophagus, llama",MONDO,disease,DISEASE_8997
8998,8998,8998,8998,8998,8998,8998,8998,MONDO:0007136,hereditary anorectal anomalies,MONDO,disease,DISEASE_8998
8999,8999,8999,8999,8999,8999,8999,8999,MONDO:0010880_MONDO:0012532_MONDO:0014217_MONDO:0008535_MONDO:0019180_MONDO:0010996,"telangiectasia, hereditary hemorrhagic,",MONDO_grouped,disease,DISEASE_8999
9000,9000,9000,9000,9000,9000,9000,9000,MONDO:0010610,holoprosencephaly-hypokinesia-congenital contractures syndrome,MONDO,disease,DISEASE_9000
9001,9001,9001,9001,9001,9001,9001,9001,MONDO:0006533_MONDO:0006532,cholesteatoma of middle ear,MONDO_grouped,disease,DISEASE_9001
9002,9002,9002,9002,9002,9002,9002,9002,MONDO:0014175,"mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive",MONDO,disease,DISEASE_9002
9003,9003,9003,9003,9003,9003,9003,9003,MONDO:0018002_MONDO:0018206,adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy,MONDO_grouped,disease,DISEASE_9003
9004,9004,9004,9004,9004,9004,9004,9004,MONDO:0008579,"toes, relative length of first and second",MONDO,disease,DISEASE_9004
9005,9005,9005,9005,9005,9005,9005,9005,MONDO:0001096,mediastinum ganglioneuroblastoma,MONDO,disease,DISEASE_9005
9006,9006,9006,9006,9006,9006,9006,9006,MONDO:0019133,visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome,MONDO,disease,DISEASE_9006
9007,9007,9007,9007,9007,9007,9007,9007,MONDO:0859141,neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia,MONDO,disease,DISEASE_9007
9008,9008,9008,9008,9008,9008,9008,9008,MONDO:0009311,grouped pigmentation of the retina,MONDO,disease,DISEASE_9008
9009,9009,9009,9009,9009,9009,9009,9009,MONDO:0018368,primary peritoneal serous/papillary carcinoma,MONDO,disease,DISEASE_9009
9010,9010,9010,9010,9010,9010,9010,9010,MONDO:0035521_MONDO:0035524_MONDO:0035525,blepharophimosis-ptosis-epicanthus inversus syndrome,MONDO_grouped,disease,DISEASE_9010
9011,9011,9011,9011,9011,9011,9011,9011,MONDO:0021445,benign neoplasm of oral cavity,MONDO,disease,DISEASE_9011
9012,9012,9012,9012,9012,9012,9012,9012,MONDO:0007716,alpha thalassemia-intellectual disability syndrome type 1,MONDO,disease,DISEASE_9012
9013,9013,9013,9013,9013,9013,9013,9013,MONDO:0030375_MONDO:8000012_MONDO:0024189,"neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset",MONDO_grouped,disease,DISEASE_9013
9014,9014,9014,9014,9014,9014,9014,9014,MONDO:0018607,combined hamartoma of the retina and retinal pigment epithelium,MONDO,disease,DISEASE_9014
9015,9015,9015,9015,9015,9015,9015,9015,MONDO:0018999,LCAT deficiency,MONDO,disease,DISEASE_9015
9016,9016,9016,9016,9016,9016,9016,9016,MONDO:1012593,"oculocutaneous albinism, TYR-related, red fox",MONDO,disease,DISEASE_9016
9017,9017,9017,9017,9017,9017,9017,9017,MONDO:0021527,benign neoplasm of meninges,MONDO,disease,DISEASE_9017
9018,9018,9018,9018,9018,9018,9018,9018,MONDO:0002136,eczematous dermatitis of eyelid,MONDO,disease,DISEASE_9018
9019,9019,9019,9019,9019,9019,9019,9019,MONDO:0003965,Capgras syndrome,MONDO,disease,DISEASE_9019
9020,9020,9020,9020,9020,9020,9020,9020,MONDO:0004568,paralytic ileus,MONDO,disease,DISEASE_9020
9021,9021,9021,9021,9021,9021,9021,9021,MONDO:0021879,small cell variant anaplastic large cell lymphoma,MONDO,disease,DISEASE_9021
9022,9022,9022,9022,9022,9022,9022,9022,MONDO:0011321,expansile bone lesions,MONDO,disease,DISEASE_9022
9023,9023,9023,9023,9023,9023,9023,9023,MONDO:0020605,X-linked recessive disease,MONDO,disease,DISEASE_9023
9024,9024,9024,9024,9024,9024,9024,9024,MONDO:0023567,Kozlowski Brown Hardwick syndrome,MONDO,disease,DISEASE_9024
9025,9025,9025,9025,9025,9025,9025,9025,MONDO:0013088,"follicular lymphoma, susceptibility to, 1",MONDO,disease,DISEASE_9025
9026,9026,9026,9026,9026,9026,9026,9026,MONDO:0019077,warty dyskeratoma,MONDO,disease,DISEASE_9026
9027,9027,9027,9027,9027,9027,9027,9027,MONDO:0000395,alcohol-related birth defect,MONDO,disease,DISEASE_9027
9028,9028,9028,9028,9028,9028,9028,9028,MONDO:0012390,"arthrogryposis multiplex with deafness, inguinal hernias, and early death",MONDO,disease,DISEASE_9028
9029,9029,9029,9029,9029,9029,9029,9029,MONDO:0002370,ovarian Brenner tumor,MONDO,disease,DISEASE_9029
9030,9030,9030,9030,9030,9030,9030,9030,MONDO:0022403,Ahumada Del Castillo syndrome,MONDO,disease,DISEASE_9030
9031,9031,9031,9031,9031,9031,9031,9031,MONDO:0001331,conjunctival deposit,MONDO,disease,DISEASE_9031
9032,9032,9032,9032,9032,9032,9032,9032,MONDO:0020382,multifocal pattern dystrophy simulating fundus flavimaculatus,MONDO,disease,DISEASE_9032
9033,9033,9033,9033,9033,9033,9033,9033,MONDO:0800418_MONDO:0800419_MONDO:0800420,"breast cancer, familial, susceptibility to",MONDO_grouped,disease,DISEASE_9033
9034,9034,9034,9034,9034,9034,9034,9034,MONDO:0005709,common cold,MONDO,disease,DISEASE_9034
9035,9035,9035,9035,9035,9035,9035,9035,MONDO:0001412,conjunctival concretion,MONDO,disease,DISEASE_9035
9036,9036,9036,9036,9036,9036,9036,9036,MONDO:0010308,"thrombocytopenia, X-linked, with or without dyserythropoietic anemia",MONDO,disease,DISEASE_9036
9037,9037,9037,9037,9037,9037,9037,9037,MONDO:0019245,lysosomal lipid storage disorder,MONDO,disease,DISEASE_9037
9038,9038,9038,9038,9038,9038,9038,9038,MONDO:0005857,morbillivirus infectious disease,MONDO,disease,DISEASE_9038
9039,9039,9039,9039,9039,9039,9039,9039,MONDO:0014658,severe achondroplasia-developmental delay-acanthosis nigricans syndrome,MONDO,disease,DISEASE_9039
9040,9040,9040,9040,9040,9040,9040,9040,MONDO:0016855,Mowat-Wilson syndrome due to monosomy 2q22,MONDO,disease,DISEASE_9040
9041,9041,9041,9041,9041,9041,9041,9041,MONDO:0035584,punctate inner choroidopathy,MONDO,disease,DISEASE_9041
9042,9042,9042,9042,9042,9042,9042,9042,MONDO:0008797,anodontia,MONDO,disease,DISEASE_9042
9043,9043,9043,9043,9043,9043,9043,9043,MONDO:0044792,large congenital melanocytic nevus,MONDO,disease,DISEASE_9043
9044,9044,9044,9044,9044,9044,9044,9044,MONDO:0018095,Weaver-Williams syndrome,MONDO,disease,DISEASE_9044
9045,9045,9045,9045,9045,9045,9045,9045,MONDO:0021660,deep seated dermatophytosis,MONDO,disease,DISEASE_9045
9046,9046,9046,9046,9046,9046,9046,9046,MONDO:0036688_MONDO:0006123,rhabdomyoma,MONDO_grouped,disease,DISEASE_9046
9047,9047,9047,9047,9047,9047,9047,9047,MONDO:0100072,"neonatal diabetes, congenital sensorineural hearing loss and congenital cataracts",MONDO,disease,DISEASE_9047
9048,9048,9048,9048,9048,9048,9048,9048,MONDO:1011546,"intervertebral disc disease, dog",MONDO,disease,DISEASE_9048
9049,9049,9049,9049,9049,9049,9049,9049,MONDO:0016914,partial deletion of the long arm of chromosome 16,MONDO,disease,DISEASE_9049
9050,9050,9050,9050,9050,9050,9050,9050,MONDO:0800428,"dengue shock syndrome, susceptibility to",MONDO,disease,DISEASE_9050
9051,9051,9051,9051,9051,9051,9051,9051,MONDO:0014670_MONDO:0014549_MONDO:0014965_MONDO:0012656_MONDO:0014570_MONDO:0011868_MONDO:0014569_MONDO:0013965_MONDO:0009670_MONDO:0017436,lethal congenital contracture syndrome,MONDO_grouped,disease,DISEASE_9051
9052,9052,9052,9052,9052,9052,9052,9052,MONDO:0006547,exanthem,MONDO,disease,DISEASE_9052
9053,9053,9053,9053,9053,9053,9053,9053,MONDO:1010101,"galactosemia, non-human animal",MONDO,disease,DISEASE_9053
9054,9054,9054,9054,9054,9054,9054,9054,MONDO:0010220,Young syndrome,MONDO,disease,DISEASE_9054
9055,9055,9055,9055,9055,9055,9055,9055,MONDO:0006320,non-cutaneous melanoma,MONDO,disease,DISEASE_9055
9056,9056,9056,9056,9056,9056,9056,9056,MONDO:0007626,familial congenital palsy of trochlear nerve,MONDO,disease,DISEASE_9056
9057,9057,9057,9057,9057,9057,9057,9057,MONDO:0007085,alopecia-epilepsy-pyorrhea-intellectual disability syndrome,MONDO,disease,DISEASE_9057
9058,9058,9058,9058,9058,9058,9058,9058,MONDO:0015070,laryngeal neuroendocrine neoplasm,MONDO,disease,DISEASE_9058
9059,9059,9059,9059,9059,9059,9059,9059,MONDO:1010463,"mitral valve stenosis, domestic cat",MONDO,disease,DISEASE_9059
9060,9060,9060,9060,9060,9060,9060,9060,MONDO:1010832,"Wilson disease, dog",MONDO,disease,DISEASE_9060
9061,9061,9061,9061,9061,9061,9061,9061,MONDO:0957519,diffuse gastric cancer,MONDO,disease,DISEASE_9061
9062,9062,9062,9062,9062,9062,9062,9062,MONDO:0030036,"leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome",MONDO,disease,DISEASE_9062
9063,9063,9063,9063,9063,9063,9063,9063,MONDO:0009748,hereditary sensory and autonomic neuropathy with spastic paraplegia,MONDO,disease,DISEASE_9063
9064,9064,9064,9064,9064,9064,9064,9064,MONDO:0016208,solitary rectal ulcer syndrome,MONDO,disease,DISEASE_9064
9065,9065,9065,9065,9065,9065,9065,9065,MONDO:0016009,fetal trimethadione syndrome,MONDO,disease,DISEASE_9065
9066,9066,9066,9066,9066,9066,9066,9066,MONDO:0007235,branchiooculofacial syndrome,MONDO,disease,DISEASE_9066
9067,9067,9067,9067,9067,9067,9067,9067,MONDO:1012689,"GM2 gangliosidosis, Muntjak deer",MONDO,disease,DISEASE_9067
9068,9068,9068,9068,9068,9068,9068,9068,MONDO:0019861,thyroid hypoplasia,MONDO,disease,DISEASE_9068
9069,9069,9069,9069,9069,9069,9069,9069,MONDO:0010024,Beemer-Langer syndrome,MONDO,disease,DISEASE_9069
9070,9070,9070,9070,9070,9070,9070,9070,MONDO:1010676_MONDO:1010677,"microtia, pig",MONDO_grouped,disease,DISEASE_9070
9071,9071,9071,9071,9071,9071,9071,9071,MONDO:0018670,symptomatic form of fragile X syndrome in female carrier,MONDO,disease,DISEASE_9071
9072,9072,9072,9072,9072,9072,9072,9072,MONDO:1012731,"progressive early-onset cerebellar ataxia, SEL1L-related, dog",MONDO,disease,DISEASE_9072
9073,9073,9073,9073,9073,9073,9073,9073,MONDO:0018659,partial duplication of the short arm of chromosome 19,MONDO,disease,DISEASE_9073
9074,9074,9074,9074,9074,9074,9074,9074,MONDO:1010291,"achondroplasia, non-human animal",MONDO,disease,DISEASE_9074
9075,9075,9075,9075,9075,9075,9075,9075,MONDO:0100098,"dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive",MONDO,disease,DISEASE_9075
9076,9076,9076,9076,9076,9076,9076,9076,MONDO:0016289,malignant germ cell tumor of cervix uteri,MONDO,disease,DISEASE_9076
9077,9077,9077,9077,9077,9077,9077,9077,MONDO:0016479,silver-Russell syndrome due to 7p11.2p13 microduplication,MONDO,disease,DISEASE_9077
9078,9078,9078,9078,9078,9078,9078,9078,MONDO:0004505,central breast papilloma,MONDO,disease,DISEASE_9078
9079,9079,9079,9079,9079,9079,9079,9079,MONDO:0100579,GRHL3-related orofacial clefting,MONDO,disease,DISEASE_9079
9080,9080,9080,9080,9080,9080,9080,9080,MONDO:0008518,calcaneonavicular coalition,MONDO,disease,DISEASE_9080
9081,9081,9081,9081,9081,9081,9081,9081,MONDO:0017945,ABetaL34V amyloidosis,MONDO,disease,DISEASE_9081
9082,9082,9082,9082,9082,9082,9082,9082,MONDO:0009809,"multicentric osteolysis, nodulosis, and arthropathy",MONDO,disease,DISEASE_9082
9083,9083,9083,9083,9083,9083,9083,9083,MONDO:0017199,osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome,MONDO,disease,DISEASE_9083
9084,9084,9084,9084,9084,9084,9084,9084,MONDO:0006462,thyroid gland diffuse large B-cell lymphoma,MONDO,disease,DISEASE_9084
9085,9085,9085,9085,9085,9085,9085,9085,MONDO:0018612_MONDO:0016410_MONDO:0016408_MONDO:0015792,congenital hypothyroidism,MONDO_grouped,disease,DISEASE_9085
9086,9086,9086,9086,9086,9086,9086,9086,MONDO:0859570_MONDO:0859569,braddock-carey syndrome,MONDO_grouped,disease,DISEASE_9086
9087,9087,9087,9087,9087,9087,9087,9087,MONDO:0003760,pediatric ovarian germ cell tumor,MONDO,disease,DISEASE_9087
9088,9088,9088,9088,9088,9088,9088,9088,MONDO:0100310,hereditary cerebellar ataxia,MONDO,disease,DISEASE_9088
9089,9089,9089,9089,9089,9089,9089,9089,MONDO:0957443,autosomal recessive ataxia due to PEX2 deficiency,MONDO,disease,DISEASE_9089
9090,9090,9090,9090,9090,9090,9090,9090,MONDO:0023662_MONDO:0014797_MONDO:0013278_MONDO:0007920_MONDO:0032907_MONDO:0957954_MONDO:0030270_MONDO:0014393_MONDO:0031043_MONDO:0007919_MONDO:0012765_MONDO:0015009_MONDO:0859379_MONDO:0030316_MONDO:0019313,lymphatic malformation,MONDO_grouped,disease,DISEASE_9090
9091,9091,9091,9091,9091,9091,9091,9091,MONDO:0017136,omodysplasia,MONDO,disease,DISEASE_9091
9092,9092,9092,9092,9092,9092,9092,9092,MONDO:0007565,familial cylindromatosis,MONDO,disease,DISEASE_9092
9093,9093,9093,9093,9093,9093,9093,9093,MONDO:0016760,"microcephaly-microcornea syndrome, Seemanova type",MONDO,disease,DISEASE_9093
9094,9094,9094,9094,9094,9094,9094,9094,MONDO:0020728_MONDO:0012793_MONDO:0968951,"hypouricemia, renal",MONDO_grouped,disease,DISEASE_9094
9095,9095,9095,9095,9095,9095,9095,9095,MONDO:0005396,thoracic aortic aneurysm,MONDO,disease,DISEASE_9095
9096,9096,9096,9096,9096,9096,9096,9096,MONDO:0024454,sacral nerve plexus disorder,MONDO,disease,DISEASE_9096
9097,9097,9097,9097,9097,9097,9097,9097,MONDO:0006077,adrenal medullary hyperplasia,MONDO,disease,DISEASE_9097
9098,9098,9098,9098,9098,9098,9098,9098,MONDO:0014249,multiple fibroadenoma of the breast,MONDO,disease,DISEASE_9098
9099,9099,9099,9099,9099,9099,9099,9099,MONDO:1010502,"Budd-chiari syndrome, domestic cat",MONDO,disease,DISEASE_9099
9100,9100,9100,9100,9100,9100,9100,9100,MONDO:0700025,chromosome 20 disorder,MONDO,disease,DISEASE_9100
9101,9101,9101,9101,9101,9101,9101,9101,MONDO:0005914,Picornaviridae infectious disease,MONDO,disease,DISEASE_9101
9102,9102,9102,9102,9102,9102,9102,9102,MONDO:0013837,deafness-encephaloneuropathy-obesity-valvulopathy syndrome,MONDO,disease,DISEASE_9102
9103,9103,9103,9103,9103,9103,9103,9103,MONDO:0031002,Baralle-Macken syndrome,MONDO,disease,DISEASE_9103
9104,9104,9104,9104,9104,9104,9104,9104,MONDO:0007528,"Ehlers-Danlos syndrome, autosomal dominant, type unspecified",MONDO,disease,DISEASE_9104
9105,9105,9105,9105,9105,9105,9105,9105,MONDO:0021038,Ewing sarcoma/peripheral primitive neuroectodermal tumor,MONDO,disease,DISEASE_9105
9106,9106,9106,9106,9106,9106,9106,9106,MONDO:1012891,"deafness, OTOF-related, sheep",MONDO,disease,DISEASE_9106
9107,9107,9107,9107,9107,9107,9107,9107,MONDO:1011780,"gallbladder mucocele, non-human animal",MONDO,disease,DISEASE_9107
9108,9108,9108,9108,9108,9108,9108,9108,MONDO:0045070,digestive system melanoma,MONDO,disease,DISEASE_9108
9109,9109,9109,9109,9109,9109,9109,9109,MONDO:0019186,Q fever,MONDO,disease,DISEASE_9109
9110,9110,9110,9110,9110,9110,9110,9110,MONDO:0016897,partial deletion of the short arm of chromosome 19,MONDO,disease,DISEASE_9110
9111,9111,9111,9111,9111,9111,9111,9111,MONDO:0020680,acute bronchiolitis,MONDO,disease,DISEASE_9111
9112,9112,9112,9112,9112,9112,9112,9112,MONDO:0003933,chest wall bone cancer,MONDO,disease,DISEASE_9112
9113,9113,9113,9113,9113,9113,9113,9113,MONDO:0975754,pseudomyogenic hemangioendothelioma,MONDO,disease,DISEASE_9113
9114,9114,9114,9114,9114,9114,9114,9114,MONDO:0001626,traumatic glaucoma,MONDO,disease,DISEASE_9114
9115,9115,9115,9115,9115,9115,9115,9115,MONDO:0015689,myeloid neoplasm associated with PDGFRA rearrangement,MONDO,disease,DISEASE_9115
9116,9116,9116,9116,9116,9116,9116,9116,MONDO:0003772_MONDO:0001275_MONDO:0003638,cerebral meningioma,MONDO_grouped,disease,DISEASE_9116
9117,9117,9117,9117,9117,9117,9117,9117,MONDO:0002766,larynx verrucous carcinoma,MONDO,disease,DISEASE_9117
9118,9118,9118,9118,9118,9118,9118,9118,MONDO:1012662_MONDO:1012663,"dwarfism, ACAN-related, horse",MONDO_grouped,disease,DISEASE_9118
9119,9119,9119,9119,9119,9119,9119,9119,MONDO:0002165,rectal neoplasm,MONDO,disease,DISEASE_9119
9120,9120,9120,9120,9120,9120,9120,9120,MONDO:0100415,"acute myeloid leukemia, FLT3 internal tandem duplication",MONDO,disease,DISEASE_9120
9121,9121,9121,9121,9121,9121,9121,9121,MONDO:0018500,cutaneous larva migrans,MONDO,disease,DISEASE_9121
9122,9122,9122,9122,9122,9122,9122,9122,MONDO:0005140_MONDO:0002225_MONDO:0000543_MONDO:0002227,ovarian carcinoma,MONDO_grouped,disease,DISEASE_9122
9123,9123,9123,9123,9123,9123,9123,9123,MONDO:0017197,osteopathia striata-pigmentary dermopathy-white forelock syndrome,MONDO,disease,DISEASE_9123
9124,9124,9124,9124,9124,9124,9124,9124,MONDO:0004896,esotropia,MONDO,disease,DISEASE_9124
9125,9125,9125,9125,9125,9125,9125,9125,MONDO:0000334,multinodular goiter,MONDO,disease,DISEASE_9125
9126,9126,9126,9126,9126,9126,9126,9126,MONDO:0004028,small intestinal fibrosarcoma,MONDO,disease,DISEASE_9126
9127,9127,9127,9127,9127,9127,9127,9127,MONDO:1012871,"deafness, LOXHD1-related, dog",MONDO,disease,DISEASE_9127
9128,9128,9128,9128,9128,9128,9128,9128,MONDO:0009221,femur-fibula-ulna complex,MONDO,disease,DISEASE_9128
9129,9129,9129,9129,9129,9129,9129,9129,MONDO:0001853,contact blepharoconjunctivitis,MONDO,disease,DISEASE_9129
9130,9130,9130,9130,9130,9130,9130,9130,MONDO:0005133_MONDO:0000931,endometriosis,MONDO_grouped,disease,DISEASE_9130
9131,9131,9131,9131,9131,9131,9131,9131,MONDO:1012394,"growth-hormone deficiency dwarfism, zebu cattle",MONDO,disease,DISEASE_9131
9132,9132,9132,9132,9132,9132,9132,9132,MONDO:0045068,minor salivary gland adenoid cystic carcinoma,MONDO,disease,DISEASE_9132
9133,9133,9133,9133,9133,9133,9133,9133,MONDO:0700016,chromosome 9 disorder,MONDO,disease,DISEASE_9133
9134,9134,9134,9134,9134,9134,9134,9134,MONDO:0002325,"tooth erosion, non-bacterial",MONDO,disease,DISEASE_9134
9135,9135,9135,9135,9135,9135,9135,9135,MONDO:0016262_MONDO:0016283,leiomyosarcoma of the corpus uteri,MONDO_grouped,disease,DISEASE_9135
9136,9136,9136,9136,9136,9136,9136,9136,MONDO:0044925,oral cavity carcinoma,MONDO,disease,DISEASE_9136
9137,9137,9137,9137,9137,9137,9137,9137,MONDO:0010132,familial thyroid dyshormonogenesis,MONDO,disease,DISEASE_9137
9138,9138,9138,9138,9138,9138,9138,9138,MONDO:1010713,"pyruvate dehydrogenase deficiency, dog",MONDO,disease,DISEASE_9138
9139,9139,9139,9139,9139,9139,9139,9139,MONDO:1010572,"diabetes mellitus, long-tailed chinchilla",MONDO,disease,DISEASE_9139
9140,9140,9140,9140,9140,9140,9140,9140,MONDO:0850473,A53 diffuse large B-cell lymphoma,MONDO,disease,DISEASE_9140
9141,9141,9141,9141,9141,9141,9141,9141,MONDO:0008904,"camptomelic syndrome, long-limb type",MONDO,disease,DISEASE_9141
9142,9142,9142,9142,9142,9142,9142,9142,MONDO:0014835_MONDO:0000211,"striatal degeneration, autosomal dominant 2",MONDO_grouped,disease,DISEASE_9142
9143,9143,9143,9143,9143,9143,9143,9143,MONDO:0020354,coloboma of choroid and retina,MONDO,disease,DISEASE_9143
9144,9144,9144,9144,9144,9144,9144,9144,MONDO:0003225_MONDO:0021138,bone marrow disorder,MONDO_grouped,disease,DISEASE_9144
9145,9145,9145,9145,9145,9145,9145,9145,MONDO:0007905,"lip, hamartomatous",MONDO,disease,DISEASE_9145
9146,9146,9146,9146,9146,9146,9146,9146,MONDO:0022070,Cantu Sanchez-Corona Hernandez syndrome,MONDO,disease,DISEASE_9146
9147,9147,9147,9147,9147,9147,9147,9147,MONDO:0006763,frozen shoulder,MONDO,disease,DISEASE_9147
9148,9148,9148,9148,9148,9148,9148,9148,MONDO:0008549,"thoracic dysostosis, isolated",MONDO,disease,DISEASE_9148
9149,9149,9149,9149,9149,9149,9149,9149,MONDO:1012035,"cardiomyopathy and woolly haircoat syndrome, cattle",MONDO,disease,DISEASE_9149
9150,9150,9150,9150,9150,9150,9150,9150,MONDO:1011348_MONDO:1011349_MONDO:1011346,"post-infectious disorder, non-human animal",MONDO_grouped,disease,DISEASE_9150
9151,9151,9151,9151,9151,9151,9151,9151,MONDO:0035823,KLHL7-related Bohring-Opitz-like syndrome,MONDO,disease,DISEASE_9151
9152,9152,9152,9152,9152,9152,9152,9152,MONDO:0000621,immune system cancer,MONDO,disease,DISEASE_9152
9153,9153,9153,9153,9153,9153,9153,9153,MONDO:0013234_MONDO:0008224_MONDO:0042979_MONDO:1011536,"hypokalemic periodic paralysis,",MONDO_grouped,disease,DISEASE_9153
9154,9154,9154,9154,9154,9154,9154,9154,MONDO:0003500,squamous cell bile duct carcinoma,MONDO,disease,DISEASE_9154
9155,9155,9155,9155,9155,9155,9155,9155,MONDO:0800043,Stüve-Wiedemann syndrome 1,MONDO,disease,DISEASE_9155
9156,9156,9156,9156,9156,9156,9156,9156,MONDO:0030066,"granulomatous disease, chronic, autosomal recessive, 5",MONDO,disease,DISEASE_9156
9157,9157,9157,9157,9157,9157,9157,9157,MONDO:0019950_MONDO:0023595,congenital muscular dystrophy,MONDO_grouped,disease,DISEASE_9157
9158,9158,9158,9158,9158,9158,9158,9158,MONDO:0859206,neurodevelopmental disorder with hearing loss and spasticity,MONDO,disease,DISEASE_9158
9159,9159,9159,9159,9159,9159,9159,9159,MONDO:0005918,placenta praevia,MONDO,disease,DISEASE_9159
9160,9160,9160,9160,9160,9160,9160,9160,MONDO:0016371,combined hyperactive dysfunction syndrome of the cranial nerves,MONDO,disease,DISEASE_9160
9161,9161,9161,9161,9161,9161,9161,9161,MONDO:0010684,X-linked myopathy with excessive autophagy,MONDO,disease,DISEASE_9161
9162,9162,9162,9162,9162,9162,9162,9162,MONDO:0010025,short stature-obesity syndrome,MONDO,disease,DISEASE_9162
9163,9163,9163,9163,9163,9163,9163,9163,MONDO:1011775_MONDO:1011781,"idiopathic hepatic fibrosis, non-human animal",MONDO_grouped,disease,DISEASE_9163
9164,9164,9164,9164,9164,9164,9164,9164,MONDO:0005644,amebiasis,MONDO,disease,DISEASE_9164
9165,9165,9165,9165,9165,9165,9165,9165,MONDO:0005723,Cryptococcal meningitis,MONDO,disease,DISEASE_9165
9166,9166,9166,9166,9166,9166,9166,9166,MONDO:0100512,"mitochondrial DNA depletion syndrome, hepatocerebral form",MONDO,disease,DISEASE_9166
9167,9167,9167,9167,9167,9167,9167,9167,MONDO:0001129,nasal cavity olfactory neuroblastoma,MONDO,disease,DISEASE_9167
9168,9168,9168,9168,9168,9168,9168,9168,MONDO:0019614,pituitary deficiency due to Rathke's pouch cysts,MONDO,disease,DISEASE_9168
9169,9169,9169,9169,9169,9169,9169,9169,MONDO:0004991,minimally invasive lung adenocarcinoma,MONDO,disease,DISEASE_9169
9170,9170,9170,9170,9170,9170,9170,9170,MONDO:0019314_MONDO:0019023_MONDO:0002726,cutaneous mastocytoma,MONDO_grouped,disease,DISEASE_9170
9171,9171,9171,9171,9171,9171,9171,9171,MONDO:0019505,obsolete hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome,MONDO,disease,DISEASE_9171
9172,9172,9172,9172,9172,9172,9172,9172,MONDO:0021129,microphthalmia,MONDO,disease,DISEASE_9172
9173,9173,9173,9173,9173,9173,9173,9173,MONDO:0002868,bile duct mucinous cystic neoplasm with an associated invasive carcinoma,MONDO,disease,DISEASE_9173
9174,9174,9174,9174,9174,9174,9174,9174,MONDO:0003515,fallopian tube teratoma,MONDO,disease,DISEASE_9174
9175,9175,9175,9175,9175,9175,9175,9175,MONDO:0017807,growing teratoma syndrome,MONDO,disease,DISEASE_9175
9176,9176,9176,9176,9176,9176,9176,9176,MONDO:0007922,lymphedema-distichiasis syndrome,MONDO,disease,DISEASE_9176
9177,9177,9177,9177,9177,9177,9177,9177,MONDO:0009970,renal tubular dysgenesis of genetic origin,MONDO,disease,DISEASE_9177
9178,9178,9178,9178,9178,9178,9178,9178,MONDO:0007434,primary failure of tooth eruption,MONDO,disease,DISEASE_9178
9179,9179,9179,9179,9179,9179,9179,9179,MONDO:0021808,acute cholinergic dysautonomia,MONDO,disease,DISEASE_9179
9180,9180,9180,9180,9180,9180,9180,9180,MONDO:0018882,vasculitis,MONDO,disease,DISEASE_9180
9181,9181,9181,9181,9181,9181,9181,9181,MONDO:0859313,neurodevelopmental disorder with speech impairment and with or without seizures,MONDO,disease,DISEASE_9181
9182,9182,9182,9182,9182,9182,9182,9182,MONDO:0019979_MONDO:1011064_MONDO:1011065_MONDO:1011066,"renal hypoplasia, unilateral",MONDO_grouped,disease,DISEASE_9182
9183,9183,9183,9183,9183,9183,9183,9183,MONDO:0021979,Basaran Yilmaz syndrome,MONDO,disease,DISEASE_9183
9184,9184,9184,9184,9184,9184,9184,9184,MONDO:0017698,"glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form",MONDO,disease,DISEASE_9184
9185,9185,9185,9185,9185,9185,9185,9185,MONDO:0003130,mesoblastic nephroma,MONDO,disease,DISEASE_9185
9186,9186,9186,9186,9186,9186,9186,9186,MONDO:1011667,"Lundehund syndrome, non-human animal",MONDO,disease,DISEASE_9186
9187,9187,9187,9187,9187,9187,9187,9187,MONDO:0005593_MONDO:0004508_MONDO:0001251_MONDO:0001338,chronic periodontitis,MONDO_grouped,disease,DISEASE_9187
9188,9188,9188,9188,9188,9188,9188,9188,MONDO:0035734,hereditary angioedema with normal C1inh not related to F12 or PLG variant,MONDO,disease,DISEASE_9188
9189,9189,9189,9189,9189,9189,9189,9189,MONDO:0015161,multiple congenital anomalies/dysmorphic syndrome without intellectual disability,MONDO,disease,DISEASE_9189
9190,9190,9190,9190,9190,9190,9190,9190,MONDO:0005980,tick infestation,MONDO,disease,DISEASE_9190
9191,9191,9191,9191,9191,9191,9191,9191,MONDO:0033006,"Galloway-Mowat syndrome 2, X-linked",MONDO,disease,DISEASE_9191
9192,9192,9192,9192,9192,9192,9192,9192,MONDO:0859303,intellectual developmental disorder with ocular anomalies and distinctive facial features,MONDO,disease,DISEASE_9192
9193,9193,9193,9193,9193,9193,9193,9193,MONDO:0013798,chromosome 16q22 deletion syndrome,MONDO,disease,DISEASE_9193
9194,9194,9194,9194,9194,9194,9194,9194,MONDO:0015605,distal monosomy 9p,MONDO,disease,DISEASE_9194
9195,9195,9195,9195,9195,9195,9195,9195,MONDO:0017850,sirenomelia,MONDO,disease,DISEASE_9195
9196,9196,9196,9196,9196,9196,9196,9196,MONDO:1011629,"quaking, non-human animal",MONDO,disease,DISEASE_9196
9197,9197,9197,9197,9197,9197,9197,9197,MONDO:0034028,obsolete symptomatic form of hemochromatosis type 1,MONDO,disease,DISEASE_9197
9198,9198,9198,9198,9198,9198,9198,9198,MONDO:0003812_MONDO:0006337,ovarian endometrial cancer,MONDO_grouped,disease,DISEASE_9198
9199,9199,9199,9199,9199,9199,9199,9199,MONDO:1011312,"disease related to transplantation, non-human animal",MONDO,disease,DISEASE_9199
9200,9200,9200,9200,9200,9200,9200,9200,MONDO:0021509,benign neoplasm of myocardium,MONDO,disease,DISEASE_9200
9201,9201,9201,9201,9201,9201,9201,9201,MONDO:1010016,"mitral valve stenosis, non-human animal",MONDO,disease,DISEASE_9201
9202,9202,9202,9202,9202,9202,9202,9202,MONDO:0015409,isolated congenital syngnathia,MONDO,disease,DISEASE_9202
9203,9203,9203,9203,9203,9203,9203,9203,MONDO:0003682,localized chondrosarcoma,MONDO,disease,DISEASE_9203
9204,9204,9204,9204,9204,9204,9204,9204,MONDO:0016362_MONDO:0018426_MONDO:0016613_MONDO:0021057,attenuated familial adenomatous polyposis,MONDO_grouped,disease,DISEASE_9204
9205,9205,9205,9205,9205,9205,9205,9205,MONDO:0009241,fountain syndrome,MONDO,disease,DISEASE_9205
9206,9206,9206,9206,9206,9206,9206,9206,MONDO:0013726_MONDO:0014905_MONDO:0054865,"encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1",MONDO_grouped,disease,DISEASE_9206
9207,9207,9207,9207,9207,9207,9207,9207,MONDO:0018573,intrauterine growth restriction-short stature-early adult-onset diabetes syndrome,MONDO,disease,DISEASE_9207
9208,9208,9208,9208,9208,9208,9208,9208,MONDO:0009778,"olivopontocerebellar atrophy II, autosomal recessive",MONDO,disease,DISEASE_9208
9209,9209,9209,9209,9209,9209,9209,9209,MONDO:0100346,microcephaly with or without short stature,MONDO,disease,DISEASE_9209
9210,9210,9210,9210,9210,9210,9210,9210,MONDO:0014243,Schaaf-Yang syndrome,MONDO,disease,DISEASE_9210
9211,9211,9211,9211,9211,9211,9211,9211,MONDO:0018199,new-onset refractory status epilepticus,MONDO,disease,DISEASE_9211
9212,9212,9212,9212,9212,9212,9212,9212,MONDO:0004193,pediatric ovarian dysgerminoma,MONDO,disease,DISEASE_9212
9213,9213,9213,9213,9213,9213,9213,9213,MONDO:0006015,Waterhouse-Friderichsen syndrome,MONDO,disease,DISEASE_9213
9214,9214,9214,9214,9214,9214,9214,9214,MONDO:1010086,"myeloperoxidase deficiency, non-human animal",MONDO,disease,DISEASE_9214
9215,9215,9215,9215,9215,9215,9215,9215,MONDO:0016564,progressive supranuclear palsy-progressive non-fluent aphasia syndrome,MONDO,disease,DISEASE_9215
9216,9216,9216,9216,9216,9216,9216,9216,MONDO:0009754,"neutropenia, lethal congenital, with eosinophilia",MONDO,disease,DISEASE_9216
9217,9217,9217,9217,9217,9217,9217,9217,MONDO:0016931,partial duplication of chromosome 10,MONDO,disease,DISEASE_9217
9218,9218,9218,9218,9218,9218,9218,9218,MONDO:0003294,pericardium leiomyoma,MONDO,disease,DISEASE_9218
9219,9219,9219,9219,9219,9219,9219,9219,MONDO:0004409,nipple duct carcinoma,MONDO,disease,DISEASE_9219
9220,9220,9220,9220,9220,9220,9220,9220,MONDO:0023079,epidermal nevus vitamin D resistant rickets,MONDO,disease,DISEASE_9220
9221,9221,9221,9221,9221,9221,9221,9221,MONDO:1011997,"recurrent uveitis, non-human animal",MONDO,disease,DISEASE_9221
9222,9222,9222,9222,9222,9222,9222,9222,MONDO:0017844,Sezary syndrome,MONDO,disease,DISEASE_9222
9223,9223,9223,9223,9223,9223,9223,9223,MONDO:0859188,neurodevelopmental disorder with seizures and brain abnormalities,MONDO,disease,DISEASE_9223
9224,9224,9224,9224,9224,9224,9224,9224,MONDO:0859763,mosaic neurofibromatosis type 1,MONDO,disease,DISEASE_9224
9225,9225,9225,9225,9225,9225,9225,9225,MONDO:1010687,"AA amyloidosis, red fox",MONDO,disease,DISEASE_9225
9226,9226,9226,9226,9226,9226,9226,9226,MONDO:0020593,trichoblastoma,MONDO,disease,DISEASE_9226
9227,9227,9227,9227,9227,9227,9227,9227,MONDO:0015515,carnitine palmitoyltransferase II deficiency,MONDO,disease,DISEASE_9227
9228,9228,9228,9228,9228,9228,9228,9228,MONDO:0002605,hepatic angiomyolipoma,MONDO,disease,DISEASE_9228
9229,9229,9229,9229,9229,9229,9229,9229,MONDO:0019084_MONDO:0004112,radiation proctitis,MONDO_grouped,disease,DISEASE_9229
9230,9230,9230,9230,9230,9230,9230,9230,MONDO:0011061,"chorea, remitting, with nystagmus and cataract",MONDO,disease,DISEASE_9230
9231,9231,9231,9231,9231,9231,9231,9231,MONDO:0017865_MONDO:0019993_MONDO:0957556,congenital pulmonary valve stenosis,MONDO_grouped,disease,DISEASE_9231
9232,9232,9232,9232,9232,9232,9232,9232,MONDO:0017052,intermediate maple syrup urine disease,MONDO,disease,DISEASE_9232
9233,9233,9233,9233,9233,9233,9233,9233,MONDO:0957487,idiopathic catatonia,MONDO,disease,DISEASE_9233
9234,9234,9234,9234,9234,9234,9234,9234,MONDO:0002950,skin clear cell basal cell carcinoma,MONDO,disease,DISEASE_9234
9235,9235,9235,9235,9235,9235,9235,9235,MONDO:0043953,burkholderia infectious disease,MONDO,disease,DISEASE_9235
9236,9236,9236,9236,9236,9236,9236,9236,MONDO:0030065,"agenesis of corpus callosum, cardiac, ocular, and genital syndrome",MONDO,disease,DISEASE_9236
9237,9237,9237,9237,9237,9237,9237,9237,MONDO:0015198,aniridia-ptosis-intellectual disability-familial obesity syndrome,MONDO,disease,DISEASE_9237
9238,9238,9238,9238,9238,9238,9238,9238,MONDO:0015832,true unicornuate uterus,MONDO,disease,DISEASE_9238
9239,9239,9239,9239,9239,9239,9239,9239,MONDO:0010177,vascular hyalinosis,MONDO,disease,DISEASE_9239
9240,9240,9240,9240,9240,9240,9240,9240,MONDO:1010031,"triploidy, non-human animal",MONDO,disease,DISEASE_9240
9241,9241,9241,9241,9241,9241,9241,9241,MONDO:0100347_MONDO:0041167,carcinoid syndrome,MONDO_grouped,disease,DISEASE_9241
9242,9242,9242,9242,9242,9242,9242,9242,MONDO:0001095,mediastinum neuroblastoma,MONDO,disease,DISEASE_9242
9243,9243,9243,9243,9243,9243,9243,9243,MONDO:0013233,"spondyloepimetaphyseal dysplasia, Handigodu type",MONDO,disease,DISEASE_9243
9244,9244,9244,9244,9244,9244,9244,9244,MONDO:0957018,autoinflammatory syndrome of childhood,MONDO,disease,DISEASE_9244
9245,9245,9245,9245,9245,9245,9245,9245,MONDO:0008005,cardiospondylocarpofacial syndrome,MONDO,disease,DISEASE_9245
9246,9246,9246,9246,9246,9246,9246,9246,MONDO:0008723,very long chain acyl-CoA dehydrogenase deficiency,MONDO,disease,DISEASE_9246
9247,9247,9247,9247,9247,9247,9247,9247,MONDO:0006326,ocular melanoma with extraocular extension,MONDO,disease,DISEASE_9247
9248,9248,9248,9248,9248,9248,9248,9248,MONDO:0100110,adenovirus renal infection,MONDO,disease,DISEASE_9248
9249,9249,9249,9249,9249,9249,9249,9249,MONDO:0020856_MONDO:0014887_MONDO:0032573_MONDO:0030015_MONDO:0000159,bone marrow failure syndrome,MONDO_grouped,disease,DISEASE_9249
9250,9250,9250,9250,9250,9250,9250,9250,MONDO:0000679,social emotional agnosia,MONDO,disease,DISEASE_9250
9251,9251,9251,9251,9251,9251,9251,9251,MONDO:0024644,myocardial ischemia,MONDO,disease,DISEASE_9251
9252,9252,9252,9252,9252,9252,9252,9252,MONDO:0012544,brachydactyly-syndactyly syndrome,MONDO,disease,DISEASE_9252
9253,9253,9253,9253,9253,9253,9253,9253,MONDO:0020718,"congenital short bowel syndrome, autosomal recessive",MONDO,disease,DISEASE_9253
9254,9254,9254,9254,9254,9254,9254,9254,MONDO:0002012,methylmalonic acidemia,MONDO,disease,DISEASE_9254
9255,9255,9255,9255,9255,9255,9255,9255,MONDO:0006214,follicular variant thyroid gland papillary carcinoma,MONDO,disease,DISEASE_9255
9256,9256,9256,9256,9256,9256,9256,9256,MONDO:0019547,Wells syndrome,MONDO,disease,DISEASE_9256
9257,9257,9257,9257,9257,9257,9257,9257,MONDO:0022458,annular constricting bands,MONDO,disease,DISEASE_9257
9258,9258,9258,9258,9258,9258,9258,9258,MONDO:0005952,scarlet fever,MONDO,disease,DISEASE_9258
9259,9259,9259,9259,9259,9259,9259,9259,MONDO:0043988,zoster sine herpete,MONDO,disease,DISEASE_9259
9260,9260,9260,9260,9260,9260,9260,9260,MONDO:0019880,distal trisomy 5q,MONDO,disease,DISEASE_9260
9261,9261,9261,9261,9261,9261,9261,9261,MONDO:1010998_MONDO:1010999_MONDO:1011000,"syringomyelia, dog",MONDO_grouped,disease,DISEASE_9261
9262,9262,9262,9262,9262,9262,9262,9262,MONDO:0018155,lateral sclerosis,MONDO,disease,DISEASE_9262
9263,9263,9263,9263,9263,9263,9263,9263,MONDO:0004897,hypotropia,MONDO,disease,DISEASE_9263
9264,9264,9264,9264,9264,9264,9264,9264,MONDO:0006868,neurogenic bowel,MONDO,disease,DISEASE_9264
9265,9265,9265,9265,9265,9265,9265,9265,MONDO:0035945,B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3),MONDO,disease,DISEASE_9265
9266,9266,9266,9266,9266,9266,9266,9266,MONDO:0002159_MONDO:0003285,fallopian tube leiomyosarcoma,MONDO_grouped,disease,DISEASE_9266
9267,9267,9267,9267,9267,9267,9267,9267,MONDO:0008704,short-limb skeletal dysplasia with severe combined immunodeficiency,MONDO,disease,DISEASE_9267
9268,9268,9268,9268,9268,9268,9268,9268,MONDO:0005607,chronic bronchitis,MONDO,disease,DISEASE_9268
9269,9269,9269,9269,9269,9269,9269,9269,MONDO:0010681,myelolymphatic insufficiency,MONDO,disease,DISEASE_9269
9270,9270,9270,9270,9270,9270,9270,9270,MONDO:0006385,primary intraosseous squamous cell carcinoma,MONDO,disease,DISEASE_9270
9271,9271,9271,9271,9271,9271,9271,9271,MONDO:0010586,X-linked Ehlers-Danlos syndrome,MONDO,disease,DISEASE_9271
9272,9272,9272,9272,9272,9272,9272,9272,MONDO:0957599,"epilepsy, early-onset",MONDO,disease,DISEASE_9272
9273,9273,9273,9273,9273,9273,9273,9273,MONDO:0006907,pilar sheath acanthoma,MONDO,disease,DISEASE_9273
9274,9274,9274,9274,9274,9274,9274,9274,MONDO:0013906_MONDO:0012926_MONDO:0013181_MONDO:0014385,amelogenesis imperfecta hypomaturation type 2A4,MONDO_grouped,disease,DISEASE_9274
9275,9275,9275,9275,9275,9275,9275,9275,MONDO:0000485,spasmodic dystonia,MONDO,disease,DISEASE_9275
9276,9276,9276,9276,9276,9276,9276,9276,MONDO:0043523,cadmium poisoning,MONDO,disease,DISEASE_9276
9277,9277,9277,9277,9277,9277,9277,9277,MONDO:0015014,"coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness",MONDO,disease,DISEASE_9277
9278,9278,9278,9278,9278,9278,9278,9278,MONDO:0003938,bladder colonic type adenocarcinoma,MONDO,disease,DISEASE_9278
9279,9279,9279,9279,9279,9279,9279,9279,MONDO:0968947,neurodevelopmental disorder plus optic atrophy,MONDO,disease,DISEASE_9279
9280,9280,9280,9280,9280,9280,9280,9280,MONDO:0004759,zoophilia,MONDO,disease,DISEASE_9280
9281,9281,9281,9281,9281,9281,9281,9281,MONDO:0957267,"neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity",MONDO,disease,DISEASE_9281
9282,9282,9282,9282,9282,9282,9282,9282,MONDO:0017330,malignancy diagnosed during pregnancy,MONDO,disease,DISEASE_9282
9283,9283,9283,9283,9283,9283,9283,9283,MONDO:0007655,fissured tongue,MONDO,disease,DISEASE_9283
9284,9284,9284,9284,9284,9284,9284,9284,MONDO:0014062,mitochondrial DNA deletion syndrome with progressive myopathy,MONDO,disease,DISEASE_9284
9285,9285,9285,9285,9285,9285,9285,9285,MONDO:0957097,hereditary hemolytic uremic syndrome,MONDO,disease,DISEASE_9285
9286,9286,9286,9286,9286,9286,9286,9286,MONDO:0016091,adult Krabbe disease,MONDO,disease,DISEASE_9286
9287,9287,9287,9287,9287,9287,9287,9287,MONDO:0005485_MONDO:0006730_MONDO:0002330,psychotic disorder,MONDO_grouped,disease,DISEASE_9287
9288,9288,9288,9288,9288,9288,9288,9288,MONDO:0014255,complement factor b deficiency,MONDO,disease,DISEASE_9288
9289,9289,9289,9289,9289,9289,9289,9289,MONDO:0013229,hot water reflex epilepsy,MONDO,disease,DISEASE_9289
9290,9290,9290,9290,9290,9290,9290,9290,MONDO:0016751,malignant perineurioma,MONDO,disease,DISEASE_9290
9291,9291,9291,9291,9291,9291,9291,9291,MONDO:0044323,Rahman syndrome,MONDO,disease,DISEASE_9291
9292,9292,9292,9292,9292,9292,9292,9292,MONDO:0003222,central nervous system melanocytic neoplasm,MONDO,disease,DISEASE_9292
9293,9293,9293,9293,9293,9293,9293,9293,MONDO:0005262,central nervous system cyst,MONDO,disease,DISEASE_9293
9294,9294,9294,9294,9294,9294,9294,9294,MONDO:0035357,portosinusoidal vascular disease,MONDO,disease,DISEASE_9294
9295,9295,9295,9295,9295,9295,9295,9295,MONDO:1011041,"oculocutaneous albinism, OCA2-related, Mexican tetra",MONDO,disease,DISEASE_9295
9296,9296,9296,9296,9296,9296,9296,9296,MONDO:0011157,Gomez-Lopez-Hernandez syndrome,MONDO,disease,DISEASE_9296
9297,9297,9297,9297,9297,9297,9297,9297,MONDO:0023022,dwarfism thin bones multiple fractures,MONDO,disease,DISEASE_9297
9298,9298,9298,9298,9298,9298,9298,9298,MONDO:0018005,spastic paraplegia-Paget disease of bone syndrome,MONDO,disease,DISEASE_9298
9299,9299,9299,9299,9299,9299,9299,9299,MONDO:1010477,"arrhythmogenic right ventricular cardiomyopathy, chimpanzee",MONDO,disease,DISEASE_9299
9300,9300,9300,9300,9300,9300,9300,9300,MONDO:0009285,gamma-glutamyl transpeptidase deficiency,MONDO,disease,DISEASE_9300
9301,9301,9301,9301,9301,9301,9301,9301,MONDO:0019972,dural sinus malformation,MONDO,disease,DISEASE_9301
9302,9302,9302,9302,9302,9302,9302,9302,MONDO:0009591_MONDO:0017730_MONDO:0017729,"metachromatic leukodystrophy, juvenile form",MONDO_grouped,disease,DISEASE_9302
9303,9303,9303,9303,9303,9303,9303,9303,MONDO:0011897,leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome,MONDO,disease,DISEASE_9303
9304,9304,9304,9304,9304,9304,9304,9304,MONDO:1010296,"Marfan syndrome, non-human animal",MONDO,disease,DISEASE_9304
9305,9305,9305,9305,9305,9305,9305,9305,MONDO:0018540,PFAPA syndrome,MONDO,disease,DISEASE_9305
9306,9306,9306,9306,9306,9306,9306,9306,MONDO:0011148,Spondylospinal thoracic dysostosis,MONDO,disease,DISEASE_9306
9307,9307,9307,9307,9307,9307,9307,9307,MONDO:0011508,"lymphoma, non-Hodgkin, familial",MONDO,disease,DISEASE_9307
9308,9308,9308,9308,9308,9308,9308,9308,MONDO:0019368,florid cemento-osseous dysplasia,MONDO,disease,DISEASE_9308
9309,9309,9309,9309,9309,9309,9309,9309,MONDO:0015855,isolated congenital breast hypoplasia/aplasia,MONDO,disease,DISEASE_9309
9310,9310,9310,9310,9310,9310,9310,9310,MONDO:0002283_MONDO:1011565_MONDO:1011564,neuroaxonal dystrophy,MONDO_grouped,disease,DISEASE_9310
9311,9311,9311,9311,9311,9311,9311,9311,MONDO:0009526,"fibular aplasia, tibial campomelia, and oligosyndactyly syndrome",MONDO,disease,DISEASE_9311
9312,9312,9312,9312,9312,9312,9312,9312,MONDO:0800502,childhood-onset self-limited focal epilepsy syndrome,MONDO,disease,DISEASE_9312
9313,9313,9313,9313,9313,9313,9313,9313,MONDO:0001390,transient refractive change,MONDO,disease,DISEASE_9313
9314,9314,9314,9314,9314,9314,9314,9314,MONDO:0004565_MONDO:0002803_MONDO:0002801,intestinal obstruction,MONDO_grouped,disease,DISEASE_9314
9315,9315,9315,9315,9315,9315,9315,9315,MONDO:0017277,partial deletion of chromosome 12,MONDO,disease,DISEASE_9315
9316,9316,9316,9316,9316,9316,9316,9316,MONDO:0011139,preaxial hallucal polydactyly,MONDO,disease,DISEASE_9316
9317,9317,9317,9317,9317,9317,9317,9317,MONDO:0003575,comedocarcinoma,MONDO,disease,DISEASE_9317
9318,9318,9318,9318,9318,9318,9318,9318,MONDO:0007502,"ear pits, posterior helical",MONDO,disease,DISEASE_9318
9319,9319,9319,9319,9319,9319,9319,9319,MONDO:0005505,dysembryoplastic neuroepithelial tumor,MONDO,disease,DISEASE_9319
9320,9320,9320,9320,9320,9320,9320,9320,MONDO:0000114,cerebelloparenchymal disorder,MONDO,disease,DISEASE_9320
9321,9321,9321,9321,9321,9321,9321,9321,MONDO:0044701,childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder,MONDO,disease,DISEASE_9321
9322,9322,9322,9322,9322,9322,9322,9322,MONDO:0007465,distichiasis with congenital anomalies of the heart and peripheral vasculature,MONDO,disease,DISEASE_9322
9323,9323,9323,9323,9323,9323,9323,9323,MONDO:0015254,schistosomiasis,MONDO,disease,DISEASE_9323
9324,9324,9324,9324,9324,9324,9324,9324,MONDO:0030705,Trichomonas prostatitis,MONDO,disease,DISEASE_9324
9325,9325,9325,9325,9325,9325,9325,9325,MONDO:0003365_MONDO:0003586_MONDO:0004832,esophagus leiomyosarcoma,MONDO_grouped,disease,DISEASE_9325
9326,9326,9326,9326,9326,9326,9326,9326,MONDO:0013359_MONDO:0011576_MONDO:0035321_MONDO:0035320_MONDO:0014875_MONDO:0016525,familial hyperaldosteronism,MONDO_grouped,disease,DISEASE_9326
9327,9327,9327,9327,9327,9327,9327,9327,MONDO:1011957,"hypochondroplastic dwarfism, non-human animal",MONDO,disease,DISEASE_9327
9328,9328,9328,9328,9328,9328,9328,9328,MONDO:0003058,microcystic meningioma,MONDO,disease,DISEASE_9328
9329,9329,9329,9329,9329,9329,9329,9329,MONDO:0003505,femoral cancer,MONDO,disease,DISEASE_9329
9330,9330,9330,9330,9330,9330,9330,9330,MONDO:0012257,Cerebrorenodigital syndrome,MONDO,disease,DISEASE_9330
9331,9331,9331,9331,9331,9331,9331,9331,MONDO:0005610,Kashin-Beck disease,MONDO,disease,DISEASE_9331
9332,9332,9332,9332,9332,9332,9332,9332,MONDO:0006732,drug-induced dyskinesia,MONDO,disease,DISEASE_9332
9333,9333,9333,9333,9333,9333,9333,9333,MONDO:0007865,knuckle pads,MONDO,disease,DISEASE_9333
9334,9334,9334,9334,9334,9334,9334,9334,MONDO:0003951,scrotal hemangioma,MONDO,disease,DISEASE_9334
9335,9335,9335,9335,9335,9335,9335,9335,MONDO:0010464,X-linked cerebral-cerebellar-coloboma syndrome syndrome,MONDO,disease,DISEASE_9335
9336,9336,9336,9336,9336,9336,9336,9336,MONDO:0012276,generalized epilepsy-paroxysmal dyskinesia syndrome,MONDO,disease,DISEASE_9336
9337,9337,9337,9337,9337,9337,9337,9337,MONDO:0700187,feline progressive histiocytosis,MONDO,disease,DISEASE_9337
9338,9338,9338,9338,9338,9338,9338,9338,MONDO:0002669,ampullary signet ring cell adenocarcinoma,MONDO,disease,DISEASE_9338
9339,9339,9339,9339,9339,9339,9339,9339,MONDO:0003917,heart lymphoma,MONDO,disease,DISEASE_9339
9340,9340,9340,9340,9340,9340,9340,9340,MONDO:0007746,"orthostatic hypotensive disorder, Streeten type",MONDO,disease,DISEASE_9340
9341,9341,9341,9341,9341,9341,9341,9341,MONDO:0018208,neurofibromatosis type 1 due to NF1 mutation or intragenic deletion,MONDO,disease,DISEASE_9341
9342,9342,9342,9342,9342,9342,9342,9342,MONDO:1011786,"perinatal weak calf syndrome, non-human animal",MONDO,disease,DISEASE_9342
9343,9343,9343,9343,9343,9343,9343,9343,MONDO:0018591,ITM2B amyloidosis,MONDO,disease,DISEASE_9343
9344,9344,9344,9344,9344,9344,9344,9344,MONDO:0019639_MONDO:0019646_MONDO:0019647,congenital megacalycosis,MONDO_grouped,disease,DISEASE_9344
9345,9345,9345,9345,9345,9345,9345,9345,MONDO:0005479,atrial tachycardia,MONDO,disease,DISEASE_9345
9346,9346,9346,9346,9346,9346,9346,9346,MONDO:0024304_MONDO:0100474_MONDO:0100475,ichthyosis vulgaris,MONDO_grouped,disease,DISEASE_9346
9347,9347,9347,9347,9347,9347,9347,9347,MONDO:0009602,"metaphyseal modeling abnormality, skin lesions, and spastic paraplegia",MONDO,disease,DISEASE_9347
9348,9348,9348,9348,9348,9348,9348,9348,MONDO:0045033_MONDO:0002312,opportunistic systemic mycosis,MONDO_grouped,disease,DISEASE_9348
9349,9349,9349,9349,9349,9349,9349,9349,MONDO:1010111,loin pain hematuria syndrome,MONDO,disease,DISEASE_9349
9350,9350,9350,9350,9350,9350,9350,9350,MONDO:0011290,"dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disability",MONDO,disease,DISEASE_9350
9351,9351,9351,9351,9351,9351,9351,9351,MONDO:0021945,hearing disorder,MONDO,disease,DISEASE_9351
9352,9352,9352,9352,9352,9352,9352,9352,MONDO:0009682,"muscular dystrophy, congenital, with rapid progression",MONDO,disease,DISEASE_9352
9353,9353,9353,9353,9353,9353,9353,9353,MONDO:0030266,immunodeficiency 80 with or without congenital cardiomyopathy,MONDO,disease,DISEASE_9353
9354,9354,9354,9354,9354,9354,9354,9354,MONDO:0009939,pulmonic stenosis and congenital nephrosis,MONDO,disease,DISEASE_9354
9355,9355,9355,9355,9355,9355,9355,9355,MONDO:0013300,commissural facial cleft,MONDO,disease,DISEASE_9355
9356,9356,9356,9356,9356,9356,9356,9356,MONDO:0018984,Oroya fever,MONDO,disease,DISEASE_9356
9357,9357,9357,9357,9357,9357,9357,9357,MONDO:0008975,otospondylomegaepiphyseal dysplasia,MONDO,disease,DISEASE_9357
9358,9358,9358,9358,9358,9358,9358,9358,MONDO:0018339,PrP systemic amyloidosis,MONDO,disease,DISEASE_9358
9359,9359,9359,9359,9359,9359,9359,9359,MONDO:0020682_MONDO:0014139_MONDO:0007526,"Ehlers-Danlos syndrome, spondylodysplastic type",MONDO_grouped,disease,DISEASE_9359
9360,9360,9360,9360,9360,9360,9360,9360,MONDO:0005699,cervicofacial actinomycosis,MONDO,disease,DISEASE_9360
9361,9361,9361,9361,9361,9361,9361,9361,MONDO:0021443,benign neoplasm of lymph node,MONDO,disease,DISEASE_9361
9362,9362,9362,9362,9362,9362,9362,9362,MONDO:0032575_MONDO:0957253,diarrhea,MONDO_grouped,disease,DISEASE_9362
9363,9363,9363,9363,9363,9363,9363,9363,MONDO:0014555_MONDO:0024548_MONDO:0011937_MONDO:0014923_MONDO:0054852_MONDO:0019347,peeling skin syndrome,MONDO_grouped,disease,DISEASE_9363
9364,9364,9364,9364,9364,9364,9364,9364,MONDO:0006551,alopecia mucinosa,MONDO,disease,DISEASE_9364
9365,9365,9365,9365,9365,9365,9365,9365,MONDO:0018570_MONDO:0000313_MONDO:0600009_MONDO:1011207_MONDO:1011208,hypophosphatasia,MONDO_grouped,disease,DISEASE_9365
9366,9366,9366,9366,9366,9366,9366,9366,MONDO:0005721,coxsackievirus infectious disease,MONDO,disease,DISEASE_9366
9367,9367,9367,9367,9367,9367,9367,9367,MONDO:0017521_MONDO:0017522,"hyperphalangy, unilateral",MONDO_grouped,disease,DISEASE_9367
9368,9368,9368,9368,9368,9368,9368,9368,MONDO:0023530,kallikrein hypertension,MONDO,disease,DISEASE_9368
9369,9369,9369,9369,9369,9369,9369,9369,MONDO:0000662,amusia,MONDO,disease,DISEASE_9369
9370,9370,9370,9370,9370,9370,9370,9370,MONDO:0700096,human disease,MONDO,disease,DISEASE_9370
9371,9371,9371,9371,9371,9371,9371,9371,MONDO:0003621,small intestinal vasoactive intestinal peptide producing tumor,MONDO,disease,DISEASE_9371
9372,9372,9372,9372,9372,9372,9372,9372,MONDO:0020696,vitamin B12 deficiency,MONDO,disease,DISEASE_9372
9373,9373,9373,9373,9373,9373,9373,9373,MONDO:1012845,"neuropathy with splayed forelimbs, UCHL1-related, cattle",MONDO,disease,DISEASE_9373
9374,9374,9374,9374,9374,9374,9374,9374,MONDO:0004428,alveoli adenoma,MONDO,disease,DISEASE_9374
9375,9375,9375,9375,9375,9375,9375,9375,MONDO:1012339,"reduced glutathione deficiency, sheep",MONDO,disease,DISEASE_9375
9376,9376,9376,9376,9376,9376,9376,9376,MONDO:0000284,"Hantavirus hemorrhagic fever with renal syndrome, Puumala virus type",MONDO,disease,DISEASE_9376
9377,9377,9377,9377,9377,9377,9377,9377,MONDO:0015524,hyperplastic polyposis syndrome,MONDO,disease,DISEASE_9377
9378,9378,9378,9378,9378,9378,9378,9378,MONDO:0002568,tracheal stenosis,MONDO,disease,DISEASE_9378
9379,9379,9379,9379,9379,9379,9379,9379,MONDO:0016757,malignant triton tumor,MONDO,disease,DISEASE_9379
9380,9380,9380,9380,9380,9380,9380,9380,MONDO:0006306,mixed lobular and ductal breast carcinoma,MONDO,disease,DISEASE_9380
9381,9381,9381,9381,9381,9381,9381,9381,MONDO:1010162,"radial hemimelia, non-human animal",MONDO,disease,DISEASE_9381
9382,9382,9382,9382,9382,9382,9382,9382,MONDO:0014978_MONDO:0014783,obsolete preimplantation embryonic lethality,MONDO_grouped,disease,DISEASE_9382
9383,9383,9383,9383,9383,9383,9383,9383,MONDO:0800149,"immunodeficiency, common variable, due to APRIL deficiency",MONDO,disease,DISEASE_9383
9384,9384,9384,9384,9384,9384,9384,9384,MONDO:0700117,SLC6A3-related dopamine transporter deficiency syndrome,MONDO,disease,DISEASE_9384
9385,9385,9385,9385,9385,9385,9385,9385,MONDO:0001522,pyromania,MONDO,disease,DISEASE_9385
9386,9386,9386,9386,9386,9386,9386,9386,MONDO:0015159,multiple congenital anomalies/dysmorphic syndrome-intellectual disability,MONDO,disease,DISEASE_9386
9387,9387,9387,9387,9387,9387,9387,9387,MONDO:0006505,basal ganglia cerebrovascular disorder,MONDO,disease,DISEASE_9387
9388,9388,9388,9388,9388,9388,9388,9388,MONDO:0021054_MONDO:0002397_MONDO:0004943_MONDO:0002930_MONDO:0002426_MONDO:0002216_MONDO:0002900_MONDO:0007300,bone sarcoma,MONDO_grouped,disease,DISEASE_9388
9389,9389,9389,9389,9389,9389,9389,9389,MONDO:0018935_MONDO:0018689,hairy cell leukemia,MONDO_grouped,disease,DISEASE_9389
9390,9390,9390,9390,9390,9390,9390,9390,MONDO:0021322,malignant tumor of meninges,MONDO,disease,DISEASE_9390
9391,9391,9391,9391,9391,9391,9391,9391,MONDO:0006397,renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions,MONDO,disease,DISEASE_9391
9392,9392,9392,9392,9392,9392,9392,9392,MONDO:0010802,pancreatic hypoplasia-diabetes-congenital heart disease syndrome,MONDO,disease,DISEASE_9392
9393,9393,9393,9393,9393,9393,9393,9393,MONDO:0002764,urethra squamous cell carcinoma,MONDO,disease,DISEASE_9393
9394,9394,9394,9394,9394,9394,9394,9394,MONDO:0014810,pancytopenia due to IKZF1 mutations,MONDO,disease,DISEASE_9394
9395,9395,9395,9395,9395,9395,9395,9395,MONDO:0003250,benign granular cell tumor,MONDO,disease,DISEASE_9395
9396,9396,9396,9396,9396,9396,9396,9396,MONDO:0008600,trigger thumb,MONDO,disease,DISEASE_9396
9397,9397,9397,9397,9397,9397,9397,9397,MONDO:0975751,brain abnormalities-severe developmental delay-facial dysmorphism-intellectual disability syndrome due to MEF2C mutation,MONDO,disease,DISEASE_9397
9398,9398,9398,9398,9398,9398,9398,9398,MONDO:0002320,congenital nervous system disorder,MONDO,disease,DISEASE_9398
9399,9399,9399,9399,9399,9399,9399,9399,MONDO:0008417,"sclerocornea, autosomal dominant",MONDO,disease,DISEASE_9399
9400,9400,9400,9400,9400,9400,9400,9400,MONDO:0007294,central core myopathy,MONDO,disease,DISEASE_9400
9401,9401,9401,9401,9401,9401,9401,9401,MONDO:0022759,trisomy 22,MONDO,disease,DISEASE_9401
9402,9402,9402,9402,9402,9402,9402,9402,MONDO:1012735,"Y anomaly in low reproductive females, cattle",MONDO,disease,DISEASE_9402
9403,9403,9403,9403,9403,9403,9403,9403,MONDO:0002182,communication disorder,MONDO,disease,DISEASE_9403
9404,9404,9404,9404,9404,9404,9404,9404,MONDO:0009785,opsismodysplasia,MONDO,disease,DISEASE_9404
9405,9405,9405,9405,9405,9405,9405,9405,MONDO:0002198,vulvar glandular neoplasm,MONDO,disease,DISEASE_9405
9406,9406,9406,9406,9406,9406,9406,9406,MONDO:0004820,peripheral nerve schwannoma,MONDO,disease,DISEASE_9406
9407,9407,9407,9407,9407,9407,9407,9407,MONDO:0016838,16q24.3 microdeletion syndrome,MONDO,disease,DISEASE_9407
9408,9408,9408,9408,9408,9408,9408,9408,MONDO:0003186,esophageal adenoid cystic carcinoma,MONDO,disease,DISEASE_9408
9409,9409,9409,9409,9409,9409,9409,9409,MONDO:0859267_MONDO:0014368,tumor predisposition syndrome,MONDO_grouped,disease,DISEASE_9409
9410,9410,9410,9410,9410,9410,9410,9410,MONDO:0009276,Bernard-Soulier syndrome,MONDO,disease,DISEASE_9410
9411,9411,9411,9411,9411,9411,9411,9411,MONDO:0011412,familial encephalopathy with neuroserpin inclusion bodies,MONDO,disease,DISEASE_9411
9412,9412,9412,9412,9412,9412,9412,9412,MONDO:0009123_MONDO:0020751_MONDO:0005469_MONDO:0021272_MONDO:0015914,orthostatic hypotension,MONDO_grouped,disease,DISEASE_9412
9413,9413,9413,9413,9413,9413,9413,9413,MONDO:0009043_MONDO:0019995_MONDO:0020711,generalized resistance to thyroid hormone,MONDO_grouped,disease,DISEASE_9413
9414,9414,9414,9414,9414,9414,9414,9414,MONDO:0005502,dengue disease,MONDO,disease,DISEASE_9414
9415,9415,9415,9415,9415,9415,9415,9415,MONDO:0008568,thyroid hormone plasma membrane transport defect,MONDO,disease,DISEASE_9415
9416,9416,9416,9416,9416,9416,9416,9416,MONDO:0016910,partial deletion of the long arm of chromosome 11,MONDO,disease,DISEASE_9416
9417,9417,9417,9417,9417,9417,9417,9417,MONDO:0004778,epididymo-orchitis,MONDO,disease,DISEASE_9417
9418,9418,9418,9418,9418,9418,9418,9418,MONDO:0010367,SHOX-related short stature,MONDO,disease,DISEASE_9418
9419,9419,9419,9419,9419,9419,9419,9419,MONDO:0009070,D-glyceric aciduria,MONDO,disease,DISEASE_9419
9420,9420,9420,9420,9420,9420,9420,9420,MONDO:0021977,basaloid follicular hamartoma,MONDO,disease,DISEASE_9420
9421,9421,9421,9421,9421,9421,9421,9421,MONDO:0012400,cortical dysplasia-focal epilepsy syndrome,MONDO,disease,DISEASE_9421
9422,9422,9422,9422,9422,9422,9422,9422,MONDO:0018044,idiopathic hypersomnia,MONDO,disease,DISEASE_9422
9423,9423,9423,9423,9423,9423,9423,9423,MONDO:0005641,aleutian mink disease,MONDO,disease,DISEASE_9423
9424,9424,9424,9424,9424,9424,9424,9424,MONDO:0014135_MONDO:0014134_MONDO:0014136_MONDO:0958334_MONDO:0024533_MONDO:1011135_MONDO:1011136,"pulmonary hypertension, primary",MONDO_grouped,disease,DISEASE_9424
9425,9425,9425,9425,9425,9425,9425,9425,MONDO:0004104,splenic manifestation of hairy cell leukemia,MONDO,disease,DISEASE_9425
9426,9426,9426,9426,9426,9426,9426,9426,MONDO:0005172_MONDO:0005046,skeletal system disorder,MONDO_grouped,disease,DISEASE_9426
9427,9427,9427,9427,9427,9427,9427,9427,MONDO:1012653_MONDO:1012655_MONDO:1012656,"XY sex reversal, SRY-related, horse",MONDO_grouped,disease,DISEASE_9427
9428,9428,9428,9428,9428,9428,9428,9428,MONDO:1012000,"sudden acquired retinal degeneration syndrome, non-human animal",MONDO,disease,DISEASE_9428
9429,9429,9429,9429,9429,9429,9429,9429,MONDO:0002685,childhood choroid plexus carcinoma,MONDO,disease,DISEASE_9429
9430,9430,9430,9430,9430,9430,9430,9430,MONDO:1012750,"cleft palate, DLX6-related, dog",MONDO,disease,DISEASE_9430
9431,9431,9431,9431,9431,9431,9431,9431,MONDO:0036990,benign Leydig cell tumor,MONDO,disease,DISEASE_9431
9432,9432,9432,9432,9432,9432,9432,9432,MONDO:0002652,anus adenocarcinoma,MONDO,disease,DISEASE_9432
9433,9433,9433,9433,9433,9433,9433,9433,MONDO:0002762,esophagus verrucous carcinoma,MONDO,disease,DISEASE_9433
9434,9434,9434,9434,9434,9434,9434,9434,MONDO:0018903,sarcocystosis,MONDO,disease,DISEASE_9434
9435,9435,9435,9435,9435,9435,9435,9435,MONDO:0017596,diffuse large B-cell lymphoma of the central nervous system,MONDO,disease,DISEASE_9435
9436,9436,9436,9436,9436,9436,9436,9436,MONDO:0012660_MONDO:0012661_MONDO:0021012,susceptibility to visceral leishmaniasis,MONDO_grouped,disease,DISEASE_9436
9437,9437,9437,9437,9437,9437,9437,9437,MONDO:1012664,"mucopolysaccharidosis II, Kaka",MONDO,disease,DISEASE_9437
9438,9438,9438,9438,9438,9438,9438,9438,MONDO:0021485,benign neoplasm of iris,MONDO,disease,DISEASE_9438
9439,9439,9439,9439,9439,9439,9439,9439,MONDO:0100311,sensory ataxia,MONDO,disease,DISEASE_9439
9440,9440,9440,9440,9440,9440,9440,9440,MONDO:0007721,hiatus hernia,MONDO,disease,DISEASE_9440
9441,9441,9441,9441,9441,9441,9441,9441,MONDO:0001861,malignant parietal pleura tumor,MONDO,disease,DISEASE_9441
9442,9442,9442,9442,9442,9442,9442,9442,MONDO:0014352_MONDO:0032837_MONDO:0000816,abdominal obesity-metabolic syndrome,MONDO_grouped,disease,DISEASE_9442
9443,9443,9443,9443,9443,9443,9443,9443,MONDO:0014277_MONDO:0958037_MONDO:0007729_MONDO:0000158,developmental dysplasia of the hip,MONDO_grouped,disease,DISEASE_9443
9444,9444,9444,9444,9444,9444,9444,9444,MONDO:0004492,mediastinitis,MONDO,disease,DISEASE_9444
9445,9445,9445,9445,9445,9445,9445,9445,MONDO:0013058_MONDO:0024555_MONDO:0013490_MONDO:0957533_MONDO:0000137_MONDO:0011391,cystic leukoencephalopathy without megalencephaly,MONDO_grouped,disease,DISEASE_9445
9446,9446,9446,9446,9446,9446,9446,9446,MONDO:0018629,focal stiff limb syndrome,MONDO,disease,DISEASE_9446
9447,9447,9447,9447,9447,9447,9447,9447,MONDO:0019167,immunoglobulin A vasculitis,MONDO,disease,DISEASE_9447
9448,9448,9448,9448,9448,9448,9448,9448,MONDO:0016922,partial duplication of chromosome 2,MONDO,disease,DISEASE_9448
9449,9449,9449,9449,9449,9449,9449,9449,MONDO:1011070,"urolithiasis, long-tailed chinchilla",MONDO,disease,DISEASE_9449
9450,9450,9450,9450,9450,9450,9450,9450,MONDO:0004605,chronic ulcer of skin,MONDO,disease,DISEASE_9450
9451,9451,9451,9451,9451,9451,9451,9451,MONDO:0024746_MONDO:0004048,immature teratoma,MONDO_grouped,disease,DISEASE_9451
9452,9452,9452,9452,9452,9452,9452,9452,MONDO:0032908,CEBALID syndrome,MONDO,disease,DISEASE_9452
9453,9453,9453,9453,9453,9453,9453,9453,MONDO:0004381,pancreatic intraductal papillary-mucinous neoplasm with low grade dysplasia,MONDO,disease,DISEASE_9453
9454,9454,9454,9454,9454,9454,9454,9454,MONDO:0014069,syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome,MONDO,disease,DISEASE_9454
9455,9455,9455,9455,9455,9455,9455,9455,MONDO:0007080,glucocorticoid-remediable aldosteronism,MONDO,disease,DISEASE_9455
9456,9456,9456,9456,9456,9456,9456,9456,MONDO:1010252,"succinic semialdehyde dehydrogenase deficiency, non-human animal",MONDO,disease,DISEASE_9456
9457,9457,9457,9457,9457,9457,9457,9457,MONDO:0005163,simian immunodeficiency virus infection,MONDO,disease,DISEASE_9457
9458,9458,9458,9458,9458,9458,9458,9458,MONDO:0005039_MONDO:0002149_MONDO:0003150_MONDO:0002263,reproductive system disorder,MONDO_grouped,disease,DISEASE_9458
9459,9459,9459,9459,9459,9459,9459,9459,MONDO:0005830,lumpy skin disease,MONDO,disease,DISEASE_9459
9460,9460,9460,9460,9460,9460,9460,9460,MONDO:0007632,"obsolete fragile site, Distamycin a type, rare, fra(16)(q22.1)",MONDO,disease,DISEASE_9460
9461,9461,9461,9461,9461,9461,9461,9461,MONDO:1012495,"symmetrical onychomadesis, dog",MONDO,disease,DISEASE_9461
9462,9462,9462,9462,9462,9462,9462,9462,MONDO:1010292,"ankylosing spondylitis, non-human animal",MONDO,disease,DISEASE_9462
9463,9463,9463,9463,9463,9463,9463,9463,MONDO:0010700,optic atrophy--spastic paraplegia syndrome,MONDO,disease,DISEASE_9463
9464,9464,9464,9464,9464,9464,9464,9464,MONDO:1012823_MONDO:1012824,"split spinal cord malformation type I, cattle",MONDO_grouped,disease,DISEASE_9464
9465,9465,9465,9465,9465,9465,9465,9465,MONDO:0023275,Graham-Boyle-Troxell syndrome,MONDO,disease,DISEASE_9465
9466,9466,9466,9466,9466,9466,9466,9466,MONDO:0004122,thymus small cell carcinoma,MONDO,disease,DISEASE_9466
9467,9467,9467,9467,9467,9467,9467,9467,MONDO:0008241,phosphoglycoprotein 1,MONDO,disease,DISEASE_9467
9468,9468,9468,9468,9468,9468,9468,9468,MONDO:0010539,X-linked mandibulofacial dysostosis,MONDO,disease,DISEASE_9468
9469,9469,9469,9469,9469,9469,9469,9469,MONDO:0700240,BEST1-related vitreoretinochoroidopathy,MONDO,disease,DISEASE_9469
9470,9470,9470,9470,9470,9470,9470,9470,MONDO:0019031,thrombocytopenia with congenital dyserythropoietic anemia,MONDO,disease,DISEASE_9470
9471,9471,9471,9471,9471,9471,9471,9471,MONDO:0021484,benign neoplasm of maxillary sinus,MONDO,disease,DISEASE_9471
9472,9472,9472,9472,9472,9472,9472,9472,MONDO:0033838,radiation-induced plexopathy,MONDO,disease,DISEASE_9472
9473,9473,9473,9473,9473,9473,9473,9473,MONDO:0016861,Alagille syndrome due to 20p12 microdeletion,MONDO,disease,DISEASE_9473
9474,9474,9474,9474,9474,9474,9474,9474,MONDO:0000297,baylisascariasis,MONDO,disease,DISEASE_9474
9475,9475,9475,9475,9475,9475,9475,9475,MONDO:0009176,epidermodysplasia verruciformis,MONDO,disease,DISEASE_9475
9476,9476,9476,9476,9476,9476,9476,9476,MONDO:0013129_MONDO:0011193_MONDO:0000455,cone dystrophy,MONDO_grouped,disease,DISEASE_9476
9477,9477,9477,9477,9477,9477,9477,9477,MONDO:0001886,midline cystocele,MONDO,disease,DISEASE_9477
9478,9478,9478,9478,9478,9478,9478,9478,MONDO:0044789,digital papillary eccrine carcinoma,MONDO,disease,DISEASE_9478
9479,9479,9479,9479,9479,9479,9479,9479,MONDO:0008937,"cerebellar ataxia, benign, with thermoanalgesia",MONDO,disease,DISEASE_9479
9480,9480,9480,9480,9480,9480,9480,9480,MONDO:0009886,pleoconial myopathy with salt craving,MONDO,disease,DISEASE_9480
9481,9481,9481,9481,9481,9481,9481,9481,MONDO:0975799,brain malformation renal syndrome,MONDO,disease,DISEASE_9481
9482,9482,9482,9482,9482,9482,9482,9482,MONDO:0002453,retrocochlear disease,MONDO,disease,DISEASE_9482
9483,9483,9483,9483,9483,9483,9483,9483,MONDO:0016070,hereditary gingival fibromatosis,MONDO,disease,DISEASE_9483
9484,9484,9484,9484,9484,9484,9484,9484,MONDO:0009694,myeloperoxidase deficiency,MONDO,disease,DISEASE_9484
9485,9485,9485,9485,9485,9485,9485,9485,MONDO:0007616,"fibula, recurrent dislocation of head of",MONDO,disease,DISEASE_9485
9486,9486,9486,9486,9486,9486,9486,9486,MONDO:0025420,"gastroenteritis, transmissible, of swine",MONDO,disease,DISEASE_9486
9487,9487,9487,9487,9487,9487,9487,9487,MONDO:0031422,familial mucolipidosis,MONDO,disease,DISEASE_9487
9488,9488,9488,9488,9488,9488,9488,9488,MONDO:0018365,malignant non-epithelial tumor of ovary,MONDO,disease,DISEASE_9488
9489,9489,9489,9489,9489,9489,9489,9489,MONDO:0000921,ampulla of vater neoplasm,MONDO,disease,DISEASE_9489
9490,9490,9490,9490,9490,9490,9490,9490,MONDO:0005146,post-traumatic stress disorder,MONDO,disease,DISEASE_9490
9491,9491,9491,9491,9491,9491,9491,9491,MONDO:0011548,"cerebral palsy, ataxic, autosomal recessive",MONDO,disease,DISEASE_9491
9492,9492,9492,9492,9492,9492,9492,9492,MONDO:0004281,vulvar eccrine porocarcinoma,MONDO,disease,DISEASE_9492
9493,9493,9493,9493,9493,9493,9493,9493,MONDO:0001291,brain compression,MONDO,disease,DISEASE_9493
9494,9494,9494,9494,9494,9494,9494,9494,MONDO:0008251,familial pityriasis rubra pilaris,MONDO,disease,DISEASE_9494
9495,9495,9495,9495,9495,9495,9495,9495,MONDO:0018625,classic stiff person syndrome,MONDO,disease,DISEASE_9495
9496,9496,9496,9496,9496,9496,9496,9496,MONDO:0019349,Sotos syndrome,MONDO,disease,DISEASE_9496
9497,9497,9497,9497,9497,9497,9497,9497,MONDO:0006142,cervical small cell carcinoma,MONDO,disease,DISEASE_9497
9498,9498,9498,9498,9498,9498,9498,9498,MONDO:0013115,RIN2 syndrome,MONDO,disease,DISEASE_9498
9499,9499,9499,9499,9499,9499,9499,9499,MONDO:1012197,"ocular squamous cell carcinoma, cattle",MONDO,disease,DISEASE_9499
9500,9500,9500,9500,9500,9500,9500,9500,MONDO:0014741,DeSanto-Shinawi syndrome due to WAC point mutation,MONDO,disease,DISEASE_9500
9501,9501,9501,9501,9501,9501,9501,9501,MONDO:0019758,obsolete midline interhemispheric variant of holoprosencephaly,MONDO,disease,DISEASE_9501
9502,9502,9502,9502,9502,9502,9502,9502,MONDO:0010115,thoracic dysplasia-hydrocephalus syndrome,MONDO,disease,DISEASE_9502
9503,9503,9503,9503,9503,9503,9503,9503,MONDO:0008089,"neutropenia, chronic familial",MONDO,disease,DISEASE_9503
9504,9504,9504,9504,9504,9504,9504,9504,MONDO:0000242,tinea barbae,MONDO,disease,DISEASE_9504
9505,9505,9505,9505,9505,9505,9505,9505,MONDO:0021158_MONDO:0001125,gonococcal epididymo-orchitis,MONDO_grouped,disease,DISEASE_9505
9506,9506,9506,9506,9506,9506,9506,9506,MONDO:0017309,neonatal Marfan syndrome,MONDO,disease,DISEASE_9506
9507,9507,9507,9507,9507,9507,9507,9507,MONDO:0032797,"myopathy, congenital, with tremor",MONDO,disease,DISEASE_9507
9508,9508,9508,9508,9508,9508,9508,9508,MONDO:1012448,"mammary tumor, dog",MONDO,disease,DISEASE_9508
9509,9509,9509,9509,9509,9509,9509,9509,MONDO:0024616,tympanitis,MONDO,disease,DISEASE_9509
9510,9510,9510,9510,9510,9510,9510,9510,MONDO:0023644,lip and oral cavity carcinoma,MONDO,disease,DISEASE_9510
9511,9511,9511,9511,9511,9511,9511,9511,MONDO:0010625,"immunodeficiency, X-linked, with deficiency of 115,000 Dalton surface glycoprotein",MONDO,disease,DISEASE_9511
9512,9512,9512,9512,9512,9512,9512,9512,MONDO:0009629_MONDO:0014343_MONDO:0015426,Desbuquois dysplasia,MONDO_grouped,disease,DISEASE_9512
9513,9513,9513,9513,9513,9513,9513,9513,MONDO:0005413,cystic fibrosis associated meconium ileus,MONDO,disease,DISEASE_9513
9514,9514,9514,9514,9514,9514,9514,9514,MONDO:0009867,lethal congenital glycogen storage disease of heart,MONDO,disease,DISEASE_9514
9515,9515,9515,9515,9515,9515,9515,9515,MONDO:0003209,thymus gland adenocarcinoma,MONDO,disease,DISEASE_9515
9516,9516,9516,9516,9516,9516,9516,9516,MONDO:0032703,"short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis",MONDO,disease,DISEASE_9516
9517,9517,9517,9517,9517,9517,9517,9517,MONDO:0008364,Raynaud disease,MONDO,disease,DISEASE_9517
9518,9518,9518,9518,9518,9518,9518,9518,MONDO:1011662,"stomach ulcer, non-human animal",MONDO,disease,DISEASE_9518
9519,9519,9519,9519,9519,9519,9519,9519,MONDO:0015007,"spastic paraplegia, intellectual disability, nystagmus, and obesity",MONDO,disease,DISEASE_9519
9520,9520,9520,9520,9520,9520,9520,9520,MONDO:1010523,"cleft palate, spectacled flying fox",MONDO,disease,DISEASE_9520
9521,9521,9521,9521,9521,9521,9521,9521,MONDO:0007217_MONDO:0007215_MONDO:0013244_MONDO:0007216_MONDO:0007223_MONDO:0014032_MONDO:0012658_MONDO:0007218_MONDO:0007221_MONDO:0014798_MONDO:0011757_MONDO:0007220_MONDO:0007222_MONDO:0019679_MONDO:0019677_MONDO:0019676_MONDO:0021004_MONDO:0019678_MONDO:0020701_MONDO:0022599_MONDO:1010800_MONDO:1010801_MONDO:1010802_MONDO:1010803,brachydactyly,MONDO_grouped,disease,DISEASE_9521
9522,9522,9522,9522,9522,9522,9522,9522,MONDO:0001165,tongue disorder,MONDO,disease,DISEASE_9522
9523,9523,9523,9523,9523,9523,9523,9523,MONDO:0009074,facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome,MONDO,disease,DISEASE_9523
9524,9524,9524,9524,9524,9524,9524,9524,MONDO:1011660,"megaesophagus, non-human animal",MONDO,disease,DISEASE_9524
9525,9525,9525,9525,9525,9525,9525,9525,MONDO:0009086,deafness-small bowel diverticulosis-neuropathy syndrome,MONDO,disease,DISEASE_9525
9526,9526,9526,9526,9526,9526,9526,9526,MONDO:0012700,"renal tubular acidosis, distal, 4, with hemolytic anemia",MONDO,disease,DISEASE_9526
9527,9527,9527,9527,9527,9527,9527,9527,MONDO:0017927,severe lateral tibial bowing with short stature,MONDO,disease,DISEASE_9527
9528,9528,9528,9528,9528,9528,9528,9528,MONDO:0030047,"microcephaly, developmental delay, and brittle hair syndrome",MONDO,disease,DISEASE_9528
9529,9529,9529,9529,9529,9529,9529,9529,MONDO:0005551,eye allergy,MONDO,disease,DISEASE_9529
9530,9530,9530,9530,9530,9530,9530,9530,MONDO:0007849,keratitis fugax hereditaria,MONDO,disease,DISEASE_9530
9531,9531,9531,9531,9531,9531,9531,9531,MONDO:0023243,glass-chapman-hockley syndrome,MONDO,disease,DISEASE_9531
9532,9532,9532,9532,9532,9532,9532,9532,MONDO:0008227,peripheral dysostosis,MONDO,disease,DISEASE_9532
9533,9533,9533,9533,9533,9533,9533,9533,MONDO:0859257,intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism,MONDO,disease,DISEASE_9533
9534,9534,9534,9534,9534,9534,9534,9534,MONDO:0011063,"hidrotic ectodermal dysplasia, Christianson-Fourie type",MONDO,disease,DISEASE_9534
9535,9535,9535,9535,9535,9535,9535,9535,MONDO:0003665_MONDO:0004487,cervical endometrioid adenocarcinoma,MONDO_grouped,disease,DISEASE_9535
9536,9536,9536,9536,9536,9536,9536,9536,MONDO:0007572,primary familial polycythemia due to EPO receptor mutation,MONDO,disease,DISEASE_9536
9537,9537,9537,9537,9537,9537,9537,9537,MONDO:1030004,Mollaret’s meningitis,MONDO,disease,DISEASE_9537
9538,9538,9538,9538,9538,9538,9538,9538,MONDO:1011330,"lymphoid system disorder, non-human animal",MONDO,disease,DISEASE_9538
9539,9539,9539,9539,9539,9539,9539,9539,MONDO:1012225,"progressive myopathy, pig",MONDO,disease,DISEASE_9539
9540,9540,9540,9540,9540,9540,9540,9540,MONDO:0015995,melorheostosis with osteopoikilosis,MONDO,disease,DISEASE_9540
9541,9541,9541,9541,9541,9541,9541,9541,MONDO:0020123,metabolic myopathy,MONDO,disease,DISEASE_9541
9542,9542,9542,9542,9542,9542,9542,9542,MONDO:0001162,impulse control disorder,MONDO,disease,DISEASE_9542
9543,9543,9543,9543,9543,9543,9543,9543,MONDO:1012294,"polymicrogyria and asymmetrical ventricular dilation, dog",MONDO,disease,DISEASE_9543
9544,9544,9544,9544,9544,9544,9544,9544,MONDO:0004337,perianal skin Paget disease,MONDO,disease,DISEASE_9544
9545,9545,9545,9545,9545,9545,9545,9545,MONDO:0011172,otofacioosseous-gonadal syndrome,MONDO,disease,DISEASE_9545
9546,9546,9546,9546,9546,9546,9546,9546,MONDO:0018063,nodular non-suppurative panniculitis,MONDO,disease,DISEASE_9546
9547,9547,9547,9547,9547,9547,9547,9547,MONDO:0010274,testicular germ cell tumor 1,MONDO,disease,DISEASE_9547
9548,9548,9548,9548,9548,9548,9548,9548,MONDO:0958192_MONDO:0958179_MONDO:0011612,glycine encephalopathy,MONDO_grouped,disease,DISEASE_9548
9549,9549,9549,9549,9549,9549,9549,9549,MONDO:0005794_MONDO:0004609_MONDO:0005780_MONDO:0005785_MONDO:0100359,Herpesviridae infectious disease,MONDO_grouped,disease,DISEASE_9549
9550,9550,9550,9550,9550,9550,9550,9550,MONDO:1011405,"Diamond-Blackfan anemia, non-human animal",MONDO,disease,DISEASE_9550
9551,9551,9551,9551,9551,9551,9551,9551,MONDO:0859598,erythroleukemia,MONDO,disease,DISEASE_9551
9552,9552,9552,9552,9552,9552,9552,9552,MONDO:1012312_MONDO:1012313_MONDO:1012314,"congenital erythropoietic porphyria, domestic cat",MONDO_grouped,disease,DISEASE_9552
9553,9553,9553,9553,9553,9553,9553,9553,MONDO:0000734,Ohdo syndrome and variants,MONDO,disease,DISEASE_9553
9554,9554,9554,9554,9554,9554,9554,9554,MONDO:0007683,Grant syndrome,MONDO,disease,DISEASE_9554
9555,9555,9555,9555,9555,9555,9555,9555,MONDO:0011670,Ehlers-Danlos syndrome due to tenascin-X deficiency,MONDO,disease,DISEASE_9555
9556,9556,9556,9556,9556,9556,9556,9556,MONDO:0012805,childhood onset GLUT1 deficiency syndrome 2,MONDO,disease,DISEASE_9556
9557,9557,9557,9557,9557,9557,9557,9557,MONDO:0021010_MONDO:0024673,skin lymphangiosarcoma,MONDO_grouped,disease,DISEASE_9557
9558,9558,9558,9558,9558,9558,9558,9558,MONDO:0008643,"veins, pattern of, on anterior thorax",MONDO,disease,DISEASE_9558
9559,9559,9559,9559,9559,9559,9559,9559,MONDO:0012155,choanal atresia,MONDO,disease,DISEASE_9559
9560,9560,9560,9560,9560,9560,9560,9560,MONDO:0017325,early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation,MONDO,disease,DISEASE_9560
9561,9561,9561,9561,9561,9561,9561,9561,MONDO:0002884,nail disorder,MONDO,disease,DISEASE_9561
9562,9562,9562,9562,9562,9562,9562,9562,MONDO:0020732,progeria,MONDO,disease,DISEASE_9562
9563,9563,9563,9563,9563,9563,9563,9563,MONDO:0010886,2q37 microdeletion syndrome,MONDO,disease,DISEASE_9563
9564,9564,9564,9564,9564,9564,9564,9564,MONDO:0012138_MONDO:0011688_MONDO:0000171_MONDO:0018276_MONDO:0000172_MONDO:0000173,muscular dystrophy-dystroglycanopathy,MONDO_grouped,disease,DISEASE_9564
9565,9565,9565,9565,9565,9565,9565,9565,MONDO:0003318,mixed cell type kidney Wilms' tumor,MONDO,disease,DISEASE_9565
9566,9566,9566,9566,9566,9566,9566,9566,MONDO:0044788,perihilar intrahepatic cholangiocarcinoma,MONDO,disease,DISEASE_9566
9567,9567,9567,9567,9567,9567,9567,9567,MONDO:0100209_MONDO:0026404_MONDO:0026426,"X inactivation, familial skewed",MONDO_grouped,disease,DISEASE_9567
9568,9568,9568,9568,9568,9568,9568,9568,MONDO:0020383,fundus pulverulentus,MONDO,disease,DISEASE_9568
9569,9569,9569,9569,9569,9569,9569,9569,MONDO:0012964,chromosome 15q26-qter deletion syndrome,MONDO,disease,DISEASE_9569
9570,9570,9570,9570,9570,9570,9570,9570,MONDO:0014273,microcephaly-thin corpus callosum-intellectual disability syndrome,MONDO,disease,DISEASE_9570
9571,9571,9571,9571,9571,9571,9571,9571,MONDO:0016580_MONDO:0017248_MONDO:0017249_MONDO:0017250_MONDO:0017251_MONDO:0017252,congenital pulmonary airway malformation,MONDO_grouped,disease,DISEASE_9571
9572,9572,9572,9572,9572,9572,9572,9572,MONDO:0001260,cercarial dermatitis,MONDO,disease,DISEASE_9572
9573,9573,9573,9573,9573,9573,9573,9573,MONDO:0007038,Achoo syndrome,MONDO,disease,DISEASE_9573
9574,9574,9574,9574,9574,9574,9574,9574,MONDO:0700121,ACTL6A-related BAFopathy,MONDO,disease,DISEASE_9574
9575,9575,9575,9575,9575,9575,9575,9575,MONDO:0004411,duodenal gastrin-producing neuroendocrine tumor,MONDO,disease,DISEASE_9575
9576,9576,9576,9576,9576,9576,9576,9576,MONDO:0003849,clivus chordoma,MONDO,disease,DISEASE_9576
9577,9577,9577,9577,9577,9577,9577,9577,MONDO:0018642,NIK deficiency,MONDO,disease,DISEASE_9577
9578,9578,9578,9578,9578,9578,9578,9578,MONDO:0005684,bulbar polio,MONDO,disease,DISEASE_9578
9579,9579,9579,9579,9579,9579,9579,9579,MONDO:0019071,pure hair and nail ectodermal dysplasia,MONDO,disease,DISEASE_9579
9580,9580,9580,9580,9580,9580,9580,9580,MONDO:0006022,acidosis disorder,MONDO,disease,DISEASE_9580
9581,9581,9581,9581,9581,9581,9581,9581,MONDO:0011036,porencephaly-cerebellar hypoplasia-internal malformations syndrome,MONDO,disease,DISEASE_9581
9582,9582,9582,9582,9582,9582,9582,9582,MONDO:0014309,obesity due to CEP19 deficiency,MONDO,disease,DISEASE_9582
9583,9583,9583,9583,9583,9583,9583,9583,MONDO:0001353,Bordetella parapertussis infectious disease,MONDO,disease,DISEASE_9583
9584,9584,9584,9584,9584,9584,9584,9584,MONDO:0009708,"myopathy, myosin storage, autosomal recessive",MONDO,disease,DISEASE_9584
9585,9585,9585,9585,9585,9585,9585,9585,MONDO:0018608,pure autonomic failure,MONDO,disease,DISEASE_9585
9586,9586,9586,9586,9586,9586,9586,9586,MONDO:0008932,premature centromere division,MONDO,disease,DISEASE_9586
9587,9587,9587,9587,9587,9587,9587,9587,MONDO:0016994,microcephalic osteodysplastic primordial dwarfism types I and III,MONDO,disease,DISEASE_9587
9588,9588,9588,9588,9588,9588,9588,9588,MONDO:0006861,myeloid sarcoma,MONDO,disease,DISEASE_9588
9589,9589,9589,9589,9589,9589,9589,9589,MONDO:0004979,asthma,MONDO,disease,DISEASE_9589
9590,9590,9590,9590,9590,9590,9590,9590,MONDO:0001509,endocrine exophthalmos,MONDO,disease,DISEASE_9590
9591,9591,9591,9591,9591,9591,9591,9591,MONDO:0010812,"macrocytosis, familial",MONDO,disease,DISEASE_9591
9592,9592,9592,9592,9592,9592,9592,9592,MONDO:0060549,"congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay",MONDO,disease,DISEASE_9592
9593,9593,9593,9593,9593,9593,9593,9593,MONDO:0003747,telangiectatic glomangioma,MONDO,disease,DISEASE_9593
9594,9594,9594,9594,9594,9594,9594,9594,MONDO:0019456,acute myeloid leukemia with multilineage dysplasia,MONDO,disease,DISEASE_9594
9595,9595,9595,9595,9595,9595,9595,9595,MONDO:0017188,diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency,MONDO,disease,DISEASE_9595
9596,9596,9596,9596,9596,9596,9596,9596,MONDO:0015435,ring chromosome 19,MONDO,disease,DISEASE_9596
9597,9597,9597,9597,9597,9597,9597,9597,MONDO:0859214,Marbach-Schaaf neurodevelopmental syndrome,MONDO,disease,DISEASE_9597
9598,9598,9598,9598,9598,9598,9598,9598,MONDO:0013980_MONDO:0007047_MONDO:0008292_MONDO:0007858_MONDO:0019332_MONDO:0017675,"palmoplantar keratoderma, punctate",MONDO_grouped,disease,DISEASE_9598
9599,9599,9599,9599,9599,9599,9599,9599,MONDO:0015493,"lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy",MONDO,disease,DISEASE_9599
9600,9600,9600,9600,9600,9600,9600,9600,MONDO:0100175,TTN-related myopathy,MONDO,disease,DISEASE_9600
9601,9601,9601,9601,9601,9601,9601,9601,MONDO:0015535,xanthoma disseminatum,MONDO,disease,DISEASE_9601
9602,9602,9602,9602,9602,9602,9602,9602,MONDO:0020010,infectious disorder of the nervous system,MONDO,disease,DISEASE_9602
9603,9603,9603,9603,9603,9603,9603,9603,MONDO:0005810,infectious mononucleosis,MONDO,disease,DISEASE_9603
9604,9604,9604,9604,9604,9604,9604,9604,MONDO:1011796,"high-frequency tremor, non-human animal",MONDO,disease,DISEASE_9604
9605,9605,9605,9605,9605,9605,9605,9605,MONDO:0007971,delayed membranous cranial ossification,MONDO,disease,DISEASE_9605
9606,9606,9606,9606,9606,9606,9606,9606,MONDO:0003169,diencephalic astrocytomas,MONDO,disease,DISEASE_9606
9607,9607,9607,9607,9607,9607,9607,9607,MONDO:0008412,intestinal schistosomiasis,MONDO,disease,DISEASE_9607
9608,9608,9608,9608,9608,9608,9608,9608,MONDO:0958231,"neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism",MONDO,disease,DISEASE_9608
9609,9609,9609,9609,9609,9609,9609,9609,MONDO:1011203,"osteopetrosis with gingival hamartomas, cattle",MONDO,disease,DISEASE_9609
9610,9610,9610,9610,9610,9610,9610,9610,MONDO:0017502,"acheiria, unilateral",MONDO,disease,DISEASE_9610
9611,9611,9611,9611,9611,9611,9611,9611,MONDO:0017519_MONDO:0017520,"symbrachydactyly of hand and foot, unilateral",MONDO_grouped,disease,DISEASE_9611
9612,9612,9612,9612,9612,9612,9612,9612,MONDO:0016529,duplication of urethra,MONDO,disease,DISEASE_9612
9613,9613,9613,9613,9613,9613,9613,9613,MONDO:0020690_MONDO:0002501_MONDO:0000457_MONDO:0004363_MONDO:0016712,adult glioblastoma,MONDO_grouped,disease,DISEASE_9613
9614,9614,9614,9614,9614,9614,9614,9614,MONDO:0005594,severe cutaneous adverse reaction,MONDO,disease,DISEASE_9614
9615,9615,9615,9615,9615,9615,9615,9615,MONDO:0024971,parturient paresis,MONDO,disease,DISEASE_9615
9616,9616,9616,9616,9616,9616,9616,9616,MONDO:0000381,infiltrating renal pelvis transitional cell carcinoma,MONDO,disease,DISEASE_9616
9617,9617,9617,9617,9617,9617,9617,9617,MONDO:0000461,nutritional biotin deficiency,MONDO,disease,DISEASE_9617
9618,9618,9618,9618,9618,9618,9618,9618,MONDO:0001116,mesenteric lymphadenitis,MONDO,disease,DISEASE_9618
9619,9619,9619,9619,9619,9619,9619,9619,MONDO:0958204_MONDO:0031031_MONDO:0032860_MONDO:0958203_MONDO:0032665_MONDO:0032789_MONDO:0014951_MONDO:0023657_MONDO:0029465_MONDO:0032729_MONDO:0957397_MONDO:0030891_MONDO:0030969_MONDO:0957288_MONDO:0032715_MONDO:0975838_MONDO:0030964_MONDO:0859333_MONDO:0968944_MONDO:0859373_MONDO:0030533_MONDO:0030968_MONDO:0030934_MONDO:0032662_MONDO:0957536,"intellectual developmental disorder, autosomal recessive",MONDO_grouped,disease,DISEASE_9619
9620,9620,9620,9620,9620,9620,9620,9620,MONDO:0100489_MONDO:0011314,"Graves disease, susceptibility to",MONDO_grouped,disease,DISEASE_9620
9621,9621,9621,9621,9621,9621,9621,9621,MONDO:0018043,Thomas syndrome,MONDO,disease,DISEASE_9621
9622,9622,9622,9622,9622,9622,9622,9622,MONDO:0023083,epimetaphyseal dysplasia cataract,MONDO,disease,DISEASE_9622
9623,9623,9623,9623,9623,9623,9623,9623,MONDO:0020579,mucositis,MONDO,disease,DISEASE_9623
9624,9624,9624,9624,9624,9624,9624,9624,MONDO:0018356,secondary neonatal autoimmune disease,MONDO,disease,DISEASE_9624
9625,9625,9625,9625,9625,9625,9625,9625,MONDO:0008958,"Klippel-Feil syndrome 2, autosomal recessive",MONDO,disease,DISEASE_9625
9626,9626,9626,9626,9626,9626,9626,9626,MONDO:0005538,proctitis,MONDO,disease,DISEASE_9626
9627,9627,9627,9627,9627,9627,9627,9627,MONDO:0004534,microglandular adenosis of breast,MONDO,disease,DISEASE_9627
9628,9628,9628,9628,9628,9628,9628,9628,MONDO:0006191,endometrial clear cell adenocarcinoma,MONDO,disease,DISEASE_9628
9629,9629,9629,9629,9629,9629,9629,9629,MONDO:0017413,Reunion island Larsen syndrome,MONDO,disease,DISEASE_9629
9630,9630,9630,9630,9630,9630,9630,9630,MONDO:0004275,osteosarcoma arising in bone Paget disease,MONDO,disease,DISEASE_9630
9631,9631,9631,9631,9631,9631,9631,9631,MONDO:0859181,DEGCAGS syndrome,MONDO,disease,DISEASE_9631
9632,9632,9632,9632,9632,9632,9632,9632,MONDO:0958122,idiopathic small fibers neuropathy,MONDO,disease,DISEASE_9632
9633,9633,9633,9633,9633,9633,9633,9633,MONDO:0001536_MONDO:0003369,vaginal leiomyoma,MONDO_grouped,disease,DISEASE_9633
9634,9634,9634,9634,9634,9634,9634,9634,MONDO:0007385,idiopathic spontaneous coronary artery dissection,MONDO,disease,DISEASE_9634
9635,9635,9635,9635,9635,9635,9635,9635,MONDO:0037398,pneumonia caused by pseudomonas aeruginosa infection,MONDO,disease,DISEASE_9635
9636,9636,9636,9636,9636,9636,9636,9636,MONDO:0020246,inherited vitreoretinopathy,MONDO,disease,DISEASE_9636
9637,9637,9637,9637,9637,9637,9637,9637,MONDO:0001812,parasitic eyelid infestation,MONDO,disease,DISEASE_9637
9638,9638,9638,9638,9638,9638,9638,9638,MONDO:0006899,pericoronitis,MONDO,disease,DISEASE_9638
9639,9639,9639,9639,9639,9639,9639,9639,MONDO:0004148,gallbladder papillary neoplasm with an associated invasive carcinoma,MONDO,disease,DISEASE_9639
9640,9640,9640,9640,9640,9640,9640,9640,MONDO:0003700,brachial plexus neoplasm,MONDO,disease,DISEASE_9640
9641,9641,9641,9641,9641,9641,9641,9641,MONDO:0008730,congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency,MONDO,disease,DISEASE_9641
9642,9642,9642,9642,9642,9642,9642,9642,MONDO:0044635,DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome,MONDO,disease,DISEASE_9642
9643,9643,9643,9643,9643,9643,9643,9643,MONDO:0016044_MONDO:0016064,cleft lip/palate,MONDO_grouped,disease,DISEASE_9643
9644,9644,9644,9644,9644,9644,9644,9644,MONDO:0000377,malignant Leydig cell tumor,MONDO,disease,DISEASE_9644
9645,9645,9645,9645,9645,9645,9645,9645,MONDO:0009468,pseudotumor cerebri,MONDO,disease,DISEASE_9645
9646,9646,9646,9646,9646,9646,9646,9646,MONDO:0018654,idiopathic dropped head syndrome,MONDO,disease,DISEASE_9646
9647,9647,9647,9647,9647,9647,9647,9647,MONDO:0002778,epidural spinal canal meningioma,MONDO,disease,DISEASE_9647
9648,9648,9648,9648,9648,9648,9648,9648,MONDO:0020396,anomaly of the tricuspid valve chordae,MONDO,disease,DISEASE_9648
9649,9649,9649,9649,9649,9649,9649,9649,MONDO:0043075,neuroaxonal dystrophy renal tubular acidosis,MONDO,disease,DISEASE_9649
9650,9650,9650,9650,9650,9650,9650,9650,MONDO:1011724,"immunodeficiency disease, non-human animal",MONDO,disease,DISEASE_9650
9651,9651,9651,9651,9651,9651,9651,9651,MONDO:0019455,acute panmyelosis with myelofibrosis,MONDO,disease,DISEASE_9651
9652,9652,9652,9652,9652,9652,9652,9652,MONDO:0011656_MONDO:0014792_MONDO:0008176,paget disease of bone,MONDO_grouped,disease,DISEASE_9652
9653,9653,9653,9653,9653,9653,9653,9653,MONDO:0012287,"Stickler syndrome, type I, nonsyndromic ocular",MONDO,disease,DISEASE_9653
9654,9654,9654,9654,9654,9654,9654,9654,MONDO:0025030,digital dermatitis in cattle,MONDO,disease,DISEASE_9654
9655,9655,9655,9655,9655,9655,9655,9655,MONDO:0017233_MONDO:0100087,familial Alzheimer-like prion disease,MONDO_grouped,disease,DISEASE_9655
9656,9656,9656,9656,9656,9656,9656,9656,MONDO:0005983,tinea favosa,MONDO,disease,DISEASE_9656
9657,9657,9657,9657,9657,9657,9657,9657,MONDO:1012667_MONDO:1012668,"von Willebrand disease II, dog",MONDO_grouped,disease,DISEASE_9657
9658,9658,9658,9658,9658,9658,9658,9658,MONDO:0021114_MONDO:0002829_MONDO:0003853_MONDO:0003419_MONDO:0003909_MONDO:0004120,Bartholin gland neoplasm,MONDO_grouped,disease,DISEASE_9658
9659,9659,9659,9659,9659,9659,9659,9659,MONDO:0005091,severe acute respiratory syndrome,MONDO,disease,DISEASE_9659
9660,9660,9660,9660,9660,9660,9660,9660,MONDO:0019211,isolated congenital anonychia,MONDO,disease,DISEASE_9660
9661,9661,9661,9661,9661,9661,9661,9661,MONDO:0850123,autonomic nervous system benign neoplasm,MONDO,disease,DISEASE_9661
9662,9662,9662,9662,9662,9662,9662,9662,MONDO:0012099,AICA-ribosiduria,MONDO,disease,DISEASE_9662
9663,9663,9663,9663,9663,9663,9663,9663,MONDO:0016833,14q12 microdeletion syndrome,MONDO,disease,DISEASE_9663
9664,9664,9664,9664,9664,9664,9664,9664,MONDO:0019934,polyploidy,MONDO,disease,DISEASE_9664
9665,9665,9665,9665,9665,9665,9665,9665,MONDO:0100133,mitochondrial complex I deficiency,MONDO,disease,DISEASE_9665
9666,9666,9666,9666,9666,9666,9666,9666,MONDO:1012783_MONDO:1012784_MONDO:1012785_MONDO:1012805_MONDO:1012827,"spinocerebellar ataxia, KCNJ10-related, dog",MONDO_grouped,disease,DISEASE_9666
9667,9667,9667,9667,9667,9667,9667,9667,MONDO:0007831,"insect Stings, hypersensitivity to",MONDO,disease,DISEASE_9667
9668,9668,9668,9668,9668,9668,9668,9668,MONDO:0007529,elastosis perforans serpiginosa,MONDO,disease,DISEASE_9668
9669,9669,9669,9669,9669,9669,9669,9669,MONDO:0017307,disorder of tyrosine metabolism,MONDO,disease,DISEASE_9669
9670,9670,9670,9670,9670,9670,9670,9670,MONDO:0008013,chromosome 9p deletion syndrome,MONDO,disease,DISEASE_9670
9671,9671,9671,9671,9671,9671,9671,9671,MONDO:0006325,ocular melanoma,MONDO,disease,DISEASE_9671
9672,9672,9672,9672,9672,9672,9672,9672,MONDO:1012442_MONDO:1012443,"malignant melanoma, dog",MONDO_grouped,disease,DISEASE_9672
9673,9673,9673,9673,9673,9673,9673,9673,MONDO:0002509,non-specific granulomatous orchitis,MONDO,disease,DISEASE_9673
9674,9674,9674,9674,9674,9674,9674,9674,MONDO:0011287,craniosynostosis-anal anomalies-porokeratosis syndrome,MONDO,disease,DISEASE_9674
9675,9675,9675,9675,9675,9675,9675,9675,MONDO:1012264,"androgen insensitivity syndrome, dog",MONDO,disease,DISEASE_9675
9676,9676,9676,9676,9676,9676,9676,9676,MONDO:0003343_MONDO:0024340,retinal hemangioblastoma,MONDO_grouped,disease,DISEASE_9676
9677,9677,9677,9677,9677,9677,9677,9677,MONDO:0005688,campylobacteriosis,MONDO,disease,DISEASE_9677
9678,9678,9678,9678,9678,9678,9678,9678,MONDO:0008282,"polyposis, intestinal, with multiple exostoses",MONDO,disease,DISEASE_9678
9679,9679,9679,9679,9679,9679,9679,9679,MONDO:0859574_MONDO:0100303_MONDO:0011870,"ichthyosis, annular epidermolytic",MONDO_grouped,disease,DISEASE_9679
9680,9680,9680,9680,9680,9680,9680,9680,MONDO:0007032,prune belly syndrome,MONDO,disease,DISEASE_9680
9681,9681,9681,9681,9681,9681,9681,9681,MONDO:0017303,qualitative or quantitative defects of tropomyosin,MONDO,disease,DISEASE_9681
9682,9682,9682,9682,9682,9682,9682,9682,MONDO:0004042_MONDO:0004043,urethra inverted papilloma,MONDO_grouped,disease,DISEASE_9682
9683,9683,9683,9683,9683,9683,9683,9683,MONDO:0010073_MONDO:0012019_MONDO:0014701_MONDO:0010068_MONDO:0032835_MONDO:0032721_MONDO:0012716_MONDO:0008472,"spondyloepiphyseal dysplasia tarda, Kohn type",MONDO_grouped,disease,DISEASE_9683
9684,9684,9684,9684,9684,9684,9684,9684,MONDO:0014918,tall stature-intellectual disability-renal anomalies syndrome,MONDO,disease,DISEASE_9684
9685,9685,9685,9685,9685,9685,9685,9685,MONDO:0003412,retroperitoneal hemangiopericytoma,MONDO,disease,DISEASE_9685
9686,9686,9686,9686,9686,9686,9686,9686,MONDO:0056819,nasal cavity and paranasal sinus carcinoma,MONDO,disease,DISEASE_9686
9687,9687,9687,9687,9687,9687,9687,9687,MONDO:0008105,"nose, anomalous shape of",MONDO,disease,DISEASE_9687
9688,9688,9688,9688,9688,9688,9688,9688,MONDO:0001750,non-renal secondary hyperparathyroidism,MONDO,disease,DISEASE_9688
9689,9689,9689,9689,9689,9689,9689,9689,MONDO:0010239,lissencephaly type 1 due to doublecortin gene mutation,MONDO,disease,DISEASE_9689
9690,9690,9690,9690,9690,9690,9690,9690,MONDO:0100155,retinal dystrophy-ataxia-pituitary hormone abnormality-hypogonadism syndrome,MONDO,disease,DISEASE_9690
9691,9691,9691,9691,9691,9691,9691,9691,MONDO:0010151,"tricarboxylic acid cycle, defect of",MONDO,disease,DISEASE_9691
9692,9692,9692,9692,9692,9692,9692,9692,MONDO:0030048,harderoporphyria,MONDO,disease,DISEASE_9692
9693,9693,9693,9693,9693,9693,9693,9693,MONDO:0004808,benign mammary dysplasia,MONDO,disease,DISEASE_9693
9694,9694,9694,9694,9694,9694,9694,9694,MONDO:0009318,Hallermann-Streiff syndrome,MONDO,disease,DISEASE_9694
9695,9695,9695,9695,9695,9695,9695,9695,MONDO:0022394_MONDO:0042491_MONDO:0060777,cervical intraepithelial neoplasia,MONDO_grouped,disease,DISEASE_9695
9696,9696,9696,9696,9696,9696,9696,9696,MONDO:0013478_MONDO:0019192,PLIN1-related familial partial lipodystrophy,MONDO_grouped,disease,DISEASE_9696
9697,9697,9697,9697,9697,9697,9697,9697,MONDO:0042970,disorder of glutamate decarboxylase,MONDO,disease,DISEASE_9697
9698,9698,9698,9698,9698,9698,9698,9698,MONDO:0014760,TFRC-related combined immunodeficiency,MONDO,disease,DISEASE_9698
9699,9699,9699,9699,9699,9699,9699,9699,MONDO:0021667,neuralgia,MONDO,disease,DISEASE_9699
9700,9700,9700,9700,9700,9700,9700,9700,MONDO:0030428,immunodeficiency 85 and autoimmunity,MONDO,disease,DISEASE_9700
9701,9701,9701,9701,9701,9701,9701,9701,MONDO:0005287,developmental disability,MONDO,disease,DISEASE_9701
9702,9702,9702,9702,9702,9702,9702,9702,MONDO:0004158,pancreatic mucinous-cystic neoplasm with an associated invasive carcinoma,MONDO,disease,DISEASE_9702
9703,9703,9703,9703,9703,9703,9703,9703,MONDO:0000632,uterine benign neoplasm,MONDO,disease,DISEASE_9703
9704,9704,9704,9704,9704,9704,9704,9704,MONDO:0010564,red-green color blindness,MONDO,disease,DISEASE_9704
9705,9705,9705,9705,9705,9705,9705,9705,MONDO:0005213_MONDO:0006485_MONDO:0004710_MONDO:0004491,uterine carcinoma,MONDO_grouped,disease,DISEASE_9705
9706,9706,9706,9706,9706,9706,9706,9706,MONDO:0014488_MONDO:0011027_MONDO:0011072_MONDO:0011363_MONDO:0011955,"diabetes mellitus, noninsulin-dependent",MONDO_grouped,disease,DISEASE_9706
9707,9707,9707,9707,9707,9707,9707,9707,MONDO:0022401,agyria pachygyria polymicrogyria,MONDO,disease,DISEASE_9707
9708,9708,9708,9708,9708,9708,9708,9708,MONDO:0800452_MONDO:0957575_MONDO:0800451,congenital amegakaryocytic thrombocytopenia,MONDO_grouped,disease,DISEASE_9708
9709,9709,9709,9709,9709,9709,9709,9709,MONDO:0005341,skin basal cell carcinoma,MONDO,disease,DISEASE_9709
9710,9710,9710,9710,9710,9710,9710,9710,MONDO:0810000,choroidal neovascularization,MONDO,disease,DISEASE_9710
9711,9711,9711,9711,9711,9711,9711,9711,MONDO:0006652_MONDO:0003679,anterolateral myocardial infarction,MONDO_grouped,disease,DISEASE_9711
9712,9712,9712,9712,9712,9712,9712,9712,MONDO:0027069,"mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1",MONDO,disease,DISEASE_9712
9713,9713,9713,9713,9713,9713,9713,9713,MONDO:0016015,phenobarbital embryopathy,MONDO,disease,DISEASE_9713
9714,9714,9714,9714,9714,9714,9714,9714,MONDO:0011571,"deafness, autosomal dominant 39, with dentinogenesis imperfecta 1",MONDO,disease,DISEASE_9714
9715,9715,9715,9715,9715,9715,9715,9715,MONDO:0009001,macular coloboma-cleft palate-hallux valgus syndrome,MONDO,disease,DISEASE_9715
9716,9716,9716,9716,9716,9716,9716,9716,MONDO:0013282,alpha 1-antitrypsin deficiency,MONDO,disease,DISEASE_9716
9717,9717,9717,9717,9717,9717,9717,9717,MONDO:0100274,alkylglycerone-phosphate synthase deficiency,MONDO,disease,DISEASE_9717
9718,9718,9718,9718,9718,9718,9718,9718,MONDO:0700037,testicular fibrothecoma,MONDO,disease,DISEASE_9718
9719,9719,9719,9719,9719,9719,9719,9719,MONDO:0009994_MONDO:0002978,alveolar rhabdomyosarcoma,MONDO_grouped,disease,DISEASE_9719
9720,9720,9720,9720,9720,9720,9720,9720,MONDO:0850470,MCD diffuse large B-cell lymphoma,MONDO,disease,DISEASE_9720
9721,9721,9721,9721,9721,9721,9721,9721,MONDO:1010772_MONDO:1010774_MONDO:1010775_MONDO:1010776,"pemphigus, dog",MONDO_grouped,disease,DISEASE_9721
9722,9722,9722,9722,9722,9722,9722,9722,MONDO:0100319,COVID-19–associated multisystem inflammatory syndrome in adults,MONDO,disease,DISEASE_9722
9723,9723,9723,9723,9723,9723,9723,9723,MONDO:0009447,"ichthyosis, split hairs, and amino aciduria",MONDO,disease,DISEASE_9723
9724,9724,9724,9724,9724,9724,9724,9724,MONDO:0002239,post-surgical hypoinsulinemia,MONDO,disease,DISEASE_9724
9725,9725,9725,9725,9725,9725,9725,9725,MONDO:0004747,cleft lip,MONDO,disease,DISEASE_9725
9726,9726,9726,9726,9726,9726,9726,9726,MONDO:0007237,familial juvenile hypertrophy of the breast,MONDO,disease,DISEASE_9726
9727,9727,9727,9727,9727,9727,9727,9727,MONDO:0022636,candida glabrata infection,MONDO,disease,DISEASE_9727
9728,9728,9728,9728,9728,9728,9728,9728,MONDO:0018696,corticobasal syndrome,MONDO,disease,DISEASE_9728
9729,9729,9729,9729,9729,9729,9729,9729,MONDO:0008253,"platelet aggregation, spontaneous",MONDO,disease,DISEASE_9729
9730,9730,9730,9730,9730,9730,9730,9730,MONDO:0001117,methemoglobinemia,MONDO,disease,DISEASE_9730
9731,9731,9731,9731,9731,9731,9731,9731,MONDO:0000309,aniseikonia,MONDO,disease,DISEASE_9731
9732,9732,9732,9732,9732,9732,9732,9732,MONDO:0009884,platelet prostacyclin receptor defect,MONDO,disease,DISEASE_9732
9733,9733,9733,9733,9733,9733,9733,9733,MONDO:0010415_MONDO:0010414,"myopathy, reducing body, X-linked, childhood-onset",MONDO_grouped,disease,DISEASE_9733
9734,9734,9734,9734,9734,9734,9734,9734,MONDO:0040673,malignant peritoneal germ cell tumor,MONDO,disease,DISEASE_9734
9735,9735,9735,9735,9735,9735,9735,9735,MONDO:0003091,cutaneous mucoepidermoid carcinoma,MONDO,disease,DISEASE_9735
9736,9736,9736,9736,9736,9736,9736,9736,MONDO:0001517,dysentery,MONDO,disease,DISEASE_9736
9737,9737,9737,9737,9737,9737,9737,9737,MONDO:0006715,coronary stenosis,MONDO,disease,DISEASE_9737
9738,9738,9738,9738,9738,9738,9738,9738,MONDO:0014250,familial hyperprolactinemia,MONDO,disease,DISEASE_9738
9739,9739,9739,9739,9739,9739,9739,9739,MONDO:0016514,epidermolysis bullosa simplex with anodontia/hypodontia,MONDO,disease,DISEASE_9739
9740,9740,9740,9740,9740,9740,9740,9740,MONDO:1010429,"atherosclerosis, Japanese quail",MONDO,disease,DISEASE_9740
9741,9741,9741,9741,9741,9741,9741,9741,MONDO:0001938,vulvar dystrophy,MONDO,disease,DISEASE_9741
9742,9742,9742,9742,9742,9742,9742,9742,MONDO:0016145,qualitative or quantitative defects of dysferlin,MONDO,disease,DISEASE_9742
9743,9743,9743,9743,9743,9743,9743,9743,MONDO:1012063,"ocular-skeletal dysplasia, dog",MONDO,disease,DISEASE_9743
9744,9744,9744,9744,9744,9744,9744,9744,MONDO:0016943,partial duplication of the short arm of chromosome 6,MONDO,disease,DISEASE_9744
9745,9745,9745,9745,9745,9745,9745,9745,MONDO:0014272,"palmoplantar keratoderma, Nagashima type",MONDO,disease,DISEASE_9745
9746,9746,9746,9746,9746,9746,9746,9746,MONDO:0015200,anisakiasis,MONDO,disease,DISEASE_9746
9747,9747,9747,9747,9747,9747,9747,9747,MONDO:0003251,esophageal granular cell tumor,MONDO,disease,DISEASE_9747
9748,9748,9748,9748,9748,9748,9748,9748,MONDO:0001551,ulceration of vulva,MONDO,disease,DISEASE_9748
9749,9749,9749,9749,9749,9749,9749,9749,MONDO:0958159_MONDO:0958297,sarcoma with BCOR genetic alterations,MONDO_grouped,disease,DISEASE_9749
9750,9750,9750,9750,9750,9750,9750,9750,MONDO:1011012,"Horner syndrome, cattle",MONDO,disease,DISEASE_9750
9751,9751,9751,9751,9751,9751,9751,9751,MONDO:0100238,inherited Fanconi renotubular syndrome,MONDO,disease,DISEASE_9751
9752,9752,9752,9752,9752,9752,9752,9752,MONDO:1010172_MONDO:1011432,"alpha-mannosidosis, non-human animal",MONDO_grouped,disease,DISEASE_9752
9753,9753,9753,9753,9753,9753,9753,9753,MONDO:0007148,"appendicitis, proneness to",MONDO,disease,DISEASE_9753
9754,9754,9754,9754,9754,9754,9754,9754,MONDO:0008427,"sister chromatid exchange, frequency of",MONDO,disease,DISEASE_9754
9755,9755,9755,9755,9755,9755,9755,9755,MONDO:0002318,trachea leiomyoma,MONDO,disease,DISEASE_9755
9756,9756,9756,9756,9756,9756,9756,9756,MONDO:0017238,hemoglobinopathy Toms River,MONDO,disease,DISEASE_9756
9757,9757,9757,9757,9757,9757,9757,9757,MONDO:1010725,"c8 deficiency, rabbit",MONDO,disease,DISEASE_9757
9758,9758,9758,9758,9758,9758,9758,9758,MONDO:0044210,thalassemia minor,MONDO,disease,DISEASE_9758
9759,9759,9759,9759,9759,9759,9759,9759,MONDO:0002710,infiltrating angiolipoma,MONDO,disease,DISEASE_9759
9760,9760,9760,9760,9760,9760,9760,9760,MONDO:0000104,"anemia, hypochromic microcytic with iron overload",MONDO,disease,DISEASE_9760
9761,9761,9761,9761,9761,9761,9761,9761,MONDO:0012876,heparin cofactor 2 deficiency,MONDO,disease,DISEASE_9761
9762,9762,9762,9762,9762,9762,9762,9762,MONDO:0007705,Heinz body anemia,MONDO,disease,DISEASE_9762
9763,9763,9763,9763,9763,9763,9763,9763,MONDO:0000664,apperceptive agnosia,MONDO,disease,DISEASE_9763
9764,9764,9764,9764,9764,9764,9764,9764,MONDO:0019886,distal trisomy 13q,MONDO,disease,DISEASE_9764
9765,9765,9765,9765,9765,9765,9765,9765,MONDO:1012488,"ACTH-independent adrenal Cushing syndrome, dog",MONDO,disease,DISEASE_9765
9766,9766,9766,9766,9766,9766,9766,9766,MONDO:0009326,congenital heart block,MONDO,disease,DISEASE_9766
9767,9767,9767,9767,9767,9767,9767,9767,MONDO:0001527,conjugate gaze palsy,MONDO,disease,DISEASE_9767
9768,9768,9768,9768,9768,9768,9768,9768,MONDO:0016906,partial deletion of the long arm of chromosome 7,MONDO,disease,DISEASE_9768
9769,9769,9769,9769,9769,9769,9769,9769,MONDO:0016912,partial deletion of the long arm of chromosome 14,MONDO,disease,DISEASE_9769
9770,9770,9770,9770,9770,9770,9770,9770,MONDO:0019377,Mycoplasma encephalitis,MONDO,disease,DISEASE_9770
9771,9771,9771,9771,9771,9771,9771,9771,MONDO:0017315,short stature-webbed neck-heart disease syndrome,MONDO,disease,DISEASE_9771
9772,9772,9772,9772,9772,9772,9772,9772,MONDO:0016426,fusariosis,MONDO,disease,DISEASE_9772
9773,9773,9773,9773,9773,9773,9773,9773,MONDO:0045013,disorder of extraembryonic membrane,MONDO,disease,DISEASE_9773
9774,9774,9774,9774,9774,9774,9774,9774,MONDO:0100366,occupational disorder,MONDO,disease,DISEASE_9774
9775,9775,9775,9775,9775,9775,9775,9775,MONDO:0008365,recombinant 8 syndrome,MONDO,disease,DISEASE_9775
9776,9776,9776,9776,9776,9776,9776,9776,MONDO:0012048,endogenous depression,MONDO,disease,DISEASE_9776
9777,9777,9777,9777,9777,9777,9777,9777,MONDO:0000488_MONDO:0004465,periampullary adenoma,MONDO_grouped,disease,DISEASE_9777
9778,9778,9778,9778,9778,9778,9778,9778,MONDO:0024518,reactive thrombocytosis,MONDO,disease,DISEASE_9778
9779,9779,9779,9779,9779,9779,9779,9779,MONDO:0003585,adult liposarcoma,MONDO,disease,DISEASE_9779
9780,9780,9780,9780,9780,9780,9780,9780,MONDO:0013732,"glucocorticoid therapy, response to",MONDO,disease,DISEASE_9780
9781,9781,9781,9781,9781,9781,9781,9781,MONDO:0020301,Prader-Willi syndrome due to paternal 15q11q13 deletion,MONDO,disease,DISEASE_9781
9782,9782,9782,9782,9782,9782,9782,9782,MONDO:0016882,partial deletion of chromosome 20,MONDO,disease,DISEASE_9782
9783,9783,9783,9783,9783,9783,9783,9783,MONDO:0858974,breast implant illness,MONDO,disease,DISEASE_9783
9784,9784,9784,9784,9784,9784,9784,9784,MONDO:0004891,hyperopia,MONDO,disease,DISEASE_9784
9785,9785,9785,9785,9785,9785,9785,9785,MONDO:0002687,superior mesenteric artery syndrome,MONDO,disease,DISEASE_9785
9786,9786,9786,9786,9786,9786,9786,9786,MONDO:0017603,ALK-negative anaplastic large cell lymphoma,MONDO,disease,DISEASE_9786
9787,9787,9787,9787,9787,9787,9787,9787,MONDO:0004453,"testicular yolk sac tumor, myxomatous pattern",MONDO,disease,DISEASE_9787
9788,9788,9788,9788,9788,9788,9788,9788,MONDO:0100523,SPAST-related motor disorder,MONDO,disease,DISEASE_9788
9789,9789,9789,9789,9789,9789,9789,9789,MONDO:0850332,IDH-mutant anaplastic astrocytoma,MONDO,disease,DISEASE_9789
9790,9790,9790,9790,9790,9790,9790,9790,MONDO:0005825,leptospirosis,MONDO,disease,DISEASE_9790
9791,9791,9791,9791,9791,9791,9791,9791,MONDO:0007798,obsolete adult hypophosphatasia,MONDO,disease,DISEASE_9791
9792,9792,9792,9792,9792,9792,9792,9792,MONDO:0013025,chromosome 6q24-q25 deletion syndrome,MONDO,disease,DISEASE_9792
9793,9793,9793,9793,9793,9793,9793,9793,MONDO:1011139,"choanal atresia, dog",MONDO,disease,DISEASE_9793
9794,9794,9794,9794,9794,9794,9794,9794,MONDO:0014892,micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome,MONDO,disease,DISEASE_9794
9795,9795,9795,9795,9795,9795,9795,9795,MONDO:0044079,cardio-renal syndrome,MONDO,disease,DISEASE_9795
9796,9796,9796,9796,9796,9796,9796,9796,MONDO:0012622,leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome,MONDO,disease,DISEASE_9796
9797,9797,9797,9797,9797,9797,9797,9797,MONDO:0014526_MONDO:0000192,polyglucosan body myopathy type 2,MONDO_grouped,disease,DISEASE_9797
9798,9798,9798,9798,9798,9798,9798,9798,MONDO:0010022,senile plaque formation,MONDO,disease,DISEASE_9798
9799,9799,9799,9799,9799,9799,9799,9799,MONDO:0007318,Alagille syndrome,MONDO,disease,DISEASE_9799
9800,9800,9800,9800,9800,9800,9800,9800,MONDO:0012726,autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome,MONDO,disease,DISEASE_9800
9801,9801,9801,9801,9801,9801,9801,9801,MONDO:0011246,megaconial type congenital muscular dystrophy,MONDO,disease,DISEASE_9801
9802,9802,9802,9802,9802,9802,9802,9802,MONDO:0016583,familial intestinal malrotation-facial anomalies syndrome,MONDO,disease,DISEASE_9802
9803,9803,9803,9803,9803,9803,9803,9803,MONDO:0015701,T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency,MONDO,disease,DISEASE_9803
9804,9804,9804,9804,9804,9804,9804,9804,MONDO:0014289,macrocephaly-developmental delay syndrome,MONDO,disease,DISEASE_9804
9805,9805,9805,9805,9805,9805,9805,9805,MONDO:1011759,"hypotrichosis with short life expectancy, non-human animal",MONDO,disease,DISEASE_9805
9806,9806,9806,9806,9806,9806,9806,9806,MONDO:0012755_MONDO:0030064_MONDO:0008047_MONDO:0007163_MONDO:0011681_MONDO:0012982_MONDO:0011682_MONDO:0013464_MONDO:0014476,episodic ataxia,MONDO_grouped,disease,DISEASE_9806
9807,9807,9807,9807,9807,9807,9807,9807,MONDO:0019457,therapy related acute myeloid leukemia and myelodysplastic syndrome,MONDO,disease,DISEASE_9807
9808,9808,9808,9808,9808,9808,9808,9808,MONDO:0023193,Friedman Goodman syndrome,MONDO,disease,DISEASE_9808
9809,9809,9809,9809,9809,9809,9809,9809,MONDO:1011911,"renal insufficiency, non-human animal",MONDO,disease,DISEASE_9809
9810,9810,9810,9810,9810,9810,9810,9810,MONDO:0022644,cardiac hydatid cysts with intracavitary expansion,MONDO,disease,DISEASE_9810
9811,9811,9811,9811,9811,9811,9811,9811,MONDO:0016081,coronary arterial fistulas,MONDO,disease,DISEASE_9811
9812,9812,9812,9812,9812,9812,9812,9812,MONDO:0004944,neurosyphilis,MONDO,disease,DISEASE_9812
9813,9813,9813,9813,9813,9813,9813,9813,MONDO:0011357,eccrine syringofibroadenomatosis with eyelid abnormalities,MONDO,disease,DISEASE_9813
9814,9814,9814,9814,9814,9814,9814,9814,MONDO:0700252,parneoplastic endocrine syndrome,MONDO,disease,DISEASE_9814
9815,9815,9815,9815,9815,9815,9815,9815,MONDO:0023100,facial clefting corpus callosum agenesis,MONDO,disease,DISEASE_9815
9816,9816,9816,9816,9816,9816,9816,9816,MONDO:0700223_MONDO:0045046,hereditary skeletal muscle disorder,MONDO_grouped,disease,DISEASE_9816
9817,9817,9817,9817,9817,9817,9817,9817,MONDO:0003435,microcystic adenoma,MONDO,disease,DISEASE_9817
9818,9818,9818,9818,9818,9818,9818,9818,MONDO:0011331,congenital chylothorax,MONDO,disease,DISEASE_9818
9819,9819,9819,9819,9819,9819,9819,9819,MONDO:0006323,non-seminomatous lesion,MONDO,disease,DISEASE_9819
9820,9820,9820,9820,9820,9820,9820,9820,MONDO:0013172,polymicrogyria with optic nerve hypoplasia,MONDO,disease,DISEASE_9820
9821,9821,9821,9821,9821,9821,9821,9821,MONDO:0008416,palmoplantar keratoderma-sclerodactyly syndrome,MONDO,disease,DISEASE_9821
9822,9822,9822,9822,9822,9822,9822,9822,MONDO:0010661,"severe X-linked intellectual disability, Gustavson type",MONDO,disease,DISEASE_9822
9823,9823,9823,9823,9823,9823,9823,9823,MONDO:0007852_MONDO:0017672_MONDO:0019272,palmoplantar keratoderma-deafness syndrome,MONDO_grouped,disease,DISEASE_9823
9824,9824,9824,9824,9824,9824,9824,9824,MONDO:0040698,subacute bursitis,MONDO,disease,DISEASE_9824
9825,9825,9825,9825,9825,9825,9825,9825,MONDO:0033646_MONDO:0033645_MONDO:0033639_MONDO:0033638_MONDO:0033635_MONDO:0033637_MONDO:0033651_MONDO:0033636_MONDO:0033652_MONDO:0033654_MONDO:0033653_MONDO:0033650_MONDO:0033656_MONDO:0033655_MONDO:0033649,"mitochondrial complex 4 deficiency, nuclear",MONDO_grouped,disease,DISEASE_9825
9826,9826,9826,9826,9826,9826,9826,9826,MONDO:0032903,"arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum",MONDO,disease,DISEASE_9826
9827,9827,9827,9827,9827,9827,9827,9827,MONDO:0958278,neurodevelopmental disorder with hypotonia and characteristic brain abnormalities,MONDO,disease,DISEASE_9827
9828,9828,9828,9828,9828,9828,9828,9828,MONDO:0001736,neonatal infective mastitis,MONDO,disease,DISEASE_9828
9829,9829,9829,9829,9829,9829,9829,9829,MONDO:0014077,cobblestone lissencephaly without muscular or ocular involvement,MONDO,disease,DISEASE_9829
9830,9830,9830,9830,9830,9830,9830,9830,MONDO:1012317_MONDO:1012241,"retinal and skeletal dysplasia, dog",MONDO_grouped,disease,DISEASE_9830
9831,9831,9831,9831,9831,9831,9831,9831,MONDO:0000939,intracranial abscess,MONDO,disease,DISEASE_9831
9832,9832,9832,9832,9832,9832,9832,9832,MONDO:0004287,pancreatic foamy gland adenocarcinoma,MONDO,disease,DISEASE_9832
9833,9833,9833,9833,9833,9833,9833,9833,MONDO:0022648,cardiomyopathy and deafness due to tRNA lysine gene mutation,MONDO,disease,DISEASE_9833
9834,9834,9834,9834,9834,9834,9834,9834,MONDO:0006613,stromal corneal pigmentation,MONDO,disease,DISEASE_9834
9835,9835,9835,9835,9835,9835,9835,9835,MONDO:0019949,zebra body myopathy,MONDO,disease,DISEASE_9835
9836,9836,9836,9836,9836,9836,9836,9836,MONDO:1011663,"displaced abomasum, non-human animal",MONDO,disease,DISEASE_9836
9837,9837,9837,9837,9837,9837,9837,9837,MONDO:0012387,osteosclerosis-ichthyosis-premature ovarian failure syndrome,MONDO,disease,DISEASE_9837
9838,9838,9838,9838,9838,9838,9838,9838,MONDO:0020461,epiblepharon,MONDO,disease,DISEASE_9838
9839,9839,9839,9839,9839,9839,9839,9839,MONDO:0100017,pityriasis rubra pilaris,MONDO,disease,DISEASE_9839
9840,9840,9840,9840,9840,9840,9840,9840,MONDO:0000265,aspiration pneumonia,MONDO,disease,DISEASE_9840
9841,9841,9841,9841,9841,9841,9841,9841,MONDO:0007352,renal coloboma syndrome,MONDO,disease,DISEASE_9841
9842,9842,9842,9842,9842,9842,9842,9842,MONDO:0032897,intellectual developmental disorder with hypotonia and behavioral abnormalities,MONDO,disease,DISEASE_9842
9843,9843,9843,9843,9843,9843,9843,9843,MONDO:0013919_MONDO:0012113_MONDO:0100519_MONDO:0011491_MONDO:0011892_MONDO:0030434_MONDO:0032699_MONDO:0013032_MONDO:0032827_MONDO:0013103_MONDO:0014734_MONDO:0011875_MONDO:0010918_MONDO:0012627_MONDO:0011753_MONDO:0012338_MONDO:0012760_MONDO:0800279,"epilepsy, idiopathic generalized, susceptibility to",MONDO_grouped,disease,DISEASE_9843
9844,9844,9844,9844,9844,9844,9844,9844,MONDO:0033554,immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia,MONDO,disease,DISEASE_9844
9845,9845,9845,9845,9845,9845,9845,9845,MONDO:0957247,"congenital myopathy 22A, classic",MONDO,disease,DISEASE_9845
9846,9846,9846,9846,9846,9846,9846,9846,MONDO:1011198,"hypophosphatemic rickets, DMP1-related, rabbit",MONDO,disease,DISEASE_9846
9847,9847,9847,9847,9847,9847,9847,9847,MONDO:0019638,renal dysplasia,MONDO,disease,DISEASE_9847
9848,9848,9848,9848,9848,9848,9848,9848,MONDO:0005846,microsporidiosis,MONDO,disease,DISEASE_9848
9849,9849,9849,9849,9849,9849,9849,9849,MONDO:0020983,myocardial rupture,MONDO,disease,DISEASE_9849
9850,9850,9850,9850,9850,9850,9850,9850,MONDO:0010662,paraplegia-intellectual disability-hyperkeratosis syndrome,MONDO,disease,DISEASE_9850
9851,9851,9851,9851,9851,9851,9851,9851,MONDO:0016911,partial deletion of the long arm of chromosome 13,MONDO,disease,DISEASE_9851
9852,9852,9852,9852,9852,9852,9852,9852,MONDO:0700060,"leukemia, acute, X-linked",MONDO,disease,DISEASE_9852
9853,9853,9853,9853,9853,9853,9853,9853,MONDO:1011818,"invasive transitional cell carcinoma, non-human animal",MONDO,disease,DISEASE_9853
9854,9854,9854,9854,9854,9854,9854,9854,MONDO:0021046,breast fibroepithelial neoplasm,MONDO,disease,DISEASE_9854
9855,9855,9855,9855,9855,9855,9855,9855,MONDO:0014307_MONDO:0014130_MONDO:0024534_MONDO:0014301_MONDO:0008371,Dowling-Degos disease,MONDO_grouped,disease,DISEASE_9855
9856,9856,9856,9856,9856,9856,9856,9856,MONDO:0011023,hereditary mixed polyposis syndrome,MONDO,disease,DISEASE_9856
9857,9857,9857,9857,9857,9857,9857,9857,MONDO:0004679_MONDO:0006830,leukoplakia of vagina,MONDO_grouped,disease,DISEASE_9857
9858,9858,9858,9858,9858,9858,9858,9858,MONDO:0012479,congenital malabsorptive diarrhea 4,MONDO,disease,DISEASE_9858
9859,9859,9859,9859,9859,9859,9859,9859,MONDO:0018676,eosinophilic angiocentric fibrosis,MONDO,disease,DISEASE_9859
9860,9860,9860,9860,9860,9860,9860,9860,MONDO:0011768,myasthenia gravis with thymus hyperplasia,MONDO,disease,DISEASE_9860
9861,9861,9861,9861,9861,9861,9861,9861,MONDO:0008622,tricho-retino-dento-digital syndrome,MONDO,disease,DISEASE_9861
9862,9862,9862,9862,9862,9862,9862,9862,MONDO:0007125,ankyloglossia,MONDO,disease,DISEASE_9862
9863,9863,9863,9863,9863,9863,9863,9863,MONDO:0007018,vulvitis,MONDO,disease,DISEASE_9863
9864,9864,9864,9864,9864,9864,9864,9864,MONDO:1011529_MONDO:1011528,"histiocytosis, pig",MONDO_grouped,disease,DISEASE_9864
9865,9865,9865,9865,9865,9865,9865,9865,MONDO:0009168,Fowler syndrome,MONDO,disease,DISEASE_9865
9866,9866,9866,9866,9866,9866,9866,9866,MONDO:0005272,myelodysplastic syndrome with single lineage dysplasia,MONDO,disease,DISEASE_9866
9867,9867,9867,9867,9867,9867,9867,9867,MONDO:0022551,Basedow's coma,MONDO,disease,DISEASE_9867
9868,9868,9868,9868,9868,9868,9868,9868,MONDO:1012487,"zinc deficiency-like syndrome, cattle",MONDO,disease,DISEASE_9868
9869,9869,9869,9869,9869,9869,9869,9869,MONDO:0013892,C3 glomerulonephritis,MONDO,disease,DISEASE_9869
9870,9870,9870,9870,9870,9870,9870,9870,MONDO:1011121,"orchitis, domestic cat",MONDO,disease,DISEASE_9870
9871,9871,9871,9871,9871,9871,9871,9871,MONDO:0100038_MONDO:0100516,complex neurodevelopmental disorder,MONDO_grouped,disease,DISEASE_9871
9872,9872,9872,9872,9872,9872,9872,9872,MONDO:0100520,NKX2-1 related choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction,MONDO,disease,DISEASE_9872
9873,9873,9873,9873,9873,9873,9873,9873,MONDO:0012557,cardiomyopathy-hypotonia-lactic acidosis syndrome,MONDO,disease,DISEASE_9873
9874,9874,9874,9874,9874,9874,9874,9874,MONDO:0019229_MONDO:0019218,inborn disorder of ketolysis,MONDO_grouped,disease,DISEASE_9874
9875,9875,9875,9875,9875,9875,9875,9875,MONDO:0004370,sphenocavernous meningioma,MONDO,disease,DISEASE_9875
9876,9876,9876,9876,9876,9876,9876,9876,MONDO:0060490,"neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies",MONDO,disease,DISEASE_9876
9877,9877,9877,9877,9877,9877,9877,9877,MONDO:0011128,Sheldon-hall syndrome,MONDO,disease,DISEASE_9877
9878,9878,9878,9878,9878,9878,9878,9878,MONDO:0004422,cerebral falx meningioma,MONDO,disease,DISEASE_9878
9879,9879,9879,9879,9879,9879,9879,9879,MONDO:0007199,"blepharochalasis, superior",MONDO,disease,DISEASE_9879
9880,9880,9880,9880,9880,9880,9880,9880,MONDO:0016395,foveal hypoplasia-presenile cataract syndrome,MONDO,disease,DISEASE_9880
9881,9881,9881,9881,9881,9881,9881,9881,MONDO:0019651,idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation,MONDO,disease,DISEASE_9881
9882,9882,9882,9882,9882,9882,9882,9882,MONDO:0025956,ovarian remnant syndrome,MONDO,disease,DISEASE_9882
9883,9883,9883,9883,9883,9883,9883,9883,MONDO:0006975,smooth muscle tumor,MONDO,disease,DISEASE_9883
9884,9884,9884,9884,9884,9884,9884,9884,MONDO:0002555,trigeminal schwannoma,MONDO,disease,DISEASE_9884
9885,9885,9885,9885,9885,9885,9885,9885,MONDO:0850257,mucinous pancreas adenocarcinoma,MONDO,disease,DISEASE_9885
9886,9886,9886,9886,9886,9886,9886,9886,MONDO:0004180,benign urinary system neoplasm,MONDO,disease,DISEASE_9886
9887,9887,9887,9887,9887,9887,9887,9887,MONDO:0015371,linear atrophoderma of Moulin,MONDO,disease,DISEASE_9887
9888,9888,9888,9888,9888,9888,9888,9888,MONDO:0005466_MONDO:0004617,hypersomnia,MONDO_grouped,disease,DISEASE_9888
9889,9889,9889,9889,9889,9889,9889,9889,MONDO:0000476,generalized dystonia,MONDO,disease,DISEASE_9889
9890,9890,9890,9890,9890,9890,9890,9890,MONDO:0005937,REM sleep behavior disorder,MONDO,disease,DISEASE_9890
9891,9891,9891,9891,9891,9891,9891,9891,MONDO:0006163,colorectal serrated adenocarcinoma,MONDO,disease,DISEASE_9891
9892,9892,9892,9892,9892,9892,9892,9892,MONDO:0006498,adenomatous colon polyp,MONDO,disease,DISEASE_9892
9893,9893,9893,9893,9893,9893,9893,9893,MONDO:0014274,L-ferritin deficiency,MONDO,disease,DISEASE_9893
9894,9894,9894,9894,9894,9894,9894,9894,MONDO:0002816_MONDO:0005495,adrenal cortex disorder,MONDO_grouped,disease,DISEASE_9894
9895,9895,9895,9895,9895,9895,9895,9895,MONDO:0006774,habitual spontaneous abortion,MONDO,disease,DISEASE_9895
9896,9896,9896,9896,9896,9896,9896,9896,MONDO:0014946,Sifrim-Hitz-Weiss syndrome,MONDO,disease,DISEASE_9896
9897,9897,9897,9897,9897,9897,9897,9897,MONDO:0016231,capillary malformation,MONDO,disease,DISEASE_9897
9898,9898,9898,9898,9898,9898,9898,9898,MONDO:0005643_MONDO:0005985_MONDO:0005949_MONDO:0005652_MONDO:0005740,Alphavirus infectious disease,MONDO_grouped,disease,DISEASE_9898
9899,9899,9899,9899,9899,9899,9899,9899,MONDO:0005198_MONDO:0006274,vulvar intraepithelial neoplasia,MONDO_grouped,disease,DISEASE_9899
9900,9900,9900,9900,9900,9900,9900,9900,MONDO:0011492,"mandibulofacial dysostosis syndrome, Bauru type",MONDO,disease,DISEASE_9900
9901,9901,9901,9901,9901,9901,9901,9901,MONDO:1010657,"prekallikrein deficiency, dog",MONDO,disease,DISEASE_9901
9902,9902,9902,9902,9902,9902,9902,9902,MONDO:0016913,partial deletion of the long arm of chromosome 15,MONDO,disease,DISEASE_9902
9903,9903,9903,9903,9903,9903,9903,9903,MONDO:0043179,piepkorn karp hickok syndrome,MONDO,disease,DISEASE_9903
9904,9904,9904,9904,9904,9904,9904,9904,MONDO:0001416,female reproductive organ cancer,MONDO,disease,DISEASE_9904
9905,9905,9905,9905,9905,9905,9905,9905,MONDO:0020505,ravine syndrome,MONDO,disease,DISEASE_9905
9906,9906,9906,9906,9906,9906,9906,9906,MONDO:0021102,prostate phyllodes tumor,MONDO,disease,DISEASE_9906
9907,9907,9907,9907,9907,9907,9907,9907,MONDO:0030701_MONDO:0022519,autoimmune cardiomyopathy,MONDO_grouped,disease,DISEASE_9907
9908,9908,9908,9908,9908,9908,9908,9908,MONDO:0005044,hypertensive disorder,MONDO,disease,DISEASE_9908
9909,9909,9909,9909,9909,9909,9909,9909,MONDO:0100033_MONDO:0015650_MONDO:0005027_MONDO:0015653,metabolic epilepsy,MONDO_grouped,disease,DISEASE_9909
9910,9910,9910,9910,9910,9910,9910,9910,MONDO:0001323,infant gynecomastia,MONDO,disease,DISEASE_9910
9911,9911,9911,9911,9911,9911,9911,9911,MONDO:0017267_MONDO:0017268,self-healing collodion baby,MONDO_grouped,disease,DISEASE_9911
9912,9912,9912,9912,9912,9912,9912,9912,MONDO:0014164_MONDO:0012626_MONDO:0013609_MONDO:0011296_MONDO:0012695_MONDO:0013630_MONDO:0030819_MONDO:0012848_MONDO:0011821_MONDO:0033044_MONDO:0013482_MONDO:0009571,"Meckel syndrome,",MONDO_grouped,disease,DISEASE_9912
9913,9913,9913,9913,9913,9913,9913,9913,MONDO:0859155,"chromosome 1p36 deletion syndrome, proximal",MONDO,disease,DISEASE_9913
9914,9914,9914,9914,9914,9914,9914,9914,MONDO:0019612,functioning gonadotropic adenoma,MONDO,disease,DISEASE_9914
9915,9915,9915,9915,9915,9915,9915,9915,MONDO:0010873,band heterotopia of brain,MONDO,disease,DISEASE_9915
9916,9916,9916,9916,9916,9916,9916,9916,MONDO:0700245_MONDO:0700248,"epidermolytic hyperkeratosis 2B, autosomal recessive",MONDO_grouped,disease,DISEASE_9916
9917,9917,9917,9917,9917,9917,9917,9917,MONDO:1011073,"urolithiasis, Francois's langur",MONDO,disease,DISEASE_9917
9918,9918,9918,9918,9918,9918,9918,9918,MONDO:0004149,gallbladder pleomorphic giant cell adenocarcinoma,MONDO,disease,DISEASE_9918
9919,9919,9919,9919,9919,9919,9919,9919,MONDO:0002554,sympathetic neurilemmoma,MONDO,disease,DISEASE_9919
9920,9920,9920,9920,9920,9920,9920,9920,MONDO:0009421_MONDO:1011118,"hypogonadism, male",MONDO_grouped,disease,DISEASE_9920
9921,9921,9921,9921,9921,9921,9921,9921,MONDO:0008515_MONDO:0008512_MONDO:0008516_MONDO:0008514_MONDO:0010669_MONDO:0021002_MONDO:0017460_MONDO:1010824_MONDO:1010825_MONDO:1010827_MONDO:1010828,syndactyly,MONDO_grouped,disease,DISEASE_9921
9922,9922,9922,9922,9922,9922,9922,9922,MONDO:0001562,displacement of cardia through esophageal hiatus,MONDO,disease,DISEASE_9922
9923,9923,9923,9923,9923,9923,9923,9923,MONDO:0012708,"primary lateral sclerosis, adult, 1",MONDO,disease,DISEASE_9923
9924,9924,9924,9924,9924,9924,9924,9924,MONDO:0850472,ST2 diffuse large B-cell lymphoma,MONDO,disease,DISEASE_9924
9925,9925,9925,9925,9925,9925,9925,9925,MONDO:0006054,reproductive system neoplasm,MONDO,disease,DISEASE_9925
9926,9926,9926,9926,9926,9926,9926,9926,MONDO:0015908,chromomycosis,MONDO,disease,DISEASE_9926
9927,9927,9927,9927,9927,9927,9927,9927,MONDO:0009450,ciliary dyskinesia with excessively long cilia,MONDO,disease,DISEASE_9927
9928,9928,9928,9928,9928,9928,9928,9928,MONDO:0011317,"microcephaly, severe, with skeletal anomalies including posterior rib-Gap defects",MONDO,disease,DISEASE_9928
9929,9929,9929,9929,9929,9929,9929,9929,MONDO:0008790,"anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism",MONDO,disease,DISEASE_9929
9930,9930,9930,9930,9930,9930,9930,9930,MONDO:1011929,"guttural pouch tympany, non-human animal",MONDO,disease,DISEASE_9930
9931,9931,9931,9931,9931,9931,9931,9931,MONDO:0002406,dermatitis,MONDO,disease,DISEASE_9931
9932,9932,9932,9932,9932,9932,9932,9932,MONDO:0008759,oxoglutaricaciduria,MONDO,disease,DISEASE_9932
9933,9933,9933,9933,9933,9933,9933,9933,MONDO:0006871,non-gestational choriocarcinoma,MONDO,disease,DISEASE_9933
9934,9934,9934,9934,9934,9934,9934,9934,MONDO:0014510_MONDO:0100275,fatty acyl-CoA reductase 1 deficiency,MONDO_grouped,disease,DISEASE_9934
9935,9935,9935,9935,9935,9935,9935,9935,MONDO:0060622,neurodevelopmental disorder with severe motor impairment and absent language,MONDO,disease,DISEASE_9935
9936,9936,9936,9936,9936,9936,9936,9936,MONDO:0013626,"psoriasis 14, pustular",MONDO,disease,DISEASE_9936
9937,9937,9937,9937,9937,9937,9937,9937,MONDO:0004397,benign mediastinal psammomatous neurilemmoma,MONDO,disease,DISEASE_9937
9938,9938,9938,9938,9938,9938,9938,9938,MONDO:0100125,hallucinogen-persisting perception disorder,MONDO,disease,DISEASE_9938
9939,9939,9939,9939,9939,9939,9939,9939,MONDO:0014423,severe combined immunodeficiency due to DNA-PKcs deficiency,MONDO,disease,DISEASE_9939
9940,9940,9940,9940,9940,9940,9940,9940,MONDO:0008006,Mobius syndrome,MONDO,disease,DISEASE_9940
9941,9941,9941,9941,9941,9941,9941,9941,MONDO:0015644,audiogenic seizures,MONDO,disease,DISEASE_9941
9942,9942,9942,9942,9942,9942,9942,9942,MONDO:0015764,mosaic trisomy 20,MONDO,disease,DISEASE_9942
9943,9943,9943,9943,9943,9943,9943,9943,MONDO:0003562,rete testis neoplasm,MONDO,disease,DISEASE_9943
9944,9944,9944,9944,9944,9944,9944,9944,MONDO:0000405,anal canal cancer,MONDO,disease,DISEASE_9944
9945,9945,9945,9945,9945,9945,9945,9945,MONDO:0001480,malignant tumor of undescended testis,MONDO,disease,DISEASE_9945
9946,9946,9946,9946,9946,9946,9946,9946,MONDO:0032894,"neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy",MONDO,disease,DISEASE_9946
9947,9947,9947,9947,9947,9947,9947,9947,MONDO:0016468,toxin-mediated infectious botulism,MONDO,disease,DISEASE_9947
9948,9948,9948,9948,9948,9948,9948,9948,MONDO:0016066,sternal cleft,MONDO,disease,DISEASE_9948
9949,9949,9949,9949,9949,9949,9949,9949,MONDO:0016093,borderline epithelial tumor of ovary,MONDO,disease,DISEASE_9949
9950,9950,9950,9950,9950,9950,9950,9950,MONDO:0009719_MONDO:0007909,familial atrial myxoma,MONDO_grouped,disease,DISEASE_9950
9951,9951,9951,9951,9951,9951,9951,9951,MONDO:0009409,"hypervitaminosis a, susceptibility to",MONDO,disease,DISEASE_9951
9952,9952,9952,9952,9952,9952,9952,9952,MONDO:0018146_MONDO:0018147,idiopathic macular telangiectasia,MONDO_grouped,disease,DISEASE_9952
9953,9953,9953,9953,9953,9953,9953,9953,MONDO:0005665,Bell's palsy,MONDO,disease,DISEASE_9953
9954,9954,9954,9954,9954,9954,9954,9954,MONDO:0005508,hereditary multiple osteochondromas,MONDO,disease,DISEASE_9954
9955,9955,9955,9955,9955,9955,9955,9955,MONDO:0029134,severe combined immunodeficiency due to CARMIL2 deficiency,MONDO,disease,DISEASE_9955
9956,9956,9956,9956,9956,9956,9956,9956,MONDO:0019484,hypothalamic hamartomas with gelastic seizures,MONDO,disease,DISEASE_9956
9957,9957,9957,9957,9957,9957,9957,9957,MONDO:0002547,nerve sheath neoplasm,MONDO,disease,DISEASE_9957
9958,9958,9958,9958,9958,9958,9958,9958,MONDO:0010620,"hypouricemia, familial renal, due to tubular hypersecretion",MONDO,disease,DISEASE_9958
9959,9959,9959,9959,9959,9959,9959,9959,MONDO:1010053,"familial goiter, non-human animal",MONDO,disease,DISEASE_9959
9960,9960,9960,9960,9960,9960,9960,9960,MONDO:0007355,uveal coloboma-cleft lip and palate-intellectual disability,MONDO,disease,DISEASE_9960
9961,9961,9961,9961,9961,9961,9961,9961,MONDO:1011858,"progressive spinal myelopathy, non-human animal",MONDO,disease,DISEASE_9961
9962,9962,9962,9962,9962,9962,9962,9962,MONDO:0019131,ossification anomalies-psychomotor developmental delay syndrome,MONDO,disease,DISEASE_9962
9963,9963,9963,9963,9963,9963,9963,9963,MONDO:0009347,familial lipochrome histiocytosis,MONDO,disease,DISEASE_9963
9964,9964,9964,9964,9964,9964,9964,9964,MONDO:0014086_MONDO:0013924_MONDO:0013460_MONDO:0013459_MONDO:0012592_MONDO:0009804_MONDO:0014672_MONDO:0008148_MONDO:0049223_MONDO:0957988_MONDO:0009805_MONDO:0014544_MONDO:0030861_MONDO:0013515_MONDO:0012536_MONDO:0008146_MONDO:0014029_MONDO:0008147_MONDO:0012581_MONDO:0032846_MONDO:0012591_MONDO:0044329_MONDO:0019019_MONDO:1011581_MONDO:1011580_MONDO:1011582_MONDO:1011583,osteogenesis imperfecta,MONDO_grouped,disease,DISEASE_9964
9965,9965,9965,9965,9965,9965,9965,9965,MONDO:0008536,temperature-sensitive lethal mutation,MONDO,disease,DISEASE_9965
9966,9966,9966,9966,9966,9966,9966,9966,MONDO:0019388,pelvis syndrome,MONDO,disease,DISEASE_9966
9967,9967,9967,9967,9967,9967,9967,9967,MONDO:0021642,vulval varices,MONDO,disease,DISEASE_9967
9968,9968,9968,9968,9968,9968,9968,9968,MONDO:0013899_MONDO:0010194_MONDO:0018096,Weill-Marchesani syndrome,MONDO_grouped,disease,DISEASE_9968
9969,9969,9969,9969,9969,9969,9969,9969,MONDO:0022308,corticobasal degeneration disorder,MONDO,disease,DISEASE_9969
9970,9970,9970,9970,9970,9970,9970,9970,MONDO:0010106,"testes, rudimentary",MONDO,disease,DISEASE_9970
9971,9971,9971,9971,9971,9971,9971,9971,MONDO:0010006,Sandhoff disease,MONDO,disease,DISEASE_9971
9972,9972,9972,9972,9972,9972,9972,9972,MONDO:0859136,Alzahrani-Kuwahara syndrome,MONDO,disease,DISEASE_9972
9973,9973,9973,9973,9973,9973,9973,9973,MONDO:0859148,neurodevelopmental disorder with seizures and gingival overgrowth,MONDO,disease,DISEASE_9973
9974,9974,9974,9974,9974,9974,9974,9974,MONDO:0010679,Duchenne muscular dystrophy,MONDO,disease,DISEASE_9974
9975,9975,9975,9975,9975,9975,9975,9975,MONDO:0012693,glycogen storage disease due to muscle and heart glycogen synthase deficiency,MONDO,disease,DISEASE_9975
9976,9976,9976,9976,9976,9976,9976,9976,MONDO:0035876,belinostat toxicity or dose selection,MONDO,disease,DISEASE_9976
9977,9977,9977,9977,9977,9977,9977,9977,MONDO:0009465,multiple intestinal atresia,MONDO,disease,DISEASE_9977
9978,9978,9978,9978,9978,9978,9978,9978,MONDO:0009029,"cranial nerves, congenital paresis of",MONDO,disease,DISEASE_9978
9979,9979,9979,9979,9979,9979,9979,9979,MONDO:0001428,pylorospasm,MONDO,disease,DISEASE_9979
9980,9980,9980,9980,9980,9980,9980,9980,MONDO:0021120,functioning endocrine neoplasm,MONDO,disease,DISEASE_9980
9981,9981,9981,9981,9981,9981,9981,9981,MONDO:0007183,"azotemia, familial",MONDO,disease,DISEASE_9981
9982,9982,9982,9982,9982,9982,9982,9982,MONDO:0014973,"sudden cardiac failure, infantile",MONDO,disease,DISEASE_9982
9983,9983,9983,9983,9983,9983,9983,9983,MONDO:0012910_MONDO:0013068,age-related hearing impairment,MONDO_grouped,disease,DISEASE_9983
9984,9984,9984,9984,9984,9984,9984,9984,MONDO:0006155,colon neuroendocrine tumor G1,MONDO,disease,DISEASE_9984
9985,9985,9985,9985,9985,9985,9985,9985,MONDO:0014912,"autoinflammation, panniculitis, and dermatosis syndrome, autosomal recessive",MONDO,disease,DISEASE_9985
9986,9986,9986,9986,9986,9986,9986,9986,MONDO:0037254,transitional cell neoplasm,MONDO,disease,DISEASE_9986
9987,9987,9987,9987,9987,9987,9987,9987,MONDO:0010181,oculogastrointestinal muscular dystrophy,MONDO,disease,DISEASE_9987
9988,9988,9988,9988,9988,9988,9988,9988,MONDO:0016642_MONDO:0004146,meningioma,MONDO_grouped,disease,DISEASE_9988
9989,9989,9989,9989,9989,9989,9989,9989,MONDO:0007689,guanylate kinase 3,MONDO,disease,DISEASE_9989
9990,9990,9990,9990,9990,9990,9990,9990,MONDO:0010078,spondyloperipheral dysplasia,MONDO,disease,DISEASE_9990
9991,9991,9991,9991,9991,9991,9991,9991,MONDO:0017958,magic syndrome,MONDO,disease,DISEASE_9991
9992,9992,9992,9992,9992,9992,9992,9992,MONDO:0008711,Goodman syndrome,MONDO,disease,DISEASE_9992
9993,9993,9993,9993,9993,9993,9993,9993,MONDO:0021698_MONDO:0002494,alcohol-related disorders,MONDO_grouped,disease,DISEASE_9993
9994,9994,9994,9994,9994,9994,9994,9994,MONDO:0020323,primary mediastinal large B-cell lymphoma,MONDO,disease,DISEASE_9994
9995,9995,9995,9995,9995,9995,9995,9995,MONDO:0005420_MONDO:0016412,hypothyroidism,MONDO_grouped,disease,DISEASE_9995
9996,9996,9996,9996,9996,9996,9996,9996,MONDO:1011669,"spina bifida with myelomeningocele, non-human animal",MONDO,disease,DISEASE_9996
9997,9997,9997,9997,9997,9997,9997,9997,MONDO:0011424,Carney triad,MONDO,disease,DISEASE_9997
9998,9998,9998,9998,9998,9998,9998,9998,MONDO:0009722,Bailey-Bloch congenital myopathy,MONDO,disease,DISEASE_9998
9999,9999,9999,9999,9999,9999,9999,9999,MONDO:0017100,neutropenia-monocytopenia-deafness syndrome,MONDO,disease,DISEASE_9999
10000,10000,10000,10000,10000,10000,10000,10000,MONDO:0006983,subclavian steal syndrome,MONDO,disease,DISEASE_10000
10001,10001,10001,10001,10001,10001,10001,10001,MONDO:0005722,croup,MONDO,disease,DISEASE_10001
10002,10002,10002,10002,10002,10002,10002,10002,MONDO:0003556,endometrial adenosquamous carcinoma,MONDO,disease,DISEASE_10002
10003,10003,10003,10003,10003,10003,10003,10003,MONDO:0035660,GNAO1-related developmental delay-seizures-movement disorder spectrum,MONDO,disease,DISEASE_10003
10004,10004,10004,10004,10004,10004,10004,10004,MONDO:0020664,spindle cell neoplasm,MONDO,disease,DISEASE_10004
10005,10005,10005,10005,10005,10005,10005,10005,MONDO:0008409,"congenital myopathy 7A, myosin storage, autosomal dominant",MONDO,disease,DISEASE_10005
10006,10006,10006,10006,10006,10006,10006,10006,MONDO:0000462,eye adnexa disorder,MONDO,disease,DISEASE_10006
10007,10007,10007,10007,10007,10007,10007,10007,MONDO:0015962,inherited renal tubular disease,MONDO,disease,DISEASE_10007
10008,10008,10008,10008,10008,10008,10008,10008,MONDO:0700082,Robertsonian translocation Down syndrome,MONDO,disease,DISEASE_10008
10009,10009,10009,10009,10009,10009,10009,10009,MONDO:0011245,"ichthyosis, hystrix-like, with hearing loss",MONDO,disease,DISEASE_10009
10010,10010,10010,10010,10010,10010,10010,10010,MONDO:1011266,"cone-rod dystrophy, PDE6B-related dog",MONDO,disease,DISEASE_10010
10011,10011,10011,10011,10011,10011,10011,10011,MONDO:0007383,Stern-Lubinsky-Durrie syndrome,MONDO,disease,DISEASE_10011
10012,10012,10012,10012,10012,10012,10012,10012,MONDO:0020336_MONDO:0014676_MONDO:0013677_MONDO:0021569_MONDO:0013072_MONDO:0013071,autosomal dominant Emery-Dreifuss muscular dystrophy,MONDO_grouped,disease,DISEASE_10012
10013,10013,10013,10013,10013,10013,10013,10013,MONDO:0002682,cerebral ventricle cancer,MONDO,disease,DISEASE_10013
10014,10014,10014,10014,10014,10014,10014,10014,MONDO:0700268,BRCA1-related cancer predisposition,MONDO,disease,DISEASE_10014
10015,10015,10015,10015,10015,10015,10015,10015,MONDO:0015809,localized pagetoid reticulosis,MONDO,disease,DISEASE_10015
10016,10016,10016,10016,10016,10016,10016,10016,MONDO:0022854,congenital unilateral pulmonary hypoplasia,MONDO,disease,DISEASE_10016
10017,10017,10017,10017,10017,10017,10017,10017,MONDO:0020466,monosomy X,MONDO,disease,DISEASE_10017
10018,10018,10018,10018,10018,10018,10018,10018,MONDO:0044067,"candidiasis, invasive",MONDO,disease,DISEASE_10018
10019,10019,10019,10019,10019,10019,10019,10019,MONDO:0001685,chronic follicular conjunctivitis,MONDO,disease,DISEASE_10019
10020,10020,10020,10020,10020,10020,10020,10020,MONDO:0013903_MONDO:0012015_MONDO:0009762_MONDO:0008106,"nystagmus 7, congenital, autosomal dominant",MONDO_grouped,disease,DISEASE_10020
10021,10021,10021,10021,10021,10021,10021,10021,MONDO:0008936,cerebellar ataxia and neurosensory deafness,MONDO,disease,DISEASE_10021
10022,10022,10022,10022,10022,10022,10022,10022,MONDO:0022761,chromosome 3 duplication syndrome,MONDO,disease,DISEASE_10022
10023,10023,10023,10023,10023,10023,10023,10023,MONDO:0020866,nasopharyngeal diphtheria,MONDO,disease,DISEASE_10023
10024,10024,10024,10024,10024,10024,10024,10024,MONDO:0006035,gastric tubular adenocarcinoma,MONDO,disease,DISEASE_10024
10025,10025,10025,10025,10025,10025,10025,10025,MONDO:0002770,vaginal discharge,MONDO,disease,DISEASE_10025
10026,10026,10026,10026,10026,10026,10026,10026,MONDO:0010400,X-linked scapuloperoneal muscular dystrophy,MONDO,disease,DISEASE_10026
10027,10027,10027,10027,10027,10027,10027,10027,MONDO:0003993_MONDO:0004013,childhood vagina botryoid rhabdomyosarcoma,MONDO_grouped,disease,DISEASE_10027
10028,10028,10028,10028,10028,10028,10028,10028,MONDO:0013311,ectodermal dysplasia-syndactyly syndrome,MONDO,disease,DISEASE_10028
10029,10029,10029,10029,10029,10029,10029,10029,MONDO:0005375,nasopharyngeal neoplasm,MONDO,disease,DISEASE_10029
10030,10030,10030,10030,10030,10030,10030,10030,MONDO:0001883,blue toe syndrome,MONDO,disease,DISEASE_10030
10031,10031,10031,10031,10031,10031,10031,10031,MONDO:0035314,obsolete congenital tricuspid valve dysplasia,MONDO,disease,DISEASE_10031
10032,10032,10032,10032,10032,10032,10032,10032,MONDO:0007145_MONDO:0021908,aplasia cutis congenita,MONDO_grouped,disease,DISEASE_10032
10033,10033,10033,10033,10033,10033,10033,10033,MONDO:0030931_MONDO:0054700_MONDO:0054699_MONDO:0968983_MONDO:0030924_MONDO:0054698,proteasome-associated autoinflammatory syndrome,MONDO_grouped,disease,DISEASE_10033
10034,10034,10034,10034,10034,10034,10034,10034,MONDO:0005395,movement disorder,MONDO,disease,DISEASE_10034
10035,10035,10035,10035,10035,10035,10035,10035,MONDO:0001094_MONDO:0001864,residual stage of open angle glaucoma,MONDO_grouped,disease,DISEASE_10035
10036,10036,10036,10036,10036,10036,10036,10036,MONDO:0014404,Webb-Dattani syndrome,MONDO,disease,DISEASE_10036
10037,10037,10037,10037,10037,10037,10037,10037,MONDO:0010182,"hypercarotenemia and vitamin A deficiency, autosomal recessive",MONDO,disease,DISEASE_10037
10038,10038,10038,10038,10038,10038,10038,10038,MONDO:0100320,post-COVID-19 disorder,MONDO,disease,DISEASE_10038
10039,10039,10039,10039,10039,10039,10039,10039,MONDO:0008154,osteomas of mandible,MONDO,disease,DISEASE_10039
10040,10040,10040,10040,10040,10040,10040,10040,MONDO:1011123,"persistent Mullerian duct syndrome, domestic cat",MONDO,disease,DISEASE_10040
10041,10041,10041,10041,10041,10041,10041,10041,MONDO:0100012_MONDO:0100013,paratenonitis,MONDO_grouped,disease,DISEASE_10041
10042,10042,10042,10042,10042,10042,10042,10042,MONDO:0018858,Graham Little-Piccardi-Lassueur syndrome,MONDO,disease,DISEASE_10042
10043,10043,10043,10043,10043,10043,10043,10043,MONDO:0001772,ulcer of anus and rectum,MONDO,disease,DISEASE_10043
10044,10044,10044,10044,10044,10044,10044,10044,MONDO:0008301,Guttmacher syndrome,MONDO,disease,DISEASE_10044
10045,10045,10045,10045,10045,10045,10045,10045,MONDO:0003516,adult teratoma,MONDO,disease,DISEASE_10045
10046,10046,10046,10046,10046,10046,10046,10046,MONDO:0020366,congenital glaucoma,MONDO,disease,DISEASE_10046
10047,10047,10047,10047,10047,10047,10047,10047,MONDO:1011114,"cryptorchidism, llama",MONDO,disease,DISEASE_10047
10048,10048,10048,10048,10048,10048,10048,10048,MONDO:0020290,familial atrioventricular septal defect,MONDO,disease,DISEASE_10048
10049,10049,10049,10049,10049,10049,10049,10049,MONDO:1011973,"pyknodysostosis, non-human animal",MONDO,disease,DISEASE_10049
10050,10050,10050,10050,10050,10050,10050,10050,MONDO:0011149,"premature aging syndrome, Okamoto type",MONDO,disease,DISEASE_10050
10051,10051,10051,10051,10051,10051,10051,10051,MONDO:0020115_MONDO:0002438_MONDO:0004563,secondary polycythemia,MONDO_grouped,disease,DISEASE_10051
10052,10052,10052,10052,10052,10052,10052,10052,MONDO:0017577,spontaneous periodic hypothermia,MONDO,disease,DISEASE_10052
10053,10053,10053,10053,10053,10053,10053,10053,MONDO:0007593,facial spasm,MONDO,disease,DISEASE_10053
10054,10054,10054,10054,10054,10054,10054,10054,MONDO:1012929_MONDO:1012938_MONDO:1012949,"Alzheimer disease, APP-related, pig",MONDO_grouped,disease,DISEASE_10054
10055,10055,10055,10055,10055,10055,10055,10055,MONDO:0017867,distal 17p13.1 microdeletion syndrome,MONDO,disease,DISEASE_10055
10056,10056,10056,10056,10056,10056,10056,10056,MONDO:1011442,"enteropathy-associated T cell lymphoma, non-human animal",MONDO,disease,DISEASE_10056
10057,10057,10057,10057,10057,10057,10057,10057,MONDO:0020669_MONDO:0001735,paranasal sinus cancer,MONDO_grouped,disease,DISEASE_10057
10058,10058,10058,10058,10058,10058,10058,10058,MONDO:0018648,Keratocystic odontogenic tumor,MONDO,disease,DISEASE_10058
10059,10059,10059,10059,10059,10059,10059,10059,MONDO:0044972_MONDO:0004802,eosinophil disorder,MONDO_grouped,disease,DISEASE_10059
10060,10060,10060,10060,10060,10060,10060,10060,MONDO:0019782_MONDO:0017548_MONDO:0017549_MONDO:0017551_MONDO:0017553,humero-ulnar synostosis,MONDO_grouped,disease,DISEASE_10060
10061,10061,10061,10061,10061,10061,10061,10061,MONDO:0024387,benign ovarian sex cord-stromal tumor,MONDO,disease,DISEASE_10061
10062,10062,10062,10062,10062,10062,10062,10062,MONDO:1040033,congenital muscular dystrophy without intellectual disability,MONDO,disease,DISEASE_10062
10063,10063,10063,10063,10063,10063,10063,10063,MONDO:0031054_MONDO:0859353,"ciliary dyskinesia, primary, 48, without situs inversus",MONDO_grouped,disease,DISEASE_10063
10064,10064,10064,10064,10064,10064,10064,10064,MONDO:0006303,middle ear squamous cell carcinoma,MONDO,disease,DISEASE_10064
10065,10065,10065,10065,10065,10065,10065,10065,MONDO:1011125,"priapism, dog",MONDO,disease,DISEASE_10065
10066,10066,10066,10066,10066,10066,10066,10066,MONDO:0008452,"spinal muscular atrophy, facioscapulohumeral type",MONDO,disease,DISEASE_10066
10067,10067,10067,10067,10067,10067,10067,10067,MONDO:1010636,"factor XI deficiency, dog",MONDO,disease,DISEASE_10067
10068,10068,10068,10068,10068,10068,10068,10068,MONDO:0010064,spastic ataxia-corneal dystrophy syndrome,MONDO,disease,DISEASE_10068
10069,10069,10069,10069,10069,10069,10069,10069,MONDO:0002618_MONDO:0006480,undifferentiated high grade pleomorphic sarcoma of bone,MONDO_grouped,disease,DISEASE_10069
10070,10070,10070,10070,10070,10070,10070,10070,MONDO:0021482,benign neoplasm of middle ear,MONDO,disease,DISEASE_10070
10071,10071,10071,10071,10071,10071,10071,10071,MONDO:0002386,mixed epithelial stromal tumor of the kidney,MONDO,disease,DISEASE_10071
10072,10072,10072,10072,10072,10072,10072,10072,MONDO:0016087,progressive non-infectious anterior vertebral fusion,MONDO,disease,DISEASE_10072
10073,10073,10073,10073,10073,10073,10073,10073,MONDO:0002486,lobular neoplasia,MONDO,disease,DISEASE_10073
10074,10074,10074,10074,10074,10074,10074,10074,MONDO:0007807,hypoxanthine guanine phosphoribosyltransferase suppressor,MONDO,disease,DISEASE_10074
10075,10075,10075,10075,10075,10075,10075,10075,MONDO:0008194,Paramolar tubercle of bolk,MONDO,disease,DISEASE_10075
10076,10076,10076,10076,10076,10076,10076,10076,MONDO:0043283,silicosiderosis,MONDO,disease,DISEASE_10076
10077,10077,10077,10077,10077,10077,10077,10077,MONDO:0007101,familial primary localized cutaneous amyloidosis,MONDO,disease,DISEASE_10077
10078,10078,10078,10078,10078,10078,10078,10078,MONDO:1012477,"disproportionate short-limbed chondrodysplasia, ITGA10-related, dog",MONDO,disease,DISEASE_10078
10079,10079,10079,10079,10079,10079,10079,10079,MONDO:0044997,midbrain disorder,MONDO,disease,DISEASE_10079
10080,10080,10080,10080,10080,10080,10080,10080,MONDO:0005837,mandibular cancer,MONDO,disease,DISEASE_10080
10081,10081,10081,10081,10081,10081,10081,10081,MONDO:0017789,idiopathic linear interstitial keratitis,MONDO,disease,DISEASE_10081
10082,10082,10082,10082,10082,10082,10082,10082,MONDO:0009328,"hemangiomatosis, cutaneous, with associated features",MONDO,disease,DISEASE_10082
10083,10083,10083,10083,10083,10083,10083,10083,MONDO:0014839,"chorea, childhood-onset, with psychomotor retardation",MONDO,disease,DISEASE_10083
10084,10084,10084,10084,10084,10084,10084,10084,MONDO:0700110,"pneumonia, non-human animal",MONDO,disease,DISEASE_10084
10085,10085,10085,10085,10085,10085,10085,10085,MONDO:1011919,"androgen insensitivity syndrome, non-human animal",MONDO,disease,DISEASE_10085
10086,10086,10086,10086,10086,10086,10086,10086,MONDO:0001308,corneal deposit,MONDO,disease,DISEASE_10086
10087,10087,10087,10087,10087,10087,10087,10087,MONDO:0001706_MONDO:0001707_MONDO:0001708,cerebral sarcoidosis,MONDO_grouped,disease,DISEASE_10087
10088,10088,10088,10088,10088,10088,10088,10088,MONDO:0019317,follicular atrophoderma-basal cell carcinoma,MONDO,disease,DISEASE_10088
10089,10089,10089,10089,10089,10089,10089,10089,MONDO:1010640,"factor XII deficiency, domestic cat",MONDO,disease,DISEASE_10089
10090,10090,10090,10090,10090,10090,10090,10090,MONDO:0035407,furuncular myiasis due to Cordylobia anthropophaga,MONDO,disease,DISEASE_10090
10091,10091,10091,10091,10091,10091,10091,10091,MONDO:0000563,GRID2-related autosomal dominant spinocerebellar ataxia,MONDO,disease,DISEASE_10091
10092,10092,10092,10092,10092,10092,10092,10092,MONDO:0001698,tinea profunda,MONDO,disease,DISEASE_10092
10093,10093,10093,10093,10093,10093,10093,10093,MONDO:0800139,HELIOS deficiency,MONDO,disease,DISEASE_10093
10094,10094,10094,10094,10094,10094,10094,10094,MONDO:0016490,hemoglobin C-beta-thalassemia syndrome,MONDO,disease,DISEASE_10094
10095,10095,10095,10095,10095,10095,10095,10095,MONDO:0004041_MONDO:0021109_MONDO:0044906,urothelial papilloma,MONDO_grouped,disease,DISEASE_10095
10096,10096,10096,10096,10096,10096,10096,10096,MONDO:1012940,"deafness, CDH23-related, dog",MONDO,disease,DISEASE_10096
10097,10097,10097,10097,10097,10097,10097,10097,MONDO:0018890,Lyell syndrome,MONDO,disease,DISEASE_10097
10098,10098,10098,10098,10098,10098,10098,10098,MONDO:0021070,sublingual gland carcinoma,MONDO,disease,DISEASE_10098
10099,10099,10099,10099,10099,10099,10099,10099,MONDO:0004212,vulvar keratoacanthoma-like carcinoma,MONDO,disease,DISEASE_10099
10100,10100,10100,10100,10100,10100,10100,10100,MONDO:0009020_MONDO:1011278,macular corneal dystrophy,MONDO_grouped,disease,DISEASE_10100
10101,10101,10101,10101,10101,10101,10101,10101,MONDO:0000110,bifid nose,MONDO,disease,DISEASE_10101
10102,10102,10102,10102,10102,10102,10102,10102,MONDO:0021511,benign neoplasm of adrenal gland,MONDO,disease,DISEASE_10102
10103,10103,10103,10103,10103,10103,10103,10103,MONDO:1012284,"stomach ulcer, pig",MONDO,disease,DISEASE_10103
10104,10104,10104,10104,10104,10104,10104,10104,MONDO:0009883,alpha-2-plasmin inhibitor deficiency,MONDO,disease,DISEASE_10104
10105,10105,10105,10105,10105,10105,10105,10105,MONDO:1012815,"laryngeal paralysis, RAPGEF6-related, dog",MONDO,disease,DISEASE_10105
10106,10106,10106,10106,10106,10106,10106,10106,MONDO:0014803,spasticity-ataxia-gait anomalies syndrome,MONDO,disease,DISEASE_10106
10107,10107,10107,10107,10107,10107,10107,10107,MONDO:0012203,familial hyperthyroidism due to mutations in TSH receptor,MONDO,disease,DISEASE_10107
10108,10108,10108,10108,10108,10108,10108,10108,MONDO:0001789,neurofibroma of spinal cord,MONDO,disease,DISEASE_10108
10109,10109,10109,10109,10109,10109,10109,10109,MONDO:0019823,premature closure of the arterial duct,MONDO,disease,DISEASE_10109
10110,10110,10110,10110,10110,10110,10110,10110,MONDO:1012287_MONDO:1012351,"progressive ataxia, dog",MONDO_grouped,disease,DISEASE_10110
10111,10111,10111,10111,10111,10111,10111,10111,MONDO:0971058,verruga peruana,MONDO,disease,DISEASE_10111
10112,10112,10112,10112,10112,10112,10112,10112,MONDO:0001515,corneal degeneration,MONDO,disease,DISEASE_10112
10113,10113,10113,10113,10113,10113,10113,10113,MONDO:1011790,"dysphagia-associated muscular dystrophy, non-human animal",MONDO,disease,DISEASE_10113
10114,10114,10114,10114,10114,10114,10114,10114,MONDO:1011074,"urolithiasis, Dusky leaf-monkey",MONDO,disease,DISEASE_10114
10115,10115,10115,10115,10115,10115,10115,10115,MONDO:0025505,mink viral enteritis,MONDO,disease,DISEASE_10115
10116,10116,10116,10116,10116,10116,10116,10116,MONDO:0021148,female reproductive system neoplasm,MONDO,disease,DISEASE_10116
10117,10117,10117,10117,10117,10117,10117,10117,MONDO:0002287,glandular cystitis,MONDO,disease,DISEASE_10117
10118,10118,10118,10118,10118,10118,10118,10118,MONDO:0000261,adenoiditis,MONDO,disease,DISEASE_10118
10119,10119,10119,10119,10119,10119,10119,10119,MONDO:0002805,hidradenoma,MONDO,disease,DISEASE_10119
10120,10120,10120,10120,10120,10120,10120,10120,MONDO:0024621_MONDO:0005177,serous cystadenocarcinoma,MONDO_grouped,disease,DISEASE_10120
10121,10121,10121,10121,10121,10121,10121,10121,MONDO:0006487,vaginal adenoid cystic carcinoma,MONDO,disease,DISEASE_10121
10122,10122,10122,10122,10122,10122,10122,10122,MONDO:0032566,squalene synthase deficiency,MONDO,disease,DISEASE_10122
10123,10123,10123,10123,10123,10123,10123,10123,MONDO:0020636,Mendelian susceptibility to mycobacterial diseases due to a complete deficiency,MONDO,disease,DISEASE_10123
10124,10124,10124,10124,10124,10124,10124,10124,MONDO:0005601_MONDO:0003887_MONDO:0002583_MONDO:0002701_MONDO:0003839_MONDO:0004032,ovarian mucinous adenocarcinoma,MONDO_grouped,disease,DISEASE_10124
10125,10125,10125,10125,10125,10125,10125,10125,MONDO:0013268,frontonasal dysplasia with alopecia and genital anomaly,MONDO,disease,DISEASE_10125
10126,10126,10126,10126,10126,10126,10126,10126,MONDO:0957225_MONDO:0958240,"neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities",MONDO_grouped,disease,DISEASE_10126
10127,10127,10127,10127,10127,10127,10127,10127,MONDO:0007128,annular erythema,MONDO,disease,DISEASE_10127
10128,10128,10128,10128,10128,10128,10128,10128,MONDO:0004417,nested variant infiltrating bladder urothelial carcinoma,MONDO,disease,DISEASE_10128
10129,10129,10129,10129,10129,10129,10129,10129,MONDO:0019290,hypopigmentation of the skin,MONDO,disease,DISEASE_10129
10130,10130,10130,10130,10130,10130,10130,10130,MONDO:0001084_MONDO:0001086,primary optic atrophy,MONDO_grouped,disease,DISEASE_10130
10131,10131,10131,10131,10131,10131,10131,10131,MONDO:1030002,dysplasia of the proximal femoral epiphyses,MONDO,disease,DISEASE_10131
10132,10132,10132,10132,10132,10132,10132,10132,MONDO:1010586,"familial goiter, domestic cat",MONDO,disease,DISEASE_10132
10133,10133,10133,10133,10133,10133,10133,10133,MONDO:0012342,7q11.23 microduplication syndrome,MONDO,disease,DISEASE_10133
10134,10134,10134,10134,10134,10134,10134,10134,MONDO:0015924,pulmonary arterial hypertension,MONDO,disease,DISEASE_10134
10135,10135,10135,10135,10135,10135,10135,10135,MONDO:0970962,terminal myelocystocele,MONDO,disease,DISEASE_10135
10136,10136,10136,10136,10136,10136,10136,10136,MONDO:0005510,hydronephrosis,MONDO,disease,DISEASE_10136
10137,10137,10137,10137,10137,10137,10137,10137,MONDO:0958352,true myeloschisis,MONDO,disease,DISEASE_10137
10138,10138,10138,10138,10138,10138,10138,10138,MONDO:0044970,mitochondrial disease,MONDO,disease,DISEASE_10138
10139,10139,10139,10139,10139,10139,10139,10139,MONDO:0002765,plantar verrucous skin carcinoma,MONDO,disease,DISEASE_10139
10140,10140,10140,10140,10140,10140,10140,10140,MONDO:0012816_MONDO:0012678_MONDO:0013544_MONDO:0013100_MONDO:0011857_MONDO:0012677_MONDO:0014156_MONDO:0015001_MONDO:0012066_MONDO:0012828_MONDO:0013513_MONDO:0013530_MONDO:0012167_MONDO:0014340_MONDO:0014155_MONDO:0013545_MONDO:0018054_MONDO:0800345_MONDO:0800349,"atrial fibrillation, familial",MONDO_grouped,disease,DISEASE_10140
10141,10141,10141,10141,10141,10141,10141,10141,MONDO:0031003_MONDO:0011374_MONDO:0007750_MONDO:0031446_MONDO:0100327,"hypercholanemia, familial",MONDO_grouped,disease,DISEASE_10141
10142,10142,10142,10142,10142,10142,10142,10142,MONDO:0044696,early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome,MONDO,disease,DISEASE_10142
10143,10143,10143,10143,10143,10143,10143,10143,MONDO:0010567,"cone dystrophy, X-linked, with tapetal-like sheen",MONDO,disease,DISEASE_10143
10144,10144,10144,10144,10144,10144,10144,10144,MONDO:0020708,brachial amyotrophic diplegia,MONDO,disease,DISEASE_10144
10145,10145,10145,10145,10145,10145,10145,10145,MONDO:1010571_MONDO:1011601,"diabetes mellitus, domestic guinea pig",MONDO_grouped,disease,DISEASE_10145
10146,10146,10146,10146,10146,10146,10146,10146,MONDO:1010022,"ventricular septal defect, non-human animal",MONDO,disease,DISEASE_10146
10147,10147,10147,10147,10147,10147,10147,10147,MONDO:0023133,Faye-Petersen-Ward-Carey syndrome,MONDO,disease,DISEASE_10147
10148,10148,10148,10148,10148,10148,10148,10148,MONDO:0002289,iris disorder,MONDO,disease,DISEASE_10148
10149,10149,10149,10149,10149,10149,10149,10149,MONDO:0800109_MONDO:0800111,persistent tachypnoe of infancy,MONDO_grouped,disease,DISEASE_10149
10150,10150,10150,10150,10150,10150,10150,10150,MONDO:0011524,Dianzani autoimmune lymphoproliferative disease,MONDO,disease,DISEASE_10150
10151,10151,10151,10151,10151,10151,10151,10151,MONDO:0015236,aortic arch defects,MONDO,disease,DISEASE_10151
10152,10152,10152,10152,10152,10152,10152,10152,MONDO:0002948,skin fibroepithelial basal cell carcinoma,MONDO,disease,DISEASE_10152
10153,10153,10153,10153,10153,10153,10153,10153,MONDO:0011805_MONDO:0012607_MONDO:0012067_MONDO:0012379_MONDO:0012577_MONDO:0012666_MONDO:0012771_MONDO:0013180,"asthma-related traits, susceptibility to",MONDO_grouped,disease,DISEASE_10153
10154,10154,10154,10154,10154,10154,10154,10154,MONDO:0958117,autosomal dominant combined immunodeficiency due to partial IL6ST deficiency,MONDO,disease,DISEASE_10154
10155,10155,10155,10155,10155,10155,10155,10155,MONDO:0100391_MONDO:0100392_MONDO:0100393_MONDO:0100394,"acute myeloid leukemia, t(2;12)",MONDO_grouped,disease,DISEASE_10155
10156,10156,10156,10156,10156,10156,10156,10156,MONDO:0003910,mixed cell uveal melanoma,MONDO,disease,DISEASE_10156
10157,10157,10157,10157,10157,10157,10157,10157,MONDO:0000892,colon medullary carcinoma,MONDO,disease,DISEASE_10157
10158,10158,10158,10158,10158,10158,10158,10158,MONDO:0004116,esophageal small cell neuroendocrine carcinoma,MONDO,disease,DISEASE_10158
10159,10159,10159,10159,10159,10159,10159,10159,MONDO:0001712,alexia,MONDO,disease,DISEASE_10159
10160,10160,10160,10160,10160,10160,10160,10160,MONDO:0007781_MONDO:1010455,"essential hypertension, genetic",MONDO_grouped,disease,DISEASE_10160
10161,10161,10161,10161,10161,10161,10161,10161,MONDO:0008228,pernicious anemia,MONDO,disease,DISEASE_10161
10162,10162,10162,10162,10162,10162,10162,10162,MONDO:0019854,thyroid ectopia,MONDO,disease,DISEASE_10162
10163,10163,10163,10163,10163,10163,10163,10163,MONDO:0009071,hereditary renal hypouricemia,MONDO,disease,DISEASE_10163
10164,10164,10164,10164,10164,10164,10164,10164,MONDO:0015785,Prader-Willi syndrome due to translocation,MONDO,disease,DISEASE_10164
10165,10165,10165,10165,10165,10165,10165,10165,MONDO:0011740,Carney-Stratakis syndrome,MONDO,disease,DISEASE_10165
10166,10166,10166,10166,10166,10166,10166,10166,MONDO:0008024_MONDO:0957875_MONDO:0010839_MONDO:0008025_MONDO:0060585_MONDO:0011879_MONDO:0013243_MONDO:0012080_MONDO:0013884_MONDO:0030860_MONDO:0008451_MONDO:0014259_MONDO:0015353_MONDO:0859300_MONDO:0100350_MONDO:0015362,"neuronopathy, distal hereditary motor,",MONDO_grouped,disease,DISEASE_10166
10167,10167,10167,10167,10167,10167,10167,10167,MONDO:0032770,intellectual developmental disorder with severe speech and ambulation defects,MONDO,disease,DISEASE_10167
10168,10168,10168,10168,10168,10168,10168,10168,MONDO:0006878,Moraxellaceae infectious disease,MONDO,disease,DISEASE_10168
10169,10169,10169,10169,10169,10169,10169,10169,MONDO:0017451_MONDO:0017452,non-syndromic brachydactyly of fingers,MONDO_grouped,disease,DISEASE_10169
10170,10170,10170,10170,10170,10170,10170,10170,MONDO:0013245,syndromic multisystem autoimmune disease due to ITCH deficiency,MONDO,disease,DISEASE_10170
10171,10171,10171,10171,10171,10171,10171,10171,MONDO:0016664,drug-induced vasculitis,MONDO,disease,DISEASE_10171
10172,10172,10172,10172,10172,10172,10172,10172,MONDO:0004389,mite infestation,MONDO,disease,DISEASE_10172
10173,10173,10173,10173,10173,10173,10173,10173,MONDO:0020492,hemimegalencephaly,MONDO,disease,DISEASE_10173
10174,10174,10174,10174,10174,10174,10174,10174,MONDO:0002565,myelitis,MONDO,disease,DISEASE_10174
10175,10175,10175,10175,10175,10175,10175,10175,MONDO:0007588,extrasystoles-short stature-hyperpigmentation-microcephaly syndrome,MONDO,disease,DISEASE_10175
10176,10176,10176,10176,10176,10176,10176,10176,MONDO:0004949,neoplasm of mature B-cells,MONDO,disease,DISEASE_10176
10177,10177,10177,10177,10177,10177,10177,10177,MONDO:1012316,"stomatocytosis and gastrits, dog",MONDO,disease,DISEASE_10177
10178,10178,10178,10178,10178,10178,10178,10178,MONDO:0011835,"sensory ataxic neuropathy, dysarthria, and ophthalmoparesis",MONDO,disease,DISEASE_10178
10179,10179,10179,10179,10179,10179,10179,10179,MONDO:0008733,familial glucocorticoid deficiency,MONDO,disease,DISEASE_10179
10180,10180,10180,10180,10180,10180,10180,10180,MONDO:0800414,"aplastic anemia, susceptibility to",MONDO,disease,DISEASE_10180
10181,10181,10181,10181,10181,10181,10181,10181,MONDO:0001978,regional ureteric cancer,MONDO,disease,DISEASE_10181
10182,10182,10182,10182,10182,10182,10182,10182,MONDO:0020816_MONDO:0024227,miliaria papulosa,MONDO_grouped,disease,DISEASE_10182
10183,10183,10183,10183,10183,10183,10183,10183,MONDO:0019607,unspecified juvenile idiopathic arthritis,MONDO,disease,DISEASE_10183
10184,10184,10184,10184,10184,10184,10184,10184,MONDO:1010929,"myotubular myopathy 1, dog",MONDO,disease,DISEASE_10184
10185,10185,10185,10185,10185,10185,10185,10185,MONDO:0005802,hymenolepiasis,MONDO,disease,DISEASE_10185
10186,10186,10186,10186,10186,10186,10186,10186,MONDO:0018829,familial schizencephaly,MONDO,disease,DISEASE_10186
10187,10187,10187,10187,10187,10187,10187,10187,MONDO:0001048,orbital granuloma,MONDO,disease,DISEASE_10187
10188,10188,10188,10188,10188,10188,10188,10188,MONDO:0020083,immunodeficiency-associated lymphoproliferative disease,MONDO,disease,DISEASE_10188
10189,10189,10189,10189,10189,10189,10189,10189,MONDO:0008949,"cerebral malformation, seizures, hypertrichosis, and overlapping fingers",MONDO,disease,DISEASE_10189
10190,10190,10190,10190,10190,10190,10190,10190,MONDO:0020590,mycobacterial infectious disease,MONDO,disease,DISEASE_10190
10191,10191,10191,10191,10191,10191,10191,10191,MONDO:0000162_MONDO:0011980_MONDO:0011981_MONDO:0011982_MONDO:0011983_MONDO:0800261,"autoimmune thyroid disease, susceptibility",MONDO_grouped,disease,DISEASE_10191
10192,10192,10192,10192,10192,10192,10192,10192,MONDO:1010297,"osteoarthritis, non-human animal",MONDO,disease,DISEASE_10192
10193,10193,10193,10193,10193,10193,10193,10193,MONDO:0018712,composite hemangioendothelioma,MONDO,disease,DISEASE_10193
10194,10194,10194,10194,10194,10194,10194,10194,MONDO:1012021_MONDO:1012022,"spontaneous autoimmune thyroiditis, chicken",MONDO_grouped,disease,DISEASE_10194
10195,10195,10195,10195,10195,10195,10195,10195,MONDO:0036212,spastic paraparesis-cataracts-speech delay syndrome,MONDO,disease,DISEASE_10195
10196,10196,10196,10196,10196,10196,10196,10196,MONDO:0015031,extraneural perineurioma,MONDO,disease,DISEASE_10196
10197,10197,10197,10197,10197,10197,10197,10197,MONDO:0004872_MONDO:0004873,hemorrhoid,MONDO_grouped,disease,DISEASE_10197
10198,10198,10198,10198,10198,10198,10198,10198,MONDO:0017765,disorder of magnesium transport,MONDO,disease,DISEASE_10198
10199,10199,10199,10199,10199,10199,10199,10199,MONDO:0013843,intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency,MONDO,disease,DISEASE_10199
10200,10200,10200,10200,10200,10200,10200,10200,MONDO:1010406,"hyperphagia leading to hepatic steatosis, pig",MONDO,disease,DISEASE_10200
10201,10201,10201,10201,10201,10201,10201,10201,MONDO:1011127,"testicular regression syndrome, horse",MONDO,disease,DISEASE_10201
10202,10202,10202,10202,10202,10202,10202,10202,MONDO:0015660_MONDO:0023142,sporadic fetal brain disruption sequence,MONDO_grouped,disease,DISEASE_10202
10203,10203,10203,10203,10203,10203,10203,10203,MONDO:0024571,AIDS-related disorder,MONDO,disease,DISEASE_10203
10204,10204,10204,10204,10204,10204,10204,10204,MONDO:0025138,vesicular exanthema of swine,MONDO,disease,DISEASE_10204
10205,10205,10205,10205,10205,10205,10205,10205,MONDO:1012262,"stringhalt, cattle",MONDO,disease,DISEASE_10205
10206,10206,10206,10206,10206,10206,10206,10206,MONDO:0010443,"macular degeneration, X-linked atrophic",MONDO,disease,DISEASE_10206
10207,10207,10207,10207,10207,10207,10207,10207,MONDO:0015892,growth hormone insensitivity syndrome,MONDO,disease,DISEASE_10207
10208,10208,10208,10208,10208,10208,10208,10208,MONDO:1011934,"dynamic laryngeal collapse, non-human animal",MONDO,disease,DISEASE_10208
10209,10209,10209,10209,10209,10209,10209,10209,MONDO:0010776,"hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial",MONDO,disease,DISEASE_10209
10210,10210,10210,10210,10210,10210,10210,10210,MONDO:0018263,fetal carbamazepine syndrome,MONDO,disease,DISEASE_10210
10211,10211,10211,10211,10211,10211,10211,10211,MONDO:0009115,congenital lactase deficiency,MONDO,disease,DISEASE_10211
10212,10212,10212,10212,10212,10212,10212,10212,MONDO:0015066,"neuroendocrine tumor of the appendix, well differentiated, low or intermediate grade",MONDO,disease,DISEASE_10212
10213,10213,10213,10213,10213,10213,10213,10213,MONDO:0006746,endomyocardial fibrosis,MONDO,disease,DISEASE_10213
10214,10214,10214,10214,10214,10214,10214,10214,MONDO:0017008,partial duplication of chromosome X,MONDO,disease,DISEASE_10214
10215,10215,10215,10215,10215,10215,10215,10215,MONDO:1012679,"hereditary vitamin D-resistant rickets, VDR-related, dog",MONDO,disease,DISEASE_10215
10216,10216,10216,10216,10216,10216,10216,10216,MONDO:0037939,porphyria,MONDO,disease,DISEASE_10216
10217,10217,10217,10217,10217,10217,10217,10217,MONDO:0100284,X-linked intellectual disability,MONDO,disease,DISEASE_10217
10218,10218,10218,10218,10218,10218,10218,10218,MONDO:0011263,"skeletal dysplasia and progressive central nervous system degeneration, lethal",MONDO,disease,DISEASE_10218
10219,10219,10219,10219,10219,10219,10219,10219,MONDO:1010742,"immunodeficiency IL17RA-related, cattle",MONDO,disease,DISEASE_10219
10220,10220,10220,10220,10220,10220,10220,10220,MONDO:0015753,cap myopathy,MONDO,disease,DISEASE_10220
10221,10221,10221,10221,10221,10221,10221,10221,MONDO:0004407_MONDO:0004408,stroma-dominant and stroma-poor composite ganglioneuroblastoma,MONDO_grouped,disease,DISEASE_10221
10222,10222,10222,10222,10222,10222,10222,10222,MONDO:1012256,"spina bifida with myelomeningocele, cattle",MONDO,disease,DISEASE_10222
10223,10223,10223,10223,10223,10223,10223,10223,MONDO:0011497,hereditary North American Indian childhood cirrhosis,MONDO,disease,DISEASE_10223
10224,10224,10224,10224,10224,10224,10224,10224,MONDO:0010288,adrenomyodystrophy,MONDO,disease,DISEASE_10224
10225,10225,10225,10225,10225,10225,10225,10225,MONDO:0016651,maternal uniparental disomy of chromosome 1,MONDO,disease,DISEASE_10225
10226,10226,10226,10226,10226,10226,10226,10226,MONDO:0017161,frontotemporal dementia with motor neuron disease,MONDO,disease,DISEASE_10226
10227,10227,10227,10227,10227,10227,10227,10227,MONDO:0007863,Kleine-Levin syndrome,MONDO,disease,DISEASE_10227
10228,10228,10228,10228,10228,10228,10228,10228,MONDO:0009565,microcephaly-glomerulonephritis-marfanoid habitus syndrome,MONDO,disease,DISEASE_10228
10229,10229,10229,10229,10229,10229,10229,10229,MONDO:0015300,cataract - microcornea syndrome,MONDO,disease,DISEASE_10229
10230,10230,10230,10230,10230,10230,10230,10230,MONDO:0013833_MONDO:0013832_MONDO:0054771_MONDO:0007851_MONDO:0013831_MONDO:0013830_MONDO:0015486_MONDO:0012069_MONDO:0012158_MONDO:0012236,keratoconus,MONDO_grouped,disease,DISEASE_10230
10231,10231,10231,10231,10231,10231,10231,10231,MONDO:0018559,fetal lower urinary tract obstruction,MONDO,disease,DISEASE_10231
10232,10232,10232,10232,10232,10232,10232,10232,MONDO:0024857,immature extragonadal teratoma,MONDO,disease,DISEASE_10232
10233,10233,10233,10233,10233,10233,10233,10233,MONDO:0011494,"hyaluronan metabolism, defect 1N",MONDO,disease,DISEASE_10233
10234,10234,10234,10234,10234,10234,10234,10234,MONDO:0100450,CAPN5-related vitreoretinopathy,MONDO,disease,DISEASE_10234
10235,10235,10235,10235,10235,10235,10235,10235,MONDO:0010141,tiglic acidemia,MONDO,disease,DISEASE_10235
10236,10236,10236,10236,10236,10236,10236,10236,MONDO:0013324,lymphedema-posterior choanal atresia syndrome,MONDO,disease,DISEASE_10236
10237,10237,10237,10237,10237,10237,10237,10237,MONDO:1010755_MONDO:1010792,"X-linked hypohidrotic ectodermal dysplasia, EDA-related, cattle",MONDO_grouped,disease,DISEASE_10237
10238,10238,10238,10238,10238,10238,10238,10238,MONDO:0006510_MONDO:0021568,renal tubular transport disease,MONDO_grouped,disease,DISEASE_10238
10239,10239,10239,10239,10239,10239,10239,10239,MONDO:0040654,autosomal dominant oculocutaneous albinism,MONDO,disease,DISEASE_10239
10240,10240,10240,10240,10240,10240,10240,10240,MONDO:0017869,chondroectodermal dysplasia with night blindness,MONDO,disease,DISEASE_10240
10241,10241,10241,10241,10241,10241,10241,10241,MONDO:0007754,hyperhidrosis palmaris ET plantaris,MONDO,disease,DISEASE_10241
10242,10242,10242,10242,10242,10242,10242,10242,MONDO:0005591,pit and fissure surface dental caries,MONDO,disease,DISEASE_10242
10243,10243,10243,10243,10243,10243,10243,10243,MONDO:0008153,progressive osseous heteroplasia,MONDO,disease,DISEASE_10243
10244,10244,10244,10244,10244,10244,10244,10244,MONDO:0020334_MONDO:0001482_MONDO:0035444_MONDO:0035445,mast cell leukemia,MONDO_grouped,disease,DISEASE_10244
10245,10245,10245,10245,10245,10245,10245,10245,MONDO:0011320,radioulnar synostosis-microcephaly-scoliosis syndrome,MONDO,disease,DISEASE_10245
10246,10246,10246,10246,10246,10246,10246,10246,MONDO:0800143,cytomegalovirus pneumonia due to NOS2 deficiency,MONDO,disease,DISEASE_10246
10247,10247,10247,10247,10247,10247,10247,10247,MONDO:0017360_MONDO:0019267,vitamin B12-unresponsive methylmalonic acidemia type mut0,MONDO_grouped,disease,DISEASE_10247
10248,10248,10248,10248,10248,10248,10248,10248,MONDO:0100107_MONDO:0100456,non-neonatal early infantile epileptic encephalopathy,MONDO_grouped,disease,DISEASE_10248
10249,10249,10249,10249,10249,10249,10249,10249,MONDO:0020637,Mendelian susceptibility to mycobacterial diseases due to a partial deficiency,MONDO,disease,DISEASE_10249
10250,10250,10250,10250,10250,10250,10250,10250,MONDO:0008391,Robinow-Sorauf syndrome,MONDO,disease,DISEASE_10250
10251,10251,10251,10251,10251,10251,10251,10251,MONDO:0004900,peripheral vertigo,MONDO,disease,DISEASE_10251
10252,10252,10252,10252,10252,10252,10252,10252,MONDO:0005164_MONDO:0002675,fibrosarcoma,MONDO_grouped,disease,DISEASE_10252
10253,10253,10253,10253,10253,10253,10253,10253,MONDO:0011853,"Camptosynpolydactyly, complex",MONDO,disease,DISEASE_10253
10254,10254,10254,10254,10254,10254,10254,10254,MONDO:0800301,Friedreich ataxia with retained reflexes,MONDO,disease,DISEASE_10254
10255,10255,10255,10255,10255,10255,10255,10255,MONDO:0014197,combined immunodeficiency due to MALT1 deficiency,MONDO,disease,DISEASE_10255
10256,10256,10256,10256,10256,10256,10256,10256,MONDO:0020143,cerebral lipidosis with dementia,MONDO,disease,DISEASE_10256
10257,10257,10257,10257,10257,10257,10257,10257,MONDO:0858998,mesomelic dysplasia-digital anomalies-intellectual disability syndrome,MONDO,disease,DISEASE_10257
10258,10258,10258,10258,10258,10258,10258,10258,MONDO:0956977,near-fatal asthma,MONDO,disease,DISEASE_10258
10259,10259,10259,10259,10259,10259,10259,10259,MONDO:0002402,malignant giant cell tumor,MONDO,disease,DISEASE_10259
10260,10260,10260,10260,10260,10260,10260,10260,MONDO:0850450,mixed phenotype acute leukemia with MLL rearranged,MONDO,disease,DISEASE_10260
10261,10261,10261,10261,10261,10261,10261,10261,MONDO:0000495,oppositional defiant disorder,MONDO,disease,DISEASE_10261
10262,10262,10262,10262,10262,10262,10262,10262,MONDO:0011766,"46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome",MONDO,disease,DISEASE_10262
10263,10263,10263,10263,10263,10263,10263,10263,MONDO:0007587,external auditory canal atresia-vertical talus-hypertelorism syndrome,MONDO,disease,DISEASE_10263
10264,10264,10264,10264,10264,10264,10264,10264,MONDO:0030781_MONDO:0800042_MONDO:0031213,restrictive dermopathy,MONDO_grouped,disease,DISEASE_10264
10265,10265,10265,10265,10265,10265,10265,10265,MONDO:0017103,encephaloclastic disorder,MONDO,disease,DISEASE_10265
10266,10266,10266,10266,10266,10266,10266,10266,MONDO:0012786,juvenile cataract-microcornea-renal glucosuria syndrome,MONDO,disease,DISEASE_10266
10267,10267,10267,10267,10267,10267,10267,10267,MONDO:0008741,PAGOD syndrome,MONDO,disease,DISEASE_10267
10268,10268,10268,10268,10268,10268,10268,10268,MONDO:0024498_MONDO:0013093_MONDO:0013092_MONDO:0100242_MONDO:0011800_MONDO:0013094_MONDO:0013095_MONDO:0013096_MONDO:0013097,glioma susceptibility,MONDO_grouped,disease,DISEASE_10268
10269,10269,10269,10269,10269,10269,10269,10269,MONDO:0018081,hemorrhagic fever-renal syndrome,MONDO,disease,DISEASE_10269
10270,10270,10270,10270,10270,10270,10270,10270,MONDO:0001015_MONDO:0023073,eosinophilic meningitis,MONDO_grouped,disease,DISEASE_10270
10271,10271,10271,10271,10271,10271,10271,10271,MONDO:0005076_MONDO:0002635,periodontitis,MONDO_grouped,disease,DISEASE_10271
10272,10272,10272,10272,10272,10272,10272,10272,MONDO:0009376,carbamoyl phosphate synthetase I deficiency disease,MONDO,disease,DISEASE_10272
10273,10273,10273,10273,10273,10273,10273,10273,MONDO:0008533,"teeth, supernumerary",MONDO,disease,DISEASE_10273
10274,10274,10274,10274,10274,10274,10274,10274,MONDO:1010982,"hydrocephalus, golden hamster",MONDO,disease,DISEASE_10274
10275,10275,10275,10275,10275,10275,10275,10275,MONDO:1011883,"dilute coat color with neurological defects, non-human animal",MONDO,disease,DISEASE_10275
10276,10276,10276,10276,10276,10276,10276,10276,MONDO:0004629,subacute delirium,MONDO,disease,DISEASE_10276
10277,10277,10277,10277,10277,10277,10277,10277,MONDO:0010813,pancreatic beta cell agenesis with neonatal diabetes mellitus,MONDO,disease,DISEASE_10277
10278,10278,10278,10278,10278,10278,10278,10278,MONDO:0019890,non-distal trisomy 9q,MONDO,disease,DISEASE_10278
10279,10279,10279,10279,10279,10279,10279,10279,MONDO:1012414,"pulmonary hypoplasia with anasarca, cattle",MONDO,disease,DISEASE_10279
10280,10280,10280,10280,10280,10280,10280,10280,MONDO:0014650_MONDO:0700090_MONDO:0013741_MONDO:0012706_MONDO:0012705_MONDO:0014308_MONDO:0014639_MONDO:0011965_MONDO:0017704_MONDO:0800493,familial temporal lobe epilepsy,MONDO_grouped,disease,DISEASE_10280
10281,10281,10281,10281,10281,10281,10281,10281,MONDO:0021471,benign neoplasm of endometrium,MONDO,disease,DISEASE_10281
10282,10282,10282,10282,10282,10282,10282,10282,MONDO:0015068,rectal neuroendocrine tumor,MONDO,disease,DISEASE_10282
10283,10283,10283,10283,10283,10283,10283,10283,MONDO:0016338,non-familial dilated cardiomyopathy,MONDO,disease,DISEASE_10283
10284,10284,10284,10284,10284,10284,10284,10284,MONDO:0009969,renal-genital-middle ear anomalies,MONDO,disease,DISEASE_10284
10285,10285,10285,10285,10285,10285,10285,10285,MONDO:0003517,mature teratoma,MONDO,disease,DISEASE_10285
10286,10286,10286,10286,10286,10286,10286,10286,MONDO:0030608_MONDO:0800029_MONDO:0015925_MONDO:0031199,interstitial lung disease,MONDO_grouped,disease,DISEASE_10286
10287,10287,10287,10287,10287,10287,10287,10287,MONDO:0017864,congenital pulmonary veins atresia or stenosis,MONDO,disease,DISEASE_10287
10288,10288,10288,10288,10288,10288,10288,10288,MONDO:0005202,atopic IgE-mediated allergic disorder,MONDO,disease,DISEASE_10288
10289,10289,10289,10289,10289,10289,10289,10289,MONDO:1012183,"subacute progressive myopathy, dog",MONDO,disease,DISEASE_10289
10290,10290,10290,10290,10290,10290,10290,10290,MONDO:0019365,scrub typhus,MONDO,disease,DISEASE_10290
10291,10291,10291,10291,10291,10291,10291,10291,MONDO:0019957,PPoma,MONDO,disease,DISEASE_10291
10292,10292,10292,10292,10292,10292,10292,10292,MONDO:0003115,subglottic hemangioma,MONDO,disease,DISEASE_10292
10293,10293,10293,10293,10293,10293,10293,10293,MONDO:0800321,"congenital heart defects, multiple types, 1, X-linked",MONDO,disease,DISEASE_10293
10294,10294,10294,10294,10294,10294,10294,10294,MONDO:1011526_MONDO:1011527,"hepatic lipidosis, cattle",MONDO_grouped,disease,DISEASE_10294
10295,10295,10295,10295,10295,10295,10295,10295,MONDO:0006217,gallbladder adenosquamous carcinoma,MONDO,disease,DISEASE_10295
10296,10296,10296,10296,10296,10296,10296,10296,MONDO:0024651,corticosteroid-induced osteoporosis,MONDO,disease,DISEASE_10296
10297,10297,10297,10297,10297,10297,10297,10297,MONDO:1011634,"self-mutilation syndrome, non-human animal",MONDO,disease,DISEASE_10297
10298,10298,10298,10298,10298,10298,10298,10298,MONDO:0004378,pediatric cerebral ependymoblastoma,MONDO,disease,DISEASE_10298
10299,10299,10299,10299,10299,10299,10299,10299,MONDO:0019339,"47,XYY syndrome",MONDO,disease,DISEASE_10299
10300,10300,10300,10300,10300,10300,10300,10300,MONDO:1010513,"triploidy, tench",MONDO,disease,DISEASE_10300
10301,10301,10301,10301,10301,10301,10301,10301,MONDO:0017350_MONDO:0017356_MONDO:0019231,inborn disorder of tryptophan metabolism,MONDO_grouped,disease,DISEASE_10301
10302,10302,10302,10302,10302,10302,10302,10302,MONDO:1012730,"hemifacial microsomia, domestic cat",MONDO,disease,DISEASE_10302
10303,10303,10303,10303,10303,10303,10303,10303,MONDO:0100287,POLE-related polyposis and colorectal cancer syndrome,MONDO,disease,DISEASE_10303
10304,10304,10304,10304,10304,10304,10304,10304,MONDO:0700184,feline large granular lymphocyte lymphoma,MONDO,disease,DISEASE_10304
10305,10305,10305,10305,10305,10305,10305,10305,MONDO:0007119,isolated aniridia,MONDO,disease,DISEASE_10305
10306,10306,10306,10306,10306,10306,10306,10306,MONDO:0030514,"leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy",MONDO,disease,DISEASE_10306
10307,10307,10307,10307,10307,10307,10307,10307,MONDO:0000669,color agnosia,MONDO,disease,DISEASE_10307
10308,10308,10308,10308,10308,10308,10308,10308,MONDO:0013661,combined malonic and methylmalonic acidemia,MONDO,disease,DISEASE_10308
10309,10309,10309,10309,10309,10309,10309,10309,MONDO:1040012,PI4KA-related disorder,MONDO,disease,DISEASE_10309
10310,10310,10310,10310,10310,10310,10310,10310,MONDO:0007450,neurohypophyseal diabetes insipidus,MONDO,disease,DISEASE_10310
10311,10311,10311,10311,10311,10311,10311,10311,MONDO:0008329,autosomal dominant pseudohypoaldosteronism type 1,MONDO,disease,DISEASE_10311
10312,10312,10312,10312,10312,10312,10312,10312,MONDO:0009872,Bjornstad syndrome,MONDO,disease,DISEASE_10312
10313,10313,10313,10313,10313,10313,10313,10313,MONDO:0015131,combined immunodeficiency,MONDO,disease,DISEASE_10313
10314,10314,10314,10314,10314,10314,10314,10314,MONDO:0028737,obsolete biliary atresia disorder,MONDO,disease,DISEASE_10314
10315,10315,10315,10315,10315,10315,10315,10315,MONDO:0009012,multiple pterygium-malignant hyperthermia syndrome,MONDO,disease,DISEASE_10315
10316,10316,10316,10316,10316,10316,10316,10316,MONDO:0010473,X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome,MONDO,disease,DISEASE_10316
10317,10317,10317,10317,10317,10317,10317,10317,MONDO:0004354,neonatal leukemia,MONDO,disease,DISEASE_10317
10318,10318,10318,10318,10318,10318,10318,10318,MONDO:0016752,benign peripheral nerve sheath tumor,MONDO,disease,DISEASE_10318
10319,10319,10319,10319,10319,10319,10319,10319,MONDO:0013575,plasma fibronectin deficiency,MONDO,disease,DISEASE_10319
10320,10320,10320,10320,10320,10320,10320,10320,MONDO:0958325,thrombocytopenia 12 with or without myopathy,MONDO,disease,DISEASE_10320
10321,10321,10321,10321,10321,10321,10321,10321,MONDO:0007114,Angel-shaped phalango-epiphyseal dysplasia,MONDO,disease,DISEASE_10321
10322,10322,10322,10322,10322,10322,10322,10322,MONDO:1012635_MONDO:1012636_MONDO:1012637_MONDO:1012638,"XX difference of sexual development, horse",MONDO_grouped,disease,DISEASE_10322
10323,10323,10323,10323,10323,10323,10323,10323,MONDO:1010552,"patent urachus, mountain zebra",MONDO,disease,DISEASE_10323
10324,10324,10324,10324,10324,10324,10324,10324,MONDO:0002719,conus medullaris neoplasm,MONDO,disease,DISEASE_10324
10325,10325,10325,10325,10325,10325,10325,10325,MONDO:0009126,duodenal atresia,MONDO,disease,DISEASE_10325
10326,10326,10326,10326,10326,10326,10326,10326,MONDO:0003233,essential tremor,MONDO,disease,DISEASE_10326
10327,10327,10327,10327,10327,10327,10327,10327,MONDO:0006354,parathyroid hyperplasia,MONDO,disease,DISEASE_10327
10328,10328,10328,10328,10328,10328,10328,10328,MONDO:0003570,lipid-rich carcinoma,MONDO,disease,DISEASE_10328
10329,10329,10329,10329,10329,10329,10329,10329,MONDO:0019506,obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome,MONDO,disease,DISEASE_10329
10330,10330,10330,10330,10330,10330,10330,10330,MONDO:1011902,"neuropathy and feather color dilution, non-human animal",MONDO,disease,DISEASE_10330
10331,10331,10331,10331,10331,10331,10331,10331,MONDO:1011251,"leber congenital amaurosis, domestic cat",MONDO,disease,DISEASE_10331
10332,10332,10332,10332,10332,10332,10332,10332,MONDO:0015498,oromandibular-limb anomalies syndrome,MONDO,disease,DISEASE_10332
10333,10333,10333,10333,10333,10333,10333,10333,MONDO:0001421,frontal lobe neoplasm,MONDO,disease,DISEASE_10333
10334,10334,10334,10334,10334,10334,10334,10334,MONDO:0042961,sacral hemangiomas multiple congenital abnormalities,MONDO,disease,DISEASE_10334
10335,10335,10335,10335,10335,10335,10335,10335,MONDO:0012980,endocrine-cerebro-osteodysplasia syndrome,MONDO,disease,DISEASE_10335
10336,10336,10336,10336,10336,10336,10336,10336,MONDO:0004100,lung mixed small cell and squamous cell carcinoma,MONDO,disease,DISEASE_10336
10337,10337,10337,10337,10337,10337,10337,10337,MONDO:0010520,X-linked Alport syndrome,MONDO,disease,DISEASE_10337
10338,10338,10338,10338,10338,10338,10338,10338,MONDO:0010092,Filippi syndrome,MONDO,disease,DISEASE_10338
10339,10339,10339,10339,10339,10339,10339,10339,MONDO:0024608,dientamoebiasis,MONDO,disease,DISEASE_10339
10340,10340,10340,10340,10340,10340,10340,10340,MONDO:0020640_MONDO:0005134,autoimmune encephalitis,MONDO_grouped,disease,DISEASE_10340
10341,10341,10341,10341,10341,10341,10341,10341,MONDO:0800479,self-limited neonatal seizures,MONDO,disease,DISEASE_10341
10342,10342,10342,10342,10342,10342,10342,10342,MONDO:0032876,neurodevelopmental disorder with absent language and variable seizures,MONDO,disease,DISEASE_10342
10343,10343,10343,10343,10343,10343,10343,10343,MONDO:1011319,"hematologic disorder, non-human animal",MONDO,disease,DISEASE_10343
10344,10344,10344,10344,10344,10344,10344,10344,MONDO:0002620,localized osteosarcoma,MONDO,disease,DISEASE_10344
10345,10345,10345,10345,10345,10345,10345,10345,MONDO:0000994,malignant prostate phyllodes tumor,MONDO,disease,DISEASE_10345
10346,10346,10346,10346,10346,10346,10346,10346,MONDO:0007755,hyperimmunoglobulin G1(A1) syndrome,MONDO,disease,DISEASE_10346
10347,10347,10347,10347,10347,10347,10347,10347,MONDO:0021424,hemangiopericytoma of skin,MONDO,disease,DISEASE_10347
10348,10348,10348,10348,10348,10348,10348,10348,MONDO:0043226,postpartum amenorrhea-galactorrhea syndrome,MONDO,disease,DISEASE_10348
10349,10349,10349,10349,10349,10349,10349,10349,MONDO:0024318,viral infection of central nervous system,MONDO,disease,DISEASE_10349
10350,10350,10350,10350,10350,10350,10350,10350,MONDO:0011431,MASS syndrome,MONDO,disease,DISEASE_10350
10351,10351,10351,10351,10351,10351,10351,10351,MONDO:0018136,minimal pigment oculocutaneous albinism type 1,MONDO,disease,DISEASE_10351
10352,10352,10352,10352,10352,10352,10352,10352,MONDO:0010003,Rowley-Rosenberg syndrome,MONDO,disease,DISEASE_10352
10353,10353,10353,10353,10353,10353,10353,10353,MONDO:0060642,"neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features",MONDO,disease,DISEASE_10353
10354,10354,10354,10354,10354,10354,10354,10354,MONDO:0003962,Froelich syndrome,MONDO,disease,DISEASE_10354
10355,10355,10355,10355,10355,10355,10355,10355,MONDO:0014968,"encephalopathy, progressive, with amyotrophy and optic atrophy",MONDO,disease,DISEASE_10355
10356,10356,10356,10356,10356,10356,10356,10356,MONDO:0019165_MONDO:0015791_MONDO:0015714,central precocious puberty,MONDO_grouped,disease,DISEASE_10356
10357,10357,10357,10357,10357,10357,10357,10357,MONDO:0016924,partial duplication of chromosome 4,MONDO,disease,DISEASE_10357
10358,10358,10358,10358,10358,10358,10358,10358,MONDO:0008754,alopecia - contractures - dwarfism - intellectual disability syndrome,MONDO,disease,DISEASE_10358
10359,10359,10359,10359,10359,10359,10359,10359,MONDO:0032755,neurodevelopmental disorder with or without variable brain abnormalities; NEDBA,MONDO,disease,DISEASE_10359
10360,10360,10360,10360,10360,10360,10360,10360,MONDO:0006821,kidney papillary necrosis,MONDO,disease,DISEASE_10360
10361,10361,10361,10361,10361,10361,10361,10361,MONDO:0005137,nutritional disorder,MONDO,disease,DISEASE_10361
10362,10362,10362,10362,10362,10362,10362,10362,MONDO:0010562_MONDO:0003409,colonic atresia,MONDO_grouped,disease,DISEASE_10362
10363,10363,10363,10363,10363,10363,10363,10363,MONDO:0006857_MONDO:0006647_MONDO:0006917,middle cerebral artery infarction,MONDO_grouped,disease,DISEASE_10363
10364,10364,10364,10364,10364,10364,10364,10364,MONDO:0012856,Birk-Barel syndrome,MONDO,disease,DISEASE_10364
10365,10365,10365,10365,10365,10365,10365,10365,MONDO:0017214,vitamin B12-responsive methylmalonic acidemia,MONDO,disease,DISEASE_10365
10366,10366,10366,10366,10366,10366,10366,10366,MONDO:0013026,subepithelial mucinous corneal dystrophy,MONDO,disease,DISEASE_10366
10367,10367,10367,10367,10367,10367,10367,10367,MONDO:0054750_MONDO:0060670_MONDO:0800224,"amyotrophic lateral sclerosis, susceptibility to",MONDO_grouped,disease,DISEASE_10367
10368,10368,10368,10368,10368,10368,10368,10368,MONDO:0032854_MONDO:0024526_MONDO:0014646,zimmermann-laband syndrome,MONDO_grouped,disease,DISEASE_10368
10369,10369,10369,10369,10369,10369,10369,10369,MONDO:0018614,undetermined early-onset epileptic encephalopathy,MONDO,disease,DISEASE_10369
10370,10370,10370,10370,10370,10370,10370,10370,MONDO:0009169,endocardial fibroelastosis,MONDO,disease,DISEASE_10370
10371,10371,10371,10371,10371,10371,10371,10371,MONDO:0002795,adult central nervous system primitive neuroectodermal neoplasm,MONDO,disease,DISEASE_10371
10372,10372,10372,10372,10372,10372,10372,10372,MONDO:0018702,Castleman-Kojima disease,MONDO,disease,DISEASE_10372
10373,10373,10373,10373,10373,10373,10373,10373,MONDO:0800113,necrotizing vasculitis,MONDO,disease,DISEASE_10373
10374,10374,10374,10374,10374,10374,10374,10374,MONDO:0859205,"delayed puberty, self-limited",MONDO,disease,DISEASE_10374
10375,10375,10375,10375,10375,10375,10375,10375,MONDO:0020504,hereditary recurrent myoglobinuria,MONDO,disease,DISEASE_10375
10376,10376,10376,10376,10376,10376,10376,10376,MONDO:1010322,"ectropion, non-human animal",MONDO,disease,DISEASE_10376
10377,10377,10377,10377,10377,10377,10377,10377,MONDO:0957961_MONDO:0957278_MONDO:0957220_MONDO:0957230_MONDO:0957231,oocyte/zygote/embryo maturation arrest,MONDO_grouped,disease,DISEASE_10377
10378,10378,10378,10378,10378,10378,10378,10378,MONDO:0700274,RAD51D-related cancer predisposition,MONDO,disease,DISEASE_10378
10379,10379,10379,10379,10379,10379,10379,10379,MONDO:0970998,auroneurodental syndrome,MONDO,disease,DISEASE_10379
10380,10380,10380,10380,10380,10380,10380,10380,MONDO:0100443_MONDO:0800099_MONDO:0800100,RDH5-related retinopathy,MONDO_grouped,disease,DISEASE_10380
10381,10381,10381,10381,10381,10381,10381,10381,MONDO:0022567,bhaskar jagannathan syndrome,MONDO,disease,DISEASE_10381
10382,10382,10382,10382,10382,10382,10382,10382,MONDO:0008055_MONDO:0009715,"myotonia congenita, autosomal dominant",MONDO_grouped,disease,DISEASE_10382
10383,10383,10383,10383,10383,10383,10383,10383,MONDO:0010000,"rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction",MONDO,disease,DISEASE_10383
10384,10384,10384,10384,10384,10384,10384,10384,MONDO:0006560,obsolete hypohidrosis,MONDO,disease,DISEASE_10384
10385,10385,10385,10385,10385,10385,10385,10385,MONDO:0002643_MONDO:0006008,vestibular disorder,MONDO_grouped,disease,DISEASE_10385
10386,10386,10386,10386,10386,10386,10386,10386,MONDO:0017940_MONDO:0018567_MONDO:0044625,autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation,MONDO_grouped,disease,DISEASE_10386
10387,10387,10387,10387,10387,10387,10387,10387,MONDO:0100109,Zinner syndrome,MONDO,disease,DISEASE_10387
10388,10388,10388,10388,10388,10388,10388,10388,MONDO:0019617,pituitary deficiency due to empty sella turcica syndrome,MONDO,disease,DISEASE_10388
10389,10389,10389,10389,10389,10389,10389,10389,MONDO:0000649,sensory system cancer,MONDO,disease,DISEASE_10389
10390,10390,10390,10390,10390,10390,10390,10390,MONDO:0006835,lipoid nephrosis,MONDO,disease,DISEASE_10390
10391,10391,10391,10391,10391,10391,10391,10391,MONDO:0003206,acquired hemangioma,MONDO,disease,DISEASE_10391
10392,10392,10392,10392,10392,10392,10392,10392,MONDO:0016098,immune-mediated necrotizing myopathy,MONDO,disease,DISEASE_10392
10393,10393,10393,10393,10393,10393,10393,10393,MONDO:0032871,"leukodystrophy, hypomyelinating, 19, transient infantile",MONDO,disease,DISEASE_10393
10394,10394,10394,10394,10394,10394,10394,10394,MONDO:0700183,feline reticulum cell sarcoma,MONDO,disease,DISEASE_10394
10395,10395,10395,10395,10395,10395,10395,10395,MONDO:0850151,lymph node carcinoma,MONDO,disease,DISEASE_10395
10396,10396,10396,10396,10396,10396,10396,10396,MONDO:0024643,myocardial disorder,MONDO,disease,DISEASE_10396
10397,10397,10397,10397,10397,10397,10397,10397,MONDO:0011505_MONDO:0014252,familial hypobetalipoproteinemia,MONDO_grouped,disease,DISEASE_10397
10398,10398,10398,10398,10398,10398,10398,10398,MONDO:0020854_MONDO:0020607_MONDO:0029132_MONDO:0008323,Liddle syndrome,MONDO_grouped,disease,DISEASE_10398
10399,10399,10399,10399,10399,10399,10399,10399,MONDO:0700215,NTRK fusion positive cancer,MONDO,disease,DISEASE_10399
10400,10400,10400,10400,10400,10400,10400,10400,MONDO:0020518,Hashimoto-Pritzker syndrome,MONDO,disease,DISEASE_10400
10401,10401,10401,10401,10401,10401,10401,10401,MONDO:1012491,"lethal arthrogryposis syndrome, cattle",MONDO,disease,DISEASE_10401
10402,10402,10402,10402,10402,10402,10402,10402,MONDO:0017803,primary progressive apraxia of speech,MONDO,disease,DISEASE_10402
10403,10403,10403,10403,10403,10403,10403,10403,MONDO:0024622_MONDO:0004483,thyroid gland adenocarcinoma,MONDO_grouped,disease,DISEASE_10403
10404,10404,10404,10404,10404,10404,10404,10404,MONDO:0011131,tricho-oculo-dermo-vertebral syndrome,MONDO,disease,DISEASE_10404
10405,10405,10405,10405,10405,10405,10405,10405,MONDO:0859159,"deafness, cataract, impaired intellectual development, and polyneuropathy",MONDO,disease,DISEASE_10405
10406,10406,10406,10406,10406,10406,10406,10406,MONDO:0016299,holoprosencephaly-caudal dysgenesis syndrome,MONDO,disease,DISEASE_10406
10407,10407,10407,10407,10407,10407,10407,10407,MONDO:0000545,sublingual gland adenoid cystic carcinoma,MONDO,disease,DISEASE_10407
10408,10408,10408,10408,10408,10408,10408,10408,MONDO:0012277_MONDO:0013061_MONDO:0030927_MONDO:0011076_MONDO:0033620_MONDO:0012289_MONDO:0012130_MONDO:0014993_MONDO:0014922_MONDO:0012215_MONDO:0018943_MONDO:1010936,myofibrillar myopathy,MONDO_grouped,disease,DISEASE_10408
10409,10409,10409,10409,10409,10409,10409,10409,MONDO:0011746,"symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch",MONDO,disease,DISEASE_10409
10410,10410,10410,10410,10410,10410,10410,10410,MONDO:0018528,congenital myopathy with myasthenic-like onset,MONDO,disease,DISEASE_10410
10411,10411,10411,10411,10411,10411,10411,10411,MONDO:0100314,GYG1-related disorder of glycogen metabolism,MONDO,disease,DISEASE_10411
10412,10412,10412,10412,10412,10412,10412,10412,MONDO:1012889,"cleft lip, GADD45G-related, rabbit",MONDO,disease,DISEASE_10412
10413,10413,10413,10413,10413,10413,10413,10413,MONDO:1010658,"prekallikrein deficiency, horse",MONDO,disease,DISEASE_10413
10414,10414,10414,10414,10414,10414,10414,10414,MONDO:0000225,human monocytic ehrlichiosis,MONDO,disease,DISEASE_10414
10415,10415,10415,10415,10415,10415,10415,10415,MONDO:0003512,mediastinal mesenchymal tumor,MONDO,disease,DISEASE_10415
10416,10416,10416,10416,10416,10416,10416,10416,MONDO:0020805,benign basal cell neoplasm,MONDO,disease,DISEASE_10416
10417,10417,10417,10417,10417,10417,10417,10417,MONDO:0003432_MONDO:0004753_MONDO:0020252,strabismus,MONDO_grouped,disease,DISEASE_10417
10418,10418,10418,10418,10418,10418,10418,10418,MONDO:0007037_MONDO:0008702_MONDO:0008701_MONDO:0010966_MONDO:0019648,achondroplasia,MONDO_grouped,disease,DISEASE_10418
10419,10419,10419,10419,10419,10419,10419,10419,MONDO:0001284,endometriosis of intestine,MONDO,disease,DISEASE_10419
10420,10420,10420,10420,10420,10420,10420,10420,MONDO:0030900,intellectual developmental disorder with paroxysmal dyskinesia or seizures,MONDO,disease,DISEASE_10420
10421,10421,10421,10421,10421,10421,10421,10421,MONDO:0018583,human infection by orthopoxvirus,MONDO,disease,DISEASE_10421
10422,10422,10422,10422,10422,10422,10422,10422,MONDO:0011706,Kufor-Rakeb syndrome,MONDO,disease,DISEASE_10422
10423,10423,10423,10423,10423,10423,10423,10423,MONDO:0007510,Clouston syndrome,MONDO,disease,DISEASE_10423
10424,10424,10424,10424,10424,10424,10424,10424,MONDO:1010009,"atrial septal defect, non-human animal",MONDO,disease,DISEASE_10424
10425,10425,10425,10425,10425,10425,10425,10425,MONDO:0022113,central centrifugal cicatricial alopecia,MONDO,disease,DISEASE_10425
10426,10426,10426,10426,10426,10426,10426,10426,MONDO:0014778,Lamb-Shaffer syndrome,MONDO,disease,DISEASE_10426
10427,10427,10427,10427,10427,10427,10427,10427,MONDO:1010594,"hyperthyroidism, domestic guinea pig",MONDO,disease,DISEASE_10427
10428,10428,10428,10428,10428,10428,10428,10428,MONDO:0003103,nerve root neoplasm,MONDO,disease,DISEASE_10428
10429,10429,10429,10429,10429,10429,10429,10429,MONDO:0000302_MONDO:0045038_MONDO:0045039,basidiobolomycosis,MONDO_grouped,disease,DISEASE_10429
10430,10430,10430,10430,10430,10430,10430,10430,MONDO:0008127,ophthalmomandibulomelic dysplasia,MONDO,disease,DISEASE_10430
10431,10431,10431,10431,10431,10431,10431,10431,MONDO:0013382,progressive demyelinating neuropathy with bilateral striatal necrosis,MONDO,disease,DISEASE_10431
10432,10432,10432,10432,10432,10432,10432,10432,MONDO:1010550,"patent urachus, dog",MONDO,disease,DISEASE_10432
10433,10433,10433,10433,10433,10433,10433,10433,MONDO:1010643_MONDO:1010644_MONDO:1010645_MONDO:1010646_MONDO:1011522,"hemophilia B, dog",MONDO_grouped,disease,DISEASE_10433
10434,10434,10434,10434,10434,10434,10434,10434,MONDO:0014914,Dias-Logan syndrome,MONDO,disease,DISEASE_10434
10435,10435,10435,10435,10435,10435,10435,10435,MONDO:0019928,"48,XXXY syndrome",MONDO,disease,DISEASE_10435
10436,10436,10436,10436,10436,10436,10436,10436,MONDO:0035290,atypical hemolytic uremic syndrome with complement gene abnormality,MONDO,disease,DISEASE_10436
10437,10437,10437,10437,10437,10437,10437,10437,MONDO:0958200_MONDO:0957203_MONDO:0957496_MONDO:0026723_MONDO:0975828_MONDO:0859086,"intellectual developmental disorder, x-linked",MONDO_grouped,disease,DISEASE_10437
10438,10438,10438,10438,10438,10438,10438,10438,MONDO:0009552,mal de Meleda,MONDO,disease,DISEASE_10438
10439,10439,10439,10439,10439,10439,10439,10439,MONDO:0019472,extranodal nasal NK/T cell lymphoma,MONDO,disease,DISEASE_10439
10440,10440,10440,10440,10440,10440,10440,10440,MONDO:0022173,chromosome 11q trisomy,MONDO,disease,DISEASE_10440
10441,10441,10441,10441,10441,10441,10441,10441,MONDO:0008124,"omphalocele, autosomal",MONDO,disease,DISEASE_10441
10442,10442,10442,10442,10442,10442,10442,10442,MONDO:0022642,childhood carcinoid tumor,MONDO,disease,DISEASE_10442
10443,10443,10443,10443,10443,10443,10443,10443,MONDO:0005294,peripheral vascular disease,MONDO,disease,DISEASE_10443
10444,10444,10444,10444,10444,10444,10444,10444,MONDO:0013291_MONDO:0009868_MONDO:0009288_MONDO:0009295_MONDO:0013091_MONDO:0009293_MONDO:0010598_MONDO:0009291_MONDO:0010362_MONDO:0009294_MONDO:0009290_MONDO:0002413_MONDO:0100439_MONDO:0800302,glycogen storage disease,MONDO_grouped,disease,DISEASE_10444
10445,10445,10445,10445,10445,10445,10445,10445,MONDO:1012962_MONDO:1010343,"cataract, non-human animal",MONDO_grouped,disease,DISEASE_10445
10446,10446,10446,10446,10446,10446,10446,10446,MONDO:1010008,"atherosclerosis, non-human animal",MONDO,disease,DISEASE_10446
10447,10447,10447,10447,10447,10447,10447,10447,MONDO:0002290,clitoris cancer,MONDO,disease,DISEASE_10447
10448,10448,10448,10448,10448,10448,10448,10448,MONDO:0007398,craniorhiny,MONDO,disease,DISEASE_10448
10449,10449,10449,10449,10449,10449,10449,10449,MONDO:1011141_MONDO:1011142_MONDO:1011144,"choanal atresia, ass",MONDO_grouped,disease,DISEASE_10449
10450,10450,10450,10450,10450,10450,10450,10450,MONDO:1012119,"hypothalamic dysplasia, dog",MONDO,disease,DISEASE_10450
10451,10451,10451,10451,10451,10451,10451,10451,MONDO:0018490,cono-spondylar dysplasia,MONDO,disease,DISEASE_10451
10452,10452,10452,10452,10452,10452,10452,10452,MONDO:0010538,Mononen-Karnes-Senac syndrome,MONDO,disease,DISEASE_10452
10453,10453,10453,10453,10453,10453,10453,10453,MONDO:1012692,"canine multiple system degeneration, SERAC1-related, dog",MONDO,disease,DISEASE_10453
10454,10454,10454,10454,10454,10454,10454,10454,MONDO:0021234,spinal cord neoplasm,MONDO,disease,DISEASE_10454
10455,10455,10455,10455,10455,10455,10455,10455,MONDO:1010094,"analphalipoproteinaemia, non-human animal",MONDO,disease,DISEASE_10455
10456,10456,10456,10456,10456,10456,10456,10456,MONDO:0012465,hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency,MONDO,disease,DISEASE_10456
10457,10457,10457,10457,10457,10457,10457,10457,MONDO:0009927_MONDO:0009770_MONDO:0009554_MONDO:0017398,3MC syndrome,MONDO_grouped,disease,DISEASE_10457
10458,10458,10458,10458,10458,10458,10458,10458,MONDO:1012433,"proportionate dwarfism with inflammatory lesions, cattle",MONDO,disease,DISEASE_10458
10459,10459,10459,10459,10459,10459,10459,10459,MONDO:0003946_MONDO:0004461,vaginal villous adenoma,MONDO_grouped,disease,DISEASE_10459
10460,10460,10460,10460,10460,10460,10460,10460,MONDO:0016671,sickle cell-hemoglobin E disease syndrome,MONDO,disease,DISEASE_10460
10461,10461,10461,10461,10461,10461,10461,10461,MONDO:0008237,phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome,MONDO,disease,DISEASE_10461
10462,10462,10462,10462,10462,10462,10462,10462,MONDO:0011846_MONDO:0011727,"bulimia nervosa, susceptibility to, 1",MONDO_grouped,disease,DISEASE_10462
10463,10463,10463,10463,10463,10463,10463,10463,MONDO:0001266,erysipelas,MONDO,disease,DISEASE_10463
10464,10464,10464,10464,10464,10464,10464,10464,MONDO:0009755,neutrophil actin dysfunction,MONDO,disease,DISEASE_10464
10465,10465,10465,10465,10465,10465,10465,10465,MONDO:0008918,carnitine-acylcarnitine translocase deficiency,MONDO,disease,DISEASE_10465
10466,10466,10466,10466,10466,10466,10466,10466,MONDO:0006580,miliaria,MONDO,disease,DISEASE_10466
10467,10467,10467,10467,10467,10467,10467,10467,MONDO:0012524,corticosterone methyloxidase type 2 deficiency,MONDO,disease,DISEASE_10467
10468,10468,10468,10468,10468,10468,10468,10468,MONDO:0009434,"hypoproteinemia, hypercatabolic",MONDO,disease,DISEASE_10468
10469,10469,10469,10469,10469,10469,10469,10469,MONDO:0023693_MONDO:0023692_MONDO:0023691_MONDO:0009563_MONDO:0017051_MONDO:0017053,maple syrup urine disease,MONDO_grouped,disease,DISEASE_10469
10470,10470,10470,10470,10470,10470,10470,10470,MONDO:0022832,congenital heart disease radio ulnar synostosis intellectual disability,MONDO,disease,DISEASE_10470
10471,10471,10471,10471,10471,10471,10471,10471,MONDO:0020835,"methemoglobinemia, alpha type",MONDO,disease,DISEASE_10471
10472,10472,10472,10472,10472,10472,10472,10472,MONDO:0019251,oligosaccharidosis,MONDO,disease,DISEASE_10472
10473,10473,10473,10473,10473,10473,10473,10473,MONDO:0957341,secondary early-onset glaucoma,MONDO,disease,DISEASE_10473
10474,10474,10474,10474,10474,10474,10474,10474,MONDO:0013393,distal 7q11.23 microdeletion syndrome,MONDO,disease,DISEASE_10474
10475,10475,10475,10475,10475,10475,10475,10475,MONDO:1012583_MONDO:1012719,"ametapodia-1, chicken",MONDO_grouped,disease,DISEASE_10475
10476,10476,10476,10476,10476,10476,10476,10476,MONDO:0007527,"Ehlers-Danlos syndrome, periodontitis type",MONDO,disease,DISEASE_10476
10477,10477,10477,10477,10477,10477,10477,10477,MONDO:0000690,body dysmorphic disorder,MONDO,disease,DISEASE_10477
10478,10478,10478,10478,10478,10478,10478,10478,MONDO:0009584,"intellectual disability, Buenos-Aires type",MONDO,disease,DISEASE_10478
10479,10479,10479,10479,10479,10479,10479,10479,MONDO:0002129,bone cancer,MONDO,disease,DISEASE_10479
10480,10480,10480,10480,10480,10480,10480,10480,MONDO:0018589_MONDO:0019731,AApoAIV amyloidosis,MONDO_grouped,disease,DISEASE_10480
10481,10481,10481,10481,10481,10481,10481,10481,MONDO:0010434_MONDO:0003465_MONDO:0004519,synovial sarcoma,MONDO_grouped,disease,DISEASE_10481
10482,10482,10482,10482,10482,10482,10482,10482,MONDO:0004797,mononeuritis of lower limb,MONDO,disease,DISEASE_10482
10483,10483,10483,10483,10483,10483,10483,10483,MONDO:0006964_MONDO:0001530_MONDO:0016165_MONDO:0016166_MONDO:0010837_MONDO:0021132,secondary hyperparathyroidism,MONDO_grouped,disease,DISEASE_10483
10484,10484,10484,10484,10484,10484,10484,10484,MONDO:0859003,PAICS deficiency,MONDO,disease,DISEASE_10484
10485,10485,10485,10485,10485,10485,10485,10485,MONDO:0009196,ermine phenotype,MONDO,disease,DISEASE_10485
10486,10486,10486,10486,10486,10486,10486,10486,MONDO:0013659,microcephaly-capillary malformation syndrome,MONDO,disease,DISEASE_10486
10487,10487,10487,10487,10487,10487,10487,10487,MONDO:0019906,ring chromosome 11,MONDO,disease,DISEASE_10487
10488,10488,10488,10488,10488,10488,10488,10488,MONDO:0010183,methylmalonic aciduria and homocystinuria type cblF,MONDO,disease,DISEASE_10488
10489,10489,10489,10489,10489,10489,10489,10489,MONDO:0019512_MONDO:0019054_MONDO:0024287,congenital heart malformation,MONDO_grouped,disease,DISEASE_10489
10490,10490,10490,10490,10490,10490,10490,10490,MONDO:0003205,renal pelvis adenocarcinoma,MONDO,disease,DISEASE_10490
10491,10491,10491,10491,10491,10491,10491,10491,MONDO:0000988,discharging ear,MONDO,disease,DISEASE_10491
10492,10492,10492,10492,10492,10492,10492,10492,MONDO:0013182,chromosome 17p13.3 duplication syndrome,MONDO,disease,DISEASE_10492
10493,10493,10493,10493,10493,10493,10493,10493,MONDO:0014115,hypomyelination with brain stem and spinal cord involvement and leg spasticity,MONDO,disease,DISEASE_10493
10494,10494,10494,10494,10494,10494,10494,10494,MONDO:0800410,"UV-induced skin damage, susceptibility to",MONDO,disease,DISEASE_10494
10495,10495,10495,10495,10495,10495,10495,10495,MONDO:0017467,tibio-fibular synostosis,MONDO,disease,DISEASE_10495
10496,10496,10496,10496,10496,10496,10496,10496,MONDO:0007619,isolated congenital adermatoglyphia,MONDO,disease,DISEASE_10496
10497,10497,10497,10497,10497,10497,10497,10497,MONDO:0008719,"acrorenal syndrome, autosomal recessive",MONDO,disease,DISEASE_10497
10498,10498,10498,10498,10498,10498,10498,10498,MONDO:0858966,central nervous system tumor with bcor internal tandem duplication,MONDO,disease,DISEASE_10498
10499,10499,10499,10499,10499,10499,10499,10499,MONDO:0016355,obsolete semilobar holoprosencephaly,MONDO,disease,DISEASE_10499
10500,10500,10500,10500,10500,10500,10500,10500,MONDO:0007950_MONDO:0003079,mastocytosis,MONDO_grouped,disease,DISEASE_10500
10501,10501,10501,10501,10501,10501,10501,10501,MONDO:0019035_MONDO:0002114_MONDO:0024677,pancreatoblastoma,MONDO_grouped,disease,DISEASE_10501
10502,10502,10502,10502,10502,10502,10502,10502,MONDO:0019445,trichofolliculoma,MONDO,disease,DISEASE_10502
10503,10503,10503,10503,10503,10503,10503,10503,MONDO:0004779,epididymitis,MONDO,disease,DISEASE_10503
10504,10504,10504,10504,10504,10504,10504,10504,MONDO:1012984,"Parkinson disease, non-human animal",MONDO,disease,DISEASE_10504
10505,10505,10505,10505,10505,10505,10505,10505,MONDO:0010729_MONDO:0019422_MONDO:0019423_MONDO:0017616,"X-linked intellectual disability, Schimke type",MONDO_grouped,disease,DISEASE_10505
10506,10506,10506,10506,10506,10506,10506,10506,MONDO:1010708,"eclampsia, dog",MONDO,disease,DISEASE_10506
10507,10507,10507,10507,10507,10507,10507,10507,MONDO:0035943,B-lymphoblastic leukemia/lymphoma with hyperdiploidy,MONDO,disease,DISEASE_10507
10508,10508,10508,10508,10508,10508,10508,10508,MONDO:0017727_MONDO:0006729_MONDO:0020394,fixed subaortic stenosis,MONDO_grouped,disease,DISEASE_10508
10509,10509,10509,10509,10509,10509,10509,10509,MONDO:0018270,extraskeletal Ewing sarcoma,MONDO,disease,DISEASE_10509
10510,10510,10510,10510,10510,10510,10510,10510,MONDO:0030979,"ENDOVE syndrome, limb-brain type",MONDO,disease,DISEASE_10510
10511,10511,10511,10511,10511,10511,10511,10511,MONDO:0001273,megacolon,MONDO,disease,DISEASE_10511
10512,10512,10512,10512,10512,10512,10512,10512,MONDO:0002672,"acinar prostate adenocarcinoma, signet ring variant",MONDO,disease,DISEASE_10512
10513,10513,10513,10513,10513,10513,10513,10513,MONDO:0013171,purine nucleoside phosphorylase deficiency,MONDO,disease,DISEASE_10513
10514,10514,10514,10514,10514,10514,10514,10514,MONDO:0009341,Mowat-Wilson syndrome,MONDO,disease,DISEASE_10514
10515,10515,10515,10515,10515,10515,10515,10515,MONDO:0004094,multiple skull base meningioma,MONDO,disease,DISEASE_10515
10516,10516,10516,10516,10516,10516,10516,10516,MONDO:0015844,agenesis and aplasia of uterine body,MONDO,disease,DISEASE_10516
10517,10517,10517,10517,10517,10517,10517,10517,MONDO:0005809,infectious ectromelia,MONDO,disease,DISEASE_10517
10518,10518,10518,10518,10518,10518,10518,10518,MONDO:1010072,"factor X deficiency, non-human animal",MONDO,disease,DISEASE_10518
10519,10519,10519,10519,10519,10519,10519,10519,MONDO:1012846,"laryngeal paralysis and polyneuropathy, CNTNAP1-related, dog",MONDO,disease,DISEASE_10519
10520,10520,10520,10520,10520,10520,10520,10520,MONDO:0018009,non-hypoproteinemic hypertrophic gastropathy,MONDO,disease,DISEASE_10520
10521,10521,10521,10521,10521,10521,10521,10521,MONDO:0018085,umbilical cord ulceration-intestinal atresia syndrome,MONDO,disease,DISEASE_10521
10522,10522,10522,10522,10522,10522,10522,10522,MONDO:0002959_MONDO:0021765,radiculopathy,MONDO_grouped,disease,DISEASE_10522
10523,10523,10523,10523,10523,10523,10523,10523,MONDO:0006790,hypercementosis,MONDO,disease,DISEASE_10523
10524,10524,10524,10524,10524,10524,10524,10524,MONDO:0006013,visna disease,MONDO,disease,DISEASE_10524
10525,10525,10525,10525,10525,10525,10525,10525,MONDO:0004624,uvula cancer,MONDO,disease,DISEASE_10525
10526,10526,10526,10526,10526,10526,10526,10526,MONDO:0017774,hypobetalipoproteinemia,MONDO,disease,DISEASE_10526
10527,10527,10527,10527,10527,10527,10527,10527,MONDO:0001227,chronic tympanitis,MONDO,disease,DISEASE_10527
10528,10528,10528,10528,10528,10528,10528,10528,MONDO:0019783,neovascular glaucoma,MONDO,disease,DISEASE_10528
10529,10529,10529,10529,10529,10529,10529,10529,MONDO:0015410,nasal dorsum fistula/cyst,MONDO,disease,DISEASE_10529
10530,10530,10530,10530,10530,10530,10530,10530,MONDO:0007112,interventricular septum aneurysm,MONDO,disease,DISEASE_10530
10531,10531,10531,10531,10531,10531,10531,10531,MONDO:0017875_MONDO:0017877,Bolivian hemorrhagic fever,MONDO_grouped,disease,DISEASE_10531
10532,10532,10532,10532,10532,10532,10532,10532,MONDO:0021444,benign neoplasm of large intestine,MONDO,disease,DISEASE_10532
10533,10533,10533,10533,10533,10533,10533,10533,MONDO:0003474,tanycytic ependymoma,MONDO,disease,DISEASE_10533
10534,10534,10534,10534,10534,10534,10534,10534,MONDO:0021366,neoplasm of middle ear,MONDO,disease,DISEASE_10534
10535,10535,10535,10535,10535,10535,10535,10535,MONDO:0008553_MONDO:0014078_MONDO:0032765_MONDO:0054577_MONDO:0011588_MONDO:0013622_MONDO:0014386_MONDO:0008552_MONDO:0013623_MONDO:0014518_MONDO:0012031_MONDO:0030996_MONDO:0014830_MONDO:0012354_MONDO:0957580_MONDO:0013597,platelet-type bleeding disorder,MONDO_grouped,disease,DISEASE_10535
10536,10536,10536,10536,10536,10536,10536,10536,MONDO:0014862_MONDO:0013033_MONDO:0016215_MONDO:0022700_MONDO:0022699,"cerebral palsy, spastic quadriplegic",MONDO_grouped,disease,DISEASE_10536
10537,10537,10537,10537,10537,10537,10537,10537,MONDO:0958228_MONDO:0033198_MONDO:0030719_MONDO:0030724_MONDO:0032732_MONDO:0859374_MONDO:0033665_MONDO:0033200_MONDO:0033201_MONDO:0033202_MONDO:0033670_MONDO:0033668_MONDO:0033260_MONDO:0029137_MONDO:0859366_MONDO:0030998_MONDO:0032917_MONDO:0032911_MONDO:0032740_MONDO:0958277_MONDO:0957825_MONDO:0029142_MONDO:0030549_MONDO:0032749_MONDO:0054860_MONDO:0032802_MONDO:0030058_MONDO:0030905_MONDO:0030723_MONDO:0032639_MONDO:0859528_MONDO:0859524_MONDO:0033259_MONDO:0859525_MONDO:0859527_MONDO:0033258_MONDO:0033199_MONDO:0971152_MONDO:0032761_MONDO:0032776_MONDO:0032762_MONDO:0030480_MONDO:0019588_MONDO:0958232,"hearing loss, autosomal recessive",MONDO_grouped,disease,DISEASE_10537
10538,10538,10538,10538,10538,10538,10538,10538,MONDO:0009892,Chuvash polycythemia,MONDO,disease,DISEASE_10538
10539,10539,10539,10539,10539,10539,10539,10539,MONDO:0010102,taurodontia-absent teeth-sparse hair syndrome,MONDO,disease,DISEASE_10539
10540,10540,10540,10540,10540,10540,10540,10540,MONDO:0002214_MONDO:0004217,brain germinoma,MONDO_grouped,disease,DISEASE_10540
10541,10541,10541,10541,10541,10541,10541,10541,MONDO:0006126,cecum neuroendocrine tumor G1,MONDO,disease,DISEASE_10541
10542,10542,10542,10542,10542,10542,10542,10542,MONDO:0021005,faciodigitogenital syndrome,MONDO,disease,DISEASE_10542
10543,10543,10543,10543,10543,10543,10543,10543,MONDO:0004980,atopic eczema,MONDO,disease,DISEASE_10543
10544,10544,10544,10544,10544,10544,10544,10544,MONDO:0009444,ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome,MONDO,disease,DISEASE_10544
10545,10545,10545,10545,10545,10545,10545,10545,MONDO:0006972,silo filler disease,MONDO,disease,DISEASE_10545
10546,10546,10546,10546,10546,10546,10546,10546,MONDO:0014401,tall stature-scoliosis-macrodactyly of the great toes syndrome,MONDO,disease,DISEASE_10546
10547,10547,10547,10547,10547,10547,10547,10547,MONDO:1012409,"gallbladder mucocele, dog",MONDO,disease,DISEASE_10547
10548,10548,10548,10548,10548,10548,10548,10548,MONDO:0012330,talo-patello-scaphoid osteolysis,MONDO,disease,DISEASE_10548
10549,10549,10549,10549,10549,10549,10549,10549,MONDO:0005106,lipoma,MONDO,disease,DISEASE_10549
10550,10550,10550,10550,10550,10550,10550,10550,MONDO:0003980,schwannoma of jugular foramen,MONDO,disease,DISEASE_10550
10551,10551,10551,10551,10551,10551,10551,10551,MONDO:0005942,Reye syndrome,MONDO,disease,DISEASE_10551
10552,10552,10552,10552,10552,10552,10552,10552,MONDO:0018152,serpiginous choroiditis,MONDO,disease,DISEASE_10552
10553,10553,10553,10553,10553,10553,10553,10553,MONDO:0859689,hepatobiliary benign neoplasm,MONDO,disease,DISEASE_10553
10554,10554,10554,10554,10554,10554,10554,10554,MONDO:0010939,low phospholipid associated cholelithiasis,MONDO,disease,DISEASE_10554
10555,10555,10555,10555,10555,10555,10555,10555,MONDO:0859258,neurodevelopmental disorder with dystonia and seizures,MONDO,disease,DISEASE_10555
10556,10556,10556,10556,10556,10556,10556,10556,MONDO:0100056_MONDO:0100057,exercise-induced anaphylaxis,MONDO_grouped,disease,DISEASE_10556
10557,10557,10557,10557,10557,10557,10557,10557,MONDO:0003795,ovarian small cell carcinoma,MONDO,disease,DISEASE_10557
10558,10558,10558,10558,10558,10558,10558,10558,MONDO:0017292,well-differentiated fetal adenocarcinoma of the lung,MONDO,disease,DISEASE_10558
10559,10559,10559,10559,10559,10559,10559,10559,MONDO:0024625,disorder of lacrimal gland,MONDO,disease,DISEASE_10559
10560,10560,10560,10560,10560,10560,10560,10560,MONDO:0007708,Kasabach-Merritt syndrome,MONDO,disease,DISEASE_10560
10561,10561,10561,10561,10561,10561,10561,10561,MONDO:1012173,"dysphagia-associated muscular dystrophy, dog",MONDO,disease,DISEASE_10561
10562,10562,10562,10562,10562,10562,10562,10562,MONDO:1012058,"degenerative myopathy of obturator-externus, dog",MONDO,disease,DISEASE_10562
10563,10563,10563,10563,10563,10563,10563,10563,MONDO:0000500,tongue squamous cell carcinoma,MONDO,disease,DISEASE_10563
10564,10564,10564,10564,10564,10564,10564,10564,MONDO:0100233,long COVID-19,MONDO,disease,DISEASE_10564
10565,10565,10565,10565,10565,10565,10565,10565,MONDO:0024317,chronic pain syndrome,MONDO,disease,DISEASE_10565
10566,10566,10566,10566,10566,10566,10566,10566,MONDO:0007079_MONDO:0002491_MONDO:0005433_MONDO:0002046_MONDO:0005689_MONDO:0004456_MONDO:0005186_MONDO:0005367,alcohol dependence,MONDO_grouped,disease,DISEASE_10566
10567,10567,10567,10567,10567,10567,10567,10567,MONDO:0002030,chronic cervicitis,MONDO,disease,DISEASE_10567
10568,10568,10568,10568,10568,10568,10568,10568,MONDO:0017441,congenital absence of upper arm and forearm with hand present,MONDO,disease,DISEASE_10568
10569,10569,10569,10569,10569,10569,10569,10569,MONDO:0020559,O'Sullivan-McLeod syndrome,MONDO,disease,DISEASE_10569
10570,10570,10570,10570,10570,10570,10570,10570,MONDO:0013483,"obesity, hyperphagia, and developmental delay",MONDO,disease,DISEASE_10570
10571,10571,10571,10571,10571,10571,10571,10571,MONDO:0023603,hereditary disorder of connective tissue,MONDO,disease,DISEASE_10571
10572,10572,10572,10572,10572,10572,10572,10572,MONDO:0017321,pili torti-onychodysplasia syndrome,MONDO,disease,DISEASE_10572
10573,10573,10573,10573,10573,10573,10573,10573,MONDO:0008314,"pronation-supination of the forearm, impairment of",MONDO,disease,DISEASE_10573
10574,10574,10574,10574,10574,10574,10574,10574,MONDO:0009426,hypoparathyroidism-retardation-dysmorphism syndrome,MONDO,disease,DISEASE_10574
10575,10575,10575,10575,10575,10575,10575,10575,MONDO:0010652,X-linked intellectual disability-seizures-psoriasis syndrome,MONDO,disease,DISEASE_10575
10576,10576,10576,10576,10576,10576,10576,10576,MONDO:0005072_MONDO:0006316_MONDO:0004024,neuroblastoma,MONDO_grouped,disease,DISEASE_10576
10577,10577,10577,10577,10577,10577,10577,10577,MONDO:1040030,"GBA1-related Parkinson disease, susceptibility",MONDO,disease,DISEASE_10577
10578,10578,10578,10578,10578,10578,10578,10578,MONDO:1010763,"vitiligo, water buffalo",MONDO,disease,DISEASE_10578
10579,10579,10579,10579,10579,10579,10579,10579,MONDO:1010243_MONDO:1011836_MONDO:1012956,"cerebellar degeneration, non-human animal",MONDO_grouped,disease,DISEASE_10579
10580,10580,10580,10580,10580,10580,10580,10580,MONDO:0008169,"osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension",MONDO,disease,DISEASE_10580
10581,10581,10581,10581,10581,10581,10581,10581,MONDO:0024757,cardiovascular neoplasm,MONDO,disease,DISEASE_10581
10582,10582,10582,10582,10582,10582,10582,10582,MONDO:1010439,"cardiomyopathy, chicken",MONDO,disease,DISEASE_10582
10583,10583,10583,10583,10583,10583,10583,10583,MONDO:0001256,arteriovenous hemangioma/malformation,MONDO,disease,DISEASE_10583
10584,10584,10584,10584,10584,10584,10584,10584,MONDO:0007969,Melkersson-Rosenthal syndrome,MONDO,disease,DISEASE_10584
10585,10585,10585,10585,10585,10585,10585,10585,MONDO:0018260,scalp syndrome,MONDO,disease,DISEASE_10585
10586,10586,10586,10586,10586,10586,10586,10586,MONDO:0037149,"HSD10 disease, atypical type",MONDO,disease,DISEASE_10586
10587,10587,10587,10587,10587,10587,10587,10587,MONDO:0000456,cerebral creatine deficiency syndrome,MONDO,disease,DISEASE_10587
10588,10588,10588,10588,10588,10588,10588,10588,MONDO:0016853,ring chromosome Y,MONDO,disease,DISEASE_10588
10589,10589,10589,10589,10589,10589,10589,10589,MONDO:0008726,Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis,MONDO,disease,DISEASE_10589
10590,10590,10590,10590,10590,10590,10590,10590,MONDO:0009420,primary hypergonadotropic hypogonadism-partial alopecia syndrome,MONDO,disease,DISEASE_10590
10591,10591,10591,10591,10591,10591,10591,10591,MONDO:1010512,"hypertrophic cardiomyopathy, SGCD-related, pig",MONDO,disease,DISEASE_10591
10592,10592,10592,10592,10592,10592,10592,10592,MONDO:0010425,Lisch epithelial corneal dystrophy,MONDO,disease,DISEASE_10592
10593,10593,10593,10593,10593,10593,10593,10593,MONDO:0009151,cleft lip/palate-ectodermal dysplasia syndrome,MONDO,disease,DISEASE_10593
10594,10594,10594,10594,10594,10594,10594,10594,MONDO:0010536,"tubulin, beta",MONDO,disease,DISEASE_10594
10595,10595,10595,10595,10595,10595,10595,10595,MONDO:0021223_MONDO:0006180,digestive system neoplasm,MONDO_grouped,disease,DISEASE_10595
10596,10596,10596,10596,10596,10596,10596,10596,MONDO:0011126,acute insulin response,MONDO,disease,DISEASE_10596
10597,10597,10597,10597,10597,10597,10597,10597,MONDO:0008642,VACTERL/vater association,MONDO,disease,DISEASE_10597
10598,10598,10598,10598,10598,10598,10598,10598,MONDO:0035441,congenital autosomal recessive small-platelet thrombocytopenia,MONDO,disease,DISEASE_10598
10599,10599,10599,10599,10599,10599,10599,10599,MONDO:0003031_MONDO:0003030_MONDO:0003313,endometrioid stromal and related neoplasms of the cervix,MONDO_grouped,disease,DISEASE_10599
10600,10600,10600,10600,10600,10600,10600,10600,MONDO:0850102_MONDO:0850103,non-specific autoimmune supratentorial encephalitis with characteristic antibodies,MONDO_grouped,disease,DISEASE_10600
10601,10601,10601,10601,10601,10601,10601,10601,MONDO:0027068,"mitochondrial complex 1 deficiency, mitochondrial type 1",MONDO,disease,DISEASE_10601
10602,10602,10602,10602,10602,10602,10602,10602,MONDO:0002093,acanthoma,MONDO,disease,DISEASE_10602
10603,10603,10603,10603,10603,10603,10603,10603,MONDO:0957408,type 1 interferonopathy of childhood,MONDO,disease,DISEASE_10603
10604,10604,10604,10604,10604,10604,10604,10604,MONDO:1012291,"neonatal hepatitis, dog",MONDO,disease,DISEASE_10604
10605,10605,10605,10605,10605,10605,10605,10605,MONDO:1010170,"Krabbe disease, non-human animal",MONDO,disease,DISEASE_10605
10606,10606,10606,10606,10606,10606,10606,10606,MONDO:0859144,Buratti-Harel syndrome,MONDO,disease,DISEASE_10606
10607,10607,10607,10607,10607,10607,10607,10607,MONDO:0021154,dermis disorder,MONDO,disease,DISEASE_10607
10608,10608,10608,10608,10608,10608,10608,10608,MONDO:0011255,mandibulofacial dysostosis-macroblepharon-macrostomia syndrome,MONDO,disease,DISEASE_10608
10609,10609,10609,10609,10609,10609,10609,10609,MONDO:0010268,X-linked lissencephaly with abnormal genitalia,MONDO,disease,DISEASE_10609
10610,10610,10610,10610,10610,10610,10610,10610,MONDO:0001270,stone in bladder diverticulum,MONDO,disease,DISEASE_10610
10611,10611,10611,10611,10611,10611,10611,10611,MONDO:0007201,"blepharophimosis, ptosis, and epicanthus inversus syndrome",MONDO,disease,DISEASE_10611
10612,10612,10612,10612,10612,10612,10612,10612,MONDO:0009585,encephalopathy due to beta-mercaptolactate-cysteine disulfiduria,MONDO,disease,DISEASE_10612
10613,10613,10613,10613,10613,10613,10613,10613,MONDO:0042489,disease susceptibility,MONDO,disease,DISEASE_10613
10614,10614,10614,10614,10614,10614,10614,10614,MONDO:0018636,autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome,MONDO,disease,DISEASE_10614
10615,10615,10615,10615,10615,10615,10615,10615,MONDO:0700256_MONDO:0700262,TREX1-related type 1 interferonopathy,MONDO_grouped,disease,DISEASE_10615
10616,10616,10616,10616,10616,10616,10616,10616,MONDO:0018312,histoplasmosis,MONDO,disease,DISEASE_10616
10617,10617,10617,10617,10617,10617,10617,10617,MONDO:0005569,obsolete cartilage disease,MONDO,disease,DISEASE_10617
10618,10618,10618,10618,10618,10618,10618,10618,MONDO:0018378,osteonecrosis of the jaw,MONDO,disease,DISEASE_10618
10619,10619,10619,10619,10619,10619,10619,10619,MONDO:0041775,intraoperative floppy iris syndrome,MONDO,disease,DISEASE_10619
10620,10620,10620,10620,10620,10620,10620,10620,MONDO:0016659,8p23.1 duplication syndrome,MONDO,disease,DISEASE_10620
10621,10621,10621,10621,10621,10621,10621,10621,MONDO:0044037,livedo reticularis,MONDO,disease,DISEASE_10621
10622,10622,10622,10622,10622,10622,10622,10622,MONDO:0004170,nodular episcleritis,MONDO,disease,DISEASE_10622
10623,10623,10623,10623,10623,10623,10623,10623,MONDO:0010607,"heterotaxy, visceral, 1, X-linked",MONDO,disease,DISEASE_10623
10624,10624,10624,10624,10624,10624,10624,10624,MONDO:1012057,"degenerative myopathy of deep pectoral muscle, turkey",MONDO,disease,DISEASE_10624
10625,10625,10625,10625,10625,10625,10625,10625,MONDO:0001155,gastrojejunal ulcer,MONDO,disease,DISEASE_10625
10626,10626,10626,10626,10626,10626,10626,10626,MONDO:0100325_MONDO:0031169,odontochondrodysplasia 1,MONDO_grouped,disease,DISEASE_10626
10627,10627,10627,10627,10627,10627,10627,10627,MONDO:0023068,Engelhard Yatziv syndrome,MONDO,disease,DISEASE_10627
10628,10628,10628,10628,10628,10628,10628,10628,MONDO:0007891,familial generalized lentiginosis,MONDO,disease,DISEASE_10628
10629,10629,10629,10629,10629,10629,10629,10629,MONDO:0005911,pharyngoconjunctival fever,MONDO,disease,DISEASE_10629
10630,10630,10630,10630,10630,10630,10630,10630,MONDO:0009416,hypoinsulinemic hypoglycemia and body hemihypertrophy,MONDO,disease,DISEASE_10630
10631,10631,10631,10631,10631,10631,10631,10631,MONDO:0008571,"Blount disease, infantile",MONDO,disease,DISEASE_10631
10632,10632,10632,10632,10632,10632,10632,10632,MONDO:0006927,Rickettsiaceae infectious disease,MONDO,disease,DISEASE_10632
10633,10633,10633,10633,10633,10633,10633,10633,MONDO:0060631,Alkuraya-Kucinskas syndrome,MONDO,disease,DISEASE_10633
10634,10634,10634,10634,10634,10634,10634,10634,MONDO:1010445,"dilated cardiomyopathy, golden hamster",MONDO,disease,DISEASE_10634
10635,10635,10635,10635,10635,10635,10635,10635,MONDO:0100306,disorder of defective peroxisome oxidative status,MONDO,disease,DISEASE_10635
10636,10636,10636,10636,10636,10636,10636,10636,MONDO:0004026,skin tag,MONDO,disease,DISEASE_10636
10637,10637,10637,10637,10637,10637,10637,10637,MONDO:0022180,chromosome 16 trisomy,MONDO,disease,DISEASE_10637
10638,10638,10638,10638,10638,10638,10638,10638,MONDO:0002645,cerebritis,MONDO,disease,DISEASE_10638
10639,10639,10639,10639,10639,10639,10639,10639,MONDO:0850285,environmental induced asthma,MONDO,disease,DISEASE_10639
10640,10640,10640,10640,10640,10640,10640,10640,MONDO:0021134,acquired factor X deficiency,MONDO,disease,DISEASE_10640
10641,10641,10641,10641,10641,10641,10641,10641,MONDO:0005867,Mycoplasma pneumoniae pneumonia,MONDO,disease,DISEASE_10641
10642,10642,10642,10642,10642,10642,10642,10642,MONDO:0004875,xanthogranulomatous cholecystitis,MONDO,disease,DISEASE_10642
10643,10643,10643,10643,10643,10643,10643,10643,MONDO:0700145,canine lymphoma,MONDO,disease,DISEASE_10643
10644,10644,10644,10644,10644,10644,10644,10644,MONDO:0002223,ovarian malignant mesothelioma,MONDO,disease,DISEASE_10644
10645,10645,10645,10645,10645,10645,10645,10645,MONDO:0700129,mosaic translocation Down syndrome,MONDO,disease,DISEASE_10645
10646,10646,10646,10646,10646,10646,10646,10646,MONDO:0060533,"microcephaly, short stature, and limb abnormalities",MONDO,disease,DISEASE_10646
10647,10647,10647,10647,10647,10647,10647,10647,MONDO:0037792_MONDO:0000224,carbohydrate metabolism disease,MONDO_grouped,disease,DISEASE_10647
10648,10648,10648,10648,10648,10648,10648,10648,MONDO:0007082_MONDO:0012551_MONDO:0005340_MONDO:1010778_MONDO:1010780_MONDO:1010781_MONDO:1010782,alopecia areata,MONDO_grouped,disease,DISEASE_10648
10649,10649,10649,10649,10649,10649,10649,10649,MONDO:0021546,ependymal tumor of spinal cord,MONDO,disease,DISEASE_10649
10650,10650,10650,10650,10650,10650,10650,10650,MONDO:0008557,Paris-Trousseau thrombocytopenia,MONDO,disease,DISEASE_10650
10651,10651,10651,10651,10651,10651,10651,10651,MONDO:1012423,"vitamin D-deficiency rickets, non-type I, non-type II, domestic cat",MONDO,disease,DISEASE_10651
10652,10652,10652,10652,10652,10652,10652,10652,MONDO:0032714,"facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome",MONDO,disease,DISEASE_10652
10653,10653,10653,10653,10653,10653,10653,10653,MONDO:0021001_MONDO:0014225_MONDO:0011417_MONDO:0011216_MONDO:0011631_MONDO:0013220_MONDO:0019257,hemochromatosis,MONDO_grouped,disease,DISEASE_10653
10654,10654,10654,10654,10654,10654,10654,10654,MONDO:0008641,retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations,MONDO,disease,DISEASE_10654
10655,10655,10655,10655,10655,10655,10655,10655,MONDO:0007856,palmoplantar keratoderma-esophageal carcinoma syndrome,MONDO,disease,DISEASE_10655
10656,10656,10656,10656,10656,10656,10656,10656,MONDO:1011169,"osteochondrosis, raccoon dog",MONDO,disease,DISEASE_10656
10657,10657,10657,10657,10657,10657,10657,10657,MONDO:0020950,viral eye infection,MONDO,disease,DISEASE_10657
10658,10658,10658,10658,10658,10658,10658,10658,MONDO:0018069,distal trisomy 17q,MONDO,disease,DISEASE_10658
10659,10659,10659,10659,10659,10659,10659,10659,MONDO:1011196,"osteogenesis imperfecta SERPINH1-related, dog",MONDO,disease,DISEASE_10659
10660,10660,10660,10660,10660,10660,10660,10660,MONDO:0006444,teratoma with malignant transformation,MONDO,disease,DISEASE_10660
10661,10661,10661,10661,10661,10661,10661,10661,MONDO:0034146,spastic ataxia-dysarthria due to glutaminase deficiency,MONDO,disease,DISEASE_10661
10662,10662,10662,10662,10662,10662,10662,10662,MONDO:0002479,Sertoli-Leydig cell tumor,MONDO,disease,DISEASE_10662
10663,10663,10663,10663,10663,10663,10663,10663,MONDO:0019460,acute leukemia of ambiguous lineage,MONDO,disease,DISEASE_10663
10664,10664,10664,10664,10664,10664,10664,10664,MONDO:0011978,CoQ-responsive OXPHOS deficiency,MONDO,disease,DISEASE_10664
10665,10665,10665,10665,10665,10665,10665,10665,MONDO:0010255,"diabetes mellitus, insulin-dependent, X-linked, susceptibility to",MONDO,disease,DISEASE_10665
10666,10666,10666,10666,10666,10666,10666,10666,MONDO:0031520,familial severe combined immunodeficiency,MONDO,disease,DISEASE_10666
10667,10667,10667,10667,10667,10667,10667,10667,MONDO:0011486,congenital muscular dystrophy 1B,MONDO,disease,DISEASE_10667
10668,10668,10668,10668,10668,10668,10668,10668,MONDO:0005998,trombiculiasis,MONDO,disease,DISEASE_10668
10669,10669,10669,10669,10669,10669,10669,10669,MONDO:0025397,canine distemper,MONDO,disease,DISEASE_10669
10670,10670,10670,10670,10670,10670,10670,10670,MONDO:0033642,neurodevelopmental disorder with alopecia and brain abnormalities,MONDO,disease,DISEASE_10670
10671,10671,10671,10671,10671,10671,10671,10671,MONDO:0024282,mucinous ovarian cancer,MONDO,disease,DISEASE_10671
10672,10672,10672,10672,10672,10672,10672,10672,MONDO:1012718,"muscular dystrophy with reduced β-sarcoglycan, domestic cat",MONDO,disease,DISEASE_10672
10673,10673,10673,10673,10673,10673,10673,10673,MONDO:0023155,fibula aplasia complex brachydactyly,MONDO,disease,DISEASE_10673
10674,10674,10674,10674,10674,10674,10674,10674,MONDO:0002940,anal margin basal cell carcinoma,MONDO,disease,DISEASE_10674
10675,10675,10675,10675,10675,10675,10675,10675,MONDO:0975745,neurodevelopmental disorder with characteristic facial and ectodermal features and tetraparesis 1,MONDO,disease,DISEASE_10675
10676,10676,10676,10676,10676,10676,10676,10676,MONDO:1012756,"congenital liver fibrosis, PKHD1-related, horse",MONDO,disease,DISEASE_10676
10677,10677,10677,10677,10677,10677,10677,10677,MONDO:0021396,polyp of vulva,MONDO,disease,DISEASE_10677
10678,10678,10678,10678,10678,10678,10678,10678,MONDO:0044782_MONDO:0001221,esophageal ulcer,MONDO_grouped,disease,DISEASE_10678
10679,10679,10679,10679,10679,10679,10679,10679,MONDO:0005987,toxascariasis,MONDO,disease,DISEASE_10679
10680,10680,10680,10680,10680,10680,10680,10680,MONDO:0000647,benign vaginal neoplasm,MONDO,disease,DISEASE_10680
10681,10681,10681,10681,10681,10681,10681,10681,MONDO:0009039,Baller-Gerold syndrome,MONDO,disease,DISEASE_10681
10682,10682,10682,10682,10682,10682,10682,10682,MONDO:0007666,glaucoma-sleep apnea syndrome,MONDO,disease,DISEASE_10682
10683,10683,10683,10683,10683,10683,10683,10683,MONDO:0004416,plasmacytoid variant infiltrating bladder urothelial carcinoma,MONDO,disease,DISEASE_10683
10684,10684,10684,10684,10684,10684,10684,10684,MONDO:0019620_MONDO:0957459,congenital esophageal diverticulum,MONDO_grouped,disease,DISEASE_10684
10685,10685,10685,10685,10685,10685,10685,10685,MONDO:0017913,pure or complex hereditary spastic paraplegia,MONDO,disease,DISEASE_10685
10686,10686,10686,10686,10686,10686,10686,10686,MONDO:0022220,Parinaud syndrome,MONDO,disease,DISEASE_10686
10687,10687,10687,10687,10687,10687,10687,10687,MONDO:0019912,maternal uniparental disomy of chromosome 6,MONDO,disease,DISEASE_10687
10688,10688,10688,10688,10688,10688,10688,10688,MONDO:0043726,multiple organ dysfunction syndrome,MONDO,disease,DISEASE_10688
10689,10689,10689,10689,10689,10689,10689,10689,MONDO:0002739,extrahepatic bile duct mucinous adenocarcinoma,MONDO,disease,DISEASE_10689
10690,10690,10690,10690,10690,10690,10690,10690,MONDO:0005571,polycythemia,MONDO,disease,DISEASE_10690
10691,10691,10691,10691,10691,10691,10691,10691,MONDO:0018907,craniopharyngioma,MONDO,disease,DISEASE_10691
10692,10692,10692,10692,10692,10692,10692,10692,MONDO:0014415,"kallikrein, decreased urinary activity of",MONDO,disease,DISEASE_10692
10693,10693,10693,10693,10693,10693,10693,10693,MONDO:0016834,16p11.2p12.2 microduplication syndrome,MONDO,disease,DISEASE_10693
10694,10694,10694,10694,10694,10694,10694,10694,MONDO:0700008,chromosome 1 disorder,MONDO,disease,DISEASE_10694
10695,10695,10695,10695,10695,10695,10695,10695,MONDO:0007828,"indifference to pain, congenital, autosomal dominant",MONDO,disease,DISEASE_10695
10696,10696,10696,10696,10696,10696,10696,10696,MONDO:0015096_MONDO:0014452_MONDO:0016638,familial hypofibrinogenemia,MONDO_grouped,disease,DISEASE_10696
10697,10697,10697,10697,10697,10697,10697,10697,MONDO:0000849,fibrogenesis imperfecta ossium,MONDO,disease,DISEASE_10697
10698,10698,10698,10698,10698,10698,10698,10698,MONDO:0005284_MONDO:0000450,chronic progressive multiple sclerosis,MONDO_grouped,disease,DISEASE_10698
10699,10699,10699,10699,10699,10699,10699,10699,MONDO:0010499_MONDO:0030331_MONDO:0030864_MONDO:0009073_MONDO:0019078,Ritscher-Schinzel syndrome,MONDO_grouped,disease,DISEASE_10699
10700,10700,10700,10700,10700,10700,10700,10700,MONDO:0016141,qualitative or quantitative defects of alpha-sarcoglycan,MONDO,disease,DISEASE_10700
10701,10701,10701,10701,10701,10701,10701,10701,MONDO:1011282,"Stargardt disease, ABCA4-related, dog",MONDO,disease,DISEASE_10701
10702,10702,10702,10702,10702,10702,10702,10702,MONDO:0100111,focal segmental glomerulosclerosis and neurodevelopmental syndrome,MONDO,disease,DISEASE_10702
10703,10703,10703,10703,10703,10703,10703,10703,MONDO:1012915_MONDO:1012916,"amyotrophic lateral sclerosis, TARDBP-related, Rhesus monkey",MONDO_grouped,disease,DISEASE_10703
10704,10704,10704,10704,10704,10704,10704,10704,MONDO:0018014,transient neonatal multiple acyl-CoA dehydrogenase deficiency,MONDO,disease,DISEASE_10704
10705,10705,10705,10705,10705,10705,10705,10705,MONDO:0003327_MONDO:0005035_MONDO:0003325_MONDO:0002293,peripheral ganglioneuroblastoma,MONDO_grouped,disease,DISEASE_10705
10706,10706,10706,10706,10706,10706,10706,10706,MONDO:0004506,microscopic breast papilloma,MONDO,disease,DISEASE_10706
10707,10707,10707,10707,10707,10707,10707,10707,MONDO:0015702,T-B+ severe combined immunodeficiency due to CD45 deficiency,MONDO,disease,DISEASE_10707
10708,10708,10708,10708,10708,10708,10708,10708,MONDO:0010525,"neural tube defects, X-linked",MONDO,disease,DISEASE_10708
10709,10709,10709,10709,10709,10709,10709,10709,MONDO:0006283,lymphoepithelioma-like lung carcinoma,MONDO,disease,DISEASE_10709
10710,10710,10710,10710,10710,10710,10710,10710,MONDO:0006709,common bile duct neoplasm,MONDO,disease,DISEASE_10710
10711,10711,10711,10711,10711,10711,10711,10711,MONDO:0002311_MONDO:0005283_MONDO:0008375_MONDO:0003072,retinal vascular disorder,MONDO_grouped,disease,DISEASE_10711
10712,10712,10712,10712,10712,10712,10712,10712,MONDO:0004237,large cell carcinoma with rhabdoid phenotype,MONDO,disease,DISEASE_10712
10713,10713,10713,10713,10713,10713,10713,10713,MONDO:0017808,duplication of the pituitary gland,MONDO,disease,DISEASE_10713
10714,10714,10714,10714,10714,10714,10714,10714,MONDO:0003954_MONDO:0003712,angiokeratoma of Fordyce,MONDO_grouped,disease,DISEASE_10714
10715,10715,10715,10715,10715,10715,10715,10715,MONDO:0001801,staphyloma posticum,MONDO,disease,DISEASE_10715
10716,10716,10716,10716,10716,10716,10716,10716,MONDO:0013053,"microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type",MONDO,disease,DISEASE_10716
10717,10717,10717,10717,10717,10717,10717,10717,MONDO:0007631,"chromosome 16p12.1 deletion syndrome, 520kb",MONDO,disease,DISEASE_10717
10718,10718,10718,10718,10718,10718,10718,10718,MONDO:0011354,situs inversus totalis with cystic dysplasia of kidneys and pancreas,MONDO,disease,DISEASE_10718
10719,10719,10719,10719,10719,10719,10719,10719,MONDO:1012388,"unilateral subcortical heterotopia, California sea lion",MONDO,disease,DISEASE_10719
10720,10720,10720,10720,10720,10720,10720,10720,MONDO:0019018,Tako-tsubo cardiomyopathy,MONDO,disease,DISEASE_10720
10721,10721,10721,10721,10721,10721,10721,10721,MONDO:0024969_MONDO:0700056,"parasitic disease, non-human animal",MONDO_grouped,disease,DISEASE_10721
10722,10722,10722,10722,10722,10722,10722,10722,MONDO:1012571,"cancer, domestic cat",MONDO,disease,DISEASE_10722
10723,10723,10723,10723,10723,10723,10723,10723,MONDO:0001436,hemosiderosis,MONDO,disease,DISEASE_10723
10724,10724,10724,10724,10724,10724,10724,10724,MONDO:0017757,disorder of metabolite absorption and transport,MONDO,disease,DISEASE_10724
10725,10725,10725,10725,10725,10725,10725,10725,MONDO:0957458,adermatopathic dermatomyositis,MONDO,disease,DISEASE_10725
10726,10726,10726,10726,10726,10726,10726,10726,MONDO:0022899,crawfurd syndrome,MONDO,disease,DISEASE_10726
10727,10727,10727,10727,10727,10727,10727,10727,MONDO:1010610,"thyroiditis, domestic guinea pig",MONDO,disease,DISEASE_10727
10728,10728,10728,10728,10728,10728,10728,10728,MONDO:0007466,"DNA, satellite, 3",MONDO,disease,DISEASE_10728
10729,10729,10729,10729,10729,10729,10729,10729,MONDO:0037738,cauda equina cancer,MONDO,disease,DISEASE_10729
10730,10730,10730,10730,10730,10730,10730,10730,MONDO:0001112,bubonic plague,MONDO,disease,DISEASE_10730
10731,10731,10731,10731,10731,10731,10731,10731,MONDO:0014389,polyglucosan body myopathy 1 with or without immunodeficiency,MONDO,disease,DISEASE_10731
10732,10732,10732,10732,10732,10732,10732,10732,MONDO:0012242,"syncope, familial vasovagal",MONDO,disease,DISEASE_10732
10733,10733,10733,10733,10733,10733,10733,10733,MONDO:0014661_MONDO:1011500_MONDO:1010750_MONDO:1011501,epidermolysis bullosa simplex with nail dystrophy,MONDO_grouped,disease,DISEASE_10733
10734,10734,10734,10734,10734,10734,10734,10734,MONDO:0009161,"Ehlers-Danlos syndrome, dermatosparaxis type",MONDO,disease,DISEASE_10734
10735,10735,10735,10735,10735,10735,10735,10735,MONDO:0002508,gingivitis,MONDO,disease,DISEASE_10735
10736,10736,10736,10736,10736,10736,10736,10736,MONDO:0021540,hamartoma of lung,MONDO,disease,DISEASE_10736
10737,10737,10737,10737,10737,10737,10737,10737,MONDO:0007696,Emery-Nelson syndrome,MONDO,disease,DISEASE_10737
10738,10738,10738,10738,10738,10738,10738,10738,MONDO:0006157,colorectal adenosquamous carcinoma,MONDO,disease,DISEASE_10738
10739,10739,10739,10739,10739,10739,10739,10739,MONDO:0010144_MONDO:1010829,tibial hemimelia,MONDO_grouped,disease,DISEASE_10739
10740,10740,10740,10740,10740,10740,10740,10740,MONDO:0035764,idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance,MONDO,disease,DISEASE_10740
10741,10741,10741,10741,10741,10741,10741,10741,MONDO:0017316,short stature-deafness-neutrophil dysfunction-dysmorphism syndrome,MONDO,disease,DISEASE_10741
10742,10742,10742,10742,10742,10742,10742,10742,MONDO:0003155_MONDO:0006267,cavernous hemangioma,MONDO_grouped,disease,DISEASE_10742
10743,10743,10743,10743,10743,10743,10743,10743,MONDO:1011518,"glycogen storage disease, ring-tailed coati",MONDO,disease,DISEASE_10743
10744,10744,10744,10744,10744,10744,10744,10744,MONDO:0019685_MONDO:1011199_MONDO:1011200,FGFR3-related chondrodysplasia,MONDO_grouped,disease,DISEASE_10744
10745,10745,10745,10745,10745,10745,10745,10745,MONDO:0007615,laurin-Sandrow syndrome,MONDO,disease,DISEASE_10745
10746,10746,10746,10746,10746,10746,10746,10746,MONDO:0009667_MONDO:0014071_MONDO:0014683_MONDO:0014140_MONDO:0013158_MONDO:0014022_MONDO:0009678_MONDO:0014120_MONDO:0013157_MONDO:0013904_MONDO:0013154_MONDO:0009364_MONDO:0014101_MONDO:0013835,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies),",MONDO_grouped,disease,DISEASE_10746
10747,10747,10747,10747,10747,10747,10747,10747,MONDO:1012176,"myasthenia, domestic cat",MONDO,disease,DISEASE_10747
10748,10748,10748,10748,10748,10748,10748,10748,MONDO:0859248,"corneal dystrophy, punctiform and polychromatic pre-descemet",MONDO,disease,DISEASE_10748
10749,10749,10749,10749,10749,10749,10749,10749,MONDO:0044209,disorder of lectin complement activation pathway,MONDO,disease,DISEASE_10749
10750,10750,10750,10750,10750,10750,10750,10750,MONDO:0859282,"neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures",MONDO,disease,DISEASE_10750
10751,10751,10751,10751,10751,10751,10751,10751,MONDO:0017454,triphalangeal thumb-polysyndactyly syndrome,MONDO,disease,DISEASE_10751
10752,10752,10752,10752,10752,10752,10752,10752,MONDO:0019328_MONDO:0019329,macrocystic lymphatic malformation,MONDO_grouped,disease,DISEASE_10752
10753,10753,10753,10753,10753,10753,10753,10753,MONDO:0003791,prostatic urethral cancer,MONDO,disease,DISEASE_10753
10754,10754,10754,10754,10754,10754,10754,10754,MONDO:0700014,chromosome 7 disorder,MONDO,disease,DISEASE_10754
10755,10755,10755,10755,10755,10755,10755,10755,MONDO:0002526,dermal unilateral segmental cavernous angioma,MONDO,disease,DISEASE_10755
10756,10756,10756,10756,10756,10756,10756,10756,MONDO:0013130_MONDO:0012605_MONDO:0012604_MONDO:0009631_MONDO:0012409_MONDO:0014050_MONDO:0013377_MONDO:0013293_MONDO:0000062,isolated microphthalmia,MONDO_grouped,disease,DISEASE_10756
10757,10757,10757,10757,10757,10757,10757,10757,MONDO:0000327,Buruli ulcer disease,MONDO,disease,DISEASE_10757
10758,10758,10758,10758,10758,10758,10758,10758,MONDO:0019644,"renal dysplasia, unilateral",MONDO,disease,DISEASE_10758
10759,10759,10759,10759,10759,10759,10759,10759,MONDO:0005142_MONDO:0005143,Pseudomonas aeruginosa CF5 infection,MONDO_grouped,disease,DISEASE_10759
10760,10760,10760,10760,10760,10760,10760,10760,MONDO:0009540_MONDO:0009645,chronic mucocutaneous candidiasis due to lymphokine deficiency,MONDO_grouped,disease,DISEASE_10760
10761,10761,10761,10761,10761,10761,10761,10761,MONDO:1011954,"tibial dyschondroplasia, non-human animal",MONDO,disease,DISEASE_10761
10762,10762,10762,10762,10762,10762,10762,10762,MONDO:0020058,gonosome anomaly,MONDO,disease,DISEASE_10762
10763,10763,10763,10763,10763,10763,10763,10763,MONDO:1012026,"black hair follicular dysplasia, cattle",MONDO,disease,DISEASE_10763
10764,10764,10764,10764,10764,10764,10764,10764,MONDO:0971006_MONDO:0971011_MONDO:0971012_MONDO:0011476,MHC class I deficiency,MONDO_grouped,disease,DISEASE_10764
10765,10765,10765,10765,10765,10765,10765,10765,MONDO:0004325,testicular thecoma,MONDO,disease,DISEASE_10765
10766,10766,10766,10766,10766,10766,10766,10766,MONDO:0002260,hidradenitis,MONDO,disease,DISEASE_10766
10767,10767,10767,10767,10767,10767,10767,10767,MONDO:0019873,4p16.3 microduplication syndrome,MONDO,disease,DISEASE_10767
10768,10768,10768,10768,10768,10768,10768,10768,MONDO:0015641,benign infantile focal epilepsy with midline spikes and wave during sleep,MONDO,disease,DISEASE_10768
10769,10769,10769,10769,10769,10769,10769,10769,MONDO:0019828,pituitary stalk interruption syndrome,MONDO,disease,DISEASE_10769
10770,10770,10770,10770,10770,10770,10770,10770,MONDO:0100147,SATB2 associated disorder,MONDO,disease,DISEASE_10770
10771,10771,10771,10771,10771,10771,10771,10771,MONDO:1010361,"hyperphagia leading to hepatic steatosis, non-human animal",MONDO,disease,DISEASE_10771
10772,10772,10772,10772,10772,10772,10772,10772,MONDO:0859274,"neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies",MONDO,disease,DISEASE_10772
10773,10773,10773,10773,10773,10773,10773,10773,MONDO:0000953,cancer of short bone of lower limb,MONDO,disease,DISEASE_10773
10774,10774,10774,10774,10774,10774,10774,10774,MONDO:0006219,gallbladder small cell neuroendocrine carcinoma,MONDO,disease,DISEASE_10774
10775,10775,10775,10775,10775,10775,10775,10775,MONDO:0014560_MONDO:0008770_MONDO:0008771_MONDO:0010521_MONDO:0015008_MONDO:0007092_MONDO:0007094_MONDO:0014540_MONDO:0032717_MONDO:0007538_MONDO:0008772_MONDO:0021547_MONDO:0019507_MONDO:0015047_MONDO:0015048,amelogenesis imperfecta,MONDO_grouped,disease,DISEASE_10775
10776,10776,10776,10776,10776,10776,10776,10776,MONDO:0022151,Chitty Hall Webb syndrome,MONDO,disease,DISEASE_10776
10777,10777,10777,10777,10777,10777,10777,10777,MONDO:0019404,perineurioma,MONDO,disease,DISEASE_10777
10778,10778,10778,10778,10778,10778,10778,10778,MONDO:0006825,kuru,MONDO,disease,DISEASE_10778
10779,10779,10779,10779,10779,10779,10779,10779,MONDO:0007759,"hyperlipidemia, familial combined, LPL related",MONDO,disease,DISEASE_10779
10780,10780,10780,10780,10780,10780,10780,10780,MONDO:0020040_MONDO:0017576,"46,XY disorder of sex development",MONDO_grouped,disease,DISEASE_10780
10781,10781,10781,10781,10781,10781,10781,10781,MONDO:0018844,urachal cyst,MONDO,disease,DISEASE_10781
10782,10782,10782,10782,10782,10782,10782,10782,MONDO:0010302,Ito hypomelanosis,MONDO,disease,DISEASE_10782
10783,10783,10783,10783,10783,10783,10783,10783,MONDO:0017783,congenital pancreatic cyst,MONDO,disease,DISEASE_10783
10784,10784,10784,10784,10784,10784,10784,10784,MONDO:0015735,severe congenital nemaline myopathy,MONDO,disease,DISEASE_10784
10785,10785,10785,10785,10785,10785,10785,10785,MONDO:0100576_MONDO:0100575,hereditary generalized epilepsy,MONDO_grouped,disease,DISEASE_10785
10786,10786,10786,10786,10786,10786,10786,10786,MONDO:0013256,chromosome 15q24 deletion syndrome,MONDO,disease,DISEASE_10786
10787,10787,10787,10787,10787,10787,10787,10787,MONDO:0016523,bronchogenic cyst,MONDO,disease,DISEASE_10787
10788,10788,10788,10788,10788,10788,10788,10788,MONDO:0005969,st. Louis encephalitis,MONDO,disease,DISEASE_10788
10789,10789,10789,10789,10789,10789,10789,10789,MONDO:0034204,syndromic congenital sodium diarrhea,MONDO,disease,DISEASE_10789
10790,10790,10790,10790,10790,10790,10790,10790,MONDO:0005507,gingival cancer,MONDO,disease,DISEASE_10790
10791,10791,10791,10791,10791,10791,10791,10791,MONDO:0005043,hyperplasia,MONDO,disease,DISEASE_10791
10792,10792,10792,10792,10792,10792,10792,10792,MONDO:0002388,intracystic papillary adenoma,MONDO,disease,DISEASE_10792
10793,10793,10793,10793,10793,10793,10793,10793,MONDO:0024532_MONDO:0014254_MONDO:0008163,otofaciocervical syndrome,MONDO_grouped,disease,DISEASE_10793
10794,10794,10794,10794,10794,10794,10794,10794,MONDO:1011304,"mammary fibrocystic disease, non-human animal",MONDO,disease,DISEASE_10794
10795,10795,10795,10795,10795,10795,10795,10795,MONDO:0007048,acrokeratosis verruciformis,MONDO,disease,DISEASE_10795
10796,10796,10796,10796,10796,10796,10796,10796,MONDO:0010581,"diabetes insipidus, nephrogenic, X-linked",MONDO,disease,DISEASE_10796
10797,10797,10797,10797,10797,10797,10797,10797,MONDO:0009028,Crane-Heise syndrome,MONDO,disease,DISEASE_10797
10798,10798,10798,10798,10798,10798,10798,10798,MONDO:0013889,short stature-optic atrophy-Pelger-HuC+t anomaly syndrome,MONDO,disease,DISEASE_10798
10799,10799,10799,10799,10799,10799,10799,10799,MONDO:0021383,neoplasm of floor of mouth,MONDO,disease,DISEASE_10799
10800,10800,10800,10800,10800,10800,10800,10800,MONDO:0000890,Zika virus congenital syndrome,MONDO,disease,DISEASE_10800
10801,10801,10801,10801,10801,10801,10801,10801,MONDO:0003302_MONDO:0044795,epithelioid neurofibroma,MONDO_grouped,disease,DISEASE_10801
10802,10802,10802,10802,10802,10802,10802,10802,MONDO:0018824_MONDO:0035235,pyoderma gangrenosum,MONDO_grouped,disease,DISEASE_10802
10803,10803,10803,10803,10803,10803,10803,10803,MONDO:1010090_MONDO:1010293,"anotia, non-human animal",MONDO_grouped,disease,DISEASE_10803
10804,10804,10804,10804,10804,10804,10804,10804,MONDO:0024360,central sleep apnea caused by high altitude,MONDO,disease,DISEASE_10804
10805,10805,10805,10805,10805,10805,10805,10805,MONDO:0013796,chromosome 17q12 duplication syndrome,MONDO,disease,DISEASE_10805
10806,10806,10806,10806,10806,10806,10806,10806,MONDO:0024529,MVP1,MONDO,disease,DISEASE_10806
10807,10807,10807,10807,10807,10807,10807,10807,MONDO:0025163,white heifer disease,MONDO,disease,DISEASE_10807
10808,10808,10808,10808,10808,10808,10808,10808,MONDO:0009363,hydrocephaly-tall stature-joint laxity syndrome,MONDO,disease,DISEASE_10808
10809,10809,10809,10809,10809,10809,10809,10809,MONDO:0004614_MONDO:1010947_MONDO:1010960_MONDO:1012405_MONDO:1012406,chronic monocytic leukemia,MONDO_grouped,disease,DISEASE_10809
10810,10810,10810,10810,10810,10810,10810,10810,MONDO:0035112_MONDO:0850449,acute myeloid leukemia with BCR-ABL1,MONDO_grouped,disease,DISEASE_10810
10811,10811,10811,10811,10811,10811,10811,10811,MONDO:0700086,uniparental disomy,MONDO,disease,DISEASE_10811
10812,10812,10812,10812,10812,10812,10812,10812,MONDO:0002285,pupil disorder,MONDO,disease,DISEASE_10812
10813,10813,10813,10813,10813,10813,10813,10813,MONDO:0019578_MONDO:0019579,nodular lichen myxedematosus,MONDO_grouped,disease,DISEASE_10813
10814,10814,10814,10814,10814,10814,10814,10814,MONDO:0002943,external ear basal cell carcinoma,MONDO,disease,DISEASE_10814
10815,10815,10815,10815,10815,10815,10815,10815,MONDO:0024506_MONDO:0014124_MONDO:0014703_MONDO:0014459_MONDO:0013895_MONDO:0013635_MONDO:0007034,Adams-Oliver syndrome,MONDO_grouped,disease,DISEASE_10815
10816,10816,10816,10816,10816,10816,10816,10816,MONDO:0004288,scirrhous breast carcinoma,MONDO,disease,DISEASE_10816
10817,10817,10817,10817,10817,10817,10817,10817,MONDO:0004889,total central choroidal atrophy,MONDO,disease,DISEASE_10817
10818,10818,10818,10818,10818,10818,10818,10818,MONDO:0019378,la Crosse encephalitis,MONDO,disease,DISEASE_10818
10819,10819,10819,10819,10819,10819,10819,10819,MONDO:0009006,complement component 2 deficiency,MONDO,disease,DISEASE_10819
10820,10820,10820,10820,10820,10820,10820,10820,MONDO:0014180,"epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency",MONDO,disease,DISEASE_10820
10821,10821,10821,10821,10821,10821,10821,10821,MONDO:0019903,ring chromosome 2,MONDO,disease,DISEASE_10821
10822,10822,10822,10822,10822,10822,10822,10822,MONDO:0011874,neonatal ichthyosis-sclerosing cholangitis syndrome,MONDO,disease,DISEASE_10822
10823,10823,10823,10823,10823,10823,10823,10823,MONDO:0009557,mandibuloacral dysplasia with type A lipodystrophy,MONDO,disease,DISEASE_10823
10824,10824,10824,10824,10824,10824,10824,10824,MONDO:1010805,"polydactyly, domestic guinea pig",MONDO,disease,DISEASE_10824
10825,10825,10825,10825,10825,10825,10825,10825,MONDO:0014336,intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency,MONDO,disease,DISEASE_10825
10826,10826,10826,10826,10826,10826,10826,10826,MONDO:0004472,breast columnar cell mucinous carcinoma,MONDO,disease,DISEASE_10826
10827,10827,10827,10827,10827,10827,10827,10827,MONDO:0008523,Blau syndrome,MONDO,disease,DISEASE_10827
10828,10828,10828,10828,10828,10828,10828,10828,MONDO:0012129,"leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema",MONDO,disease,DISEASE_10828
10829,10829,10829,10829,10829,10829,10829,10829,MONDO:0004450_MONDO:0004763,carotid artery occlusion,MONDO_grouped,disease,DISEASE_10829
10830,10830,10830,10830,10830,10830,10830,10830,MONDO:0850156,B-lymphoblastic leukemia/lymphoma MLL rearranged,MONDO,disease,DISEASE_10830
10831,10831,10831,10831,10831,10831,10831,10831,MONDO:0016472,dracunculiasis,MONDO,disease,DISEASE_10831
10832,10832,10832,10832,10832,10832,10832,10832,MONDO:0015455,gonococcal conjunctivitis,MONDO,disease,DISEASE_10832
10833,10833,10833,10833,10833,10833,10833,10833,MONDO:0017575,mitochondrial neurogastrointestinal encephalomyopathy,MONDO,disease,DISEASE_10833
10834,10834,10834,10834,10834,10834,10834,10834,MONDO:0012235_MONDO:0033116_MONDO:0014159_MONDO:0033115_MONDO:0014339_MONDO:0030323_MONDO:0008943_MONDO:0014934_MONDO:0013645_MONDO:0859245_MONDO:0014530_MONDO:0013905_MONDO:0032923_MONDO:0014311_MONDO:0032706_MONDO:0859360_MONDO:0014601_MONDO:0014846_MONDO:0014845_MONDO:0014503_MONDO:0030312_MONDO:0013687_MONDO:0016163_MONDO:0030318_MONDO:0013392_MONDO:0020380_MONDO:0019792_MONDO:0019793_MONDO:0019794_MONDO:0020043,autosomal recessive spinocerebellar ataxia,MONDO_grouped,disease,DISEASE_10834
10835,10835,10835,10835,10835,10835,10835,10835,MONDO:0000762,syndrome caused by partial chromosomal duplication,MONDO,disease,DISEASE_10835
10836,10836,10836,10836,10836,10836,10836,10836,MONDO:0005061,lung adenocarcinoma,MONDO,disease,DISEASE_10836
10837,10837,10837,10837,10837,10837,10837,10837,MONDO:0005667,biliary dyskinesia,MONDO,disease,DISEASE_10837
10838,10838,10838,10838,10838,10838,10838,10838,MONDO:0859263,"developmental delay, impaired speech, and behavioral abnormalities, with or without seizures",MONDO,disease,DISEASE_10838
10839,10839,10839,10839,10839,10839,10839,10839,MONDO:0018100,familial primary hypomagnesemia,MONDO,disease,DISEASE_10839
10840,10840,10840,10840,10840,10840,10840,10840,MONDO:0975953,Pan-Chung-Bellen syndrome,MONDO,disease,DISEASE_10840
10841,10841,10841,10841,10841,10841,10841,10841,MONDO:0013000,porphyria due to ALA dehydratase deficiency,MONDO,disease,DISEASE_10841
10842,10842,10842,10842,10842,10842,10842,10842,MONDO:0017295,"glycerol kinase deficiency, juvenile form",MONDO,disease,DISEASE_10842
10843,10843,10843,10843,10843,10843,10843,10843,MONDO:0100341,fire ant poisoning,MONDO,disease,DISEASE_10843
10844,10844,10844,10844,10844,10844,10844,10844,MONDO:0004168,cribriform variant testicular seminoma,MONDO,disease,DISEASE_10844
10845,10845,10845,10845,10845,10845,10845,10845,MONDO:0016027_MONDO:0015642_MONDO:0018981,benign neonatal seizures,MONDO_grouped,disease,DISEASE_10845
10846,10846,10846,10846,10846,10846,10846,10846,MONDO:0001761,favism,MONDO,disease,DISEASE_10846
10847,10847,10847,10847,10847,10847,10847,10847,MONDO:0700040,neonatal jaundice due to ABO incompatibility,MONDO,disease,DISEASE_10847
10848,10848,10848,10848,10848,10848,10848,10848,MONDO:1011732,"autosomal T cell-negative, B cell-negative, NK cell-positive severe combined immunodeficiency disease with sensitivity to ionizing radiation, non-human animal",MONDO,disease,DISEASE_10848
10849,10849,10849,10849,10849,10849,10849,10849,MONDO:0700125,chromosome 18 disorder,MONDO,disease,DISEASE_10849
10850,10850,10850,10850,10850,10850,10850,10850,MONDO:0013531,PSPH deficiency,MONDO,disease,DISEASE_10850
10851,10851,10851,10851,10851,10851,10851,10851,MONDO:0958299_MONDO:0958300_MONDO:0958301,round cell sarcoma with EWSR1-NFATC2 gene fusion,MONDO_grouped,disease,DISEASE_10851
10852,10852,10852,10852,10852,10852,10852,10852,MONDO:0005843,mediastinal cancer,MONDO,disease,DISEASE_10852
10853,10853,10853,10853,10853,10853,10853,10853,MONDO:0017400,hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome,MONDO,disease,DISEASE_10853
10854,10854,10854,10854,10854,10854,10854,10854,MONDO:0021168,hibernoma,MONDO,disease,DISEASE_10854
10855,10855,10855,10855,10855,10855,10855,10855,MONDO:0006387,primary pulmonary diffuse large B-cell lymphoma,MONDO,disease,DISEASE_10855
10856,10856,10856,10856,10856,10856,10856,10856,MONDO:0017696,"glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form",MONDO,disease,DISEASE_10856
10857,10857,10857,10857,10857,10857,10857,10857,MONDO:0003108,cervicomedullary junction neoplasm,MONDO,disease,DISEASE_10857
10858,10858,10858,10858,10858,10858,10858,10858,MONDO:0968987,extramedullary conus spinal cord lipoma,MONDO,disease,DISEASE_10858
10859,10859,10859,10859,10859,10859,10859,10859,MONDO:0012572,Sakoda complex,MONDO,disease,DISEASE_10859
10860,10860,10860,10860,10860,10860,10860,10860,MONDO:1011007_MONDO:1011008,"peripheral neuropathy, dog",MONDO_grouped,disease,DISEASE_10860
10861,10861,10861,10861,10861,10861,10861,10861,MONDO:0018912,Cushing syndrome,MONDO,disease,DISEASE_10861
10862,10862,10862,10862,10862,10862,10862,10862,MONDO:0014863,"macrocephaly, dysmorphic facies, and psychomotor retardation",MONDO,disease,DISEASE_10862
10863,10863,10863,10863,10863,10863,10863,10863,MONDO:0001585_MONDO:0004939,hallucinogen abuse,MONDO_grouped,disease,DISEASE_10863
10864,10864,10864,10864,10864,10864,10864,10864,MONDO:0003000,central nervous system germ cell tumor,MONDO,disease,DISEASE_10864
10865,10865,10865,10865,10865,10865,10865,10865,MONDO:0034676,overgrowth syndrome with 2q37 translocation,MONDO,disease,DISEASE_10865
10866,10866,10866,10866,10866,10866,10866,10866,MONDO:0003271,iodine hypothyroidism,MONDO,disease,DISEASE_10866
10867,10867,10867,10867,10867,10867,10867,10867,MONDO:1011416,"calcinosis circumscripta, non-human animal",MONDO,disease,DISEASE_10867
10868,10868,10868,10868,10868,10868,10868,10868,MONDO:0002000_MONDO:0024414,anaerobic meningitis,MONDO_grouped,disease,DISEASE_10868
10869,10869,10869,10869,10869,10869,10869,10869,MONDO:0040653,autosomal recessive ocular albinism,MONDO,disease,DISEASE_10869
10870,10870,10870,10870,10870,10870,10870,10870,MONDO:0004046,childhood brain meningioma,MONDO,disease,DISEASE_10870
10871,10871,10871,10871,10871,10871,10871,10871,MONDO:0012272,"intellectual disability, keratoconus, febrile seizures, and sinoatrial block",MONDO,disease,DISEASE_10871
10872,10872,10872,10872,10872,10872,10872,10872,MONDO:0030720,trichomonal vulvovaginitis,MONDO,disease,DISEASE_10872
10873,10873,10873,10873,10873,10873,10873,10873,MONDO:0007322,"chondrodysplasia punctata, tibial-metacarpal type",MONDO,disease,DISEASE_10873
10874,10874,10874,10874,10874,10874,10874,10874,MONDO:0009791,"oral sensibility, disturbance of",MONDO,disease,DISEASE_10874
10875,10875,10875,10875,10875,10875,10875,10875,MONDO:0006839,Lutembacher syndrome,MONDO,disease,DISEASE_10875
10876,10876,10876,10876,10876,10876,10876,10876,MONDO:0007571,primary erythermalgia,MONDO,disease,DISEASE_10876
10877,10877,10877,10877,10877,10877,10877,10877,MONDO:0013955,Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency,MONDO,disease,DISEASE_10877
10878,10878,10878,10878,10878,10878,10878,10878,MONDO:0016949,partial duplication of the short arm of chromosome 16,MONDO,disease,DISEASE_10878
10879,10879,10879,10879,10879,10879,10879,10879,MONDO:0013169,chromosome 5p13 duplication syndrome,MONDO,disease,DISEASE_10879
10880,10880,10880,10880,10880,10880,10880,10880,MONDO:1010510,"dilated cardiomyopathy PLN-related, dog",MONDO,disease,DISEASE_10880
10881,10881,10881,10881,10881,10881,10881,10881,MONDO:1012028,"bleeding disorder, domestic cat",MONDO,disease,DISEASE_10881
10882,10882,10882,10882,10882,10882,10882,10882,MONDO:0005056,keratinizing squamous cell carcinoma,MONDO,disease,DISEASE_10882
10883,10883,10883,10883,10883,10883,10883,10883,MONDO:0012719,combined PSAP deficiency,MONDO,disease,DISEASE_10883
10884,10884,10884,10884,10884,10884,10884,10884,MONDO:0850231,erythema nodosum,MONDO,disease,DISEASE_10884
10885,10885,10885,10885,10885,10885,10885,10885,MONDO:0004152,chronic lymphocytic leukemia/small lymphocytic lymphoma with immunoglobulin heavy chain variable-region gene somatic hypermutation,MONDO,disease,DISEASE_10885
10886,10886,10886,10886,10886,10886,10886,10886,MONDO:0008582,tooth and nail syndrome,MONDO,disease,DISEASE_10886
10887,10887,10887,10887,10887,10887,10887,10887,MONDO:1012952,"amelogenesis imperfecta, non-human animal",MONDO,disease,DISEASE_10887
10888,10888,10888,10888,10888,10888,10888,10888,MONDO:0003288,bizarre leiomyoma,MONDO,disease,DISEASE_10888
10889,10889,10889,10889,10889,10889,10889,10889,MONDO:0018070,familial multiple fibrofolliculoma,MONDO,disease,DISEASE_10889
10890,10890,10890,10890,10890,10890,10890,10890,MONDO:0018569,X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome,MONDO,disease,DISEASE_10890
10891,10891,10891,10891,10891,10891,10891,10891,MONDO:0002043,ectropion,MONDO,disease,DISEASE_10891
10892,10892,10892,10892,10892,10892,10892,10892,MONDO:0023543,Katsantoni-Papadakou-Lagoyanni syndrome,MONDO,disease,DISEASE_10892
10893,10893,10893,10893,10893,10893,10893,10893,MONDO:0005579,idiopathic generalized epilepsy,MONDO,disease,DISEASE_10893
10894,10894,10894,10894,10894,10894,10894,10894,MONDO:0015667,acute myeloid leukemia by FAB classification,MONDO,disease,DISEASE_10894
10895,10895,10895,10895,10895,10895,10895,10895,MONDO:0005060_MONDO:0003431_MONDO:0004510,liposarcoma,MONDO_grouped,disease,DISEASE_10895
10896,10896,10896,10896,10896,10896,10896,10896,MONDO:0008603_MONDO:0013774_MONDO:0000156,trigonocephaly,MONDO_grouped,disease,DISEASE_10896
10897,10897,10897,10897,10897,10897,10897,10897,MONDO:0018598,obsolete neonatal adrenoleukodystrophy,MONDO,disease,DISEASE_10897
10898,10898,10898,10898,10898,10898,10898,10898,MONDO:0012076,"midface hypoplasia, obesity, developmental delay, and neonatal hypotonia",MONDO,disease,DISEASE_10898
10899,10899,10899,10899,10899,10899,10899,10899,MONDO:0010017,sea-blue histiocyte syndrome,MONDO,disease,DISEASE_10899
10900,10900,10900,10900,10900,10900,10900,10900,MONDO:1010524,"cleft palate, American mink",MONDO,disease,DISEASE_10900
10901,10901,10901,10901,10901,10901,10901,10901,MONDO:0004130,anus basaloid carcinoma,MONDO,disease,DISEASE_10901
10902,10902,10902,10902,10902,10902,10902,10902,MONDO:0001855,rubeosis iridis,MONDO,disease,DISEASE_10902
10903,10903,10903,10903,10903,10903,10903,10903,MONDO:0018752,exercise-induced malignant hyperthermia,MONDO,disease,DISEASE_10903
10904,10904,10904,10904,10904,10904,10904,10904,MONDO:0010947,Budd-Chiari syndrome,MONDO,disease,DISEASE_10904
10905,10905,10905,10905,10905,10905,10905,10905,MONDO:0004958,oral cavity squamous cell carcinoma,MONDO,disease,DISEASE_10905
10906,10906,10906,10906,10906,10906,10906,10906,MONDO:0700093,balanced Robertsonian translocation Down syndrome,MONDO,disease,DISEASE_10906
10907,10907,10907,10907,10907,10907,10907,10907,MONDO:0019799,hepatoerythropoietic porphyria,MONDO,disease,DISEASE_10907
10908,10908,10908,10908,10908,10908,10908,10908,MONDO:0001603,paralytic lagophthalmos,MONDO,disease,DISEASE_10908
10909,10909,10909,10909,10909,10909,10909,10909,MONDO:0018153,Erdheim-Chester disease,MONDO,disease,DISEASE_10909
10910,10910,10910,10910,10910,10910,10910,10910,MONDO:0014501,"macular degeneration, early-onset",MONDO,disease,DISEASE_10910
10911,10911,10911,10911,10911,10911,10911,10911,MONDO:0957783,ichthyosis with erythrokeratoderma,MONDO,disease,DISEASE_10911
10912,10912,10912,10912,10912,10912,10912,10912,MONDO:0015664,idiopathic pulmonary artery dilatation,MONDO,disease,DISEASE_10912
10913,10913,10913,10913,10913,10913,10913,10913,MONDO:1010007_MONDO:1010020,"subvalvular aortic stenosis, non-human animal",MONDO_grouped,disease,DISEASE_10913
10914,10914,10914,10914,10914,10914,10914,10914,MONDO:0012035,craniosynostosis-intracranial calcifications syndrome,MONDO,disease,DISEASE_10914
10915,10915,10915,10915,10915,10915,10915,10915,MONDO:0001241,transient neonatal neutropenia,MONDO,disease,DISEASE_10915
10916,10916,10916,10916,10916,10916,10916,10916,MONDO:0015167,amniotic band syndrome,MONDO,disease,DISEASE_10916
10917,10917,10917,10917,10917,10917,10917,10917,MONDO:0007584,exostoses-anetodermia-brachydactyly type E syndrome,MONDO,disease,DISEASE_10917
10918,10918,10918,10918,10918,10918,10918,10918,MONDO:0020977,granulomatous prostatitis,MONDO,disease,DISEASE_10918
10919,10919,10919,10919,10919,10919,10919,10919,MONDO:0042600,Sammartino-Decreccio syndrome,MONDO,disease,DISEASE_10919
10920,10920,10920,10920,10920,10920,10920,10920,MONDO:0008108,oculocerebrocutaneous syndrome,MONDO,disease,DISEASE_10920
10921,10921,10921,10921,10921,10921,10921,10921,MONDO:0010280_MONDO:0011407_MONDO:0013880_MONDO:0008340_MONDO:0024466,"ptosis, hereditary congenital",MONDO_grouped,disease,DISEASE_10921
10922,10922,10922,10922,10922,10922,10922,10922,MONDO:0001119,premature menopause,MONDO,disease,DISEASE_10922
10923,10923,10923,10923,10923,10923,10923,10923,MONDO:0008118,odontomatosis-aortae esophagus stenosis syndrome,MONDO,disease,DISEASE_10923
10924,10924,10924,10924,10924,10924,10924,10924,MONDO:0011369_MONDO:0007751,"hypercholesterolemia, autosomal dominant",MONDO_grouped,disease,DISEASE_10924
10925,10925,10925,10925,10925,10925,10925,10925,MONDO:0018672,IgG4-related aortitis,MONDO,disease,DISEASE_10925
10926,10926,10926,10926,10926,10926,10926,10926,MONDO:0015474,cryptosporidiosis,MONDO,disease,DISEASE_10926
10927,10927,10927,10927,10927,10927,10927,10927,MONDO:0015994,muscular dystrophy-white matter spongiosis syndrome,MONDO,disease,DISEASE_10927
10928,10928,10928,10928,10928,10928,10928,10928,MONDO:0003038,dysgraphia,MONDO,disease,DISEASE_10928
10929,10929,10929,10929,10929,10929,10929,10929,MONDO:0005028,esophageal adenocarcinoma,MONDO,disease,DISEASE_10929
10930,10930,10930,10930,10930,10930,10930,10930,MONDO:0006923,Bacillaceae infectious disease,MONDO,disease,DISEASE_10930
10931,10931,10931,10931,10931,10931,10931,10931,MONDO:0014489,limb-girdle muscular dystrophy due to POMK deficiency,MONDO,disease,DISEASE_10931
10932,10932,10932,10932,10932,10932,10932,10932,MONDO:0019925,paternal uniparental disomy of chromosome 21,MONDO,disease,DISEASE_10932
10933,10933,10933,10933,10933,10933,10933,10933,MONDO:1010745,"dermatomyositis, dog",MONDO,disease,DISEASE_10933
10934,10934,10934,10934,10934,10934,10934,10934,MONDO:0001328,thyroid hormone resistance syndrome,MONDO,disease,DISEASE_10934
10935,10935,10935,10935,10935,10935,10935,10935,MONDO:0042911,Schwartz-Cohen-addad-Lambert syndrome,MONDO,disease,DISEASE_10935
10936,10936,10936,10936,10936,10936,10936,10936,MONDO:0004276,ceruminoma,MONDO,disease,DISEASE_10936
10937,10937,10937,10937,10937,10937,10937,10937,MONDO:0018336,obsolete Silver-Russell syndrome due to a point mutation,MONDO,disease,DISEASE_10937
10938,10938,10938,10938,10938,10938,10938,10938,MONDO:0007681,"goiter, multinodular 1, with or without Sertoli-Leydig cell tumors",MONDO,disease,DISEASE_10938
10939,10939,10939,10939,10939,10939,10939,10939,MONDO:0004203,female urethral cancer,MONDO,disease,DISEASE_10939
10940,10940,10940,10940,10940,10940,10940,10940,MONDO:0009353,homocystinuria due to methylene tetrahydrofolate reductase deficiency,MONDO,disease,DISEASE_10940
10941,10941,10941,10941,10941,10941,10941,10941,MONDO:0010887,isolated anterior cervical hypertrichosis,MONDO,disease,DISEASE_10941
10942,10942,10942,10942,10942,10942,10942,10942,MONDO:0003680,periosteal chondrosarcoma,MONDO,disease,DISEASE_10942
10943,10943,10943,10943,10943,10943,10943,10943,MONDO:0017988,multifocal atrial tachycardia,MONDO,disease,DISEASE_10943
10944,10944,10944,10944,10944,10944,10944,10944,MONDO:0859231,"macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin",MONDO,disease,DISEASE_10944
10945,10945,10945,10945,10945,10945,10945,10945,MONDO:0018816,isolated neonatal sclerosing cholangitis,MONDO,disease,DISEASE_10945
10946,10946,10946,10946,10946,10946,10946,10946,MONDO:0043789,serum sickness,MONDO,disease,DISEASE_10946
10947,10947,10947,10947,10947,10947,10947,10947,MONDO:0022428,aluminosis,MONDO,disease,DISEASE_10947
10948,10948,10948,10948,10948,10948,10948,10948,MONDO:0024884,metastatic carcinoma in the bone,MONDO,disease,DISEASE_10948
10949,10949,10949,10949,10949,10949,10949,10949,MONDO:0037743,mediastinal soft tissue cancer,MONDO,disease,DISEASE_10949
10950,10950,10950,10950,10950,10950,10950,10950,MONDO:0005386,peripheral arterial disease,MONDO,disease,DISEASE_10950
10951,10951,10951,10951,10951,10951,10951,10951,MONDO:0020989,hereditary persistence of fetal hemoglobin,MONDO,disease,DISEASE_10951
10952,10952,10952,10952,10952,10952,10952,10952,MONDO:0003989,polyembryoma of the ovary,MONDO,disease,DISEASE_10952
10953,10953,10953,10953,10953,10953,10953,10953,MONDO:0800445_MONDO:0800455_MONDO:0800444,Birt-Hogg-Dube syndrome,MONDO_grouped,disease,DISEASE_10953
10954,10954,10954,10954,10954,10954,10954,10954,MONDO:0010559,MASA syndrome,MONDO,disease,DISEASE_10954
10955,10955,10955,10955,10955,10955,10955,10955,MONDO:0009701,"myopathy, granulovacuolar lobular, with electrical myotonia",MONDO,disease,DISEASE_10955
10956,10956,10956,10956,10956,10956,10956,10956,MONDO:1011936,"arthritis deformans, non-human animal",MONDO,disease,DISEASE_10956
10957,10957,10957,10957,10957,10957,10957,10957,MONDO:1010837,"copper toxicosis, COMMD1-related, dog",MONDO,disease,DISEASE_10957
10958,10958,10958,10958,10958,10958,10958,10958,MONDO:0018499,"double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy",MONDO,disease,DISEASE_10958
10959,10959,10959,10959,10959,10959,10959,10959,MONDO:0018685,incessant infant ventricular tachycardia,MONDO,disease,DISEASE_10959
10960,10960,10960,10960,10960,10960,10960,10960,MONDO:0018766,chronic enteropathy associated with SLCO2A1 gene,MONDO,disease,DISEASE_10960
10961,10961,10961,10961,10961,10961,10961,10961,MONDO:1010614,"congenital adrenal hyperplasia due to 11-beta hydroxylase deficiency, domestic cat",MONDO,disease,DISEASE_10961
10962,10962,10962,10962,10962,10962,10962,10962,MONDO:0008423,sinus node disease and myopia,MONDO,disease,DISEASE_10962
10963,10963,10963,10963,10963,10963,10963,10963,MONDO:0001222,congenital T-cell immunodeficiency,MONDO,disease,DISEASE_10963
10964,10964,10964,10964,10964,10964,10964,10964,MONDO:0007336,isolated cleft palate,MONDO,disease,DISEASE_10964
10965,10965,10965,10965,10965,10965,10965,10965,MONDO:0001040,nasopharyngitis,MONDO,disease,DISEASE_10965
10966,10966,10966,10966,10966,10966,10966,10966,MONDO:0007390_MONDO:0011993,coumarin resistance,MONDO_grouped,disease,DISEASE_10966
10967,10967,10967,10967,10967,10967,10967,10967,MONDO:0021488,benign neoplasm of lacrimal gland,MONDO,disease,DISEASE_10967
10968,10968,10968,10968,10968,10968,10968,10968,MONDO:0020633,anaplastic cancer,MONDO,disease,DISEASE_10968
10969,10969,10969,10969,10969,10969,10969,10969,MONDO:0016951,partial trisomy/tetrasomy of the short arm of chromosome 18,MONDO,disease,DISEASE_10969
10970,10970,10970,10970,10970,10970,10970,10970,MONDO:0021190,DNA repair disease,MONDO,disease,DISEASE_10970
10971,10971,10971,10971,10971,10971,10971,10971,MONDO:0021348,neoplasm of testis,MONDO,disease,DISEASE_10971
10972,10972,10972,10972,10972,10972,10972,10972,MONDO:0021537,undifferentiated carcinoma of nasopharynx,MONDO,disease,DISEASE_10972
10973,10973,10973,10973,10973,10973,10973,10973,MONDO:0035824,KLHL7-related cold-induced sweating-like syndrome,MONDO,disease,DISEASE_10973
10974,10974,10974,10974,10974,10974,10974,10974,MONDO:0700238_MONDO:0700239,BEST1-related dominant retinopathy,MONDO_grouped,disease,DISEASE_10974
10975,10975,10975,10975,10975,10975,10975,10975,MONDO:0016443,papular elastorrhexis,MONDO,disease,DISEASE_10975
10976,10976,10976,10976,10976,10976,10976,10976,MONDO:0007787,Ambras type hypertrichosis universalis congenita,MONDO,disease,DISEASE_10976
10977,10977,10977,10977,10977,10977,10977,10977,MONDO:0018891,familial tumoral calcinosis,MONDO,disease,DISEASE_10977
10978,10978,10978,10978,10978,10978,10978,10978,MONDO:0800322,membranous obstruction of inferior vena cava,MONDO,disease,DISEASE_10978
10979,10979,10979,10979,10979,10979,10979,10979,MONDO:0032868,lessel-kubisch syndrome,MONDO,disease,DISEASE_10979
10980,10980,10980,10980,10980,10980,10980,10980,MONDO:1012036,"spontaneous cardiomyopathy, turkey",MONDO,disease,DISEASE_10980
10981,10981,10981,10981,10981,10981,10981,10981,MONDO:0016099_MONDO:0018011,overlap myositis,MONDO_grouped,disease,DISEASE_10981
10982,10982,10982,10982,10982,10982,10982,10982,MONDO:0005737,Ebola hemorrhagic fever,MONDO,disease,DISEASE_10982
10983,10983,10983,10983,10983,10983,10983,10983,MONDO:0001747,tibial collateral ligament bursitis,MONDO,disease,DISEASE_10983
10984,10984,10984,10984,10984,10984,10984,10984,MONDO:0001249,trachoma,MONDO,disease,DISEASE_10984
10985,10985,10985,10985,10985,10985,10985,10985,MONDO:0005755,equine infectious anemia,MONDO,disease,DISEASE_10985
10986,10986,10986,10986,10986,10986,10986,10986,MONDO:0003799_MONDO:0001214_MONDO:0005808,conjunctivitis,MONDO_grouped,disease,DISEASE_10986
10987,10987,10987,10987,10987,10987,10987,10987,MONDO:0035136,isolated melanotic schwannoma,MONDO,disease,DISEASE_10987
10988,10988,10988,10988,10988,10988,10988,10988,MONDO:0009889_MONDO:0004691_MONDO:0000447,autosomal recessive polycystic kidney disease,MONDO_grouped,disease,DISEASE_10988
10989,10989,10989,10989,10989,10989,10989,10989,MONDO:0020469,"48,XYYY syndrome",MONDO,disease,DISEASE_10989
10990,10990,10990,10990,10990,10990,10990,10990,MONDO:1010316,"hypophosphatasia, non-human animal",MONDO,disease,DISEASE_10990
10991,10991,10991,10991,10991,10991,10991,10991,MONDO:0850419,diffuse large B-cell lymphoma germinal center B-cell type,MONDO,disease,DISEASE_10991
10992,10992,10992,10992,10992,10992,10992,10992,MONDO:0001504,fetishistic disorder,MONDO,disease,DISEASE_10992
10993,10993,10993,10993,10993,10993,10993,10993,MONDO:1010112,isolated short stature,MONDO,disease,DISEASE_10993
10994,10994,10994,10994,10994,10994,10994,10994,MONDO:0015464,craniofrontonasal dysplasia-Poland anomaly syndrome,MONDO,disease,DISEASE_10994
10995,10995,10995,10995,10995,10995,10995,10995,MONDO:0021121,hemangioendothelioma,MONDO,disease,DISEASE_10995
10996,10996,10996,10996,10996,10996,10996,10996,MONDO:0008456,spinocerebellar ataxia with rigidity and peripheral neuropathy,MONDO,disease,DISEASE_10996
10997,10997,10997,10997,10997,10997,10997,10997,MONDO:1010411,"epilepsy, dog",MONDO,disease,DISEASE_10997
10998,10998,10998,10998,10998,10998,10998,10998,MONDO:0020452,inferior vena cava interruption,MONDO,disease,DISEASE_10998
10999,10999,10999,10999,10999,10999,10999,10999,MONDO:0006302,micropapillary serous carcinoma,MONDO,disease,DISEASE_10999
11000,11000,11000,11000,11000,11000,11000,11000,MONDO:0001198,acquired thrombocytopenia,MONDO,disease,DISEASE_11000
11001,11001,11001,11001,11001,11001,11001,11001,MONDO:1012118,"congenital hypoplasia of mammary gland, sheep",MONDO,disease,DISEASE_11001
11002,11002,11002,11002,11002,11002,11002,11002,MONDO:0005878,ocular onchocerciasis,MONDO,disease,DISEASE_11002
11003,11003,11003,11003,11003,11003,11003,11003,MONDO:0012794,ANE syndrome,MONDO,disease,DISEASE_11003
11004,11004,11004,11004,11004,11004,11004,11004,MONDO:0060564,HELIX syndrome,MONDO,disease,DISEASE_11004
11005,11005,11005,11005,11005,11005,11005,11005,MONDO:0019468_MONDO:0019461,T-cell prolymphocytic leukemia,MONDO_grouped,disease,DISEASE_11005
11006,11006,11006,11006,11006,11006,11006,11006,MONDO:0012280,Goldberg-Shprintzen syndrome,MONDO,disease,DISEASE_11006
11007,11007,11007,11007,11007,11007,11007,11007,MONDO:0018874_MONDO:0004996,acute myeloid leukemia,MONDO_grouped,disease,DISEASE_11007
11008,11008,11008,11008,11008,11008,11008,11008,MONDO:0014429,autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency,MONDO,disease,DISEASE_11008
11009,11009,11009,11009,11009,11009,11009,11009,MONDO:0859201,neurodevelopmental disorder with impaired language and ataxia and with or without seizures,MONDO,disease,DISEASE_11009
11010,11010,11010,11010,11010,11010,11010,11010,MONDO:0002926_MONDO:0005006,clear cell sarcoma,MONDO_grouped,disease,DISEASE_11010
11011,11011,11011,11011,11011,11011,11011,11011,MONDO:0006795,hypersplenism,MONDO,disease,DISEASE_11011
11012,11012,11012,11012,11012,11012,11012,11012,MONDO:0971124,perifoveal exudative vascular anomalous complex,MONDO,disease,DISEASE_11012
11013,11013,11013,11013,11013,11013,11013,11013,MONDO:0021530,benign neoplasm of subglottis,MONDO,disease,DISEASE_11013
11014,11014,11014,11014,11014,11014,11014,11014,MONDO:0005975,suppurative otitis media,MONDO,disease,DISEASE_11014
11015,11015,11015,11015,11015,11015,11015,11015,MONDO:0003755,urinary tract non-invasive transitional cell neoplasm,MONDO,disease,DISEASE_11015
11016,11016,11016,11016,11016,11016,11016,11016,MONDO:0022535,autonomic facial cephalgia,MONDO,disease,DISEASE_11016
11017,11017,11017,11017,11017,11017,11017,11017,MONDO:0036781,benign axillary neoplasm,MONDO,disease,DISEASE_11017
11018,11018,11018,11018,11018,11018,11018,11018,MONDO:0010983_MONDO:0014019_MONDO:0030486_MONDO:0030513_MONDO:0013813_MONDO:0012789_MONDO:0014627_MONDO:0025691_MONDO:0007495_MONDO:0007496_MONDO:0014033_MONDO:0030455_MONDO:0013928_MONDO:0003441_MONDO:0044807,dystonia,MONDO_grouped,disease,DISEASE_11018
11019,11019,11019,11019,11019,11019,11019,11019,MONDO:0001029,Klippel-Feil syndrome,MONDO,disease,DISEASE_11019
11020,11020,11020,11020,11020,11020,11020,11020,MONDO:0015583,2p21 microdeletion syndrome,MONDO,disease,DISEASE_11020
11021,11021,11021,11021,11021,11021,11021,11021,MONDO:0009551,"magnesium, elevated red cell",MONDO,disease,DISEASE_11021
11022,11022,11022,11022,11022,11022,11022,11022,MONDO:0060664,"neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities",MONDO,disease,DISEASE_11022
11023,11023,11023,11023,11023,11023,11023,11023,MONDO:0020308,childhood occipital visual epilepsy,MONDO,disease,DISEASE_11023
11024,11024,11024,11024,11024,11024,11024,11024,MONDO:0700200,atypical dopamine transporter deficiency syndrome,MONDO,disease,DISEASE_11024
11025,11025,11025,11025,11025,11025,11025,11025,MONDO:0011939,Spondyloenchondrodysplasia with immune dysregulation,MONDO,disease,DISEASE_11025
11026,11026,11026,11026,11026,11026,11026,11026,MONDO:0700182,feline erythroleukemia,MONDO,disease,DISEASE_11026
11027,11027,11027,11027,11027,11027,11027,11027,MONDO:0003057,pediatric meningioma,MONDO,disease,DISEASE_11027
11028,11028,11028,11028,11028,11028,11028,11028,MONDO:0044874,refractory cytopenia of childhood,MONDO,disease,DISEASE_11028
11029,11029,11029,11029,11029,11029,11029,11029,MONDO:0001848,Morgagni cataract,MONDO,disease,DISEASE_11029
11030,11030,11030,11030,11030,11030,11030,11030,MONDO:0700109,"skin disease caused by bacterial infection, non-human animal",MONDO,disease,DISEASE_11030
11031,11031,11031,11031,11031,11031,11031,11031,MONDO:0044638,hypopharynx squamous cell carcinoma,MONDO,disease,DISEASE_11031
11032,11032,11032,11032,11032,11032,11032,11032,MONDO:0007629,fragile site 10Q23,MONDO,disease,DISEASE_11032
11033,11033,11033,11033,11033,11033,11033,11033,MONDO:0016456,5q14.3 microdeletion syndrome,MONDO,disease,DISEASE_11033
11034,11034,11034,11034,11034,11034,11034,11034,MONDO:0017041,osteochondrodysplatic nanism-deafness-retinitis pigmentosa syndrome,MONDO,disease,DISEASE_11034
11035,11035,11035,11035,11035,11035,11035,11035,MONDO:1011504,"Fanconi syndrome, horse",MONDO,disease,DISEASE_11035
11036,11036,11036,11036,11036,11036,11036,11036,MONDO:0002463,lacrimal gland carcinoma,MONDO,disease,DISEASE_11036
11037,11037,11037,11037,11037,11037,11037,11037,MONDO:0003892,acinar lung adenocarcinoma,MONDO,disease,DISEASE_11037
11038,11038,11038,11038,11038,11038,11038,11038,MONDO:0044783,solid papillary breast carcinoma,MONDO,disease,DISEASE_11038
11039,11039,11039,11039,11039,11039,11039,11039,MONDO:0007977_MONDO:0011530,"mesomelic dysplasia, Kantaputra type",MONDO_grouped,disease,DISEASE_11039
11040,11040,11040,11040,11040,11040,11040,11040,MONDO:0003534,papillary thymic adenocarcinoma,MONDO,disease,DISEASE_11040
11041,11041,11041,11041,11041,11041,11041,11041,MONDO:0021032,herpes zoster with dermatitis of eyelid,MONDO,disease,DISEASE_11041
11042,11042,11042,11042,11042,11042,11042,11042,MONDO:0000763,epithelial and subepithelial corneal dystrophy,MONDO,disease,DISEASE_11042
11043,11043,11043,11043,11043,11043,11043,11043,MONDO:0004234,chronic lymphoproliferative disorder of NK-cells,MONDO,disease,DISEASE_11043
11044,11044,11044,11044,11044,11044,11044,11044,MONDO:0016674_MONDO:0010765,"46,XY partial gonadal dysgenesis",MONDO_grouped,disease,DISEASE_11044
11045,11045,11045,11045,11045,11045,11045,11045,MONDO:0004499,lung hilum carcinoma,MONDO,disease,DISEASE_11045
11046,11046,11046,11046,11046,11046,11046,11046,MONDO:0002481,ovarian neuroendocrine neoplasm,MONDO,disease,DISEASE_11046
11047,11047,11047,11047,11047,11047,11047,11047,MONDO:0013956,Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency,MONDO,disease,DISEASE_11047
11048,11048,11048,11048,11048,11048,11048,11048,MONDO:0033559,intellectual developmental disorder with seizures and language delay,MONDO,disease,DISEASE_11048
11049,11049,11049,11049,11049,11049,11049,11049,MONDO:1012102_MONDO:1012543,"idiopathic hepatic fibrosis, dog",MONDO_grouped,disease,DISEASE_11049
11050,11050,11050,11050,11050,11050,11050,11050,MONDO:0014162,infantile hypertrophic cardiomyopathy due to MRPL44 deficiency,MONDO,disease,DISEASE_11050
11051,11051,11051,11051,11051,11051,11051,11051,MONDO:0850368,immunoglobulin heavy-and-light chain,MONDO,disease,DISEASE_11051
11052,11052,11052,11052,11052,11052,11052,11052,MONDO:0011327,neuronal intranuclear inclusion disease,MONDO,disease,DISEASE_11052
11053,11053,11053,11053,11053,11053,11053,11053,MONDO:0014313,autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity,MONDO,disease,DISEASE_11053
11054,11054,11054,11054,11054,11054,11054,11054,MONDO:0005467,occupation-related stress disorder,MONDO,disease,DISEASE_11054
11055,11055,11055,11055,11055,11055,11055,11055,MONDO:0001854,lacrimal apparatus disorder,MONDO,disease,DISEASE_11055
11056,11056,11056,11056,11056,11056,11056,11056,MONDO:0023054,klumpke's paralysis,MONDO,disease,DISEASE_11056
11057,11057,11057,11057,11057,11057,11057,11057,MONDO:0015816,indolent primary cutaneous T-cell lymphoma,MONDO,disease,DISEASE_11057
11058,11058,11058,11058,11058,11058,11058,11058,MONDO:0017018,isolated pulmonary capillaritis,MONDO,disease,DISEASE_11058
11059,11059,11059,11059,11059,11059,11059,11059,MONDO:1010562_MONDO:1010563,"acromegaly, dog",MONDO_grouped,disease,DISEASE_11059
11060,11060,11060,11060,11060,11060,11060,11060,MONDO:0002561_MONDO:1010860_MONDO:1010862,lysosomal storage disease,MONDO_grouped,disease,DISEASE_11060
11061,11061,11061,11061,11061,11061,11061,11061,MONDO:0859571,"diaphragmatic hernia 4, with cardiovascular defects",MONDO,disease,DISEASE_11061
11062,11062,11062,11062,11062,11062,11062,11062,MONDO:0016729,mixed neuronal-glial tumor,MONDO,disease,DISEASE_11062
11063,11063,11063,11063,11063,11063,11063,11063,MONDO:0005883,ophthalmic herpes zoster,MONDO,disease,DISEASE_11063
11064,11064,11064,11064,11064,11064,11064,11064,MONDO:0100285,extrahepatic biliary atresia,MONDO,disease,DISEASE_11064
11065,11065,11065,11065,11065,11065,11065,11065,MONDO:0800503,TMEM63B-related developmental and epileptic encephalopathy with anemia,MONDO,disease,DISEASE_11065
11066,11066,11066,11066,11066,11066,11066,11066,MONDO:1010966,"Dandy-Walker syndrome, domestic cat",MONDO,disease,DISEASE_11066
11067,11067,11067,11067,11067,11067,11067,11067,MONDO:0006369,pineal parenchymal tumor of intermediate differentiation,MONDO,disease,DISEASE_11067
11068,11068,11068,11068,11068,11068,11068,11068,MONDO:0022672_MONDO:0022673,autosomal dominant cataract,MONDO_grouped,disease,DISEASE_11068
11069,11069,11069,11069,11069,11069,11069,11069,MONDO:0009898,"polysaccharide, storage of unusual",MONDO,disease,DISEASE_11069
11070,11070,11070,11070,11070,11070,11070,11070,MONDO:0007332_MONDO:0012537,split-hand/foot malformation with long bone deficiency,MONDO_grouped,disease,DISEASE_11070
11071,11071,11071,11071,11071,11071,11071,11071,MONDO:0012254,"multiple epiphyseal dysplasia, with miniepiphyses",MONDO,disease,DISEASE_11071
11072,11072,11072,11072,11072,11072,11072,11072,MONDO:0958160_MONDO:0958298,round cell sarcoma with EWSR1-non-ETS fusion,MONDO_grouped,disease,DISEASE_11072
11073,11073,11073,11073,11073,11073,11073,11073,MONDO:0007776,"hypersensitivity pneumonitis, familial",MONDO,disease,DISEASE_11073
11074,11074,11074,11074,11074,11074,11074,11074,MONDO:0013335,"tuberculin skin test reactivity, absence of",MONDO,disease,DISEASE_11074
11075,11075,11075,11075,11075,11075,11075,11075,MONDO:0850127,epithelioid inflammatory myofibroblastic sarcoma,MONDO,disease,DISEASE_11075
11076,11076,11076,11076,11076,11076,11076,11076,MONDO:1010514,"triploidy, chicken",MONDO,disease,DISEASE_11076
11077,11077,11077,11077,11077,11077,11077,11077,MONDO:0025013,non-human primate disease,MONDO,disease,DISEASE_11077
11078,11078,11078,11078,11078,11078,11078,11078,MONDO:0002894_MONDO:0958349,spinal chordoma,MONDO_grouped,disease,DISEASE_11078
11079,11079,11079,11079,11079,11079,11079,11079,MONDO:0002941,anal margin carcinoma,MONDO,disease,DISEASE_11079
11080,11080,11080,11080,11080,11080,11080,11080,MONDO:0014786_MONDO:0008072_MONDO:0013496_MONDO:0100555,"IgA nephropathy, susceptibility to",MONDO_grouped,disease,DISEASE_11080
11081,11081,11081,11081,11081,11081,11081,11081,MONDO:0025095,"malaria, avian",MONDO,disease,DISEASE_11081
11082,11082,11082,11082,11082,11082,11082,11082,MONDO:0003754,Brown-Sequard syndrome,MONDO,disease,DISEASE_11082
11083,11083,11083,11083,11083,11083,11083,11083,MONDO:1011151,"anodontia, dog",MONDO,disease,DISEASE_11083
11084,11084,11084,11084,11084,11084,11084,11084,MONDO:0000320,glandular tularemia,MONDO,disease,DISEASE_11084
11085,11085,11085,11085,11085,11085,11085,11085,MONDO:0005399,venous thromboembolism,MONDO,disease,DISEASE_11085
11086,11086,11086,11086,11086,11086,11086,11086,MONDO:0008088,"neuropathy, with paraprotein in serum, cerebrospinal fluid and urine",MONDO,disease,DISEASE_11086
11087,11087,11087,11087,11087,11087,11087,11087,MONDO:0035669_MONDO:0035670,acute disseminated encephalomyelitis with anti-MOG antibodies,MONDO_grouped,disease,DISEASE_11087
11088,11088,11088,11088,11088,11088,11088,11088,MONDO:0859162,neurodevelopmental disorder with infantile epileptic spasms,MONDO,disease,DISEASE_11088
11089,11089,11089,11089,11089,11089,11089,11089,MONDO:0005928,post-thrombotic syndrome,MONDO,disease,DISEASE_11089
11090,11090,11090,11090,11090,11090,11090,11090,MONDO:0014711_MONDO:0020558_MONDO:0019548_MONDO:0017058_MONDO:0017937_MONDO:0016431,autosomal dominant Charcot-Marie-Tooth disease,MONDO_grouped,disease,DISEASE_11090
11091,11091,11091,11091,11091,11091,11091,11091,MONDO:0008946,"cerebral angiopathy, dysphoric",MONDO,disease,DISEASE_11091
11092,11092,11092,11092,11092,11092,11092,11092,MONDO:0060758,"spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits",MONDO,disease,DISEASE_11092
11093,11093,11093,11093,11093,11093,11093,11093,MONDO:0000594,pervasive developmental disorder,MONDO,disease,DISEASE_11093
11094,11094,11094,11094,11094,11094,11094,11094,MONDO:0002022,disorder of orbital region,MONDO,disease,DISEASE_11094
11095,11095,11095,11095,11095,11095,11095,11095,MONDO:1012439,"ear necrosis syndrome, pig",MONDO,disease,DISEASE_11095
11096,11096,11096,11096,11096,11096,11096,11096,MONDO:0018381,osteochondrosis,MONDO,disease,DISEASE_11096
11097,11097,11097,11097,11097,11097,11097,11097,MONDO:0007866,Bart-Pumphrey syndrome,MONDO,disease,DISEASE_11097
11098,11098,11098,11098,11098,11098,11098,11098,MONDO:0001986,Argyll Robertson pupil,MONDO,disease,DISEASE_11098
11099,11099,11099,11099,11099,11099,11099,11099,MONDO:0016190,qualitative or quantitative defects of protein ZASP,MONDO,disease,DISEASE_11099
11100,11100,11100,11100,11100,11100,11100,11100,MONDO:0007508,Rapp-Hodgkin syndrome,MONDO,disease,DISEASE_11100
11101,11101,11101,11101,11101,11101,11101,11101,MONDO:0007457,"diastema, dental medial",MONDO,disease,DISEASE_11101
11102,11102,11102,11102,11102,11102,11102,11102,MONDO:0007845,"Kaposi sarcoma, susceptibility to",MONDO,disease,DISEASE_11102
11103,11103,11103,11103,11103,11103,11103,11103,MONDO:0043759,abdominal ectopic pregnancy,MONDO,disease,DISEASE_11103
11104,11104,11104,11104,11104,11104,11104,11104,MONDO:0017786,2q23.1 microduplication syndrome,MONDO,disease,DISEASE_11104
11105,11105,11105,11105,11105,11105,11105,11105,MONDO:0021394,polyp of vagina,MONDO,disease,DISEASE_11105
11106,11106,11106,11106,11106,11106,11106,11106,MONDO:0006029,cecum carcinoma,MONDO,disease,DISEASE_11106
11107,11107,11107,11107,11107,11107,11107,11107,MONDO:0010739,Taqi polymorphism,MONDO,disease,DISEASE_11107
11108,11108,11108,11108,11108,11108,11108,11108,MONDO:1011454,"osteogenesis imperfecta, non-human animal",MONDO,disease,DISEASE_11108
11109,11109,11109,11109,11109,11109,11109,11109,MONDO:0100372,disorder of peroxisomal transporter,MONDO,disease,DISEASE_11109
11110,11110,11110,11110,11110,11110,11110,11110,MONDO:0021514,benign neoplasm of pericardium,MONDO,disease,DISEASE_11110
11111,11111,11111,11111,11111,11111,11111,11111,MONDO:0012580,hereditary pulmonary alveolar proteinosis,MONDO,disease,DISEASE_11111
11112,11112,11112,11112,11112,11112,11112,11112,MONDO:0042458,Trichinella spiralis infectious disease,MONDO,disease,DISEASE_11112
11113,11113,11113,11113,11113,11113,11113,11113,MONDO:0013534,apolipoprotein c-III deficiency,MONDO,disease,DISEASE_11113
11114,11114,11114,11114,11114,11114,11114,11114,MONDO:0019771,oromandibular dystonia,MONDO,disease,DISEASE_11114
11115,11115,11115,11115,11115,11115,11115,11115,MONDO:0015206,short stature-heart defect-craniofacial anomalies syndrome,MONDO,disease,DISEASE_11115
11116,11116,11116,11116,11116,11116,11116,11116,MONDO:0010260,"arthrogryposis, congenital, lower limb, X-linked",MONDO,disease,DISEASE_11116
11117,11117,11117,11117,11117,11117,11117,11117,MONDO:0000483,oculogyric crisis,MONDO,disease,DISEASE_11117
11118,11118,11118,11118,11118,11118,11118,11118,MONDO:0011794,obsolete Dravet syndrome,MONDO,disease,DISEASE_11118
11119,11119,11119,11119,11119,11119,11119,11119,MONDO:0032584,"ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis",MONDO,disease,DISEASE_11119
11120,11120,11120,11120,11120,11120,11120,11120,MONDO:0004675,mitochondrial encephalomyopathy,MONDO,disease,DISEASE_11120
11121,11121,11121,11121,11121,11121,11121,11121,MONDO:0007802,"hypospadias 3, autosomal",MONDO,disease,DISEASE_11121
11122,11122,11122,11122,11122,11122,11122,11122,MONDO:0009128,"dwarfism, intellectual disability, and eye abnormality",MONDO,disease,DISEASE_11122
11123,11123,11123,11123,11123,11123,11123,11123,MONDO:0015405_MONDO:0015406_MONDO:0015407,cerebrofacial arteriovenous metameric syndrome,MONDO_grouped,disease,DISEASE_11123
11124,11124,11124,11124,11124,11124,11124,11124,MONDO:0001888,anus lymphoma,MONDO,disease,DISEASE_11124
11125,11125,11125,11125,11125,11125,11125,11125,MONDO:0020321,acute undifferentiated leukemia,MONDO,disease,DISEASE_11125
11126,11126,11126,11126,11126,11126,11126,11126,MONDO:0100485,KCNH1 associated disorder,MONDO,disease,DISEASE_11126
11127,11127,11127,11127,11127,11127,11127,11127,MONDO:0003666,fallopian tube endometrioid adenocarcinoma,MONDO,disease,DISEASE_11127
11128,11128,11128,11128,11128,11128,11128,11128,MONDO:0005493,carbon monoxide-induced delayed encephalopathy,MONDO,disease,DISEASE_11128
11129,11129,11129,11129,11129,11129,11129,11129,MONDO:0008714,acrofacial dysostosis Rodriguez type,MONDO,disease,DISEASE_11129
11130,11130,11130,11130,11130,11130,11130,11130,MONDO:0001056,gastric cancer,MONDO,disease,DISEASE_11130
11131,11131,11131,11131,11131,11131,11131,11131,MONDO:0009999,autosomal recessive Robinow syndrome,MONDO,disease,DISEASE_11131
11132,11132,11132,11132,11132,11132,11132,11132,MONDO:0001972,Brucella melitensis brucellosis,MONDO,disease,DISEASE_11132
11133,11133,11133,11133,11133,11133,11133,11133,MONDO:0009463,"internal carotid arteries, hypoplasia of",MONDO,disease,DISEASE_11133
11134,11134,11134,11134,11134,11134,11134,11134,MONDO:0016971,limb-girdle muscular dystrophy,MONDO,disease,DISEASE_11134
11135,11135,11135,11135,11135,11135,11135,11135,MONDO:0700337,renal tubular dysgenesis - ACE,MONDO,disease,DISEASE_11135
11136,11136,11136,11136,11136,11136,11136,11136,MONDO:0019862,levocardia,MONDO,disease,DISEASE_11136
11137,11137,11137,11137,11137,11137,11137,11137,MONDO:0002242,coagulation protein disease,MONDO,disease,DISEASE_11137
11138,11138,11138,11138,11138,11138,11138,11138,MONDO:0015268,medullary sponge kidney,MONDO,disease,DISEASE_11138
11139,11139,11139,11139,11139,11139,11139,11139,MONDO:0004863,purulent endophthalmitis,MONDO,disease,DISEASE_11139
11140,11140,11140,11140,11140,11140,11140,11140,MONDO:1011031,"succinic semialdehyde dehydrogenase deficiency, dog",MONDO,disease,DISEASE_11140
11141,11141,11141,11141,11141,11141,11141,11141,MONDO:0012897,congenital factor XI deficiency,MONDO,disease,DISEASE_11141
11142,11142,11142,11142,11142,11142,11142,11142,MONDO:0023246,linear porokeratosis,MONDO,disease,DISEASE_11142
11143,11143,11143,11143,11143,11143,11143,11143,MONDO:1012040_MONDO:1012041_MONDO:1012042_MONDO:1012043_MONDO:1012224,"cerebellar abiotrophy, horse",MONDO_grouped,disease,DISEASE_11143
11144,11144,11144,11144,11144,11144,11144,11144,MONDO:0044717,4q25 proximal deletion syndrome,MONDO,disease,DISEASE_11144
11145,11145,11145,11145,11145,11145,11145,11145,MONDO:0017244,pseudoxanthomatous diffuse cutaneous mastocytosis,MONDO,disease,DISEASE_11145
11146,11146,11146,11146,11146,11146,11146,11146,MONDO:0009723,Leigh syndrome,MONDO,disease,DISEASE_11146
11147,11147,11147,11147,11147,11147,11147,11147,MONDO:0007695,hairy palms and soles,MONDO,disease,DISEASE_11147
11148,11148,11148,11148,11148,11148,11148,11148,MONDO:0025487,murine acquired immunodeficiency syndrome,MONDO,disease,DISEASE_11148
11149,11149,11149,11149,11149,11149,11149,11149,MONDO:1010328,"retinoschisis, non-human animal",MONDO,disease,DISEASE_11149
11150,11150,11150,11150,11150,11150,11150,11150,MONDO:0031068,"Charcot-Marie-Tooth disease, axonal, IIa 2II",MONDO,disease,DISEASE_11150
11151,11151,11151,11151,11151,11151,11151,11151,MONDO:0957217_MONDO:0032866_MONDO:0032578_MONDO:0014116_MONDO:0013541_MONDO:0859332_MONDO:0014341_MONDO:0014171_MONDO:0014170_MONDO:0012399_MONDO:0014337_MONDO:0000904,"cortical dysplasia, complex, with other brain malformations",MONDO_grouped,disease,DISEASE_11151
11152,11152,11152,11152,11152,11152,11152,11152,MONDO:0000925,hyperlucent lung,MONDO,disease,DISEASE_11152
11153,11153,11153,11153,11153,11153,11153,11153,MONDO:0009495,Keutel syndrome,MONDO,disease,DISEASE_11153
11154,11154,11154,11154,11154,11154,11154,11154,MONDO:0012000,specific phobia,MONDO,disease,DISEASE_11154
11155,11155,11155,11155,11155,11155,11155,11155,MONDO:0005313_MONDO:0002845,necrotizing enterocolitis,MONDO_grouped,disease,DISEASE_11155
11156,11156,11156,11156,11156,11156,11156,11156,MONDO:0011976,lipodystrophy-intellectual disability-deafness syndrome,MONDO,disease,DISEASE_11156
11157,11157,11157,11157,11157,11157,11157,11157,MONDO:0020817,miliaria vesiculosa,MONDO,disease,DISEASE_11157
11158,11158,11158,11158,11158,11158,11158,11158,MONDO:0003196_MONDO:0006088_MONDO:0006087_MONDO:0001237,appendix carcinoma,MONDO_grouped,disease,DISEASE_11158
11159,11159,11159,11159,11159,11159,11159,11159,MONDO:1010666,"Scott Syndrome, dog",MONDO,disease,DISEASE_11159
11160,11160,11160,11160,11160,11160,11160,11160,MONDO:0001345,antidepressant type abuse,MONDO,disease,DISEASE_11160
11161,11161,11161,11161,11161,11161,11161,11161,MONDO:0019729,light and heavy chain deposition disease,MONDO,disease,DISEASE_11161
11162,11162,11162,11162,11162,11162,11162,11162,MONDO:0010019,secretory component deficiency,MONDO,disease,DISEASE_11162
11163,11163,11163,11163,11163,11163,11163,11163,MONDO:0000088,precocious puberty,MONDO,disease,DISEASE_11163
11164,11164,11164,11164,11164,11164,11164,11164,MONDO:0010809,familial chronic myelocytic leukemia-like syndrome,MONDO,disease,DISEASE_11164
11165,11165,11165,11165,11165,11165,11165,11165,MONDO:0011789_MONDO:0016995,familial meningioma,MONDO_grouped,disease,DISEASE_11165
11166,11166,11166,11166,11166,11166,11166,11166,MONDO:0100479,rifampicin-resistant tuberculosis,MONDO,disease,DISEASE_11166
11167,11167,11167,11167,11167,11167,11167,11167,MONDO:0001247,social phobia,MONDO,disease,DISEASE_11167
11168,11168,11168,11168,11168,11168,11168,11168,MONDO:1011719,"intestinal cobalamin (vitamin B12) malabsorption, non-human animal",MONDO,disease,DISEASE_11168
11169,11169,11169,11169,11169,11169,11169,11169,MONDO:0024336,vulvar adenocarcinoma,MONDO,disease,DISEASE_11169
11170,11170,11170,11170,11170,11170,11170,11170,MONDO:0001497,male genital organ vascular disease,MONDO,disease,DISEASE_11170
11171,11171,11171,11171,11171,11171,11171,11171,MONDO:0008977_MONDO:0000515_MONDO:0002342,chondrosarcoma,MONDO_grouped,disease,DISEASE_11171
11172,11172,11172,11172,11172,11172,11172,11172,MONDO:0016765,19p13.12 microdeletion syndrome,MONDO,disease,DISEASE_11172
11173,11173,11173,11173,11173,11173,11173,11173,MONDO:0002029,chronic gonorrhea of cervix,MONDO,disease,DISEASE_11173
11174,11174,11174,11174,11174,11174,11174,11174,MONDO:0001340,heart cancer,MONDO,disease,DISEASE_11174
11175,11175,11175,11175,11175,11175,11175,11175,MONDO:0018684,idiopathic neonatal atrial flutter,MONDO,disease,DISEASE_11175
11176,11176,11176,11176,11176,11176,11176,11176,MONDO:0700272,PALB2-related cancer predisposition,MONDO,disease,DISEASE_11176
11177,11177,11177,11177,11177,11177,11177,11177,MONDO:0019025,extracutaneous mastocytoma,MONDO,disease,DISEASE_11177
11178,11178,11178,11178,11178,11178,11178,11178,MONDO:0007698,hand-foot-genital syndrome,MONDO,disease,DISEASE_11178
11179,11179,11179,11179,11179,11179,11179,11179,MONDO:1010412,"epilepsy, domestic cat",MONDO,disease,DISEASE_11179
11180,11180,11180,11180,11180,11180,11180,11180,MONDO:0009081,"deafness, congenital, with total albinism",MONDO,disease,DISEASE_11180
11181,11181,11181,11181,11181,11181,11181,11181,MONDO:0015150,complex hereditary spastic paraplegia,MONDO,disease,DISEASE_11181
11182,11182,11182,11182,11182,11182,11182,11182,MONDO:0002691,liver cancer,MONDO,disease,DISEASE_11182
11183,11183,11183,11183,11183,11183,11183,11183,MONDO:1012373,"retinal dysplasia and degeneration, chicken",MONDO,disease,DISEASE_11183
11184,11184,11184,11184,11184,11184,11184,11184,MONDO:0016186,qualitative or quantitative defects of myofibrillar proteins,MONDO,disease,DISEASE_11184
11185,11185,11185,11185,11185,11185,11185,11185,MONDO:0014971,"amelogenesis imperfecta, hypomaturation type, IIa6",MONDO,disease,DISEASE_11185
11186,11186,11186,11186,11186,11186,11186,11186,MONDO:0017246,extralobar congenital pulmonary sequestration,MONDO,disease,DISEASE_11186
11187,11187,11187,11187,11187,11187,11187,11187,MONDO:1011800,"contractural arachnodactyly, non-human animal",MONDO,disease,DISEASE_11187
11188,11188,11188,11188,11188,11188,11188,11188,MONDO:0003340,malignant glomus tumor,MONDO,disease,DISEASE_11188
11189,11189,11189,11189,11189,11189,11189,11189,MONDO:0015801,hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation,MONDO,disease,DISEASE_11189
11190,11190,11190,11190,11190,11190,11190,11190,MONDO:0001487_MONDO:0003444_MONDO:0003445_MONDO:0003979,intrahepatic bile duct cancer,MONDO_grouped,disease,DISEASE_11190
11191,11191,11191,11191,11191,11191,11191,11191,MONDO:0002291,cutaneous granular cell tumor,MONDO,disease,DISEASE_11191
11192,11192,11192,11192,11192,11192,11192,11192,MONDO:0014663_MONDO:0020795_MONDO:0020796_MONDO:0030116_MONDO:0030118_MONDO:0008394,Silver-Russell syndrome,MONDO_grouped,disease,DISEASE_11192
11193,11193,11193,11193,11193,11193,11193,11193,MONDO:0006659,arteriosclerosis obliterans,MONDO,disease,DISEASE_11193
11194,11194,11194,11194,11194,11194,11194,11194,MONDO:0018474,13q12.3 microdeletion syndrome,MONDO,disease,DISEASE_11194
11195,11195,11195,11195,11195,11195,11195,11195,MONDO:0007042,Saethre-Chotzen syndrome,MONDO,disease,DISEASE_11195
11196,11196,11196,11196,11196,11196,11196,11196,MONDO:0017437_MONDO:0017438,amelia of upper limb,MONDO_grouped,disease,DISEASE_11196
11197,11197,11197,11197,11197,11197,11197,11197,MONDO:0010416,"deafness, cataract, retinitis pigmentosa, and sperm abnormalities",MONDO,disease,DISEASE_11197
11198,11198,11198,11198,11198,11198,11198,11198,MONDO:0025028,vesicular stomatitis,MONDO,disease,DISEASE_11198
11199,11199,11199,11199,11199,11199,11199,11199,MONDO:0003120,mixed testicular germ cell cancer,MONDO,disease,DISEASE_11199
11200,11200,11200,11200,11200,11200,11200,11200,MONDO:0010639,laryngeal abductor paralysis-intellectual disability syndrome,MONDO,disease,DISEASE_11200
11201,11201,11201,11201,11201,11201,11201,11201,MONDO:0018034,thalidomide embryopathy,MONDO,disease,DISEASE_11201
11202,11202,11202,11202,11202,11202,11202,11202,MONDO:0009257,galactose epimerase deficiency,MONDO,disease,DISEASE_11202
11203,11203,11203,11203,11203,11203,11203,11203,MONDO:1010139,"atrichia with papular lesions, non-human animal",MONDO,disease,DISEASE_11203
11204,11204,11204,11204,11204,11204,11204,11204,MONDO:0016996,NK-cell enteropathy,MONDO,disease,DISEASE_11204
11205,11205,11205,11205,11205,11205,11205,11205,MONDO:0004447,pituitary stalk meningioma,MONDO,disease,DISEASE_11205
11206,11206,11206,11206,11206,11206,11206,11206,MONDO:0859260,Dworschak-Punetha neurodevelopmental syndrome,MONDO,disease,DISEASE_11206
11207,11207,11207,11207,11207,11207,11207,11207,MONDO:0021507,benign neoplasm of brain stem,MONDO,disease,DISEASE_11207
11208,11208,11208,11208,11208,11208,11208,11208,MONDO:0019524,Bartter syndrome type 4,MONDO,disease,DISEASE_11208
11209,11209,11209,11209,11209,11209,11209,11209,MONDO:0011559_MONDO:0009469_MONDO:0019008,benign recurrent intrahepatic cholestasis,MONDO_grouped,disease,DISEASE_11209
11210,11210,11210,11210,11210,11210,11210,11210,MONDO:0800308,orotic aciduria without megaloblastic anemia,MONDO,disease,DISEASE_11210
11211,11211,11211,11211,11211,11211,11211,11211,MONDO:1011741,"cutaneous papillomatosis, non-human animal",MONDO,disease,DISEASE_11211
11212,11212,11212,11212,11212,11212,11212,11212,MONDO:0800484,PRKAG2-related cardiomyopathy,MONDO,disease,DISEASE_11212
11213,11213,11213,11213,11213,11213,11213,11213,MONDO:0005402_MONDO:0004643,lymphoid leukemia,MONDO_grouped,disease,DISEASE_11213
11214,11214,11214,11214,11214,11214,11214,11214,MONDO:0002363,papilloma,MONDO,disease,DISEASE_11214
11215,11215,11215,11215,11215,11215,11215,11215,MONDO:0043195,Rubinstein Taybi like syndrome,MONDO,disease,DISEASE_11215
11216,11216,11216,11216,11216,11216,11216,11216,MONDO:0008218,Hailey-Hailey disease,MONDO,disease,DISEASE_11216
11217,11217,11217,11217,11217,11217,11217,11217,MONDO:0018416_MONDO:0018423_MONDO:0014975_MONDO:0014827_MONDO:0018417_MONDO:0018418_MONDO:0018419_MONDO:0018421_MONDO:0018422_MONDO:0018420,autosomal recessive spastic paraplegia,MONDO_grouped,disease,DISEASE_11217
11218,11218,11218,11218,11218,11218,11218,11218,MONDO:0000243,ectothrix infectious disease,MONDO,disease,DISEASE_11218
11219,11219,11219,11219,11219,11219,11219,11219,MONDO:0018940_MONDO:0957215_MONDO:0014578_MONDO:0012157_MONDO:0009690_MONDO:0014581_MONDO:0014582_MONDO:0859264_MONDO:0014939_MONDO:0012240_MONDO:0014052_MONDO:0013620_MONDO:0014543_MONDO:0009689_MONDO:0011281_MONDO:0859335_MONDO:0014542_MONDO:0044299_MONDO:0013883_MONDO:0014745_MONDO:0014586_MONDO:0014590_MONDO:0012518_MONDO:0014983_MONDO:0014587_MONDO:0859514_MONDO:0014588_MONDO:0014468_MONDO:0014584_MONDO:0011600_MONDO:0014585_MONDO:0014583_MONDO:0011088_MONDO:0019952_MONDO:0002921_MONDO:1040021_MONDO:1010918_MONDO:0975808_MONDO:1010919,congenital myasthenic syndrome,MONDO_grouped,disease,DISEASE_11219
11220,11220,11220,11220,11220,11220,11220,11220,MONDO:0002883,intestinal neuroendocrine neoplasm,MONDO,disease,DISEASE_11220
11221,11221,11221,11221,11221,11221,11221,11221,MONDO:0015484,cysticercosis,MONDO,disease,DISEASE_11221
11222,11222,11222,11222,11222,11222,11222,11222,MONDO:0009544,"macrocephaly/megalencephaly syndrome, autosomal recessive",MONDO,disease,DISEASE_11222
11223,11223,11223,11223,11223,11223,11223,11223,MONDO:0009283_MONDO:0000129_MONDO:0700073_MONDO:0700074_MONDO:0700076,glutaric acidemia,MONDO_grouped,disease,DISEASE_11223
11224,11224,11224,11224,11224,11224,11224,11224,MONDO:0858921,EWSR1-negative small round cell tumor,MONDO,disease,DISEASE_11224
11225,11225,11225,11225,11225,11225,11225,11225,MONDO:0011060,early-onset non-syndromic cataract,MONDO,disease,DISEASE_11225
11226,11226,11226,11226,11226,11226,11226,11226,MONDO:0009384_MONDO:0019155,"Leydig cell hypoplasia, type 1",MONDO_grouped,disease,DISEASE_11226
11227,11227,11227,11227,11227,11227,11227,11227,MONDO:0015601,"X-linked intellectual disability, van Esch type",MONDO,disease,DISEASE_11227
11228,11228,11228,11228,11228,11228,11228,11228,MONDO:1010585,"familial goiter, American black bear",MONDO,disease,DISEASE_11228
11229,11229,11229,11229,11229,11229,11229,11229,MONDO:0006438_MONDO:1011192,synovial chondromatosis,MONDO_grouped,disease,DISEASE_11229
11230,11230,11230,11230,11230,11230,11230,11230,MONDO:0014005_MONDO:0018013,immunoglobulin-mediated membranoproliferative glomerulonephritis,MONDO_grouped,disease,DISEASE_11230
11231,11231,11231,11231,11231,11231,11231,11231,MONDO:0006343,ovarian transitional cell carcinoma,MONDO,disease,DISEASE_11231
11232,11232,11232,11232,11232,11232,11232,11232,MONDO:0008342,pubic bone dysplasia,MONDO,disease,DISEASE_11232
11233,11233,11233,11233,11233,11233,11233,11233,MONDO:0006423,soft tissue chondroma,MONDO,disease,DISEASE_11233
11234,11234,11234,11234,11234,11234,11234,11234,MONDO:0024771,"myopathy, distal, 7, adult-onset, X-linked",MONDO,disease,DISEASE_11234
11235,11235,11235,11235,11235,11235,11235,11235,MONDO:0009019,congenital hereditary endothelial dystrophy of cornea,MONDO,disease,DISEASE_11235
11236,11236,11236,11236,11236,11236,11236,11236,MONDO:0008180,congenital velopharyngeal incompetence,MONDO,disease,DISEASE_11236
11237,11237,11237,11237,11237,11237,11237,11237,MONDO:0009825,5-oxoprolinase deficiency,MONDO,disease,DISEASE_11237
11238,11238,11238,11238,11238,11238,11238,11238,MONDO:0100286,respiratory syncytial virus bronchiolitis,MONDO,disease,DISEASE_11238
11239,11239,11239,11239,11239,11239,11239,11239,MONDO:0019467,CD4+/CD56+ hematodermic neoplasm,MONDO,disease,DISEASE_11239
11240,11240,11240,11240,11240,11240,11240,11240,MONDO:0005720,cowpox,MONDO,disease,DISEASE_11240
11241,11241,11241,11241,11241,11241,11241,11241,MONDO:0023272,goniodysgenesis intellectual disability short stature,MONDO,disease,DISEASE_11241
11242,11242,11242,11242,11242,11242,11242,11242,MONDO:1010132,AARS1-related leukoencephalopathy,MONDO,disease,DISEASE_11242
11243,11243,11243,11243,11243,11243,11243,11243,MONDO:1012286,"warts between hooves, cattle",MONDO,disease,DISEASE_11243
11244,11244,11244,11244,11244,11244,11244,11244,MONDO:0006553,Fox-Fordyce disease,MONDO,disease,DISEASE_11244
11245,11245,11245,11245,11245,11245,11245,11245,MONDO:0006117,breast diffuse large B-cell lymphoma,MONDO,disease,DISEASE_11245
11246,11246,11246,11246,11246,11246,11246,11246,MONDO:0011606,baby rattle pelvis dysplasia,MONDO,disease,DISEASE_11246
11247,11247,11247,11247,11247,11247,11247,11247,MONDO:0015500,facial arteriovenous malformation,MONDO,disease,DISEASE_11247
11248,11248,11248,11248,11248,11248,11248,11248,MONDO:0043264,post-traumatic epilepsy,MONDO,disease,DISEASE_11248
11249,11249,11249,11249,11249,11249,11249,11249,MONDO:0006977,spermatocele,MONDO,disease,DISEASE_11249
11250,11250,11250,11250,11250,11250,11250,11250,MONDO:0008879,Bowen-Conradi syndrome,MONDO,disease,DISEASE_11250
11251,11251,11251,11251,11251,11251,11251,11251,MONDO:0019309,late-onset junctional epidermolysis bullosa,MONDO,disease,DISEASE_11251
11252,11252,11252,11252,11252,11252,11252,11252,MONDO:0003907,"ovarian yolk sac tumor, polyvesicular vitelline pattern",MONDO,disease,DISEASE_11252
11253,11253,11253,11253,11253,11253,11253,11253,MONDO:0004431,hemarthrosis,MONDO,disease,DISEASE_11253
11254,11254,11254,11254,11254,11254,11254,11254,MONDO:1011485,"calcinosis circumscripta, dog",MONDO,disease,DISEASE_11254
11255,11255,11255,11255,11255,11255,11255,11255,MONDO:0100039,CDKL5 disorder,MONDO,disease,DISEASE_11255
11256,11256,11256,11256,11256,11256,11256,11256,MONDO:0003966,testicular monophasic choriocarcinoma,MONDO,disease,DISEASE_11256
11257,11257,11257,11257,11257,11257,11257,11257,MONDO:1012652_MONDO:1012935,"osteochondromatosis, EXT2-related, dog",MONDO_grouped,disease,DISEASE_11257
11258,11258,11258,11258,11258,11258,11258,11258,MONDO:0009085,deafness-vitiligo-achalasia syndrome,MONDO,disease,DISEASE_11258
11259,11259,11259,11259,11259,11259,11259,11259,MONDO:0004888_MONDO:0004898,partial circumpapillary choroid dystrophy,MONDO_grouped,disease,DISEASE_11259
11260,11260,11260,11260,11260,11260,11260,11260,MONDO:0005941,retroperitoneal cancer,MONDO,disease,DISEASE_11260
11261,11261,11261,11261,11261,11261,11261,11261,MONDO:1012395,"rupture of the cranial cruciate ligament, dog",MONDO,disease,DISEASE_11261
11262,11262,11262,11262,11262,11262,11262,11262,MONDO:0971010_MONDO:0971009_MONDO:0971004_MONDO:0971008,"amyloidosis, hereditary systemic",MONDO_grouped,disease,DISEASE_11262
11263,11263,11263,11263,11263,11263,11263,11263,MONDO:0002086_MONDO:0002961,clear cell acanthoma,MONDO_grouped,disease,DISEASE_11263
11264,11264,11264,11264,11264,11264,11264,11264,MONDO:0007644,IgAD1,MONDO,disease,DISEASE_11264
11265,11265,11265,11265,11265,11265,11265,11265,MONDO:0012269,chromosome 3q29 microdeletion syndrome,MONDO,disease,DISEASE_11265
11266,11266,11266,11266,11266,11266,11266,11266,MONDO:0011493_MONDO:0007160_MONDO:0031047_MONDO:0013590_MONDO:0013666_MONDO:0019354,Stickler syndrome,MONDO_grouped,disease,DISEASE_11266
11267,11267,11267,11267,11267,11267,11267,11267,MONDO:0019473,enteropathy-associated T-cell lymphoma,MONDO,disease,DISEASE_11267
11268,11268,11268,11268,11268,11268,11268,11268,MONDO:0018088,familial Mediterranean fever,MONDO,disease,DISEASE_11268
11269,11269,11269,11269,11269,11269,11269,11269,MONDO:0043164,palmer pagon syndrome,MONDO,disease,DISEASE_11269
11270,11270,11270,11270,11270,11270,11270,11270,MONDO:1011856_MONDO:1011793_MONDO:1011868_MONDO:1011871,"progressive axonopathy, non-human animal",MONDO_grouped,disease,DISEASE_11270
11271,11271,11271,11271,11271,11271,11271,11271,MONDO:1010511,"hypertrophic cardiomyopathy, SGCD-related, golden hamster",MONDO,disease,DISEASE_11271
11272,11272,11272,11272,11272,11272,11272,11272,MONDO:0015389,supernumerary nostril,MONDO,disease,DISEASE_11272
11273,11273,11273,11273,11273,11273,11273,11273,MONDO:0016079_MONDO:0005357_MONDO:0006518,sporadic Creutzfeldt-Jakob disease,MONDO_grouped,disease,DISEASE_11273
11274,11274,11274,11274,11274,11274,11274,11274,MONDO:0030914,Clark-Baraitser syndrome,MONDO,disease,DISEASE_11274
11275,11275,11275,11275,11275,11275,11275,11275,MONDO:0001219,serous conjunctivitis except viral,MONDO,disease,DISEASE_11275
11276,11276,11276,11276,11276,11276,11276,11276,MONDO:0044645,familial monosomy 7 syndrome,MONDO,disease,DISEASE_11276
11277,11277,11277,11277,11277,11277,11277,11277,MONDO:0006597,photosensitivity disease,MONDO,disease,DISEASE_11277
11278,11278,11278,11278,11278,11278,11278,11278,MONDO:0009695,"myeloproliferative disease, autosomal recessive",MONDO,disease,DISEASE_11278
11279,11279,11279,11279,11279,11279,11279,11279,MONDO:1010428,"atherosclerosis, rock pigeon",MONDO,disease,DISEASE_11279
11280,11280,11280,11280,11280,11280,11280,11280,MONDO:0008563,thumb stiffness-brachydactyly-intellectual disability syndrome,MONDO,disease,DISEASE_11280
11281,11281,11281,11281,11281,11281,11281,11281,MONDO:0033262_MONDO:0010974_MONDO:0033280_MONDO:0030895_MONDO:0014817_MONDO:0014818_MONDO:0009733_MONDO:0014373_MONDO:0032580_MONDO:0032581_MONDO:0026726_MONDO:0014099_MONDO:0031008_MONDO:0013619_MONDO:0012546_MONDO:0032826_MONDO:0032582_MONDO:0014257_MONDO:0030962_MONDO:0033203_MONDO:0014752_MONDO:0005377_MONDO:1011047,nephrotic syndrome,MONDO_grouped,disease,DISEASE_11281
11282,11282,11282,11282,11282,11282,11282,11282,MONDO:0004441,childhood ovarian embryonal carcinoma,MONDO,disease,DISEASE_11282
11283,11283,11283,11283,11283,11283,11283,11283,MONDO:0003408,ovarian primitive germ cell tumor,MONDO,disease,DISEASE_11283
11284,11284,11284,11284,11284,11284,11284,11284,MONDO:1012886_MONDO:1012904_MONDO:1012926_MONDO:1012950,"Parkinson disease, LRRK2-related, white-tufted-ear marmoset",MONDO_grouped,disease,DISEASE_11284
11285,11285,11285,11285,11285,11285,11285,11285,MONDO:0003848,ectopic thymus,MONDO,disease,DISEASE_11285
11286,11286,11286,11286,11286,11286,11286,11286,MONDO:0010876,recessive aplasia cutis congenita of limbs,MONDO,disease,DISEASE_11286
11287,11287,11287,11287,11287,11287,11287,11287,MONDO:0003544_MONDO:0002545,spinal cord cancer,MONDO_grouped,disease,DISEASE_11287
11288,11288,11288,11288,11288,11288,11288,11288,MONDO:0001429_MONDO:0002204,transient arthropathy,MONDO_grouped,disease,DISEASE_11288
11289,11289,11289,11289,11289,11289,11289,11289,MONDO:0005748,enzootic pneumonia of calves,MONDO,disease,DISEASE_11289
11290,11290,11290,11290,11290,11290,11290,11290,MONDO:0023069,enlarged vestibular aqueduct syndrome,MONDO,disease,DISEASE_11290
11291,11291,11291,11291,11291,11291,11291,11291,MONDO:0958226,"leukoencephalopathy, porphyria-related",MONDO,disease,DISEASE_11291
11292,11292,11292,11292,11292,11292,11292,11292,MONDO:0700036,fibrothecoma,MONDO,disease,DISEASE_11292
11293,11293,11293,11293,11293,11293,11293,11293,MONDO:0018111,idiopathic severe pneumococcemia,MONDO,disease,DISEASE_11293
11294,11294,11294,11294,11294,11294,11294,11294,MONDO:0002113,peritoneal carcinoma,MONDO,disease,DISEASE_11294
11295,11295,11295,11295,11295,11295,11295,11295,MONDO:0014890,PERCHING syndrome,MONDO,disease,DISEASE_11295
11296,11296,11296,11296,11296,11296,11296,11296,MONDO:0006229,gastric small cell neuroendocrine carcinoma,MONDO,disease,DISEASE_11296
11297,11297,11297,11297,11297,11297,11297,11297,MONDO:0008576,"toe, fifth, number of phalanges 1N",MONDO,disease,DISEASE_11297
11298,11298,11298,11298,11298,11298,11298,11298,MONDO:0003260,adult cerebellar neoplasm,MONDO,disease,DISEASE_11298
11299,11299,11299,11299,11299,11299,11299,11299,MONDO:1011488,"complement component 3 deficiency, domestic guinea pig",MONDO,disease,DISEASE_11299
11300,11300,11300,11300,11300,11300,11300,11300,MONDO:1011907_MONDO:1011912_MONDO:1011914,"nephropathy, non-human animal",MONDO_grouped,disease,DISEASE_11300
11301,11301,11301,11301,11301,11301,11301,11301,MONDO:0008390,Rombo syndrome,MONDO,disease,DISEASE_11301
11302,11302,11302,11302,11302,11302,11302,11302,MONDO:0007888,hereditary leiomyomatosis and renal cell cancer,MONDO,disease,DISEASE_11302
11303,11303,11303,11303,11303,11303,11303,11303,MONDO:0019549,severe early-onset axonal neuropathy due to MFN2 deficiency,MONDO,disease,DISEASE_11303
11304,11304,11304,11304,11304,11304,11304,11304,MONDO:0060659,neurodevelopmental disorder with poor language and loss of hand skills,MONDO,disease,DISEASE_11304
11305,11305,11305,11305,11305,11305,11305,11305,MONDO:0015473,cryptorchidism-arachnodactyly-intellectual disability syndrome,MONDO,disease,DISEASE_11305
11306,11306,11306,11306,11306,11306,11306,11306,MONDO:0003122,striatonigral degeneration,MONDO,disease,DISEASE_11306
11307,11307,11307,11307,11307,11307,11307,11307,MONDO:0023581,Kuster syndrome,MONDO,disease,DISEASE_11307
11308,11308,11308,11308,11308,11308,11308,11308,MONDO:0018383,osteonecrosis of genetic origin,MONDO,disease,DISEASE_11308
11309,11309,11309,11309,11309,11309,11309,11309,MONDO:0054838_MONDO:0030317,"cardiomyopathy, familial hypertrophic",MONDO_grouped,disease,DISEASE_11309
11310,11310,11310,11310,11310,11310,11310,11310,MONDO:1012386,"recurrent airway obstruction, horse",MONDO,disease,DISEASE_11310
11311,11311,11311,11311,11311,11311,11311,11311,MONDO:0007188,primary basilar invagination,MONDO,disease,DISEASE_11311
11312,11312,11312,11312,11312,11312,11312,11312,MONDO:0003684,clear cell chondrosarcoma,MONDO,disease,DISEASE_11312
11313,11313,11313,11313,11313,11313,11313,11313,MONDO:0021321,malignant tumor of extrahepatic bile duct,MONDO,disease,DISEASE_11313
11314,11314,11314,11314,11314,11314,11314,11314,MONDO:0006896,peptic esophagitis,MONDO,disease,DISEASE_11314
11315,11315,11315,11315,11315,11315,11315,11315,MONDO:0014284_MONDO:0014287_MONDO:0014577_MONDO:0030356_MONDO:0009894_MONDO:0009964_MONDO:0033485_MONDO:0014915_MONDO:0014214_MONDO:0054565_MONDO:0013569,short-rib thoracic dysplasia 10 with or without polydactyly,MONDO_grouped,disease,DISEASE_11315
11316,11316,11316,11316,11316,11316,11316,11316,MONDO:1010034,"cleft lip with or without cleft palate, non-human animal",MONDO,disease,DISEASE_11316
11317,11317,11317,11317,11317,11317,11317,11317,MONDO:0008177,extramammary Paget disease,MONDO,disease,DISEASE_11317
11318,11318,11318,11318,11318,11318,11318,11318,MONDO:0021311,malignant tumor of parathyroid gland,MONDO,disease,DISEASE_11318
11319,11319,11319,11319,11319,11319,11319,11319,MONDO:1012736_MONDO:1012946,"skeletal dysplasia, COL11A2-related, dog",MONDO_grouped,disease,DISEASE_11319
11320,11320,11320,11320,11320,11320,11320,11320,MONDO:1011744,"cutaneous and renal vasculopathy, non-human animal",MONDO,disease,DISEASE_11320
11321,11321,11321,11321,11321,11321,11321,11321,MONDO:0001037,ring corneal ulcer,MONDO,disease,DISEASE_11321
11322,11322,11322,11322,11322,11322,11322,11322,MONDO:0007904,median nodule of the upper lip,MONDO,disease,DISEASE_11322
11323,11323,11323,11323,11323,11323,11323,11323,MONDO:0009697,Lafora disease,MONDO,disease,DISEASE_11323
11324,11324,11324,11324,11324,11324,11324,11324,MONDO:0015183,short bowel syndrome,MONDO,disease,DISEASE_11324
11325,11325,11325,11325,11325,11325,11325,11325,MONDO:0010399,chromosome Xp21 deletion syndrome,MONDO,disease,DISEASE_11325
11326,11326,11326,11326,11326,11326,11326,11326,MONDO:0005303_MONDO:0004938,drug dependence,MONDO_grouped,disease,DISEASE_11326
11327,11327,11327,11327,11327,11327,11327,11327,MONDO:0015645_MONDO:0015647,eating seizures,MONDO_grouped,disease,DISEASE_11327
11328,11328,11328,11328,11328,11328,11328,11328,MONDO:0018521,squamous cell carcinoma of pancreas,MONDO,disease,DISEASE_11328
11329,11329,11329,11329,11329,11329,11329,11329,MONDO:0004851,toxic myocarditis,MONDO,disease,DISEASE_11329
11330,11330,11330,11330,11330,11330,11330,11330,MONDO:0007030,autosomal dominant Aarskog syndrome,MONDO,disease,DISEASE_11330
11331,11331,11331,11331,11331,11331,11331,11331,MONDO:0859280,"developmental delay, hypotonia, and impaired language",MONDO,disease,DISEASE_11331
11332,11332,11332,11332,11332,11332,11332,11332,MONDO:0020303,Angelman syndrome due to paternal uniparental disomy of chromosome 15,MONDO,disease,DISEASE_11332
11333,11333,11333,11333,11333,11333,11333,11333,MONDO:0004257,childhood central nervous system mixed germ cell tumor,MONDO,disease,DISEASE_11333
11334,11334,11334,11334,11334,11334,11334,11334,MONDO:0013336,chromosome 19p13.13 deletion syndrome,MONDO,disease,DISEASE_11334
11335,11335,11335,11335,11335,11335,11335,11335,MONDO:0958296,BCOR-CCNB3 sarcoma,MONDO,disease,DISEASE_11335
11336,11336,11336,11336,11336,11336,11336,11336,MONDO:0018229,Stevens-Johnson syndrome,MONDO,disease,DISEASE_11336
11337,11337,11337,11337,11337,11337,11337,11337,MONDO:0015061,neurogenic thoracic outlet syndrome,MONDO,disease,DISEASE_11337
11338,11338,11338,11338,11338,11338,11338,11338,MONDO:0016787,epithelioid trophoblastic tumor,MONDO,disease,DISEASE_11338
11339,11339,11339,11339,11339,11339,11339,11339,MONDO:1011925,"primary ciliary dyskinesia, non-human animal",MONDO,disease,DISEASE_11339
11340,11340,11340,11340,11340,11340,11340,11340,MONDO:0011867,"microphthalmia with cyst, bilateral facial clefts, and limb anomalies",MONDO,disease,DISEASE_11340
11341,11341,11341,11341,11341,11341,11341,11341,MONDO:0859204,"fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies",MONDO,disease,DISEASE_11341
11342,11342,11342,11342,11342,11342,11342,11342,MONDO:1011645,"ventricular arrhythmias and sudden death, non-human animal",MONDO,disease,DISEASE_11342
11343,11343,11343,11343,11343,11343,11343,11343,MONDO:0003248,adult pineal parenchymal tumor,MONDO,disease,DISEASE_11343
11344,11344,11344,11344,11344,11344,11344,11344,MONDO:1012883,"congenital disorder of glycosylation, GALNT2-related, cattle",MONDO,disease,DISEASE_11344
11345,11345,11345,11345,11345,11345,11345,11345,MONDO:1012601,"sex-linked dwarfism, GHR-related, chicken",MONDO,disease,DISEASE_11345
11346,11346,11346,11346,11346,11346,11346,11346,MONDO:0009150,hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome,MONDO,disease,DISEASE_11346
11347,11347,11347,11347,11347,11347,11347,11347,MONDO:0859218,developmental delay with variable neurologic and brain abnormalities,MONDO,disease,DISEASE_11347
11348,11348,11348,11348,11348,11348,11348,11348,MONDO:0012624,acyl-CoA dehydrogenase 9 deficiency,MONDO,disease,DISEASE_11348
11349,11349,11349,11349,11349,11349,11349,11349,MONDO:0020587,factor XI deficiency,MONDO,disease,DISEASE_11349
11350,11350,11350,11350,11350,11350,11350,11350,MONDO:0018662,autosomal recessive brachyolmia,MONDO,disease,DISEASE_11350
11351,11351,11351,11351,11351,11351,11351,11351,MONDO:0001654,spermatic cord cancer,MONDO,disease,DISEASE_11351
11352,11352,11352,11352,11352,11352,11352,11352,MONDO:0001901,selective IgG subclass deficiency,MONDO,disease,DISEASE_11352
11353,11353,11353,11353,11353,11353,11353,11353,MONDO:0005711,congenital diaphragmatic hernia,MONDO,disease,DISEASE_11353
11354,11354,11354,11354,11354,11354,11354,11354,MONDO:0030995,global developmental delay with speech and behavioral abnormalities,MONDO,disease,DISEASE_11354
11355,11355,11355,11355,11355,11355,11355,11355,MONDO:1010627,"Chediak-Higashi syndrome, American mink",MONDO,disease,DISEASE_11355
11356,11356,11356,11356,11356,11356,11356,11356,MONDO:0005619_MONDO:0018626,typhoid fever,MONDO_grouped,disease,DISEASE_11356
11357,11357,11357,11357,11357,11357,11357,11357,MONDO:0975757,anastomosing haemangioma,MONDO,disease,DISEASE_11357
11358,11358,11358,11358,11358,11358,11358,11358,MONDO:0019667_MONDO:0008471,spondyloepiphyseal dysplasia tarda,MONDO_grouped,disease,DISEASE_11358
11359,11359,11359,11359,11359,11359,11359,11359,MONDO:0018481,undifferentiated carcinoma of esophagus,MONDO,disease,DISEASE_11359
11360,11360,11360,11360,11360,11360,11360,11360,MONDO:1010217,"schwannomatosis, non-human animal",MONDO,disease,DISEASE_11360
11361,11361,11361,11361,11361,11361,11361,11361,MONDO:0005567,substance withdrawal syndrome,MONDO,disease,DISEASE_11361
11362,11362,11362,11362,11362,11362,11362,11362,MONDO:0010709,early-onset parkinsonism-intellectual disability syndrome,MONDO,disease,DISEASE_11362
11363,11363,11363,11363,11363,11363,11363,11363,MONDO:1040009,TRIP11-related skeletal dysplasia,MONDO,disease,DISEASE_11363
11364,11364,11364,11364,11364,11364,11364,11364,MONDO:0007491,dystelephalangy,MONDO,disease,DISEASE_11364
11365,11365,11365,11365,11365,11365,11365,11365,MONDO:1010823,"syndactyly, Swainson's hawk",MONDO,disease,DISEASE_11365
11366,11366,11366,11366,11366,11366,11366,11366,MONDO:0002056,breast fibroadenoma,MONDO,disease,DISEASE_11366
11367,11367,11367,11367,11367,11367,11367,11367,MONDO:0032705,"neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination",MONDO,disease,DISEASE_11367
11368,11368,11368,11368,11368,11368,11368,11368,MONDO:0023176,formaldehyde poisoning,MONDO,disease,DISEASE_11368
11369,11369,11369,11369,11369,11369,11369,11369,MONDO:0859597,cns neuroblastoma with FOXR2 activation,MONDO,disease,DISEASE_11369
11370,11370,11370,11370,11370,11370,11370,11370,MONDO:0003761_MONDO:0003765_MONDO:0004330,leptomeningeal melanoma,MONDO_grouped,disease,DISEASE_11370
11371,11371,11371,11371,11371,11371,11371,11371,MONDO:0000336,meningovascular neurosyphilis,MONDO,disease,DISEASE_11371
11372,11372,11372,11372,11372,11372,11372,11372,MONDO:0006616,toxicodendron dermatitis,MONDO,disease,DISEASE_11372
11373,11373,11373,11373,11373,11373,11373,11373,MONDO:0002245,blood platelet disease,MONDO,disease,DISEASE_11373
11374,11374,11374,11374,11374,11374,11374,11374,MONDO:1012295_MONDO:1012398,"axonopathy, cattle",MONDO_grouped,disease,DISEASE_11374
11375,11375,11375,11375,11375,11375,11375,11375,MONDO:0002230,ovarian Wilms tumor,MONDO,disease,DISEASE_11375
11376,11376,11376,11376,11376,11376,11376,11376,MONDO:0005067,monophasic synovial sarcoma,MONDO,disease,DISEASE_11376
11377,11377,11377,11377,11377,11377,11377,11377,MONDO:0975955,"autoinflammation, panniculitis, and dermatosis syndrome",MONDO,disease,DISEASE_11377
11378,11378,11378,11378,11378,11378,11378,11378,MONDO:0018461,Angelman syndrome due to a point mutation,MONDO,disease,DISEASE_11378
11379,11379,11379,11379,11379,11379,11379,11379,MONDO:0006212,flat urothelial hyperplasia,MONDO,disease,DISEASE_11379
11380,11380,11380,11380,11380,11380,11380,11380,MONDO:0012998,faciocardiomelic syndrome,MONDO,disease,DISEASE_11380
11381,11381,11381,11381,11381,11381,11381,11381,MONDO:0002962_MONDO:0044656,epidermolytic acanthoma,MONDO_grouped,disease,DISEASE_11381
11382,11382,11382,11382,11382,11382,11382,11382,MONDO:0800340,"seasonal affective disorder, susceptibility to",MONDO,disease,DISEASE_11382
11383,11383,11383,11383,11383,11383,11383,11383,MONDO:0008849,atrophoderma vermiculata,MONDO,disease,DISEASE_11383
11384,11384,11384,11384,11384,11384,11384,11384,MONDO:0041403,toxic amblyopia,MONDO,disease,DISEASE_11384
11385,11385,11385,11385,11385,11385,11385,11385,MONDO:0016936,partial trisomy/tetrasomy of chromosome 18,MONDO,disease,DISEASE_11385
11386,11386,11386,11386,11386,11386,11386,11386,MONDO:0016941,partial duplication of the short arm of chromosome 4,MONDO,disease,DISEASE_11386
11387,11387,11387,11387,11387,11387,11387,11387,MONDO:0003878_MONDO:0003912_MONDO:0004550,malignant choroid melanoma,MONDO_grouped,disease,DISEASE_11387
11388,11388,11388,11388,11388,11388,11388,11388,MONDO:0011008,cleft lip/palate-intestinal malrotation-cardiopathy syndrome,MONDO,disease,DISEASE_11388
11389,11389,11389,11389,11389,11389,11389,11389,MONDO:0013008,combined immunodeficiency due to STIM1 deficiency,MONDO,disease,DISEASE_11389
11390,11390,11390,11390,11390,11390,11390,11390,MONDO:0018207,2p13.2 microdeletion syndrome,MONDO,disease,DISEASE_11390
11391,11391,11391,11391,11391,11391,11391,11391,MONDO:0003727,animal phobia,MONDO,disease,DISEASE_11391
11392,11392,11392,11392,11392,11392,11392,11392,MONDO:1040003,KCND2-related neurodevelopmental disorder with or without seizures,MONDO,disease,DISEASE_11392
11393,11393,11393,11393,11393,11393,11393,11393,MONDO:0002695,sagittal sinus thrombosis,MONDO,disease,DISEASE_11393
11394,11394,11394,11394,11394,11394,11394,11394,MONDO:0001216,pulp degeneration,MONDO,disease,DISEASE_11394
11395,11395,11395,11395,11395,11395,11395,11395,MONDO:0010305,creatine transporter deficiency,MONDO,disease,DISEASE_11395
11396,11396,11396,11396,11396,11396,11396,11396,MONDO:0018810,lethal hydranencephaly-diaphragmatic hernia syndrome,MONDO,disease,DISEASE_11396
11397,11397,11397,11397,11397,11397,11397,11397,MONDO:0018546,serotonin syndrome,MONDO,disease,DISEASE_11397
11398,11398,11398,11398,11398,11398,11398,11398,MONDO:1010014,"essential hypertension, non-human animal",MONDO,disease,DISEASE_11398
11399,11399,11399,11399,11399,11399,11399,11399,MONDO:0859340,"spinocerebellar ataxia 27B, late-onset",MONDO,disease,DISEASE_11399
11400,11400,11400,11400,11400,11400,11400,11400,MONDO:0031615,familial bent bone dysplasia syndrome,MONDO,disease,DISEASE_11400
11401,11401,11401,11401,11401,11401,11401,11401,MONDO:0100075,jaw fracture,MONDO,disease,DISEASE_11401
11402,11402,11402,11402,11402,11402,11402,11402,MONDO:0700052,intersphincteric abscess,MONDO,disease,DISEASE_11402
11403,11403,11403,11403,11403,11403,11403,11403,MONDO:0019202,myxofibrosarcoma,MONDO,disease,DISEASE_11403
11404,11404,11404,11404,11404,11404,11404,11404,MONDO:0022691,cerebello-olivary atrophy,MONDO,disease,DISEASE_11404
11405,11405,11405,11405,11405,11405,11405,11405,MONDO:1011498,"enteropathy-associated T cell lymphoma, domestic cat",MONDO,disease,DISEASE_11405
11406,11406,11406,11406,11406,11406,11406,11406,MONDO:0010208,wrinkly skin syndrome,MONDO,disease,DISEASE_11406
11407,11407,11407,11407,11407,11407,11407,11407,MONDO:0008850,Cooper-Jabs syndrome,MONDO,disease,DISEASE_11407
11408,11408,11408,11408,11408,11408,11408,11408,MONDO:0005757,eumycotic mycetoma,MONDO,disease,DISEASE_11408
11409,11409,11409,11409,11409,11409,11409,11409,MONDO:0005476,atrioventricular node disorder,MONDO,disease,DISEASE_11409
11410,11410,11410,11410,11410,11410,11410,11410,MONDO:0005552,ocular vascular disorder,MONDO,disease,DISEASE_11410
11411,11411,11411,11411,11411,11411,11411,11411,MONDO:0005879,ocular toxoplasmosis,MONDO,disease,DISEASE_11411
11412,11412,11412,11412,11412,11412,11412,11412,MONDO:0019387,macrostomia-preauricular tags-external ophthalmoplegia syndrome,MONDO,disease,DISEASE_11412
11413,11413,11413,11413,11413,11413,11413,11413,MONDO:0019927,growth hormone-producing pituitary gland neoplasm,MONDO,disease,DISEASE_11413
11414,11414,11414,11414,11414,11414,11414,11414,MONDO:0001704,vaginal glandular neoplasm,MONDO,disease,DISEASE_11414
11415,11415,11415,11415,11415,11415,11415,11415,MONDO:1010049,"acromegaly, non-human animal",MONDO,disease,DISEASE_11415
11416,11416,11416,11416,11416,11416,11416,11416,MONDO:1012582,"cone-rod dystrophy, non-human animal",MONDO,disease,DISEASE_11416
11417,11417,11417,11417,11417,11417,11417,11417,MONDO:0005805,hypodermyiasis,MONDO,disease,DISEASE_11417
11418,11418,11418,11418,11418,11418,11418,11418,MONDO:0971138,progressive hypotonia-intellectual disability-facial dysmorphism syndrome due to FYVE-defective RBSN,MONDO,disease,DISEASE_11418
11419,11419,11419,11419,11419,11419,11419,11419,MONDO:0013890,congenital myopathy with internal nuclei and atypical cores,MONDO,disease,DISEASE_11419
11420,11420,11420,11420,11420,11420,11420,11420,MONDO:0009702,myopathy due to malate-aspartate shuttle defect,MONDO,disease,DISEASE_11420
11421,11421,11421,11421,11421,11421,11421,11421,MONDO:0006411,sinonasal undifferentiated carcinoma,MONDO,disease,DISEASE_11421
11422,11422,11422,11422,11422,11422,11422,11422,MONDO:0006751,Erysipelothrix infectious disease,MONDO,disease,DISEASE_11422
11423,11423,11423,11423,11423,11423,11423,11423,MONDO:0008344,"pulmonary edema of mountaineers, susceptibility to",MONDO,disease,DISEASE_11423
11424,11424,11424,11424,11424,11424,11424,11424,MONDO:0008168_MONDO:0005183_MONDO:0005602_MONDO:0005179_MONDO:0037255,ovarian fibroma,MONDO_grouped,disease,DISEASE_11424
11425,11425,11425,11425,11425,11425,11425,11425,MONDO:0015596,non-herpetic acute limbic encephalitis,MONDO,disease,DISEASE_11425
11426,11426,11426,11426,11426,11426,11426,11426,MONDO:0018959,potassium-aggravated myotonia,MONDO,disease,DISEASE_11426
11427,11427,11427,11427,11427,11427,11427,11427,MONDO:1010157,"hyperostosis, non-human animal",MONDO,disease,DISEASE_11427
11428,11428,11428,11428,11428,11428,11428,11428,MONDO:0001702,labia majora carcinoma,MONDO,disease,DISEASE_11428
11429,11429,11429,11429,11429,11429,11429,11429,MONDO:0010756,"Von Willebrand disease, X-linked form",MONDO,disease,DISEASE_11429
11430,11430,11430,11430,11430,11430,11430,11430,MONDO:0002071,supratentorial cancer,MONDO,disease,DISEASE_11430
11431,11431,11431,11431,11431,11431,11431,11431,MONDO:0035105,diaphragmatic hernia-short bowel-asplenia syndrome,MONDO,disease,DISEASE_11431
11432,11432,11432,11432,11432,11432,11432,11432,MONDO:0700220_MONDO:0700221,disease related to transplantation,MONDO_grouped,disease,DISEASE_11432
11433,11433,11433,11433,11433,11433,11433,11433,MONDO:0009537,lymphoid interstitial pneumonia,MONDO,disease,DISEASE_11433
11434,11434,11434,11434,11434,11434,11434,11434,MONDO:0018842,primary effusion lymphoma,MONDO,disease,DISEASE_11434
11435,11435,11435,11435,11435,11435,11435,11435,MONDO:0017581,obsolete familial infantile gigantism,MONDO,disease,DISEASE_11435
11436,11436,11436,11436,11436,11436,11436,11436,MONDO:0008043,myoclonus-cerebellar ataxia-deafness syndrome,MONDO,disease,DISEASE_11436
11437,11437,11437,11437,11437,11437,11437,11437,MONDO:0004339,tuberculum sellae meningioma,MONDO,disease,DISEASE_11437
11438,11438,11438,11438,11438,11438,11438,11438,MONDO:0100061,PRPS1 deficiency disorder,MONDO,disease,DISEASE_11438
11439,11439,11439,11439,11439,11439,11439,11439,MONDO:0040674,orgasm disorder,MONDO,disease,DISEASE_11439
11440,11440,11440,11440,11440,11440,11440,11440,MONDO:0045045,selective IgG immunodeficiency,MONDO,disease,DISEASE_11440
11441,11441,11441,11441,11441,11441,11441,11441,MONDO:0032649_MONDO:0100522_MONDO:0013017_MONDO:0007805_MONDO:0011932_MONDO:0859341_MONDO:0013650_MONDO:0014390_MONDO:0013649_MONDO:0013514_MONDO:0011452_MONDO:0014384_MONDO:0014027_MONDO:0010206_MONDO:0011549_MONDO:0018914_MONDO:0003037,hypotrichosis,MONDO_grouped,disease,DISEASE_11441
11442,11442,11442,11442,11442,11442,11442,11442,MONDO:0008255,platelet factor 3 deficiency,MONDO,disease,DISEASE_11442
11443,11443,11443,11443,11443,11443,11443,11443,MONDO:0018541_MONDO:0011754,familial hypoaldosteronism,MONDO_grouped,disease,DISEASE_11443
11444,11444,11444,11444,11444,11444,11444,11444,MONDO:0014825,"chromosome 11p13 deletion syndrome, distal",MONDO,disease,DISEASE_11444
11445,11445,11445,11445,11445,11445,11445,11445,MONDO:0024461_MONDO:0010481,angiomatosis,MONDO_grouped,disease,DISEASE_11445
11446,11446,11446,11446,11446,11446,11446,11446,MONDO:0018606,extensive peripapillary myelinated nerve fibers,MONDO,disease,DISEASE_11446
11447,11447,11447,11447,11447,11447,11447,11447,MONDO:1012755_MONDO:1012790_MONDO:1012923,"cataract, NID1-related, cattle",MONDO_grouped,disease,DISEASE_11447
11448,11448,11448,11448,11448,11448,11448,11448,MONDO:0030831,gastrointestinal defect and immunodeficiency syndrome,MONDO,disease,DISEASE_11448
11449,11449,11449,11449,11449,11449,11449,11449,MONDO:0007525_MONDO:0040501,"ehlers-danlos syndrome, arthrochalasia type",MONDO_grouped,disease,DISEASE_11449
11450,11450,11450,11450,11450,11450,11450,11450,MONDO:1011077,"urolithiasis, Rhesus monkey",MONDO,disease,DISEASE_11450
11451,11451,11451,11451,11451,11451,11451,11451,MONDO:0008645,ventricular extrasystoles with syncopal episodes-perodactyly-robin sequence syndrome,MONDO,disease,DISEASE_11451
11452,11452,11452,11452,11452,11452,11452,11452,MONDO:1010117,sudden unexplained death in childhood,MONDO,disease,DISEASE_11452
11453,11453,11453,11453,11453,11453,11453,11453,MONDO:0021080,blood vessel neoplasm,MONDO,disease,DISEASE_11453
11454,11454,11454,11454,11454,11454,11454,11454,MONDO:0008634,"urticaria, familial localized heat",MONDO,disease,DISEASE_11454
11455,11455,11455,11455,11455,11455,11455,11455,MONDO:0044312,immunoskeletal dysplasia with neurodevelopmental abnormalities,MONDO,disease,DISEASE_11455
11456,11456,11456,11456,11456,11456,11456,11456,MONDO:0016685_MONDO:0016680_MONDO:0021638,low-grade astrocytoma,MONDO_grouped,disease,DISEASE_11456
11457,11457,11457,11457,11457,11457,11457,11457,MONDO:0004187,nodular fasciitis,MONDO,disease,DISEASE_11457
11458,11458,11458,11458,11458,11458,11458,11458,MONDO:0009464,immunodeficiency with defective T-cell response to interleukin 1,MONDO,disease,DISEASE_11458
11459,11459,11459,11459,11459,11459,11459,11459,MONDO:0006761,fibromuscular dysplasia,MONDO,disease,DISEASE_11459
11460,11460,11460,11460,11460,11460,11460,11460,MONDO:0019781,astrocytoma (excluding glioblastoma),MONDO,disease,DISEASE_11460
11461,11461,11461,11461,11461,11461,11461,11461,MONDO:0032875,short stature and microcephaly with genital anomalies,MONDO,disease,DISEASE_11461
11462,11462,11462,11462,11462,11462,11462,11462,MONDO:0012850_MONDO:0012851_MONDO:0000079,hypophosphatemic nephrolithiasis/osteoporosis,MONDO_grouped,disease,DISEASE_11462
11463,11463,11463,11463,11463,11463,11463,11463,MONDO:1011545,"immunoglobulin A glomerulonephropathy, dog",MONDO,disease,DISEASE_11463
11464,11464,11464,11464,11464,11464,11464,11464,MONDO:0017087,neurenteric cyst,MONDO,disease,DISEASE_11464
11465,11465,11465,11465,11465,11465,11465,11465,MONDO:0009852,hereditary intrinsic factor deficiency,MONDO,disease,DISEASE_11465
11466,11466,11466,11466,11466,11466,11466,11466,MONDO:0030756,Stuve-Wiedemann syndrome 2,MONDO,disease,DISEASE_11466
11467,11467,11467,11467,11467,11467,11467,11467,MONDO:0005631,actinomycosis,MONDO,disease,DISEASE_11467
11468,11468,11468,11468,11468,11468,11468,11468,MONDO:0800180,CPOX-related hereditary coproporphyria,MONDO,disease,DISEASE_11468
11469,11469,11469,11469,11469,11469,11469,11469,MONDO:0004767,vesiculitis,MONDO,disease,DISEASE_11469
11470,11470,11470,11470,11470,11470,11470,11470,MONDO:0018453,familial atypical multiple mole melanoma syndrome,MONDO,disease,DISEASE_11470
11471,11471,11471,11471,11471,11471,11471,11471,MONDO:0020291,hypoplastic right heart syndrome,MONDO,disease,DISEASE_11471
11472,11472,11472,11472,11472,11472,11472,11472,MONDO:0007878_MONDO:0015316,congenital laryngomalacia,MONDO_grouped,disease,DISEASE_11472
11473,11473,11473,11473,11473,11473,11473,11473,MONDO:0017478_MONDO:0017479_MONDO:0017480_MONDO:0017481,"amelia of upper limb, unilateral",MONDO_grouped,disease,DISEASE_11473
11474,11474,11474,11474,11474,11474,11474,11474,MONDO:0009110,dicarboxylic aminoaciduria,MONDO,disease,DISEASE_11474
11475,11475,11475,11475,11475,11475,11475,11475,MONDO:0009258,classic galactosemia,MONDO,disease,DISEASE_11475
11476,11476,11476,11476,11476,11476,11476,11476,MONDO:0011100,"microcephaly, retinitis pigmentosa, and sutural cataract",MONDO,disease,DISEASE_11476
11477,11477,11477,11477,11477,11477,11477,11477,MONDO:0030281_MONDO:0008825_MONDO:0100218_MONDO:0032778_MONDO:0008823_MONDO:0015168_MONDO:1011474_MONDO:1011475_MONDO:1011476,arthrogryposis multiplex congenita,MONDO_grouped,disease,DISEASE_11477
11478,11478,11478,11478,11478,11478,11478,11478,MONDO:0100582,TOR1AIP1-related myopathy,MONDO,disease,DISEASE_11478
11479,11479,11479,11479,11479,11479,11479,11479,MONDO:0010067,splenoportal vascular anomalies,MONDO,disease,DISEASE_11479
11480,11480,11480,11480,11480,11480,11480,11480,MONDO:0006237,granulocytic sarcoma,MONDO,disease,DISEASE_11480
11481,11481,11481,11481,11481,11481,11481,11481,MONDO:0008921,carnosinemia,MONDO,disease,DISEASE_11481
11482,11482,11482,11482,11482,11482,11482,11482,MONDO:0021522,benign neoplasm of lower jaw bone,MONDO,disease,DISEASE_11482
11483,11483,11483,11483,11483,11483,11483,11483,MONDO:1010272_MONDO:1010290,"renal agenesis, non-human animal",MONDO_grouped,disease,DISEASE_11483
11484,11484,11484,11484,11484,11484,11484,11484,MONDO:0016531,digestive duplication,MONDO,disease,DISEASE_11484
11485,11485,11485,11485,11485,11485,11485,11485,MONDO:0013855,"influenza, severe, susceptibility to",MONDO,disease,DISEASE_11485
11486,11486,11486,11486,11486,11486,11486,11486,MONDO:0003066,submandibular adenitis,MONDO,disease,DISEASE_11486
11487,11487,11487,11487,11487,11487,11487,11487,MONDO:0008976,"chondroitin-6-sulfaturia, defective cellular immunity, nephrotic syndrome",MONDO,disease,DISEASE_11487
11488,11488,11488,11488,11488,11488,11488,11488,MONDO:0008434,Smith-Magenis syndrome,MONDO,disease,DISEASE_11488
11489,11489,11489,11489,11489,11489,11489,11489,MONDO:0020022,central nervous system malformation,MONDO,disease,DISEASE_11489
11490,11490,11490,11490,11490,11490,11490,11490,MONDO:0003461_MONDO:0004501,fallopian tube serous adenofibroma,MONDO_grouped,disease,DISEASE_11490
11491,11491,11491,11491,11491,11491,11491,11491,MONDO:0002616,mesenchymal cell neoplasm,MONDO,disease,DISEASE_11491
11492,11492,11492,11492,11492,11492,11492,11492,MONDO:0040676,great vessel cancer,MONDO,disease,DISEASE_11492
11493,11493,11493,11493,11493,11493,11493,11493,MONDO:0003258,hobnail hemangioma,MONDO,disease,DISEASE_11493
11494,11494,11494,11494,11494,11494,11494,11494,MONDO:0009934_MONDO:0600014,alveolar capillary dysplasia with misalignment of pulmonary veins,MONDO_grouped,disease,DISEASE_11494
11495,11495,11495,11495,11495,11495,11495,11495,MONDO:0100503,DPH5-related diphthamide-deficiency syndrome,MONDO,disease,DISEASE_11495
11496,11496,11496,11496,11496,11496,11496,11496,MONDO:0002322,angiodysplasia,MONDO,disease,DISEASE_11496
11497,11497,11497,11497,11497,11497,11497,11497,MONDO:0700192,chicken hepatoma,MONDO,disease,DISEASE_11497
11498,11498,11498,11498,11498,11498,11498,11498,MONDO:0015175_MONDO:0017227_MONDO:0017228,autoimmune pancreatitis,MONDO_grouped,disease,DISEASE_11498
11499,11499,11499,11499,11499,11499,11499,11499,MONDO:0017407,deficiency in anterior pituitary function - variable immunodeficiency syndrome,MONDO,disease,DISEASE_11499
11500,11500,11500,11500,11500,11500,11500,11500,MONDO:0017300,congenital pericardium anomaly,MONDO,disease,DISEASE_11500
11501,11501,11501,11501,11501,11501,11501,11501,MONDO:0008271,polydactyly of an index finger,MONDO,disease,DISEASE_11501
11502,11502,11502,11502,11502,11502,11502,11502,MONDO:1011704,"exercise-induced pulmonary hemorrhage, non-human animal",MONDO,disease,DISEASE_11502
11503,11503,11503,11503,11503,11503,11503,11503,MONDO:0015295,intractable diarrhea-choanal atresia-eye anomalies syndrome,MONDO,disease,DISEASE_11503
11504,11504,11504,11504,11504,11504,11504,11504,MONDO:0009528,chylomicron retention disease,MONDO,disease,DISEASE_11504
11505,11505,11505,11505,11505,11505,11505,11505,MONDO:0859526,immunodeficiency 109 with lymphoproliferation,MONDO,disease,DISEASE_11505
11506,11506,11506,11506,11506,11506,11506,11506,MONDO:0002432,malignant neoplasm of acoustic nerve,MONDO,disease,DISEASE_11506
11507,11507,11507,11507,11507,11507,11507,11507,MONDO:0007198,Ascher syndrome,MONDO,disease,DISEASE_11507
11508,11508,11508,11508,11508,11508,11508,11508,MONDO:0009430_MONDO:0010358_MONDO:0010619_MONDO:0013219_MONDO:0020720,"hypophosphatemic rickets, autosomal recessive",MONDO_grouped,disease,DISEASE_11508
11509,11509,11509,11509,11509,11509,11509,11509,MONDO:0021133,acquired factor XIII deficiency,MONDO,disease,DISEASE_11509
11510,11510,11510,11510,11510,11510,11510,11510,MONDO:0010846_MONDO:0007586_MONDO:0007585_MONDO:1012073_MONDO:1012074_MONDO:1012075,"exostoses, multiple,",MONDO_grouped,disease,DISEASE_11510
11511,11511,11511,11511,11511,11511,11511,11511,MONDO:0010599,"granulomas, congenital cerebral",MONDO,disease,DISEASE_11511
11512,11512,11512,11512,11512,11512,11512,11512,MONDO:0016504,primary unilateral adrenal hyperplasia,MONDO,disease,DISEASE_11512
11513,11513,11513,11513,11513,11513,11513,11513,MONDO:0006520,Achenbach syndrome,MONDO,disease,DISEASE_11513
11514,11514,11514,11514,11514,11514,11514,11514,MONDO:0005374,bone marrow neoplasm,MONDO,disease,DISEASE_11514
11515,11515,11515,11515,11515,11515,11515,11515,MONDO:0007870,"labia minora, incomplete adhesion of",MONDO,disease,DISEASE_11515
11516,11516,11516,11516,11516,11516,11516,11516,MONDO:0024530_MONDO:0034022_MONDO:0958234_MONDO:0958233_MONDO:0008029,Bethlem myopathy,MONDO_grouped,disease,DISEASE_11516
11517,11517,11517,11517,11517,11517,11517,11517,MONDO:0005739,echinostomiasis,MONDO,disease,DISEASE_11517
11518,11518,11518,11518,11518,11518,11518,11518,MONDO:0001466,punctate epithelial keratoconjunctivitis,MONDO,disease,DISEASE_11518
11519,11519,11519,11519,11519,11519,11519,11519,MONDO:0021964,bagatelle Cassidy syndrome,MONDO,disease,DISEASE_11519
11520,11520,11520,11520,11520,11520,11520,11520,MONDO:0009735,Netherton syndrome,MONDO,disease,DISEASE_11520
11521,11521,11521,11521,11521,11521,11521,11521,MONDO:0016605,perinatal lethal hypophosphatasia,MONDO,disease,DISEASE_11521
11522,11522,11522,11522,11522,11522,11522,11522,MONDO:0006994,tarsal tunnel syndrome,MONDO,disease,DISEASE_11522
11523,11523,11523,11523,11523,11523,11523,11523,MONDO:0400005,refeeding syndrome,MONDO,disease,DISEASE_11523
11524,11524,11524,11524,11524,11524,11524,11524,MONDO:0013568,"sick sinus syndrome 3, susceptibility to",MONDO,disease,DISEASE_11524
11525,11525,11525,11525,11525,11525,11525,11525,MONDO:0007647,"gastric volvulus, intrathoracic",MONDO,disease,DISEASE_11525
11526,11526,11526,11526,11526,11526,11526,11526,MONDO:0008165,southeast Asian ovalocytosis,MONDO,disease,DISEASE_11526
11527,11527,11527,11527,11527,11527,11527,11527,MONDO:0011669,hypotonia-cystinuria syndrome,MONDO,disease,DISEASE_11527
11528,11528,11528,11528,11528,11528,11528,11528,MONDO:0002871,testicular trophoblastic tumor,MONDO,disease,DISEASE_11528
11529,11529,11529,11529,11529,11529,11529,11529,MONDO:0700134,bovine neoplasm,MONDO,disease,DISEASE_11529
11530,11530,11530,11530,11530,11530,11530,11530,MONDO:0001064_MONDO:0002170,acute eustachian salpingitis,MONDO_grouped,disease,DISEASE_11530
11531,11531,11531,11531,11531,11531,11531,11531,MONDO:0009599,metaphyseal dysostosis-intellectual disability-conductive deafness syndrome,MONDO,disease,DISEASE_11531
11532,11532,11532,11532,11532,11532,11532,11532,MONDO:0016521,muscular pseudohypertrophy-hypothyroidism syndrome,MONDO,disease,DISEASE_11532
11533,11533,11533,11533,11533,11533,11533,11533,MONDO:0003775,lateral ventricle meningioma,MONDO,disease,DISEASE_11533
11534,11534,11534,11534,11534,11534,11534,11534,MONDO:0002798,childhood central nervous system primitive neuroectodermal neoplasm,MONDO,disease,DISEASE_11534
11535,11535,11535,11535,11535,11535,11535,11535,MONDO:0006181,digestive system carcinoma,MONDO,disease,DISEASE_11535
11536,11536,11536,11536,11536,11536,11536,11536,MONDO:0002594,monkeypox,MONDO,disease,DISEASE_11536
11537,11537,11537,11537,11537,11537,11537,11537,MONDO:0015239,abnormal origin of the pulmonary artery,MONDO,disease,DISEASE_11537
11538,11538,11538,11538,11538,11538,11538,11538,MONDO:0004890,partial central choroid dystrophy,MONDO,disease,DISEASE_11538
11539,11539,11539,11539,11539,11539,11539,11539,MONDO:0958161,B acute lymphoblastic leukemia with PAX5 P80R mutation,MONDO,disease,DISEASE_11539
11540,11540,11540,11540,11540,11540,11540,11540,MONDO:0006554,granuloma annulare,MONDO,disease,DISEASE_11540
11541,11541,11541,11541,11541,11541,11541,11541,MONDO:0015745,microcephaly-polymicrogyria-corpus callosum agenesis syndrome,MONDO,disease,DISEASE_11541
11542,11542,11542,11542,11542,11542,11542,11542,MONDO:0007379,Meesmann corneal dystrophy,MONDO,disease,DISEASE_11542
11543,11543,11543,11543,11543,11543,11543,11543,MONDO:0019885,distal trisomy 11q,MONDO,disease,DISEASE_11543
11544,11544,11544,11544,11544,11544,11544,11544,MONDO:0009993_MONDO:0859046_MONDO:0002579_MONDO:1010952,embryonal rhabdomyosarcoma,MONDO_grouped,disease,DISEASE_11544
11545,11545,11545,11545,11545,11545,11545,11545,MONDO:0022645,cardioencephalomyopathy,MONDO,disease,DISEASE_11545
11546,11546,11546,11546,11546,11546,11546,11546,MONDO:0021221,vestibulocochlear nerve neoplasm,MONDO,disease,DISEASE_11546
11547,11547,11547,11547,11547,11547,11547,11547,MONDO:0957583,neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities,MONDO,disease,DISEASE_11547
11548,11548,11548,11548,11548,11548,11548,11548,MONDO:0018877,retinitis punctata albescens,MONDO,disease,DISEASE_11548
11549,11549,11549,11549,11549,11549,11549,11549,MONDO:0007113,Angelman syndrome,MONDO,disease,DISEASE_11549
11550,11550,11550,11550,11550,11550,11550,11550,MONDO:0007036,Achard syndrome,MONDO,disease,DISEASE_11550
11551,11551,11551,11551,11551,11551,11551,11551,MONDO:0018968,iniencephaly,MONDO,disease,DISEASE_11551
11552,11552,11552,11552,11552,11552,11552,11552,MONDO:0022067,Cantu Sanchez-Corona Fragoso syndrome,MONDO,disease,DISEASE_11552
11553,11553,11553,11553,11553,11553,11553,11553,MONDO:8000014,familial antiphospholipid syndrome,MONDO,disease,DISEASE_11553
11554,11554,11554,11554,11554,11554,11554,11554,MONDO:0002337,intra-abdominal hemangioma,MONDO,disease,DISEASE_11554
11555,11555,11555,11555,11555,11555,11555,11555,MONDO:0025514,livedoid vasculopathy,MONDO,disease,DISEASE_11555
11556,11556,11556,11556,11556,11556,11556,11556,MONDO:0002455,exocervical carcinoma,MONDO,disease,DISEASE_11556
11557,11557,11557,11557,11557,11557,11557,11557,MONDO:1011924,"brachycephalic airway obstruction syndrome, non-human animal",MONDO,disease,DISEASE_11557
11558,11558,11558,11558,11558,11558,11558,11558,MONDO:0008776,"amyloidosis of gingiva and conjunctiva, with intellectual disability",MONDO,disease,DISEASE_11558
11559,11559,11559,11559,11559,11559,11559,11559,MONDO:0016890,partial deletion of the short arm of chromosome 8,MONDO,disease,DISEASE_11559
11560,11560,11560,11560,11560,11560,11560,11560,MONDO:0009202,Thakker-Donnai syndrome,MONDO,disease,DISEASE_11560
11561,11561,11561,11561,11561,11561,11561,11561,MONDO:0100322,non-Zellweger spectrum disorder,MONDO,disease,DISEASE_11561
11562,11562,11562,11562,11562,11562,11562,11562,MONDO:0005771,geographic tongue,MONDO,disease,DISEASE_11562
11563,11563,11563,11563,11563,11563,11563,11563,MONDO:0003321,hereditary Wilms tumor,MONDO,disease,DISEASE_11563
11564,11564,11564,11564,11564,11564,11564,11564,MONDO:0010040,"ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and intellectual disability",MONDO,disease,DISEASE_11564
11565,11565,11565,11565,11565,11565,11565,11565,MONDO:0003307,multiple mucosal neuroma,MONDO,disease,DISEASE_11565
11566,11566,11566,11566,11566,11566,11566,11566,MONDO:0015718,mosaic trisomy 12,MONDO,disease,DISEASE_11566
11567,11567,11567,11567,11567,11567,11567,11567,MONDO:0015237,arrhinia,MONDO,disease,DISEASE_11567
11568,11568,11568,11568,11568,11568,11568,11568,MONDO:0006377,pleural biphasic mesothelioma,MONDO,disease,DISEASE_11568
11569,11569,11569,11569,11569,11569,11569,11569,MONDO:0016312,5-fluorouracil poisoning,MONDO,disease,DISEASE_11569
11570,11570,11570,11570,11570,11570,11570,11570,MONDO:1012143,"multiple lipomatosis, cattle",MONDO,disease,DISEASE_11570
11571,11571,11571,11571,11571,11571,11571,11571,MONDO:0014789,CCDC115-CDG,MONDO,disease,DISEASE_11571
11572,11572,11572,11572,11572,11572,11572,11572,MONDO:0014268,combined immunodeficiency due to OX40 deficiency,MONDO,disease,DISEASE_11572
11573,11573,11573,11573,11573,11573,11573,11573,MONDO:0005651,arenavirus hemorrhagic fever,MONDO,disease,DISEASE_11573
11574,11574,11574,11574,11574,11574,11574,11574,MONDO:0021071,laryngeal neoplasm,MONDO,disease,DISEASE_11574
11575,11575,11575,11575,11575,11575,11575,11575,MONDO:0001540,bagassosis,MONDO,disease,DISEASE_11575
11576,11576,11576,11576,11576,11576,11576,11576,MONDO:0020421,coronary artery intramyocardial course,MONDO,disease,DISEASE_11576
11577,11577,11577,11577,11577,11577,11577,11577,MONDO:0003499,sarcomatoid squamous cell skin carcinoma,MONDO,disease,DISEASE_11577
11578,11578,11578,11578,11578,11578,11578,11578,MONDO:0011062,aprosencephaly cerebellar dysgenesis,MONDO,disease,DISEASE_11578
11579,11579,11579,11579,11579,11579,11579,11579,MONDO:0017989,His bundle tachycardia,MONDO,disease,DISEASE_11579
11580,11580,11580,11580,11580,11580,11580,11580,MONDO:0020845_MONDO:0012241_MONDO:0012238_MONDO:0014898_MONDO:0014899_MONDO:0012415_MONDO:0013117_MONDO:0009783_MONDO:0957993_MONDO:0014656_MONDO:0024528_MONDO:0000090,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive",MONDO_grouped,disease,DISEASE_11580
11581,11581,11581,11581,11581,11581,11581,11581,MONDO:0008648,"ventricular tachycardia, familial",MONDO,disease,DISEASE_11581
11582,11582,11582,11582,11582,11582,11582,11582,MONDO:0006799,hypothalamic neoplasm,MONDO,disease,DISEASE_11582
11583,11583,11583,11583,11583,11583,11583,11583,MONDO:0005432,alcohol and nicotine codependence,MONDO,disease,DISEASE_11583
11584,11584,11584,11584,11584,11584,11584,11584,MONDO:0007017,vitreous detachment,MONDO,disease,DISEASE_11584
11585,11585,11585,11585,11585,11585,11585,11585,MONDO:0005151,endocrine system disorder,MONDO,disease,DISEASE_11585
11586,11586,11586,11586,11586,11586,11586,11586,MONDO:0018773,autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome,MONDO,disease,DISEASE_11586
11587,11587,11587,11587,11587,11587,11587,11587,MONDO:1011513,"glaucoma, Japanese quail",MONDO,disease,DISEASE_11587
11588,11588,11588,11588,11588,11588,11588,11588,MONDO:0017094,cerebral cortical dysplasia,MONDO,disease,DISEASE_11588
11589,11589,11589,11589,11589,11589,11589,11589,MONDO:0010589,"Aarskog-Scott syndrome, X-linked",MONDO,disease,DISEASE_11589
11590,11590,11590,11590,11590,11590,11590,11590,MONDO:0015712,non-distal trisomy 10q,MONDO,disease,DISEASE_11590
11591,11591,11591,11591,11591,11591,11591,11591,MONDO:0017515_MONDO:0017516_MONDO:0017517_MONDO:0017518,"brachydactyly of fingers, unilateral",MONDO_grouped,disease,DISEASE_11591
11592,11592,11592,11592,11592,11592,11592,11592,MONDO:0859147,Marbach-Rustad progeroid syndrome,MONDO,disease,DISEASE_11592
11593,11593,11593,11593,11593,11593,11593,11593,MONDO:0004641,skin carcinoma in situ,MONDO,disease,DISEASE_11593
11594,11594,11594,11594,11594,11594,11594,11594,MONDO:0011717,hyperinsulinism-hyperammonemia syndrome,MONDO,disease,DISEASE_11594
11595,11595,11595,11595,11595,11595,11595,11595,MONDO:0003578,extragonadal nonseminomatous germ cell tumor,MONDO,disease,DISEASE_11595
11596,11596,11596,11596,11596,11596,11596,11596,MONDO:0005490,large artery stroke,MONDO,disease,DISEASE_11596
11597,11597,11597,11597,11597,11597,11597,11597,MONDO:0021454,benign neoplasm of eye,MONDO,disease,DISEASE_11597
11598,11598,11598,11598,11598,11598,11598,11598,MONDO:0003898,pediatric myxoid chondrosarcoma,MONDO,disease,DISEASE_11598
11599,11599,11599,11599,11599,11599,11599,11599,MONDO:0021042,glioma,MONDO,disease,DISEASE_11599
11600,11600,11600,11600,11600,11600,11600,11600,MONDO:0005859,mucocutaneous leishmaniasis,MONDO,disease,DISEASE_11600
11601,11601,11601,11601,11601,11601,11601,11601,MONDO:0018601,autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome,MONDO,disease,DISEASE_11601
11602,11602,11602,11602,11602,11602,11602,11602,MONDO:0002965,parovarian cyst,MONDO,disease,DISEASE_11602
11603,11603,11603,11603,11603,11603,11603,11603,MONDO:0007812,"ichthyosis, lamellar, autosomal dominant",MONDO,disease,DISEASE_11603
11604,11604,11604,11604,11604,11604,11604,11604,MONDO:0010214,xeroderma pigmentosum variant type,MONDO,disease,DISEASE_11604
11605,11605,11605,11605,11605,11605,11605,11605,MONDO:0007687,"graying of hair, precocious",MONDO,disease,DISEASE_11605
11606,11606,11606,11606,11606,11606,11606,11606,MONDO:0000050,isolated congenital growth hormone deficiency,MONDO,disease,DISEASE_11606
11607,11607,11607,11607,11607,11607,11607,11607,MONDO:0001183,contact lens corneal edema,MONDO,disease,DISEASE_11607
11608,11608,11608,11608,11608,11608,11608,11608,MONDO:0003595,sclerosing liposarcoma,MONDO,disease,DISEASE_11608
11609,11609,11609,11609,11609,11609,11609,11609,MONDO:0032574,"osteochondrodysplasia, brachydactyly, and overlapping malformed digits",MONDO,disease,DISEASE_11609
11610,11610,11610,11610,11610,11610,11610,11610,MONDO:0060556,"joint laxity, short stature, and myopia",MONDO,disease,DISEASE_11610
11611,11611,11611,11611,11611,11611,11611,11611,MONDO:0019174,obsolete infantile Refsum disease,MONDO,disease,DISEASE_11611
11612,11612,11612,11612,11612,11612,11612,11612,MONDO:0016864,Okihiro syndrome due to a point mutation,MONDO,disease,DISEASE_11612
11613,11613,11613,11613,11613,11613,11613,11613,MONDO:0016463,syndromic agammaglobulinemia,MONDO,disease,DISEASE_11613
11614,11614,11614,11614,11614,11614,11614,11614,MONDO:0014157,mandibular hypoplasia-deafness-progeroid syndrome,MONDO,disease,DISEASE_11614
11615,11615,11615,11615,11615,11615,11615,11615,MONDO:1012792,"hypotrichosis, KRT71-related, cattle",MONDO,disease,DISEASE_11615
11616,11616,11616,11616,11616,11616,11616,11616,MONDO:0009216,glycogen storage disease due to GLUT2 deficiency,MONDO,disease,DISEASE_11616
11617,11617,11617,11617,11617,11617,11617,11617,MONDO:0010654,Partington syndrome,MONDO,disease,DISEASE_11617
11618,11618,11618,11618,11618,11618,11618,11618,MONDO:0007049,"acroleukopathy, symmetric",MONDO,disease,DISEASE_11618
11619,11619,11619,11619,11619,11619,11619,11619,MONDO:0008713_MONDO:1010757_MONDO:1010758_MONDO:1010759,acrodermatitis enteropathica,MONDO_grouped,disease,DISEASE_11619
11620,11620,11620,11620,11620,11620,11620,11620,MONDO:0007187,nevoid basal cell carcinoma syndrome,MONDO,disease,DISEASE_11620
11621,11621,11621,11621,11621,11621,11621,11621,MONDO:0019159,Loeffler endocarditis,MONDO,disease,DISEASE_11621
11622,11622,11622,11622,11622,11622,11622,11622,MONDO:0022815,congenital absence of the sternocleidomastoid muscle,MONDO,disease,DISEASE_11622
11623,11623,11623,11623,11623,11623,11623,11623,MONDO:0011230,ossification of the posterior longitudinal ligament of the spine,MONDO,disease,DISEASE_11623
11624,11624,11624,11624,11624,11624,11624,11624,MONDO:0005384_MONDO:0001386_MONDO:0100574_MONDO:0006710_MONDO:0003290_MONDO:0006892_MONDO:0100035,focal epilepsy,MONDO_grouped,disease,DISEASE_11624
11625,11625,11625,11625,11625,11625,11625,11625,MONDO:0014035,severe intellectual disability-progressive spastic diplegia syndrome,MONDO,disease,DISEASE_11625
11626,11626,11626,11626,11626,11626,11626,11626,MONDO:0017609,renal tubular dysgenesis,MONDO,disease,DISEASE_11626
11627,11627,11627,11627,11627,11627,11627,11627,MONDO:0010634,"jaundice, familial obstructive, of infancy",MONDO,disease,DISEASE_11627
11628,11628,11628,11628,11628,11628,11628,11628,MONDO:0014494,"psoriasis 15, pustular, susceptibility to",MONDO,disease,DISEASE_11628
11629,11629,11629,11629,11629,11629,11629,11629,MONDO:0009992,"myoglobinuria, acute recurrent, autosomal recessive",MONDO,disease,DISEASE_11629
11630,11630,11630,11630,11630,11630,11630,11630,MONDO:0019203,acute interstitial pneumonia,MONDO,disease,DISEASE_11630
11631,11631,11631,11631,11631,11631,11631,11631,MONDO:0032597,"myasthenic syndrome, congenital, 24, presynaptic",MONDO,disease,DISEASE_11631
11632,11632,11632,11632,11632,11632,11632,11632,MONDO:0033621,"spinal muscular atrophy, infantile, James type",MONDO,disease,DISEASE_11632
11633,11633,11633,11633,11633,11633,11633,11633,MONDO:0004950_MONDO:0003834_MONDO:0006221_MONDO:0003972_MONDO:0000938_MONDO:0003592,gastric carcinoma,MONDO_grouped,disease,DISEASE_11633
11634,11634,11634,11634,11634,11634,11634,11634,MONDO:0006770,giant cell reparative granuloma,MONDO,disease,DISEASE_11634
11635,11635,11635,11635,11635,11635,11635,11635,MONDO:0008387,ring dermoid of cornea,MONDO,disease,DISEASE_11635
11636,11636,11636,11636,11636,11636,11636,11636,MONDO:0005336,myopathy,MONDO,disease,DISEASE_11636
11637,11637,11637,11637,11637,11637,11637,11637,MONDO:0700029,partial duplication of chromosome 13,MONDO,disease,DISEASE_11637
11638,11638,11638,11638,11638,11638,11638,11638,MONDO:0004529,non-ossifying fibromyxoid tumor,MONDO,disease,DISEASE_11638
11639,11639,11639,11639,11639,11639,11639,11639,MONDO:0015347,multicentric reticulohistiocytosis,MONDO,disease,DISEASE_11639
11640,11640,11640,11640,11640,11640,11640,11640,MONDO:0008623,Undritz anomaly,MONDO,disease,DISEASE_11640
11641,11641,11641,11641,11641,11641,11641,11641,MONDO:0004847,senile cataract,MONDO,disease,DISEASE_11641
11642,11642,11642,11642,11642,11642,11642,11642,MONDO:0022587,bone dysplasia corpus callosum agenesis,MONDO,disease,DISEASE_11642
11643,11643,11643,11643,11643,11643,11643,11643,MONDO:0004195,thymic dysplasia,MONDO,disease,DISEASE_11643
11644,11644,11644,11644,11644,11644,11644,11644,MONDO:0009453,immune deficiency disease,MONDO,disease,DISEASE_11644
11645,11645,11645,11645,11645,11645,11645,11645,MONDO:0020715,"multiple system atrophy 1, susceptibility to",MONDO,disease,DISEASE_11645
11646,11646,11646,11646,11646,11646,11646,11646,MONDO:0032579,warburg-cinotti syndrome,MONDO,disease,DISEASE_11646
11647,11647,11647,11647,11647,11647,11647,11647,MONDO:0001989,atrophic glossitis,MONDO,disease,DISEASE_11647
11648,11648,11648,11648,11648,11648,11648,11648,MONDO:0100089,GATA1-Related X-Linked Cytopenia,MONDO,disease,DISEASE_11648
11649,11649,11649,11649,11649,11649,11649,11649,MONDO:0008045,spinal muscular atrophy-progressive myoclonic epilepsy syndrome,MONDO,disease,DISEASE_11649
11650,11650,11650,11650,11650,11650,11650,11650,MONDO:0018445,global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome,MONDO,disease,DISEASE_11650
11651,11651,11651,11651,11651,11651,11651,11651,MONDO:0100551,AFG2B-related complex neurodevelopmental disorder with motor features and hearing loss,MONDO,disease,DISEASE_11651
11652,11652,11652,11652,11652,11652,11652,11652,MONDO:0008463,split-hand and split-foot with hypodontia,MONDO,disease,DISEASE_11652
11653,11653,11653,11653,11653,11653,11653,11653,MONDO:0023619,lentigo maligna melanoma,MONDO,disease,DISEASE_11653
11654,11654,11654,11654,11654,11654,11654,11654,MONDO:0016532,Lennox-Gastaut syndrome,MONDO,disease,DISEASE_11654
11655,11655,11655,11655,11655,11655,11655,11655,MONDO:0022756,chromosome 1q deletion,MONDO,disease,DISEASE_11655
11656,11656,11656,11656,11656,11656,11656,11656,MONDO:0003336,acute necrotizing encephalitis,MONDO,disease,DISEASE_11656
11657,11657,11657,11657,11657,11657,11657,11657,MONDO:0013664,"46,XY disorder of sex development due to testicular 17,20-desmolase deficiency",MONDO,disease,DISEASE_11657
11658,11658,11658,11658,11658,11658,11658,11658,MONDO:0021783,streptococcal sore throat,MONDO,disease,DISEASE_11658
11659,11659,11659,11659,11659,11659,11659,11659,MONDO:0023232,giant cell myocarditis,MONDO,disease,DISEASE_11659
11660,11660,11660,11660,11660,11660,11660,11660,MONDO:0015537,necrobiotic xanthogranuloma,MONDO,disease,DISEASE_11660
11661,11661,11661,11661,11661,11661,11661,11661,MONDO:0002142_MONDO:0002141,undifferentiated pleomorphic sarcoma,MONDO_grouped,disease,DISEASE_11661
11662,11662,11662,11662,11662,11662,11662,11662,MONDO:0000967,conventional lipoma,MONDO,disease,DISEASE_11662
11663,11663,11663,11663,11663,11663,11663,11663,MONDO:0014963,Shashi-Pena syndrome,MONDO,disease,DISEASE_11663
11664,11664,11664,11664,11664,11664,11664,11664,MONDO:0014300,proximal myopathy with extrapyramidal signs,MONDO,disease,DISEASE_11664
11665,11665,11665,11665,11665,11665,11665,11665,MONDO:0010558,choroideremia-deafness-obesity syndrome,MONDO,disease,DISEASE_11665
11666,11666,11666,11666,11666,11666,11666,11666,MONDO:0021915,arakawa syndrome 2,MONDO,disease,DISEASE_11666
11667,11667,11667,11667,11667,11667,11667,11667,MONDO:0017819,atypical dentin dysplasia due to SMOC2 deficiency,MONDO,disease,DISEASE_11667
11668,11668,11668,11668,11668,11668,11668,11668,MONDO:0002195,vulvar squamous neoplasm,MONDO,disease,DISEASE_11668
11669,11669,11669,11669,11669,11669,11669,11669,MONDO:0958191,"nephrolithiasis, calcium oxalate, 2, with or without nephrocalcinosis",MONDO,disease,DISEASE_11669
11670,11670,11670,11670,11670,11670,11670,11670,MONDO:0010852,chromosome 8Q12.1-q21.2 deletion syndrome,MONDO,disease,DISEASE_11670
11671,11671,11671,11671,11671,11671,11671,11671,MONDO:1011468_MONDO:1010509_MONDO:1010694_MONDO:1012010,"amyloidosis, domestic cat",MONDO_grouped,disease,DISEASE_11671
11672,11672,11672,11672,11672,11672,11672,11672,MONDO:1010634,"factor X deficiency, dog",MONDO,disease,DISEASE_11672
11673,11673,11673,11673,11673,11673,11673,11673,MONDO:0020298,Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15,MONDO,disease,DISEASE_11673
11674,11674,11674,11674,11674,11674,11674,11674,MONDO:0013360,"brachyolmia, Maroteaux type",MONDO,disease,DISEASE_11674
11675,11675,11675,11675,11675,11675,11675,11675,MONDO:0002728,rhabdoid tumor,MONDO,disease,DISEASE_11675
11676,11676,11676,11676,11676,11676,11676,11676,MONDO:0003725_MONDO:0006118,breast adenosis,MONDO_grouped,disease,DISEASE_11676
11677,11677,11677,11677,11677,11677,11677,11677,MONDO:0004368,sphenoorbital meningioma,MONDO,disease,DISEASE_11677
11678,11678,11678,11678,11678,11678,11678,11678,MONDO:0700007,idiopathic disease,MONDO,disease,DISEASE_11678
11679,11679,11679,11679,11679,11679,11679,11679,MONDO:0001559,perineocele,MONDO,disease,DISEASE_11679
11680,11680,11680,11680,11680,11680,11680,11680,MONDO:0004075,infiltrating lipoma,MONDO,disease,DISEASE_11680
11681,11681,11681,11681,11681,11681,11681,11681,MONDO:0007438,dentin dysplasia-sclerotic bones syndrome,MONDO,disease,DISEASE_11681
11682,11682,11682,11682,11682,11682,11682,11682,MONDO:0007319_MONDO:0010917_MONDO:0001314,chondrocalcinosis,MONDO_grouped,disease,DISEASE_11682
11683,11683,11683,11683,11683,11683,11683,11683,MONDO:0000351,disorder of methionine catabolism,MONDO,disease,DISEASE_11683
11684,11684,11684,11684,11684,11684,11684,11684,MONDO:0017320,phosphoenolpyruvate carboxykinase deficiency,MONDO,disease,DISEASE_11684
11685,11685,11685,11685,11685,11685,11685,11685,MONDO:0013775,thrombomodulin-related bleeding disorder,MONDO,disease,DISEASE_11685
11686,11686,11686,11686,11686,11686,11686,11686,MONDO:0015783_MONDO:0015784,Prader-Willi syndrome due to paternal deletion of 15q11q13,MONDO_grouped,disease,DISEASE_11686
11687,11687,11687,11687,11687,11687,11687,11687,MONDO:0005838,mansonelliasis,MONDO,disease,DISEASE_11687
11688,11688,11688,11688,11688,11688,11688,11688,MONDO:0022981,die Smulders droog van dijk syndrome,MONDO,disease,DISEASE_11688
11689,11689,11689,11689,11689,11689,11689,11689,MONDO:0017798,Spigelian hernia-cryptorchidism syndrome,MONDO,disease,DISEASE_11689
11690,11690,11690,11690,11690,11690,11690,11690,MONDO:0018394_MONDO:0018393_MONDO:0015746,male infertility with teratozoospermia due to single gene mutation,MONDO_grouped,disease,DISEASE_11690
11691,11691,11691,11691,11691,11691,11691,11691,MONDO:0011760,Scheie syndrome,MONDO,disease,DISEASE_11691
11692,11692,11692,11692,11692,11692,11692,11692,MONDO:0007314,"chemodectoma, intraabdominal, with cutaneous angiolipomas",MONDO,disease,DISEASE_11692
11693,11693,11693,11693,11693,11693,11693,11693,MONDO:0007353,coloboma of macula-brachydactyly type B syndrome,MONDO,disease,DISEASE_11693
11694,11694,11694,11694,11694,11694,11694,11694,MONDO:0006903,peroneal nerve paralysis,MONDO,disease,DISEASE_11694
11695,11695,11695,11695,11695,11695,11695,11695,MONDO:0009383,transient familial neonatal hyperbilirubinemia,MONDO,disease,DISEASE_11695
11696,11696,11696,11696,11696,11696,11696,11696,MONDO:0019911,maternal uniparental disomy of chromosome 4,MONDO,disease,DISEASE_11696
11697,11697,11697,11697,11697,11697,11697,11697,MONDO:0015695,combined immunodeficiency due to CRAC channel dysfunction,MONDO,disease,DISEASE_11697
11698,11698,11698,11698,11698,11698,11698,11698,MONDO:0009686,"musk, inability to smell",MONDO,disease,DISEASE_11698
11699,11699,11699,11699,11699,11699,11699,11699,MONDO:0044343,cervical disk degenerative disorder,MONDO,disease,DISEASE_11699
11700,11700,11700,11700,11700,11700,11700,11700,MONDO:0014072_MONDO:0013345_MONDO:0024554_MONDO:0010924,"D,L-2-hydroxyglutaric aciduria",MONDO_grouped,disease,DISEASE_11700
11701,11701,11701,11701,11701,11701,11701,11701,MONDO:0020742,"obsolete cataract, microcephaly, failure to thrive, kyphoscoliosis syndrome",MONDO,disease,DISEASE_11701
11702,11702,11702,11702,11702,11702,11702,11702,MONDO:0006419,small intestinal intraepithelial neoplasia,MONDO,disease,DISEASE_11702
11703,11703,11703,11703,11703,11703,11703,11703,MONDO:0023158,Fitz-Hugh-Curtis syndrome,MONDO,disease,DISEASE_11703
11704,11704,11704,11704,11704,11704,11704,11704,MONDO:0020351,Blake pouch cyst,MONDO,disease,DISEASE_11704
11705,11705,11705,11705,11705,11705,11705,11705,MONDO:0007190_MONDO:0013108_MONDO:0012318_MONDO:0012934_MONDO:0012935_MONDO:0012936_MONDO:0013109_MONDO:0100173,"leukemia, chronic lymphocytic, susceptibility to",MONDO_grouped,disease,DISEASE_11705
11706,11706,11706,11706,11706,11706,11706,11706,MONDO:0001775,chronic duodenal ileus,MONDO,disease,DISEASE_11706
11707,11707,11707,11707,11707,11707,11707,11707,MONDO:0024361,circadian rhythm sleep disorder,MONDO,disease,DISEASE_11707
11708,11708,11708,11708,11708,11708,11708,11708,MONDO:1010142,"pyoderma, non-human animal",MONDO,disease,DISEASE_11708
11709,11709,11709,11709,11709,11709,11709,11709,MONDO:0021441,benign neoplasm of exocrine pancreas,MONDO,disease,DISEASE_11709
11710,11710,11710,11710,11710,11710,11710,11710,MONDO:0018151,coenzyme Q10 deficiency,MONDO,disease,DISEASE_11710
11711,11711,11711,11711,11711,11711,11711,11711,MONDO:0006595,perinatal jaundice due to hepatocellular damage,MONDO,disease,DISEASE_11711
11712,11712,11712,11712,11712,11712,11712,11712,MONDO:0008638,varicose disease,MONDO,disease,DISEASE_11712
11713,11713,11713,11713,11713,11713,11713,11713,MONDO:1012811,"hypertrophic cardiomyopathy, MYH7-related, rabbit",MONDO,disease,DISEASE_11713
11714,11714,11714,11714,11714,11714,11714,11714,MONDO:0021515,benign neoplasm of ethmoidal sinus,MONDO,disease,DISEASE_11714
11715,11715,11715,11715,11715,11715,11715,11715,MONDO:0958350,conus spinal cord lipoma,MONDO,disease,DISEASE_11715
11716,11716,11716,11716,11716,11716,11716,11716,MONDO:1011948,"navicular disease, non-human animal",MONDO,disease,DISEASE_11716
11717,11717,11717,11717,11717,11717,11717,11717,MONDO:0007623,flushing of ears and somnolence,MONDO,disease,DISEASE_11717
11718,11718,11718,11718,11718,11718,11718,11718,MONDO:0000371,oral cavity carcinoma in situ,MONDO,disease,DISEASE_11718
11719,11719,11719,11719,11719,11719,11719,11719,MONDO:0021258,choroid neoplasm,MONDO,disease,DISEASE_11719
11720,11720,11720,11720,11720,11720,11720,11720,MONDO:0016901,partial deletion of the long arm of chromosome 2,MONDO,disease,DISEASE_11720
11721,11721,11721,11721,11721,11721,11721,11721,MONDO:0022504,arthrogryposis spinal muscular atrophy,MONDO,disease,DISEASE_11721
11722,11722,11722,11722,11722,11722,11722,11722,MONDO:0004055_MONDO:0004923,acute inflammation of lacrimal passage,MONDO_grouped,disease,DISEASE_11722
11723,11723,11723,11723,11723,11723,11723,11723,MONDO:0009543,prominent glabella-microcephaly-hypogenitalism syndrome,MONDO,disease,DISEASE_11723
11724,11724,11724,11724,11724,11724,11724,11724,MONDO:0002475,lacrimal gland adenocarcinoma,MONDO,disease,DISEASE_11724
11725,11725,11725,11725,11725,11725,11725,11725,MONDO:0002718,central nervous system teratoma,MONDO,disease,DISEASE_11725
11726,11726,11726,11726,11726,11726,11726,11726,MONDO:0036918,punctate acrokeratoderma freckle-like pigmentation,MONDO,disease,DISEASE_11726
11727,11727,11727,11727,11727,11727,11727,11727,MONDO:0016205,IRVAN syndrome,MONDO,disease,DISEASE_11727
11728,11728,11728,11728,11728,11728,11728,11728,MONDO:1012330_MONDO:1012331,"laminitis, horse",MONDO_grouped,disease,DISEASE_11728
11729,11729,11729,11729,11729,11729,11729,11729,MONDO:0021075,neoplastic polyp,MONDO,disease,DISEASE_11729
11730,11730,11730,11730,11730,11730,11730,11730,MONDO:0019770,X-linked dominant intellectual disability-epilepsy syndrome,MONDO,disease,DISEASE_11730
11731,11731,11731,11731,11731,11731,11731,11731,MONDO:0008275,familial expansile osteolysis,MONDO,disease,DISEASE_11731
11732,11732,11732,11732,11732,11732,11732,11732,MONDO:1010059,"thyroiditis, non-human animal",MONDO,disease,DISEASE_11732
11733,11733,11733,11733,11733,11733,11733,11733,MONDO:0850812,dendritic cell deficiency,MONDO,disease,DISEASE_11733
11734,11734,11734,11734,11734,11734,11734,11734,MONDO:0700022,chromosome 15 disorder,MONDO,disease,DISEASE_11734
11735,11735,11735,11735,11735,11735,11735,11735,MONDO:0010223,"ichthyosis, X-linked, without steroid sulfatase deficiency",MONDO,disease,DISEASE_11735
11736,11736,11736,11736,11736,11736,11736,11736,MONDO:0012712,dystonia with cerebellar atrophy,MONDO,disease,DISEASE_11736
11737,11737,11737,11737,11737,11737,11737,11737,MONDO:0019489,diffuse palmoplantar keratoderma - acrocyanosis syndrome,MONDO,disease,DISEASE_11737
11738,11738,11738,11738,11738,11738,11738,11738,MONDO:0004109,epiglottis neoplasm,MONDO,disease,DISEASE_11738
11739,11739,11739,11739,11739,11739,11739,11739,MONDO:0022821,congenital benign spinal muscular atrophy dominant,MONDO,disease,DISEASE_11739
11740,11740,11740,11740,11740,11740,11740,11740,MONDO:0014480_MONDO:0013120_MONDO:0020712_MONDO:0100250_MONDO:0007938_MONDO:0010226_MONDO:8000015_MONDO:0060489_MONDO:0010218_MONDO:0013410_MONDO:0014634_MONDO:0009301_MONDO:0030049_MONDO:0010442_MONDO:0013066,"46,XY sex reversal",MONDO_grouped,disease,DISEASE_11740
11741,11741,11741,11741,11741,11741,11741,11741,MONDO:0001148,iliac vein thrombophlebitis,MONDO,disease,DISEASE_11741
11742,11742,11742,11742,11742,11742,11742,11742,MONDO:0022778,cleft lip palate intellectual disability corneal opacity,MONDO,disease,DISEASE_11742
11743,11743,11743,11743,11743,11743,11743,11743,MONDO:0005496_MONDO:0003193_MONDO:0006108_MONDO:0002862,bile duct carcinoma,MONDO_grouped,disease,DISEASE_11743
11744,11744,11744,11744,11744,11744,11744,11744,MONDO:1012460_MONDO:1012461_MONDO:1012462_MONDO:1012463_MONDO:1012464,"hemangiosarcoma, domestic cat",MONDO_grouped,disease,DISEASE_11744
11745,11745,11745,11745,11745,11745,11745,11745,MONDO:0019650,idiopathic steroid-sensitive nephrotic syndrome with minimal change,MONDO,disease,DISEASE_11745
11746,11746,11746,11746,11746,11746,11746,11746,MONDO:1010618,"microcephaly, sheep",MONDO,disease,DISEASE_11746
11747,11747,11747,11747,11747,11747,11747,11747,MONDO:0958077,collagen 6-related congenital muscular dystrophy,MONDO,disease,DISEASE_11747
11748,11748,11748,11748,11748,11748,11748,11748,MONDO:0020457,6-phosphogluconate dehydrogenase deficiency,MONDO,disease,DISEASE_11748
11749,11749,11749,11749,11749,11749,11749,11749,MONDO:0012502,normophosphatemic familial tumoral calcinosis,MONDO,disease,DISEASE_11749
11750,11750,11750,11750,11750,11750,11750,11750,MONDO:0024715,benign synovial neoplasm,MONDO,disease,DISEASE_11750
11751,11751,11751,11751,11751,11751,11751,11751,MONDO:0002034,cecum lymphoma,MONDO,disease,DISEASE_11751
11752,11752,11752,11752,11752,11752,11752,11752,MONDO:0700211,"Erysipelothrix infectious disease, non-human animal",MONDO,disease,DISEASE_11752
11753,11753,11753,11753,11753,11753,11753,11753,MONDO:0003545,intradural extramedullary spinal canal neoplasm,MONDO,disease,DISEASE_11753
11754,11754,11754,11754,11754,11754,11754,11754,MONDO:0008910,carboxypeptidase N deficiency,MONDO,disease,DISEASE_11754
11755,11755,11755,11755,11755,11755,11755,11755,MONDO:1010211,"mycosis fungoides, non-human animal",MONDO,disease,DISEASE_11755
11756,11756,11756,11756,11756,11756,11756,11756,MONDO:0018843,embryonal carcinoma of the central nervous system,MONDO,disease,DISEASE_11756
11757,11757,11757,11757,11757,11757,11757,11757,MONDO:0017189,adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia,MONDO,disease,DISEASE_11757
11758,11758,11758,11758,11758,11758,11758,11758,MONDO:0016703,anaplastic oligoastrocytoma,MONDO,disease,DISEASE_11758
11759,11759,11759,11759,11759,11759,11759,11759,MONDO:0006169_MONDO:0006410,complex endometrial hyperplasia,MONDO_grouped,disease,DISEASE_11759
11760,11760,11760,11760,11760,11760,11760,11760,MONDO:0021331,carcinoma of parotid gland,MONDO,disease,DISEASE_11760
11761,11761,11761,11761,11761,11761,11761,11761,MONDO:0044984,nasolacrimal duct disorder,MONDO,disease,DISEASE_11761
11762,11762,11762,11762,11762,11762,11762,11762,MONDO:0800387,sulfur mustard poisoning,MONDO,disease,DISEASE_11762
11763,11763,11763,11763,11763,11763,11763,11763,MONDO:0956988,EZB-MYC- diffuse large B-cell lymphoma,MONDO,disease,DISEASE_11763
11764,11764,11764,11764,11764,11764,11764,11764,MONDO:0957467,primary genito-urinary tuberculosis,MONDO,disease,DISEASE_11764
11765,11765,11765,11765,11765,11765,11765,11765,MONDO:0045052,benign osteogenic neoplasm,MONDO,disease,DISEASE_11765
11766,11766,11766,11766,11766,11766,11766,11766,MONDO:0009938,pulmonic stenosis,MONDO,disease,DISEASE_11766
11767,11767,11767,11767,11767,11767,11767,11767,MONDO:1010131,encapsulating peritoneal sclerosis,MONDO,disease,DISEASE_11767
11768,11768,11768,11768,11768,11768,11768,11768,MONDO:0018248,intellectual disability-seizures-macrocephaly-obesity syndrome,MONDO,disease,DISEASE_11768
11769,11769,11769,11769,11769,11769,11769,11769,MONDO:0012500_MONDO:0013739_MONDO:0019557,chilblain lupus,MONDO_grouped,disease,DISEASE_11769
11770,11770,11770,11770,11770,11770,11770,11770,MONDO:0002383,Pacinian tumor,MONDO,disease,DISEASE_11770
11771,11771,11771,11771,11771,11771,11771,11771,MONDO:0015062,"gastric neuroendocrine tumor, well differentiated, low or intermediate grade",MONDO,disease,DISEASE_11771
11772,11772,11772,11772,11772,11772,11772,11772,MONDO:0033672,Duane anomaly-myopathy-scoliosis syndrome,MONDO,disease,DISEASE_11772
11773,11773,11773,11773,11773,11773,11773,11773,MONDO:0007997,microspherophakia with hernia,MONDO,disease,DISEASE_11773
11774,11774,11774,11774,11774,11774,11774,11774,MONDO:0022865,corneal dystrophy ichthyosis microcephaly intellectual disability,MONDO,disease,DISEASE_11774
11775,11775,11775,11775,11775,11775,11775,11775,MONDO:0022909,cutis laxa osteoporosis,MONDO,disease,DISEASE_11775
11776,11776,11776,11776,11776,11776,11776,11776,MONDO:0700171_MONDO:0700196,horse melanoma,MONDO_grouped,disease,DISEASE_11776
11777,11777,11777,11777,11777,11777,11777,11777,MONDO:0001403,labium majus cancer,MONDO,disease,DISEASE_11777
11778,11778,11778,11778,11778,11778,11778,11778,MONDO:0016352,obsolete idiopathic inherited hypercalciuria,MONDO,disease,DISEASE_11778
11779,11779,11779,11779,11779,11779,11779,11779,MONDO:0035423,triglyceride deposit cardiomyovasculopathy,MONDO,disease,DISEASE_11779
11780,11780,11780,11780,11780,11780,11780,11780,MONDO:0032864_MONDO:0032672_MONDO:0859197_MONDO:0032851,"intellectual developmental disorder with speech delay, autism, and dysmorphic facies",MONDO_grouped,disease,DISEASE_11780
11781,11781,11781,11781,11781,11781,11781,11781,MONDO:0019653,familial idiopathic steroid-resistant nephrotic syndrome with minimal changes,MONDO,disease,DISEASE_11781
11782,11782,11782,11782,11782,11782,11782,11782,MONDO:0008786,pyridoxine-responsive sideroblastic anemia,MONDO,disease,DISEASE_11782
11783,11783,11783,11783,11783,11783,11783,11783,MONDO:0030293_MONDO:0025712_MONDO:0023660_MONDO:0030298_MONDO:0025713_MONDO:0012526_MONDO:0015053_MONDO:0015054,"angioedema, hereditary",MONDO_grouped,disease,DISEASE_11783
11784,11784,11784,11784,11784,11784,11784,11784,MONDO:0007942,Mammastatin,MONDO,disease,DISEASE_11784
11785,11785,11785,11785,11785,11785,11785,11785,MONDO:0014227,hypopigmentation-punctate palmoplantar keratoderma syndrome,MONDO,disease,DISEASE_11785
11786,11786,11786,11786,11786,11786,11786,11786,MONDO:0036595,ovarian Sertoli-Leydig cell tumor,MONDO,disease,DISEASE_11786
11787,11787,11787,11787,11787,11787,11787,11787,MONDO:0016198,qualitative or quantitative defects of plectin,MONDO,disease,DISEASE_11787
11788,11788,11788,11788,11788,11788,11788,11788,MONDO:0006235,granular cell tumor,MONDO,disease,DISEASE_11788
11789,11789,11789,11789,11789,11789,11789,11789,MONDO:0017588,nail tumor,MONDO,disease,DISEASE_11789
11790,11790,11790,11790,11790,11790,11790,11790,MONDO:0007545,Eosinophilopenia,MONDO,disease,DISEASE_11790
11791,11791,11791,11791,11791,11791,11791,11791,MONDO:0012145,"macular degeneration, age-related, 3",MONDO,disease,DISEASE_11791
11792,11792,11792,11792,11792,11792,11792,11792,MONDO:0007377_MONDO:0011855_MONDO:0001490,granular corneal dystrophy,MONDO_grouped,disease,DISEASE_11792
11793,11793,11793,11793,11793,11793,11793,11793,MONDO:0007213,Ballard syndrome,MONDO,disease,DISEASE_11793
11794,11794,11794,11794,11794,11794,11794,11794,MONDO:0009059,cysteine Peptiduria,MONDO,disease,DISEASE_11794
11795,11795,11795,11795,11795,11795,11795,11795,MONDO:0005121,Enterococcus faecalis infection,MONDO,disease,DISEASE_11795
11796,11796,11796,11796,11796,11796,11796,11796,MONDO:0021582,lentigo,MONDO,disease,DISEASE_11796
11797,11797,11797,11797,11797,11797,11797,11797,MONDO:0858940,infant-type hemispheric glioma,MONDO,disease,DISEASE_11797
11798,11798,11798,11798,11798,11798,11798,11798,MONDO:0017362,neuralgic amyotrophy,MONDO,disease,DISEASE_11798
11799,11799,11799,11799,11799,11799,11799,11799,MONDO:1011681,"ACTH-independent adrenal Cushing syndrome, non-human animal",MONDO,disease,DISEASE_11799
11800,11800,11800,11800,11800,11800,11800,11800,MONDO:0006593,pelvic lipomatosis,MONDO,disease,DISEASE_11800
11801,11801,11801,11801,11801,11801,11801,11801,MONDO:0002153,telogen effluvium,MONDO,disease,DISEASE_11801
11802,11802,11802,11802,11802,11802,11802,11802,MONDO:0006005,Venezuelan equine encephalitis,MONDO,disease,DISEASE_11802
11803,11803,11803,11803,11803,11803,11803,11803,MONDO:0006418,small intestinal enteropathy-associated T-cell lymphoma,MONDO,disease,DISEASE_11803
11804,11804,11804,11804,11804,11804,11804,11804,MONDO:0013584,hereditary sensory neuropathy-deafness-dementia syndrome,MONDO,disease,DISEASE_11804
11805,11805,11805,11805,11805,11805,11805,11805,MONDO:0017881,Kyasanur forest disease,MONDO,disease,DISEASE_11805
11806,11806,11806,11806,11806,11806,11806,11806,MONDO:1010061,"hyperaldosteronism, non-human animal",MONDO,disease,DISEASE_11806
11807,11807,11807,11807,11807,11807,11807,11807,MONDO:0035220,PLG-related hereditary angioedema with normal C1inh,MONDO,disease,DISEASE_11807
11808,11808,11808,11808,11808,11808,11808,11808,MONDO:0010084,"sucrosuria, hiatus hernia and intellectual disability",MONDO,disease,DISEASE_11808
11809,11809,11809,11809,11809,11809,11809,11809,MONDO:0021297,carcinoma in situ of nasopharynx,MONDO,disease,DISEASE_11809
11810,11810,11810,11810,11810,11810,11810,11810,MONDO:0002995,"small intestine neuroendocrine tumor, well differentiated, low or intermediate grade",MONDO,disease,DISEASE_11810
11811,11811,11811,11811,11811,11811,11811,11811,MONDO:0011652,Phelan-McDermid syndrome,MONDO,disease,DISEASE_11811
11812,11812,11812,11812,11812,11812,11812,11812,MONDO:0006105,benign conjunctival neoplasm,MONDO,disease,DISEASE_11812
11813,11813,11813,11813,11813,11813,11813,11813,MONDO:0008182,nasopalpebral lipoma-coloboma syndrome,MONDO,disease,DISEASE_11813
11814,11814,11814,11814,11814,11814,11814,11814,MONDO:0014085_MONDO:0009360,"hydrocephalus, nonsyndromic, autosomal recessive",MONDO_grouped,disease,DISEASE_11814
11815,11815,11815,11815,11815,11815,11815,11815,MONDO:0017706,disorder of carbohydrate transmembrane transport and absorption,MONDO,disease,DISEASE_11815
11816,11816,11816,11816,11816,11816,11816,11816,MONDO:0005886,oral candidiasis,MONDO,disease,DISEASE_11816
11817,11817,11817,11817,11817,11817,11817,11817,MONDO:0700201,"tick-borne infectious disease, non-human animal",MONDO,disease,DISEASE_11817
11818,11818,11818,11818,11818,11818,11818,11818,MONDO:0002924,smooth muscle cancer,MONDO,disease,DISEASE_11818
11819,11819,11819,11819,11819,11819,11819,11819,MONDO:0009650_MONDO:0009653_MONDO:0019248,mucolipidosis,MONDO_grouped,disease,DISEASE_11819
11820,11820,11820,11820,11820,11820,11820,11820,MONDO:0008584,torus palatinus and torus mandibularis,MONDO,disease,DISEASE_11820
11821,11821,11821,11821,11821,11821,11821,11821,MONDO:0006718_MONDO:0005976,cutaneous syphilis,MONDO_grouped,disease,DISEASE_11821
11822,11822,11822,11822,11822,11822,11822,11822,MONDO:0043254,papular urticaria,MONDO,disease,DISEASE_11822
11823,11823,11823,11823,11823,11823,11823,11823,MONDO:0007953,Binder syndrome,MONDO,disease,DISEASE_11823
11824,11824,11824,11824,11824,11824,11824,11824,MONDO:0002963,acantholytic acanthoma,MONDO,disease,DISEASE_11824
11825,11825,11825,11825,11825,11825,11825,11825,MONDO:0007732,Holt-Oram syndrome,MONDO,disease,DISEASE_11825
11826,11826,11826,11826,11826,11826,11826,11826,MONDO:0009069,"congenital lactic acidosis, Saguenay-Lac-Saint-Jean type",MONDO,disease,DISEASE_11826
11827,11827,11827,11827,11827,11827,11827,11827,MONDO:0015049,solitary necrotic nodule of the liver,MONDO,disease,DISEASE_11827
11828,11828,11828,11828,11828,11828,11828,11828,MONDO:0006610,skin atrophy,MONDO,disease,DISEASE_11828
11829,11829,11829,11829,11829,11829,11829,11829,MONDO:1012447,"gyrate atrophy of choroid and retina, domestic cat",MONDO,disease,DISEASE_11829
11830,11830,11830,11830,11830,11830,11830,11830,MONDO:0014637,DOCK2 deficiency,MONDO,disease,DISEASE_11830
11831,11831,11831,11831,11831,11831,11831,11831,MONDO:0020671,obsolete susceptibility to ischemic stroke,MONDO,disease,DISEASE_11831
11832,11832,11832,11832,11832,11832,11832,11832,MONDO:0033543_MONDO:0012490,"cone-rod synaptic disorder syndrome, congenital nonprogressive",MONDO_grouped,disease,DISEASE_11832
11833,11833,11833,11833,11833,11833,11833,11833,MONDO:0971173_MONDO:0060457_MONDO:0957204,autoinflammation with arthritis and vasculitis,MONDO_grouped,disease,DISEASE_11833
11834,11834,11834,11834,11834,11834,11834,11834,MONDO:0007058,Acropectorovertebral dysplasia,MONDO,disease,DISEASE_11834
11835,11835,11835,11835,11835,11835,11835,11835,MONDO:1010045,"diprosopus, non-human animal",MONDO,disease,DISEASE_11835
11836,11836,11836,11836,11836,11836,11836,11836,MONDO:0018735,multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome,MONDO,disease,DISEASE_11836
11837,11837,11837,11837,11837,11837,11837,11837,MONDO:0009595,cartilage-hair hypoplasia,MONDO,disease,DISEASE_11837
11838,11838,11838,11838,11838,11838,11838,11838,MONDO:0019930_MONDO:0019931,Leydig cell hypoplasia due to complete LH resistance,MONDO_grouped,disease,DISEASE_11838
11839,11839,11839,11839,11839,11839,11839,11839,MONDO:0018361,neonatal scleroderma,MONDO,disease,DISEASE_11839
11840,11840,11840,11840,11840,11840,11840,11840,MONDO:0800494,variable-age onset combined generalized and focal epilepsy syndrome,MONDO,disease,DISEASE_11840
11841,11841,11841,11841,11841,11841,11841,11841,MONDO:0005105_MONDO:0004141,melanoma,MONDO_grouped,disease,DISEASE_11841
11842,11842,11842,11842,11842,11842,11842,11842,MONDO:0012396,exercise-induced hyperinsulinism,MONDO,disease,DISEASE_11842
11843,11843,11843,11843,11843,11843,11843,11843,MONDO:0005301,multiple sclerosis,MONDO,disease,DISEASE_11843
11844,11844,11844,11844,11844,11844,11844,11844,MONDO:0009303_MONDO:0003136,anti-glomerular basement membrane disease,MONDO_grouped,disease,DISEASE_11844
11845,11845,11845,11845,11845,11845,11845,11845,MONDO:0023554,acquired testicular failure,MONDO,disease,DISEASE_11845
11846,11846,11846,11846,11846,11846,11846,11846,MONDO:1010166,"galactosialidosis, non-human animal",MONDO,disease,DISEASE_11846
11847,11847,11847,11847,11847,11847,11847,11847,MONDO:0013194,Pseudopili annulati,MONDO,disease,DISEASE_11847
11848,11848,11848,11848,11848,11848,11848,11848,MONDO:0958076,myeloschisis,MONDO,disease,DISEASE_11848
11849,11849,11849,11849,11849,11849,11849,11849,MONDO:0016835,14q11.2 microduplication syndrome,MONDO,disease,DISEASE_11849
11850,11850,11850,11850,11850,11850,11850,11850,MONDO:0044141_MONDO:0044144,panic disorder without agoraphobia,MONDO_grouped,disease,DISEASE_11850
11851,11851,11851,11851,11851,11851,11851,11851,MONDO:0007374,Schnyder corneal dystrophy,MONDO,disease,DISEASE_11851
11852,11852,11852,11852,11852,11852,11852,11852,MONDO:0017840,"classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form",MONDO,disease,DISEASE_11852
11853,11853,11853,11853,11853,11853,11853,11853,MONDO:0017064,thoracolumbosacral spina bifida aperta,MONDO,disease,DISEASE_11853
11854,11854,11854,11854,11854,11854,11854,11854,MONDO:1012095_MONDO:1012096_MONDO:1012097_MONDO:1012100,"hemolytic anemia, dog",MONDO_grouped,disease,DISEASE_11854
11855,11855,11855,11855,11855,11855,11855,11855,MONDO:0021764,acrofacial dysostosis Preis type,MONDO,disease,DISEASE_11855
11856,11856,11856,11856,11856,11856,11856,11856,MONDO:0016919,partial deletion of the long arm of chromosome 21,MONDO,disease,DISEASE_11856
11857,11857,11857,11857,11857,11857,11857,11857,MONDO:0009068,obsolete cytochrome-c oxidase deficiency disease,MONDO,disease,DISEASE_11857
11858,11858,11858,11858,11858,11858,11858,11858,MONDO:0019986,sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy,MONDO,disease,DISEASE_11858
11859,11859,11859,11859,11859,11859,11859,11859,MONDO:0957795,arrhythmogenic cardiomyopathy with variable ectodermal abnormalities,MONDO,disease,DISEASE_11859
11860,11860,11860,11860,11860,11860,11860,11860,MONDO:0021531,fibroma of lung,MONDO,disease,DISEASE_11860
11861,11861,11861,11861,11861,11861,11861,11861,MONDO:0010580,immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome,MONDO,disease,DISEASE_11861
11862,11862,11862,11862,11862,11862,11862,11862,MONDO:0850426,high-grade B-cell lymphoma double-hit/triple-hit,MONDO,disease,DISEASE_11862
11863,11863,11863,11863,11863,11863,11863,11863,MONDO:0017351_MONDO:0800156_MONDO:0800157,inborn disorder of lysine and hydroxylysine metabolism,MONDO_grouped,disease,DISEASE_11863
11864,11864,11864,11864,11864,11864,11864,11864,MONDO:0001745,subserous uterine fibroid,MONDO,disease,DISEASE_11864
11865,11865,11865,11865,11865,11865,11865,11865,MONDO:0006496,palsy,MONDO,disease,DISEASE_11865
11866,11866,11866,11866,11866,11866,11866,11866,MONDO:0002419,transient tic disorder,MONDO,disease,DISEASE_11866
11867,11867,11867,11867,11867,11867,11867,11867,MONDO:0958110,atrophic papulosis,MONDO,disease,DISEASE_11867
11868,11868,11868,11868,11868,11868,11868,11868,MONDO:0001890,pulp erosion,MONDO,disease,DISEASE_11868
11869,11869,11869,11869,11869,11869,11869,11869,MONDO:0011433,"anemia, congenital hypoplastic, with multiple congenital anomalies/intellectual disability syndrome",MONDO,disease,DISEASE_11869
11870,11870,11870,11870,11870,11870,11870,11870,MONDO:0023607,Laurence-Prosser-Rocker syndrome,MONDO,disease,DISEASE_11870
11871,11871,11871,11871,11871,11871,11871,11871,MONDO:1012717,"early-onset retinal dystrophy, Bengal, domestic cat",MONDO,disease,DISEASE_11871
11872,11872,11872,11872,11872,11872,11872,11872,MONDO:0010147,"tongue, pigmented fungiform papillae of",MONDO,disease,DISEASE_11872
11873,11873,11873,11873,11873,11873,11873,11873,MONDO:0008221,prolidase deficiency,MONDO,disease,DISEASE_11873
11874,11874,11874,11874,11874,11874,11874,11874,MONDO:0006605_MONDO:0006556_MONDO:0006569,scalp dermatosis,MONDO_grouped,disease,DISEASE_11874
11875,11875,11875,11875,11875,11875,11875,11875,MONDO:0026771,"developmental and epileptic encephalopathy, 85, with or without midline brain defects",MONDO,disease,DISEASE_11875
11876,11876,11876,11876,11876,11876,11876,11876,MONDO:0006152_MONDO:0006153,colon inflammatory polyp,MONDO_grouped,disease,DISEASE_11876
11877,11877,11877,11877,11877,11877,11877,11877,MONDO:0013111,acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins,MONDO,disease,DISEASE_11877
11878,11878,11878,11878,11878,11878,11878,11878,MONDO:0025062,"encephalomyelitis, enzootic porcine",MONDO,disease,DISEASE_11878
11879,11879,11879,11879,11879,11879,11879,11879,MONDO:0009828,palant cleft palate syndrome,MONDO,disease,DISEASE_11879
11880,11880,11880,11880,11880,11880,11880,11880,MONDO:0032884,"ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies",MONDO,disease,DISEASE_11880
11881,11881,11881,11881,11881,11881,11881,11881,MONDO:0007426,"deafness, unilateral",MONDO,disease,DISEASE_11881
11882,11882,11882,11882,11882,11882,11882,11882,MONDO:0043125,mcpherson robertson cammarano syndrome,MONDO,disease,DISEASE_11882
11883,11883,11883,11883,11883,11883,11883,11883,MONDO:0007406,"cryofibrinogenemia, familial primary",MONDO,disease,DISEASE_11883
11884,11884,11884,11884,11884,11884,11884,11884,MONDO:0006643,alcoholic cardiomyopathy,MONDO,disease,DISEASE_11884
11885,11885,11885,11885,11885,11885,11885,11885,MONDO:0003097,childhood mediastinal neurogenic neoplasm,MONDO,disease,DISEASE_11885
11886,11886,11886,11886,11886,11886,11886,11886,MONDO:0600024_MONDO:0700335_MONDO:0024573_MONDO:0016340_MONDO:0016333_MONDO:0005217,familial idiopathic inflammatory myopathy,MONDO_grouped,disease,DISEASE_11886
11887,11887,11887,11887,11887,11887,11887,11887,MONDO:0100428_MONDO:0008890,progressive bulbar palsy of childhood,MONDO_grouped,disease,DISEASE_11887
11888,11888,11888,11888,11888,11888,11888,11888,MONDO:0044877,paraneoplastic cerebellar degeneration,MONDO,disease,DISEASE_11888
11889,11889,11889,11889,11889,11889,11889,11889,MONDO:0019109,CANOMAD syndrome,MONDO,disease,DISEASE_11889
11890,11890,11890,11890,11890,11890,11890,11890,MONDO:1011890,"leukoencephalomyelopathy, non-human animal",MONDO,disease,DISEASE_11890
11891,11891,11891,11891,11891,11891,11891,11891,MONDO:0800136,non-severe combined immunodeficiency due to COPG1 deficiency,MONDO,disease,DISEASE_11891
11892,11892,11892,11892,11892,11892,11892,11892,MONDO:0000645,fallopian tube benign neoplasm,MONDO,disease,DISEASE_11892
11893,11893,11893,11893,11893,11893,11893,11893,MONDO:0005959,sick building syndrome,MONDO,disease,DISEASE_11893
11894,11894,11894,11894,11894,11894,11894,11894,MONDO:0007295,self-limited epilepsy with centrotemporal spikes,MONDO,disease,DISEASE_11894
11895,11895,11895,11895,11895,11895,11895,11895,MONDO:0014765,"wooly hair, autosomal recessive 3",MONDO,disease,DISEASE_11895
11896,11896,11896,11896,11896,11896,11896,11896,MONDO:0016670,sickle cell-hemoglobin d disease syndrome,MONDO,disease,DISEASE_11896
11897,11897,11897,11897,11897,11897,11897,11897,MONDO:1012377,"nasal parakeratosis, dog",MONDO,disease,DISEASE_11897
11898,11898,11898,11898,11898,11898,11898,11898,MONDO:0020863,laryngeal diphtheria,MONDO,disease,DISEASE_11898
11899,11899,11899,11899,11899,11899,11899,11899,MONDO:0013769_MONDO:0013747_MONDO:0859565,atrioventricular septal defect,MONDO_grouped,disease,DISEASE_11899
11900,11900,11900,11900,11900,11900,11900,11900,MONDO:0018156,3q26q27 microdeletion syndrome,MONDO,disease,DISEASE_11900
11901,11901,11901,11901,11901,11901,11901,11901,MONDO:8000000,infectious discitis,MONDO,disease,DISEASE_11901
11902,11902,11902,11902,11902,11902,11902,11902,MONDO:0024228,miliaria profunda,MONDO,disease,DISEASE_11902
11903,11903,11903,11903,11903,11903,11903,11903,MONDO:0005355_MONDO:0006716,coronary restenosis,MONDO_grouped,disease,DISEASE_11903
11904,11904,11904,11904,11904,11904,11904,11904,MONDO:0016981,infantile spams-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome,MONDO,disease,DISEASE_11904
11905,11905,11905,11905,11905,11905,11905,11905,MONDO:0100573,combined generalized and focal epilepsy,MONDO,disease,DISEASE_11905
11906,11906,11906,11906,11906,11906,11906,11906,MONDO:0017391,Grayson-Wilbrandt corneal dystrophy,MONDO,disease,DISEASE_11906
11907,11907,11907,11907,11907,11907,11907,11907,MONDO:0018552,urachal sinus,MONDO,disease,DISEASE_11907
11908,11908,11908,11908,11908,11908,11908,11908,MONDO:0100326_MONDO:0031332_MONDO:0031009,Glanzmann thrombasthenia,MONDO_grouped,disease,DISEASE_11908
11909,11909,11909,11909,11909,11909,11909,11909,MONDO:0024412,Peptostreptococcus infectious disease,MONDO,disease,DISEASE_11909
11910,11910,11910,11910,11910,11910,11910,11910,MONDO:1012419,"episodic falling, dog",MONDO,disease,DISEASE_11910
11911,11911,11911,11911,11911,11911,11911,11911,MONDO:0002705,breast mucinous cystadenocarcinoma,MONDO,disease,DISEASE_11911
11912,11912,11912,11912,11912,11912,11912,11912,MONDO:0100095,"neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures",MONDO,disease,DISEASE_11912
11913,11913,11913,11913,11913,11913,11913,11913,MONDO:0011132,"T-cell immunodeficiency, congenital alopecia, and nail dystrophy",MONDO,disease,DISEASE_11913
11914,11914,11914,11914,11914,11914,11914,11914,MONDO:0006997,tibial neuropathy,MONDO,disease,DISEASE_11914
11915,11915,11915,11915,11915,11915,11915,11915,MONDO:0008017,hereditary mucoepithelial dysplasia,MONDO,disease,DISEASE_11915
11916,11916,11916,11916,11916,11916,11916,11916,MONDO:0850087,primary hypomagnesemia-generalized seizures-intellectual disability-obesity syndrome,MONDO,disease,DISEASE_11916
11917,11917,11917,11917,11917,11917,11917,11917,MONDO:1010262_MONDO:1011908,"polycystic kidney disease, non-human animal",MONDO_grouped,disease,DISEASE_11917
11918,11918,11918,11918,11918,11918,11918,11918,MONDO:1010681,"AA amyloidosis, northern tree shrew",MONDO,disease,DISEASE_11918
11919,11919,11919,11919,11919,11919,11919,11919,MONDO:0012282,Al-Gazali syndrome,MONDO,disease,DISEASE_11919
11920,11920,11920,11920,11920,11920,11920,11920,MONDO:0000756,parameningeal embryonal rhabdomyosarcoma,MONDO,disease,DISEASE_11920
11921,11921,11921,11921,11921,11921,11921,11921,MONDO:0859614,"diffuse low-grade glioma, MAPK pathway–altered",MONDO,disease,DISEASE_11921
11922,11922,11922,11922,11922,11922,11922,11922,MONDO:0026724,Paganini-Miozzo syndrome,MONDO,disease,DISEASE_11922
11923,11923,11923,11923,11923,11923,11923,11923,MONDO:0003778,inborn error of immunity,MONDO,disease,DISEASE_11923
11924,11924,11924,11924,11924,11924,11924,11924,MONDO:0009538,"lymphoid system deterioration, progressive",MONDO,disease,DISEASE_11924
11925,11925,11925,11925,11925,11925,11925,11925,MONDO:0001259,pituitary gland infarction,MONDO,disease,DISEASE_11925
11926,11926,11926,11926,11926,11926,11926,11926,MONDO:0014342,female infertility due to zona pellucida defect,MONDO,disease,DISEASE_11926
11927,11927,11927,11927,11927,11927,11927,11927,MONDO:0019654,familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis,MONDO,disease,DISEASE_11927
11928,11928,11928,11928,11928,11928,11928,11928,MONDO:1012964,"Charcot-Marie-Tooth disease, non-human animal",MONDO,disease,DISEASE_11928
11929,11929,11929,11929,11929,11929,11929,11929,MONDO:1012360,"neuronal vacuolar disorder, dog",MONDO,disease,DISEASE_11929
11930,11930,11930,11930,11930,11930,11930,11930,MONDO:0957787,Fliedner-Zweier syndrome,MONDO,disease,DISEASE_11930
11931,11931,11931,11931,11931,11931,11931,11931,MONDO:1011962,"vitamin D-deficiency rickets, non-type I, non-type II, non-human animal",MONDO,disease,DISEASE_11931
11932,11932,11932,11932,11932,11932,11932,11932,MONDO:1012353,"hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome, horse",MONDO,disease,DISEASE_11932
11933,11933,11933,11933,11933,11933,11933,11933,MONDO:0023609,le Marec-Bracq-Picaud syndrome,MONDO,disease,DISEASE_11933
11934,11934,11934,11934,11934,11934,11934,11934,MONDO:0859306,developmental delay with variable intellectual disability and dysmorphic facies,MONDO,disease,DISEASE_11934
11935,11935,11935,11935,11935,11935,11935,11935,MONDO:0010853,"Helicobacter pylori infection, susceptibility to",MONDO,disease,DISEASE_11935
11936,11936,11936,11936,11936,11936,11936,11936,MONDO:0021440,benign neoplasm of skin,MONDO,disease,DISEASE_11936
11937,11937,11937,11937,11937,11937,11937,11937,MONDO:0021316,malignant tumor of minor salivary gland,MONDO,disease,DISEASE_11937
11938,11938,11938,11938,11938,11938,11938,11938,MONDO:0006360,penile carcinoma,MONDO,disease,DISEASE_11938
11939,11939,11939,11939,11939,11939,11939,11939,MONDO:1011126,"priapism, domestic cat",MONDO,disease,DISEASE_11939
11940,11940,11940,11940,11940,11940,11940,11940,MONDO:0021722,vulvodynia,MONDO,disease,DISEASE_11940
11941,11941,11941,11941,11941,11941,11941,11941,MONDO:0013680,cognitive impairment with or without cerebellar ataxia,MONDO,disease,DISEASE_11941
11942,11942,11942,11942,11942,11942,11942,11942,MONDO:0009104,Donnai-Barrow syndrome,MONDO,disease,DISEASE_11942
11943,11943,11943,11943,11943,11943,11943,11943,MONDO:0859518,"leukodystrophy, hypomyelinating, 26, with chondrodysplasia",MONDO,disease,DISEASE_11943
11944,11944,11944,11944,11944,11944,11944,11944,MONDO:0017379,polyneuropathy-intellectual disability-acromicria-premature menopause syndrome,MONDO,disease,DISEASE_11944
11945,11945,11945,11945,11945,11945,11945,11945,MONDO:0007166,ataxia with fasciculations,MONDO,disease,DISEASE_11945
11946,11946,11946,11946,11946,11946,11946,11946,MONDO:0010920,microtia,MONDO,disease,DISEASE_11946
11947,11947,11947,11947,11947,11947,11947,11947,MONDO:0009508,Lambotte syndrome,MONDO,disease,DISEASE_11947
11948,11948,11948,11948,11948,11948,11948,11948,MONDO:0043243,leukoplakia,MONDO,disease,DISEASE_11948
11949,11949,11949,11949,11949,11949,11949,11949,MONDO:0010048,spastic paraplegia with myoclonic epilepsy,MONDO,disease,DISEASE_11949
11950,11950,11950,11950,11950,11950,11950,11950,MONDO:0010545,Nance-Horan syndrome,MONDO,disease,DISEASE_11950
11951,11951,11951,11951,11951,11951,11951,11951,MONDO:0002262,capillary lymphangioma,MONDO,disease,DISEASE_11951
11952,11952,11952,11952,11952,11952,11952,11952,MONDO:0008094,familial multiple nevi flammei,MONDO,disease,DISEASE_11952
11953,11953,11953,11953,11953,11953,11953,11953,MONDO:0001343,impaired renal function disease,MONDO,disease,DISEASE_11953
11954,11954,11954,11954,11954,11954,11954,11954,MONDO:0009943,Pyle disease,MONDO,disease,DISEASE_11954
11955,11955,11955,11955,11955,11955,11955,11955,MONDO:0014448,"hyperthyroxinemia, familial dysalbuminemic",MONDO,disease,DISEASE_11955
11956,11956,11956,11956,11956,11956,11956,11956,MONDO:0021069,malignant endocrine neoplasm,MONDO,disease,DISEASE_11956
11957,11957,11957,11957,11957,11957,11957,11957,MONDO:0001422,primary aldosteronism,MONDO,disease,DISEASE_11957
11958,11958,11958,11958,11958,11958,11958,11958,MONDO:0007359,commissural lip pits,MONDO,disease,DISEASE_11958
11959,11959,11959,11959,11959,11959,11959,11959,MONDO:0018429,14q24.1q24.3 microdeletion syndrome,MONDO,disease,DISEASE_11959
11960,11960,11960,11960,11960,11960,11960,11960,MONDO:0008376,retinal venous beading,MONDO,disease,DISEASE_11960
11961,11961,11961,11961,11961,11961,11961,11961,MONDO:0004535,childhood choriocarcinoma of the ovary,MONDO,disease,DISEASE_11961
11962,11962,11962,11962,11962,11962,11962,11962,MONDO:0044725,combined immunodeficiency due to GINS1 deficiency,MONDO,disease,DISEASE_11962
11963,11963,11963,11963,11963,11963,11963,11963,MONDO:0008400,salivary duct calculi,MONDO,disease,DISEASE_11963
11964,11964,11964,11964,11964,11964,11964,11964,MONDO:0019241,inborn disorder of the gamma-glutamyl cycle,MONDO,disease,DISEASE_11964
11965,11965,11965,11965,11965,11965,11965,11965,MONDO:0100432,FNIP1-associated syndrome,MONDO,disease,DISEASE_11965
11966,11966,11966,11966,11966,11966,11966,11966,MONDO:0013561,"chondrodysplasia with joint dislocations, gPAPP type",MONDO,disease,DISEASE_11966
11967,11967,11967,11967,11967,11967,11967,11967,MONDO:0021233,ear neoplasm,MONDO,disease,DISEASE_11967
11968,11968,11968,11968,11968,11968,11968,11968,MONDO:0012084,aromatic L-amino acid decarboxylase deficiency,MONDO,disease,DISEASE_11968
11969,11969,11969,11969,11969,11969,11969,11969,MONDO:0005315,bone fracture,MONDO,disease,DISEASE_11969
11970,11970,11970,11970,11970,11970,11970,11970,MONDO:0008522,"synovial chondromatosis, familial, with dwarfism",MONDO,disease,DISEASE_11970
11971,11971,11971,11971,11971,11971,11971,11971,MONDO:0017184,autosomal dominant hyperinsulinism due to SUR1 deficiency,MONDO,disease,DISEASE_11971
11972,11972,11972,11972,11972,11972,11972,11972,MONDO:0009691_MONDO:0015821_MONDO:0045071,mycosis fungoides,MONDO_grouped,disease,DISEASE_11972
11973,11973,11973,11973,11973,11973,11973,11973,MONDO:0008969,cholesterol pneumonia,MONDO,disease,DISEASE_11973
11974,11974,11974,11974,11974,11974,11974,11974,MONDO:0958227,polydactyly-macrocephaly syndrome,MONDO,disease,DISEASE_11974
11975,11975,11975,11975,11975,11975,11975,11975,MONDO:0021111,ureter neoplasm,MONDO,disease,DISEASE_11975
11976,11976,11976,11976,11976,11976,11976,11976,MONDO:0009152_MONDO:0007514,"ectopia lentis 2, isolated, autosomal recessive",MONDO_grouped,disease,DISEASE_11976
11977,11977,11977,11977,11977,11977,11977,11977,MONDO:1010958,"ameloblastoma, dog",MONDO,disease,DISEASE_11977
11978,11978,11978,11978,11978,11978,11978,11978,MONDO:0012204,familial pseudohyperkalemia,MONDO,disease,DISEASE_11978
11979,11979,11979,11979,11979,11979,11979,11979,MONDO:0009520,3-hydroxy-3-methylglutaric aciduria,MONDO,disease,DISEASE_11979
11980,11980,11980,11980,11980,11980,11980,11980,MONDO:0100166,PPP2R1A-related intellectual disability,MONDO,disease,DISEASE_11980
11981,11981,11981,11981,11981,11981,11981,11981,MONDO:0004596,cor pulmonale,MONDO,disease,DISEASE_11981
11982,11982,11982,11982,11982,11982,11982,11982,MONDO:0859198,"short stature, impaired intellectual development, microcephaly, hypotonia, and ocular anomalies",MONDO,disease,DISEASE_11982
11983,11983,11983,11983,11983,11983,11983,11983,MONDO:1010766,"vitiligo, domestic cat",MONDO,disease,DISEASE_11983
11984,11984,11984,11984,11984,11984,11984,11984,MONDO:0012313_MONDO:0012312_MONDO:0012314_MONDO:0859368_MONDO:0000453,short QT syndrome,MONDO_grouped,disease,DISEASE_11984
11985,11985,11985,11985,11985,11985,11985,11985,MONDO:0008847,atrichia with papular lesions,MONDO,disease,DISEASE_11985
11986,11986,11986,11986,11986,11986,11986,11986,MONDO:0017802,ovarian fibrothecoma,MONDO,disease,DISEASE_11986
11987,11987,11987,11987,11987,11987,11987,11987,MONDO:0956964,medulloblastoma SHH activated and TP53 mutant,MONDO,disease,DISEASE_11987
11988,11988,11988,11988,11988,11988,11988,11988,MONDO:1010050,"congenital adrenal hyperplasia, non-human animal",MONDO,disease,DISEASE_11988
11989,11989,11989,11989,11989,11989,11989,11989,MONDO:0022410,retinal ciliopathy,MONDO,disease,DISEASE_11989
11990,11990,11990,11990,11990,11990,11990,11990,MONDO:0004731,central sleep apnea syndrome,MONDO,disease,DISEASE_11990
11991,11991,11991,11991,11991,11991,11991,11991,MONDO:0019326,phakomatosis cesiomarmorata,MONDO,disease,DISEASE_11991
11992,11992,11992,11992,11992,11992,11992,11992,MONDO:1011099,"alkaptonuria, rabbit",MONDO,disease,DISEASE_11992
11993,11993,11993,11993,11993,11993,11993,11993,MONDO:0018582,GCGR-related hyperglucagonemia,MONDO,disease,DISEASE_11993
11994,11994,11994,11994,11994,11994,11994,11994,MONDO:0021462,benign neoplasm of rectum,MONDO,disease,DISEASE_11994
11995,11995,11995,11995,11995,11995,11995,11995,MONDO:0020974,laryngeal granuloma,MONDO,disease,DISEASE_11995
11996,11996,11996,11996,11996,11996,11996,11996,MONDO:0005327,hip fracture,MONDO,disease,DISEASE_11996
11997,11997,11997,11997,11997,11997,11997,11997,MONDO:0010004,EEC syndrome,MONDO,disease,DISEASE_11997
11998,11998,11998,11998,11998,11998,11998,11998,MONDO:0003342,benign perivascular tumor,MONDO,disease,DISEASE_11998
11999,11999,11999,11999,11999,11999,11999,11999,MONDO:0019100,neuromyelitis optica,MONDO,disease,DISEASE_11999
12000,12000,12000,12000,12000,12000,12000,12000,MONDO:1010245,"hyperekplexia, non-human animal",MONDO,disease,DISEASE_12000
12001,12001,12001,12001,12001,12001,12001,12001,MONDO:1011338,"nutritional disorder, non-human animal",MONDO,disease,DISEASE_12001
12002,12002,12002,12002,12002,12002,12002,12002,MONDO:0007880,congenital laryngeal web,MONDO,disease,DISEASE_12002
12003,12003,12003,12003,12003,12003,12003,12003,MONDO:0018047,familial thrombomodulin anomalies,MONDO,disease,DISEASE_12003
12004,12004,12004,12004,12004,12004,12004,12004,MONDO:0002189,nodular hidradenoma,MONDO,disease,DISEASE_12004
12005,12005,12005,12005,12005,12005,12005,12005,MONDO:0004914,celiac artery stenosis from compression by median arcuate ligament of diaphragm,MONDO,disease,DISEASE_12005
12006,12006,12006,12006,12006,12006,12006,12006,MONDO:0012725,lipoprotein glomerulopathy,MONDO,disease,DISEASE_12006
12007,12007,12007,12007,12007,12007,12007,12007,MONDO:0044916,extrarenal rhabdoid tumor,MONDO,disease,DISEASE_12007
12008,12008,12008,12008,12008,12008,12008,12008,MONDO:0010087,Sugarman brachydactyly,MONDO,disease,DISEASE_12008
12009,12009,12009,12009,12009,12009,12009,12009,MONDO:0001911,tracheal calcification,MONDO,disease,DISEASE_12009
12010,12010,12010,12010,12010,12010,12010,12010,MONDO:0021429,squamous cell carcinoma of floor of mouth,MONDO,disease,DISEASE_12010
12011,12011,12011,12011,12011,12011,12011,12011,MONDO:0957815,developmental delay with or without epilepsy,MONDO,disease,DISEASE_12011
12012,12012,12012,12012,12012,12012,12012,12012,MONDO:0005714_MONDO:0000333_MONDO:0005821,congenital syphilis,MONDO_grouped,disease,DISEASE_12012
12013,12013,12013,12013,12013,12013,12013,12013,MONDO:0859220,Ferguson-Bonni neurodevelopmental syndrome,MONDO,disease,DISEASE_12013
12014,12014,12014,12014,12014,12014,12014,12014,MONDO:0027655,allopurinol toxicity,MONDO,disease,DISEASE_12014
12015,12015,12015,12015,12015,12015,12015,12015,MONDO:0004525,scabies,MONDO,disease,DISEASE_12015
12016,12016,12016,12016,12016,12016,12016,12016,MONDO:1011511,"glaucoma, domestic cat",MONDO,disease,DISEASE_12016
12017,12017,12017,12017,12017,12017,12017,12017,MONDO:0800144,autoimmune pulmonary disease due to PD-1 deficiency,MONDO,disease,DISEASE_12017
12018,12018,12018,12018,12018,12018,12018,12018,MONDO:0044641,9q33.3q34.11 microdeletion syndrome,MONDO,disease,DISEASE_12018
12019,12019,12019,12019,12019,12019,12019,12019,MONDO:0021378,neoplasm of endocardium,MONDO,disease,DISEASE_12019
12020,12020,12020,12020,12020,12020,12020,12020,MONDO:0003845,corpus callosum lipoma,MONDO,disease,DISEASE_12020
12021,12021,12021,12021,12021,12021,12021,12021,MONDO:0030849,intellectual developmental disorder with speech delay and axonal peripheral neuropathy,MONDO,disease,DISEASE_12021
12022,12022,12022,12022,12022,12022,12022,12022,MONDO:0010526,Fabry disease,MONDO,disease,DISEASE_12022
12023,12023,12023,12023,12023,12023,12023,12023,MONDO:0000200,Zimmermann-Laband syndrome,MONDO,disease,DISEASE_12023
12024,12024,12024,12024,12024,12024,12024,12024,MONDO:1040053_MONDO:1040052_MONDO:0800400,PROM1-related dominant retinopathy,MONDO_grouped,disease,DISEASE_12024
12025,12025,12025,12025,12025,12025,12025,12025,MONDO:0032658,"macrocephaly, acquired, with impaired intellectual development",MONDO,disease,DISEASE_12025
12026,12026,12026,12026,12026,12026,12026,12026,MONDO:1010709_MONDO:1010712,"trimethylaminuria (fishy taint), mallard",MONDO_grouped,disease,DISEASE_12026
12027,12027,12027,12027,12027,12027,12027,12027,MONDO:0009272,German syndrome,MONDO,disease,DISEASE_12027
12028,12028,12028,12028,12028,12028,12028,12028,MONDO:0002459_MONDO:0007004_MONDO:0025512,type IV hypersensitivity disease,MONDO_grouped,disease,DISEASE_12028
12029,12029,12029,12029,12029,12029,12029,12029,MONDO:0007569,"erythema nodosum, familial",MONDO,disease,DISEASE_12029
12030,12030,12030,12030,12030,12030,12030,12030,MONDO:0015029,reticular perineurioma,MONDO,disease,DISEASE_12030
12031,12031,12031,12031,12031,12031,12031,12031,MONDO:1010029,"aleutian mink disease, human",MONDO,disease,DISEASE_12031
12032,12032,12032,12032,12032,12032,12032,12032,MONDO:0018600,congenital abducens nerve palsy,MONDO,disease,DISEASE_12032
12033,12033,12033,12033,12033,12033,12033,12033,MONDO:0016062,median cleft lip/mandibule,MONDO,disease,DISEASE_12033
12034,12034,12034,12034,12034,12034,12034,12034,MONDO:0020360_MONDO:0020361,complete cryptophthalmia,MONDO_grouped,disease,DISEASE_12034
12035,12035,12035,12035,12035,12035,12035,12035,MONDO:0010780,mitochondrial myopathy with reversible cytochrome C oxidase deficiency,MONDO,disease,DISEASE_12035
12036,12036,12036,12036,12036,12036,12036,12036,MONDO:0001062,pyloric antrum cancer,MONDO,disease,DISEASE_12036
12037,12037,12037,12037,12037,12037,12037,12037,MONDO:0006696,cervix erosion,MONDO,disease,DISEASE_12037
12038,12038,12038,12038,12038,12038,12038,12038,MONDO:0008945,myoclonic cerebellar dyssynergia,MONDO,disease,DISEASE_12038
12039,12039,12039,12039,12039,12039,12039,12039,MONDO:0016586,systemic mastocytosis,MONDO,disease,DISEASE_12039
12040,12040,12040,12040,12040,12040,12040,12040,MONDO:0021164,posthitis,MONDO,disease,DISEASE_12040
12041,12041,12041,12041,12041,12041,12041,12041,MONDO:0003402,testicular yolk sac tumor,MONDO,disease,DISEASE_12041
12042,12042,12042,12042,12042,12042,12042,12042,MONDO:0016008,fetal hydantoin syndrome,MONDO,disease,DISEASE_12042
12043,12043,12043,12043,12043,12043,12043,12043,MONDO:0035782_MONDO:0035783,"non-syndromic anorectal malformation with rectourethral fistula, bulbar type",MONDO_grouped,disease,DISEASE_12043
12044,12044,12044,12044,12044,12044,12044,12044,MONDO:1011344,"perinatal disease, non-human animal",MONDO,disease,DISEASE_12044
12045,12045,12045,12045,12045,12045,12045,12045,MONDO:0700177,feline mammary carcinoma,MONDO,disease,DISEASE_12045
12046,12046,12046,12046,12046,12046,12046,12046,MONDO:1010717,"glycogen storage disease, AGL-related, dog",MONDO,disease,DISEASE_12046
12047,12047,12047,12047,12047,12047,12047,12047,MONDO:0019029,segmental odontomaxillary dysplasia,MONDO,disease,DISEASE_12047
12048,12048,12048,12048,12048,12048,12048,12048,MONDO:0044720,cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome,MONDO,disease,DISEASE_12048
12049,12049,12049,12049,12049,12049,12049,12049,MONDO:0010546,"central incisors, absence of",MONDO,disease,DISEASE_12049
12050,12050,12050,12050,12050,12050,12050,12050,MONDO:0003633_MONDO:0003691_MONDO:0003692,malignant mesenchymoma,MONDO_grouped,disease,DISEASE_12050
12051,12051,12051,12051,12051,12051,12051,12051,MONDO:1011797,"myopathy of the diaphragmatic muscles, non-human animal",MONDO,disease,DISEASE_12051
12052,12052,12052,12052,12052,12052,12052,12052,MONDO:0009185,amelocerebrohypohidrotic syndrome,MONDO,disease,DISEASE_12052
12053,12053,12053,12053,12053,12053,12053,12053,MONDO:0020423,stenosis or atrophy of the coronary ostium,MONDO,disease,DISEASE_12053
12054,12054,12054,12054,12054,12054,12054,12054,MONDO:0032832_MONDO:0030988_MONDO:0957810,"intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies",MONDO_grouped,disease,DISEASE_12054
12055,12055,12055,12055,12055,12055,12055,12055,MONDO:0003480_MONDO:0004216,pineal region dysgerminoma,MONDO_grouped,disease,DISEASE_12055
12056,12056,12056,12056,12056,12056,12056,12056,MONDO:0009901_MONDO:0859154,Bartsocas-Papas syndrome,MONDO_grouped,disease,DISEASE_12056
12057,12057,12057,12057,12057,12057,12057,12057,MONDO:0018065,isolated trigonocephaly,MONDO,disease,DISEASE_12057
12058,12058,12058,12058,12058,12058,12058,12058,MONDO:0005917_MONDO:0002178,placenta disorder,MONDO_grouped,disease,DISEASE_12058
12059,12059,12059,12059,12059,12059,12059,12059,MONDO:0958263,isolated micronodular adrenocortical disease,MONDO,disease,DISEASE_12059
12060,12060,12060,12060,12060,12060,12060,12060,MONDO:0100211_MONDO:0100219,"growth hormone insensitivity with immune dysregulation 1, autosomal recessive",MONDO_grouped,disease,DISEASE_12060
12061,12061,12061,12061,12061,12061,12061,12061,MONDO:1012913,"amyotrophic lateral sclerosis, SOD1-related, pig",MONDO,disease,DISEASE_12061
12062,12062,12062,12062,12062,12062,12062,12062,MONDO:0800478,trigeminal trophic syndrome,MONDO,disease,DISEASE_12062
12063,12063,12063,12063,12063,12063,12063,12063,MONDO:0019022,sensorineural hearing loss-early graying-essential tremor syndrome,MONDO,disease,DISEASE_12063
12064,12064,12064,12064,12064,12064,12064,12064,MONDO:0001766,eversion of lacrimal punctum,MONDO,disease,DISEASE_12064
12065,12065,12065,12065,12065,12065,12065,12065,MONDO:1010424,"autism spectrum disorder, zebra finch",MONDO,disease,DISEASE_12065
12066,12066,12066,12066,12066,12066,12066,12066,MONDO:0008490_MONDO:0008474_MONDO:0010072,"otospondylomegaepiphyseal dysplasia, autosomal dominant",MONDO_grouped,disease,DISEASE_12066
12067,12067,12067,12067,12067,12067,12067,12067,MONDO:0042717,Saul-Wilkes-Stevenson syndrome,MONDO,disease,DISEASE_12067
12068,12068,12068,12068,12068,12068,12068,12068,MONDO:0019559,hypertrophic or verrucous lupus erythematosus,MONDO,disease,DISEASE_12068
12069,12069,12069,12069,12069,12069,12069,12069,MONDO:0014952,intellectual disability-epilepsy-extrapyramidal syndrome,MONDO,disease,DISEASE_12069
12070,12070,12070,12070,12070,12070,12070,12070,MONDO:0021856,Alsing syndrome,MONDO,disease,DISEASE_12070
12071,12071,12071,12071,12071,12071,12071,12071,MONDO:0031400,Tessadori-Van-Haaften neurodevelopmental syndrome,MONDO,disease,DISEASE_12071
12072,12072,12072,12072,12072,12072,12072,12072,MONDO:0011830_MONDO:0012703,lissencephaly due to LIS1 mutation,MONDO_grouped,disease,DISEASE_12072
12073,12073,12073,12073,12073,12073,12073,12073,MONDO:0034143,early-onset calcifying leukoencephalopathy-skeletal dysplasia,MONDO,disease,DISEASE_12073
12074,12074,12074,12074,12074,12074,12074,12074,MONDO:0021260,sensory ganglionopathy,MONDO,disease,DISEASE_12074
12075,12075,12075,12075,12075,12075,12075,12075,MONDO:1012496,"Dahlem dwarfism, rabbit",MONDO,disease,DISEASE_12075
12076,12076,12076,12076,12076,12076,12076,12076,MONDO:0010011,schizencephaly,MONDO,disease,DISEASE_12076
12077,12077,12077,12077,12077,12077,12077,12077,MONDO:1030003,Mycoplasmoides infection,MONDO,disease,DISEASE_12077
12078,12078,12078,12078,12078,12078,12078,12078,MONDO:0957534_MONDO:0013491,"megalencephalic leukoencephalopathy with subcortical cysts 4, remitting",MONDO_grouped,disease,DISEASE_12078
12079,12079,12079,12079,12079,12079,12079,12079,MONDO:0016867,partial deletion of chromosome 2,MONDO,disease,DISEASE_12079
12080,12080,12080,12080,12080,12080,12080,12080,MONDO:0100571,CTNNB1-related neurodevelopmental disorder and/or vitreoretinopathy,MONDO,disease,DISEASE_12080
12081,12081,12081,12081,12081,12081,12081,12081,MONDO:0019045,obsolete rare sleep disorder,MONDO,disease,DISEASE_12081
12082,12082,12082,12082,12082,12082,12082,12082,MONDO:0958005,Hoxha-Aliu syndrome,MONDO,disease,DISEASE_12082
12083,12083,12083,12083,12083,12083,12083,12083,MONDO:0002042,mechanical ectropion,MONDO,disease,DISEASE_12083
12084,12084,12084,12084,12084,12084,12084,12084,MONDO:0100023_MONDO:0100024_MONDO:0100208,self-limited familial neonatal epilepsy,MONDO_grouped,disease,DISEASE_12084
12085,12085,12085,12085,12085,12085,12085,12085,MONDO:0030966,neurofacioskeletal syndrome with or without renal agenesis,MONDO,disease,DISEASE_12085
12086,12086,12086,12086,12086,12086,12086,12086,MONDO:0008219,pemphigus vulgaris,MONDO,disease,DISEASE_12086
12087,12087,12087,12087,12087,12087,12087,12087,MONDO:1010908,"muscular dystrophy, American mink",MONDO,disease,DISEASE_12087
12088,12088,12088,12088,12088,12088,12088,12088,MONDO:1011430,"neuronal ceroid lipofuscinosis, non-human animal",MONDO,disease,DISEASE_12088
12089,12089,12089,12089,12089,12089,12089,12089,MONDO:0022875,cortada Koussef Matsumoto syndrome,MONDO,disease,DISEASE_12089
12090,12090,12090,12090,12090,12090,12090,12090,MONDO:0012397,"brachydactyly, coloboma, and anterior segment dysgenesis",MONDO,disease,DISEASE_12090
12091,12091,12091,12091,12091,12091,12091,12091,MONDO:0003751,childhood germ cell tumor,MONDO,disease,DISEASE_12091
12092,12092,12092,12092,12092,12092,12092,12092,MONDO:1010577_MONDO:1010574_MONDO:1010576,"diabetes mellitus, pig",MONDO_grouped,disease,DISEASE_12092
12093,12093,12093,12093,12093,12093,12093,12093,MONDO:1012578,"achromatopsia, non-human animal",MONDO,disease,DISEASE_12093
12094,12094,12094,12094,12094,12094,12094,12094,MONDO:0007302,cervical hypertrichosis with underlying kyphoscoliosis,MONDO,disease,DISEASE_12094
12095,12095,12095,12095,12095,12095,12095,12095,MONDO:0012164,Meacham syndrome,MONDO,disease,DISEASE_12095
12096,12096,12096,12096,12096,12096,12096,12096,MONDO:1011801,"type 2 polysaccharide storage myopathy, non-human animal",MONDO,disease,DISEASE_12096
12097,12097,12097,12097,12097,12097,12097,12097,MONDO:0016887,partial deletion of the short arm of chromosome 5,MONDO,disease,DISEASE_12097
12098,12098,12098,12098,12098,12098,12098,12098,MONDO:0016934,partial duplication of chromosome 16,MONDO,disease,DISEASE_12098
12099,12099,12099,12099,12099,12099,12099,12099,MONDO:0044302,"congenital heart defects, dysmorphic facial features, and intellectual developmental disorder",MONDO,disease,DISEASE_12099
12100,12100,12100,12100,12100,12100,12100,12100,MONDO:0003771,jugular foramen meningioma,MONDO,disease,DISEASE_12100
12101,12101,12101,12101,12101,12101,12101,12101,MONDO:1011841,"faded shaker, non-human animal",MONDO,disease,DISEASE_12101
12102,12102,12102,12102,12102,12102,12102,12102,MONDO:0007814,"immune deficiency, familial variable",MONDO,disease,DISEASE_12102
12103,12103,12103,12103,12103,12103,12103,12103,MONDO:0700164,canine nephroblastoma,MONDO,disease,DISEASE_12103
12104,12104,12104,12104,12104,12104,12104,12104,MONDO:0100455_MONDO:0800490,neonatal-onset developmental and epileptic encephalopathy,MONDO_grouped,disease,DISEASE_12104
12105,12105,12105,12105,12105,12105,12105,12105,MONDO:0002592,invasive malignant thymoma,MONDO,disease,DISEASE_12105
12106,12106,12106,12106,12106,12106,12106,12106,MONDO:0019933,acromegaly,MONDO,disease,DISEASE_12106
12107,12107,12107,12107,12107,12107,12107,12107,MONDO:0021091_MONDO:0006149,papillary cystadenoma,MONDO_grouped,disease,DISEASE_12107
12108,12108,12108,12108,12108,12108,12108,12108,MONDO:0024455_MONDO:0014819_MONDO:0014591_MONDO:0008389,autosomal dominant Robinow syndrome,MONDO_grouped,disease,DISEASE_12108
12109,12109,12109,12109,12109,12109,12109,12109,MONDO:0958101,lymphocytic mastitis,MONDO,disease,DISEASE_12109
12110,12110,12110,12110,12110,12110,12110,12110,MONDO:0001179,pinguecula,MONDO,disease,DISEASE_12110
12111,12111,12111,12111,12111,12111,12111,12111,MONDO:0044649,omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome,MONDO,disease,DISEASE_12111
12112,12112,12112,12112,12112,12112,12112,12112,MONDO:0014195,microcornea-myopic chorioretinal atrophy,MONDO,disease,DISEASE_12112
12113,12113,12113,12113,12113,12113,12113,12113,MONDO:0021181,inherited blood coagulation disorder,MONDO,disease,DISEASE_12113
12114,12114,12114,12114,12114,12114,12114,12114,MONDO:0020397,parachute tricuspid valve,MONDO,disease,DISEASE_12114
12115,12115,12115,12115,12115,12115,12115,12115,MONDO:0958009_MONDO:0032753,"spastic ataxia 10, autosomal recessive",MONDO_grouped,disease,DISEASE_12115
12116,12116,12116,12116,12116,12116,12116,12116,MONDO:0018620,hypothalamic adipsic hypernatraemia syndrome,MONDO,disease,DISEASE_12116
12117,12117,12117,12117,12117,12117,12117,12117,MONDO:0001869,paraurethral gland cancer,MONDO,disease,DISEASE_12117
12118,12118,12118,12118,12118,12118,12118,12118,MONDO:0044637,infantile-onset generalized dyskinesia with orofacial involvement,MONDO,disease,DISEASE_12118
12119,12119,12119,12119,12119,12119,12119,12119,MONDO:0037250,childhood testicular neoplasm,MONDO,disease,DISEASE_12119
12120,12120,12120,12120,12120,12120,12120,12120,MONDO:0007233_MONDO:0015376_MONDO:0015377_MONDO:0015378,second branchial cleft anomaly,MONDO_grouped,disease,DISEASE_12120
12121,12121,12121,12121,12121,12121,12121,12121,MONDO:0014060,progressive retinal dystrophy due to retinol transport defect,MONDO,disease,DISEASE_12121
12122,12122,12122,12122,12122,12122,12122,12122,MONDO:0006653,anthracosilicosis,MONDO,disease,DISEASE_12122
12123,12123,12123,12123,12123,12123,12123,12123,MONDO:0003107,infratentorial cancer,MONDO,disease,DISEASE_12123
12124,12124,12124,12124,12124,12124,12124,12124,MONDO:0020398_MONDO:0001298_MONDO:0020403,congenital mitral stenosis,MONDO_grouped,disease,DISEASE_12124
12125,12125,12125,12125,12125,12125,12125,12125,MONDO:0017392,pre-descemet corneal dystrophy,MONDO,disease,DISEASE_12125
12126,12126,12126,12126,12126,12126,12126,12126,MONDO:0003844,central nervous system lipoma,MONDO,disease,DISEASE_12126
12127,12127,12127,12127,12127,12127,12127,12127,MONDO:0004348,retinal telangiectasia,MONDO,disease,DISEASE_12127
12128,12128,12128,12128,12128,12128,12128,12128,MONDO:0020683,acute disease,MONDO,disease,DISEASE_12128
12129,12129,12129,12129,12129,12129,12129,12129,MONDO:0006926_MONDO:0000889,haemophilus infectious disease,MONDO_grouped,disease,DISEASE_12129
12130,12130,12130,12130,12130,12130,12130,12130,MONDO:0016944,partial duplication of the short arm of chromosome 7,MONDO,disease,DISEASE_12130
12131,12131,12131,12131,12131,12131,12131,12131,MONDO:0017924,central nervous system calcification-deafness-tubular acidosis-anemia syndrome,MONDO,disease,DISEASE_12131
12132,12132,12132,12132,12132,12132,12132,12132,MONDO:0001795,plantar wart,MONDO,disease,DISEASE_12132
12133,12133,12133,12133,12133,12133,12133,12133,MONDO:0005532,Crohn's colitis,MONDO,disease,DISEASE_12133
12134,12134,12134,12134,12134,12134,12134,12134,MONDO:0009173,congenital enteropathy due to enteropeptidase deficiency,MONDO,disease,DISEASE_12134
12135,12135,12135,12135,12135,12135,12135,12135,MONDO:0010278,Christianson syndrome,MONDO,disease,DISEASE_12135
12136,12136,12136,12136,12136,12136,12136,12136,MONDO:0044621,16p12.1p12.3 triplication syndrome,MONDO,disease,DISEASE_12136
12137,12137,12137,12137,12137,12137,12137,12137,MONDO:0022208,crystal arthropathy,MONDO,disease,DISEASE_12137
12138,12138,12138,12138,12138,12138,12138,12138,MONDO:0001606,central nervous system leukemia,MONDO,disease,DISEASE_12138
12139,12139,12139,12139,12139,12139,12139,12139,MONDO:0023240,gigantism advanced bone age hoarse cry,MONDO,disease,DISEASE_12139
12140,12140,12140,12140,12140,12140,12140,12140,MONDO:1010080,"thrombocytopenia, non-human animal",MONDO,disease,DISEASE_12140
12141,12141,12141,12141,12141,12141,12141,12141,MONDO:0016011_MONDO:0000408_MONDO:0000815,fetal alcohol syndrome,MONDO_grouped,disease,DISEASE_12141
12142,12142,12142,12142,12142,12142,12142,12142,MONDO:0005578,arthritic joint disease,MONDO,disease,DISEASE_12142
12143,12143,12143,12143,12143,12143,12143,12143,MONDO:0000188,GLUT1 deficiency syndrome,MONDO,disease,DISEASE_12143
12144,12144,12144,12144,12144,12144,12144,12144,MONDO:0800472,CYP1B1-related glaucoma with or without anterior segment dysgenesis,MONDO,disease,DISEASE_12144
12145,12145,12145,12145,12145,12145,12145,12145,MONDO:0008283,Cronkhite-Canada syndrome,MONDO,disease,DISEASE_12145
12146,12146,12146,12146,12146,12146,12146,12146,MONDO:0003011,mucinous tubular and spindle renal cell carcinoma,MONDO,disease,DISEASE_12146
12147,12147,12147,12147,12147,12147,12147,12147,MONDO:0017780,20p13 microdeletion syndrome,MONDO,disease,DISEASE_12147
12148,12148,12148,12148,12148,12148,12148,12148,MONDO:0006081,anal melanoma,MONDO,disease,DISEASE_12148
12149,12149,12149,12149,12149,12149,12149,12149,MONDO:0002244,factor VII deficiency,MONDO,disease,DISEASE_12149
12150,12150,12150,12150,12150,12150,12150,12150,MONDO:0017920,deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome,MONDO,disease,DISEASE_12150
12151,12151,12151,12151,12151,12151,12151,12151,MONDO:0009016_MONDO:0001180,band keratopathy,MONDO_grouped,disease,DISEASE_12151
12152,12152,12152,12152,12152,12152,12152,12152,MONDO:0100123,toxic bronchiolitis,MONDO,disease,DISEASE_12152
12153,12153,12153,12153,12153,12153,12153,12153,MONDO:0018449,acquired cystic disease-associated renal cell carcinoma,MONDO,disease,DISEASE_12153
12154,12154,12154,12154,12154,12154,12154,12154,MONDO:0006476,undifferentiated gallbladder carcinoma,MONDO,disease,DISEASE_12154
12155,12155,12155,12155,12155,12155,12155,12155,MONDO:0017687,disorder of neutral amino acid transport,MONDO,disease,DISEASE_12155
12156,12156,12156,12156,12156,12156,12156,12156,MONDO:0006230,gastric squamous cell carcinoma,MONDO,disease,DISEASE_12156
12157,12157,12157,12157,12157,12157,12157,12157,MONDO:0005812,influenza,MONDO,disease,DISEASE_12157
12158,12158,12158,12158,12158,12158,12158,12158,MONDO:0006755,euthyroid sick syndrome,MONDO,disease,DISEASE_12158
12159,12159,12159,12159,12159,12159,12159,12159,MONDO:0100230,fatty acyl-CoA reductase 1 upregulation,MONDO,disease,DISEASE_12159
12160,12160,12160,12160,12160,12160,12160,12160,MONDO:0009589,mesomelic dwarfism-cleft palate-camptodactyly syndrome,MONDO,disease,DISEASE_12160
12161,12161,12161,12161,12161,12161,12161,12161,MONDO:0010439,"cardiomyopathy, fatal fetal, due to myocardial calcification",MONDO,disease,DISEASE_12161
12162,12162,12162,12162,12162,12162,12162,12162,MONDO:0017763_MONDO:0017313,disorder of iron metabolism and transport,MONDO_grouped,disease,DISEASE_12162
12163,12163,12163,12163,12163,12163,12163,12163,MONDO:0012997,cholestasis-pigmentary retinopathy-cleft palate syndrome,MONDO,disease,DISEASE_12163
12164,12164,12164,12164,12164,12164,12164,12164,MONDO:0020179,palpebral nevus,MONDO,disease,DISEASE_12164
12165,12165,12165,12165,12165,12165,12165,12165,MONDO:0017395,fixed pigmented erythema,MONDO,disease,DISEASE_12165
12166,12166,12166,12166,12166,12166,12166,12166,MONDO:0010281,Danon disease,MONDO,disease,DISEASE_12166
12167,12167,12167,12167,12167,12167,12167,12167,MONDO:0012013,"Weill-Marchesani syndrome 2, dominant",MONDO,disease,DISEASE_12167
12168,12168,12168,12168,12168,12168,12168,12168,MONDO:0032926,sandestig-stefanova syndrome,MONDO,disease,DISEASE_12168
12169,12169,12169,12169,12169,12169,12169,12169,MONDO:0003262,rhabdoid meningioma,MONDO,disease,DISEASE_12169
12170,12170,12170,12170,12170,12170,12170,12170,MONDO:1011413,"paroxysmal nocturnal hemoglobinuria, non-human animal",MONDO,disease,DISEASE_12170
12171,12171,12171,12171,12171,12171,12171,12171,MONDO:0009262_MONDO:0009261_MONDO:0009260_MONDO:0018149_MONDO:0017720_MONDO:1010847_MONDO:1012691,GM1 gangliosidosis,MONDO_grouped,disease,DISEASE_12171
12172,12172,12172,12172,12172,12172,12172,12172,MONDO:0009801,"familial osteodysplasia, Anderson type",MONDO,disease,DISEASE_12172
12173,12173,12173,12173,12173,12173,12173,12173,MONDO:0010323,Atkin-Flaitz syndrome,MONDO,disease,DISEASE_12173
12174,12174,12174,12174,12174,12174,12174,12174,MONDO:0009582,Mietens syndrome,MONDO,disease,DISEASE_12174
12175,12175,12175,12175,12175,12175,12175,12175,MONDO:0850096,SBDS-related severe neonatal spondylometaphyseal dysplasia,MONDO,disease,DISEASE_12175
12176,12176,12176,12176,12176,12176,12176,12176,MONDO:0022560,benign metastasizing leiomyoma,MONDO,disease,DISEASE_12176
12177,12177,12177,12177,12177,12177,12177,12177,MONDO:0008392,Roussy-Levy syndrome,MONDO,disease,DISEASE_12177
12178,12178,12178,12178,12178,12178,12178,12178,MONDO:0009567,Marinesco-Sjogren syndrome,MONDO,disease,DISEASE_12178
12179,12179,12179,12179,12179,12179,12179,12179,MONDO:0015269,symmetrical thalamic calcifications,MONDO,disease,DISEASE_12179
12180,12180,12180,12180,12180,12180,12180,12180,MONDO:0009577,megalocornea-intellectual disability syndrome,MONDO,disease,DISEASE_12180
12181,12181,12181,12181,12181,12181,12181,12181,MONDO:0000316,opportunistic bacterial infectious disease,MONDO,disease,DISEASE_12181
12182,12182,12182,12182,12182,12182,12182,12182,MONDO:0022892,craniosynostosis alopecia brain defect,MONDO,disease,DISEASE_12182
12183,12183,12183,12183,12183,12183,12183,12183,MONDO:0015492_MONDO:0005435,anti-neutrophil cytoplasmic antibody-associated vasculitis,MONDO_grouped,disease,DISEASE_12183
12184,12184,12184,12184,12184,12184,12184,12184,MONDO:0043077,weinstein kliman scully syndrome,MONDO,disease,DISEASE_12184
12185,12185,12185,12185,12185,12185,12185,12185,MONDO:0035009,isolated mesenteric vein thrombosis,MONDO,disease,DISEASE_12185
12186,12186,12186,12186,12186,12186,12186,12186,MONDO:0015134,constitutional neutropenia,MONDO,disease,DISEASE_12186
12187,12187,12187,12187,12187,12187,12187,12187,MONDO:0018740,drug-induced methemoglobinemia,MONDO,disease,DISEASE_12187
12188,12188,12188,12188,12188,12188,12188,12188,MONDO:0014877_MONDO:0008049,"myopathy, distal",MONDO_grouped,disease,DISEASE_12188
12189,12189,12189,12189,12189,12189,12189,12189,MONDO:0007335_MONDO:0014772_MONDO:0013466_MONDO:0013378_MONDO:0010906_MONDO:0010927_MONDO:0012142_MONDO:0000358_MONDO:0029145_MONDO:0011276_MONDO:0012022_MONDO:0012478_MONDO:0013023_MONDO:0700251,orofacial cleft,MONDO_grouped,disease,DISEASE_12189
12190,12190,12190,12190,12190,12190,12190,12190,MONDO:0007980,metachromasia of fibroblasts,MONDO,disease,DISEASE_12190
12191,12191,12191,12191,12191,12191,12191,12191,MONDO:0007231,brachytelephalangy-dysmorphism-Kallmann syndrome,MONDO,disease,DISEASE_12191
12192,12192,12192,12192,12192,12192,12192,12192,MONDO:1012134,"immunoglobulin G2 deficiency, cattle",MONDO,disease,DISEASE_12192
12193,12193,12193,12193,12193,12193,12193,12193,MONDO:0012159_MONDO:0012942_MONDO:0012955_MONDO:0013631,lung cancer susceptibility,MONDO_grouped,disease,DISEASE_12193
12194,12194,12194,12194,12194,12194,12194,12194,MONDO:0006477,undifferentiated ovarian carcinoma,MONDO,disease,DISEASE_12194
12195,12195,12195,12195,12195,12195,12195,12195,MONDO:0013808,Maffucci syndrome,MONDO,disease,DISEASE_12195
12196,12196,12196,12196,12196,12196,12196,12196,MONDO:0002585,"breast fibrocystic change, proliferative type",MONDO,disease,DISEASE_12196
12197,12197,12197,12197,12197,12197,12197,12197,MONDO:0022749,non-neoplastic nevus,MONDO,disease,DISEASE_12197
12198,12198,12198,12198,12198,12198,12198,12198,MONDO:0001560_MONDO:0100239_MONDO:0001878,hypertrophic pyloric stenosis,MONDO_grouped,disease,DISEASE_12198
12199,12199,12199,12199,12199,12199,12199,12199,MONDO:0013170,"cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies",MONDO,disease,DISEASE_12199
12200,12200,12200,12200,12200,12200,12200,12200,MONDO:0100367,port-wine nevi-mega cisterna magna-hydrocephalus syndrome,MONDO,disease,DISEASE_12200
12201,12201,12201,12201,12201,12201,12201,12201,MONDO:0002360,chondroma,MONDO,disease,DISEASE_12201
12202,12202,12202,12202,12202,12202,12202,12202,MONDO:0100368_MONDO:0100452_MONDO:0800399,RPE65-related recessive retinopathy,MONDO_grouped,disease,DISEASE_12202
12203,12203,12203,12203,12203,12203,12203,12203,MONDO:0042602,Samson-Viljoen syndrome,MONDO,disease,DISEASE_12203
12204,12204,12204,12204,12204,12204,12204,12204,MONDO:0003850,clivus chondroid chordoma,MONDO,disease,DISEASE_12204
12205,12205,12205,12205,12205,12205,12205,12205,MONDO:0859156,"dysostosis multiplex, Ain-Naz type",MONDO,disease,DISEASE_12205
12206,12206,12206,12206,12206,12206,12206,12206,MONDO:0011249,torsion dystonia with onset in infancy,MONDO,disease,DISEASE_12206
12207,12207,12207,12207,12207,12207,12207,12207,MONDO:0000383,benign reproductive system neoplasm,MONDO,disease,DISEASE_12207
12208,12208,12208,12208,12208,12208,12208,12208,MONDO:0040732,Pseudomonas aeruginosa infectious disease,MONDO,disease,DISEASE_12208
12209,12209,12209,12209,12209,12209,12209,12209,MONDO:0009414,glycogen storage disorder due to hepatic glycogen synthase deficiency,MONDO,disease,DISEASE_12209
12210,12210,12210,12210,12210,12210,12210,12210,MONDO:0023214,gas bloat syndrome,MONDO,disease,DISEASE_12210
12211,12211,12211,12211,12211,12211,12211,12211,MONDO:0019884,distal trisomy 10q,MONDO,disease,DISEASE_12211
12212,12212,12212,12212,12212,12212,12212,12212,MONDO:0022791,coarse face hypotonia constipation,MONDO,disease,DISEASE_12212
12213,12213,12213,12213,12213,12213,12213,12213,MONDO:0042452,tertiary lesion of yaws,MONDO,disease,DISEASE_12213
12214,12214,12214,12214,12214,12214,12214,12214,MONDO:0007908,multiple symmetric lipomatosis,MONDO,disease,DISEASE_12214
12215,12215,12215,12215,12215,12215,12215,12215,MONDO:0019561,lupus erythematosus panniculitis,MONDO,disease,DISEASE_12215
12216,12216,12216,12216,12216,12216,12216,12216,MONDO:0021538,verrucous carcinoma of oral cavity,MONDO,disease,DISEASE_12216
12217,12217,12217,12217,12217,12217,12217,12217,MONDO:1010840_MONDO:1010843_MONDO:1010842,"gangliosidosis, dog",MONDO_grouped,disease,DISEASE_12217
12218,12218,12218,12218,12218,12218,12218,12218,MONDO:0019509,cutaneous leukocytoclastic angiitis,MONDO,disease,DISEASE_12218
12219,12219,12219,12219,12219,12219,12219,12219,MONDO:0017387_MONDO:0004060_MONDO:0004105_MONDO:0004521_MONDO:0004540,epithelioid sarcoma,MONDO_grouped,disease,DISEASE_12219
12220,12220,12220,12220,12220,12220,12220,12220,MONDO:0007887,leiomyoma of vulva and esophagus,MONDO,disease,DISEASE_12220
12221,12221,12221,12221,12221,12221,12221,12221,MONDO:0024675,adult kidney Wilms tumor,MONDO,disease,DISEASE_12221
12222,12222,12222,12222,12222,12222,12222,12222,MONDO:0000918_MONDO:0042451,endometritis,MONDO_grouped,disease,DISEASE_12222
12223,12223,12223,12223,12223,12223,12223,12223,MONDO:0004772,glaucomatocyclitic crisis,MONDO,disease,DISEASE_12223
12224,12224,12224,12224,12224,12224,12224,12224,MONDO:0001991,malignant cardiac germ cell tumor,MONDO,disease,DISEASE_12224
12225,12225,12225,12225,12225,12225,12225,12225,MONDO:0017461,familial isolated clinodactyly of fingers,MONDO,disease,DISEASE_12225
12226,12226,12226,12226,12226,12226,12226,12226,MONDO:0019913,silver-Russell syndrome due to maternal uniparental disomy of chromosome 7,MONDO,disease,DISEASE_12226
12227,12227,12227,12227,12227,12227,12227,12227,MONDO:0006272,low grade fibromyxoid sarcoma,MONDO,disease,DISEASE_12227
12228,12228,12228,12228,12228,12228,12228,12228,MONDO:0020754_MONDO:0859157,visceral myopathy,MONDO_grouped,disease,DISEASE_12228
12229,12229,12229,12229,12229,12229,12229,12229,MONDO:1040015_MONDO:0005229,infectious disease with sepsis,MONDO_grouped,disease,DISEASE_12229
12230,12230,12230,12230,12230,12230,12230,12230,MONDO:0032850,neurooculocardiogenitourinary syndrome,MONDO,disease,DISEASE_12230
12231,12231,12231,12231,12231,12231,12231,12231,MONDO:1010039,"megacolon, non-human animal",MONDO,disease,DISEASE_12231
12232,12232,12232,12232,12232,12232,12232,12232,MONDO:0958180_MONDO:0958190,prolonged electroretinal response suppression,MONDO_grouped,disease,DISEASE_12232
12233,12233,12233,12233,12233,12233,12233,12233,MONDO:0007916_MONDO:0019574_MONDO:0018178,primary intestinal lymphangiectasia,MONDO_grouped,disease,DISEASE_12233
12234,12234,12234,12234,12234,12234,12234,12234,MONDO:0004601,ulcer of lower limbs,MONDO,disease,DISEASE_12234
12235,12235,12235,12235,12235,12235,12235,12235,MONDO:0017546_MONDO:0017547,"congenital vertical talus, unilateral",MONDO_grouped,disease,DISEASE_12235
12236,12236,12236,12236,12236,12236,12236,12236,MONDO:0021699,alcohol-induced disorders,MONDO,disease,DISEASE_12236
12237,12237,12237,12237,12237,12237,12237,12237,MONDO:0007007,Ureaplasma urethritis,MONDO,disease,DISEASE_12237
12238,12238,12238,12238,12238,12238,12238,12238,MONDO:1012478,"upper airway syndrome, dog",MONDO,disease,DISEASE_12238
12239,12239,12239,12239,12239,12239,12239,12239,MONDO:0010298,Lesch-Nyhan syndrome,MONDO,disease,DISEASE_12239
12240,12240,12240,12240,12240,12240,12240,12240,MONDO:0008367,red cell phospholipid defect with hemolysis,MONDO,disease,DISEASE_12240
12241,12241,12241,12241,12241,12241,12241,12241,MONDO:0024288,hyperbilirubinemia,MONDO,disease,DISEASE_12241
12242,12242,12242,12242,12242,12242,12242,12242,MONDO:0018304,Schnitzler syndrome,MONDO,disease,DISEASE_12242
12243,12243,12243,12243,12243,12243,12243,12243,MONDO:0017361,congenital rubella syndrome,MONDO,disease,DISEASE_12243
12244,12244,12244,12244,12244,12244,12244,12244,MONDO:0020449,persistent eustachian valve,MONDO,disease,DISEASE_12244
12245,12245,12245,12245,12245,12245,12245,12245,MONDO:0003828,growth hormone-producing pituitary gland carcinoma,MONDO,disease,DISEASE_12245
12246,12246,12246,12246,12246,12246,12246,12246,MONDO:0004489,fallopian tube gestational choriocarcinoma,MONDO,disease,DISEASE_12246
12247,12247,12247,12247,12247,12247,12247,12247,MONDO:0850303,supratentorial meningioma,MONDO,disease,DISEASE_12247
12248,12248,12248,12248,12248,12248,12248,12248,MONDO:0009847,"pericardial effusion, chronic",MONDO,disease,DISEASE_12248
12249,12249,12249,12249,12249,12249,12249,12249,MONDO:0012315,distal 10q deletion syndrome,MONDO,disease,DISEASE_12249
12250,12250,12250,12250,12250,12250,12250,12250,MONDO:0001808,chronic subinvolution of uterus,MONDO,disease,DISEASE_12250
12251,12251,12251,12251,12251,12251,12251,12251,MONDO:1011328,"integumentary system disorder, non-human animal",MONDO,disease,DISEASE_12251
12252,12252,12252,12252,12252,12252,12252,12252,MONDO:0043895,ankle injury,MONDO,disease,DISEASE_12252
12253,12253,12253,12253,12253,12253,12253,12253,MONDO:0019914,maternal uniparental disomy of chromosome 9,MONDO,disease,DISEASE_12253
12254,12254,12254,12254,12254,12254,12254,12254,MONDO:0013868_MONDO:0014713,"porokeratosis 7, multiple types",MONDO_grouped,disease,DISEASE_12254
12255,12255,12255,12255,12255,12255,12255,12255,MONDO:0001485,atypical depressive disorder,MONDO,disease,DISEASE_12255
12256,12256,12256,12256,12256,12256,12256,12256,MONDO:0005015,diabetes mellitus,MONDO,disease,DISEASE_12256
12257,12257,12257,12257,12257,12257,12257,12257,MONDO:0018913,malakoplakia,MONDO,disease,DISEASE_12257
12258,12258,12258,12258,12258,12258,12258,12258,MONDO:0009345,histidinemia,MONDO,disease,DISEASE_12258
12259,12259,12259,12259,12259,12259,12259,12259,MONDO:1012034,"brachygnathia superior and degenerative joint disease, cattle",MONDO,disease,DISEASE_12259
12260,12260,12260,12260,12260,12260,12260,12260,MONDO:0008236,phlebectasia of lips,MONDO,disease,DISEASE_12260
12261,12261,12261,12261,12261,12261,12261,12261,MONDO:0017853,hypersensitivity pneumonitis,MONDO,disease,DISEASE_12261
12262,12262,12262,12262,12262,12262,12262,12262,MONDO:0971126,isolated angioid streaks,MONDO,disease,DISEASE_12262
12263,12263,12263,12263,12263,12263,12263,12263,MONDO:0007995,"microphthalmia, isolated, with cataract 1",MONDO,disease,DISEASE_12263
12264,12264,12264,12264,12264,12264,12264,12264,MONDO:0001623,cicatricial lagophthalmos,MONDO,disease,DISEASE_12264
12265,12265,12265,12265,12265,12265,12265,12265,MONDO:0018202,gonadal germ cell tumor,MONDO,disease,DISEASE_12265
12266,12266,12266,12266,12266,12266,12266,12266,MONDO:0018628,HIV-associated cancer,MONDO,disease,DISEASE_12266
12267,12267,12267,12267,12267,12267,12267,12267,MONDO:0012773,Hunter-Macdonald syndrome,MONDO,disease,DISEASE_12267
12268,12268,12268,12268,12268,12268,12268,12268,MONDO:0005907,persian gulf syndrome,MONDO,disease,DISEASE_12268
12269,12269,12269,12269,12269,12269,12269,12269,MONDO:0009539,"lymphoblastic leukemia, acute, with lymphomatous features",MONDO,disease,DISEASE_12269
12270,12270,12270,12270,12270,12270,12270,12270,MONDO:1010109,"dihydropyrimidinase deficiency, non-human animal",MONDO,disease,DISEASE_12270
12271,12271,12271,12271,12271,12271,12271,12271,MONDO:0016543,hyperphenylalaninemia due to tetrahydrobiopterin deficiency,MONDO,disease,DISEASE_12271
12272,12272,12272,12272,12272,12272,12272,12272,MONDO:0041806_MONDO:0005861,drug-resistant tuberculosis,MONDO_grouped,disease,DISEASE_12272
12273,12273,12273,12273,12273,12273,12273,12273,MONDO:0002559,plexiform schwannoma,MONDO,disease,DISEASE_12273
12274,12274,12274,12274,12274,12274,12274,12274,MONDO:1010134,"pityriasis rosea, non-human animal",MONDO,disease,DISEASE_12274
12275,12275,12275,12275,12275,12275,12275,12275,MONDO:0002595,vaccinia,MONDO,disease,DISEASE_12275
12276,12276,12276,12276,12276,12276,12276,12276,MONDO:0021839,spirochaetales infections,MONDO,disease,DISEASE_12276
12277,12277,12277,12277,12277,12277,12277,12277,MONDO:0010730,"combined immunodeficiency, X-linked",MONDO,disease,DISEASE_12277
12278,12278,12278,12278,12278,12278,12278,12278,MONDO:0001302,hypertensive heart disease,MONDO,disease,DISEASE_12278
12279,12279,12279,12279,12279,12279,12279,12279,MONDO:1012457,"hemangiosarcoma, cockatiel",MONDO,disease,DISEASE_12279
12280,12280,12280,12280,12280,12280,12280,12280,MONDO:0012309_MONDO:0008197_MONDO:0012302_MONDO:0018953,parietal foramina,MONDO_grouped,disease,DISEASE_12280
12281,12281,12281,12281,12281,12281,12281,12281,MONDO:0004668,fascioliasis,MONDO,disease,DISEASE_12281
12282,12282,12282,12282,12282,12282,12282,12282,MONDO:0010707,Paine syndrome,MONDO,disease,DISEASE_12282
12283,12283,12283,12283,12283,12283,12283,12283,MONDO:0011958,"bile and pancreatic ducts, complete absence of",MONDO,disease,DISEASE_12283
12284,12284,12284,12284,12284,12284,12284,12284,MONDO:0002738,acute transudative otitis media,MONDO,disease,DISEASE_12284
12285,12285,12285,12285,12285,12285,12285,12285,MONDO:0005718_MONDO:0005762_MONDO:0005939,Coronaviridae infectious disease,MONDO_grouped,disease,DISEASE_12285
12286,12286,12286,12286,12286,12286,12286,12286,MONDO:0011989_MONDO:0005446,leishmaniasis,MONDO_grouped,disease,DISEASE_12286
12287,12287,12287,12287,12287,12287,12287,12287,MONDO:0003835,gastric cardia adenocarcinoma,MONDO,disease,DISEASE_12287
12288,12288,12288,12288,12288,12288,12288,12288,MONDO:0003316,nonanaplastic kidney Wilms tumor,MONDO,disease,DISEASE_12288
12289,12289,12289,12289,12289,12289,12289,12289,MONDO:0001409_MONDO:0001832_MONDO:0003846,esophagitis,MONDO_grouped,disease,DISEASE_12289
12290,12290,12290,12290,12290,12290,12290,12290,MONDO:0004558,thyroid gland macrofollicular adenoma,MONDO,disease,DISEASE_12290
12291,12291,12291,12291,12291,12291,12291,12291,MONDO:1012968,"cystinuria, non-human animal",MONDO,disease,DISEASE_12291
12292,12292,12292,12292,12292,12292,12292,12292,MONDO:0100217_MONDO:0800438_MONDO:0031632,"developmental delay with short stature, dysmorphic facial features, and sparse hair",MONDO_grouped,disease,DISEASE_12292
12293,12293,12293,12293,12293,12293,12293,12293,MONDO:0014523,juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome,MONDO,disease,DISEASE_12293
12294,12294,12294,12294,12294,12294,12294,12294,MONDO:0958097_MONDO:0958098,primary superior vena cava aneurysm,MONDO_grouped,disease,DISEASE_12294
12295,12295,12295,12295,12295,12295,12295,12295,MONDO:0008868,biliary malformation with renal tubular insufficiency,MONDO,disease,DISEASE_12295
12296,12296,12296,12296,12296,12296,12296,12296,MONDO:0011581,arrhythmogenic cardiomyopathy with wooly hair and keratoderma,MONDO,disease,DISEASE_12296
12297,12297,12297,12297,12297,12297,12297,12297,MONDO:0020831,congenital vertebral-cardiac-renal anomalies syndrome,MONDO,disease,DISEASE_12297
12298,12298,12298,12298,12298,12298,12298,12298,MONDO:0009299,46 XX gonadal dysgenesis,MONDO,disease,DISEASE_12298
12299,12299,12299,12299,12299,12299,12299,12299,MONDO:0001213,serous glue ear,MONDO,disease,DISEASE_12299
12300,12300,12300,12300,12300,12300,12300,12300,MONDO:0020426,malposition of the coronary ostium,MONDO,disease,DISEASE_12300
12301,12301,12301,12301,12301,12301,12301,12301,MONDO:0001640,gonococcal spondylitis,MONDO,disease,DISEASE_12301
12302,12302,12302,12302,12302,12302,12302,12302,MONDO:0010821,familial developmental dysphasia,MONDO,disease,DISEASE_12302
12303,12303,12303,12303,12303,12303,12303,12303,MONDO:0009796,ornithine aminotransferase deficiency,MONDO,disease,DISEASE_12303
12304,12304,12304,12304,12304,12304,12304,12304,MONDO:0005406,gestational diabetes,MONDO,disease,DISEASE_12304
12305,12305,12305,12305,12305,12305,12305,12305,MONDO:0012913,"Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome",MONDO,disease,DISEASE_12305
12306,12306,12306,12306,12306,12306,12306,12306,MONDO:0019373,desmoplastic small round cell tumor,MONDO,disease,DISEASE_12306
12307,12307,12307,12307,12307,12307,12307,12307,MONDO:0020497,Turcot syndrome with polyposis,MONDO,disease,DISEASE_12307
12308,12308,12308,12308,12308,12308,12308,12308,MONDO:0033644_MONDO:0800296,"microcornea, rod-cone dystrophy, cataract, and posterior staphyloma",MONDO_grouped,disease,DISEASE_12308
12309,12309,12309,12309,12309,12309,12309,12309,MONDO:0003859,bilateral meningioma of optic nerve,MONDO,disease,DISEASE_12309
12310,12310,12310,12310,12310,12310,12310,12310,MONDO:0044749,X-linked congenital stationary night blindness,MONDO,disease,DISEASE_12310
12311,12311,12311,12311,12311,12311,12311,12311,MONDO:1011788,"degenerative myopathy of obturator-externus, non-human animal",MONDO,disease,DISEASE_12311
12312,12312,12312,12312,12312,12312,12312,12312,MONDO:0010156,Troyer syndrome,MONDO,disease,DISEASE_12312
12313,12313,12313,12313,12313,12313,12313,12313,MONDO:0006672,balanitis,MONDO,disease,DISEASE_12313
12314,12314,12314,12314,12314,12314,12314,12314,MONDO:0016276,high-grade neuroendocrine carcinoma of the cervix uteri,MONDO,disease,DISEASE_12314
12315,12315,12315,12315,12315,12315,12315,12315,MONDO:0000249,secretory diarrhea,MONDO,disease,DISEASE_12315
12316,12316,12316,12316,12316,12316,12316,12316,MONDO:0016024,shoulder and thorax deformity-congenital heart disease syndrome,MONDO,disease,DISEASE_12316
12317,12317,12317,12317,12317,12317,12317,12317,MONDO:0008827,progressive pseudorheumatoid arthropathy of childhood,MONDO,disease,DISEASE_12317
12318,12318,12318,12318,12318,12318,12318,12318,MONDO:0021355,neoplasm of esophagus,MONDO,disease,DISEASE_12318
12319,12319,12319,12319,12319,12319,12319,12319,MONDO:0030077_MONDO:0060554_MONDO:0060555,"vertebral, cardiac, renal, and limb defects syndrome",MONDO_grouped,disease,DISEASE_12319
12320,12320,12320,12320,12320,12320,12320,12320,MONDO:0016367_MONDO:0002040,dermatomyositis,MONDO_grouped,disease,DISEASE_12320
12321,12321,12321,12321,12321,12321,12321,12321,MONDO:0008564,DiGeorge syndrome,MONDO,disease,DISEASE_12321
12322,12322,12322,12322,12322,12322,12322,12322,MONDO:1011758,"zinc deficiency-like syndrome, non-human animal",MONDO,disease,DISEASE_12322
12323,12323,12323,12323,12323,12323,12323,12323,MONDO:1011845,"congenital hypomyelinogenesis, non-human animal",MONDO,disease,DISEASE_12323
12324,12324,12324,12324,12324,12324,12324,12324,MONDO:0100193,chronic liver failure,MONDO,disease,DISEASE_12324
12325,12325,12325,12325,12325,12325,12325,12325,MONDO:0012865,Pseudofolliculitis barbae,MONDO,disease,DISEASE_12325
12326,12326,12326,12326,12326,12326,12326,12326,MONDO:0100533,"hemorrhage, intracerebral, susceptibility to",MONDO,disease,DISEASE_12326
12327,12327,12327,12327,12327,12327,12327,12327,MONDO:0024472,boutonneuse fever,MONDO,disease,DISEASE_12327
12328,12328,12328,12328,12328,12328,12328,12328,MONDO:0006561,eyelid hypopigmentation,MONDO,disease,DISEASE_12328
12329,12329,12329,12329,12329,12329,12329,12329,MONDO:0011185,Thiel-Behnke corneal dystrophy,MONDO,disease,DISEASE_12329
12330,12330,12330,12330,12330,12330,12330,12330,MONDO:0008330,pseudomonilethrix,MONDO,disease,DISEASE_12330
12331,12331,12331,12331,12331,12331,12331,12331,MONDO:0007771,"hyperpigmentation with or without hypopigmentation, familial progressive",MONDO,disease,DISEASE_12331
12332,12332,12332,12332,12332,12332,12332,12332,MONDO:0007050,"acromegaloid changes, cutis verticis gyrata, and corneal leukoma",MONDO,disease,DISEASE_12332
12333,12333,12333,12333,12333,12333,12333,12333,MONDO:0007407,Cryoglobulinemic vasculitis,MONDO,disease,DISEASE_12333
12334,12334,12334,12334,12334,12334,12334,12334,MONDO:0100185,immune reconstitution inflammatory syndrome,MONDO,disease,DISEASE_12334
12335,12335,12335,12335,12335,12335,12335,12335,MONDO:0958199_MONDO:0800306,myoclonic epilepsy of Lafora,MONDO_grouped,disease,DISEASE_12335
12336,12336,12336,12336,12336,12336,12336,12336,MONDO:0859372,"cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies",MONDO,disease,DISEASE_12336
12337,12337,12337,12337,12337,12337,12337,12337,MONDO:0010264,X-linked adrenal hypoplasia congenita,MONDO,disease,DISEASE_12337
12338,12338,12338,12338,12338,12338,12338,12338,MONDO:0019324,pemphigus foliaceus,MONDO,disease,DISEASE_12338
12339,12339,12339,12339,12339,12339,12339,12339,MONDO:0020406,complete atrioventricular canal-left heart obstruction syndrome,MONDO,disease,DISEASE_12339
12340,12340,12340,12340,12340,12340,12340,12340,MONDO:1011644,"persistent right aortic arch, non-human animal",MONDO,disease,DISEASE_12340
12341,12341,12341,12341,12341,12341,12341,12341,MONDO:0007855,"keratosis, familial actinic",MONDO,disease,DISEASE_12341
12342,12342,12342,12342,12342,12342,12342,12342,MONDO:1010003,"narcolepsy, non-human animal",MONDO,disease,DISEASE_12342
12343,12343,12343,12343,12343,12343,12343,12343,MONDO:0700233,TOPORS-related retinopathy,MONDO,disease,DISEASE_12343
12344,12344,12344,12344,12344,12344,12344,12344,MONDO:0957318,"nephrolithiasis, calcium oxalate",MONDO,disease,DISEASE_12344
12345,12345,12345,12345,12345,12345,12345,12345,MONDO:0018951,distal myopathy with vocal cord weakness,MONDO,disease,DISEASE_12345
12346,12346,12346,12346,12346,12346,12346,12346,MONDO:0006598,phototoxic dermatitis,MONDO,disease,DISEASE_12346
12347,12347,12347,12347,12347,12347,12347,12347,MONDO:0009855,d-bifunctional protein deficiency,MONDO,disease,DISEASE_12347
12348,12348,12348,12348,12348,12348,12348,12348,MONDO:0004880,bowel dysfunction,MONDO,disease,DISEASE_12348
12349,12349,12349,12349,12349,12349,12349,12349,MONDO:0016639,lower limb deficiency-hypospadias syndrome,MONDO,disease,DISEASE_12349
12350,12350,12350,12350,12350,12350,12350,12350,MONDO:0018924,"microphthalmia, Lenz type",MONDO,disease,DISEASE_12350
12351,12351,12351,12351,12351,12351,12351,12351,MONDO:0002279_MONDO:0000226_MONDO:0056803_MONDO:0024301,iron metabolism disease,MONDO_grouped,disease,DISEASE_12351
12352,12352,12352,12352,12352,12352,12352,12352,MONDO:0001666,retinal dystrophies primarily involving Bruch's membrane,MONDO,disease,DISEASE_12352
12353,12353,12353,12353,12353,12353,12353,12353,MONDO:0025382,"sarcoma, avian",MONDO,disease,DISEASE_12353
12354,12354,12354,12354,12354,12354,12354,12354,MONDO:0016089,infantile Krabbe disease,MONDO,disease,DISEASE_12354
12355,12355,12355,12355,12355,12355,12355,12355,MONDO:0007126_MONDO:0008468_MONDO:0024512_MONDO:0013192,"spondyloarthropathy, susceptibility to",MONDO_grouped,disease,DISEASE_12355
12356,12356,12356,12356,12356,12356,12356,12356,MONDO:0006744,endolymphatic hydrops,MONDO,disease,DISEASE_12356
12357,12357,12357,12357,12357,12357,12357,12357,MONDO:0043693,alcoholic liver diseases,MONDO,disease,DISEASE_12357
12358,12358,12358,12358,12358,12358,12358,12358,MONDO:0859530,"myopathy, sarcoplasmic body",MONDO,disease,DISEASE_12358
12359,12359,12359,12359,12359,12359,12359,12359,MONDO:0002653_MONDO:0015873,Paget disease of the penis,MONDO_grouped,disease,DISEASE_12359
12360,12360,12360,12360,12360,12360,12360,12360,MONDO:0021222,lacrimal gland neoplasm,MONDO,disease,DISEASE_12360
12361,12361,12361,12361,12361,12361,12361,12361,MONDO:0045051_MONDO:0001749,cortical cataract,MONDO_grouped,disease,DISEASE_12361
12362,12362,12362,12362,12362,12362,12362,12362,MONDO:0009319_MONDO:0016305_MONDO:0016304,pantothenate kinase-associated neurodegeneration,MONDO_grouped,disease,DISEASE_12362
12363,12363,12363,12363,12363,12363,12363,12363,MONDO:0023045,ectodermal dysplasia arthrogryposis diabetes mellitus,MONDO,disease,DISEASE_12363
12364,12364,12364,12364,12364,12364,12364,12364,MONDO:0003261,papillary meningioma of the cerebellum,MONDO,disease,DISEASE_12364
12365,12365,12365,12365,12365,12365,12365,12365,MONDO:0005554_MONDO:0006955_MONDO:0003627,rheumatic disorder,MONDO_grouped,disease,DISEASE_12365
12366,12366,12366,12366,12366,12366,12366,12366,MONDO:1011647,"chronic valvular disease, non-human animal",MONDO,disease,DISEASE_12366
12367,12367,12367,12367,12367,12367,12367,12367,MONDO:0015094,subependymal nodular heterotopia,MONDO,disease,DISEASE_12367
12368,12368,12368,12368,12368,12368,12368,12368,MONDO:0002601,teratoma,MONDO,disease,DISEASE_12368
12369,12369,12369,12369,12369,12369,12369,12369,MONDO:0017476_MONDO:0017477,upper limb hypertrophy,MONDO_grouped,disease,DISEASE_12369
12370,12370,12370,12370,12370,12370,12370,12370,MONDO:0060507,retinal dystrophy with or without macular staphyloma,MONDO,disease,DISEASE_12370
12371,12371,12371,12371,12371,12371,12371,12371,MONDO:0957807,"hyper-IgE syndrome 6, autosomal dominant, with recurrent infections",MONDO,disease,DISEASE_12371
12372,12372,12372,12372,12372,12372,12372,12372,MONDO:0001134_MONDO:0005149_MONDO:0005080,essential hypertension,MONDO_grouped,disease,DISEASE_12372
12373,12373,12373,12373,12373,12373,12373,12373,MONDO:0020562_MONDO:0003573_MONDO:0000966,pleomorphic liposarcoma,MONDO_grouped,disease,DISEASE_12373
12374,12374,12374,12374,12374,12374,12374,12374,MONDO:0000666,associative visual agnosia,MONDO,disease,DISEASE_12374
12375,12375,12375,12375,12375,12375,12375,12375,MONDO:0035838_MONDO:0019754,idiopathic multicentric Castleman disease,MONDO_grouped,disease,DISEASE_12375
12376,12376,12376,12376,12376,12376,12376,12376,MONDO:0008079,neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome,MONDO,disease,DISEASE_12376
12377,12377,12377,12377,12377,12377,12377,12377,MONDO:0010228_MONDO:0010484_MONDO:0010238_MONDO:0010577,"hearing loss, X-linked",MONDO_grouped,disease,DISEASE_12377
12378,12378,12378,12378,12378,12378,12378,12378,MONDO:0800106,disruptive behavior disorder,MONDO,disease,DISEASE_12378
12379,12379,12379,12379,12379,12379,12379,12379,MONDO:0014234,reticulate acropigmentation of Kitamura,MONDO,disease,DISEASE_12379
12380,12380,12380,12380,12380,12380,12380,12380,MONDO:0004443,chest wall parachordoma,MONDO,disease,DISEASE_12380
12381,12381,12381,12381,12381,12381,12381,12381,MONDO:0013725_MONDO:0013695,"colorectal cancer, hereditary nonpolyposis,",MONDO_grouped,disease,DISEASE_12381
12382,12382,12382,12382,12382,12382,12382,12382,MONDO:0008672,Watson syndrome,MONDO,disease,DISEASE_12382
12383,12383,12383,12383,12383,12383,12383,12383,MONDO:0020705,"neural tube defects, susceptibility to",MONDO,disease,DISEASE_12383
12384,12384,12384,12384,12384,12384,12384,12384,MONDO:0009051,cutaneous photosensitivity-lethal colitis syndrome,MONDO,disease,DISEASE_12384
12385,12385,12385,12385,12385,12385,12385,12385,MONDO:0022843,congenital mumps,MONDO,disease,DISEASE_12385
12386,12386,12386,12386,12386,12386,12386,12386,MONDO:0008693,ablepharon macrostomia syndrome,MONDO,disease,DISEASE_12386
12387,12387,12387,12387,12387,12387,12387,12387,MONDO:0004745,priapism,MONDO,disease,DISEASE_12387
12388,12388,12388,12388,12388,12388,12388,12388,MONDO:0016722,pineoblastoma,MONDO,disease,DISEASE_12388
12389,12389,12389,12389,12389,12389,12389,12389,MONDO:0001844_MONDO:0003928_MONDO:0004161,uterine corpus myxoid leiomyoma,MONDO_grouped,disease,DISEASE_12389
12390,12390,12390,12390,12390,12390,12390,12390,MONDO:0008325,Pseudoatrophoderma colli,MONDO,disease,DISEASE_12390
12391,12391,12391,12391,12391,12391,12391,12391,MONDO:0010708,Pallister-W syndrome,MONDO,disease,DISEASE_12391
12392,12392,12392,12392,12392,12392,12392,12392,MONDO:0017752,defect in V-ATPase,MONDO,disease,DISEASE_12392
12393,12393,12393,12393,12393,12393,12393,12393,MONDO:0031057_MONDO:0015780,"dyskeratosis congenita, digenic",MONDO_grouped,disease,DISEASE_12393
12394,12394,12394,12394,12394,12394,12394,12394,MONDO:0100502,NTHL1-deficiency tumor predisposition syndrome,MONDO,disease,DISEASE_12394
12395,12395,12395,12395,12395,12395,12395,12395,MONDO:1012981_MONDO:1011689,"anemia, non-human animal",MONDO_grouped,disease,DISEASE_12395
12396,12396,12396,12396,12396,12396,12396,12396,MONDO:0859151,"fibromuscular dysplasia, multifocal",MONDO,disease,DISEASE_12396
12397,12397,12397,12397,12397,12397,12397,12397,MONDO:0859692,immune-mediated cerebellar ataxia,MONDO,disease,DISEASE_12397
12398,12398,12398,12398,12398,12398,12398,12398,MONDO:0018744,oligodendroglial tumor,MONDO,disease,DISEASE_12398
12399,12399,12399,12399,12399,12399,12399,12399,MONDO:0001081,acute cervicitis,MONDO,disease,DISEASE_12399
12400,12400,12400,12400,12400,12400,12400,12400,MONDO:0007965,"melanoma, malignant familial intraocular",MONDO,disease,DISEASE_12400
12401,12401,12401,12401,12401,12401,12401,12401,MONDO:0010178,congenital bilateral aplasia of vas deferens from CFTR mutation,MONDO,disease,DISEASE_12401
12402,12402,12402,12402,12402,12402,12402,12402,MONDO:0013223,"autosomal recessive spondylometaphyseal dysplasia, Megarbane type",MONDO,disease,DISEASE_12402
12403,12403,12403,12403,12403,12403,12403,12403,MONDO:0010636,Kallmann syndrome with spastic paraplegia,MONDO,disease,DISEASE_12403
12404,12404,12404,12404,12404,12404,12404,12404,MONDO:0005084,mental disorder,MONDO,disease,DISEASE_12404
12405,12405,12405,12405,12405,12405,12405,12405,MONDO:0001525,thyrocalcitonin secretion disease,MONDO,disease,DISEASE_12405
12406,12406,12406,12406,12406,12406,12406,12406,MONDO:0009396,"hyperparathyroidism, neonatal self-limited primary, with hypercalciuria",MONDO,disease,DISEASE_12406
12407,12407,12407,12407,12407,12407,12407,12407,MONDO:0012761,chromosome 3q29 microduplication syndrome,MONDO,disease,DISEASE_12407
12408,12408,12408,12408,12408,12408,12408,12408,MONDO:0013189,trichotillomania,MONDO,disease,DISEASE_12408
12409,12409,12409,12409,12409,12409,12409,12409,MONDO:0001773,post-vaccinal encephalitis,MONDO,disease,DISEASE_12409
12410,12410,12410,12410,12410,12410,12410,12410,MONDO:0032887,"neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity",MONDO,disease,DISEASE_12410
12411,12411,12411,12411,12411,12411,12411,12411,MONDO:0019977,parkinsonism with dementia of Guadeloupe,MONDO,disease,DISEASE_12411
12412,12412,12412,12412,12412,12412,12412,12412,MONDO:0042966,inherited mitral valve disease,MONDO,disease,DISEASE_12412
12413,12413,12413,12413,12413,12413,12413,12413,MONDO:0001306,obsolete recurrent corneal erosion,MONDO,disease,DISEASE_12413
12414,12414,12414,12414,12414,12414,12414,12414,MONDO:0004346,signet ring cell intrahepatic cholangiocarcinoma,MONDO,disease,DISEASE_12414
12415,12415,12415,12415,12415,12415,12415,12415,MONDO:0013050,"lethal polymalformative syndrome, Boissel type",MONDO,disease,DISEASE_12415
12416,12416,12416,12416,12416,12416,12416,12416,MONDO:0022752,chromosome 16p13.3 deletion syndrome,MONDO,disease,DISEASE_12416
12417,12417,12417,12417,12417,12417,12417,12417,MONDO:0011641,"baculum, congenital absence of",MONDO,disease,DISEASE_12417
12418,12418,12418,12418,12418,12418,12418,12418,MONDO:0017066,cervical spina bifida aperta,MONDO,disease,DISEASE_12418
12419,12419,12419,12419,12419,12419,12419,12419,MONDO:0015379,cervical dermoid cyst,MONDO,disease,DISEASE_12419
12420,12420,12420,12420,12420,12420,12420,12420,MONDO:0044322,intellectual developmental disorder with neuropsychiatric features,MONDO,disease,DISEASE_12420
12421,12421,12421,12421,12421,12421,12421,12421,MONDO:0019469,T-cell large granular lymphocyte leukemia,MONDO,disease,DISEASE_12421
12422,12422,12422,12422,12422,12422,12422,12422,MONDO:0002359,periosteal chondroma,MONDO,disease,DISEASE_12422
12423,12423,12423,12423,12423,12423,12423,12423,MONDO:0018657,pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome,MONDO,disease,DISEASE_12423
12424,12424,12424,12424,12424,12424,12424,12424,MONDO:0002849_MONDO:0002580_MONDO:0002859_MONDO:0850346,liver rhabdomyosarcoma,MONDO_grouped,disease,DISEASE_12424
12425,12425,12425,12425,12425,12425,12425,12425,MONDO:0016980,ATR-X-related syndrome,MONDO,disease,DISEASE_12425
12426,12426,12426,12426,12426,12426,12426,12426,MONDO:0020159,congenital entropion,MONDO,disease,DISEASE_12426
12427,12427,12427,12427,12427,12427,12427,12427,MONDO:8000018,benign paroxysmal positional vertigo,MONDO,disease,DISEASE_12427
12428,12428,12428,12428,12428,12428,12428,12428,MONDO:0005233,non-small cell lung carcinoma,MONDO,disease,DISEASE_12428
12429,12429,12429,12429,12429,12429,12429,12429,MONDO:0013164,beta-ureidopropionase deficiency,MONDO,disease,DISEASE_12429
12430,12430,12430,12430,12430,12430,12430,12430,MONDO:0015589_MONDO:0015590_MONDO:0850104,paraneoplastic limbic encephalitis,MONDO_grouped,disease,DISEASE_12430
12431,12431,12431,12431,12431,12431,12431,12431,MONDO:0030961_MONDO:0010486_MONDO:0100296_MONDO:0031421,Olmsted syndrome,MONDO_grouped,disease,DISEASE_12431
12432,12432,12432,12432,12432,12432,12432,12432,MONDO:1010565_MONDO:1010567_MONDO:1010568_MONDO:1010569_MONDO:1010570,"diabetes insipidus, chicken",MONDO_grouped,disease,DISEASE_12432
12433,12433,12433,12433,12433,12433,12433,12433,MONDO:0012044_MONDO:0007380_MONDO:1011219_MONDO:1011220,"corneal dystrophy, lattice",MONDO_grouped,disease,DISEASE_12433
12434,12434,12434,12434,12434,12434,12434,12434,MONDO:0850084,non-syndromic pansynostosis,MONDO,disease,DISEASE_12434
12435,12435,12435,12435,12435,12435,12435,12435,MONDO:0003279,testicular infarct,MONDO,disease,DISEASE_12435
12436,12436,12436,12436,12436,12436,12436,12436,MONDO:0800331,"hyperglycinemia, transient neonatal",MONDO,disease,DISEASE_12436
12437,12437,12437,12437,12437,12437,12437,12437,MONDO:1011212,"coloboma, Mexican tetra",MONDO,disease,DISEASE_12437
12438,12438,12438,12438,12438,12438,12438,12438,MONDO:0021478,benign neoplasm of nasopharynx,MONDO,disease,DISEASE_12438
12439,12439,12439,12439,12439,12439,12439,12439,MONDO:0015235,arachnodactyly-intellectual disability-dysmorphism syndrome,MONDO,disease,DISEASE_12439
12440,12440,12440,12440,12440,12440,12440,12440,MONDO:0012383,primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency,MONDO,disease,DISEASE_12440
12441,12441,12441,12441,12441,12441,12441,12441,MONDO:0006692,central pontine myelinolysis,MONDO,disease,DISEASE_12441
12442,12442,12442,12442,12442,12442,12442,12442,MONDO:0019394,Senior-Boichis syndrome,MONDO,disease,DISEASE_12442
12443,12443,12443,12443,12443,12443,12443,12443,MONDO:0850445,benign peritoneal solitary fibrous tumor,MONDO,disease,DISEASE_12443
12444,12444,12444,12444,12444,12444,12444,12444,MONDO:0005736_MONDO:0019380,eastern equine encephalitis,MONDO_grouped,disease,DISEASE_12444
12445,12445,12445,12445,12445,12445,12445,12445,MONDO:0015358_MONDO:0015364,hereditary motor and sensory neuropathy,MONDO_grouped,disease,DISEASE_12445
12446,12446,12446,12446,12446,12446,12446,12446,MONDO:0044631,early-onset familial noncirrhotic portal hypertension,MONDO,disease,DISEASE_12446
12447,12447,12447,12447,12447,12447,12447,12447,MONDO:0010980,"midline malformations, multiple, with limb abnormalities and hypopituitarism",MONDO,disease,DISEASE_12447
12448,12448,12448,12448,12448,12448,12448,12448,MONDO:0020485,King-Denborough syndrome,MONDO,disease,DISEASE_12448
12449,12449,12449,12449,12449,12449,12449,12449,MONDO:0043300_MONDO:0000741,actinic cheilitis,MONDO_grouped,disease,DISEASE_12449
12450,12450,12450,12450,12450,12450,12450,12450,MONDO:1030007,hypertensive urgency,MONDO,disease,DISEASE_12450
12451,12451,12451,12451,12451,12451,12451,12451,MONDO:0100161,hyperkalemic renal tubular acidosis,MONDO,disease,DISEASE_12451
12452,12452,12452,12452,12452,12452,12452,12452,MONDO:0002807,bronchial neoplasm,MONDO,disease,DISEASE_12452
12453,12453,12453,12453,12453,12453,12453,12453,MONDO:0009890,Gillessen-Kaesbach-Nishimura syndrome,MONDO,disease,DISEASE_12453
12454,12454,12454,12454,12454,12454,12454,12454,MONDO:0014957,language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia,MONDO,disease,DISEASE_12454
12455,12455,12455,12455,12455,12455,12455,12455,MONDO:1012231_MONDO:1012232,"pulmonary adenomatosis, dog",MONDO_grouped,disease,DISEASE_12455
12456,12456,12456,12456,12456,12456,12456,12456,MONDO:0004756,nasal cavity neoplasm,MONDO,disease,DISEASE_12456
12457,12457,12457,12457,12457,12457,12457,12457,MONDO:0009485,"oculocerebrofacial syndrome, Kaufman type",MONDO,disease,DISEASE_12457
12458,12458,12458,12458,12458,12458,12458,12458,MONDO:0022790,cleft tongue,MONDO,disease,DISEASE_12458
12459,12459,12459,12459,12459,12459,12459,12459,MONDO:0001100,hypertrophy of breast,MONDO,disease,DISEASE_12459
12460,12460,12460,12460,12460,12460,12460,12460,MONDO:0020726,"tubulointerstitial kidney disease, autosomal dominant, 2",MONDO,disease,DISEASE_12460
12461,12461,12461,12461,12461,12461,12461,12461,MONDO:0010592,focal dermal hypoplasia,MONDO,disease,DISEASE_12461
12462,12462,12462,12462,12462,12462,12462,12462,MONDO:0003245,aflatoxin-related hepatocellular carcinoma,MONDO,disease,DISEASE_12462
12463,12463,12463,12463,12463,12463,12463,12463,MONDO:0006040,lactic acidosis,MONDO,disease,DISEASE_12463
12464,12464,12464,12464,12464,12464,12464,12464,MONDO:0003475,papillary ependymoma,MONDO,disease,DISEASE_12464
12465,12465,12465,12465,12465,12465,12465,12465,MONDO:0004626,obsolete Hodgkin's paragranuloma,MONDO,disease,DISEASE_12465
12466,12466,12466,12466,12466,12466,12466,12466,MONDO:1012279_MONDO:1012280,"tremor, dog",MONDO_grouped,disease,DISEASE_12466
12467,12467,12467,12467,12467,12467,12467,12467,MONDO:0027664,cisplatin toxicity,MONDO,disease,DISEASE_12467
12468,12468,12468,12468,12468,12468,12468,12468,MONDO:0009058,cystathioninuria,MONDO,disease,DISEASE_12468
12469,12469,12469,12469,12469,12469,12469,12469,MONDO:0015614_MONDO:0006565,dermatitis herpetiformis,MONDO_grouped,disease,DISEASE_12469
12470,12470,12470,12470,12470,12470,12470,12470,MONDO:0850196,medulloblastoma WNT activated,MONDO,disease,DISEASE_12470
12471,12471,12471,12471,12471,12471,12471,12471,MONDO:0006158,colorectal diffuse large B-cell lymphoma,MONDO,disease,DISEASE_12471
12472,12472,12472,12472,12472,12472,12472,12472,MONDO:0017799,Meigs syndrome,MONDO,disease,DISEASE_12472
12473,12473,12473,12473,12473,12473,12473,12473,MONDO:0859265,neurodevelopmental disorder with epilepsy and brain atrophy,MONDO,disease,DISEASE_12473
12474,12474,12474,12474,12474,12474,12474,12474,MONDO:0006916,postcholecystectomy syndrome,MONDO,disease,DISEASE_12474
12475,12475,12475,12475,12475,12475,12475,12475,MONDO:0015840_MONDO:0015841,complete septate uterus,MONDO_grouped,disease,DISEASE_12475
12476,12476,12476,12476,12476,12476,12476,12476,MONDO:0024278,proctocolitis,MONDO,disease,DISEASE_12476
12477,12477,12477,12477,12477,12477,12477,12477,MONDO:0020129,acquired motor neuron disease,MONDO,disease,DISEASE_12477
12478,12478,12478,12478,12478,12478,12478,12478,MONDO:0003065,nasal cavity inverting papilloma,MONDO,disease,DISEASE_12478
12479,12479,12479,12479,12479,12479,12479,12479,MONDO:0018585,pediatric arterial ischemic stroke,MONDO,disease,DISEASE_12479
12480,12480,12480,12480,12480,12480,12480,12480,MONDO:0002968,lymphocele,MONDO,disease,DISEASE_12480
12481,12481,12481,12481,12481,12481,12481,12481,MONDO:0800134,primary immunodeficiency due to calcium channel deficiency,MONDO,disease,DISEASE_12481
12482,12482,12482,12482,12482,12482,12482,12482,MONDO:0004965,acinar cell carcinoma,MONDO,disease,DISEASE_12482
12483,12483,12483,12483,12483,12483,12483,12483,MONDO:0008078,"neurofibromatosis, familial spinal",MONDO,disease,DISEASE_12483
12484,12484,12484,12484,12484,12484,12484,12484,MONDO:0019768,"X-linked intellectual disability, Golabi-Ito-hall type",MONDO,disease,DISEASE_12484
12485,12485,12485,12485,12485,12485,12485,12485,MONDO:0005827,lipoatrophic diabetes,MONDO,disease,DISEASE_12485
12486,12486,12486,12486,12486,12486,12486,12486,MONDO:0016048,"isolated autosomal dominant hypomagnesemia, Glaudemans type",MONDO,disease,DISEASE_12486
12487,12487,12487,12487,12487,12487,12487,12487,MONDO:0014773,cardiac anomalies - developmental delay - facial dysmorphism syndrome,MONDO,disease,DISEASE_12487
12488,12488,12488,12488,12488,12488,12488,12488,MONDO:0002578_MONDO:0003992_MONDO:0004012,botryoid rhabdomyosarcoma,MONDO_grouped,disease,DISEASE_12488
12489,12489,12489,12489,12489,12489,12489,12489,MONDO:0005314,relapsing-remitting multiple sclerosis,MONDO,disease,DISEASE_12489
12490,12490,12490,12490,12490,12490,12490,12490,MONDO:0800141,MAN2B2 deficiency,MONDO,disease,DISEASE_12490
12491,12491,12491,12491,12491,12491,12491,12491,MONDO:0019835_MONDO:0021156,primary hypophysitis,MONDO_grouped,disease,DISEASE_12491
12492,12492,12492,12492,12492,12492,12492,12492,MONDO:0006464,thyroid gland mucosa-associated lymphoid tissue lymphoma,MONDO,disease,DISEASE_12492
12493,12493,12493,12493,12493,12493,12493,12493,MONDO:0009775_MONDO:0013259,Oguchi disease-1,MONDO_grouped,disease,DISEASE_12493
12494,12494,12494,12494,12494,12494,12494,12494,MONDO:0007006_MONDO:0001459,ulnar neuropathy,MONDO_grouped,disease,DISEASE_12494
12495,12495,12495,12495,12495,12495,12495,12495,MONDO:0006585,neurodermatitis,MONDO,disease,DISEASE_12495
12496,12496,12496,12496,12496,12496,12496,12496,MONDO:0002821,trabecular follicular adenocarcinoma,MONDO,disease,DISEASE_12496
12497,12497,12497,12497,12497,12497,12497,12497,MONDO:0004611,soft palate cancer,MONDO,disease,DISEASE_12497
12498,12498,12498,12498,12498,12498,12498,12498,MONDO:0013921_MONDO:0013920_MONDO:0024563_MONDO:0014680_MONDO:0013075,"herpes simplex encephalitis, susceptibility to",MONDO_grouped,disease,DISEASE_12498
12499,12499,12499,12499,12499,12499,12499,12499,MONDO:0018669,snakebite envenomation,MONDO,disease,DISEASE_12499
12500,12500,12500,12500,12500,12500,12500,12500,MONDO:0007946,jaw-winking syndrome,MONDO,disease,DISEASE_12500
12501,12501,12501,12501,12501,12501,12501,12501,MONDO:0019582,self-healing papular mucinosis,MONDO,disease,DISEASE_12501
12502,12502,12502,12502,12502,12502,12502,12502,MONDO:0023370,neoplastic disease or syndrome,MONDO,disease,DISEASE_12502
12503,12503,12503,12503,12503,12503,12503,12503,MONDO:0002598,germinoma,MONDO,disease,DISEASE_12503
12504,12504,12504,12504,12504,12504,12504,12504,MONDO:0022178,chromosome 13q-mosaicism,MONDO,disease,DISEASE_12504
12505,12505,12505,12505,12505,12505,12505,12505,MONDO:0001828,acquired color blindness,MONDO,disease,DISEASE_12505
12506,12506,12506,12506,12506,12506,12506,12506,MONDO:0016090,late-infantile/juvenile Krabbe disease,MONDO,disease,DISEASE_12506
12507,12507,12507,12507,12507,12507,12507,12507,MONDO:0031044,"advance sleep phase syndrome, familial, 4",MONDO,disease,DISEASE_12507
12508,12508,12508,12508,12508,12508,12508,12508,MONDO:0011215,osteocraniostenosis,MONDO,disease,DISEASE_12508
12509,12509,12509,12509,12509,12509,12509,12509,MONDO:0100518,hereditary attention deficit-hyperactivity disorder,MONDO,disease,DISEASE_12509
12510,12510,12510,12510,12510,12510,12510,12510,MONDO:0002116,malignant exocrine pancreas neoplasm,MONDO,disease,DISEASE_12510
12511,12511,12511,12511,12511,12511,12511,12511,MONDO:0016968,partial trisomy of the long arm of chromosome 18,MONDO,disease,DISEASE_12511
12512,12512,12512,12512,12512,12512,12512,12512,MONDO:0011966,"periventricular heterotopia with microcephaly, autosomal recessive",MONDO,disease,DISEASE_12512
12513,12513,12513,12513,12513,12513,12513,12513,MONDO:0021451,benign neoplasm of brain,MONDO,disease,DISEASE_12513
12514,12514,12514,12514,12514,12514,12514,12514,MONDO:0003697,non-invasive verrucous carcinoma of the penis,MONDO,disease,DISEASE_12514
12515,12515,12515,12515,12515,12515,12515,12515,MONDO:0010505,intellectual disability-balding-patella luxation-acromicria syndrome,MONDO,disease,DISEASE_12515
12516,12516,12516,12516,12516,12516,12516,12516,MONDO:0014870,NEK9-related lethal skeletal dysplasia,MONDO,disease,DISEASE_12516
12517,12517,12517,12517,12517,12517,12517,12517,MONDO:1012348_MONDO:1012349,"recessive hypotrichosis, dog",MONDO_grouped,disease,DISEASE_12517
12518,12518,12518,12518,12518,12518,12518,12518,MONDO:0020820_MONDO:0007157_MONDO:0032751_MONDO:0957819_MONDO:0014028_MONDO:0032750_MONDO:0016675_MONDO:0030847_MONDO:0013698_MONDO:0007364_MONDO:0800200,"arthrogryposis, distal,",MONDO_grouped,disease,DISEASE_12518
12519,12519,12519,12519,12519,12519,12519,12519,MONDO:0013424,3p- syndrome,MONDO,disease,DISEASE_12519
12520,12520,12520,12520,12520,12520,12520,12520,MONDO:0010754,van den Bosch syndrome,MONDO,disease,DISEASE_12520
12521,12521,12521,12521,12521,12521,12521,12521,MONDO:0002164_MONDO:0001393,focal chorioretinitis,MONDO_grouped,disease,DISEASE_12521
12522,12522,12522,12522,12522,12522,12522,12522,MONDO:0014872_MONDO:0013807_MONDO:0014614_MONDO:0013183_MONDO:0009758_MONDO:0010690_MONDO:0010241_MONDO:0032811_MONDO:0014026_MONDO:0013450_MONDO:0016293,congenital stationary night blindness,MONDO_grouped,disease,DISEASE_12522
12523,12523,12523,12523,12523,12523,12523,12523,MONDO:0009509,Landau-Kleffner syndrome,MONDO,disease,DISEASE_12523
12524,12524,12524,12524,12524,12524,12524,12524,MONDO:0008585,HELLP syndrome,MONDO,disease,DISEASE_12524
12525,12525,12525,12525,12525,12525,12525,12525,MONDO:0100447,ATF6-related retinopathy,MONDO,disease,DISEASE_12525
12526,12526,12526,12526,12526,12526,12526,12526,MONDO:0013615,craniosynostosis and dental anomalies,MONDO,disease,DISEASE_12526
12527,12527,12527,12527,12527,12527,12527,12527,MONDO:0018027,duplication/inversion 15q11,MONDO,disease,DISEASE_12527
12528,12528,12528,12528,12528,12528,12528,12528,MONDO:0015521,juvenile or adult CACH syndrome,MONDO,disease,DISEASE_12528
12529,12529,12529,12529,12529,12529,12529,12529,MONDO:0024377_MONDO:0024378,"circadian rhythm sleep disorder, delayed sleep phase type",MONDO_grouped,disease,DISEASE_12529
12530,12530,12530,12530,12530,12530,12530,12530,MONDO:0010436,chromosome Xq28 duplication syndrome,MONDO,disease,DISEASE_12530
12531,12531,12531,12531,12531,12531,12531,12531,MONDO:0009854,"peroneus tertius muscle, absence of",MONDO,disease,DISEASE_12531
12532,12532,12532,12532,12532,12532,12532,12532,MONDO:0011915_MONDO:0012569,"mitral valve prolapse, myxomatous",MONDO_grouped,disease,DISEASE_12532
12533,12533,12533,12533,12533,12533,12533,12533,MONDO:0017372,congenital varicella syndrome,MONDO,disease,DISEASE_12533
12534,12534,12534,12534,12534,12534,12534,12534,MONDO:0800140,ITPKB deficiency,MONDO,disease,DISEASE_12534
12535,12535,12535,12535,12535,12535,12535,12535,MONDO:0007657,giant neutrophil leukocytes,MONDO,disease,DISEASE_12535
12536,12536,12536,12536,12536,12536,12536,12536,MONDO:0019129,global developmental delay-osteopenia-ectodermal defect syndrome,MONDO,disease,DISEASE_12536
12537,12537,12537,12537,12537,12537,12537,12537,MONDO:0010334,severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome,MONDO,disease,DISEASE_12537
12538,12538,12538,12538,12538,12538,12538,12538,MONDO:0009354,methylcobalamin deficiency type cblE,MONDO,disease,DISEASE_12538
12539,12539,12539,12539,12539,12539,12539,12539,MONDO:0008931,Cenani-Lenz syndactyly syndrome,MONDO,disease,DISEASE_12539
12540,12540,12540,12540,12540,12540,12540,12540,MONDO:0005361_MONDO:0005407,eosinophilic esophagitis,MONDO_grouped,disease,DISEASE_12540
12541,12541,12541,12541,12541,12541,12541,12541,MONDO:0045054,cancer-related condition,MONDO,disease,DISEASE_12541
12542,12542,12542,12542,12542,12542,12542,12542,MONDO:0016758,microcephaly-brain defect-spasticity-hypernatremia syndrome,MONDO,disease,DISEASE_12542
12543,12543,12543,12543,12543,12543,12543,12543,MONDO:0012057,"legionnaire disease, susceptibility to",MONDO,disease,DISEASE_12543
12544,12544,12544,12544,12544,12544,12544,12544,MONDO:0003937_MONDO:0005541_MONDO:0002253,spondylitis,MONDO_grouped,disease,DISEASE_12544
12545,12545,12545,12545,12545,12545,12545,12545,MONDO:0009009,hypoplasminogenemia,MONDO,disease,DISEASE_12545
12546,12546,12546,12546,12546,12546,12546,12546,MONDO:0002249,thrombocytosis disease,MONDO,disease,DISEASE_12546
12547,12547,12547,12547,12547,12547,12547,12547,MONDO:0000271,tuberculous salpingitis,MONDO,disease,DISEASE_12547
12548,12548,12548,12548,12548,12548,12548,12548,MONDO:0010110,tetraamelia-multiple malformations syndrome,MONDO,disease,DISEASE_12548
12549,12549,12549,12549,12549,12549,12549,12549,MONDO:0007212,brachydactyly-long thumb syndrome,MONDO,disease,DISEASE_12549
12550,12550,12550,12550,12550,12550,12550,12550,MONDO:0000902,agenesis of the corpus callosum with peripheral neuropathy,MONDO,disease,DISEASE_12550
12551,12551,12551,12551,12551,12551,12551,12551,MONDO:0040797,obsolete vascular headache,MONDO,disease,DISEASE_12551
12552,12552,12552,12552,12552,12552,12552,12552,MONDO:1011955,"spondylosis deformans, non-human animal",MONDO,disease,DISEASE_12552
12553,12553,12553,12553,12553,12553,12553,12553,MONDO:0024611,orbit neoplasm,MONDO,disease,DISEASE_12553
12554,12554,12554,12554,12554,12554,12554,12554,MONDO:0001691,laryngeal cartilage cancer,MONDO,disease,DISEASE_12554
12555,12555,12555,12555,12555,12555,12555,12555,MONDO:0019210,cutaneous neuroendocrine carcinoma,MONDO,disease,DISEASE_12555
12556,12556,12556,12556,12556,12556,12556,12556,MONDO:0013624,Rafiq syndrome,MONDO,disease,DISEASE_12556
12557,12557,12557,12557,12557,12557,12557,12557,MONDO:0009668,lethal multiple pterygium syndrome,MONDO,disease,DISEASE_12557
12558,12558,12558,12558,12558,12558,12558,12558,MONDO:0008959,CHAND syndrome,MONDO,disease,DISEASE_12558
12559,12559,12559,12559,12559,12559,12559,12559,MONDO:0009547,macrosomia-microphthalmia-cleft palate syndrome,MONDO,disease,DISEASE_12559
12560,12560,12560,12560,12560,12560,12560,12560,MONDO:0003960,pulmonary large cell neuroendocrine carcinoma,MONDO,disease,DISEASE_12560
12561,12561,12561,12561,12561,12561,12561,12561,MONDO:1011812,"ocular squamous cell carcinoma, non-human animal",MONDO,disease,DISEASE_12561
12562,12562,12562,12562,12562,12562,12562,12562,MONDO:0007028,rotator cuff syndrome,MONDO,disease,DISEASE_12562
12563,12563,12563,12563,12563,12563,12563,12563,MONDO:0009607,methionine adenosyltransferase deficiency,MONDO,disease,DISEASE_12563
12564,12564,12564,12564,12564,12564,12564,12564,MONDO:0009063,ventriculomegaly-cystic kidney disease,MONDO,disease,DISEASE_12564
12565,12565,12565,12565,12565,12565,12565,12565,MONDO:0013177,congenital muscular dystrophy due to integrin alpha-7 deficiency,MONDO,disease,DISEASE_12565
12566,12566,12566,12566,12566,12566,12566,12566,MONDO:0014575_MONDO:0024535,Singleton-Merten syndrome,MONDO_grouped,disease,DISEASE_12566
12567,12567,12567,12567,12567,12567,12567,12567,MONDO:0004098,malignant melanocytic peripheral nerve sheath tumor of mediastinum,MONDO,disease,DISEASE_12567
12568,12568,12568,12568,12568,12568,12568,12568,MONDO:0002371,breast pericanalicular fibroadenoma,MONDO,disease,DISEASE_12568
12569,12569,12569,12569,12569,12569,12569,12569,MONDO:1011789,"fibrodysplasia ossificans, non-human animal",MONDO,disease,DISEASE_12569
12570,12570,12570,12570,12570,12570,12570,12570,MONDO:0015534_MONDO:0024617_MONDO:0004385,juvenile xanthogranuloma,MONDO_grouped,disease,DISEASE_12570
12571,12571,12571,12571,12571,12571,12571,12571,MONDO:0004821,nasopharyngeal disorder,MONDO,disease,DISEASE_12571
12572,12572,12572,12572,12572,12572,12572,12572,MONDO:0004805,leukocyte disorder,MONDO,disease,DISEASE_12572
12573,12573,12573,12573,12573,12573,12573,12573,MONDO:0007763,nonpapillary renal cell carcinoma,MONDO,disease,DISEASE_12573
12574,12574,12574,12574,12574,12574,12574,12574,MONDO:1012955,"arachnomelia syndrome, non-human animal",MONDO,disease,DISEASE_12574
12575,12575,12575,12575,12575,12575,12575,12575,MONDO:0005533,distal colitis,MONDO,disease,DISEASE_12575
12576,12576,12576,12576,12576,12576,12576,12576,MONDO:0009518_MONDO:0011860_MONDO:0012358_MONDO:0012595_MONDO:0013185_MONDO:0013257,"leprosy, susceptibility to",MONDO_grouped,disease,DISEASE_12576
12577,12577,12577,12577,12577,12577,12577,12577,MONDO:0009489,"hereditary palmoplantar keratoderma, Gamborg-Nielsen type",MONDO,disease,DISEASE_12577
12578,12578,12578,12578,12578,12578,12578,12578,MONDO:0001296,acquired night blindness,MONDO,disease,DISEASE_12578
12579,12579,12579,12579,12579,12579,12579,12579,MONDO:0004091,skin basaloid carcinoma,MONDO,disease,DISEASE_12579
12580,12580,12580,12580,12580,12580,12580,12580,MONDO:0044765,steroid-resistant nephrotic syndrome,MONDO,disease,DISEASE_12580
12581,12581,12581,12581,12581,12581,12581,12581,MONDO:0002361,transverse colon cancer,MONDO,disease,DISEASE_12581
12582,12582,12582,12582,12582,12582,12582,12582,MONDO:0007327,"chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase",MONDO,disease,DISEASE_12582
12583,12583,12583,12583,12583,12583,12583,12583,MONDO:0016086,osteochondritis of tarsal/metatarsal bone,MONDO,disease,DISEASE_12583
12584,12584,12584,12584,12584,12584,12584,12584,MONDO:0017177,hemihyperplasia-multiple lipomatosis syndrome,MONDO,disease,DISEASE_12584
12585,12585,12585,12585,12585,12585,12585,12585,MONDO:0700167,canine sebaceous gland epithelioma,MONDO,disease,DISEASE_12585
12586,12586,12586,12586,12586,12586,12586,12586,MONDO:0000470,endocardium disorder,MONDO,disease,DISEASE_12586
12587,12587,12587,12587,12587,12587,12587,12587,MONDO:0023138,Feingold trainer syndrome,MONDO,disease,DISEASE_12587
12588,12588,12588,12588,12588,12588,12588,12588,MONDO:0002085,benign shuddering attacks,MONDO,disease,DISEASE_12588
12589,12589,12589,12589,12589,12589,12589,12589,MONDO:0024612,manic bipolar affective disorder,MONDO,disease,DISEASE_12589
12590,12590,12590,12590,12590,12590,12590,12590,MONDO:0009512,lethal Larsen-like syndrome,MONDO,disease,DISEASE_12590
12591,12591,12591,12591,12591,12591,12591,12591,MONDO:0015432,ring chromosome 12,MONDO,disease,DISEASE_12591
12592,12592,12592,12592,12592,12592,12592,12592,MONDO:0004881,myositis fibrosa,MONDO,disease,DISEASE_12592
12593,12593,12593,12593,12593,12593,12593,12593,MONDO:0001965,sclerosing keratitis,MONDO,disease,DISEASE_12593
12594,12594,12594,12594,12594,12594,12594,12594,MONDO:0011795,anonychia-microcephaly syndrome,MONDO,disease,DISEASE_12594
12595,12595,12595,12595,12595,12595,12595,12595,MONDO:0004081,extrahepatic bile duct clear cell adenocarcinoma,MONDO,disease,DISEASE_12595
12596,12596,12596,12596,12596,12596,12596,12596,MONDO:0023040,ectodermal dysplasia Bartalos type,MONDO,disease,DISEASE_12596
12597,12597,12597,12597,12597,12597,12597,12597,MONDO:0003950,nipple carcinoma,MONDO,disease,DISEASE_12597
12598,12598,12598,12598,12598,12598,12598,12598,MONDO:0019971,melanoma of soft tissue,MONDO,disease,DISEASE_12598
12599,12599,12599,12599,12599,12599,12599,12599,MONDO:0021658,vascular ectasia,MONDO,disease,DISEASE_12599
12600,12600,12600,12600,12600,12600,12600,12600,MONDO:0019869,mosaic trisomy 22,MONDO,disease,DISEASE_12600
12601,12601,12601,12601,12601,12601,12601,12601,MONDO:0008424,"sella turcica, bridged",MONDO,disease,DISEASE_12601
12602,12602,12602,12602,12602,12602,12602,12602,MONDO:0008551,thoracolaryngopelvic dysplasia,MONDO,disease,DISEASE_12602
12603,12603,12603,12603,12603,12603,12603,12603,MONDO:0023196,frontonasal malformation cloacal exstrophy,MONDO,disease,DISEASE_12603
12604,12604,12604,12604,12604,12604,12604,12604,MONDO:0036217,lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to a point mutation,MONDO,disease,DISEASE_12604
12605,12605,12605,12605,12605,12605,12605,12605,MONDO:1011335,"musculoskeletal system disorder, non-human animal",MONDO,disease,DISEASE_12605
12606,12606,12606,12606,12606,12606,12606,12606,MONDO:0018950,3-methylcrotonyl-CoA carboxylase deficiency,MONDO,disease,DISEASE_12606
12607,12607,12607,12607,12607,12607,12607,12607,MONDO:0024654,skull disorder,MONDO,disease,DISEASE_12607
12608,12608,12608,12608,12608,12608,12608,12608,MONDO:0004837,neurofibroma of the esophagus,MONDO,disease,DISEASE_12608
12609,12609,12609,12609,12609,12609,12609,12609,MONDO:0017043_MONDO:0004454_MONDO:0004455,congenital mesoblastic nephroma,MONDO_grouped,disease,DISEASE_12609
12610,12610,12610,12610,12610,12610,12610,12610,MONDO:0006840,lymphangiectasis,MONDO,disease,DISEASE_12610
12611,12611,12611,12611,12611,12611,12611,12611,MONDO:0006226,gastric mucosa-associated lymphoid tissue lymphoma,MONDO,disease,DISEASE_12611
12612,12612,12612,12612,12612,12612,12612,12612,MONDO:0001788,nutmeg liver,MONDO,disease,DISEASE_12612
12613,12613,12613,12613,12613,12613,12613,12613,MONDO:0024350,pityriasis steatoides,MONDO,disease,DISEASE_12613
12614,12614,12614,12614,12614,12614,12614,12614,MONDO:0006213,floor of mouth mucoepidermoid carcinoma,MONDO,disease,DISEASE_12614
12615,12615,12615,12615,12615,12615,12615,12615,MONDO:0016595,inhalational anthrax,MONDO,disease,DISEASE_12615
12616,12616,12616,12616,12616,12616,12616,12616,MONDO:0008290,"porokeratosis 1, Mibelli type",MONDO,disease,DISEASE_12616
12617,12617,12617,12617,12617,12617,12617,12617,MONDO:0850461,neurobehavioral disorder with prenatal alcohol exposure,MONDO,disease,DISEASE_12617
12618,12618,12618,12618,12618,12618,12618,12618,MONDO:0014456,autosomal recessive severe congenital neutropenia due to JAGN1 deficiency,MONDO,disease,DISEASE_12618
12619,12619,12619,12619,12619,12619,12619,12619,MONDO:0012401,congenital stromal corneal dystrophy,MONDO,disease,DISEASE_12619
12620,12620,12620,12620,12620,12620,12620,12620,MONDO:0001374_MONDO:0001381,kidney sarcoma,MONDO_grouped,disease,DISEASE_12620
12621,12621,12621,12621,12621,12621,12621,12621,MONDO:0018226,infantile epileptic-dyskinetic encephalopathy,MONDO,disease,DISEASE_12621
12622,12622,12622,12622,12622,12622,12622,12622,MONDO:0009864,"phosphoenolpyruvate carboxykinase deficiency, mitochondrial",MONDO,disease,DISEASE_12622
12623,12623,12623,12623,12623,12623,12623,12623,MONDO:0100442_MONDO:0100445_MONDO:0700235,RP2-related retinopathy,MONDO_grouped,disease,DISEASE_12623
12624,12624,12624,12624,12624,12624,12624,12624,MONDO:0015986,bilateral renal agenesis,MONDO,disease,DISEASE_12624
12625,12625,12625,12625,12625,12625,12625,12625,MONDO:0008886,Sabinas brittle hair syndrome,MONDO,disease,DISEASE_12625
12626,12626,12626,12626,12626,12626,12626,12626,MONDO:0013267,distal 16p11.2 microdeletion syndrome,MONDO,disease,DISEASE_12626
12627,12627,12627,12627,12627,12627,12627,12627,MONDO:0003524,gastric gastrin-producing neuroendocrine tumor,MONDO,disease,DISEASE_12627
12628,12628,12628,12628,12628,12628,12628,12628,MONDO:0002954,superficial multifocal basal cell carcinoma,MONDO,disease,DISEASE_12628
12629,12629,12629,12629,12629,12629,12629,12629,MONDO:0006290,malignant germ cell tumor,MONDO,disease,DISEASE_12629
12630,12630,12630,12630,12630,12630,12630,12630,MONDO:0014220,myopathy due to myoadenylate deaminase deficiency,MONDO,disease,DISEASE_12630
12631,12631,12631,12631,12631,12631,12631,12631,MONDO:0016609,inflammatory myopathy with abundant macrophages,MONDO,disease,DISEASE_12631
12632,12632,12632,12632,12632,12632,12632,12632,MONDO:0016483,intracranial berry aneurysm,MONDO,disease,DISEASE_12632
12633,12633,12633,12633,12633,12633,12633,12633,MONDO:0012124,sudden infant death-dysgenesis of the testes syndrome,MONDO,disease,DISEASE_12633
12634,12634,12634,12634,12634,12634,12634,12634,MONDO:1010720_MONDO:1010721,"tyrosinemia type 1, FAH-related, pig",MONDO_grouped,disease,DISEASE_12634
12635,12635,12635,12635,12635,12635,12635,12635,MONDO:0009034_MONDO:0000486,craniofacial dyssynostosis,MONDO_grouped,disease,DISEASE_12635
12636,12636,12636,12636,12636,12636,12636,12636,MONDO:0859160_MONDO:0859520_MONDO:0700250,"mitochondrial complex IV deficiency, nuclear",MONDO_grouped,disease,DISEASE_12636
12637,12637,12637,12637,12637,12637,12637,12637,MONDO:0004418,microcystic variant infiltrating bladder urothelial carcinoma,MONDO,disease,DISEASE_12637
12638,12638,12638,12638,12638,12638,12638,12638,MONDO:0019962_MONDO:0003028,thyroid lymphoma,MONDO_grouped,disease,DISEASE_12638
12639,12639,12639,12639,12639,12639,12639,12639,MONDO:0010244,CGF1,MONDO,disease,DISEASE_12639
12640,12640,12640,12640,12640,12640,12640,12640,MONDO:0100344_MONDO:0010503_MONDO:0000909_MONDO:0009424_MONDO:0011242_MONDO:0011822_MONDO:0015231,Bartter disease,MONDO_grouped,disease,DISEASE_12640
12641,12641,12641,12641,12641,12641,12641,12641,MONDO:0019408,Astley-Kendall dysplasia,MONDO,disease,DISEASE_12641
12642,12642,12642,12642,12642,12642,12642,12642,MONDO:0005212,rhabdomyosarcoma,MONDO,disease,DISEASE_12642
12643,12643,12643,12643,12643,12643,12643,12643,MONDO:0006831_MONDO:0002769,leukostasis,MONDO_grouped,disease,DISEASE_12643
12644,12644,12644,12644,12644,12644,12644,12644,MONDO:0042705,prostatic malacoplakia associated with prostatic abscess,MONDO,disease,DISEASE_12644
12645,12645,12645,12645,12645,12645,12645,12645,MONDO:0021315,malignant tumor of nasopharynx,MONDO,disease,DISEASE_12645
12646,12646,12646,12646,12646,12646,12646,12646,MONDO:0012815,Coats plus syndrome,MONDO,disease,DISEASE_12646
12647,12647,12647,12647,12647,12647,12647,12647,MONDO:0004526,mixed endometrial stromal and smooth muscle tumor,MONDO,disease,DISEASE_12647
12648,12648,12648,12648,12648,12648,12648,12648,MONDO:0014298,chromosome 5q12 deletion syndrome,MONDO,disease,DISEASE_12648
12649,12649,12649,12649,12649,12649,12649,12649,MONDO:0025086,"hip dysplasia, canine",MONDO,disease,DISEASE_12649
12650,12650,12650,12650,12650,12650,12650,12650,MONDO:0010612,hydrocephaly-cerebellar agenesis syndrome,MONDO,disease,DISEASE_12650
12651,12651,12651,12651,12651,12651,12651,12651,MONDO:1012450,"leukoencephalomyelopathy, dog",MONDO,disease,DISEASE_12651
12652,12652,12652,12652,12652,12652,12652,12652,MONDO:1011433_MONDO:1011434,"hyperkalemic periodic paralysis, non-human animal",MONDO_grouped,disease,DISEASE_12652
12653,12653,12653,12653,12653,12653,12653,12653,MONDO:0008185_MONDO:0005003,hereditary chronic pancreatitis,MONDO_grouped,disease,DISEASE_12653
12654,12654,12654,12654,12654,12654,12654,12654,MONDO:0017980,syngnathia multiple anomalies,MONDO,disease,DISEASE_12654
12655,12655,12655,12655,12655,12655,12655,12655,MONDO:0003317,metachronous kidney Wilms' tumor,MONDO,disease,DISEASE_12655
12656,12656,12656,12656,12656,12656,12656,12656,MONDO:0004390,ocular hypotension,MONDO,disease,DISEASE_12656
12657,12657,12657,12657,12657,12657,12657,12657,MONDO:0043089,acute posterior multifocal placoid pigment epitheliopathy,MONDO,disease,DISEASE_12657
12658,12658,12658,12658,12658,12658,12658,12658,MONDO:1011680,"postpartum dysgalactia syndrome, non-human animal",MONDO,disease,DISEASE_12658
12659,12659,12659,12659,12659,12659,12659,12659,MONDO:0013885,Malan overgrowth syndrome,MONDO,disease,DISEASE_12659
12660,12660,12660,12660,12660,12660,12660,12660,MONDO:0002752_MONDO:0002880_MONDO:0003035,ovarian adenocarcinoma,MONDO_grouped,disease,DISEASE_12660
12661,12661,12661,12661,12661,12661,12661,12661,MONDO:0030355_MONDO:0008030_MONDO:0008031_MONDO:0030354_MONDO:0001347,"facioscapulohumeral muscular dystrophy 4, digenic",MONDO_grouped,disease,DISEASE_12661
12662,12662,12662,12662,12662,12662,12662,12662,MONDO:0006680,blue nevus,MONDO,disease,DISEASE_12662
12663,12663,12663,12663,12663,12663,12663,12663,MONDO:1012332,"hemophagocytic syndrome, dog",MONDO,disease,DISEASE_12663
12664,12664,12664,12664,12664,12664,12664,12664,MONDO:0021637,low grade glioma,MONDO,disease,DISEASE_12664
12665,12665,12665,12665,12665,12665,12665,12665,MONDO:0010364,X-linked intellectual disability-retinitis pigmentosa syndrome,MONDO,disease,DISEASE_12665
12666,12666,12666,12666,12666,12666,12666,12666,MONDO:0011672,persistent polyclonal B-cell lymphocytosis,MONDO,disease,DISEASE_12666
12667,12667,12667,12667,12667,12667,12667,12667,MONDO:0004959,plasma cell neoplasm,MONDO,disease,DISEASE_12667
12668,12668,12668,12668,12668,12668,12668,12668,MONDO:1012959,"hereditary ataxia, non-human animal",MONDO,disease,DISEASE_12668
12669,12669,12669,12669,12669,12669,12669,12669,MONDO:0008633,Muckle-Wells syndrome,MONDO,disease,DISEASE_12669
12670,12670,12670,12670,12670,12670,12670,12670,MONDO:0030338_MONDO:0008791_MONDO:0000819,anencephaly,MONDO_grouped,disease,DISEASE_12670
12671,12671,12671,12671,12671,12671,12671,12671,MONDO:0100150_MONDO:0800462,RYR1-related myopathy,MONDO_grouped,disease,DISEASE_12671
12672,12672,12672,12672,12672,12672,12672,12672,MONDO:0034103,infection-related hemolytic uremic syndrome,MONDO,disease,DISEASE_12672
12673,12673,12673,12673,12673,12673,12673,12673,MONDO:1012791_MONDO:1012797_MONDO:1012798_MONDO:1012921,"osteogenesis imperfecta, COL1A2-related, dog",MONDO_grouped,disease,DISEASE_12673
12674,12674,12674,12674,12674,12674,12674,12674,MONDO:0957008,hereditary cerebral malformation,MONDO,disease,DISEASE_12674
12675,12675,12675,12675,12675,12675,12675,12675,MONDO:0009838,Parana hard-skin syndrome,MONDO,disease,DISEASE_12675
12676,12676,12676,12676,12676,12676,12676,12676,MONDO:1011341,"omphalitis, non-human animal",MONDO,disease,DISEASE_12676
12677,12677,12677,12677,12677,12677,12677,12677,MONDO:0012381,hyperinsulinism due to INSR deficiency,MONDO,disease,DISEASE_12677
12678,12678,12678,12678,12678,12678,12678,12678,MONDO:0011211,axial spondylometaphyseal dysplasia,MONDO,disease,DISEASE_12678
12679,12679,12679,12679,12679,12679,12679,12679,MONDO:0014031_MONDO:0009616,"microcephalic primordial dwarfism, Alazami type",MONDO_grouped,disease,DISEASE_12679
12680,12680,12680,12680,12680,12680,12680,12680,MONDO:0044702,X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome,MONDO,disease,DISEASE_12680
12681,12681,12681,12681,12681,12681,12681,12681,MONDO:1011862,"tremor syndrome with central axonopathy, non-human animal",MONDO,disease,DISEASE_12681
12682,12682,12682,12682,12682,12682,12682,12682,MONDO:0850066,SAMD9L-associated autoinflammatory syndrome,MONDO,disease,DISEASE_12682
12683,12683,12683,12683,12683,12683,12683,12683,MONDO:0003994_MONDO:0003995,botryoid-type embryonal rhabdomyosarcoma of the vagina,MONDO_grouped,disease,DISEASE_12683
12684,12684,12684,12684,12684,12684,12684,12684,MONDO:0017332,pyoderma gangrenosum-acne-suppurative hidradenitis syndrome,MONDO,disease,DISEASE_12684
12685,12685,12685,12685,12685,12685,12685,12685,MONDO:0019358,encephalopathy due to sulfite oxidase deficiency,MONDO,disease,DISEASE_12685
12686,12686,12686,12686,12686,12686,12686,12686,MONDO:0018705,infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome,MONDO,disease,DISEASE_12686
12687,12687,12687,12687,12687,12687,12687,12687,MONDO:1040055_MONDO:0700234_MONDO:0800395_MONDO:0800402,PRPH2-related retinopathy,MONDO_grouped,disease,DISEASE_12687
12688,12688,12688,12688,12688,12688,12688,12688,MONDO:0033850,autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect,MONDO,disease,DISEASE_12688
12689,12689,12689,12689,12689,12689,12689,12689,MONDO:0007959_MONDO:0002797_MONDO:0002794_MONDO:0000517,medulloblastoma,MONDO_grouped,disease,DISEASE_12689
12690,12690,12690,12690,12690,12690,12690,12690,MONDO:1010302,"scoliosis, non-human animal",MONDO,disease,DISEASE_12690
12691,12691,12691,12691,12691,12691,12691,12691,MONDO:0005826,lipid pneumonia,MONDO,disease,DISEASE_12691
12692,12692,12692,12692,12692,12692,12692,12692,MONDO:0012984,PHARC syndrome,MONDO,disease,DISEASE_12692
12693,12693,12693,12693,12693,12693,12693,12693,MONDO:0013549,N-acetylaspartate deficiency,MONDO,disease,DISEASE_12693
12694,12694,12694,12694,12694,12694,12694,12694,MONDO:0017327,primary non-gestational choriocarcinoma of ovary,MONDO,disease,DISEASE_12694
12695,12695,12695,12695,12695,12695,12695,12695,MONDO:0016481,silver-Russell syndrome due to 11p15 microduplication,MONDO,disease,DISEASE_12695
12696,12696,12696,12696,12696,12696,12696,12696,MONDO:0017110_MONDO:0017111,isolated Dandy-Walker malformation with hydrocephalus,MONDO_grouped,disease,DISEASE_12696
12697,12697,12697,12697,12697,12697,12697,12697,MONDO:0007134,Cooks syndrome,MONDO,disease,DISEASE_12697
12698,12698,12698,12698,12698,12698,12698,12698,MONDO:1012774,"cerebellar cortical degeneration, SNX14-related, dog",MONDO,disease,DISEASE_12698
12699,12699,12699,12699,12699,12699,12699,12699,MONDO:0017224,Pelizaeus-Merzbacher disease in female carriers,MONDO,disease,DISEASE_12699
12700,12700,12700,12700,12700,12700,12700,12700,MONDO:1012385,"inherited periodic spasticity, cattle",MONDO,disease,DISEASE_12700
12701,12701,12701,12701,12701,12701,12701,12701,MONDO:0015443,chromosome 8-derived supernumerary ring/marker,MONDO,disease,DISEASE_12701
12702,12702,12702,12702,12702,12702,12702,12702,MONDO:0016496,pharyngeal-cervical-brachial variant of Guillain-Barre syndrome,MONDO,disease,DISEASE_12702
12703,12703,12703,12703,12703,12703,12703,12703,MONDO:0021320,malignant tumor of floor of mouth,MONDO,disease,DISEASE_12703
12704,12704,12704,12704,12704,12704,12704,12704,MONDO:1012914,"amyotrophic lateral sclerosis, TARDBP-related, crab-eating macaque",MONDO,disease,DISEASE_12704
12705,12705,12705,12705,12705,12705,12705,12705,MONDO:0018051,Jessner lymphocytic infiltration of the skin,MONDO,disease,DISEASE_12705
12706,12706,12706,12706,12706,12706,12706,12706,MONDO:0015293,segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome,MONDO,disease,DISEASE_12706
12707,12707,12707,12707,12707,12707,12707,12707,MONDO:1011038,"oculocutaneous albinism, SLC45A2-related, western gorilla",MONDO,disease,DISEASE_12707
12708,12708,12708,12708,12708,12708,12708,12708,MONDO:0002537,inverted papilloma,MONDO,disease,DISEASE_12708
12709,12709,12709,12709,12709,12709,12709,12709,MONDO:0027668,flucloxacilline toxicity,MONDO,disease,DISEASE_12709
12710,12710,12710,12710,12710,12710,12710,12710,MONDO:1010280,"priapism, non-human animal",MONDO,disease,DISEASE_12710
12711,12711,12711,12711,12711,12711,12711,12711,MONDO:0014507,Catel-Manzke syndrome,MONDO,disease,DISEASE_12711
12712,12712,12712,12712,12712,12712,12712,12712,MONDO:0044324,Al Kaissi syndrome,MONDO,disease,DISEASE_12712
12713,12713,12713,12713,12713,12713,12713,12713,MONDO:0033551,immunodeficiency 72 with autoinflammation,MONDO,disease,DISEASE_12713
12714,12714,12714,12714,12714,12714,12714,12714,MONDO:0022174,chromosome 12p deletion,MONDO,disease,DISEASE_12714
12715,12715,12715,12715,12715,12715,12715,12715,MONDO:0015277,medullary thyroid gland carcinoma,MONDO,disease,DISEASE_12715
12716,12716,12716,12716,12716,12716,12716,12716,MONDO:0019320,acanthokeratolytic verrucous nevus,MONDO,disease,DISEASE_12716
12717,12717,12717,12717,12717,12717,12717,12717,MONDO:0957260,combined low LDL and fibrinogen,MONDO,disease,DISEASE_12717
12718,12718,12718,12718,12718,12718,12718,12718,MONDO:1011641,"cardiomyopathy and woolly haircoat syndrome, non-human animal",MONDO,disease,DISEASE_12718
12719,12719,12719,12719,12719,12719,12719,12719,MONDO:0012041_MONDO:0021056_MONDO:0014630_MONDO:0044300_MONDO:0021055_MONDO:1010950_MONDO:1010951,familial adenomatous polyposis,MONDO_grouped,disease,DISEASE_12719
12720,12720,12720,12720,12720,12720,12720,12720,MONDO:0044884,tonsillar lymphoma,MONDO,disease,DISEASE_12720
12721,12721,12721,12721,12721,12721,12721,12721,MONDO:0015149,pure hereditary spastic paraplegia,MONDO,disease,DISEASE_12721
12722,12722,12722,12722,12722,12722,12722,12722,MONDO:1011029,"congenital myasthenic syndrome, CHAT-related, dog",MONDO,disease,DISEASE_12722
12723,12723,12723,12723,12723,12723,12723,12723,MONDO:0012206,spondyloepiphyseal dysplasia with metatarsal shortening,MONDO,disease,DISEASE_12723
12724,12724,12724,12724,12724,12724,12724,12724,MONDO:0054866,sudden arrhythmia death syndrome,MONDO,disease,DISEASE_12724
12725,12725,12725,12725,12725,12725,12725,12725,MONDO:0002272,polyclonal hypergammaglobulinemia,MONDO,disease,DISEASE_12725
12726,12726,12726,12726,12726,12726,12726,12726,MONDO:0013999,"retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis, and migraine headache syndrome",MONDO,disease,DISEASE_12726
12727,12727,12727,12727,12727,12727,12727,12727,MONDO:0005580,esophageal squamous cell carcinoma,MONDO,disease,DISEASE_12727
12728,12728,12728,12728,12728,12728,12728,12728,MONDO:0020488,atypical progressive supranuclear palsy syndrome,MONDO,disease,DISEASE_12728
12729,12729,12729,12729,12729,12729,12729,12729,MONDO:0006021,Prinzmetal angina,MONDO,disease,DISEASE_12729
12730,12730,12730,12730,12730,12730,12730,12730,MONDO:1010326_MONDO:1010321_MONDO:1011977_MONDO:1011978_MONDO:1011979,"retinal degeneration, non-human animal",MONDO_grouped,disease,DISEASE_12730
12731,12731,12731,12731,12731,12731,12731,12731,MONDO:0014369,postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome,MONDO,disease,DISEASE_12731
12732,12732,12732,12732,12732,12732,12732,12732,MONDO:0009555,malocclusion and short stature,MONDO,disease,DISEASE_12732
12733,12733,12733,12733,12733,12733,12733,12733,MONDO:0016925,partial trisomy/tetrasomy of chromosome 5,MONDO,disease,DISEASE_12733
12734,12734,12734,12734,12734,12734,12734,12734,MONDO:0013415,chromosome 17p13.1 deletion syndrome,MONDO,disease,DISEASE_12734
12735,12735,12735,12735,12735,12735,12735,12735,MONDO:0007446,dermatosis papulosa nigra,MONDO,disease,DISEASE_12735
12736,12736,12736,12736,12736,12736,12736,12736,MONDO:0020733_MONDO:0014125_MONDO:0008509_MONDO:0008511,proximal symphalangism,MONDO_grouped,disease,DISEASE_12736
12737,12737,12737,12737,12737,12737,12737,12737,MONDO:0016917,partial deletion of the long arm of chromosome 19,MONDO,disease,DISEASE_12737
12738,12738,12738,12738,12738,12738,12738,12738,MONDO:1010153,"Darier disease, non-human animal",MONDO,disease,DISEASE_12738
12739,12739,12739,12739,12739,12739,12739,12739,MONDO:0003311_MONDO:0001783,endometrial stromal tumor,MONDO_grouped,disease,DISEASE_12739
12740,12740,12740,12740,12740,12740,12740,12740,MONDO:0009475,isovaleric acidemia,MONDO,disease,DISEASE_12740
12741,12741,12741,12741,12741,12741,12741,12741,MONDO:0010041,Charlevoix-Saguenay spastic ataxia,MONDO,disease,DISEASE_12741
12742,12742,12742,12742,12742,12742,12742,12742,MONDO:1012252_MONDO:1012253,"spastic paresis, pig",MONDO_grouped,disease,DISEASE_12742
12743,12743,12743,12743,12743,12743,12743,12743,MONDO:0008421,flat face-microstomia-ear anomaly syndrome,MONDO,disease,DISEASE_12743
12744,12744,12744,12744,12744,12744,12744,12744,MONDO:0014314,sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome,MONDO,disease,DISEASE_12744
12745,12745,12745,12745,12745,12745,12745,12745,MONDO:0026762,"Wieacker-Wolff syndrome, female-restricted",MONDO,disease,DISEASE_12745
12746,12746,12746,12746,12746,12746,12746,12746,MONDO:0020502_MONDO:0001195,yellow fever,MONDO_grouped,disease,DISEASE_12746
12747,12747,12747,12747,12747,12747,12747,12747,MONDO:0002674,stricture or kinking of ureter,MONDO,disease,DISEASE_12747
12748,12748,12748,12748,12748,12748,12748,12748,MONDO:0023165,florid cystic endosalpingiosis of the uterus,MONDO,disease,DISEASE_12748
12749,12749,12749,12749,12749,12749,12749,12749,MONDO:0032922,Beck-Fahrner syndrome,MONDO,disease,DISEASE_12749
12750,12750,12750,12750,12750,12750,12750,12750,MONDO:1012296_MONDO:1012297,"imperforate hymen, horse",MONDO_grouped,disease,DISEASE_12750
12751,12751,12751,12751,12751,12751,12751,12751,MONDO:0957953,Garg-Mishra progeroid syndrome,MONDO,disease,DISEASE_12751
12752,12752,12752,12752,12752,12752,12752,12752,MONDO:0009158,"Ehlers-Danlos syndrome, fibronectinemic type",MONDO,disease,DISEASE_12752
12753,12753,12753,12753,12753,12753,12753,12753,MONDO:0021957,autosomal recessive nonsyndromic congenital nuclear cataract,MONDO,disease,DISEASE_12753
12754,12754,12754,12754,12754,12754,12754,12754,MONDO:0005668,bird fancier's lung,MONDO,disease,DISEASE_12754
12755,12755,12755,12755,12755,12755,12755,12755,MONDO:0016035,Nelson syndrome,MONDO,disease,DISEASE_12755
12756,12756,12756,12756,12756,12756,12756,12756,MONDO:0009049,Cushing syndrome due to macronodular adrenal hyperplasia,MONDO,disease,DISEASE_12756
12757,12757,12757,12757,12757,12757,12757,12757,MONDO:0100064,tyrosine hydroxylase deficiency,MONDO,disease,DISEASE_12757
12758,12758,12758,12758,12758,12758,12758,12758,MONDO:0021283,malignant teratoma of mediastinum,MONDO,disease,DISEASE_12758
12759,12759,12759,12759,12759,12759,12759,12759,MONDO:0044326,developmental delay and seizures with or without movement abnormalities,MONDO,disease,DISEASE_12759
12760,12760,12760,12760,12760,12760,12760,12760,MONDO:0015967,monogenic diabetes,MONDO,disease,DISEASE_12760
12761,12761,12761,12761,12761,12761,12761,12761,MONDO:0005566,neonatal abstinence syndrome,MONDO,disease,DISEASE_12761
12762,12762,12762,12762,12762,12762,12762,12762,MONDO:0010175,van Bogaert-Hozay syndrome,MONDO,disease,DISEASE_12762
12763,12763,12763,12763,12763,12763,12763,12763,MONDO:0005075,thyroid gland papillary carcinoma,MONDO,disease,DISEASE_12763
12764,12764,12764,12764,12764,12764,12764,12764,MONDO:1012906,"congenital muscular dystrophy, LAMA2-related, dog",MONDO,disease,DISEASE_12764
12765,12765,12765,12765,12765,12765,12765,12765,MONDO:0004438,sporadic breast cancer,MONDO,disease,DISEASE_12765
12766,12766,12766,12766,12766,12766,12766,12766,MONDO:1012341,"spinal dysmyelination, cattle",MONDO,disease,DISEASE_12766
12767,12767,12767,12767,12767,12767,12767,12767,MONDO:0008059,Naegeli-Franceschetti-Jadassohn syndrome,MONDO,disease,DISEASE_12767
12768,12768,12768,12768,12768,12768,12768,12768,MONDO:0022809,Colver Steer Godman syndrome,MONDO,disease,DISEASE_12768
12769,12769,12769,12769,12769,12769,12769,12769,MONDO:0100466,butterfly-shaped pigment dystrophy,MONDO,disease,DISEASE_12769
12770,12770,12770,12770,12770,12770,12770,12770,MONDO:0020417,right aortic arch,MONDO,disease,DISEASE_12770
12771,12771,12771,12771,12771,12771,12771,12771,MONDO:0009041,craniosynostosis-intellectual disability-clefting syndrome,MONDO,disease,DISEASE_12771
12772,12772,12772,12772,12772,12772,12772,12772,MONDO:0006285,major salivary gland carcinoma ex pleomorphic adenoma,MONDO,disease,DISEASE_12772
12773,12773,12773,12773,12773,12773,12773,12773,MONDO:0014850,retinitis pigmentosa and erythrocytic microcytosis,MONDO,disease,DISEASE_12773
12774,12774,12774,12774,12774,12774,12774,12774,MONDO:0014864_MONDO:0000214,hypermanganesemia with dystonia 2,MONDO_grouped,disease,DISEASE_12774
12775,12775,12775,12775,12775,12775,12775,12775,MONDO:0000490,glomerulosclerosis,MONDO,disease,DISEASE_12775
12776,12776,12776,12776,12776,12776,12776,12776,MONDO:0021492,benign neoplasm of major salivary gland,MONDO,disease,DISEASE_12776
12777,12777,12777,12777,12777,12777,12777,12777,MONDO:0017487_MONDO:0017488_MONDO:0017489,"radial hemimelia, bilateral",MONDO_grouped,disease,DISEASE_12777
12778,12778,12778,12778,12778,12778,12778,12778,MONDO:0000306,trichosporonosis,MONDO,disease,DISEASE_12778
12779,12779,12779,12779,12779,12779,12779,12779,MONDO:0001456,cobblestone retinal degeneration,MONDO,disease,DISEASE_12779
12780,12780,12780,12780,12780,12780,12780,12780,MONDO:0032760,developmental delay with or without dysmorphic facies and autism,MONDO,disease,DISEASE_12780
12781,12781,12781,12781,12781,12781,12781,12781,MONDO:0002301,frontal sinus squamous cell carcinoma,MONDO,disease,DISEASE_12781
12782,12782,12782,12782,12782,12782,12782,12782,MONDO:0005705,clonorchiasis,MONDO,disease,DISEASE_12782
12783,12783,12783,12783,12783,12783,12783,12783,MONDO:0011516,early response to neural induction gene,MONDO,disease,DISEASE_12783
12784,12784,12784,12784,12784,12784,12784,12784,MONDO:0006557,hemangioma of subcutaneous tissue,MONDO,disease,DISEASE_12784
12785,12785,12785,12785,12785,12785,12785,12785,MONDO:0005019,diffuse scleroderma,MONDO,disease,DISEASE_12785
12786,12786,12786,12786,12786,12786,12786,12786,MONDO:0014331,Moyamoya disease with early-onset achalasia,MONDO,disease,DISEASE_12786
12787,12787,12787,12787,12787,12787,12787,12787,MONDO:0016593,acquired ataxia,MONDO,disease,DISEASE_12787
12788,12788,12788,12788,12788,12788,12788,12788,MONDO:0001754,eclampsia,MONDO,disease,DISEASE_12788
12789,12789,12789,12789,12789,12789,12789,12789,MONDO:0013228,spondylo-megaepiphyseal-metaphyseal dysplasia,MONDO,disease,DISEASE_12789
12790,12790,12790,12790,12790,12790,12790,12790,MONDO:0011934_MONDO:0023273,dermatofibrosarcoma protuberans,MONDO_grouped,disease,DISEASE_12790
12791,12791,12791,12791,12791,12791,12791,12791,MONDO:0006225,gastric mantle cell lymphoma,MONDO,disease,DISEASE_12791
12792,12792,12792,12792,12792,12792,12792,12792,MONDO:0030376_MONDO:8000008_MONDO:0023910,Martsolf syndrome,MONDO_grouped,disease,DISEASE_12792
12793,12793,12793,12793,12793,12793,12793,12793,MONDO:0012063,ulnar/fibula ray defect-brachydactyly syndrome,MONDO,disease,DISEASE_12793
12794,12794,12794,12794,12794,12794,12794,12794,MONDO:0007769,hyperpigmentation of eyelid,MONDO,disease,DISEASE_12794
12795,12795,12795,12795,12795,12795,12795,12795,MONDO:0010027,"free sialic acid storage disease, infantile form",MONDO,disease,DISEASE_12795
12796,12796,12796,12796,12796,12796,12796,12796,MONDO:0010978,"portal vein, cavernous transformation of",MONDO,disease,DISEASE_12796
12797,12797,12797,12797,12797,12797,12797,12797,MONDO:0032821,"myopathy, congenital, progressive, with scoliosis",MONDO,disease,DISEASE_12797
12798,12798,12798,12798,12798,12798,12798,12798,MONDO:0006266,Leydig cell tumor,MONDO,disease,DISEASE_12798
12799,12799,12799,12799,12799,12799,12799,12799,MONDO:0003546,third cranial nerve disorder,MONDO,disease,DISEASE_12799
12800,12800,12800,12800,12800,12800,12800,12800,MONDO:0033885,"mitochondrial complex IV deficiency, nuclear-type",MONDO,disease,DISEASE_12800
12801,12801,12801,12801,12801,12801,12801,12801,MONDO:0600016,acinar dysplasia,MONDO,disease,DISEASE_12801
12802,12802,12802,12802,12802,12802,12802,12802,MONDO:0007341,cleidorhizomelic syndrome,MONDO,disease,DISEASE_12802
12803,12803,12803,12803,12803,12803,12803,12803,MONDO:0859382,cataract 50 with or without glaucoma,MONDO,disease,DISEASE_12803
12804,12804,12804,12804,12804,12804,12804,12804,MONDO:0005465,methamphetamine-induced psychosis,MONDO,disease,DISEASE_12804
12805,12805,12805,12805,12805,12805,12805,12805,MONDO:0009232,Fuhrmann syndrome,MONDO,disease,DISEASE_12805
12806,12806,12806,12806,12806,12806,12806,12806,MONDO:0021634,epithelial skin neoplasm,MONDO,disease,DISEASE_12806
12807,12807,12807,12807,12807,12807,12807,12807,MONDO:1011743,"nodular dermatofibrosis and kidney disease, non-human animal",MONDO,disease,DISEASE_12807
12808,12808,12808,12808,12808,12808,12808,12808,MONDO:0001955,protozoal dysentery,MONDO,disease,DISEASE_12808
12809,12809,12809,12809,12809,12809,12809,12809,MONDO:0009988,retinoschisis of fovea,MONDO,disease,DISEASE_12809
12810,12810,12810,12810,12810,12810,12810,12810,MONDO:0022866,corneal dystrophy pigmentary anomaly malabsorption,MONDO,disease,DISEASE_12810
12811,12811,12811,12811,12811,12811,12811,12811,MONDO:0035151,17q24.2 microdeletion syndrome,MONDO,disease,DISEASE_12811
12812,12812,12812,12812,12812,12812,12812,12812,MONDO:0006594,pemphigus,MONDO,disease,DISEASE_12812
12813,12813,12813,12813,12813,12813,12813,12813,MONDO:0001569,acoustic neuroma,MONDO,disease,DISEASE_12813
12814,12814,12814,12814,12814,12814,12814,12814,MONDO:0060486,"arthrogryposis multiplex congenita 1, neurogenic, with myelin defect",MONDO,disease,DISEASE_12814
12815,12815,12815,12815,12815,12815,12815,12815,MONDO:0042980,Westphal disease,MONDO,disease,DISEASE_12815
12816,12816,12816,12816,12816,12816,12816,12816,MONDO:0015411,facial cleft,MONDO,disease,DISEASE_12816
12817,12817,12817,12817,12817,12817,12817,12817,MONDO:0021427,squamous cell carcinoma of lip,MONDO,disease,DISEASE_12817
12818,12818,12818,12818,12818,12818,12818,12818,MONDO:1011769_MONDO:1012371,"dysplasia epiphysealis hememelica, non-human animal",MONDO_grouped,disease,DISEASE_12818
12819,12819,12819,12819,12819,12819,12819,12819,MONDO:0000345,Oropouche fever,MONDO,disease,DISEASE_12819
12820,12820,12820,12820,12820,12820,12820,12820,MONDO:0011069,"cervical ribs, Sprengel anomaly, anal atresia, and urethral obstruction",MONDO,disease,DISEASE_12820
12821,12821,12821,12821,12821,12821,12821,12821,MONDO:0014679,"polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis",MONDO,disease,DISEASE_12821
12822,12822,12822,12822,12822,12822,12822,12822,MONDO:1011122,"persistent Mullerian duct syndrome, dog",MONDO,disease,DISEASE_12822
12823,12823,12823,12823,12823,12823,12823,12823,MONDO:0017216,calciphylaxis cutis,MONDO,disease,DISEASE_12823
12824,12824,12824,12824,12824,12824,12824,12824,MONDO:0700157,canine oral squamous cell carcinoma,MONDO,disease,DISEASE_12824
12825,12825,12825,12825,12825,12825,12825,12825,MONDO:0032862,"hydrocephalus, congenital communicating, 1",MONDO,disease,DISEASE_12825
12826,12826,12826,12826,12826,12826,12826,12826,MONDO:0018492,hereditary clear cell renal cell carcinoma,MONDO,disease,DISEASE_12826
12827,12827,12827,12827,12827,12827,12827,12827,MONDO:0009367,McKusick-Kaufman syndrome,MONDO,disease,DISEASE_12827
12828,12828,12828,12828,12828,12828,12828,12828,MONDO:0009425,hypomandibular faciocranial dysostosis,MONDO,disease,DISEASE_12828
12829,12829,12829,12829,12829,12829,12829,12829,MONDO:0009747,mitochondrial DNA depletion syndrome 6 (hepatocerebral type),MONDO,disease,DISEASE_12829
12830,12830,12830,12830,12830,12830,12830,12830,MONDO:0009389,hyperlysinemia due to defect in lysine transport into mitochondria,MONDO,disease,DISEASE_12830
12831,12831,12831,12831,12831,12831,12831,12831,MONDO:1010851,"glycogen storage disease, GAA-related, domestic cat",MONDO,disease,DISEASE_12831
12832,12832,12832,12832,12832,12832,12832,12832,MONDO:0001995,sphenoid sinus squamous cell carcinoma,MONDO,disease,DISEASE_12832
12833,12833,12833,12833,12833,12833,12833,12833,MONDO:0008322,pseudoachondroplasia,MONDO,disease,DISEASE_12833
12834,12834,12834,12834,12834,12834,12834,12834,MONDO:0020786,"obsolete short sleep, familial natural, 2",MONDO,disease,DISEASE_12834
12835,12835,12835,12835,12835,12835,12835,12835,MONDO:0017595,aggressive B-cell non-Hodgkin lymphoma,MONDO,disease,DISEASE_12835
12836,12836,12836,12836,12836,12836,12836,12836,MONDO:0013599,autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome,MONDO,disease,DISEASE_12836
12837,12837,12837,12837,12837,12837,12837,12837,MONDO:0022578,childhood bladder carcinoma,MONDO,disease,DISEASE_12837
12838,12838,12838,12838,12838,12838,12838,12838,MONDO:0003926,neurilemmoma of the pleura,MONDO,disease,DISEASE_12838
12839,12839,12839,12839,12839,12839,12839,12839,MONDO:0003172,glomeruloid hemangioma,MONDO,disease,DISEASE_12839
12840,12840,12840,12840,12840,12840,12840,12840,MONDO:0008020,multiple exostoses with spastic tetraparesis,MONDO,disease,DISEASE_12840
12841,12841,12841,12841,12841,12841,12841,12841,MONDO:1012795_MONDO:1012796,"polyneuropathy, GJA9-related, dog",MONDO_grouped,disease,DISEASE_12841
12842,12842,12842,12842,12842,12842,12842,12842,MONDO:0010498,MEND syndrome,MONDO,disease,DISEASE_12842
12843,12843,12843,12843,12843,12843,12843,12843,MONDO:0011365,"blepharophimosis - intellectual disability syndrome, SBBYS type",MONDO,disease,DISEASE_12843
12844,12844,12844,12844,12844,12844,12844,12844,MONDO:1012056,"degenerative myelopathy, dog",MONDO,disease,DISEASE_12844
12845,12845,12845,12845,12845,12845,12845,12845,MONDO:0012359,combined immunodeficiency due to partial RAG1 deficiency,MONDO,disease,DISEASE_12845
12846,12846,12846,12846,12846,12846,12846,12846,MONDO:1011334,"mouth mucosa disorder, non-human animal",MONDO,disease,DISEASE_12846
12847,12847,12847,12847,12847,12847,12847,12847,MONDO:0043233,exfoliative dermatitis,MONDO,disease,DISEASE_12847
12848,12848,12848,12848,12848,12848,12848,12848,MONDO:0016284,primitive neuroectodermal tumor of the cervix uteri,MONDO,disease,DISEASE_12848
12849,12849,12849,12849,12849,12849,12849,12849,MONDO:0018761,SMARCA4-deficient sarcoma of thorax,MONDO,disease,DISEASE_12849
12850,12850,12850,12850,12850,12850,12850,12850,MONDO:0001760,photokeratitis,MONDO,disease,DISEASE_12850
12851,12851,12851,12851,12851,12851,12851,12851,MONDO:0003891,bladder signet ring cell adenocarcinoma,MONDO,disease,DISEASE_12851
12852,12852,12852,12852,12852,12852,12852,12852,MONDO:0019123,continuous spikes and waves during sleep,MONDO,disease,DISEASE_12852
12853,12853,12853,12853,12853,12853,12853,12853,MONDO:0022932,Davenport-Donlan syndrome,MONDO,disease,DISEASE_12853
12854,12854,12854,12854,12854,12854,12854,12854,MONDO:0859244,phosphoribosylaminoimidazole carboxylase deficiency,MONDO,disease,DISEASE_12854
12855,12855,12855,12855,12855,12855,12855,12855,MONDO:0005258,autism spectrum disorder,MONDO,disease,DISEASE_12855
12856,12856,12856,12856,12856,12856,12856,12856,MONDO:0001493,chronic pulmonary heart disease,MONDO,disease,DISEASE_12856
12857,12857,12857,12857,12857,12857,12857,12857,MONDO:0019630,congenital ectropion uveae,MONDO,disease,DISEASE_12857
12858,12858,12858,12858,12858,12858,12858,12858,MONDO:0001984,candidal paronychia,MONDO,disease,DISEASE_12858
12859,12859,12859,12859,12859,12859,12859,12859,MONDO:0018733,intellectual disability syndrome due to a DYRK1A point mutation,MONDO,disease,DISEASE_12859
12860,12860,12860,12860,12860,12860,12860,12860,MONDO:0032927,triokinase and FMN cyclase deficiency syndrome,MONDO,disease,DISEASE_12860
12861,12861,12861,12861,12861,12861,12861,12861,MONDO:0011080,progressive deafness with stapes fixation,MONDO,disease,DISEASE_12861
12862,12862,12862,12862,12862,12862,12862,12862,MONDO:0013004,"hypotonia, seizures, and precocious puberty",MONDO,disease,DISEASE_12862
12863,12863,12863,12863,12863,12863,12863,12863,MONDO:0015337,isolated craniosynostosis,MONDO,disease,DISEASE_12863
12864,12864,12864,12864,12864,12864,12864,12864,MONDO:0001473,medulloadrenal hyperfunction,MONDO,disease,DISEASE_12864
12865,12865,12865,12865,12865,12865,12865,12865,MONDO:0018977,polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG,MONDO,disease,DISEASE_12865
12866,12866,12866,12866,12866,12866,12866,12866,MONDO:0001243_MONDO:0001242,disseminated intravascular coagulation,MONDO_grouped,disease,DISEASE_12866
12867,12867,12867,12867,12867,12867,12867,12867,MONDO:0011552_MONDO:0010897_MONDO:0010943_MONDO:0008414_MONDO:0005090_MONDO:0013498_MONDO:0033312_MONDO:0012054_MONDO:0011960_MONDO:0011280_MONDO:0011294_MONDO:0011295_MONDO:0011298_MONDO:0011307_MONDO:0011498_MONDO:0012879_MONDO:0013089_MONDO:0013506_MONDO:0014092_MONDO:0800358,schizophrenia,MONDO_grouped,disease,DISEASE_12867
12868,12868,12868,12868,12868,12868,12868,12868,MONDO:0005484_MONDO:0003885_MONDO:0024331_MONDO:0005008_MONDO:0006160,colorectal adenoma,MONDO_grouped,disease,DISEASE_12868
12869,12869,12869,12869,12869,12869,12869,12869,MONDO:0009274,ghosal hematodiaphyseal dysplasia,MONDO,disease,DISEASE_12869
12870,12870,12870,12870,12870,12870,12870,12870,MONDO:0013301,aromatase deficiency,MONDO,disease,DISEASE_12870
12871,12871,12871,12871,12871,12871,12871,12871,MONDO:0022037,large-cell immunoblastic lymphoma,MONDO,disease,DISEASE_12871
12872,12872,12872,12872,12872,12872,12872,12872,MONDO:0006743,endocrine tuberculosis,MONDO,disease,DISEASE_12872
12873,12873,12873,12873,12873,12873,12873,12873,MONDO:1010481,"tetralogy of fallot, snow leopard",MONDO,disease,DISEASE_12873
12874,12874,12874,12874,12874,12874,12874,12874,MONDO:0019881,distal trisomy 6q,MONDO,disease,DISEASE_12874
12875,12875,12875,12875,12875,12875,12875,12875,MONDO:0043099,Hordnes Engebretsen Knudtson syndrome,MONDO,disease,DISEASE_12875
12876,12876,12876,12876,12876,12876,12876,12876,MONDO:0700015,chromosome 8 disorder,MONDO,disease,DISEASE_12876
12877,12877,12877,12877,12877,12877,12877,12877,MONDO:0014008,phosphohydroxylysinuria,MONDO,disease,DISEASE_12877
12878,12878,12878,12878,12878,12878,12878,12878,MONDO:0019652,familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation,MONDO,disease,DISEASE_12878
12879,12879,12879,12879,12879,12879,12879,12879,MONDO:0024499,vascular bone neoplasm,MONDO,disease,DISEASE_12879
12880,12880,12880,12880,12880,12880,12880,12880,MONDO:1010071,"factor VII deficiency, non-human animal",MONDO,disease,DISEASE_12880
12881,12881,12881,12881,12881,12881,12881,12881,MONDO:0009490,Papillon-Lefevre disease,MONDO,disease,DISEASE_12881
12882,12882,12882,12882,12882,12882,12882,12882,MONDO:0006586,neurotic excoriation,MONDO,disease,DISEASE_12882
12883,12883,12883,12883,12883,12883,12883,12883,MONDO:0008950,cerebral sclerosis similar to Pelizaeus-Merzbacher disease,MONDO,disease,DISEASE_12883
12884,12884,12884,12884,12884,12884,12884,12884,MONDO:1012746,"sex-limited cystinuria, dog",MONDO,disease,DISEASE_12884
12885,12885,12885,12885,12885,12885,12885,12885,MONDO:0005899,parotid disorder,MONDO,disease,DISEASE_12885
12886,12886,12886,12886,12886,12886,12886,12886,MONDO:0006531,cholesteatoma of attic,MONDO,disease,DISEASE_12886
12887,12887,12887,12887,12887,12887,12887,12887,MONDO:0007656,Gerstmann-Straussler-Scheinker syndrome,MONDO,disease,DISEASE_12887
12888,12888,12888,12888,12888,12888,12888,12888,MONDO:0012454,"alcohol sensitivity, acute",MONDO,disease,DISEASE_12888
12889,12889,12889,12889,12889,12889,12889,12889,MONDO:0001913,oligospermia,MONDO,disease,DISEASE_12889
12890,12890,12890,12890,12890,12890,12890,12890,MONDO:0017282,alveolar echinococcosis,MONDO,disease,DISEASE_12890
12891,12891,12891,12891,12891,12891,12891,12891,MONDO:0016845,21q22.11q22.12 microdeletion syndrome,MONDO,disease,DISEASE_12891
12892,12892,12892,12892,12892,12892,12892,12892,MONDO:0009270,genito-palato-cardiac syndrome,MONDO,disease,DISEASE_12892
12893,12893,12893,12893,12893,12893,12893,12893,MONDO:0004604,"Hodgkin's lymphoma, lymphocytic-histiocytic predominance",MONDO,disease,DISEASE_12893
12894,12894,12894,12894,12894,12894,12894,12894,MONDO:0007827,inclusion body myositis,MONDO,disease,DISEASE_12894
12895,12895,12895,12895,12895,12895,12895,12895,MONDO:0018504,undifferentiated carcinoma of stomach,MONDO,disease,DISEASE_12895
12896,12896,12896,12896,12896,12896,12896,12896,MONDO:0011040,"spinal dysplasia, Anhalt type",MONDO,disease,DISEASE_12896
12897,12897,12897,12897,12897,12897,12897,12897,MONDO:0004493,"testicular yolk sac tumor, papillary pattern",MONDO,disease,DISEASE_12897
12898,12898,12898,12898,12898,12898,12898,12898,MONDO:0018631,Marie Unna hereditary hypotrichosis,MONDO,disease,DISEASE_12898
12899,12899,12899,12899,12899,12899,12899,12899,MONDO:1010359,"night blindness, non-human animal",MONDO,disease,DISEASE_12899
12900,12900,12900,12900,12900,12900,12900,12900,MONDO:0018969,craniorachischisis,MONDO,disease,DISEASE_12900
12901,12901,12901,12901,12901,12901,12901,12901,MONDO:0042603,Sanderson-Fraser syndrome,MONDO,disease,DISEASE_12901
12902,12902,12902,12902,12902,12902,12902,12902,MONDO:0009561_MONDO:0022424_MONDO:1010865_MONDO:1010866_MONDO:1010867,alpha-mannosidosis,MONDO_grouped,disease,DISEASE_12902
12903,12903,12903,12903,12903,12903,12903,12903,MONDO:0019173,rabies,MONDO,disease,DISEASE_12903
12904,12904,12904,12904,12904,12904,12904,12904,MONDO:0005915,pityriasis versicolor,MONDO,disease,DISEASE_12904
12905,12905,12905,12905,12905,12905,12905,12905,MONDO:0600025,hydrosalpinx,MONDO,disease,DISEASE_12905
12906,12906,12906,12906,12906,12906,12906,12906,MONDO:0004376,infiltrating nipple syringomatous adenoma,MONDO,disease,DISEASE_12906
12907,12907,12907,12907,12907,12907,12907,12907,MONDO:0003650,mixed hepatoblastoma,MONDO,disease,DISEASE_12907
12908,12908,12908,12908,12908,12908,12908,12908,MONDO:0002792,cerebellar vermis medulloblastoma,MONDO,disease,DISEASE_12908
12909,12909,12909,12909,12909,12909,12909,12909,MONDO:1012700,"geleophysic dysplasia, ADMATSL2-related, dog",MONDO,disease,DISEASE_12909
12910,12910,12910,12910,12910,12910,12910,12910,MONDO:0002576,embryonal extrahepatic bile duct rhabdomyosarcoma,MONDO,disease,DISEASE_12910
12911,12911,12911,12911,12911,12911,12911,12911,MONDO:0007116,hereditary neurocutaneous angioma,MONDO,disease,DISEASE_12911
12912,12912,12912,12912,12912,12912,12912,12912,MONDO:0008960,Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome,MONDO,disease,DISEASE_12912
12913,12913,12913,12913,12913,12913,12913,12913,MONDO:0009050,Cushing disease due to pituitary adenoma,MONDO,disease,DISEASE_12913
12914,12914,12914,12914,12914,12914,12914,12914,MONDO:0019208,Bickerstaff brainstem encephalitis,MONDO,disease,DISEASE_12914
12915,12915,12915,12915,12915,12915,12915,12915,MONDO:0014104_MONDO:0024542_MONDO:0013188_MONDO:0012430_MONDO:0009133,"cerebellar ataxia, intellectual disability, and dysequilibrium syndrome",MONDO_grouped,disease,DISEASE_12915
12916,12916,12916,12916,12916,12916,12916,12916,MONDO:0019888,distal trisomy 20q,MONDO,disease,DISEASE_12916
12917,12917,12917,12917,12917,12917,12917,12917,MONDO:0002670,ampulla of vater adenocarcinoma,MONDO,disease,DISEASE_12917
12918,12918,12918,12918,12918,12918,12918,12918,MONDO:0011312,"thyroid carcinoma, nonmedullary, with or without cell oxyphilia",MONDO,disease,DISEASE_12918
12919,12919,12919,12919,12919,12919,12919,12919,MONDO:0011273,H syndrome,MONDO,disease,DISEASE_12919
12920,12920,12920,12920,12920,12920,12920,12920,MONDO:0100412_MONDO:0100413,"acute myeloid leukemia, monoallelic CEBPA gene mutation",MONDO_grouped,disease,DISEASE_12920
12921,12921,12921,12921,12921,12921,12921,12921,MONDO:0010835,pterygium colli-intellectual disability-digital anomalies syndrome,MONDO,disease,DISEASE_12921
12922,12922,12922,12922,12922,12922,12922,12922,MONDO:0003504,anal canal neuroendocrine neoplasm,MONDO,disease,DISEASE_12922
12923,12923,12923,12923,12923,12923,12923,12923,MONDO:0009684,"muscular hypertonia, lethal",MONDO,disease,DISEASE_12923
12924,12924,12924,12924,12924,12924,12924,12924,MONDO:0018868,metachromatic leukodystrophy,MONDO,disease,DISEASE_12924
12925,12925,12925,12925,12925,12925,12925,12925,MONDO:0009008,heart defect - tongue hamartoma - polysyndactyly syndrome,MONDO,disease,DISEASE_12925
12926,12926,12926,12926,12926,12926,12926,12926,MONDO:0957431,endogenous Cushing syndrome,MONDO,disease,DISEASE_12926
12927,12927,12927,12927,12927,12927,12927,12927,MONDO:0007970,melorheostosis,MONDO,disease,DISEASE_12927
12928,12928,12928,12928,12928,12928,12928,12928,MONDO:0700260,SAMHD1-related type 1 interferonopathy,MONDO,disease,DISEASE_12928
12929,12929,12929,12929,12929,12929,12929,12929,MONDO:0018884,Roch-Leri mesosomatous lipomatosis,MONDO,disease,DISEASE_12929
12930,12930,12930,12930,12930,12930,12930,12930,MONDO:0019753,localized Castleman disease,MONDO,disease,DISEASE_12930
12931,12931,12931,12931,12931,12931,12931,12931,MONDO:0022898,craniosynostosis intellectual disability heart defects,MONDO,disease,DISEASE_12931
12932,12932,12932,12932,12932,12932,12932,12932,MONDO:1012510,"facial dysplasia syndrome, cattle",MONDO,disease,DISEASE_12932
12933,12933,12933,12933,12933,12933,12933,12933,MONDO:1012740,"xanthinuria, MOCOS-related, cattle",MONDO,disease,DISEASE_12933
12934,12934,12934,12934,12934,12934,12934,12934,MONDO:1012932,"chondrodysplasia, UGDH-related, domestic cat",MONDO,disease,DISEASE_12934
12935,12935,12935,12935,12935,12935,12935,12935,MONDO:1012479_MONDO:1012480_MONDO:1012481_MONDO:1012482,"cervical vertebral compressive myelopathy, dog",MONDO_grouped,disease,DISEASE_12935
12936,12936,12936,12936,12936,12936,12936,12936,MONDO:0012720,Krabbe disease due to saposin A deficiency,MONDO,disease,DISEASE_12936
12937,12937,12937,12937,12937,12937,12937,12937,MONDO:0012915,chromosome 1q21.1 duplication syndrome,MONDO,disease,DISEASE_12937
12938,12938,12938,12938,12938,12938,12938,12938,MONDO:0001415_MONDO:0006666,atrophy of testis,MONDO_grouped,disease,DISEASE_12938
12939,12939,12939,12939,12939,12939,12939,12939,MONDO:0958295,BCOR ITD sarcoma,MONDO,disease,DISEASE_12939
12940,12940,12940,12940,12940,12940,12940,12940,MONDO:0001375,bladder trigone cancer,MONDO,disease,DISEASE_12940
12941,12941,12941,12941,12941,12941,12941,12941,MONDO:0021113,respiratory failure,MONDO,disease,DISEASE_12941
12942,12942,12942,12942,12942,12942,12942,12942,MONDO:0012484,"prosopagnosia, hereditary",MONDO,disease,DISEASE_12942
12943,12943,12943,12943,12943,12943,12943,12943,MONDO:0003825_MONDO:0003824,kidney oncocytoma,MONDO_grouped,disease,DISEASE_12943
12944,12944,12944,12944,12944,12944,12944,12944,MONDO:0003774_MONDO:0004426,cerebral convexity meningioma,MONDO_grouped,disease,DISEASE_12944
12945,12945,12945,12945,12945,12945,12945,12945,MONDO:0001099,lactocele,MONDO,disease,DISEASE_12945
12946,12946,12946,12946,12946,12946,12946,12946,MONDO:0011465,infundibulocystic basal cell carcinoma,MONDO,disease,DISEASE_12946
12947,12947,12947,12947,12947,12947,12947,12947,MONDO:0004531,sclerosing adenosis of breast,MONDO,disease,DISEASE_12947
12948,12948,12948,12948,12948,12948,12948,12948,MONDO:0023021,dwarfism lethal type advanced bone age,MONDO,disease,DISEASE_12948
12949,12949,12949,12949,12949,12949,12949,12949,MONDO:1010191,"deficiency of uridine monophosphate synthase, non-human animal",MONDO,disease,DISEASE_12949
12950,12950,12950,12950,12950,12950,12950,12950,MONDO:0004380_MONDO:0005764,dendritic cell sarcoma,MONDO_grouped,disease,DISEASE_12950
12951,12951,12951,12951,12951,12951,12951,12951,MONDO:0100309_MONDO:0015547_MONDO:0016624,hereditary ataxia,MONDO_grouped,disease,DISEASE_12951
12952,12952,12952,12952,12952,12952,12952,12952,MONDO:0001262,African histoplasmosis,MONDO,disease,DISEASE_12952
12953,12953,12953,12953,12953,12953,12953,12953,MONDO:0023368,Ho-Kaufman-McAlister syndrome,MONDO,disease,DISEASE_12953
12954,12954,12954,12954,12954,12954,12954,12954,MONDO:1010334,"retinitis pigmentosa, non-human animal",MONDO,disease,DISEASE_12954
12955,12955,12955,12955,12955,12955,12955,12955,MONDO:1012288_MONDO:1012289,"progressive ataxia, pig",MONDO_grouped,disease,DISEASE_12955
12956,12956,12956,12956,12956,12956,12956,12956,MONDO:0011133,"deaf blind hypopigmentation syndrome, Yemenite type",MONDO,disease,DISEASE_12956
12957,12957,12957,12957,12957,12957,12957,12957,MONDO:0100091,inherited pseudoxanthoma elasticum,MONDO,disease,DISEASE_12957
12958,12958,12958,12958,12958,12958,12958,12958,MONDO:0021826,aerobic Actinomyces infection,MONDO,disease,DISEASE_12958
12959,12959,12959,12959,12959,12959,12959,12959,MONDO:0043114,Landy-Donnai syndrome,MONDO,disease,DISEASE_12959
12960,12960,12960,12960,12960,12960,12960,12960,MONDO:0013040,atypical hemolytic-uremic syndrome with MCP/CD46 anomaly,MONDO,disease,DISEASE_12960
12961,12961,12961,12961,12961,12961,12961,12961,MONDO:0100120,vector-borne disease,MONDO,disease,DISEASE_12961
12962,12962,12962,12962,12962,12962,12962,12962,MONDO:0002517,tenosynovitis of foot and ankle,MONDO,disease,DISEASE_12962
12963,12963,12963,12963,12963,12963,12963,12963,MONDO:0001664,submucous uterine fibroid,MONDO,disease,DISEASE_12963
12964,12964,12964,12964,12964,12964,12964,12964,MONDO:0007914,"lumbar stenosis, familial",MONDO,disease,DISEASE_12964
12965,12965,12965,12965,12965,12965,12965,12965,MONDO:0018309,Hirschsprung disease,MONDO,disease,DISEASE_12965
12966,12966,12966,12966,12966,12966,12966,12966,MONDO:0018588,ALECT2 amyloidosis,MONDO,disease,DISEASE_12966
12967,12967,12967,12967,12967,12967,12967,12967,MONDO:0021228,brainstem neoplasm,MONDO,disease,DISEASE_12967
12968,12968,12968,12968,12968,12968,12968,12968,MONDO:0019529_MONDO:0021553,radiation myelitis,MONDO_grouped,disease,DISEASE_12968
12969,12969,12969,12969,12969,12969,12969,12969,MONDO:0002048,thrombocytopenia due to immune destruction,MONDO,disease,DISEASE_12969
12970,12970,12970,12970,12970,12970,12970,12970,MONDO:0009566,marfanoid habitus-autosomal recessive intellectual disability syndrome,MONDO,disease,DISEASE_12970
12971,12971,12971,12971,12971,12971,12971,12971,MONDO:0003611,uterine ligament papillary cystadenoma associated with von Hippel-Lindau disease,MONDO,disease,DISEASE_12971
12972,12972,12972,12972,12972,12972,12972,12972,MONDO:0005842_MONDO:0002186_MONDO:0001122,maxillary sinusitis,MONDO_grouped,disease,DISEASE_12972
12973,12973,12973,12973,12973,12973,12973,12973,MONDO:0006479,undifferentiated pancreatic carcinoma with osteoclast-like giant cells,MONDO,disease,DISEASE_12973
12974,12974,12974,12974,12974,12974,12974,12974,MONDO:0100001,alpha-gal syndrome,MONDO,disease,DISEASE_12974
12975,12975,12975,12975,12975,12975,12975,12975,MONDO:0024458,disorder of visual system,MONDO,disease,DISEASE_12975
12976,12976,12976,12976,12976,12976,12976,12976,MONDO:0005078,phyllodes tumor,MONDO,disease,DISEASE_12976
12977,12977,12977,12977,12977,12977,12977,12977,MONDO:0100207,infantile-onset epilepsy,MONDO,disease,DISEASE_12977
12978,12978,12978,12978,12978,12978,12978,12978,MONDO:0014261,growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome,MONDO,disease,DISEASE_12978
12979,12979,12979,12979,12979,12979,12979,12979,MONDO:0007928,obsolete Fechtner syndrome,MONDO,disease,DISEASE_12979
12980,12980,12980,12980,12980,12980,12980,12980,MONDO:0004775,lens-induced iridocyclitis,MONDO,disease,DISEASE_12980
12981,12981,12981,12981,12981,12981,12981,12981,MONDO:0011882,skin fragility-woolly hair-palmoplantar keratoderma syndrome,MONDO,disease,DISEASE_12981
12982,12982,12982,12982,12982,12982,12982,12982,MONDO:0025598,pneumonia caused by chlamydia,MONDO,disease,DISEASE_12982
12983,12983,12983,12983,12983,12983,12983,12983,MONDO:0008313_MONDO:0013124_MONDO:0800222,"pelvic organ prolapse, susceptibility to",MONDO_grouped,disease,DISEASE_12983
12984,12984,12984,12984,12984,12984,12984,12984,MONDO:0017080_MONDO:0017081,occipital encephalocele,MONDO_grouped,disease,DISEASE_12984
12985,12985,12985,12985,12985,12985,12985,12985,MONDO:1040041_MONDO:0700228,FZD4-related exudative vitreoretinopathy,MONDO_grouped,disease,DISEASE_12985
12986,12986,12986,12986,12986,12986,12986,12986,MONDO:0000705,Clostridium difficile colitis,MONDO,disease,DISEASE_12986
12987,12987,12987,12987,12987,12987,12987,12987,MONDO:0030037,"neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures",MONDO,disease,DISEASE_12987
12988,12988,12988,12988,12988,12988,12988,12988,MONDO:0700009,chromosome 2 disorder,MONDO,disease,DISEASE_12988
12989,12989,12989,12989,12989,12989,12989,12989,MONDO:1011146,"achondroplasia, water buffalo",MONDO,disease,DISEASE_12989
12990,12990,12990,12990,12990,12990,12990,12990,MONDO:0011261,"spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability",MONDO,disease,DISEASE_12990
12991,12991,12991,12991,12991,12991,12991,12991,MONDO:0020437,"atrial septal defect, ostium primum type",MONDO,disease,DISEASE_12991
12992,12992,12992,12992,12992,12992,12992,12992,MONDO:0008014,nondisjunction,MONDO,disease,DISEASE_12992
12993,12993,12993,12993,12993,12993,12993,12993,MONDO:0100069,hearing impairment and infertile male syndrome,MONDO,disease,DISEASE_12993
12994,12994,12994,12994,12994,12994,12994,12994,MONDO:0008496,storm syndrome,MONDO,disease,DISEASE_12994
12995,12995,12995,12995,12995,12995,12995,12995,MONDO:0024474,intraepithelial neoplasia,MONDO,disease,DISEASE_12995
12996,12996,12996,12996,12996,12996,12996,12996,MONDO:0019760,terminal transverse defects of arm,MONDO,disease,DISEASE_12996
12997,12997,12997,12997,12997,12997,12997,12997,MONDO:0002647_MONDO:0001369,laryngitis,MONDO_grouped,disease,DISEASE_12997
12998,12998,12998,12998,12998,12998,12998,12998,MONDO:0007236_MONDO:0012575,branchiootorenal syndrome,MONDO_grouped,disease,DISEASE_12998
12999,12999,12999,12999,12999,12999,12999,12999,MONDO:0004542,"cervical adenosquamous carcinoma, glassy cell variant",MONDO,disease,DISEASE_12999
13000,13000,13000,13000,13000,13000,13000,13000,MONDO:0016280,sarcoma of cervix uteri,MONDO,disease,DISEASE_13000
13001,13001,13001,13001,13001,13001,13001,13001,MONDO:0004533,perineural angioma,MONDO,disease,DISEASE_13001
13002,13002,13002,13002,13002,13002,13002,13002,MONDO:0004297,lymphoepithelioma-like thymic carcinoma,MONDO,disease,DISEASE_13002
13003,13003,13003,13003,13003,13003,13003,13003,MONDO:0044704,oropharynx squamous cell carcinoma,MONDO,disease,DISEASE_13003
13004,13004,13004,13004,13004,13004,13004,13004,MONDO:0010867,PARC syndrome,MONDO,disease,DISEASE_13004
13005,13005,13005,13005,13005,13005,13005,13005,MONDO:0004785,blepharitis,MONDO,disease,DISEASE_13005
13006,13006,13006,13006,13006,13006,13006,13006,MONDO:0011927,tufted angioma,MONDO,disease,DISEASE_13006
13007,13007,13007,13007,13007,13007,13007,13007,MONDO:0956989,CIC-rearranged sarcoma,MONDO,disease,DISEASE_13007
13008,13008,13008,13008,13008,13008,13008,13008,MONDO:0008826,"arthrogryposis-hyperkeratosis syndrome, lethal form",MONDO,disease,DISEASE_13008
13009,13009,13009,13009,13009,13009,13009,13009,MONDO:0010613,inborn glycerol kinase deficiency,MONDO,disease,DISEASE_13009
13010,13010,13010,13010,13010,13010,13010,13010,MONDO:0015649,micturation-induced seizures,MONDO,disease,DISEASE_13010
13011,13011,13011,13011,13011,13011,13011,13011,MONDO:1010114,"phenylketonuria, non-human animal",MONDO,disease,DISEASE_13011
13012,13012,13012,13012,13012,13012,13012,13012,MONDO:0019000,perineural cyst,MONDO,disease,DISEASE_13012
13013,13013,13013,13013,13013,13013,13013,13013,MONDO:0022775,cleft lip and palate malrotation cardiopathy,MONDO,disease,DISEASE_13013
13014,13014,13014,13014,13014,13014,13014,13014,MONDO:0012798,"deafness, unilateral, with delayed endolymphatic hydrops",MONDO,disease,DISEASE_13014
13015,13015,13015,13015,13015,13015,13015,13015,MONDO:0011057,cerebrovascular disorder,MONDO,disease,DISEASE_13015
13016,13016,13016,13016,13016,13016,13016,13016,MONDO:0014757,macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome,MONDO,disease,DISEASE_13016
13017,13017,13017,13017,13017,13017,13017,13017,MONDO:0021952,autoimmune progesterone dermatitis,MONDO,disease,DISEASE_13017
13018,13018,13018,13018,13018,13018,13018,13018,MONDO:0003293_MONDO:0002057_MONDO:0003371,lung leiomyoma,MONDO_grouped,disease,DISEASE_13018
13019,13019,13019,13019,13019,13019,13019,13019,MONDO:0022831,congenital heart disease ptosis hypodontia craniostosis,MONDO,disease,DISEASE_13019
13020,13020,13020,13020,13020,13020,13020,13020,MONDO:0859217,Brunet-Wagner neurodevelopmental syndrome,MONDO,disease,DISEASE_13020
13021,13021,13021,13021,13021,13021,13021,13021,MONDO:0024410,infection caused by Bifidobacterium,MONDO,disease,DISEASE_13021
13022,13022,13022,13022,13022,13022,13022,13022,MONDO:0005257,advanced heart failure,MONDO,disease,DISEASE_13022
13023,13023,13023,13023,13023,13023,13023,13023,MONDO:0013865,mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency,MONDO,disease,DISEASE_13023
13024,13024,13024,13024,13024,13024,13024,13024,MONDO:0020076,myeloproliferative neoplasm,MONDO,disease,DISEASE_13024
13025,13025,13025,13025,13025,13025,13025,13025,MONDO:0002082,endocrine gland neoplasm,MONDO,disease,DISEASE_13025
13026,13026,13026,13026,13026,13026,13026,13026,MONDO:0001597_MONDO:0004724,submandibular gland disorder,MONDO_grouped,disease,DISEASE_13026
13027,13027,13027,13027,13027,13027,13027,13027,MONDO:0018084,Uhl anomaly,MONDO,disease,DISEASE_13027
13028,13028,13028,13028,13028,13028,13028,13028,MONDO:1011830,"audiogenic seizure, non-human animal",MONDO,disease,DISEASE_13028
13029,13029,13029,13029,13029,13029,13029,13029,MONDO:0011716,acute hemorrhagic leukoencephalitis,MONDO,disease,DISEASE_13029
13030,13030,13030,13030,13030,13030,13030,13030,MONDO:0020472,Turner syndrome due to structural X chromosome anomalies,MONDO,disease,DISEASE_13030
13031,13031,13031,13031,13031,13031,13031,13031,MONDO:0958165,anaplastic sarcoma of the kidney,MONDO,disease,DISEASE_13031
13032,13032,13032,13032,13032,13032,13032,13032,MONDO:0020638,superficial spreading melanoma,MONDO,disease,DISEASE_13032
13033,13033,13033,13033,13033,13033,13033,13033,MONDO:0004087,basaloid large cell lung carcinoma,MONDO,disease,DISEASE_13033
13034,13034,13034,13034,13034,13034,13034,13034,MONDO:0006617,vesiculobullous skin disease,MONDO,disease,DISEASE_13034
13035,13035,13035,13035,13035,13035,13035,13035,MONDO:0007874_MONDO:0008596_MONDO:0017951,trichorhinophalangeal syndrome,MONDO_grouped,disease,DISEASE_13035
13036,13036,13036,13036,13036,13036,13036,13036,MONDO:0017731,glycoproteinosis,MONDO,disease,DISEASE_13036
13037,13037,13037,13037,13037,13037,13037,13037,MONDO:0017380,juvenile polyposis syndrome,MONDO,disease,DISEASE_13037
13038,13038,13038,13038,13038,13038,13038,13038,MONDO:0014114_MONDO:0007265_MONDO:0014113_MONDO:0014112_MONDO:0015280,cardiofaciocutaneous syndrome,MONDO_grouped,disease,DISEASE_13038
13039,13039,13039,13039,13039,13039,13039,13039,MONDO:0030033,"seizures, early-onset, with neurodegeneration and brain calcifications",MONDO,disease,DISEASE_13039
13040,13040,13040,13040,13040,13040,13040,13040,MONDO:0100337,SEC61A1 deficiency,MONDO,disease,DISEASE_13040
13041,13041,13041,13041,13041,13041,13041,13041,MONDO:0700046,baclofen withdrawal syndrome,MONDO,disease,DISEASE_13041
13042,13042,13042,13042,13042,13042,13042,13042,MONDO:0007083_MONDO:0008923,autosomal dominant palmoplantar keratoderma and congenital alopecia,MONDO_grouped,disease,DISEASE_13042
13043,13043,13043,13043,13043,13043,13043,13043,MONDO:0019194,localized lipodystrophy,MONDO,disease,DISEASE_13043
13044,13044,13044,13044,13044,13044,13044,13044,MONDO:0019150,obsolete familial isolated restrictive cardiomyopathy,MONDO,disease,DISEASE_13044
13045,13045,13045,13045,13045,13045,13045,13045,MONDO:0008774,2-aminoadipic 2-oxoadipic aciduria,MONDO,disease,DISEASE_13045
13046,13046,13046,13046,13046,13046,13046,13046,MONDO:0007967,melanoma and neural system tumor syndrome,MONDO,disease,DISEASE_13046
13047,13047,13047,13047,13047,13047,13047,13047,MONDO:0044751,chronic diarrheal disease,MONDO,disease,DISEASE_13047
13048,13048,13048,13048,13048,13048,13048,13048,MONDO:0007873,"lactic acidosis, chronic adult form",MONDO,disease,DISEASE_13048
13049,13049,13049,13049,13049,13049,13049,13049,MONDO:0000611,pre-malignant neoplasm,MONDO,disease,DISEASE_13049
13050,13050,13050,13050,13050,13050,13050,13050,MONDO:0015692,refractory anemia with excess blasts in transformation,MONDO,disease,DISEASE_13050
13051,13051,13051,13051,13051,13051,13051,13051,MONDO:0022580,blepharo naso facial syndrome van Maldergem type,MONDO,disease,DISEASE_13051
13052,13052,13052,13052,13052,13052,13052,13052,MONDO:0008822_MONDO:0013255_MONDO:0017123,"arthrogryposis, renal dysfunction, and cholestasis",MONDO_grouped,disease,DISEASE_13052
13053,13053,13053,13053,13053,13053,13053,13053,MONDO:0100294_MONDO:0031230,"mitochondrial complex II deficiency, nuclear",MONDO_grouped,disease,DISEASE_13053
13054,13054,13054,13054,13054,13054,13054,13054,MONDO:0000992,heart conduction disease,MONDO,disease,DISEASE_13054
13055,13055,13055,13055,13055,13055,13055,13055,MONDO:0958093,non-syndromic supernumerary kidneys,MONDO,disease,DISEASE_13055
13056,13056,13056,13056,13056,13056,13056,13056,MONDO:0004861,ophthalmia nodosa,MONDO,disease,DISEASE_13056
13057,13057,13057,13057,13057,13057,13057,13057,MONDO:0018575,obsolete microcephalic primordial dwarfism-insulin resistance syndrome,MONDO,disease,DISEASE_13057
13058,13058,13058,13058,13058,13058,13058,13058,MONDO:0009473,isotretinoin-like syndrome,MONDO,disease,DISEASE_13058
13059,13059,13059,13059,13059,13059,13059,13059,MONDO:0007612,gingival fibromatosis-progressive deafness syndrome,MONDO,disease,DISEASE_13059
13060,13060,13060,13060,13060,13060,13060,13060,MONDO:0015743,idiopathic bilateral vestibulopathy,MONDO,disease,DISEASE_13060
13061,13061,13061,13061,13061,13061,13061,13061,MONDO:0004184_MONDO:0001926_MONDO:0004192_MONDO:0001730,urethral disorder,MONDO_grouped,disease,DISEASE_13061
13062,13062,13062,13062,13062,13062,13062,13062,MONDO:0002606,epithelioid type angiomyolipoma,MONDO,disease,DISEASE_13062
13063,13063,13063,13063,13063,13063,13063,13063,MONDO:0001932,obsolete atrophic vulva,MONDO,disease,DISEASE_13063
13064,13064,13064,13064,13064,13064,13064,13064,MONDO:0008708,acrocallosal syndrome,MONDO,disease,DISEASE_13064
13065,13065,13065,13065,13065,13065,13065,13065,MONDO:0021298,carcinoma in situ of oropharynx,MONDO,disease,DISEASE_13065
13066,13066,13066,13066,13066,13066,13066,13066,MONDO:0003903,benign vaginal mixed tumor,MONDO,disease,DISEASE_13066
13067,13067,13067,13067,13067,13067,13067,13067,MONDO:0009780,lethal omphalocele-cleft palate syndrome,MONDO,disease,DISEASE_13067
13068,13068,13068,13068,13068,13068,13068,13068,MONDO:0006606,scleredema adultorum,MONDO,disease,DISEASE_13068
13069,13069,13069,13069,13069,13069,13069,13069,MONDO:0007459,"dilution, pigmentary",MONDO,disease,DISEASE_13069
13070,13070,13070,13070,13070,13070,13070,13070,MONDO:1010536,"megacolon, horse",MONDO,disease,DISEASE_13070
13071,13071,13071,13071,13071,13071,13071,13071,MONDO:1010987,"hydrocephalus, puma",MONDO,disease,DISEASE_13071
13072,13072,13072,13072,13072,13072,13072,13072,MONDO:0006512,estrogen-receptor positive breast cancer,MONDO,disease,DISEASE_13072
13073,13073,13073,13073,13073,13073,13073,13073,MONDO:0005200,viral dilated cardiomyopathy,MONDO,disease,DISEASE_13073
13074,13074,13074,13074,13074,13074,13074,13074,MONDO:0009079,DOORS syndrome,MONDO,disease,DISEASE_13074
13075,13075,13075,13075,13075,13075,13075,13075,MONDO:0021663,sarcomatoid squamous cell carcinoma,MONDO,disease,DISEASE_13075
13076,13076,13076,13076,13076,13076,13076,13076,MONDO:0100348,"neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities",MONDO,disease,DISEASE_13076
13077,13077,13077,13077,13077,13077,13077,13077,MONDO:0011152,PHGDH deficiency,MONDO,disease,DISEASE_13077
13078,13078,13078,13078,13078,13078,13078,13078,MONDO:0000898,malignant hemangioma,MONDO,disease,DISEASE_13078
13079,13079,13079,13079,13079,13079,13079,13079,MONDO:0008803,Antley-Bixler syndrome,MONDO,disease,DISEASE_13079
13080,13080,13080,13080,13080,13080,13080,13080,MONDO:1040023,NDUFB11-related disorders,MONDO,disease,DISEASE_13080
13081,13081,13081,13081,13081,13081,13081,13081,MONDO:0012311,"spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctate calcifications, and deafness",MONDO,disease,DISEASE_13081
13082,13082,13082,13082,13082,13082,13082,13082,MONDO:0003602,intracranial liposarcoma,MONDO,disease,DISEASE_13082
13083,13083,13083,13083,13083,13083,13083,13083,MONDO:0019855,athyreosis,MONDO,disease,DISEASE_13083
13084,13084,13084,13084,13084,13084,13084,13084,MONDO:0002976,stomach diverticulosis,MONDO,disease,DISEASE_13084
13085,13085,13085,13085,13085,13085,13085,13085,MONDO:0008608,Down syndrome,MONDO,disease,DISEASE_13085
13086,13086,13086,13086,13086,13086,13086,13086,MONDO:0010637,"keratosis follicularis spinulosa decalvans, X-linked",MONDO,disease,DISEASE_13086
13087,13087,13087,13087,13087,13087,13087,13087,MONDO:1010141,"ectodermal dysplasia/skin fragility syndrome, non-human animal",MONDO,disease,DISEASE_13087
13088,13088,13088,13088,13088,13088,13088,13088,MONDO:0100493_MONDO:0100495,autosomal recessive titinopathy,MONDO_grouped,disease,DISEASE_13088
13089,13089,13089,13089,13089,13089,13089,13089,MONDO:0002092_MONDO:0003360,small intestine leiomyoma,MONDO_grouped,disease,DISEASE_13089
13090,13090,13090,13090,13090,13090,13090,13090,MONDO:0010252_MONDO:0100195,"intellectual disability, X-linked, with panhypopituitarism",MONDO_grouped,disease,DISEASE_13090
13091,13091,13091,13091,13091,13091,13091,13091,MONDO:0005220,collecting duct carcinoma,MONDO,disease,DISEASE_13091
13092,13092,13092,13092,13092,13092,13092,13092,MONDO:0013779,Wiskott-Aldrich syndrome 2,MONDO,disease,DISEASE_13092
13093,13093,13093,13093,13093,13093,13093,13093,MONDO:0022666,cassavism,MONDO,disease,DISEASE_13093
13094,13094,13094,13094,13094,13094,13094,13094,MONDO:0007052,growth hormone secreting pituitary adenoma 1,MONDO,disease,DISEASE_13094
13095,13095,13095,13095,13095,13095,13095,13095,MONDO:1010163,"tetradysmelia, non-human animal",MONDO,disease,DISEASE_13095
13096,13096,13096,13096,13096,13096,13096,13096,MONDO:0016316_MONDO:0016315_MONDO:0017171_MONDO:0017172,"mucopolysaccharidosis type 2, attenuated form",MONDO_grouped,disease,DISEASE_13096
13097,13097,13097,13097,13097,13097,13097,13097,MONDO:0009488,keratoconus posticus circumscriptus,MONDO,disease,DISEASE_13097
13098,13098,13098,13098,13098,13098,13098,13098,MONDO:0014520,"46,XX ovarian dysgenesis-short stature syndrome",MONDO,disease,DISEASE_13098
13099,13099,13099,13099,13099,13099,13099,13099,MONDO:0044872,dysautonomia,MONDO,disease,DISEASE_13099
13100,13100,13100,13100,13100,13100,13100,13100,MONDO:0005623_MONDO:0022518,autoimmune thyroid disease,MONDO_grouped,disease,DISEASE_13100
13101,13101,13101,13101,13101,13101,13101,13101,MONDO:1010047_MONDO:1010048,"spina bifida, non-human animal",MONDO_grouped,disease,DISEASE_13101
13102,13102,13102,13102,13102,13102,13102,13102,MONDO:0000346,"Hantavirus hemorrhagic fever with renal syndrome, Dobrava-Belgrade virus type",MONDO,disease,DISEASE_13102
13103,13103,13103,13103,13103,13103,13103,13103,MONDO:0044709,cochleovestibular dysplasia,MONDO,disease,DISEASE_13103
13104,13104,13104,13104,13104,13104,13104,13104,MONDO:0018450,spinal muscular atrophy with respiratory distress type 2,MONDO,disease,DISEASE_13104
13105,13105,13105,13105,13105,13105,13105,13105,MONDO:0022757,chromosome 20 trisomy,MONDO,disease,DISEASE_13105
13106,13106,13106,13106,13106,13106,13106,13106,MONDO:0011722,intellectual disability-obesity-prognathism-eye and skin anomalies syndrome,MONDO,disease,DISEASE_13106
13107,13107,13107,13107,13107,13107,13107,13107,MONDO:0001727,active cochleovestibular Meniere disease,MONDO,disease,DISEASE_13107
13108,13108,13108,13108,13108,13108,13108,13108,MONDO:1010685,"AA amyloidosis, white-tufted-ear marmoset",MONDO,disease,DISEASE_13108
13109,13109,13109,13109,13109,13109,13109,13109,MONDO:0010968,"glaucoma 3, primary infantile, B",MONDO,disease,DISEASE_13109
13110,13110,13110,13110,13110,13110,13110,13110,MONDO:1011010,"Horner syndrome, domestic cat",MONDO,disease,DISEASE_13110
13111,13111,13111,13111,13111,13111,13111,13111,MONDO:0003067,cervical lymphadenitis,MONDO,disease,DISEASE_13111
13112,13112,13112,13112,13112,13112,13112,13112,MONDO:0011895,idiopathic hypereosinophilic syndrome,MONDO,disease,DISEASE_13112
13113,13113,13113,13113,13113,13113,13113,13113,MONDO:0008930_MONDO:0011793_MONDO:0012339_MONDO:0012340_MONDO:0012341_MONDO:0012702_MONDO:0012776_MONDO:0012777_MONDO:0012778_MONDO:0012779_MONDO:0012780_MONDO:0012781_MONDO:0012782,"celiac disease, susceptibility to",MONDO_grouped,disease,DISEASE_13113
13114,13114,13114,13114,13114,13114,13114,13114,MONDO:0013860_MONDO:0005376,idiopathic membranous glomerulonephritis,MONDO_grouped,disease,DISEASE_13114
13115,13115,13115,13115,13115,13115,13115,13115,MONDO:0013462,fucosyltransferase 6 deficiency,MONDO,disease,DISEASE_13115
13116,13116,13116,13116,13116,13116,13116,13116,MONDO:0017620,congenital sucrase-isomaltase deficiency without starch intolerance,MONDO,disease,DISEASE_13116
13117,13117,13117,13117,13117,13117,13117,13117,MONDO:0019104,Sandifer syndrome,MONDO,disease,DISEASE_13117
13118,13118,13118,13118,13118,13118,13118,13118,MONDO:0014210,intellectual disability-hypotonia-spasticity-sleep disorder syndrome,MONDO,disease,DISEASE_13118
13119,13119,13119,13119,13119,13119,13119,13119,MONDO:0006349,papillary cystic neoplasm,MONDO,disease,DISEASE_13119
13120,13120,13120,13120,13120,13120,13120,13120,MONDO:0008503,Worster-Drought syndrome,MONDO,disease,DISEASE_13120
13121,13121,13121,13121,13121,13121,13121,13121,MONDO:0859006,proximal femoral focal deficiency,MONDO,disease,DISEASE_13121
13122,13122,13122,13122,13122,13122,13122,13122,MONDO:0020641,respiratory tract neoplasm,MONDO,disease,DISEASE_13122
13123,13123,13123,13123,13123,13123,13123,13123,MONDO:0003840,epicardium lipoma,MONDO,disease,DISEASE_13123
13124,13124,13124,13124,13124,13124,13124,13124,MONDO:0022990,diphallus rachischisis imperforate anus,MONDO,disease,DISEASE_13124
13125,13125,13125,13125,13125,13125,13125,13125,MONDO:0002740,uterine ligament mucinous adenocarcinoma,MONDO,disease,DISEASE_13125
13126,13126,13126,13126,13126,13126,13126,13126,MONDO:0012931_MONDO:0011917,"focal segmental glomerulosclerosis 4, susceptibility to",MONDO_grouped,disease,DISEASE_13126
13127,13127,13127,13127,13127,13127,13127,13127,MONDO:0013042,atypical hemolytic-uremic syndrome with B factor anomaly,MONDO,disease,DISEASE_13127
13128,13128,13128,13128,13128,13128,13128,13128,MONDO:0800495,variable-age epilepsy syndrome with developmental and/or epileptic encephalopathy or progressive neurological deterioration,MONDO,disease,DISEASE_13128
13129,13129,13129,13129,13129,13129,13129,13129,MONDO:0001460,dyshormonogenic goiter,MONDO,disease,DISEASE_13129
13130,13130,13130,13130,13130,13130,13130,13130,MONDO:0023042,ectodermal dysplasia margarita type,MONDO,disease,DISEASE_13130
13131,13131,13131,13131,13131,13131,13131,13131,MONDO:0100168,desmoid tumor caused by somatic mutation,MONDO,disease,DISEASE_13131
13132,13132,13132,13132,13132,13132,13132,13132,MONDO:0001377,vitreous syneresis,MONDO,disease,DISEASE_13132
13133,13133,13133,13133,13133,13133,13133,13133,MONDO:0013947_MONDO:0971150_MONDO:0957874_MONDO:0011771_MONDO:0957876_MONDO:0012608_MONDO:0030977_MONDO:0030055_MONDO:0015363_MONDO:0009750,"neuronopathy, distal hereditary motor, autosomal recessive",MONDO_grouped,disease,DISEASE_13133
13134,13134,13134,13134,13134,13134,13134,13134,MONDO:0009604,methemoglobin reductase deficiency,MONDO,disease,DISEASE_13134
13135,13135,13135,13135,13135,13135,13135,13135,MONDO:0005708,Colorado tick fever,MONDO,disease,DISEASE_13135
13136,13136,13136,13136,13136,13136,13136,13136,MONDO:0005418,non-compaction cardiomyopathy,MONDO,disease,DISEASE_13136
13137,13137,13137,13137,13137,13137,13137,13137,MONDO:0000471,tricuspid valve disorder,MONDO,disease,DISEASE_13137
13138,13138,13138,13138,13138,13138,13138,13138,MONDO:0024744,childhood choroid plexus neoplasm,MONDO,disease,DISEASE_13138
13139,13139,13139,13139,13139,13139,13139,13139,MONDO:0003904,lung occult squamous cell carcinoma,MONDO,disease,DISEASE_13139
13140,13140,13140,13140,13140,13140,13140,13140,MONDO:1012132,"immunoglobulin G deficiency, dog",MONDO,disease,DISEASE_13140
13141,13141,13141,13141,13141,13141,13141,13141,MONDO:0015467,"craniosynostosis, Philadelphia type",MONDO,disease,DISEASE_13141
13142,13142,13142,13142,13142,13142,13142,13142,MONDO:0016453,foodborne botulism,MONDO,disease,DISEASE_13142
13143,13143,13143,13143,13143,13143,13143,13143,MONDO:0013394,porencephaly-microcephaly-bilateral congenital cataract syndrome,MONDO,disease,DISEASE_13143
13144,13144,13144,13144,13144,13144,13144,13144,MONDO:0044687,chronic relapsing inflammatory optic neuropathy,MONDO,disease,DISEASE_13144
13145,13145,13145,13145,13145,13145,13145,13145,MONDO:0030038_MONDO:1011515,"hereditary glaucoma, primary closed-angle",MONDO_grouped,disease,DISEASE_13145
13146,13146,13146,13146,13146,13146,13146,13146,MONDO:1010868,"mucopolysaccharidosis, GNS-related, goat",MONDO,disease,DISEASE_13146
13147,13147,13147,13147,13147,13147,13147,13147,MONDO:1011765,"micromelia, non-human animal",MONDO,disease,DISEASE_13147
13148,13148,13148,13148,13148,13148,13148,13148,MONDO:0016611,lipoblastoma,MONDO,disease,DISEASE_13148
13149,13149,13149,13149,13149,13149,13149,13149,MONDO:0006650,anterior spinal artery syndrome,MONDO,disease,DISEASE_13149
13150,13150,13150,13150,13150,13150,13150,13150,MONDO:0022760,chromosome 22q deletion,MONDO,disease,DISEASE_13150
13151,13151,13151,13151,13151,13151,13151,13151,MONDO:0003836,malignant thyroid stimulating hormone producing neoplasm of pituitary gland,MONDO,disease,DISEASE_13151
13152,13152,13152,13152,13152,13152,13152,13152,MONDO:0010321_MONDO:0010342_MONDO:0010341_MONDO:0010440_MONDO:0010449,"autism, susceptibility to, X-linked",MONDO_grouped,disease,DISEASE_13152
13153,13153,13153,13153,13153,13153,13153,13153,MONDO:0009237,focal epithelial hyperplasia,MONDO,disease,DISEASE_13153
13154,13154,13154,13154,13154,13154,13154,13154,MONDO:1010358,"Leber hereditary optic neuropathy, non-human animal",MONDO,disease,DISEASE_13154
13155,13155,13155,13155,13155,13155,13155,13155,MONDO:0016209,benign familial nocturnal alternating hemiplegia of childhood,MONDO,disease,DISEASE_13155
13156,13156,13156,13156,13156,13156,13156,13156,MONDO:0100331,nerve agent poisoning,MONDO,disease,DISEASE_13156
13157,13157,13157,13157,13157,13157,13157,13157,MONDO:0021588,eyelid sebaceous gland carcinoma,MONDO,disease,DISEASE_13157
13158,13158,13158,13158,13158,13158,13158,13158,MONDO:0010128,thyrocerebrorenal syndrome,MONDO,disease,DISEASE_13158
13159,13159,13159,13159,13159,13159,13159,13159,MONDO:0015257,sino-auricular heart block,MONDO,disease,DISEASE_13159
13160,13160,13160,13160,13160,13160,13160,13160,MONDO:0000680,astereognosia,MONDO,disease,DISEASE_13160
13161,13161,13161,13161,13161,13161,13161,13161,MONDO:0006424,soft tissue neoplasm,MONDO,disease,DISEASE_13161
13162,13162,13162,13162,13162,13162,13162,13162,MONDO:0002437,dehydration polycythemia,MONDO,disease,DISEASE_13162
13163,13163,13163,13163,13163,13163,13163,13163,MONDO:0020102,hereditary stomatocytosis,MONDO,disease,DISEASE_13163
13164,13164,13164,13164,13164,13164,13164,13164,MONDO:0018677,visceral heterotaxy,MONDO,disease,DISEASE_13164
13165,13165,13165,13165,13165,13165,13165,13165,MONDO:0009823_MONDO:0009824_MONDO:0013327_MONDO:0002474,primary hyperoxaluria,MONDO_grouped,disease,DISEASE_13165
13166,13166,13166,13166,13166,13166,13166,13166,MONDO:0700255,paraneoplastic renal syndrome,MONDO,disease,DISEASE_13166
13167,13167,13167,13167,13167,13167,13167,13167,MONDO:0002423,rectosigmoid junction neoplasm,MONDO,disease,DISEASE_13167
13168,13168,13168,13168,13168,13168,13168,13168,MONDO:0003873,ovarian surface papilloma,MONDO,disease,DISEASE_13168
13169,13169,13169,13169,13169,13169,13169,13169,MONDO:0022398,aglossia and situs inversus,MONDO,disease,DISEASE_13169
13170,13170,13170,13170,13170,13170,13170,13170,MONDO:0012197,idiopathic aplastic anemia,MONDO,disease,DISEASE_13170
13171,13171,13171,13171,13171,13171,13171,13171,MONDO:1010490,"ventricular septal defect, domestic cat",MONDO,disease,DISEASE_13171
13172,13172,13172,13172,13172,13172,13172,13172,MONDO:0003810,bladder diffuse clear cell adenocarcinoma,MONDO,disease,DISEASE_13172
13173,13173,13173,13173,13173,13173,13173,13173,MONDO:0020848_MONDO:0011877_MONDO:0008156,"osteopetrosis, autosomal dominant",MONDO_grouped,disease,DISEASE_13173
13174,13174,13174,13174,13174,13174,13174,13174,MONDO:0017106,retrocerebellar cyst,MONDO,disease,DISEASE_13174
13175,13175,13175,13175,13175,13175,13175,13175,MONDO:1011898,"hypomyelinating leukodystrophy, non-human animal",MONDO,disease,DISEASE_13175
13176,13176,13176,13176,13176,13176,13176,13176,MONDO:0005575,colorectal cancer,MONDO,disease,DISEASE_13176
13177,13177,13177,13177,13177,13177,13177,13177,MONDO:1011406_MONDO:1011407_MONDO:1011690,"autoimmune hemolytic anemia, non-human animal",MONDO_grouped,disease,DISEASE_13177
13178,13178,13178,13178,13178,13178,13178,13178,MONDO:0033818,Terrien marginal degeneration,MONDO,disease,DISEASE_13178
13179,13179,13179,13179,13179,13179,13179,13179,MONDO:0012895_MONDO:0011264_MONDO:0007493_MONDO:0011200_MONDO:0011886_MONDO:0009141_MONDO:0044843,torsion dystonia,MONDO_grouped,disease,DISEASE_13179
13180,13180,13180,13180,13180,13180,13180,13180,MONDO:0975826,"arthrogryposis multiplex congenita 7, X-linked",MONDO,disease,DISEASE_13180
13181,13181,13181,13181,13181,13181,13181,13181,MONDO:0859275,"neurodevelopmental disorder with spasticity, seizures, and brain abnormalities",MONDO,disease,DISEASE_13181
13182,13182,13182,13182,13182,13182,13182,13182,MONDO:0001317,phlyctenulosis,MONDO,disease,DISEASE_13182
13183,13183,13183,13183,13183,13183,13183,13183,MONDO:0008919,systemic primary carnitine deficiency disease,MONDO,disease,DISEASE_13183
13184,13184,13184,13184,13184,13184,13184,13184,MONDO:0850105_MONDO:0850106_MONDO:0850108_MONDO:0850109,non-specific autoimmune brainstem encephalitis with characteristic antibodies,MONDO_grouped,disease,DISEASE_13184
13185,13185,13185,13185,13185,13185,13185,13185,MONDO:0009423,"hypokalemic alkalosis, familial, with specific renal tubulopathy",MONDO,disease,DISEASE_13185
13186,13186,13186,13186,13186,13186,13186,13186,MONDO:0012634,craniofacial dysplasia - osteopenia syndrome,MONDO,disease,DISEASE_13186
13187,13187,13187,13187,13187,13187,13187,13187,MONDO:0016040,harlequin syndrome,MONDO,disease,DISEASE_13187
13188,13188,13188,13188,13188,13188,13188,13188,MONDO:0015166_MONDO:0018433_MONDO:0100374_MONDO:0100375_MONDO:0100376_MONDO:0100378_MONDO:0100379_MONDO:0100380_MONDO:0100381_MONDO:0100383_MONDO:0100385_MONDO:0100395_MONDO:0100396_MONDO:0100397_MONDO:0100399_MONDO:0100407_MONDO:0100408_MONDO:0100409_MONDO:0100410_MONDO:0850492_MONDO:0850495,acute myeloid leukemia with t(8;21)(q22;q22) translocation,MONDO_grouped,disease,DISEASE_13188
13189,13189,13189,13189,13189,13189,13189,13189,MONDO:0009478,combined immunodeficiency due to DOCK8 deficiency,MONDO,disease,DISEASE_13189
13190,13190,13190,13190,13190,13190,13190,13190,MONDO:0001672,bronchus cancer,MONDO,disease,DISEASE_13190
13191,13191,13191,13191,13191,13191,13191,13191,MONDO:0024421,short stature contractures hypotonia,MONDO,disease,DISEASE_13191
13192,13192,13192,13192,13192,13192,13192,13192,MONDO:0007001,tricuspid valve prolapse,MONDO,disease,DISEASE_13192
13193,13193,13193,13193,13193,13193,13193,13193,MONDO:1011456,"rickets, non-human animal",MONDO,disease,DISEASE_13193
13194,13194,13194,13194,13194,13194,13194,13194,MONDO:0022060,calloso-genital dysplasia,MONDO,disease,DISEASE_13194
13195,13195,13195,13195,13195,13195,13195,13195,MONDO:0020248_MONDO:0001457_MONDO:0001923,vitreoretinal degeneration,MONDO_grouped,disease,DISEASE_13195
13196,13196,13196,13196,13196,13196,13196,13196,MONDO:0017997,telecanthus-hypertelorism-strabismus-pes cavus syndrome,MONDO,disease,DISEASE_13196
13197,13197,13197,13197,13197,13197,13197,13197,MONDO:1011133_MONDO:1011134,"pneumothorax, dog",MONDO_grouped,disease,DISEASE_13197
13198,13198,13198,13198,13198,13198,13198,13198,MONDO:0034895,congenital brachyesophagus-intrathoracic stomach-vertebral anomalies syndrome,MONDO,disease,DISEASE_13198
13199,13199,13199,13199,13199,13199,13199,13199,MONDO:0010641,X-linked diffuse leiomyomatosis-Alport syndrome,MONDO,disease,DISEASE_13199
13200,13200,13200,13200,13200,13200,13200,13200,MONDO:0007740,Wagner disease,MONDO,disease,DISEASE_13200
13201,13201,13201,13201,13201,13201,13201,13201,MONDO:0012590,XFE progeroid syndrome,MONDO,disease,DISEASE_13201
13202,13202,13202,13202,13202,13202,13202,13202,MONDO:0800347,"cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction",MONDO,disease,DISEASE_13202
13203,13203,13203,13203,13203,13203,13203,13203,MONDO:0006810,intracranial hypertension,MONDO,disease,DISEASE_13203
13204,13204,13204,13204,13204,13204,13204,13204,MONDO:0008010_MONDO:0008011,antigen defined by monoclonal antibody Aj9,MONDO_grouped,disease,DISEASE_13204
13205,13205,13205,13205,13205,13205,13205,13205,MONDO:0009891,acquired polycythemia vera,MONDO,disease,DISEASE_13205
13206,13206,13206,13206,13206,13206,13206,13206,MONDO:0010568,Aicardi syndrome,MONDO,disease,DISEASE_13206
13207,13207,13207,13207,13207,13207,13207,13207,MONDO:1012524,"diffuse cystic renal dysplasia and hepatic fibrosis, dog",MONDO,disease,DISEASE_13207
13208,13208,13208,13208,13208,13208,13208,13208,MONDO:0015040,myelodysplastic syndrome with excess blasts-1,MONDO,disease,DISEASE_13208
13209,13209,13209,13209,13209,13209,13209,13209,MONDO:0958270_MONDO:0958356_MONDO:0018561_MONDO:0958355_MONDO:0958357,central precocious puberty in male,MONDO_grouped,disease,DISEASE_13209
13210,13210,13210,13210,13210,13210,13210,13210,MONDO:0001723,progressive peripheral pterygium,MONDO,disease,DISEASE_13210
13211,13211,13211,13211,13211,13211,13211,13211,MONDO:0006134,cervical adenosquamous carcinoma,MONDO,disease,DISEASE_13211
13212,13212,13212,13212,13212,13212,13212,13212,MONDO:0001821,hypoactive sexual desire disorder,MONDO,disease,DISEASE_13212
13213,13213,13213,13213,13213,13213,13213,13213,MONDO:0017406,hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome,MONDO,disease,DISEASE_13213
13214,13214,13214,13214,13214,13214,13214,13214,MONDO:0019615,pituitary dermoid and epidermoid cysts,MONDO,disease,DISEASE_13214
13215,13215,13215,13215,13215,13215,13215,13215,MONDO:0008626,"ureter, bifid or double",MONDO,disease,DISEASE_13215
13216,13216,13216,13216,13216,13216,13216,13216,MONDO:0005136,malaria,MONDO,disease,DISEASE_13216
13217,13217,13217,13217,13217,13217,13217,13217,MONDO:0000914_MONDO:0014768,"cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy,",MONDO_grouped,disease,DISEASE_13217
13218,13218,13218,13218,13218,13218,13218,13218,MONDO:0008546_MONDO:0008547_MONDO:0017042,thanatophoric dysplasia,MONDO_grouped,disease,DISEASE_13218
13219,13219,13219,13219,13219,13219,13219,13219,MONDO:0044688,isolated optic neuritis,MONDO,disease,DISEASE_13219
13220,13220,13220,13220,13220,13220,13220,13220,MONDO:1010126,"atopic dermatitis, non-human animal",MONDO,disease,DISEASE_13220
13221,13221,13221,13221,13221,13221,13221,13221,MONDO:0002678_MONDO:0003022,pediatric fibrosarcoma,MONDO_grouped,disease,DISEASE_13221
13222,13222,13222,13222,13222,13222,13222,13222,MONDO:0859286,"neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures",MONDO,disease,DISEASE_13222
13223,13223,13223,13223,13223,13223,13223,13223,MONDO:0017823,somatomammotropinoma,MONDO,disease,DISEASE_13223
13224,13224,13224,13224,13224,13224,13224,13224,MONDO:0009521,"leukemia, acute myelocytic, with polyposis coli and colon cancer",MONDO,disease,DISEASE_13224
13225,13225,13225,13225,13225,13225,13225,13225,MONDO:0015951,hereditary photodermatosis,MONDO,disease,DISEASE_13225
13226,13226,13226,13226,13226,13226,13226,13226,MONDO:1010732,"X-linked severe combined immunodeficiency disease, IL2RG-related, pig",MONDO,disease,DISEASE_13226
13227,13227,13227,13227,13227,13227,13227,13227,MONDO:0009456,Immunoerythromyeloid hypoplasia,MONDO,disease,DISEASE_13227
13228,13228,13228,13228,13228,13228,13228,13228,MONDO:1010696,"analphalipoproteinaemia, chicken",MONDO,disease,DISEASE_13228
13229,13229,13229,13229,13229,13229,13229,13229,MONDO:0000774_MONDO:0100014_MONDO:0850416,autoimmune neuropathy,MONDO_grouped,disease,DISEASE_13229
13230,13230,13230,13230,13230,13230,13230,13230,MONDO:0005791,herpangina,MONDO,disease,DISEASE_13230
13231,13231,13231,13231,13231,13231,13231,13231,MONDO:0008183,annular pancreas,MONDO,disease,DISEASE_13231
13232,13232,13232,13232,13232,13232,13232,13232,MONDO:0700092,neurodevelopmental disorder,MONDO,disease,DISEASE_13232
13233,13233,13233,13233,13233,13233,13233,13233,MONDO:0021458,benign neoplasm of penis,MONDO,disease,DISEASE_13233
13234,13234,13234,13234,13234,13234,13234,13234,MONDO:0001616,lobomycosis,MONDO,disease,DISEASE_13234
13235,13235,13235,13235,13235,13235,13235,13235,MONDO:0958275,segmental spinal dysgenesis,MONDO,disease,DISEASE_13235
13236,13236,13236,13236,13236,13236,13236,13236,MONDO:0007915_MONDO:0859083_MONDO:0004670_MONDO:1010733,systemic lupus erythematosus,MONDO_grouped,disease,DISEASE_13236
13237,13237,13237,13237,13237,13237,13237,13237,MONDO:0009665,biotinidase deficiency,MONDO,disease,DISEASE_13237
13238,13238,13238,13238,13238,13238,13238,13238,MONDO:0011247,jejunal atresia with renal adysplasia,MONDO,disease,DISEASE_13238
13239,13239,13239,13239,13239,13239,13239,13239,MONDO:0010722,X-linked retinal dysplasia,MONDO,disease,DISEASE_13239
13240,13240,13240,13240,13240,13240,13240,13240,MONDO:0000600,nosophobia,MONDO,disease,DISEASE_13240
13241,13241,13241,13241,13241,13241,13241,13241,MONDO:1011950,"osteochondroma causing progressive posterior paresis, non-human animal",MONDO,disease,DISEASE_13241
13242,13242,13242,13242,13242,13242,13242,13242,MONDO:0100536,"tooth agenesis, selective, with orofacial cleft",MONDO,disease,DISEASE_13242
13243,13243,13243,13243,13243,13243,13243,13243,MONDO:1011068,"urolithiasis, Silvery lutung",MONDO,disease,DISEASE_13243
13244,13244,13244,13244,13244,13244,13244,13244,MONDO:0009963,Ulbright-Hodes syndrome,MONDO,disease,DISEASE_13244
13245,13245,13245,13245,13245,13245,13245,13245,MONDO:1011636,"compulsive disorder, non-human animal",MONDO,disease,DISEASE_13245
13246,13246,13246,13246,13246,13246,13246,13246,MONDO:1012632,"XX difference of sexual development, Japanese medaka",MONDO,disease,DISEASE_13246
13247,13247,13247,13247,13247,13247,13247,13247,MONDO:0020853,"encephalitis/encephalopathy, mild, with reversible myelin vacuolization",MONDO,disease,DISEASE_13247
13248,13248,13248,13248,13248,13248,13248,13248,MONDO:0019909,ring chromosome 16,MONDO,disease,DISEASE_13248
13249,13249,13249,13249,13249,13249,13249,13249,MONDO:0007898,"leukocyte nuclear appendages, hereditary prevalence of",MONDO,disease,DISEASE_13249
13250,13250,13250,13250,13250,13250,13250,13250,MONDO:0043475,Adams-Stokes syndrome,MONDO,disease,DISEASE_13250
13251,13251,13251,13251,13251,13251,13251,13251,MONDO:0008223,hypokalemic periodic paralysis,MONDO,disease,DISEASE_13251
13252,13252,13252,13252,13252,13252,13252,13252,MONDO:0008027,"muscular atrophy, malignant neurogenic",MONDO,disease,DISEASE_13252
13253,13253,13253,13253,13253,13253,13253,13253,MONDO:0044786,solid pseudopapillary neoplasm of the pancreas,MONDO,disease,DISEASE_13253
13254,13254,13254,13254,13254,13254,13254,13254,MONDO:0005994,trichostrongyloidiasis,MONDO,disease,DISEASE_13254
13255,13255,13255,13255,13255,13255,13255,13255,MONDO:0008178_MONDO:0000507,inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1,MONDO_grouped,disease,DISEASE_13255
13256,13256,13256,13256,13256,13256,13256,13256,MONDO:0006010,salmonid viral hemorrhagic septicemia,MONDO,disease,DISEASE_13256
13257,13257,13257,13257,13257,13257,13257,13257,MONDO:0009479,Johanson-Blizzard syndrome,MONDO,disease,DISEASE_13257
13258,13258,13258,13258,13258,13258,13258,13258,MONDO:0008373,retinal arterial tortuosity,MONDO,disease,DISEASE_13258
13259,13259,13259,13259,13259,13259,13259,13259,MONDO:1011876,"unilateral subcortical heterotopia, non-human animal",MONDO,disease,DISEASE_13259
13260,13260,13260,13260,13260,13260,13260,13260,MONDO:0021450,benign neoplasm of heart,MONDO,disease,DISEASE_13260
13261,13261,13261,13261,13261,13261,13261,13261,MONDO:0002754_MONDO:0015043,extramedullary plasmacytoma,MONDO_grouped,disease,DISEASE_13261
13262,13262,13262,13262,13262,13262,13262,13262,MONDO:1010933_MONDO:1012822,"congenital increased muscular tonus, MYBPC1-related, cattle",MONDO_grouped,disease,DISEASE_13262
13263,13263,13263,13263,13263,13263,13263,13263,MONDO:0003943,central nervous system hibernoma,MONDO,disease,DISEASE_13263
13264,13264,13264,13264,13264,13264,13264,13264,MONDO:0003077,intraocular retinoblastoma,MONDO,disease,DISEASE_13264
13265,13265,13265,13265,13265,13265,13265,13265,MONDO:0006961,scrapie,MONDO,disease,DISEASE_13265
13266,13266,13266,13266,13266,13266,13266,13266,MONDO:0014716_MONDO:0014848,macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome,MONDO_grouped,disease,DISEASE_13266
13267,13267,13267,13267,13267,13267,13267,13267,MONDO:0971118,pilocytic astrocytoma with histological features of anaplasia,MONDO,disease,DISEASE_13267
13268,13268,13268,13268,13268,13268,13268,13268,MONDO:1012038,"cerebellar abiotrophy, dog",MONDO,disease,DISEASE_13268
13269,13269,13269,13269,13269,13269,13269,13269,MONDO:1011651,"cardiomyopathy and juvenile mortality, non-human animal",MONDO,disease,DISEASE_13269
13270,13270,13270,13270,13270,13270,13270,13270,MONDO:0003736,cancerophobia,MONDO,disease,DISEASE_13270
13271,13271,13271,13271,13271,13271,13271,13271,MONDO:0004961,stage I endometrioid carcinoma,MONDO,disease,DISEASE_13271
13272,13272,13272,13272,13272,13272,13272,13272,MONDO:0009944,pyloric atresia,MONDO,disease,DISEASE_13272
13273,13273,13273,13273,13273,13273,13273,13273,MONDO:0008507,"surface polypeptides, anonymous",MONDO,disease,DISEASE_13273
13274,13274,13274,13274,13274,13274,13274,13274,MONDO:0004709,occipital lobe neoplasm,MONDO,disease,DISEASE_13274
13275,13275,13275,13275,13275,13275,13275,13275,MONDO:0004088,cervical basaloid carcinoma,MONDO,disease,DISEASE_13275
13276,13276,13276,13276,13276,13276,13276,13276,MONDO:0007573,"erythroleukemia, familial, susceptibility to",MONDO,disease,DISEASE_13276
13277,13277,13277,13277,13277,13277,13277,13277,MONDO:0001612,carotid stenosis,MONDO,disease,DISEASE_13277
13278,13278,13278,13278,13278,13278,13278,13278,MONDO:0018649,obsolete cerebral visual impairment,MONDO,disease,DISEASE_13278
13279,13279,13279,13279,13279,13279,13279,13279,MONDO:0024618,poliovirus infection,MONDO,disease,DISEASE_13279
13280,13280,13280,13280,13280,13280,13280,13280,MONDO:0021273,leiomyoma of ciliary body,MONDO,disease,DISEASE_13280
13281,13281,13281,13281,13281,13281,13281,13281,MONDO:0011676,PHACE syndrome,MONDO,disease,DISEASE_13281
13282,13282,13282,13282,13282,13282,13282,13282,MONDO:0005908,peste des petits ruminants infectious disease,MONDO,disease,DISEASE_13282
13283,13283,13283,13283,13283,13283,13283,13283,MONDO:0007492_MONDO:0100016,early-onset generalized limb-onset dystonia,MONDO_grouped,disease,DISEASE_13283
13284,13284,13284,13284,13284,13284,13284,13284,MONDO:0021047,breast phyllodes tumor,MONDO,disease,DISEASE_13284
13285,13285,13285,13285,13285,13285,13285,13285,MONDO:0016568,Lowe-Kohn-Cohen syndrome,MONDO,disease,DISEASE_13285
13286,13286,13286,13286,13286,13286,13286,13286,MONDO:0032934,genitourinary and/or brain malformation syndrome,MONDO,disease,DISEASE_13286
13287,13287,13287,13287,13287,13287,13287,13287,MONDO:0958195_MONDO:0958176_MONDO:0008116,oculopharyngeal muscular dystrophy,MONDO_grouped,disease,DISEASE_13287
13288,13288,13288,13288,13288,13288,13288,13288,MONDO:0006978_MONDO:0001787,splenic infarction,MONDO_grouped,disease,DISEASE_13288
13289,13289,13289,13289,13289,13289,13289,13289,MONDO:0021101,appendix L-cell glucagon-like peptide-producing neuroendocrine tumor,MONDO,disease,DISEASE_13289
13290,13290,13290,13290,13290,13290,13290,13290,MONDO:1012451_MONDO:1012452_MONDO:1012613_MONDO:1012737,"intestinal cobalamin (vitamin B12) malabsorption, dog",MONDO_grouped,disease,DISEASE_13290
13291,13291,13291,13291,13291,13291,13291,13291,MONDO:1012680,"vitamin D-dependent rickets, VDR-related, cat",MONDO,disease,DISEASE_13291
13292,13292,13292,13292,13292,13292,13292,13292,MONDO:0019858,idiopathic congenital hypothyroidism,MONDO,disease,DISEASE_13292
13293,13293,13293,13293,13293,13293,13293,13293,MONDO:0016964,partial duplication of the long arm of chromosome 14,MONDO,disease,DISEASE_13293
13294,13294,13294,13294,13294,13294,13294,13294,MONDO:0957476,isolated persistent urogenital sinus,MONDO,disease,DISEASE_13294
13295,13295,13295,13295,13295,13295,13295,13295,MONDO:0004174,secretory uterine corpus endometrioid adenocarcinoma,MONDO,disease,DISEASE_13295
13296,13296,13296,13296,13296,13296,13296,13296,MONDO:0005093,skin disorder,MONDO,disease,DISEASE_13296
13297,13297,13297,13297,13297,13297,13297,13297,MONDO:0008914,cardioauditory syndrome of Sanchez Cascos,MONDO,disease,DISEASE_13297
13298,13298,13298,13298,13298,13298,13298,13298,MONDO:0006359,neoplasm with perivascular epithelioid cell differentiation,MONDO,disease,DISEASE_13298
13299,13299,13299,13299,13299,13299,13299,13299,MONDO:0014119,intellectual disability-strabismus syndrome,MONDO,disease,DISEASE_13299
13300,13300,13300,13300,13300,13300,13300,13300,MONDO:0003220_MONDO:0006215_MONDO:0002857_MONDO:0006220_MONDO:0000972_MONDO:0003297_MONDO:0003364_MONDO:0004474_MONDO:0004484_MONDO:0006216,gallbladder carcinoma,MONDO_grouped,disease,DISEASE_13300
13301,13301,13301,13301,13301,13301,13301,13301,MONDO:0019830_MONDO:0020451,congenital anomaly of the inferior vena cava,MONDO_grouped,disease,DISEASE_13301
13302,13302,13302,13302,13302,13302,13302,13302,MONDO:0016511,infectious embryofetopathy,MONDO,disease,DISEASE_13302
13303,13303,13303,13303,13303,13303,13303,13303,MONDO:0018324,adult-onset myasthenia gravis,MONDO,disease,DISEASE_13303
13304,13304,13304,13304,13304,13304,13304,13304,MONDO:0000589,autoimmune disorder of musculoskeletal system,MONDO,disease,DISEASE_13304
13305,13305,13305,13305,13305,13305,13305,13305,MONDO:0017354,infantile glycine encephalopathy,MONDO,disease,DISEASE_13305
13306,13306,13306,13306,13306,13306,13306,13306,MONDO:0016802,mitochondrial protein import disorder,MONDO,disease,DISEASE_13306
13307,13307,13307,13307,13307,13307,13307,13307,MONDO:0019846,acquired central diabetes insipidus,MONDO,disease,DISEASE_13307
13308,13308,13308,13308,13308,13308,13308,13308,MONDO:0032661,"neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia",MONDO,disease,DISEASE_13308
13309,13309,13309,13309,13309,13309,13309,13309,MONDO:0021477,benign neoplasm of sphenoidal sinus,MONDO,disease,DISEASE_13309
13310,13310,13310,13310,13310,13310,13310,13310,MONDO:0003709,agoraphobia,MONDO,disease,DISEASE_13310
13311,13311,13311,13311,13311,13311,13311,13311,MONDO:0006705_MONDO:0006671,Bacteroidaceae infectious disease,MONDO_grouped,disease,DISEASE_13311
13312,13312,13312,13312,13312,13312,13312,13312,MONDO:1010259_MONDO:1010261,"nephritis, non-human animal",MONDO_grouped,disease,DISEASE_13312
13313,13313,13313,13313,13313,13313,13313,13313,MONDO:0018820,recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome,MONDO,disease,DISEASE_13313
13314,13314,13314,13314,13314,13314,13314,13314,MONDO:0020541,maligant granulosa cell tumor of ovary,MONDO,disease,DISEASE_13314
13315,13315,13315,13315,13315,13315,13315,13315,MONDO:0957576,"parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development",MONDO,disease,DISEASE_13315
13316,13316,13316,13316,13316,13316,13316,13316,MONDO:0016602,citrin deficiency,MONDO,disease,DISEASE_13316
13317,13317,13317,13317,13317,13317,13317,13317,MONDO:0008619,ulna metaphyseal dysplasia syndrome,MONDO,disease,DISEASE_13317
13318,13318,13318,13318,13318,13318,13318,13318,MONDO:0004885,choroidal sclerosis,MONDO,disease,DISEASE_13318
13319,13319,13319,13319,13319,13319,13319,13319,MONDO:0019502_MONDO:0019181_MONDO:0015802_MONDO:0000509,autosomal recessive non-syndromic intellectual disability,MONDO_grouped,disease,DISEASE_13319
13320,13320,13320,13320,13320,13320,13320,13320,MONDO:0800153,urea cycle disorder or inherited hyperammonemia,MONDO,disease,DISEASE_13320
13321,13321,13321,13321,13321,13321,13321,13321,MONDO:0012288,iridogoniodysgenesis and skeletal anomalies,MONDO,disease,DISEASE_13321
13322,13322,13322,13322,13322,13322,13322,13322,MONDO:0018164,arterial thoracic outlet syndrome,MONDO,disease,DISEASE_13322
13323,13323,13323,13323,13323,13323,13323,13323,MONDO:0008789,"anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane",MONDO,disease,DISEASE_13323
13324,13324,13324,13324,13324,13324,13324,13324,MONDO:0019289,hyperpigmentation of the skin,MONDO,disease,DISEASE_13324
13325,13325,13325,13325,13325,13325,13325,13325,MONDO:0000118,reticulate pigment disorder,MONDO,disease,DISEASE_13325
13326,13326,13326,13326,13326,13326,13326,13326,MONDO:1010097,DHDDS-related syndrome,MONDO,disease,DISEASE_13326
13327,13327,13327,13327,13327,13327,13327,13327,MONDO:0008502,"sulfhemoglobinemia, congenital",MONDO,disease,DISEASE_13327
13328,13328,13328,13328,13328,13328,13328,13328,MONDO:1011706,"atypical thrombasthenia, non-human animal",MONDO,disease,DISEASE_13328
13329,13329,13329,13329,13329,13329,13329,13329,MONDO:0019604,acquired monoclonal Ig light chain-associated Fanconi syndrome,MONDO,disease,DISEASE_13329
13330,13330,13330,13330,13330,13330,13330,13330,MONDO:0001080,acute gonococcal cervicitis,MONDO,disease,DISEASE_13330
13331,13331,13331,13331,13331,13331,13331,13331,MONDO:0011005,trisomy 18-like syndrome,MONDO,disease,DISEASE_13331
13332,13332,13332,13332,13332,13332,13332,13332,MONDO:0004258,female orgasmic disorder,MONDO,disease,DISEASE_13332
13333,13333,13333,13333,13333,13333,13333,13333,MONDO:0011513,"Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology",MONDO,disease,DISEASE_13333
13334,13334,13334,13334,13334,13334,13334,13334,MONDO:0800177,frostbite,MONDO,disease,DISEASE_13334
13335,13335,13335,13335,13335,13335,13335,13335,MONDO:0003153_MONDO:0002911_MONDO:0003869_MONDO:0003152_MONDO:0003705_MONDO:0003706_MONDO:0003870_MONDO:0003932,adult brainstem glioma,MONDO_grouped,disease,DISEASE_13335
13336,13336,13336,13336,13336,13336,13336,13336,MONDO:0859295,"neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties",MONDO,disease,DISEASE_13336
13337,13337,13337,13337,13337,13337,13337,13337,MONDO:0005887,oral tuberculosis,MONDO,disease,DISEASE_13337
13338,13338,13338,13338,13338,13338,13338,13338,MONDO:0100488,CDH1-related diffuse gastric and lobular breast cancer syndrome,MONDO,disease,DISEASE_13338
13339,13339,13339,13339,13339,13339,13339,13339,MONDO:0850269,core binding factor acute myeloid leukemia,MONDO,disease,DISEASE_13339
13340,13340,13340,13340,13340,13340,13340,13340,MONDO:0019362,epidemic louse-borne typhus,MONDO,disease,DISEASE_13340
13341,13341,13341,13341,13341,13341,13341,13341,MONDO:0003392,fallopian tube germ cell tumor,MONDO,disease,DISEASE_13341
13342,13342,13342,13342,13342,13342,13342,13342,MONDO:0015083,nuclear oculomotor paralysis,MONDO,disease,DISEASE_13342
13343,13343,13343,13343,13343,13343,13343,13343,MONDO:0019940,hypertrichosis-acromegaloid facial appearance syndrome,MONDO,disease,DISEASE_13343
13344,13344,13344,13344,13344,13344,13344,13344,MONDO:0859298,"neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-pelger-huet anomaly",MONDO,disease,DISEASE_13344
13345,13345,13345,13345,13345,13345,13345,13345,MONDO:0000946,psychologic vaginismus,MONDO,disease,DISEASE_13345
13346,13346,13346,13346,13346,13346,13346,13346,MONDO:1011792,"subacute progressive myopathy, non-human animal",MONDO,disease,DISEASE_13346
13347,13347,13347,13347,13347,13347,13347,13347,MONDO:0018832,HTRA1-related autosomal dominant cerebral small vessel disease,MONDO,disease,DISEASE_13347
13348,13348,13348,13348,13348,13348,13348,13348,MONDO:0004235,diverticulitis,MONDO,disease,DISEASE_13348
13349,13349,13349,13349,13349,13349,13349,13349,MONDO:0004859,hydrops of gallbladder,MONDO,disease,DISEASE_13349
13350,13350,13350,13350,13350,13350,13350,13350,MONDO:0007679,GMS syndrome,MONDO,disease,DISEASE_13350
13351,13351,13351,13351,13351,13351,13351,13351,MONDO:0859225,neurodevelopmental disorder with or without variable movement or behavioral abnormalities,MONDO,disease,DISEASE_13351
13352,13352,13352,13352,13352,13352,13352,13352,MONDO:0017994,severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency,MONDO,disease,DISEASE_13352
13353,13353,13353,13353,13353,13353,13353,13353,MONDO:1011626,"hyperkinesis, non-human animal",MONDO,disease,DISEASE_13353
13354,13354,13354,13354,13354,13354,13354,13354,MONDO:0032766_MONDO:0859238_MONDO:0011393_MONDO:0017773,"hypoalphalipoproteinemia, primary",MONDO_grouped,disease,DISEASE_13354
13355,13355,13355,13355,13355,13355,13355,13355,MONDO:0007014,vibrio infectious disease,MONDO,disease,DISEASE_13355
13356,13356,13356,13356,13356,13356,13356,13356,MONDO:0003698,penis verrucous carcinoma,MONDO,disease,DISEASE_13356
13357,13357,13357,13357,13357,13357,13357,13357,MONDO:0004697,esophageal leukoplakia,MONDO,disease,DISEASE_13357
13358,13358,13358,13358,13358,13358,13358,13358,MONDO:0100561_MONDO:0100562_MONDO:0100564,HBA1-related alpha thalassemia spectrum,MONDO_grouped,disease,DISEASE_13358
13359,13359,13359,13359,13359,13359,13359,13359,MONDO:0009873,pilodental dysplasia-refractive errors syndrome,MONDO,disease,DISEASE_13359
13360,13360,13360,13360,13360,13360,13360,13360,MONDO:0009492,succinyl-CoA:3-ketoacid CoA transferase deficiency,MONDO,disease,DISEASE_13360
13361,13361,13361,13361,13361,13361,13361,13361,MONDO:0023066,enchondromatosis dwarfism deafness,MONDO,disease,DISEASE_13361
13362,13362,13362,13362,13362,13362,13362,13362,MONDO:0001039,tonsillitis,MONDO,disease,DISEASE_13362
13363,13363,13363,13363,13363,13363,13363,13363,MONDO:0001816,scleroperikeratitis,MONDO,disease,DISEASE_13363
13364,13364,13364,13364,13364,13364,13364,13364,MONDO:0004698,intestine carcinoma in situ,MONDO,disease,DISEASE_13364
13365,13365,13365,13365,13365,13365,13365,13365,MONDO:1012807_MONDO:1012872,"primary ciliary dyskinesia, NME5-related, dog",MONDO_grouped,disease,DISEASE_13365
13366,13366,13366,13366,13366,13366,13366,13366,MONDO:0016238,solitary fibrous tumor,MONDO,disease,DISEASE_13366
13367,13367,13367,13367,13367,13367,13367,13367,MONDO:0043219,migraine with brainstem aura,MONDO,disease,DISEASE_13367
13368,13368,13368,13368,13368,13368,13368,13368,MONDO:0003916,overnutrition,MONDO,disease,DISEASE_13368
13369,13369,13369,13369,13369,13369,13369,13369,MONDO:0010585_MONDO:0016535,X-linked hypohidrotic ectodermal dysplasia,MONDO_grouped,disease,DISEASE_13369
13370,13370,13370,13370,13370,13370,13370,13370,MONDO:0015384,digestive duplication cyst of the tongue,MONDO,disease,DISEASE_13370
13371,13371,13371,13371,13371,13371,13371,13371,MONDO:0016788,obsolete genetic hyperferritinemia without iron overload,MONDO,disease,DISEASE_13371
13372,13372,13372,13372,13372,13372,13372,13372,MONDO:0007099_MONDO:0016829,familial visceral amyloidosis,MONDO_grouped,disease,DISEASE_13372
13373,13373,13373,13373,13373,13373,13373,13373,MONDO:0008599_MONDO:0003543,trigeminal neuralgia,MONDO_grouped,disease,DISEASE_13373
13374,13374,13374,13374,13374,13374,13374,13374,MONDO:1011861,"tremor, non-human animal",MONDO,disease,DISEASE_13374
13375,13375,13375,13375,13375,13375,13375,13375,MONDO:0004858,occlusion of gallbladder,MONDO,disease,DISEASE_13375
13376,13376,13376,13376,13376,13376,13376,13376,MONDO:0019294,mixed dermis disorder,MONDO,disease,DISEASE_13376
13377,13377,13377,13377,13377,13377,13377,13377,MONDO:0859591,childhood low-grade glioma,MONDO,disease,DISEASE_13377
13378,13378,13378,13378,13378,13378,13378,13378,MONDO:0002791,large cell medulloblastoma,MONDO,disease,DISEASE_13378
13379,13379,13379,13379,13379,13379,13379,13379,MONDO:0034024,obsolete kyphoscoliotic Ehlers-Danlos syndrome,MONDO,disease,DISEASE_13379
13380,13380,13380,13380,13380,13380,13380,13380,MONDO:0012756,proximal 16p11.2 microdeletion syndrome,MONDO,disease,DISEASE_13380
13381,13381,13381,13381,13381,13381,13381,13381,MONDO:1010167,"gangliosidosis, non-human animal",MONDO,disease,DISEASE_13381
13382,13382,13382,13382,13382,13382,13382,13382,MONDO:0008809,polyneuropathy-hand defect syndrome,MONDO,disease,DISEASE_13382
13383,13383,13383,13383,13383,13383,13383,13383,MONDO:0037938_MONDO:0019239,inborn disorder of aspartate family metabolism,MONDO_grouped,disease,DISEASE_13383
13384,13384,13384,13384,13384,13384,13384,13384,MONDO:0020561,myxoid/round cell liposarcoma,MONDO,disease,DISEASE_13384
13385,13385,13385,13385,13385,13385,13385,13385,MONDO:0009107,diastrophic dysplasia,MONDO,disease,DISEASE_13385
13386,13386,13386,13386,13386,13386,13386,13386,MONDO:0002380,myoepithelial tumor,MONDO,disease,DISEASE_13386
13387,13387,13387,13387,13387,13387,13387,13387,MONDO:0007710,facial hemiatrophy,MONDO,disease,DISEASE_13387
13388,13388,13388,13388,13388,13388,13388,13388,MONDO:0013113_MONDO:0015177,metaphyseal anadysplasia 2,MONDO_grouped,disease,DISEASE_13388
13389,13389,13389,13389,13389,13389,13389,13389,MONDO:0017165,bile acid CoA ligase deficiency and defective amidation,MONDO,disease,DISEASE_13389
13390,13390,13390,13390,13390,13390,13390,13390,MONDO:0010925,velo-facial-skeletal syndrome,MONDO,disease,DISEASE_13390
13391,13391,13391,13391,13391,13391,13391,13391,MONDO:0011034,odontomicronychial dysplasia,MONDO,disease,DISEASE_13391
13392,13392,13392,13392,13392,13392,13392,13392,MONDO:0100159,"pulmonary hypertension, neonatal",MONDO,disease,DISEASE_13392
13393,13393,13393,13393,13393,13393,13393,13393,MONDO:0700209,"Strongylida infectious disease, non-human animal",MONDO,disease,DISEASE_13393
13394,13394,13394,13394,13394,13394,13394,13394,MONDO:0002716,childhood spinal cord tumor,MONDO,disease,DISEASE_13394
13395,13395,13395,13395,13395,13395,13395,13395,MONDO:0009845,pelviscapular dysplasia,MONDO,disease,DISEASE_13395
13396,13396,13396,13396,13396,13396,13396,13396,MONDO:0012032,Braddock syndrome,MONDO,disease,DISEASE_13396
13397,13397,13397,13397,13397,13397,13397,13397,MONDO:0005412,duodenal ulcer,MONDO,disease,DISEASE_13397
13398,13398,13398,13398,13398,13398,13398,13398,MONDO:0017689_MONDO:0017690,disorder of fructose metabolism,MONDO_grouped,disease,DISEASE_13398
13399,13399,13399,13399,13399,13399,13399,13399,MONDO:0021242,sublingual gland neoplasm,MONDO,disease,DISEASE_13399
13400,13400,13400,13400,13400,13400,13400,13400,MONDO:0024237,inherited neurodegenerative disorder,MONDO,disease,DISEASE_13400
13401,13401,13401,13401,13401,13401,13401,13401,MONDO:0008821,"arthrogryposis, distal, with intellectual disability and characteristic facies",MONDO,disease,DISEASE_13401
13402,13402,13402,13402,13402,13402,13402,13402,MONDO:0008136_MONDO:0958342,isolated optic nerve hypoplasia,MONDO_grouped,disease,DISEASE_13402
13403,13403,13403,13403,13403,13403,13403,13403,MONDO:0019576,telangiectasia macularis eruptiva perstans,MONDO,disease,DISEASE_13403
13404,13404,13404,13404,13404,13404,13404,13404,MONDO:0007016,vitamin A deficiency,MONDO,disease,DISEASE_13404
13405,13405,13405,13405,13405,13405,13405,13405,MONDO:0014460,nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome,MONDO,disease,DISEASE_13405
13406,13406,13406,13406,13406,13406,13406,13406,MONDO:0018904_MONDO:0002461,primary membranoproliferative glomerulonephritis,MONDO_grouped,disease,DISEASE_13406
13407,13407,13407,13407,13407,13407,13407,13407,MONDO:1011736,"dermatosis vegetans, non-human animal",MONDO,disease,DISEASE_13407
13408,13408,13408,13408,13408,13408,13408,13408,MONDO:0700138,bovine rectal myxoma,MONDO,disease,DISEASE_13408
13409,13409,13409,13409,13409,13409,13409,13409,MONDO:0003118,testicular Brenner tumor,MONDO,disease,DISEASE_13409
13410,13410,13410,13410,13410,13410,13410,13410,MONDO:0010989,Mayer-Rokitansky-Küster-Hauser syndrome type 2,MONDO,disease,DISEASE_13410
13411,13411,13411,13411,13411,13411,13411,13411,MONDO:0009117,"obsolete disorganization, mouse, homolog of",MONDO,disease,DISEASE_13411
13412,13412,13412,13412,13412,13412,13412,13412,MONDO:0035004,"serine biosynthesis pathway deficiency, infantile/juvenile form",MONDO,disease,DISEASE_13412
13413,13413,13413,13413,13413,13413,13413,13413,MONDO:0017984,obsolete familial lambdoid synostosis,MONDO,disease,DISEASE_13413
13414,13414,13414,13414,13414,13414,13414,13414,MONDO:0019866,mosaic trisomy 5,MONDO,disease,DISEASE_13414
13415,13415,13415,13415,13415,13415,13415,13415,MONDO:0015243,allergic bronchopulmonary aspergillosis,MONDO,disease,DISEASE_13415
13416,13416,13416,13416,13416,13416,13416,13416,MONDO:0000625,benign male reproductive system neoplasm,MONDO,disease,DISEASE_13416
13417,13417,13417,13417,13417,13417,13417,13417,MONDO:0015271,idiopathic camptocormia,MONDO,disease,DISEASE_13417
13418,13418,13418,13418,13418,13418,13418,13418,MONDO:0018161,non-hereditary retinoblastoma,MONDO,disease,DISEASE_13418
13419,13419,13419,13419,13419,13419,13419,13419,MONDO:0859163,Faundes-Banka syndrome,MONDO,disease,DISEASE_13419
13420,13420,13420,13420,13420,13420,13420,13420,MONDO:0859568_MONDO:0012139_MONDO:0011957_MONDO:0031166,"macular dystrophy, retinal",MONDO_grouped,disease,DISEASE_13420
13421,13421,13421,13421,13421,13421,13421,13421,MONDO:0044811_MONDO:0044816,idiopathic torsion dystonia,MONDO_grouped,disease,DISEASE_13421
13422,13422,13422,13422,13422,13422,13422,13422,MONDO:0015523,epithelioid hemangioendothelioma,MONDO,disease,DISEASE_13422
13423,13423,13423,13423,13423,13423,13423,13423,MONDO:0000065_MONDO:0012963_MONDO:0012962_MONDO:0012966_MONDO:0012969_MONDO:0012970_MONDO:0011386_MONDO:0012971,"microvascular complications of diabetes, susceptibility",MONDO_grouped,disease,DISEASE_13423
13424,13424,13424,13424,13424,13424,13424,13424,MONDO:0035826,symptomatic form of X-linked centronuclear myopathy in female carriers,MONDO,disease,DISEASE_13424
13425,13425,13425,13425,13425,13425,13425,13425,MONDO:0001454,Blessig's cysts,MONDO,disease,DISEASE_13425
13426,13426,13426,13426,13426,13426,13426,13426,MONDO:0018224,hydroa vacciniforme-like lymphoma,MONDO,disease,DISEASE_13426
13427,13427,13427,13427,13427,13427,13427,13427,MONDO:0019773_MONDO:0012296_MONDO:0957453_MONDO:0957454,myelomeningocele,MONDO_grouped,disease,DISEASE_13427
13428,13428,13428,13428,13428,13428,13428,13428,MONDO:0004667,sublingual gland cancer,MONDO,disease,DISEASE_13428
13429,13429,13429,13429,13429,13429,13429,13429,MONDO:1011987,"photoreceptor dysplasia, non-human animal",MONDO,disease,DISEASE_13429
13430,13430,13430,13430,13430,13430,13430,13430,MONDO:0001993,seminal vesicle adenocarcinoma,MONDO,disease,DISEASE_13430
13431,13431,13431,13431,13431,13431,13431,13431,MONDO:0007343,isolated congenital digital clubbing,MONDO,disease,DISEASE_13431
13432,13432,13432,13432,13432,13432,13432,13432,MONDO:0005563,nut midline carcinoma,MONDO,disease,DISEASE_13432
13433,13433,13433,13433,13433,13433,13433,13433,MONDO:0014376,intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism,MONDO,disease,DISEASE_13433
13434,13434,13434,13434,13434,13434,13434,13434,MONDO:0006694,cerebral atherosclerosis,MONDO,disease,DISEASE_13434
13435,13435,13435,13435,13435,13435,13435,13435,MONDO:0033864,infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome,MONDO,disease,DISEASE_13435
13436,13436,13436,13436,13436,13436,13436,13436,MONDO:0859081,chromosome Xq13 duplication syndrome,MONDO,disease,DISEASE_13436
13437,13437,13437,13437,13437,13437,13437,13437,MONDO:0008636_MONDO:0023005,double uterus-hemivagina-renal agenesis syndrome,MONDO_grouped,disease,DISEASE_13437
13438,13438,13438,13438,13438,13438,13438,13438,MONDO:0015687,chronic eosinophilic leukemia,MONDO,disease,DISEASE_13438
13439,13439,13439,13439,13439,13439,13439,13439,MONDO:1012127,"immunodeficiency disease, llama",MONDO,disease,DISEASE_13439
13440,13440,13440,13440,13440,13440,13440,13440,MONDO:0011410,"Hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly",MONDO,disease,DISEASE_13440
13441,13441,13441,13441,13441,13441,13441,13441,MONDO:0859261_MONDO:0007743,attention deficit-hyperactivity disorder 8,MONDO_grouped,disease,DISEASE_13441
13442,13442,13442,13442,13442,13442,13442,13442,MONDO:1011561_MONDO:1011562_MONDO:1011563,"neuroaxonal dystrophy, dog",MONDO_grouped,disease,DISEASE_13442
13443,13443,13443,13443,13443,13443,13443,13443,MONDO:0014383_MONDO:0024531,"myopathy, tubular aggregate",MONDO_grouped,disease,DISEASE_13443
13444,13444,13444,13444,13444,13444,13444,13444,MONDO:0008028,"muscular dystrophy, Barnes type",MONDO,disease,DISEASE_13444
13445,13445,13445,13445,13445,13445,13445,13445,MONDO:1012852,"60,XX/90,XXY disorder of sexual development, cattle",MONDO,disease,DISEASE_13445
13446,13446,13446,13446,13446,13446,13446,13446,MONDO:0016042,late-onset isolated ACTH deficiency,MONDO,disease,DISEASE_13446
13447,13447,13447,13447,13447,13447,13447,13447,MONDO:0032800,"robinow syndrome, autosomal recessive 2",MONDO,disease,DISEASE_13447
13448,13448,13448,13448,13448,13448,13448,13448,MONDO:0007077,Tietz syndrome,MONDO,disease,DISEASE_13448
13449,13449,13449,13449,13449,13449,13449,13449,MONDO:0022697,athetoid cerebral palsy,MONDO,disease,DISEASE_13449
13450,13450,13450,13450,13450,13450,13450,13450,MONDO:0007501,"preauricular fistulae, congenital",MONDO,disease,DISEASE_13450
13451,13451,13451,13451,13451,13451,13451,13451,MONDO:0018922,cold agglutinin disease,MONDO,disease,DISEASE_13451
13452,13452,13452,13452,13452,13452,13452,13452,MONDO:0016270,low-grade neuroendocrine tumor of the corpus uteri,MONDO,disease,DISEASE_13452
13453,13453,13453,13453,13453,13453,13453,13453,MONDO:0007947,Marfan syndrome,MONDO,disease,DISEASE_13453
13454,13454,13454,13454,13454,13454,13454,13454,MONDO:0850162,B-lymphoblastic leukemia/lymphoma with IAMP21,MONDO,disease,DISEASE_13454
13455,13455,13455,13455,13455,13455,13455,13455,MONDO:0100257,peroxisomal single enzyme/protein defect,MONDO,disease,DISEASE_13455
13456,13456,13456,13456,13456,13456,13456,13456,MONDO:0100498,UROD-related inherited porphyria,MONDO,disease,DISEASE_13456
13457,13457,13457,13457,13457,13457,13457,13457,MONDO:0011402,congenital cataracts-facial dysmorphism-neuropathy syndrome,MONDO,disease,DISEASE_13457
13458,13458,13458,13458,13458,13458,13458,13458,MONDO:0016101,neurolymphomatosis,MONDO,disease,DISEASE_13458
13459,13459,13459,13459,13459,13459,13459,13459,MONDO:0009369,non-immune hydrops fetalis,MONDO,disease,DISEASE_13459
13460,13460,13460,13460,13460,13460,13460,13460,MONDO:0017866,subpulmonary stenosis,MONDO,disease,DISEASE_13460
13461,13461,13461,13461,13461,13461,13461,13461,MONDO:0008667,von Hippel-Lindau disease,MONDO,disease,DISEASE_13461
13462,13462,13462,13462,13462,13462,13462,13462,MONDO:1010935,"nemaline myopathy, NEB-related, dog",MONDO,disease,DISEASE_13462
13463,13463,13463,13463,13463,13463,13463,13463,MONDO:0002211,B cell deficiency,MONDO,disease,DISEASE_13463
13464,13464,13464,13464,13464,13464,13464,13464,MONDO:0014054_MONDO:0013081_MONDO:0016537,lymphoproliferative syndrome,MONDO_grouped,disease,DISEASE_13464
13465,13465,13465,13465,13465,13465,13465,13465,MONDO:0020527,ectopic Cushing syndrome,MONDO,disease,DISEASE_13465
13466,13466,13466,13466,13466,13466,13466,13466,MONDO:0003055,secretory meningioma,MONDO,disease,DISEASE_13466
13467,13467,13467,13467,13467,13467,13467,13467,MONDO:0008544,tetramelic monodactyly,MONDO,disease,DISEASE_13467
13468,13468,13468,13468,13468,13468,13468,13468,MONDO:0100210,growth hormone insensitivity syndrome with immune dysregulation,MONDO,disease,DISEASE_13468
13469,13469,13469,13469,13469,13469,13469,13469,MONDO:0014229_MONDO:0013734_MONDO:0012413_MONDO:0010261_MONDO:0010671_MONDO:0016073,"microphthalmia, syndromic",MONDO_grouped,disease,DISEASE_13469
13470,13470,13470,13470,13470,13470,13470,13470,MONDO:1011773,"degenerative suspensory ligament desmitis, non-human animal",MONDO,disease,DISEASE_13470
13471,13471,13471,13471,13471,13471,13471,13471,MONDO:0005031,fibromatosis,MONDO,disease,DISEASE_13471
13472,13472,13472,13472,13472,13472,13472,13472,MONDO:0002184,drug-induced hepatitis,MONDO,disease,DISEASE_13472
13473,13473,13473,13473,13473,13473,13473,13473,MONDO:0003857,adult intracranial malignant hemangiopericytoma,MONDO,disease,DISEASE_13473
13474,13474,13474,13474,13474,13474,13474,13474,MONDO:0005582,binge eating disorder,MONDO,disease,DISEASE_13474
13475,13475,13475,13475,13475,13475,13475,13475,MONDO:0005635_MONDO:0010888,adenomyoma,MONDO_grouped,disease,DISEASE_13475
13476,13476,13476,13476,13476,13476,13476,13476,MONDO:0033664,Kilquist syndrome,MONDO,disease,DISEASE_13476
13477,13477,13477,13477,13477,13477,13477,13477,MONDO:0003394,dental pulp disorder,MONDO,disease,DISEASE_13477
13478,13478,13478,13478,13478,13478,13478,13478,MONDO:1011155,"Marfan syndrome, pig",MONDO,disease,DISEASE_13478
13479,13479,13479,13479,13479,13479,13479,13479,MONDO:0005352,conduct disorder,MONDO,disease,DISEASE_13479
13480,13480,13480,13480,13480,13480,13480,13480,MONDO:0012901,inherited prekallikrein deficiency,MONDO,disease,DISEASE_13480
13481,13481,13481,13481,13481,13481,13481,13481,MONDO:0008695,chorea-acanthocytosis,MONDO,disease,DISEASE_13481
13482,13482,13482,13482,13482,13482,13482,13482,MONDO:0013523,Nestor-Guillermo progeria syndrome,MONDO,disease,DISEASE_13482
13483,13483,13483,13483,13483,13483,13483,13483,MONDO:1011058,"polycystic kidney disease, Western roe deer",MONDO,disease,DISEASE_13483
13484,13484,13484,13484,13484,13484,13484,13484,MONDO:0024517,SMARCB1-related schwannomatosis,MONDO,disease,DISEASE_13484
13485,13485,13485,13485,13485,13485,13485,13485,MONDO:0003100,nerve plexus neoplasm,MONDO,disease,DISEASE_13485
13486,13486,13486,13486,13486,13486,13486,13486,MONDO:0008298,postaxial tetramelic oligodactyly,MONDO,disease,DISEASE_13486
13487,13487,13487,13487,13487,13487,13487,13487,MONDO:0012173,long chain 3-hydroxyacyl-CoA dehydrogenase deficiency,MONDO,disease,DISEASE_13487
13488,13488,13488,13488,13488,13488,13488,13488,MONDO:0004239,cervical keratinizing squamous cell carcinoma,MONDO,disease,DISEASE_13488
13489,13489,13489,13489,13489,13489,13489,13489,MONDO:0700123,SMARCC1-associated developmental dysgenesis syndrome,MONDO,disease,DISEASE_13489
13490,13490,13490,13490,13490,13490,13490,13490,MONDO:0004197,male urethral cancer,MONDO,disease,DISEASE_13490
13491,13491,13491,13491,13491,13491,13491,13491,MONDO:0032893,"pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures",MONDO,disease,DISEASE_13491
13492,13492,13492,13492,13492,13492,13492,13492,MONDO:0021467,benign neoplasm of renal pelvis,MONDO,disease,DISEASE_13492
13493,13493,13493,13493,13493,13493,13493,13493,MONDO:0007381,epithelial recurrent erosion dystrophy,MONDO,disease,DISEASE_13493
13494,13494,13494,13494,13494,13494,13494,13494,MONDO:0002570,high pressure neurological syndrome,MONDO,disease,DISEASE_13494
13495,13495,13495,13495,13495,13495,13495,13495,MONDO:0003315,endometrium carcinoma in situ,MONDO,disease,DISEASE_13495
13496,13496,13496,13496,13496,13496,13496,13496,MONDO:0850273,salivary gland mucinous adenocarcinoma,MONDO,disease,DISEASE_13496
13497,13497,13497,13497,13497,13497,13497,13497,MONDO:0800431,"efavirenz central nervous system toxicity, susceptibility to",MONDO,disease,DISEASE_13497
13498,13498,13498,13498,13498,13498,13498,13498,MONDO:0008303,familial male-limited precocious puberty,MONDO,disease,DISEASE_13498
13499,13499,13499,13499,13499,13499,13499,13499,MONDO:0001997,root resorption,MONDO,disease,DISEASE_13499
13500,13500,13500,13500,13500,13500,13500,13500,MONDO:0004895,accommodative esotropia,MONDO,disease,DISEASE_13500
13501,13501,13501,13501,13501,13501,13501,13501,MONDO:0009156,ectrodactyly-polydactyly syndrome,MONDO,disease,DISEASE_13501
13502,13502,13502,13502,13502,13502,13502,13502,MONDO:0044689,recurrent idiopathic neuroretinitis,MONDO,disease,DISEASE_13502
13503,13503,13503,13503,13503,13503,13503,13503,MONDO:0002031,cecal disorder,MONDO,disease,DISEASE_13503
13504,13504,13504,13504,13504,13504,13504,13504,MONDO:0008353,pruritic urticarial papules and plaques of pregnancy,MONDO,disease,DISEASE_13504
13505,13505,13505,13505,13505,13505,13505,13505,MONDO:1011821,"malignant melanoma, non-human animal",MONDO,disease,DISEASE_13505
13506,13506,13506,13506,13506,13506,13506,13506,MONDO:1012565,"dyserythropoietic anemia and myopathy syndrome, dog",MONDO,disease,DISEASE_13506
13507,13507,13507,13507,13507,13507,13507,13507,MONDO:0004931,residual stage corticosteroid-induced glaucoma,MONDO,disease,DISEASE_13507
13508,13508,13508,13508,13508,13508,13508,13508,MONDO:0009412,scurvy,MONDO,disease,DISEASE_13508
13509,13509,13509,13509,13509,13509,13509,13509,MONDO:0021524,benign neoplasm of buccal mucosa,MONDO,disease,DISEASE_13509
13510,13510,13510,13510,13510,13510,13510,13510,MONDO:0019132,spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome,MONDO,disease,DISEASE_13510
13511,13511,13511,13511,13511,13511,13511,13511,MONDO:0010540,"bullous dystrophy, macular type",MONDO,disease,DISEASE_13511
13512,13512,13512,13512,13512,13512,13512,13512,MONDO:0100054,idiopathic anaphylaxis,MONDO,disease,DISEASE_13512
13513,13513,13513,13513,13513,13513,13513,13513,MONDO:1012844,"XY sex reversal, NR5A1-related, dog",MONDO,disease,DISEASE_13513
13514,13514,13514,13514,13514,13514,13514,13514,MONDO:0800457,HNRNPC-related neurodevelopmental disorder,MONDO,disease,DISEASE_13514
13515,13515,13515,13515,13515,13515,13515,13515,MONDO:0019624_MONDO:0015055_MONDO:0015056,acquired angioedema,MONDO_grouped,disease,DISEASE_13515
13516,13516,13516,13516,13516,13516,13516,13516,MONDO:0015530,trigeminal autonomic cephalalgia,MONDO,disease,DISEASE_13516
13517,13517,13517,13517,13517,13517,13517,13517,MONDO:0010570,craniofrontonasal syndrome,MONDO,disease,DISEASE_13517
13518,13518,13518,13518,13518,13518,13518,13518,MONDO:0019915,maternal uniparental disomy of chromosome 14,MONDO,disease,DISEASE_13518
13519,13519,13519,13519,13519,13519,13519,13519,MONDO:1012975,"hyperlipidemia, non-human animal",MONDO,disease,DISEASE_13519
13520,13520,13520,13520,13520,13520,13520,13520,MONDO:0017907,primary lymphoma of the conjunctiva,MONDO,disease,DISEASE_13520
13521,13521,13521,13521,13521,13521,13521,13521,MONDO:0007009,ureterolithiasis,MONDO,disease,DISEASE_13521
13522,13522,13522,13522,13522,13522,13522,13522,MONDO:0000425,X-linked disease,MONDO,disease,DISEASE_13522
13523,13523,13523,13523,13523,13523,13523,13523,MONDO:0021008,secondary antiphospholipid syndrome,MONDO,disease,DISEASE_13523
13524,13524,13524,13524,13524,13524,13524,13524,MONDO:0700282,POLR3-related leukodystrophy,MONDO,disease,DISEASE_13524
13525,13525,13525,13525,13525,13525,13525,13525,MONDO:0016039,infantile digital fibromatosis,MONDO,disease,DISEASE_13525
13526,13526,13526,13526,13526,13526,13526,13526,MONDO:0859309_MONDO:0032737,"spastic paraplegia 88, autosomal dominant",MONDO_grouped,disease,DISEASE_13526
13527,13527,13527,13527,13527,13527,13527,13527,MONDO:0100534,SMARCB1-deficient kidney medullary carcinoma,MONDO,disease,DISEASE_13527
13528,13528,13528,13528,13528,13528,13528,13528,MONDO:1012983_MONDO:1012953_MONDO:1011848_MONDO:1011874,"neuromuscular disease, non-human animal",MONDO_grouped,disease,DISEASE_13528
13529,13529,13529,13529,13529,13529,13529,13529,MONDO:0016281_MONDO:0017968,"46,XX ovotesticular disorder of sex development",MONDO_grouped,disease,DISEASE_13529
13530,13530,13530,13530,13530,13530,13530,13530,MONDO:0000477_MONDO:0000479,focal dystonia,MONDO_grouped,disease,DISEASE_13530
13531,13531,13531,13531,13531,13531,13531,13531,MONDO:0011990_MONDO:0007365_MONDO:0007366_MONDO:0010021,"seizures, benign familial neonatal",MONDO_grouped,disease,DISEASE_13531
13532,13532,13532,13532,13532,13532,13532,13532,MONDO:0054794,"hydrocephalus, congenital, 3, with brain anomalies",MONDO,disease,DISEASE_13532
13533,13533,13533,13533,13533,13533,13533,13533,MONDO:0054869,nondystrophic myotonia,MONDO,disease,DISEASE_13533
13534,13534,13534,13534,13534,13534,13534,13534,MONDO:0006246_MONDO:0006271,high grade surface osteosarcoma,MONDO_grouped,disease,DISEASE_13534
13535,13535,13535,13535,13535,13535,13535,13535,MONDO:0100086,perinatal disease,MONDO,disease,DISEASE_13535
13536,13536,13536,13536,13536,13536,13536,13536,MONDO:0007682,granddad syndrome,MONDO,disease,DISEASE_13536
13537,13537,13537,13537,13537,13537,13537,13537,MONDO:0030885,amyotrophic lateral sclerosis 26 with or without frontotemporal dementia,MONDO,disease,DISEASE_13537
13538,13538,13538,13538,13538,13538,13538,13538,MONDO:0005184_MONDO:0002809_MONDO:0006047_MONDO:0002867_MONDO:0006346_MONDO:0021040_MONDO:0002117_MONDO:0002808_MONDO:0003630_MONDO:0018523,pancreatic ductal adenocarcinoma,MONDO_grouped,disease,DISEASE_13538
13539,13539,13539,13539,13539,13539,13539,13539,MONDO:0010186_MONDO:0020723_MONDO:0033640_MONDO:0010931_MONDO:0019642_MONDO:0009924_MONDO:0024299,"vitamin D-dependent rickets,",MONDO_grouped,disease,DISEASE_13539
13540,13540,13540,13540,13540,13540,13540,13540,MONDO:0009437,Bamforth-Lazarus syndrome,MONDO,disease,DISEASE_13540
13541,13541,13541,13541,13541,13541,13541,13541,MONDO:0001280,choroiditis,MONDO,disease,DISEASE_13541
13542,13542,13542,13542,13542,13542,13542,13542,MONDO:0859184,ventriculomegaly and arthrogryposis,MONDO,disease,DISEASE_13542
13543,13543,13543,13543,13543,13543,13543,13543,MONDO:0016715,ependymoblastoma,MONDO,disease,DISEASE_13543
13544,13544,13544,13544,13544,13544,13544,13544,MONDO:0800393,IDH3B-related retinopathy,MONDO,disease,DISEASE_13544
13545,13545,13545,13545,13545,13545,13545,13545,MONDO:0021811,acute mountain sickness,MONDO,disease,DISEASE_13545
13546,13546,13546,13546,13546,13546,13546,13546,MONDO:0017385,malignant migrating partial seizures of infancy,MONDO,disease,DISEASE_13546
13547,13547,13547,13547,13547,13547,13547,13547,MONDO:0016533,apolipoprotein A-II amyloidosis,MONDO,disease,DISEASE_13547
13548,13548,13548,13548,13548,13548,13548,13548,MONDO:0009926,autosomal recessive multiple pterygium syndrome,MONDO,disease,DISEASE_13548
13549,13549,13549,13549,13549,13549,13549,13549,MONDO:0014479_MONDO:0008293_MONDO:0012874_MONDO:0011900_MONDO:0012857,"porokeratosis 8, disseminated superficial actinic type",MONDO_grouped,disease,DISEASE_13549
13550,13550,13550,13550,13550,13550,13550,13550,MONDO:0002004,atheroembolism of kidney,MONDO,disease,DISEASE_13550
13551,13551,13551,13551,13551,13551,13551,13551,MONDO:0005953,scirrhous adenocarcinoma,MONDO,disease,DISEASE_13551
13552,13552,13552,13552,13552,13552,13552,13552,MONDO:0010901,HEC syndrome,MONDO,disease,DISEASE_13552
13553,13553,13553,13553,13553,13553,13553,13553,MONDO:0020695,hypotonic cerebral palsy,MONDO,disease,DISEASE_13553
13554,13554,13554,13554,13554,13554,13554,13554,MONDO:0025513_MONDO:0031012,autoimmune urticaria,MONDO_grouped,disease,DISEASE_13554
13555,13555,13555,13555,13555,13555,13555,13555,MONDO:0957524,"COX deficiency, benign infantile mitochondrial myopathy",MONDO,disease,DISEASE_13555
13556,13556,13556,13556,13556,13556,13556,13556,MONDO:0043529,carcinoid heart disease,MONDO,disease,DISEASE_13556
13557,13557,13557,13557,13557,13557,13557,13557,MONDO:0011047,deafness-epiphyseal dysplasia-short stature syndrome,MONDO,disease,DISEASE_13557
13558,13558,13558,13558,13558,13558,13558,13558,MONDO:0009184,epidermolysis bullosa with diaphragmatic hernia,MONDO,disease,DISEASE_13558
13559,13559,13559,13559,13559,13559,13559,13559,MONDO:0007229,Brachymetatarsus 4,MONDO,disease,DISEASE_13559
13560,13560,13560,13560,13560,13560,13560,13560,MONDO:0006001,urinary schistosomiasis,MONDO,disease,DISEASE_13560
13561,13561,13561,13561,13561,13561,13561,13561,MONDO:0019385,steroid-responsive encephalopathy associated with autoimmune thyroiditis,MONDO,disease,DISEASE_13561
13562,13562,13562,13562,13562,13562,13562,13562,MONDO:0009417_MONDO:0018555_MONDO:0015770_MONDO:0016553,hypergonadotropic hypogonadism-cataract syndrome,MONDO_grouped,disease,DISEASE_13562
13563,13563,13563,13563,13563,13563,13563,13563,MONDO:1011076,"urolithiasis, kangaroo",MONDO,disease,DISEASE_13563
13564,13564,13564,13564,13564,13564,13564,13564,MONDO:0005639,AIDS related complex,MONDO,disease,DISEASE_13564
13565,13565,13565,13565,13565,13565,13565,13565,MONDO:0022874,corpus callosum dysgenesis hypopituitarism,MONDO,disease,DISEASE_13565
13566,13566,13566,13566,13566,13566,13566,13566,MONDO:0859293,"neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment",MONDO,disease,DISEASE_13566
13567,13567,13567,13567,13567,13567,13567,13567,MONDO:0007762_MONDO:0014412_MONDO:0018473_MONDO:0037748_MONDO:0015903,hyperlipoproteinemia,MONDO_grouped,disease,DISEASE_13567
13568,13568,13568,13568,13568,13568,13568,13568,MONDO:0003687,endocardium cancer,MONDO,disease,DISEASE_13568
13569,13569,13569,13569,13569,13569,13569,13569,MONDO:0008836,ataxia with myoclonic epilepsy and presenile dementia,MONDO,disease,DISEASE_13569
13570,13570,13570,13570,13570,13570,13570,13570,MONDO:0023153,tuberculous ascites,MONDO,disease,DISEASE_13570
13571,13571,13571,13571,13571,13571,13571,13571,MONDO:0020544,streptococcal toxic-shock syndrome,MONDO,disease,DISEASE_13571
13572,13572,13572,13572,13572,13572,13572,13572,MONDO:0002280_MONDO:0002476,anemia,MONDO_grouped,disease,DISEASE_13572
13573,13573,13573,13573,13573,13573,13573,13573,MONDO:0971056,ocular surface squamous neoplasia,MONDO,disease,DISEASE_13573
13574,13574,13574,13574,13574,13574,13574,13574,MONDO:0022855,congenital vagal hyperreflexivity,MONDO,disease,DISEASE_13574
13575,13575,13575,13575,13575,13575,13575,13575,MONDO:0015611,neutral lipid storage disease,MONDO,disease,DISEASE_13575
13576,13576,13576,13576,13576,13576,13576,13576,MONDO:0015796,acute lung injury,MONDO,disease,DISEASE_13576
13577,13577,13577,13577,13577,13577,13577,13577,MONDO:0004291,subglottis squamous cell carcinoma,MONDO,disease,DISEASE_13577
13578,13578,13578,13578,13578,13578,13578,13578,MONDO:0859310_MONDO:0014413_MONDO:0009793_MONDO:0010336_MONDO:0014932_MONDO:0009642_MONDO:0010702_MONDO:0054770_MONDO:0033375_MONDO:0010176_MONDO:0013035_MONDO:0009794_MONDO:0033045_MONDO:0008267_MONDO:0008137_MONDO:0009795_MONDO:0958230_MONDO:0015375_MONDO:0012049_MONDO:0015421_MONDO:0975827,orofaciodigital syndrome,MONDO_grouped,disease,DISEASE_13578
13579,13579,13579,13579,13579,13579,13579,13579,MONDO:0006074,adenosquamous carcinoma,MONDO,disease,DISEASE_13579
13580,13580,13580,13580,13580,13580,13580,13580,MONDO:0009010,aortic arch interruption,MONDO,disease,DISEASE_13580
13581,13581,13581,13581,13581,13581,13581,13581,MONDO:0019563,CREST syndrome,MONDO,disease,DISEASE_13581
13582,13582,13582,13582,13582,13582,13582,13582,MONDO:0006351,parachordoma,MONDO,disease,DISEASE_13582
13583,13583,13583,13583,13583,13583,13583,13583,MONDO:0010633,iris hypoplasia with glaucoma,MONDO,disease,DISEASE_13583
13584,13584,13584,13584,13584,13584,13584,13584,MONDO:0010623,ichthyosis and male hypogonadism,MONDO,disease,DISEASE_13584
13585,13585,13585,13585,13585,13585,13585,13585,MONDO:0008562,thumb deformity-alopecia-pigmentation anomaly syndrome,MONDO,disease,DISEASE_13585
13586,13586,13586,13586,13586,13586,13586,13586,MONDO:0021372,neoplasm of temporal lobe,MONDO,disease,DISEASE_13586
13587,13587,13587,13587,13587,13587,13587,13587,MONDO:0011274,Muenke syndrome,MONDO,disease,DISEASE_13587
13588,13588,13588,13588,13588,13588,13588,13588,MONDO:0016322,neuroendocrine cell hyperplasia of infancy,MONDO,disease,DISEASE_13588
13589,13589,13589,13589,13589,13589,13589,13589,MONDO:0010222,X-linked Opitz G/BBB syndrome,MONDO,disease,DISEASE_13589
13590,13590,13590,13590,13590,13590,13590,13590,MONDO:0024813,pulmonary sulcus neoplasm,MONDO,disease,DISEASE_13590
13591,13591,13591,13591,13591,13591,13591,13591,MONDO:0019591_MONDO:0005152,panhypopituitarism,MONDO_grouped,disease,DISEASE_13591
13592,13592,13592,13592,13592,13592,13592,13592,MONDO:0025425,"hepatitis, infectious canine",MONDO,disease,DISEASE_13592
13593,13593,13593,13593,13593,13593,13593,13593,MONDO:0031011,neurodevelopmental disorder with dysmorphic facies and variable seizures,MONDO,disease,DISEASE_13593
13594,13594,13594,13594,13594,13594,13594,13594,MONDO:0007121,"aniridia, microcornea, and spontaneously Reabsorbed cataract",MONDO,disease,DISEASE_13594
13595,13595,13595,13595,13595,13595,13595,13595,MONDO:0019102,dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome,MONDO,disease,DISEASE_13595
13596,13596,13596,13596,13596,13596,13596,13596,MONDO:0859288,bone marrow failure and diabetes mellitus syndrome,MONDO,disease,DISEASE_13596
13597,13597,13597,13597,13597,13597,13597,13597,MONDO:0001307,corneal abscess,MONDO,disease,DISEASE_13597
13598,13598,13598,13598,13598,13598,13598,13598,MONDO:0004552,microinvasive cervical squamous cell carcinoma,MONDO,disease,DISEASE_13598
13599,13599,13599,13599,13599,13599,13599,13599,MONDO:0958257,psoriatic arthritis-pyoderma gangrenosum-acne-hidradenitis suppurativa syndrome,MONDO,disease,DISEASE_13599
13600,13600,13600,13600,13600,13600,13600,13600,MONDO:1012551,"caudal cruciate ligament disease, dog",MONDO,disease,DISEASE_13600
13601,13601,13601,13601,13601,13601,13601,13601,MONDO:0011566,abdominal obesity-metabolic syndrome quantitative trait locus 2,MONDO,disease,DISEASE_13601
13602,13602,13602,13602,13602,13602,13602,13602,MONDO:0023642,Weber syndrome,MONDO,disease,DISEASE_13602
13603,13603,13603,13603,13603,13603,13603,13603,MONDO:0003427,bronchus adenoma,MONDO,disease,DISEASE_13603
13604,13604,13604,13604,13604,13604,13604,13604,MONDO:0971111,intraoral basal cell carcinoma,MONDO,disease,DISEASE_13604
13605,13605,13605,13605,13605,13605,13605,13605,MONDO:0002655,cutaneous Paget disease,MONDO,disease,DISEASE_13605
13606,13606,13606,13606,13606,13606,13606,13606,MONDO:0008076,amyotrophic neuralgia,MONDO,disease,DISEASE_13606
13607,13607,13607,13607,13607,13607,13607,13607,MONDO:0022586,bone dysplasia Moore type,MONDO,disease,DISEASE_13607
13608,13608,13608,13608,13608,13608,13608,13608,MONDO:0100468,Batten-Turner congenital myopathy,MONDO,disease,DISEASE_13608
13609,13609,13609,13609,13609,13609,13609,13609,MONDO:0017892,autosomal recessive myogenic arthrogryposis multiplex congenita,MONDO,disease,DISEASE_13609
13610,13610,13610,13610,13610,13610,13610,13610,MONDO:0003971,gastric pylorus carcinoma,MONDO,disease,DISEASE_13610
13611,13611,13611,13611,13611,13611,13611,13611,MONDO:0016718_MONDO:1012545,choroid plexus carcinoma,MONDO_grouped,disease,DISEASE_13611
13612,13612,13612,13612,13612,13612,13612,13612,MONDO:1012222,"primary seborrhea-oleosa, domestic cat",MONDO,disease,DISEASE_13612
13613,13613,13613,13613,13613,13613,13613,13613,MONDO:0018605,disorders of pentose/polyol metabolism,MONDO,disease,DISEASE_13613
13614,13614,13614,13614,13614,13614,13614,13614,MONDO:0009433_MONDO:0013752_MONDO:0004933,hypoplastic left heart syndrome,MONDO_grouped,disease,DISEASE_13614
13615,13615,13615,13615,13615,13615,13615,13615,MONDO:1011652,"mitral valve dysplasia, non-human animal",MONDO,disease,DISEASE_13615
13616,13616,13616,13616,13616,13616,13616,13616,MONDO:0015050,esophageal duplication cyst,MONDO,disease,DISEASE_13616
13617,13617,13617,13617,13617,13617,13617,13617,MONDO:0002529,skin squamous cell carcinoma,MONDO,disease,DISEASE_13617
13618,13618,13618,13618,13618,13618,13618,13618,MONDO:0019682,congenital sialidosis type 2,MONDO,disease,DISEASE_13618
13619,13619,13619,13619,13619,13619,13619,13619,MONDO:0017405,1p21.3 microdeletion syndrome,MONDO,disease,DISEASE_13619
13620,13620,13620,13620,13620,13620,13620,13620,MONDO:0007358,"comedones, familial Dyskeratotic",MONDO,disease,DISEASE_13620
13621,13621,13621,13621,13621,13621,13621,13621,MONDO:0021449,benign neoplasm of stomach,MONDO,disease,DISEASE_13621
13622,13622,13622,13622,13622,13622,13622,13622,MONDO:0016043,isolated cleft lip,MONDO,disease,DISEASE_13622
13623,13623,13623,13623,13623,13623,13623,13623,MONDO:0016832,distal 7q11.23 microduplication syndrome,MONDO,disease,DISEASE_13623
13624,13624,13624,13624,13624,13624,13624,13624,MONDO:0007054,acromial dimples,MONDO,disease,DISEASE_13624
13625,13625,13625,13625,13625,13625,13625,13625,MONDO:0012559,primary immunodeficiency syndrome due to p14 deficiency,MONDO,disease,DISEASE_13625
13626,13626,13626,13626,13626,13626,13626,13626,MONDO:0060611,combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia,MONDO,disease,DISEASE_13626
13627,13627,13627,13627,13627,13627,13627,13627,MONDO:0002622,multifocal osteogenic sarcoma,MONDO,disease,DISEASE_13627
13628,13628,13628,13628,13628,13628,13628,13628,MONDO:0800446,bleeding diathesis due to thromboxane synthesis deficiency,MONDO,disease,DISEASE_13628
13629,13629,13629,13629,13629,13629,13629,13629,MONDO:0008581,malposition of teeth with or without hypodontia/oligodontia,MONDO,disease,DISEASE_13629
13630,13630,13630,13630,13630,13630,13630,13630,MONDO:0035892,Mills syndrome,MONDO,disease,DISEASE_13630
13631,13631,13631,13631,13631,13631,13631,13631,MONDO:0019860,thyroid hemiagenesis,MONDO,disease,DISEASE_13631
13632,13632,13632,13632,13632,13632,13632,13632,MONDO:1012580,"leukocyte adhesion deficiency, non-human animal",MONDO,disease,DISEASE_13632
13633,13633,13633,13633,13633,13633,13633,13633,MONDO:0004357,carcinoma of supraglottis,MONDO,disease,DISEASE_13633
13634,13634,13634,13634,13634,13634,13634,13634,MONDO:0008889,thromboangiitis obliterans,MONDO,disease,DISEASE_13634
13635,13635,13635,13635,13635,13635,13635,13635,MONDO:0020781_MONDO:0014960,"encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1",MONDO_grouped,disease,DISEASE_13635
13636,13636,13636,13636,13636,13636,13636,13636,MONDO:0011338,Omenn syndrome,MONDO,disease,DISEASE_13636
13637,13637,13637,13637,13637,13637,13637,13637,MONDO:0020585,anemia due to erythrocyte enzyme disorder,MONDO,disease,DISEASE_13637
13638,13638,13638,13638,13638,13638,13638,13638,MONDO:0000716,agraphia,MONDO,disease,DISEASE_13638
13639,13639,13639,13639,13639,13639,13639,13639,MONDO:1011846,"hypothalamic dysplasia, non-human animal",MONDO,disease,DISEASE_13639
13640,13640,13640,13640,13640,13640,13640,13640,MONDO:0005219,breast fibrocystic disease,MONDO,disease,DISEASE_13640
13641,13641,13641,13641,13641,13641,13641,13641,MONDO:0001818,facial neuralgia,MONDO,disease,DISEASE_13641
13642,13642,13642,13642,13642,13642,13642,13642,MONDO:0013136,hereditary hypotrichosis with recurrent skin vesicles,MONDO,disease,DISEASE_13642
13643,13643,13643,13643,13643,13643,13643,13643,MONDO:0001172_MONDO:0001171_MONDO:0001474,salpingo-oophoritis,MONDO_grouped,disease,DISEASE_13643
13644,13644,13644,13644,13644,13644,13644,13644,MONDO:1010965,"cauda equina syndrome, dog",MONDO,disease,DISEASE_13644
13645,13645,13645,13645,13645,13645,13645,13645,MONDO:0005598,dopaminergic neuroblastoma,MONDO,disease,DISEASE_13645
13646,13646,13646,13646,13646,13646,13646,13646,MONDO:0003809,malignant mediastinum hemangiopericytoma,MONDO,disease,DISEASE_13646
13647,13647,13647,13647,13647,13647,13647,13647,MONDO:1010479,"arrhythmogenic right ventricular cardiomyopathy, domestic cat",MONDO,disease,DISEASE_13647
13648,13648,13648,13648,13648,13648,13648,13648,MONDO:0001442,dysthymic disorder,MONDO,disease,DISEASE_13648
13649,13649,13649,13649,13649,13649,13649,13649,MONDO:0005766_MONDO:0002041,fungal lung infectious disease,MONDO_grouped,disease,DISEASE_13649
13650,13650,13650,13650,13650,13650,13650,13650,MONDO:1011361,"thymus gland disorder, non-human animal",MONDO,disease,DISEASE_13650
13651,13651,13651,13651,13651,13651,13651,13651,MONDO:0009601,metaphyseal dysplasia without hypotrichosis,MONDO,disease,DISEASE_13651
13652,13652,13652,13652,13652,13652,13652,13652,MONDO:0020161,congenital ectropion,MONDO,disease,DISEASE_13652
13653,13653,13653,13653,13653,13653,13653,13653,MONDO:1011932,"recurrent inflammatory pulmonary disease, non-human animal",MONDO,disease,DISEASE_13653
13654,13654,13654,13654,13654,13654,13654,13654,MONDO:0005480,contact dermatitis,MONDO,disease,DISEASE_13654
13655,13655,13655,13655,13655,13655,13655,13655,MONDO:0018783,fibroblastic rheumatism,MONDO,disease,DISEASE_13655
13656,13656,13656,13656,13656,13656,13656,13656,MONDO:0019514,hepatic veno-occlusive disease,MONDO,disease,DISEASE_13656
13657,13657,13657,13657,13657,13657,13657,13657,MONDO:0018855_MONDO:0021036_MONDO:0859588,keratosis pilaris atrophicans,MONDO_grouped,disease,DISEASE_13657
13658,13658,13658,13658,13658,13658,13658,13658,MONDO:0016819,Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome,MONDO,disease,DISEASE_13658
13659,13659,13659,13659,13659,13659,13659,13659,MONDO:0008143_MONDO:0007704_MONDO:0011923_MONDO:0012893_MONDO:0012894_MONDO:0012568,osteoarthritis susceptibility,MONDO_grouped,disease,DISEASE_13659
13660,13660,13660,13660,13660,13660,13660,13660,MONDO:1012877,"dilated cardiomyopathy, RBM20-related, dog",MONDO,disease,DISEASE_13660
13661,13661,13661,13661,13661,13661,13661,13661,MONDO:0015793,moderate multiminicore disease with hand involvement,MONDO,disease,DISEASE_13661
13662,13662,13662,13662,13662,13662,13662,13662,MONDO:0018827,familial chilblain lupus,MONDO,disease,DISEASE_13662
13663,13663,13663,13663,13663,13663,13663,13663,MONDO:0013319,chromosome 4Q32.1-q32.2 triplication syndrome,MONDO,disease,DISEASE_13663
13664,13664,13664,13664,13664,13664,13664,13664,MONDO:0005872,nervous system cancer,MONDO,disease,DISEASE_13664
13665,13665,13665,13665,13665,13665,13665,13665,MONDO:0044750,lassa virus infectious disease,MONDO,disease,DISEASE_13665
13666,13666,13666,13666,13666,13666,13666,13666,MONDO:0011751,"COPD, severe early onset",MONDO,disease,DISEASE_13666
13667,13667,13667,13667,13667,13667,13667,13667,MONDO:0011784_MONDO:0013542_MONDO:0009649_MONDO:0958202_MONDO:0016820_MONDO:0012122,Moyamoya disease,MONDO_grouped,disease,DISEASE_13667
13668,13668,13668,13668,13668,13668,13668,13668,MONDO:0958094,adult-onset progressive leukoencephalopathy-early-onset deafness,MONDO,disease,DISEASE_13668
13669,13669,13669,13669,13669,13669,13669,13669,MONDO:0002915,childhood infratentorial neoplasm,MONDO,disease,DISEASE_13669
13670,13670,13670,13670,13670,13670,13670,13670,MONDO:0040753,latent tuberculosis infection,MONDO,disease,DISEASE_13670
13671,13671,13671,13671,13671,13671,13671,13671,MONDO:0019975,pellagra,MONDO,disease,DISEASE_13671
13672,13672,13672,13672,13672,13672,13672,13672,MONDO:0007699,Hashimoto thyroiditis,MONDO,disease,DISEASE_13672
13673,13673,13673,13673,13673,13673,13673,13673,MONDO:0009033,temtamy syndrome,MONDO,disease,DISEASE_13673
13674,13674,13674,13674,13674,13674,13674,13674,MONDO:0015794,antenatal multiminicore disease with arthrogryposis multiplex congenita,MONDO,disease,DISEASE_13674
13675,13675,13675,13675,13675,13675,13675,13675,MONDO:0042968,partial duplication of chromosome 12,MONDO,disease,DISEASE_13675
13676,13676,13676,13676,13676,13676,13676,13676,MONDO:0005608,varicella zoster infection,MONDO,disease,DISEASE_13676
13677,13677,13677,13677,13677,13677,13677,13677,MONDO:0005316,bacterial vaginosis,MONDO,disease,DISEASE_13677
13678,13678,13678,13678,13678,13678,13678,13678,MONDO:0001613,vertebrobasilar insufficiency,MONDO,disease,DISEASE_13678
13679,13679,13679,13679,13679,13679,13679,13679,MONDO:0001019,suppression amblyopia,MONDO,disease,DISEASE_13679
13680,13680,13680,13680,13680,13680,13680,13680,MONDO:0024547_MONDO:0014406_MONDO:0009832_MONDO:0975839,pancreatic agenesis,MONDO_grouped,disease,DISEASE_13680
13681,13681,13681,13681,13681,13681,13681,13681,MONDO:0005534,ileocolitis,MONDO,disease,DISEASE_13681
13682,13682,13682,13682,13682,13682,13682,13682,MONDO:0002717,spinal cord intramedullary teratoma,MONDO,disease,DISEASE_13682
13683,13683,13683,13683,13683,13683,13683,13683,MONDO:0003468,biphasic synovial sarcoma,MONDO,disease,DISEASE_13683
13684,13684,13684,13684,13684,13684,13684,13684,MONDO:0013761,childhood encephalopathy due to thiamine pyrophosphokinase deficiency,MONDO,disease,DISEASE_13684
13685,13685,13685,13685,13685,13685,13685,13685,MONDO:0019938_MONDO:0015733_MONDO:0015731_MONDO:0015732,anorectal malformation,MONDO_grouped,disease,DISEASE_13685
13686,13686,13686,13686,13686,13686,13686,13686,MONDO:0045047,neurosarcoidosis,MONDO,disease,DISEASE_13686
13687,13687,13687,13687,13687,13687,13687,13687,MONDO:0008682,Denys-Drash syndrome,MONDO,disease,DISEASE_13687
13688,13688,13688,13688,13688,13688,13688,13688,MONDO:1011465,"amyloidosis, black-footed ferret",MONDO,disease,DISEASE_13688
13689,13689,13689,13689,13689,13689,13689,13689,MONDO:0013572,Keppen-Lubinsky syndrome,MONDO,disease,DISEASE_13689
13690,13690,13690,13690,13690,13690,13690,13690,MONDO:0030484,immunodeficiency 89 and autoimmunity,MONDO,disease,DISEASE_13690
13691,13691,13691,13691,13691,13691,13691,13691,MONDO:1010121,"periodic fever syndrome, non-human animal",MONDO,disease,DISEASE_13691
13692,13692,13692,13692,13692,13692,13692,13692,MONDO:0016990,acquired prothrombin deficiency,MONDO,disease,DISEASE_13692
13693,13693,13693,13693,13693,13693,13693,13693,MONDO:0011620,"metaphyseal dysplasia, Braun-Tinschert type",MONDO,disease,DISEASE_13693
13694,13694,13694,13694,13694,13694,13694,13694,MONDO:0006988,sulfhemoglobinemia,MONDO,disease,DISEASE_13694
13695,13695,13695,13695,13695,13695,13695,13695,MONDO:0044647,kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome,MONDO,disease,DISEASE_13695
13696,13696,13696,13696,13696,13696,13696,13696,MONDO:0044793_MONDO:0006778_MONDO:0020980,spitz nevus,MONDO_grouped,disease,DISEASE_13696
13697,13697,13697,13697,13697,13697,13697,13697,MONDO:0011945,Gaucher disease perinatal lethal,MONDO,disease,DISEASE_13697
13698,13698,13698,13698,13698,13698,13698,13698,MONDO:0020470,"49,XYYYY syndrome",MONDO,disease,DISEASE_13698
13699,13699,13699,13699,13699,13699,13699,13699,MONDO:0001502_MONDO:0001501_MONDO:0000551_MONDO:0001499_MONDO:0003370,retroperitoneum carcinoma,MONDO_grouped,disease,DISEASE_13699
13700,13700,13700,13700,13700,13700,13700,13700,MONDO:0100021,photosensitive occipital lobe epilepsy,MONDO,disease,DISEASE_13700
13701,13701,13701,13701,13701,13701,13701,13701,MONDO:0971179,arterial tortuosity-bone fragility syndrome,MONDO,disease,DISEASE_13701
13702,13702,13702,13702,13702,13702,13702,13702,MONDO:0017695,"glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form",MONDO,disease,DISEASE_13702
13703,13703,13703,13703,13703,13703,13703,13703,MONDO:0010554,Abruzzo-Erickson syndrome,MONDO,disease,DISEASE_13703
13704,13704,13704,13704,13704,13704,13704,13704,MONDO:0016945,partial duplication of the short arm of chromosome 8,MONDO,disease,DISEASE_13704
13705,13705,13705,13705,13705,13705,13705,13705,MONDO:0007350_MONDO:0009002,"coloboma, ocular, autosomal dominant",MONDO_grouped,disease,DISEASE_13705
13706,13706,13706,13706,13706,13706,13706,13706,MONDO:0013391,sterol carrier protein 2 deficiency,MONDO,disease,DISEASE_13706
13707,13707,13707,13707,13707,13707,13707,13707,MONDO:0020549_MONDO:0016785,invasive hydatidiform mole,MONDO_grouped,disease,DISEASE_13707
13708,13708,13708,13708,13708,13708,13708,13708,MONDO:0001350,parametrium malignant neoplasm,MONDO,disease,DISEASE_13708
13709,13709,13709,13709,13709,13709,13709,13709,MONDO:0008498_MONDO:0800226,"strabismus, susceptibility to",MONDO_grouped,disease,DISEASE_13709
13710,13710,13710,13710,13710,13710,13710,13710,MONDO:0018323_MONDO:0018322,"HSD10 disease, neonatal type",MONDO_grouped,disease,DISEASE_13710
13711,13711,13711,13711,13711,13711,13711,13711,MONDO:1012474,"retinal degeneration, Smoky Joe, chicken",MONDO,disease,DISEASE_13711
13712,13712,13712,13712,13712,13712,13712,13712,MONDO:0007693,hypertrichosis cubiti-short stature syndrome,MONDO,disease,DISEASE_13712
13713,13713,13713,13713,13713,13713,13713,13713,MONDO:0018230,skeletal dysplasia,MONDO,disease,DISEASE_13713
13714,13714,13714,13714,13714,13714,13714,13714,MONDO:0009906,prenatal bowing,MONDO,disease,DISEASE_13714
13715,13715,13715,13715,13715,13715,13715,13715,MONDO:0018811,congenital portosystemic shunt,MONDO,disease,DISEASE_13715
13716,13716,13716,13716,13716,13716,13716,13716,MONDO:0009206,"factor V and factor VIII, combined deficiency of, type 1",MONDO,disease,DISEASE_13716
13717,13717,13717,13717,13717,13717,13717,13717,MONDO:0035236_MONDO:0035237_MONDO:0035238,pustular pyoderma gangrenosum,MONDO_grouped,disease,DISEASE_13717
13718,13718,13718,13718,13718,13718,13718,13718,MONDO:0004004,motor nerve neuritis,MONDO,disease,DISEASE_13718
13719,13719,13719,13719,13719,13719,13719,13719,MONDO:0006133,cervical adenoid cystic carcinoma,MONDO,disease,DISEASE_13719
13720,13720,13720,13720,13720,13720,13720,13720,MONDO:0011396,loricrin keratoderma,MONDO,disease,DISEASE_13720
13721,13721,13721,13721,13721,13721,13721,13721,MONDO:0018851,familial keratoacanthoma,MONDO,disease,DISEASE_13721
13722,13722,13722,13722,13722,13722,13722,13722,MONDO:1011464,"amyloidosis, black-footed cat",MONDO,disease,DISEASE_13722
13723,13723,13723,13723,13723,13723,13723,13723,MONDO:0030029,"skeletal dysplasia, mild, with joint laxity and advanced bone age",MONDO,disease,DISEASE_13723
13724,13724,13724,13724,13724,13724,13724,13724,MONDO:0002234,vaginitis,MONDO,disease,DISEASE_13724
13725,13725,13725,13725,13725,13725,13725,13725,MONDO:1011171_MONDO:1011170_MONDO:1011172_MONDO:1011173_MONDO:1011174_MONDO:1011175_MONDO:1011176_MONDO:1011177_MONDO:1012562_MONDO:1012563,"osteochondrosis, dog",MONDO_grouped,disease,DISEASE_13725
13726,13726,13726,13726,13726,13726,13726,13726,MONDO:0024477,liver and intrahepatic bile duct neoplasm,MONDO,disease,DISEASE_13726
13727,13727,13727,13727,13727,13727,13727,13727,MONDO:0023019,dwarfism bluish sclerae,MONDO,disease,DISEASE_13727
13728,13728,13728,13728,13728,13728,13728,13728,MONDO:0004015_MONDO:0004016,pineal region teratoma,MONDO_grouped,disease,DISEASE_13728
13729,13729,13729,13729,13729,13729,13729,13729,MONDO:0023013,Duker-Weiss-Siber syndrome,MONDO,disease,DISEASE_13729
13730,13730,13730,13730,13730,13730,13730,13730,MONDO:0009514,Laurence-Moon syndrome,MONDO,disease,DISEASE_13730
13731,13731,13731,13731,13731,13731,13731,13731,MONDO:0000933,subglottis neoplasm,MONDO,disease,DISEASE_13731
13732,13732,13732,13732,13732,13732,13732,13732,MONDO:0021829,agnathia-microstomia-synotia,MONDO,disease,DISEASE_13732
13733,13733,13733,13733,13733,13733,13733,13733,MONDO:0002464,lacrimal gland cancer,MONDO,disease,DISEASE_13733
13734,13734,13734,13734,13734,13734,13734,13734,MONDO:0010237,X-linked intellectual disability-plagiocephaly syndrome,MONDO,disease,DISEASE_13734
13735,13735,13735,13735,13735,13735,13735,13735,MONDO:0015565,cap polyposis,MONDO,disease,DISEASE_13735
13736,13736,13736,13736,13736,13736,13736,13736,MONDO:0019907,ring chromosome 13,MONDO,disease,DISEASE_13736
13737,13737,13737,13737,13737,13737,13737,13737,MONDO:0008362,ragweed sensitivity,MONDO,disease,DISEASE_13737
13738,13738,13738,13738,13738,13738,13738,13738,MONDO:0004166,hereditary fallopian tube carcinoma,MONDO,disease,DISEASE_13738
13739,13739,13739,13739,13739,13739,13739,13739,MONDO:0018310_MONDO:0015531_MONDO:0017025_MONDO:0017029_MONDO:0020520_MONDO:0700163,Langerhans cell histiocytosis,MONDO_grouped,disease,DISEASE_13739
13740,13740,13740,13740,13740,13740,13740,13740,MONDO:0035122,"GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder",MONDO,disease,DISEASE_13740
13741,13741,13741,13741,13741,13741,13741,13741,MONDO:0016213,leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome,MONDO,disease,DISEASE_13741
13742,13742,13742,13742,13742,13742,13742,13742,MONDO:0020352,"multiple system atrophy, parkinsonian type",MONDO,disease,DISEASE_13742
13743,13743,13743,13743,13743,13743,13743,13743,MONDO:0010784,chloramphenicol toxicity,MONDO,disease,DISEASE_13743
13744,13744,13744,13744,13744,13744,13744,13744,MONDO:0001313_MONDO:0002757_MONDO:0004864,acute allergic serous otitis media,MONDO_grouped,disease,DISEASE_13744
13745,13745,13745,13745,13745,13745,13745,13745,MONDO:0957279_MONDO:0012196_MONDO:0859235,"auditory neuropathy, autosomal dominant",MONDO_grouped,disease,DISEASE_13745
13746,13746,13746,13746,13746,13746,13746,13746,MONDO:0016211,non-papillary transitional cell carcinoma of the bladder,MONDO,disease,DISEASE_13746
13747,13747,13747,13747,13747,13747,13747,13747,MONDO:1012329,"laminitis, ass",MONDO,disease,DISEASE_13747
13748,13748,13748,13748,13748,13748,13748,13748,MONDO:0004841,kidney hypertrophy,MONDO,disease,DISEASE_13748
13749,13749,13749,13749,13749,13749,13749,13749,MONDO:1010140,"alopecia areata, non-human animal",MONDO,disease,DISEASE_13749
13750,13750,13750,13750,13750,13750,13750,13750,MONDO:0010696,"omphalocele, X-linked",MONDO,disease,DISEASE_13750
13751,13751,13751,13751,13751,13751,13751,13751,MONDO:0100003,susceptibility to angioedema induced by ACE inhibitors,MONDO,disease,DISEASE_13751
13752,13752,13752,13752,13752,13752,13752,13752,MONDO:0005255_MONDO:0005256,mild heart failure,MONDO_grouped,disease,DISEASE_13752
13753,13753,13753,13753,13753,13753,13753,13753,MONDO:0100048,"graft-versus-host disease, susceptibility to",MONDO,disease,DISEASE_13753
13754,13754,13754,13754,13754,13754,13754,13754,MONDO:0010262,"hypotonia, congenital nystagmus, ataxia, and abnormal auditory brainstem responses",MONDO,disease,DISEASE_13754
13755,13755,13755,13755,13755,13755,13755,13755,MONDO:0019095,plague,MONDO,disease,DISEASE_13755
13756,13756,13756,13756,13756,13756,13756,13756,MONDO:0015004_MONDO:0030958_MONDO:0957542_MONDO:0957539,"dystonia 28, childhood-onset",MONDO_grouped,disease,DISEASE_13756
13757,13757,13757,13757,13757,13757,13757,13757,MONDO:0975753,papillary hemangioma,MONDO,disease,DISEASE_13757
13758,13758,13758,13758,13758,13758,13758,13758,MONDO:0001951,Norwegian scabies,MONDO,disease,DISEASE_13758
13759,13759,13759,13759,13759,13759,13759,13759,MONDO:0022529,BK-virus nephropathy,MONDO,disease,DISEASE_13759
13760,13760,13760,13760,13760,13760,13760,13760,MONDO:0009280,monosodium glutamate sensitivity,MONDO,disease,DISEASE_13760
13761,13761,13761,13761,13761,13761,13761,13761,MONDO:1012425,"congenital merosin-deficient muscular dystrophy, domestic cat",MONDO,disease,DISEASE_13761
13762,13762,13762,13762,13762,13762,13762,13762,MONDO:0022662,carpo tarsal osteolysis recessive,MONDO,disease,DISEASE_13762
13763,13763,13763,13763,13763,13763,13763,13763,MONDO:0013193_MONDO:0008570_MONDO:0013908,"thyrotoxic periodic paralysis, susceptibility to",MONDO_grouped,disease,DISEASE_13763
13764,13764,13764,13764,13764,13764,13764,13764,MONDO:0013836,familial steroid-resistant nephrotic syndrome with sensorineural deafness,MONDO,disease,DISEASE_13764
13765,13765,13765,13765,13765,13765,13765,13765,MONDO:0004402,"testicular yolk sac tumor, glandular-alveolar pattern",MONDO,disease,DISEASE_13765
13766,13766,13766,13766,13766,13766,13766,13766,MONDO:0015440,ring chromosome 6,MONDO,disease,DISEASE_13766
13767,13767,13767,13767,13767,13767,13767,13767,MONDO:0010566_MONDO:0010245_MONDO:0010335_MONDO:0021155,X-linked cone-rod dystrophy,MONDO_grouped,disease,DISEASE_13767
13768,13768,13768,13768,13768,13768,13768,13768,MONDO:0019204,respiratory bronchiolitis-interstitial lung disease syndrome,MONDO,disease,DISEASE_13768
13769,13769,13769,13769,13769,13769,13769,13769,MONDO:0859236,neurodevelopmental disorder with neuromuscular and skeletal abnormalities,MONDO,disease,DISEASE_13769
13770,13770,13770,13770,13770,13770,13770,13770,MONDO:0013793,"encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency",MONDO,disease,DISEASE_13770
13771,13771,13771,13771,13771,13771,13771,13771,MONDO:0021077,cystic neoplasm,MONDO,disease,DISEASE_13771
13772,13772,13772,13772,13772,13772,13772,13772,MONDO:0016854,"49,XXXYY syndrome",MONDO,disease,DISEASE_13772
13773,13773,13773,13773,13773,13773,13773,13773,MONDO:0016826_MONDO:0018964,methylmalonic aciduria and homocystinuria type cblD,MONDO_grouped,disease,DISEASE_13773
13774,13774,13774,13774,13774,13774,13774,13774,MONDO:1010746,"Ehlers-Danlos syndrome, dermatosparaxis type, ADAMTS2-related, dog",MONDO,disease,DISEASE_13774
13775,13775,13775,13775,13775,13775,13775,13775,MONDO:0006245,hidradenocarcinoma,MONDO,disease,DISEASE_13775
13776,13776,13776,13776,13776,13776,13776,13776,MONDO:0013054,"microcephaly, growth retardation, cataract, hearing loss, and unusual appearance",MONDO,disease,DISEASE_13776
13777,13777,13777,13777,13777,13777,13777,13777,MONDO:0021747_MONDO:0006635,Acanthamoeba infectious disease,MONDO_grouped,disease,DISEASE_13777
13778,13778,13778,13778,13778,13778,13778,13778,MONDO:1012320,"high-frequency tremor, pig",MONDO,disease,DISEASE_13778
13779,13779,13779,13779,13779,13779,13779,13779,MONDO:0019414,BRESEK syndrome,MONDO,disease,DISEASE_13779
13780,13780,13780,13780,13780,13780,13780,13780,MONDO:0033938,acute radiation syndrome,MONDO,disease,DISEASE_13780
13781,13781,13781,13781,13781,13781,13781,13781,MONDO:1012522,"turning calves syndrome, cattle",MONDO,disease,DISEASE_13781
13782,13782,13782,13782,13782,13782,13782,13782,MONDO:0020134,cystic malformation of the posterior fossa,MONDO,disease,DISEASE_13782
13783,13783,13783,13783,13783,13783,13783,13783,MONDO:0004444,bladder tubulo-cystic clear cell adenocarcinoma,MONDO,disease,DISEASE_13783
13784,13784,13784,13784,13784,13784,13784,13784,MONDO:0700120,BAFopathy,MONDO,disease,DISEASE_13784
13785,13785,13785,13785,13785,13785,13785,13785,MONDO:0019960,VIPoma,MONDO,disease,DISEASE_13785
13786,13786,13786,13786,13786,13786,13786,13786,MONDO:1011420,"hyperhomocysteinemia, non-human animal",MONDO,disease,DISEASE_13786
13787,13787,13787,13787,13787,13787,13787,13787,MONDO:0000710,gastroduodenal Crohn disease,MONDO,disease,DISEASE_13787
13788,13788,13788,13788,13788,13788,13788,13788,MONDO:0023513,Jeune syndrome situs inversus,MONDO,disease,DISEASE_13788
13789,13789,13789,13789,13789,13789,13789,13789,MONDO:0021479,benign neoplasm of oropharynx,MONDO,disease,DISEASE_13789
13790,13790,13790,13790,13790,13790,13790,13790,MONDO:1011252_MONDO:1011253,"keratitis, dog",MONDO_grouped,disease,DISEASE_13790
13791,13791,13791,13791,13791,13791,13791,13791,MONDO:0005799_MONDO:0005954,hookworm infectious disease,MONDO_grouped,disease,DISEASE_13791
13792,13792,13792,13792,13792,13792,13792,13792,MONDO:0008341,ptosis-strabismus-ectopic pupils syndrome,MONDO,disease,DISEASE_13792
13793,13793,13793,13793,13793,13793,13793,13793,MONDO:0019432,rheumatoid factor-negative juvenile idiopathic arthritis,MONDO,disease,DISEASE_13793
13794,13794,13794,13794,13794,13794,13794,13794,MONDO:0001104,toxic diffuse goiter,MONDO,disease,DISEASE_13794
13795,13795,13795,13795,13795,13795,13795,13795,MONDO:0007177,auriculoosteodysplasia,MONDO,disease,DISEASE_13795
13796,13796,13796,13796,13796,13796,13796,13796,MONDO:0002998,skull base meningioma,MONDO,disease,DISEASE_13796
13797,13797,13797,13797,13797,13797,13797,13797,MONDO:0042983,neurocutaneous syndrome,MONDO,disease,DISEASE_13797
13798,13798,13798,13798,13798,13798,13798,13798,MONDO:1040022,linkeropathy,MONDO,disease,DISEASE_13798
13799,13799,13799,13799,13799,13799,13799,13799,MONDO:1012810,"hypertrophic cardiomyopathy, MYH7-related, pig",MONDO,disease,DISEASE_13799
13800,13800,13800,13800,13800,13800,13800,13800,MONDO:1010853,"glycogen storage disease II, sheep",MONDO,disease,DISEASE_13800
13801,13801,13801,13801,13801,13801,13801,13801,MONDO:0013971,leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome,MONDO,disease,DISEASE_13801
13802,13802,13802,13802,13802,13802,13802,13802,MONDO:0005161,human papilloma virus infection,MONDO,disease,DISEASE_13802
13803,13803,13803,13803,13803,13803,13803,13803,MONDO:1011703,"selective ADP deficiency, non-human animal",MONDO,disease,DISEASE_13803
13804,13804,13804,13804,13804,13804,13804,13804,MONDO:0003957,adult pineoblastoma,MONDO,disease,DISEASE_13804
13805,13805,13805,13805,13805,13805,13805,13805,MONDO:0009712,congenital multicore myopathy with external ophthalmoplegia,MONDO,disease,DISEASE_13805
13806,13806,13806,13806,13806,13806,13806,13806,MONDO:0011205,medium chain 3-ketoacyl-Coa thiolase deficiency,MONDO,disease,DISEASE_13806
13807,13807,13807,13807,13807,13807,13807,13807,MONDO:0005047,infertility disorder,MONDO,disease,DISEASE_13807
13808,13808,13808,13808,13808,13808,13808,13808,MONDO:0007475,"duodenal ulcer, hyperpepsinogenemic 1",MONDO,disease,DISEASE_13808
13809,13809,13809,13809,13809,13809,13809,13809,MONDO:0012820_MONDO:0014038_MONDO:0012953_MONDO:0012132_MONDO:0012673_MONDO:0012821_MONDO:0012822_MONDO:0012823_MONDO:0012951_MONDO:0012952_MONDO:0012954_MONDO:0800423,"colorectal cancer, susceptibility to",MONDO_grouped,disease,DISEASE_13809
13810,13810,13810,13810,13810,13810,13810,13810,MONDO:0800339,"laryngospasm, severe neonatal episodic",MONDO,disease,DISEASE_13810
13811,13811,13811,13811,13811,13811,13811,13811,MONDO:0041008,obsolete contact dermatitis caused by poison oak,MONDO,disease,DISEASE_13811
13812,13812,13812,13812,13812,13812,13812,13812,MONDO:1011840,"delta 9-tetrahydrocannabinol seizure, non-human animal",MONDO,disease,DISEASE_13812
13813,13813,13813,13813,13813,13813,13813,13813,MONDO:0700197,porcine leukemia,MONDO,disease,DISEASE_13813
13814,13814,13814,13814,13814,13814,13814,13814,MONDO:0024885_MONDO:0002224_MONDO:0002920_MONDO:0859690,malignant ovarian serous tumor,MONDO_grouped,disease,DISEASE_13814
13815,13815,13815,13815,13815,13815,13815,13815,MONDO:0003781_MONDO:0002465,bronchitis,MONDO_grouped,disease,DISEASE_13815
13816,13816,13816,13816,13816,13816,13816,13816,MONDO:1011560,"nephroma, ducks",MONDO,disease,DISEASE_13816
13817,13817,13817,13817,13817,13817,13817,13817,MONDO:0021029,hereditary sebaceous gland anomaly,MONDO,disease,DISEASE_13817
13818,13818,13818,13818,13818,13818,13818,13818,MONDO:0011594,"ovarian dysgenesis, hypergonadotropic, with short stature and recurrent metabolic acidosis",MONDO,disease,DISEASE_13818
13819,13819,13819,13819,13819,13819,13819,13819,MONDO:0005701,chlamydia trachomatis infectious disease,MONDO,disease,DISEASE_13819
13820,13820,13820,13820,13820,13820,13820,13820,MONDO:0018808_MONDO:0010913,Caroli syndrome,MONDO_grouped,disease,DISEASE_13820
13821,13821,13821,13821,13821,13821,13821,13821,MONDO:0003395,testicular granulosa cell tumor,MONDO,disease,DISEASE_13821
13822,13822,13822,13822,13822,13822,13822,13822,MONDO:0010919,"varicella, severe recurrent",MONDO,disease,DISEASE_13822
13823,13823,13823,13823,13823,13823,13823,13823,MONDO:0850347,bladder sarcomatoid transitional cell carcinoma,MONDO,disease,DISEASE_13823
13824,13824,13824,13824,13824,13824,13824,13824,MONDO:0003936,invasive tubular breast carcinoma,MONDO,disease,DISEASE_13824
13825,13825,13825,13825,13825,13825,13825,13825,MONDO:0015032,intraneural perineurioma,MONDO,disease,DISEASE_13825
13826,13826,13826,13826,13826,13826,13826,13826,MONDO:0009091,non-acquired combined pituitary hormone deficiency with spine abnormalities,MONDO,disease,DISEASE_13826
13827,13827,13827,13827,13827,13827,13827,13827,MONDO:0851105,cerebrovascular benign neoplasm,MONDO,disease,DISEASE_13827
13828,13828,13828,13828,13828,13828,13828,13828,MONDO:1010796,"Darier disease, dog",MONDO,disease,DISEASE_13828
13829,13829,13829,13829,13829,13829,13829,13829,MONDO:0001811,tetanic cataract,MONDO,disease,DISEASE_13829
13830,13830,13830,13830,13830,13830,13830,13830,MONDO:0008166,"ovalocytosis, hereditary hemolytic, with defective erythropoiesis",MONDO,disease,DISEASE_13830
13831,13831,13831,13831,13831,13831,13831,13831,MONDO:0019969,panner disease,MONDO,disease,DISEASE_13831
13832,13832,13832,13832,13832,13832,13832,13832,MONDO:0011309,familial gestational hyperthyroidism,MONDO,disease,DISEASE_13832
13833,13833,13833,13833,13833,13833,13833,13833,MONDO:1011033,"coat color dilution, MLPH-related, dog",MONDO,disease,DISEASE_13833
13834,13834,13834,13834,13834,13834,13834,13834,MONDO:0100373_MONDO:0100398_MONDO:0100406,"acute myeloid leukemia, inv(16)(p13.1;q22)",MONDO_grouped,disease,DISEASE_13834
13835,13835,13835,13835,13835,13835,13835,13835,MONDO:0017443_MONDO:0017498_MONDO:0017499_MONDO:0017500_MONDO:0017501,congenital absence of both forearm and hand,MONDO_grouped,disease,DISEASE_13835
13836,13836,13836,13836,13836,13836,13836,13836,MONDO:0002947,adamantinoid basal cell epithelioma,MONDO,disease,DISEASE_13836
13837,13837,13837,13837,13837,13837,13837,13837,MONDO:0009897,adult polyglucosan body disease,MONDO,disease,DISEASE_13837
13838,13838,13838,13838,13838,13838,13838,13838,MONDO:0006200,epithelioid cell uveal melanoma,MONDO,disease,DISEASE_13838
13839,13839,13839,13839,13839,13839,13839,13839,MONDO:0001829,lumbosacral plexus lesion,MONDO,disease,DISEASE_13839
13840,13840,13840,13840,13840,13840,13840,13840,MONDO:0019947_MONDO:0010868_MONDO:0011634,rippling muscle disease,MONDO_grouped,disease,DISEASE_13840
13841,13841,13841,13841,13841,13841,13841,13841,MONDO:0024882,secondary neoplasm,MONDO,disease,DISEASE_13841
13842,13842,13842,13842,13842,13842,13842,13842,MONDO:0001458,ulnar nerve lesion,MONDO,disease,DISEASE_13842
13843,13843,13843,13843,13843,13843,13843,13843,MONDO:0003738,selective IgE deficiency disease,MONDO,disease,DISEASE_13843
13844,13844,13844,13844,13844,13844,13844,13844,MONDO:0020483,acetazolamide-responsive myotonia,MONDO,disease,DISEASE_13844
13845,13845,13845,13845,13845,13845,13845,13845,MONDO:0017218,obsolete septopreoptic holoprosencephaly,MONDO,disease,DISEASE_13845
13846,13846,13846,13846,13846,13846,13846,13846,MONDO:0001312_MONDO:0002737,acute serous otitis media,MONDO_grouped,disease,DISEASE_13846
13847,13847,13847,13847,13847,13847,13847,13847,MONDO:0020582,benign uterine ligament neoplasm,MONDO,disease,DISEASE_13847
13848,13848,13848,13848,13848,13848,13848,13848,MONDO:0800206,epidermolysis bullosa dystrophica with subcorneal cleavage,MONDO,disease,DISEASE_13848
13849,13849,13849,13849,13849,13849,13849,13849,MONDO:0010229,"alopecia, congenital",MONDO,disease,DISEASE_13849
13850,13850,13850,13850,13850,13850,13850,13850,MONDO:0007086,autosomal dominant Alport syndrome,MONDO,disease,DISEASE_13850
13851,13851,13851,13851,13851,13851,13851,13851,MONDO:0003713,angiokeratoma circumscriptum,MONDO,disease,DISEASE_13851
13852,13852,13852,13852,13852,13852,13852,13852,MONDO:0032792,"neuropathy, hereditary motor and sensory, type VIc, with optic atrophy",MONDO,disease,DISEASE_13852
13853,13853,13853,13853,13853,13853,13853,13853,MONDO:0007706,cavernous hemangiomas of face-supraumbilical midline raphe syndrome,MONDO,disease,DISEASE_13853
13854,13854,13854,13854,13854,13854,13854,13854,MONDO:0020528,ACTH-dependent Cushing syndrome,MONDO,disease,DISEASE_13854
13855,13855,13855,13855,13855,13855,13855,13855,MONDO:0010790,MERRF syndrome,MONDO,disease,DISEASE_13855
13856,13856,13856,13856,13856,13856,13856,13856,MONDO:0023569,Kozlowski Ouvrier syndrome,MONDO,disease,DISEASE_13856
13857,13857,13857,13857,13857,13857,13857,13857,MONDO:0010146,Kerion celsi,MONDO,disease,DISEASE_13857
13858,13858,13858,13858,13858,13858,13858,13858,MONDO:0000536,pharyngeal squamous cell carcinoma,MONDO,disease,DISEASE_13858
13859,13859,13859,13859,13859,13859,13859,13859,MONDO:0016871,partial deletion of chromosome 6,MONDO,disease,DISEASE_13859
13860,13860,13860,13860,13860,13860,13860,13860,MONDO:0975705,otofacial neurodevelopmental syndrome,MONDO,disease,DISEASE_13860
13861,13861,13861,13861,13861,13861,13861,13861,MONDO:0003565,urethral villous adenoma,MONDO,disease,DISEASE_13861
13862,13862,13862,13862,13862,13862,13862,13862,MONDO:0005694,cecal neoplasm,MONDO,disease,DISEASE_13862
13863,13863,13863,13863,13863,13863,13863,13863,MONDO:0020586,factor V deficiency,MONDO,disease,DISEASE_13863
13864,13864,13864,13864,13864,13864,13864,13864,MONDO:0004899,monofixation syndrome,MONDO,disease,DISEASE_13864
13865,13865,13865,13865,13865,13865,13865,13865,MONDO:1012125,"immunodeficiency disease, dog",MONDO,disease,DISEASE_13865
13866,13866,13866,13866,13866,13866,13866,13866,MONDO:0033683,congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome,MONDO,disease,DISEASE_13866
13867,13867,13867,13867,13867,13867,13867,13867,MONDO:0009771,oculotrichodysplasia,MONDO,disease,DISEASE_13867
13868,13868,13868,13868,13868,13868,13868,13868,MONDO:0004582,rheumatic myocarditis,MONDO,disease,DISEASE_13868
13869,13869,13869,13869,13869,13869,13869,13869,MONDO:0044632,extracranial carotid artery aneurysm,MONDO,disease,DISEASE_13869
13870,13870,13870,13870,13870,13870,13870,13870,MONDO:0001903,calcific tendinitis,MONDO,disease,DISEASE_13870
13871,13871,13871,13871,13871,13871,13871,13871,MONDO:0032921,"neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation",MONDO,disease,DISEASE_13871
13872,13872,13872,13872,13872,13872,13872,13872,MONDO:0005155_MONDO:0006644,cirrhosis of liver,MONDO_grouped,disease,DISEASE_13872
13873,13873,13873,13873,13873,13873,13873,13873,MONDO:0007044_MONDO:0013822,Acrodysostosis 1 with or without hormone resistance,MONDO_grouped,disease,DISEASE_13873
13874,13874,13874,13874,13874,13874,13874,13874,MONDO:0007848,autosomal dominant keratitis,MONDO,disease,DISEASE_13874
13875,13875,13875,13875,13875,13875,13875,13875,MONDO:0000740,adenoid hypertrophy,MONDO,disease,DISEASE_13875
13876,13876,13876,13876,13876,13876,13876,13876,MONDO:0006294_MONDO:0002037,pleural cancer,MONDO_grouped,disease,DISEASE_13876
13877,13877,13877,13877,13877,13877,13877,13877,MONDO:0000984,thalassemia,MONDO,disease,DISEASE_13877
13878,13878,13878,13878,13878,13878,13878,13878,MONDO:0012320_MONDO:0020756_MONDO:0011232_MONDO:0018925_MONDO:0000700_MONDO:0800335,"migraine, familial hemiplegic",MONDO_grouped,disease,DISEASE_13878
13879,13879,13879,13879,13879,13879,13879,13879,MONDO:0009404,"hypertelorism, microtia, facial clefting syndrome",MONDO,disease,DISEASE_13879
13880,13880,13880,13880,13880,13880,13880,13880,MONDO:0018174,hereditary glaucoma,MONDO,disease,DISEASE_13880
13881,13881,13881,13881,13881,13881,13881,13881,MONDO:0004630,substance-induced psychosis,MONDO,disease,DISEASE_13881
13882,13882,13882,13882,13882,13882,13882,13882,MONDO:0013452,multisystemic smooth muscle dysfunction syndrome,MONDO,disease,DISEASE_13882
13883,13883,13883,13883,13883,13883,13883,13883,MONDO:0019610,Zollinger-Ellison syndrome,MONDO,disease,DISEASE_13883
13884,13884,13884,13884,13884,13884,13884,13884,MONDO:0008268,polydactyly-myopia syndrome,MONDO,disease,DISEASE_13884
13885,13885,13885,13885,13885,13885,13885,13885,MONDO:0008782,amyotrophic lateral sclerosis with polyglucosan bodies,MONDO,disease,DISEASE_13885
13886,13886,13886,13886,13886,13886,13886,13886,MONDO:0021583,melanocytic skin neoplasm,MONDO,disease,DISEASE_13886
13887,13887,13887,13887,13887,13887,13887,13887,MONDO:0014493,autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency,MONDO,disease,DISEASE_13887
13888,13888,13888,13888,13888,13888,13888,13888,MONDO:0017185,autosomal dominant hyperinsulinism due to Kir6.2 deficiency,MONDO,disease,DISEASE_13888
13889,13889,13889,13889,13889,13889,13889,13889,MONDO:0021218,placenta neoplasm,MONDO,disease,DISEASE_13889
13890,13890,13890,13890,13890,13890,13890,13890,MONDO:0006549_MONDO:0006550,fibroepithelial polyp of the anus,MONDO_grouped,disease,DISEASE_13890
13891,13891,13891,13891,13891,13891,13891,13891,MONDO:0035647_MONDO:0035648_MONDO:0035649_MONDO:0035650,childhood-onset Steinert myotonic dystrophy,MONDO_grouped,disease,DISEASE_13891
13892,13892,13892,13892,13892,13892,13892,13892,MONDO:0018604,familial colorectal cancer type X,MONDO,disease,DISEASE_13892
13893,13893,13893,13893,13893,13893,13893,13893,MONDO:0700034,mosaic trisomy 13,MONDO,disease,DISEASE_13893
13894,13894,13894,13894,13894,13894,13894,13894,MONDO:0007185,Banki syndrome,MONDO,disease,DISEASE_13894
13895,13895,13895,13895,13895,13895,13895,13895,MONDO:0957564,"congenital smooth muscle hamartoma, with or without hemihypertrophy",MONDO,disease,DISEASE_13895
13896,13896,13896,13896,13896,13896,13896,13896,MONDO:0006706,Bifidobacteriales infectious disease,MONDO,disease,DISEASE_13896
13897,13897,13897,13897,13897,13897,13897,13897,MONDO:0000502_MONDO:0003204,villous adenoma,MONDO_grouped,disease,DISEASE_13897
13898,13898,13898,13898,13898,13898,13898,13898,MONDO:0017237,hereditary sensorimotor neuropathy with hyperelastic skin,MONDO,disease,DISEASE_13898
13899,13899,13899,13899,13899,13899,13899,13899,MONDO:0022557,Behrens Baumann dust syndrome,MONDO,disease,DISEASE_13899
13900,13900,13900,13900,13900,13900,13900,13900,MONDO:0045057,delirium,MONDO,disease,DISEASE_13900
13901,13901,13901,13901,13901,13901,13901,13901,MONDO:0025149,"encephalopathy, bovine spongiform",MONDO,disease,DISEASE_13901
13902,13902,13902,13902,13902,13902,13902,13902,MONDO:0005068,myocardial infarction,MONDO,disease,DISEASE_13902
13903,13903,13903,13903,13903,13903,13903,13903,MONDO:0006322,non-neoplastic bile duct disorder,MONDO,disease,DISEASE_13903
13904,13904,13904,13904,13904,13904,13904,13904,MONDO:0008813,arachnoid cyst,MONDO,disease,DISEASE_13904
13905,13905,13905,13905,13905,13905,13905,13905,MONDO:0005627,head and neck cancer,MONDO,disease,DISEASE_13905
13906,13906,13906,13906,13906,13906,13906,13906,MONDO:0020113,primary acquired red cell aplasia,MONDO,disease,DISEASE_13906
13907,13907,13907,13907,13907,13907,13907,13907,MONDO:0001874_MONDO:0001688_MONDO:0004904,toxic labyrinthitis,MONDO_grouped,disease,DISEASE_13907
13908,13908,13908,13908,13908,13908,13908,13908,MONDO:0044200,T-B+ severe combined immunodeficiency,MONDO,disease,DISEASE_13908
13909,13909,13909,13909,13909,13909,13909,13909,MONDO:1010475_MONDO:1010471_MONDO:1010472_MONDO:1010473_MONDO:1010474_MONDO:1010476,"persistent truncus arteriosus, cattle",MONDO_grouped,disease,DISEASE_13909
13910,13910,13910,13910,13910,13910,13910,13910,MONDO:0002299,glomangioma,MONDO,disease,DISEASE_13910
13911,13911,13911,13911,13911,13911,13911,13911,MONDO:0019375,megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome,MONDO,disease,DISEASE_13911
13912,13912,13912,13912,13912,13912,13912,13912,MONDO:0007722,heterochromia iridis,MONDO,disease,DISEASE_13912
13913,13913,13913,13913,13913,13913,13913,13913,MONDO:0850471,N1 diffuse large B-cell lymphoma,MONDO,disease,DISEASE_13913
13914,13914,13914,13914,13914,13914,13914,13914,MONDO:0008150,osteoglophonic dwarfism,MONDO,disease,DISEASE_13914
13915,13915,13915,13915,13915,13915,13915,13915,MONDO:0011856,spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome,MONDO,disease,DISEASE_13915
13916,13916,13916,13916,13916,13916,13916,13916,MONDO:0006482,ureter small cell carcinoma,MONDO,disease,DISEASE_13916
13917,13917,13917,13917,13917,13917,13917,13917,MONDO:0700035,monosomy chromosome 8,MONDO,disease,DISEASE_13917
13918,13918,13918,13918,13918,13918,13918,13918,MONDO:0011420,short stature due to partial GHR deficiency,MONDO,disease,DISEASE_13918
13919,13919,13919,13919,13919,13919,13919,13919,MONDO:1011803,"muscular dystrophy-dystroglycanopathy (limb-girdle), non-human animal",MONDO,disease,DISEASE_13919
13920,13920,13920,13920,13920,13920,13920,13920,MONDO:0957216_MONDO:0970995_MONDO:0030870_MONDO:0957822_MONDO:0044777_MONDO:0014843_MONDO:0014322_MONDO:0014844_MONDO:0044317_MONDO:0030985_MONDO:0012861_MONDO:0044776_MONDO:0010706_MONDO:0030975_MONDO:0012169_MONDO:0014321_MONDO:0012689_MONDO:0010350_MONDO:0030939_MONDO:0010373_MONDO:0054862_MONDO:0032881_MONDO:0013065_MONDO:0975843_MONDO:0958035_MONDO:0800317,premature ovarian failure,MONDO_grouped,disease,DISEASE_13920
13921,13921,13921,13921,13921,13921,13921,13921,MONDO:1011226,"entropion, domestic cat",MONDO,disease,DISEASE_13921
13922,13922,13922,13922,13922,13922,13922,13922,MONDO:0014267,severe combined immunodeficiency due to IKK2 deficiency,MONDO,disease,DISEASE_13922
13923,13923,13923,13923,13923,13923,13923,13923,MONDO:0008179,paroxysmal extreme pain disorder,MONDO,disease,DISEASE_13923
13924,13924,13924,13924,13924,13924,13924,13924,MONDO:0024676,childhood kidney Wilms tumor,MONDO,disease,DISEASE_13924
13925,13925,13925,13925,13925,13925,13925,13925,MONDO:0005738,echinococcosis,MONDO,disease,DISEASE_13925
13926,13926,13926,13926,13926,13926,13926,13926,MONDO:0015101,Marin-Amat syndrome,MONDO,disease,DISEASE_13926
13927,13927,13927,13927,13927,13927,13927,13927,MONDO:0011509,"low density lipoprotein cholesterol, mild elevation of",MONDO,disease,DISEASE_13927
13928,13928,13928,13928,13928,13928,13928,13928,MONDO:0040679,urothelial carcinoma,MONDO,disease,DISEASE_13928
13929,13929,13929,13929,13929,13929,13929,13929,MONDO:1012675_MONDO:1012676,"osteochondrodysplasia, SLC13A1-related, dog",MONDO_grouped,disease,DISEASE_13929
13930,13930,13930,13930,13930,13930,13930,13930,MONDO:0011165_MONDO:0024527,glomerulopathy with fibronectin deposits,MONDO_grouped,disease,DISEASE_13930
13931,13931,13931,13931,13931,13931,13931,13931,MONDO:0971007,neuroocular syndrome 1,MONDO,disease,DISEASE_13931
13932,13932,13932,13932,13932,13932,13932,13932,MONDO:0001835,facial paralysis,MONDO,disease,DISEASE_13932
13933,13933,13933,13933,13933,13933,13933,13933,MONDO:0016487,beta-thalassemia intermedia,MONDO,disease,DISEASE_13933
13934,13934,13934,13934,13934,13934,13934,13934,MONDO:0018717,mixed cystic lymphatic malformation,MONDO,disease,DISEASE_13934
13935,13935,13935,13935,13935,13935,13935,13935,MONDO:0043346,progressive transformation of germinal centers,MONDO,disease,DISEASE_13935
13936,13936,13936,13936,13936,13936,13936,13936,MONDO:0004599,barbiturate abuse,MONDO,disease,DISEASE_13936
13937,13937,13937,13937,13937,13937,13937,13937,MONDO:0017832,Mycobacterium xenopi infection,MONDO,disease,DISEASE_13937
13938,13938,13938,13938,13938,13938,13938,13938,MONDO:0040870,primary polydipsia,MONDO,disease,DISEASE_13938
13939,13939,13939,13939,13939,13939,13939,13939,MONDO:0014196,Hartsfield-Bixler-Demyer syndrome,MONDO,disease,DISEASE_13939
13940,13940,13940,13940,13940,13940,13940,13940,MONDO:0970959,posterior extramedullary conus spinal cord lipoma,MONDO,disease,DISEASE_13940
13941,13941,13941,13941,13941,13941,13941,13941,MONDO:0001364_MONDO:0001831,regular astigmatism,MONDO_grouped,disease,DISEASE_13941
13942,13942,13942,13942,13942,13942,13942,13942,MONDO:0007583,obsolete exostoses of heel,MONDO,disease,DISEASE_13942
13943,13943,13943,13943,13943,13943,13943,13943,MONDO:1011971,"caudal cruciate ligament disease, non-human animal",MONDO,disease,DISEASE_13943
13944,13944,13944,13944,13944,13944,13944,13944,MONDO:0008289,brain small vessel disease 1 with or without ocular anomalies,MONDO,disease,DISEASE_13944
13945,13945,13945,13945,13945,13945,13945,13945,MONDO:0005768,gastrointestinal tuberculosis,MONDO,disease,DISEASE_13945
13946,13946,13946,13946,13946,13946,13946,13946,MONDO:0007040,Sakati-Nyhan syndrome,MONDO,disease,DISEASE_13946
13947,13947,13947,13947,13947,13947,13947,13947,MONDO:0056818,skin adenosquamous carcinoma,MONDO,disease,DISEASE_13947
13948,13948,13948,13948,13948,13948,13948,13948,MONDO:0009407,hypertrophic neuropathy and cataract,MONDO,disease,DISEASE_13948
13949,13949,13949,13949,13949,13949,13949,13949,MONDO:0034819,obsolete familial intestinal malrotation,MONDO,disease,DISEASE_13949
13950,13950,13950,13950,13950,13950,13950,13950,MONDO:0030313_MONDO:0957561_MONDO:0013633_MONDO:0054754_MONDO:0030334_MONDO:0032742_MONDO:0800174,"encephalopathy, acute, infection-induced (herpes-specific), susceptibility to",MONDO_grouped,disease,DISEASE_13950
13951,13951,13951,13951,13951,13951,13951,13951,MONDO:0018125,focal epilepsy-intellectual disability-cerebro-cerebellar malformation,MONDO,disease,DISEASE_13951
13952,13952,13952,13952,13952,13952,13952,13952,MONDO:0006837,low tension glaucoma,MONDO,disease,DISEASE_13952
13953,13953,13953,13953,13953,13953,13953,13953,MONDO:0056799_MONDO:0002403,synovium disorder,MONDO_grouped,disease,DISEASE_13953
13954,13954,13954,13954,13954,13954,13954,13954,MONDO:0002564,jejunal neoplasm,MONDO,disease,DISEASE_13954
13955,13955,13955,13955,13955,13955,13955,13955,MONDO:0009915,"46,XX disorder of sex development-skeletal anomalies syndrome",MONDO,disease,DISEASE_13955
13956,13956,13956,13956,13956,13956,13956,13956,MONDO:0006624,overactive bladder,MONDO,disease,DISEASE_13956
13957,13957,13957,13957,13957,13957,13957,13957,MONDO:0003142,intracranial primitive neuroectodermal tumor,MONDO,disease,DISEASE_13957
13958,13958,13958,13958,13958,13958,13958,13958,MONDO:0001076,glucose intolerance,MONDO,disease,DISEASE_13958
13959,13959,13959,13959,13959,13959,13959,13959,MONDO:0001224,Angelucci syndrome,MONDO,disease,DISEASE_13959
13960,13960,13960,13960,13960,13960,13960,13960,MONDO:0019772,blepharospasm-oromandibular dystonia syndrome,MONDO,disease,DISEASE_13960
13961,13961,13961,13961,13961,13961,13961,13961,MONDO:0015998,isolated ectopia lentis,MONDO,disease,DISEASE_13961
13962,13962,13962,13962,13962,13962,13962,13962,MONDO:0011146_MONDO:0018030_MONDO:0013668_MONDO:0018028_MONDO:0019525_MONDO:0030502_MONDO:0019864,tetrasomy,MONDO_grouped,disease,DISEASE_13962
13963,13963,13963,13963,13963,13963,13963,13963,MONDO:0022824,congenital craniosynostosis maternal hyperthyroiditis,MONDO,disease,DISEASE_13963
13964,13964,13964,13964,13964,13964,13964,13964,MONDO:0002917,disorder of pilosebaceous unit,MONDO,disease,DISEASE_13964
13965,13965,13965,13965,13965,13965,13965,13965,MONDO:1011143,"choanal atresia, llama",MONDO,disease,DISEASE_13965
13966,13966,13966,13966,13966,13966,13966,13966,MONDO:0019807,mesocardia,MONDO,disease,DISEASE_13966
13967,13967,13967,13967,13967,13967,13967,13967,MONDO:0008261,"hereditary sclerosing poikiloderma, Weary type",MONDO,disease,DISEASE_13967
13968,13968,13968,13968,13968,13968,13968,13968,MONDO:0005614,pancreatic adenosquamous carcinoma,MONDO,disease,DISEASE_13968
13969,13969,13969,13969,13969,13969,13969,13969,MONDO:0024965_MONDO:1010198,"muscular dystrophy, non-human animal",MONDO_grouped,disease,DISEASE_13969
13970,13970,13970,13970,13970,13970,13970,13970,MONDO:0017935,hyperinsulinism due to HNF1A deficiency,MONDO,disease,DISEASE_13970
13971,13971,13971,13971,13971,13971,13971,13971,MONDO:0013559_MONDO:0013560_MONDO:0013558_MONDO:0013557_MONDO:0008748_MONDO:0013556_MONDO:0013555_MONDO:0014885_MONDO:0013606_MONDO:0011997_MONDO:0030903_MONDO:0019312,Hermansky-Pudlak syndrome,MONDO_grouped,disease,DISEASE_13971
13972,13972,13972,13972,13972,13972,13972,13972,MONDO:0007757,hyperkeratosis-hyperpigmentation syndrome,MONDO,disease,DISEASE_13972
13973,13973,13973,13973,13973,13973,13973,13973,MONDO:0000991_MONDO:0001662,obsolete left bundle branch block,MONDO_grouped,disease,DISEASE_13973
13974,13974,13974,13974,13974,13974,13974,13974,MONDO:0100511,sudden cardiac arrest,MONDO,disease,DISEASE_13974
13975,13975,13975,13975,13975,13975,13975,13975,MONDO:1012476,"attention deficit hyperactivity disorder, dog",MONDO,disease,DISEASE_13975
13976,13976,13976,13976,13976,13976,13976,13976,MONDO:1011851_MONDO:1011975_MONDO:1011838,"congenital neuromuscular disease, non-human animal",MONDO_grouped,disease,DISEASE_13976
13977,13977,13977,13977,13977,13977,13977,13977,MONDO:0002090_MONDO:0024482,eccrine sweat gland neoplasm,MONDO_grouped,disease,DISEASE_13977
13978,13978,13978,13978,13978,13978,13978,13978,MONDO:0003010,multilocular clear cell renal cell carcinoma,MONDO,disease,DISEASE_13978
13979,13979,13979,13979,13979,13979,13979,13979,MONDO:0015755,myopathy with hexagonally cross-linked tubular arrays,MONDO,disease,DISEASE_13979
13980,13980,13980,13980,13980,13980,13980,13980,MONDO:1040046,LZTFL1-related ciliopathy,MONDO,disease,DISEASE_13980
13981,13981,13981,13981,13981,13981,13981,13981,MONDO:0043275,TORCH syndrome,MONDO,disease,DISEASE_13981
13982,13982,13982,13982,13982,13982,13982,13982,MONDO:0024637,malignant soft tissue neoplasm,MONDO,disease,DISEASE_13982
13983,13983,13983,13983,13983,13983,13983,13983,MONDO:0000292,philophthalmiasis,MONDO,disease,DISEASE_13983
13984,13984,13984,13984,13984,13984,13984,13984,MONDO:0859292,"developmental delay, behavioral abnormalities, and neuropsychiatric disorders",MONDO,disease,DISEASE_13984
13985,13985,13985,13985,13985,13985,13985,13985,MONDO:0006829,leukemoid reaction,MONDO,disease,DISEASE_13985
13986,13986,13986,13986,13986,13986,13986,13986,MONDO:0023263,glyceraldehyde-3-phosphate dehydrogenase deficiency,MONDO,disease,DISEASE_13986
13987,13987,13987,13987,13987,13987,13987,13987,MONDO:0030069,"hyper-IgE recurrent infection syndrome 5, autosomal recessive",MONDO,disease,DISEASE_13987
13988,13988,13988,13988,13988,13988,13988,13988,MONDO:0019787_MONDO:0015174_MONDO:0021950_MONDO:0033862,autoimmune enteropathy,MONDO_grouped,disease,DISEASE_13988
13989,13989,13989,13989,13989,13989,13989,13989,MONDO:0032594,intellectual developmental disorder and retinitis pigmentosa; IDDRP,MONDO,disease,DISEASE_13989
13990,13990,13990,13990,13990,13990,13990,13990,MONDO:0800123,bronchiolocentric pattern of interstitial pneumonia,MONDO,disease,DISEASE_13990
13991,13991,13991,13991,13991,13991,13991,13991,MONDO:0021517,benign neoplasm of trachea,MONDO,disease,DISEASE_13991
13992,13992,13992,13992,13992,13992,13992,13992,MONDO:0019575,hypotrichosis simplex of the scalp,MONDO,disease,DISEASE_13992
13993,13993,13993,13993,13993,13993,13993,13993,MONDO:0011646,laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy,MONDO,disease,DISEASE_13993
13994,13994,13994,13994,13994,13994,13994,13994,MONDO:0032823,intellectual developmental disorder 60 with seizures,MONDO,disease,DISEASE_13994
13995,13995,13995,13995,13995,13995,13995,13995,MONDO:0001335,hypotrichosis of eyelid,MONDO,disease,DISEASE_13995
13996,13996,13996,13996,13996,13996,13996,13996,MONDO:0011604,spondylo-ocular syndrome,MONDO,disease,DISEASE_13996
13997,13997,13997,13997,13997,13997,13997,13997,MONDO:0001728,active vestibular Meniere disease,MONDO,disease,DISEASE_13997
13998,13998,13998,13998,13998,13998,13998,13998,MONDO:1011787,"degenerative myopathy of deep pectoral muscle, non-human animal",MONDO,disease,DISEASE_13998
13999,13999,13999,13999,13999,13999,13999,13999,MONDO:1012343,"gluten-sensitive enteropathy, dog",MONDO,disease,DISEASE_13999
14000,14000,14000,14000,14000,14000,14000,14000,MONDO:0009871,pili torti-developmental delay-neurological abnormalities syndrome,MONDO,disease,DISEASE_14000
14001,14001,14001,14001,14001,14001,14001,14001,MONDO:0006264,laryngeal adenoid cystic carcinoma,MONDO,disease,DISEASE_14001
14002,14002,14002,14002,14002,14002,14002,14002,MONDO:0006956,Rickettsiosis,MONDO,disease,DISEASE_14002
14003,14003,14003,14003,14003,14003,14003,14003,MONDO:0019017,short fifth metacarpals-insulin resistance syndrome,MONDO,disease,DISEASE_14003
14004,14004,14004,14004,14004,14004,14004,14004,MONDO:0010001_MONDO:0023046_MONDO:0023048,ectodermal dysplasia-blindness syndrome,MONDO_grouped,disease,DISEASE_14004
14005,14005,14005,14005,14005,14005,14005,14005,MONDO:0020482,myotonia permanens,MONDO,disease,DISEASE_14005
14006,14006,14006,14006,14006,14006,14006,14006,MONDO:0006109,malignant biphasic mesothelioma,MONDO,disease,DISEASE_14006
14007,14007,14007,14007,14007,14007,14007,14007,MONDO:0007927,congenital macroglossia,MONDO,disease,DISEASE_14007
14008,14008,14008,14008,14008,14008,14008,14008,MONDO:0008860,"beta-aminoisobutyric acid, urinary excretion of",MONDO,disease,DISEASE_14008
14009,14009,14009,14009,14009,14009,14009,14009,MONDO:0010235,X-linked intellectual disability-psychosis-macroorchidism syndrome,MONDO,disease,DISEASE_14009
14010,14010,14010,14010,14010,14010,14010,14010,MONDO:0017147,idiopathic pulmonary arterial hypertension,MONDO,disease,DISEASE_14010
14011,14011,14011,14011,14011,14011,14011,14011,MONDO:1011224,"ectropion, dog",MONDO,disease,DISEASE_14011
14012,14012,14012,14012,14012,14012,14012,14012,MONDO:0006971,sigmoid neoplasm,MONDO,disease,DISEASE_14012
14013,14013,14013,14013,14013,14013,14013,14013,MONDO:0007256_MONDO:0018666_MONDO:0018902,hepatocellular carcinoma,MONDO_grouped,disease,DISEASE_14013
14014,14014,14014,14014,14014,14014,14014,14014,MONDO:1012137,"congenital joint laxity and dwarfism, cattle",MONDO,disease,DISEASE_14014
14015,14015,14015,14015,14015,14015,14015,14015,MONDO:0004308,meningeal sarcoma,MONDO,disease,DISEASE_14015
14016,14016,14016,14016,14016,14016,14016,14016,MONDO:0010900,intrauterine growth retardation with increased mitomycin c sensitivity,MONDO,disease,DISEASE_14016
14017,14017,14017,14017,14017,14017,14017,14017,MONDO:1012016,"progressive ataxia with degenerative thoracic myelopathy, sheep",MONDO,disease,DISEASE_14017
14018,14018,14018,14018,14018,14018,14018,14018,MONDO:0011726,peripheral arterial occlusive disease 1,MONDO,disease,DISEASE_14018
14019,14019,14019,14019,14019,14019,14019,14019,MONDO:0044721,severe combined immunodeficiency due to LAT deficiency,MONDO,disease,DISEASE_14019
14020,14020,14020,14020,14020,14020,14020,14020,MONDO:0005296,sleep apnea syndrome,MONDO,disease,DISEASE_14020
14021,14021,14021,14021,14021,14021,14021,14021,MONDO:1010360,"dacryocystitis, non-human animal",MONDO,disease,DISEASE_14021
14022,14022,14022,14022,14022,14022,14022,14022,MONDO:0009284,glutathione synthetase deficiency without 5-oxoprolinuria,MONDO,disease,DISEASE_14022
14023,14023,14023,14023,14023,14023,14023,14023,MONDO:0002009_MONDO:0012050_MONDO:0012100,major depressive disorder,MONDO_grouped,disease,DISEASE_14023
14024,14024,14024,14024,14024,14024,14024,14024,MONDO:0016697,low grade ependymoma,MONDO,disease,DISEASE_14024
14025,14025,14025,14025,14025,14025,14025,14025,MONDO:0005096,squamous cell carcinoma,MONDO,disease,DISEASE_14025
14026,14026,14026,14026,14026,14026,14026,14026,MONDO:0003410,Wolffian duct adenocarcinoma,MONDO,disease,DISEASE_14026
14027,14027,14027,14027,14027,14027,14027,14027,MONDO:0020128,motor neuron disorder,MONDO,disease,DISEASE_14027
14028,14028,14028,14028,14028,14028,14028,14028,MONDO:0013918_MONDO:0015728,distal tetrasomy 15q,MONDO_grouped,disease,DISEASE_14028
14029,14029,14029,14029,14029,14029,14029,14029,MONDO:0004720,variola minor infection,MONDO,disease,DISEASE_14029
14030,14030,14030,14030,14030,14030,14030,14030,MONDO:0020789_MONDO:0030044_MONDO:0018828_MONDO:0009626,pseudo-TORCH syndrome,MONDO_grouped,disease,DISEASE_14030
14031,14031,14031,14031,14031,14031,14031,14031,MONDO:0006256,invasive breast carcinoma,MONDO,disease,DISEASE_14031
14032,14032,14032,14032,14032,14032,14032,14032,MONDO:0700055,KIF1A related neurological disorder,MONDO,disease,DISEASE_14032
14033,14033,14033,14033,14033,14033,14033,14033,MONDO:0017986,disorder of plasmalogens biosynthesis,MONDO,disease,DISEASE_14033
14034,14034,14034,14034,14034,14034,14034,14034,MONDO:0001847,nuclear senile cataract,MONDO,disease,DISEASE_14034
14035,14035,14035,14035,14035,14035,14035,14035,MONDO:0001001,baritosis,MONDO,disease,DISEASE_14035
14036,14036,14036,14036,14036,14036,14036,14036,MONDO:0005617,undifferentiated carcinoma,MONDO,disease,DISEASE_14036
14037,14037,14037,14037,14037,14037,14037,14037,MONDO:0002516,digestive system cancer,MONDO,disease,DISEASE_14037
14038,14038,14038,14038,14038,14038,14038,14038,MONDO:0018106,hereditary xanthinuria,MONDO,disease,DISEASE_14038
14039,14039,14039,14039,14039,14039,14039,14039,MONDO:0000304,penicilliosis,MONDO,disease,DISEASE_14039
14040,14040,14040,14040,14040,14040,14040,14040,MONDO:0011254,"brachydactyly, intraventricular septal defect, and deafness",MONDO,disease,DISEASE_14040
14041,14041,14041,14041,14041,14041,14041,14041,MONDO:1010914,"muscular hypertrophy, MSTN-related, cattle",MONDO,disease,DISEASE_14041
14042,14042,14042,14042,14042,14042,14042,14042,MONDO:0015585,cryptogenic late-onset epileptic spasms,MONDO,disease,DISEASE_14042
14043,14043,14043,14043,14043,14043,14043,14043,MONDO:0001531,blood coagulation disease,MONDO,disease,DISEASE_14043
14044,14044,14044,14044,14044,14044,14044,14044,MONDO:0003326,intermixed schwannian stroma-rich ganglioneuroblastoma,MONDO,disease,DISEASE_14044
14045,14045,14045,14045,14045,14045,14045,14045,MONDO:0017688,disorder of glycolysis,MONDO,disease,DISEASE_14045
14046,14046,14046,14046,14046,14046,14046,14046,MONDO:0006735,duodenogastric reflux,MONDO,disease,DISEASE_14046
14047,14047,14047,14047,14047,14047,14047,14047,MONDO:0024245,ductal eccrine adenocarcinoma,MONDO,disease,DISEASE_14047
14048,14048,14048,14048,14048,14048,14048,14048,MONDO:0018355,SIM1-related Prader-Willi-like syndrome,MONDO,disease,DISEASE_14048
14049,14049,14049,14049,14049,14049,14049,14049,MONDO:0034989,intellectual disability-cardiac anomalies-short stature-joint laxity syndrome,MONDO,disease,DISEASE_14049
14050,14050,14050,14050,14050,14050,14050,14050,MONDO:0003628,pulmonary valve disorder,MONDO,disease,DISEASE_14050
14051,14051,14051,14051,14051,14051,14051,14051,MONDO:0005342,IgA glomerulonephritis,MONDO,disease,DISEASE_14051
14052,14052,14052,14052,14052,14052,14052,14052,MONDO:0023282,granulomatous hypophysitis,MONDO,disease,DISEASE_14052
14053,14053,14053,14053,14053,14053,14053,14053,MONDO:0021039,extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor,MONDO,disease,DISEASE_14053
14054,14054,14054,14054,14054,14054,14054,14054,MONDO:1012695,"dwarfism, PRKG2-related, cattle",MONDO,disease,DISEASE_14054
14055,14055,14055,14055,14055,14055,14055,14055,MONDO:0009741_MONDO:0700041_MONDO:0013083_MONDO:0013084_MONDO:0013085_MONDO:0013086_MONDO:0014774,"neuroblastoma, susceptibility to",MONDO_grouped,disease,DISEASE_14055
14056,14056,14056,14056,14056,14056,14056,14056,MONDO:0009097_MONDO:0019631_MONDO:0012653,"persistent hyperplastic primary vitreous, autosomal recessive",MONDO_grouped,disease,DISEASE_14056
14057,14057,14057,14057,14057,14057,14057,14057,MONDO:0008650,posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome,MONDO,disease,DISEASE_14057
14058,14058,14058,14058,14058,14058,14058,14058,MONDO:0800101_MONDO:1040056,NMNAT1-related retinopathy,MONDO_grouped,disease,DISEASE_14058
14059,14059,14059,14059,14059,14059,14059,14059,MONDO:0002802,functional colonic disease,MONDO,disease,DISEASE_14059
14060,14060,14060,14060,14060,14060,14060,14060,MONDO:0011463,"polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive",MONDO,disease,DISEASE_14060
14061,14061,14061,14061,14061,14061,14061,14061,MONDO:0019374,CAMOS syndrome,MONDO,disease,DISEASE_14061
14062,14062,14062,14062,14062,14062,14062,14062,MONDO:0012803,diarrhea-vomiting due to trehalase deficiency,MONDO,disease,DISEASE_14062
14063,14063,14063,14063,14063,14063,14063,14063,MONDO:0019449,lissencephaly type 3-familial fetal akinesia sequence syndrome,MONDO,disease,DISEASE_14063
14064,14064,14064,14064,14064,14064,14064,14064,MONDO:0016806,maternally-inherited mitochondrial dystonia,MONDO,disease,DISEASE_14064
14065,14065,14065,14065,14065,14065,14065,14065,MONDO:0019415,fetal and neonatal alloimmune thrombocytopenia,MONDO,disease,DISEASE_14065
14066,14066,14066,14066,14066,14066,14066,14066,MONDO:0001596,hypochondriasis,MONDO,disease,DISEASE_14066
14067,14067,14067,14067,14067,14067,14067,14067,MONDO:0010492,"pituitary adenoma, growth hormone-secreting, 2",MONDO,disease,DISEASE_14067
14068,14068,14068,14068,14068,14068,14068,14068,MONDO:0700246,ocular dysgenesis caused by defects in PAX6 regulation,MONDO,disease,DISEASE_14068
14069,14069,14069,14069,14069,14069,14069,14069,MONDO:0010737_MONDO:1012683,"spondyloepiphyseal dysplasia tarda, X-linked",MONDO_grouped,disease,DISEASE_14069
14070,14070,14070,14070,14070,14070,14070,14070,MONDO:1011067,"urolithiasis, domestic guinea pig",MONDO,disease,DISEASE_14070
14071,14071,14071,14071,14071,14071,14071,14071,MONDO:0001391,indeterminate leprosy,MONDO,disease,DISEASE_14071
14072,14072,14072,14072,14072,14072,14072,14072,MONDO:0021288,carcinoma in situ of hypopharynx,MONDO,disease,DISEASE_14072
14073,14073,14073,14073,14073,14073,14073,14073,MONDO:0007246,"calcific aortic disease with immunologic abnormalities, familial",MONDO,disease,DISEASE_14073
14074,14074,14074,14074,14074,14074,14074,14074,MONDO:0010496,X-linked intellectual disability-short stature-overweight syndrome,MONDO,disease,DISEASE_14074
14075,14075,14075,14075,14075,14075,14075,14075,MONDO:0011693,"glaucoma, normal tension, susceptibility to",MONDO,disease,DISEASE_14075
14076,14076,14076,14076,14076,14076,14076,14076,MONDO:0015623,cavitary myiasis,MONDO,disease,DISEASE_14076
14077,14077,14077,14077,14077,14077,14077,14077,MONDO:0001784,malignant renovascular hypertension,MONDO,disease,DISEASE_14077
14078,14078,14078,14078,14078,14078,14078,14078,MONDO:0019534,mixed-type autoimmune hemolytic anemia,MONDO,disease,DISEASE_14078
14079,14079,14079,14079,14079,14079,14079,14079,MONDO:0003502,ureter squamous cell carcinoma,MONDO,disease,DISEASE_14079
14080,14080,14080,14080,14080,14080,14080,14080,MONDO:0003481,dysgerminoma of ovary,MONDO,disease,DISEASE_14080
14081,14081,14081,14081,14081,14081,14081,14081,MONDO:0010717,pyruvate dehydrogenase E1-alpha deficiency,MONDO,disease,DISEASE_14081
14082,14082,14082,14082,14082,14082,14082,14082,MONDO:0003553,ampulla of vater adenosquamous carcinoma,MONDO,disease,DISEASE_14082
14083,14083,14083,14083,14083,14083,14083,14083,MONDO:0008202,"Parotidomegaly, hereditary bilateral",MONDO,disease,DISEASE_14083
14084,14084,14084,14084,14084,14084,14084,14084,MONDO:0700039,bladder exstrophy-epispadias-cloacal extrophy complex,MONDO,disease,DISEASE_14084
14085,14085,14085,14085,14085,14085,14085,14085,MONDO:0859200,"cerebellar ataxia, brain abnormalities, and cardiac conduction defects",MONDO,disease,DISEASE_14085
14086,14086,14086,14086,14086,14086,14086,14086,MONDO:0018062,autosomal dominant trichoodontoonychodysplasia-syndactyly,MONDO,disease,DISEASE_14086
14087,14087,14087,14087,14087,14087,14087,14087,MONDO:0010403,albinism-hearing loss syndrome,MONDO,disease,DISEASE_14087
14088,14088,14088,14088,14088,14088,14088,14088,MONDO:0035534,DONSON-related microcephaly-short stature-limb abnormalities spectrum,MONDO,disease,DISEASE_14088
14089,14089,14089,14089,14089,14089,14089,14089,MONDO:0001558,Potter sequence,MONDO,disease,DISEASE_14089
14090,14090,14090,14090,14090,14090,14090,14090,MONDO:0005589,thiopurine immunosuppressant-induced pancreatitis,MONDO,disease,DISEASE_14090
14091,14091,14091,14091,14091,14091,14091,14091,MONDO:0021024,"malaria, susceptibility to",MONDO,disease,DISEASE_14091
14092,14092,14092,14092,14092,14092,14092,14092,MONDO:0020368,Axenfeld anomaly,MONDO,disease,DISEASE_14092
14093,14093,14093,14093,14093,14093,14093,14093,MONDO:0021020_MONDO:0011725_MONDO:0009044,Crigler-Najjar syndrome,MONDO_grouped,disease,DISEASE_14093
14094,14094,14094,14094,14094,14094,14094,14094,MONDO:0022646,cardiofacial syndrome short limbs,MONDO,disease,DISEASE_14094
14095,14095,14095,14095,14095,14095,14095,14095,MONDO:0018864,Kikuchi-Fujimoto disease,MONDO,disease,DISEASE_14095
14096,14096,14096,14096,14096,14096,14096,14096,MONDO:0001441,pica disease,MONDO,disease,DISEASE_14096
14097,14097,14097,14097,14097,14097,14097,14097,MONDO:0016506,ectopic aldosterone-producing tumor,MONDO,disease,DISEASE_14097
14098,14098,14098,14098,14098,14098,14098,14098,MONDO:0056815,liver adenosquamous carcinoma,MONDO,disease,DISEASE_14098
14099,14099,14099,14099,14099,14099,14099,14099,MONDO:0043343,Chilaiditi syndrome,MONDO,disease,DISEASE_14099
14100,14100,14100,14100,14100,14100,14100,14100,MONDO:0010030,Sjogren syndrome,MONDO,disease,DISEASE_14100
14101,14101,14101,14101,14101,14101,14101,14101,MONDO:0007238,amastia,MONDO,disease,DISEASE_14101
14102,14102,14102,14102,14102,14102,14102,14102,MONDO:0004353_MONDO:0004509,extrahepatic biliary papillomatosis,MONDO_grouped,disease,DISEASE_14102
14103,14103,14103,14103,14103,14103,14103,14103,MONDO:0800107,anterior deviation infundibular septum,MONDO,disease,DISEASE_14103
14104,14104,14104,14104,14104,14104,14104,14104,MONDO:0007943_MONDO:0018237,Nager acrofacial dysostosis,MONDO_grouped,disease,DISEASE_14104
14105,14105,14105,14105,14105,14105,14105,14105,MONDO:0019462,splenic marginal zone lymphoma,MONDO,disease,DISEASE_14105
14106,14106,14106,14106,14106,14106,14106,14106,MONDO:0008369_MONDO:0015827,proximal renal tubular acidosis,MONDO_grouped,disease,DISEASE_14106
14107,14107,14107,14107,14107,14107,14107,14107,MONDO:0017824_MONDO:0017896_MONDO:0020523,familial isolated pituitary adenoma,MONDO_grouped,disease,DISEASE_14107
14108,14108,14108,14108,14108,14108,14108,14108,MONDO:0020326,lymphomatoid papulosis,MONDO,disease,DISEASE_14108
14109,14109,14109,14109,14109,14109,14109,14109,MONDO:0005247_MONDO:0100338,bacterial urinary tract infection,MONDO_grouped,disease,DISEASE_14109
14110,14110,14110,14110,14110,14110,14110,14110,MONDO:1011734,"black hair follicular dysplasia, non-human animal",MONDO,disease,DISEASE_14110
14111,14111,14111,14111,14111,14111,14111,14111,MONDO:0800110,"persistent tachypnoe of infancy, aberrant",MONDO,disease,DISEASE_14111
14112,14112,14112,14112,14112,14112,14112,14112,MONDO:0100015,adult-onset segmental dystonia,MONDO,disease,DISEASE_14112
14113,14113,14113,14113,14113,14113,14113,14113,MONDO:0035646,congenital-onset Steinert myotonic dystrophy,MONDO,disease,DISEASE_14113
14114,14114,14114,14114,14114,14114,14114,14114,MONDO:0859226,"craniotubular dysplasia, Ikegawa type",MONDO,disease,DISEASE_14114
14115,14115,14115,14115,14115,14115,14115,14115,MONDO:0001277,cerebral arteritis,MONDO,disease,DISEASE_14115
14116,14116,14116,14116,14116,14116,14116,14116,MONDO:0023288,green sandford davison syndrome,MONDO,disease,DISEASE_14116
14117,14117,14117,14117,14117,14117,14117,14117,MONDO:0013567_MONDO:0013123_MONDO:0013770_MONDO:0007173_MONDO:0013750_MONDO:0012654_MONDO:0011938_MONDO:0007172_MONDO:0013011_MONDO:0006664_MONDO:1010433_MONDO:1010434_MONDO:1010436,atrial septal defect,MONDO_grouped,disease,DISEASE_14117
14118,14118,14118,14118,14118,14118,14118,14118,MONDO:0009321,hallux varus-preaxial polysyndactyly syndrome,MONDO,disease,DISEASE_14118
14119,14119,14119,14119,14119,14119,14119,14119,MONDO:0005865,mushroom workers' lung,MONDO,disease,DISEASE_14119
14120,14120,14120,14120,14120,14120,14120,14120,MONDO:1012772_MONDO:1012800_MONDO:1012839,"arthrogryposis multiplex congenita, CHRNB1-related, cattle",MONDO_grouped,disease,DISEASE_14120
14121,14121,14121,14121,14121,14121,14121,14121,MONDO:0010065,spinocerebellar degeneration with slow eye movements,MONDO,disease,DISEASE_14121
14122,14122,14122,14122,14122,14122,14122,14122,MONDO:0017614,X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome,MONDO,disease,DISEASE_14122
14123,14123,14123,14123,14123,14123,14123,14123,MONDO:1012260,"spinal dysraphism, cattle",MONDO,disease,DISEASE_14123
14124,14124,14124,14124,14124,14124,14124,14124,MONDO:0007471,Doyne honeycomb retinal dystrophy,MONDO,disease,DISEASE_14124
14125,14125,14125,14125,14125,14125,14125,14125,MONDO:0010391,"angioma serpiginosum, X-linked",MONDO,disease,DISEASE_14125
14126,14126,14126,14126,14126,14126,14126,14126,MONDO:0002654_MONDO:0002715_MONDO:0005558_MONDO:0001786,uterine disorder,MONDO_grouped,disease,DISEASE_14126
14127,14127,14127,14127,14127,14127,14127,14127,MONDO:0859572_MONDO:0010753,cardiac valvular dysplasia,MONDO_grouped,disease,DISEASE_14127
14128,14128,14128,14128,14128,14128,14128,14128,MONDO:1012501,"hydrallantois, water buffalo",MONDO,disease,DISEASE_14128
14129,14129,14129,14129,14129,14129,14129,14129,MONDO:1010738,"severe combined immunodeficiency disease, RAG1-related, dog",MONDO,disease,DISEASE_14129
14130,14130,14130,14130,14130,14130,14130,14130,MONDO:0016706,chordoid glioma of the third ventricle,MONDO,disease,DISEASE_14130
14131,14131,14131,14131,14131,14131,14131,14131,MONDO:0010033,generalized peeling skin syndrome,MONDO,disease,DISEASE_14131
14132,14132,14132,14132,14132,14132,14132,14132,MONDO:0005358,Dengue hemorrhagic fever,MONDO,disease,DISEASE_14132
14133,14133,14133,14133,14133,14133,14133,14133,MONDO:0020428,congenital Gerbode defect,MONDO,disease,DISEASE_14133
14134,14134,14134,14134,14134,14134,14134,14134,MONDO:0060496,"neurodevelopmental disorder with hypotonia, neuropathy, and deafness",MONDO,disease,DISEASE_14134
14135,14135,14135,14135,14135,14135,14135,14135,MONDO:0005664,bartonellosis,MONDO,disease,DISEASE_14135
14136,14136,14136,14136,14136,14136,14136,14136,MONDO:0043174,Pfeiffer Tietze Welte syndrome,MONDO,disease,DISEASE_14136
14137,14137,14137,14137,14137,14137,14137,14137,MONDO:0014306,vasculitis due to ADA2 deficiency,MONDO,disease,DISEASE_14137
14138,14138,14138,14138,14138,14138,14138,14138,MONDO:0012486,"preauricular tag, isolated, autosomal dominant, 1",MONDO,disease,DISEASE_14138
14139,14139,14139,14139,14139,14139,14139,14139,MONDO:0022780,cleft lip palate pituitary deficiency,MONDO,disease,DISEASE_14139
14140,14140,14140,14140,14140,14140,14140,14140,MONDO:0024500,duodenal neuroendocrine neoplasm,MONDO,disease,DISEASE_14140
14141,14141,14141,14141,14141,14141,14141,14141,MONDO:0001238,polycythemia neonatorum,MONDO,disease,DISEASE_14141
14142,14142,14142,14142,14142,14142,14142,14142,MONDO:0011366,ovarian germ cell tumor,MONDO,disease,DISEASE_14142
14143,14143,14143,14143,14143,14143,14143,14143,MONDO:0010038,growth delay due to insulin-like growth factor I resistance,MONDO,disease,DISEASE_14143
14144,14144,14144,14144,14144,14144,14144,14144,MONDO:0016687,protoplasmic astrocytoma,MONDO,disease,DISEASE_14144
14145,14145,14145,14145,14145,14145,14145,14145,MONDO:1011277_MONDO:1012659,"progressive retinal atrophy, BBS4-related, dog",MONDO_grouped,disease,DISEASE_14145
14146,14146,14146,14146,14146,14146,14146,14146,MONDO:0001867,phaeohyphomycosis,MONDO,disease,DISEASE_14146
14147,14147,14147,14147,14147,14147,14147,14147,MONDO:0016928,partial duplication of chromosome 7,MONDO,disease,DISEASE_14147
14148,14148,14148,14148,14148,14148,14148,14148,MONDO:0004848,ulcerative stomatitis,MONDO,disease,DISEASE_14148
14149,14149,14149,14149,14149,14149,14149,14149,MONDO:0018742,familial gastric type 1 neuroendocrine tumor,MONDO,disease,DISEASE_14149
14150,14150,14150,14150,14150,14150,14150,14150,MONDO:0016573,acute fatty liver of pregnancy,MONDO,disease,DISEASE_14150
14151,14151,14151,14151,14151,14151,14151,14151,MONDO:0006244,HER2 positive breast carcinoma,MONDO,disease,DISEASE_14151
14152,14152,14152,14152,14152,14152,14152,14152,MONDO:0016546,primary orthostatic tremor,MONDO,disease,DISEASE_14152
14153,14153,14153,14153,14153,14153,14153,14153,MONDO:0100196_MONDO:0100108,TPM2-related myopathy,MONDO_grouped,disease,DISEASE_14153
14154,14154,14154,14154,14154,14154,14154,14154,MONDO:0003673_MONDO:0003677_MONDO:0006803,apical myocardial infarction,MONDO_grouped,disease,DISEASE_14154
14155,14155,14155,14155,14155,14155,14155,14155,MONDO:0007610,gingival fibromatosis-hypertrichosis syndrome,MONDO,disease,DISEASE_14155
14156,14156,14156,14156,14156,14156,14156,14156,MONDO:0010037,sodium-potassium-ATPase activity of red cell,MONDO,disease,DISEASE_14156
14157,14157,14157,14157,14157,14157,14157,14157,MONDO:0018243,intellectual disability-hyperkinetic movement-truncal ataxia syndrome,MONDO,disease,DISEASE_14157
14158,14158,14158,14158,14158,14158,14158,14158,MONDO:0003757,paraplegia,MONDO,disease,DISEASE_14158
14159,14159,14159,14159,14159,14159,14159,14159,MONDO:0003572,nasopharyngeal type undifferentiated carcinoma,MONDO,disease,DISEASE_14159
14160,14160,14160,14160,14160,14160,14160,14160,MONDO:1012246,"rod-cone dysplasia, dog",MONDO,disease,DISEASE_14160
14161,14161,14161,14161,14161,14161,14161,14161,MONDO:0024268_MONDO:0000255,superficial mycosis,MONDO_grouped,disease,DISEASE_14161
14162,14162,14162,14162,14162,14162,14162,14162,MONDO:0022792,coccygodynia,MONDO,disease,DISEASE_14162
14163,14163,14163,14163,14163,14163,14163,14163,MONDO:0011986_MONDO:0004982_MONDO:0006515_MONDO:0003232,tropical pancreatitis,MONDO_grouped,disease,DISEASE_14163
14164,14164,14164,14164,14164,14164,14164,14164,MONDO:0006820,kidney cortex necrosis,MONDO,disease,DISEASE_14164
14165,14165,14165,14165,14165,14165,14165,14165,MONDO:0004218,childhood germ cell brain tumor,MONDO,disease,DISEASE_14165
14166,14166,14166,14166,14166,14166,14166,14166,MONDO:0014320,Bosch-Boonstra-Schaaf optic atrophy syndrome,MONDO,disease,DISEASE_14166
14167,14167,14167,14167,14167,14167,14167,14167,MONDO:1010611,"thyroiditis, dog",MONDO,disease,DISEASE_14167
14168,14168,14168,14168,14168,14168,14168,14168,MONDO:0000745,cardiac arrest,MONDO,disease,DISEASE_14168
14169,14169,14169,14169,14169,14169,14169,14169,MONDO:0014310,hereditary sclerosing poikiloderma with tendon and pulmonary involvement,MONDO,disease,DISEASE_14169
14170,14170,14170,14170,14170,14170,14170,14170,MONDO:0019990,non-amyloid fibrillary glomerulopathy,MONDO,disease,DISEASE_14170
14171,14171,14171,14171,14171,14171,14171,14171,MONDO:0013390_MONDO:0014144_MONDO:0011968_MONDO:0011787_MONDO:0013297_MONDO:0029133_MONDO:0014977_MONDO:0014142_MONDO:0029136_MONDO:0011028_MONDO:0009683_MONDO:0013161_MONDO:0014788_MONDO:0012248_MONDO:0957270_MONDO:0011170_MONDO:0012699_MONDO:0014900_MONDO:0012127_MONDO:0014782_MONDO:0012034_MONDO:0971171_MONDO:0013162_MONDO:0009675_MONDO:0009676_MONDO:0013440_MONDO:0012193_MONDO:0014474_MONDO:0011423_MONDO:0030456_MONDO:0030014_MONDO:0012652_MONDO:0009677_MONDO:0015152,autosomal recessive limb-girdle muscular dystrophy,MONDO_grouped,disease,DISEASE_14171
14172,14172,14172,14172,14172,14172,14172,14172,MONDO:1010557_MONDO:1012257,"spina bifida, domestic cat",MONDO_grouped,disease,DISEASE_14172
14173,14173,14173,14173,14173,14173,14173,14173,MONDO:0001370,pericardial effusion,MONDO,disease,DISEASE_14173
14174,14174,14174,14174,14174,14174,14174,14174,MONDO:0020808,testicular sertoli cell tumor,MONDO,disease,DISEASE_14174
14175,14175,14175,14175,14175,14175,14175,14175,MONDO:0005032,follicular thyroid adenoma,MONDO,disease,DISEASE_14175
14176,14176,14176,14176,14176,14176,14176,14176,MONDO:0000682,time agnosia,MONDO,disease,DISEASE_14176
14177,14177,14177,14177,14177,14177,14177,14177,MONDO:1012255,"spastic syndrome, sheep",MONDO,disease,DISEASE_14177
14178,14178,14178,14178,14178,14178,14178,14178,MONDO:0012735,Temple-Baraitser syndrome,MONDO,disease,DISEASE_14178
14179,14179,14179,14179,14179,14179,14179,14179,MONDO:0001402_MONDO:0001433_MONDO:0015867_MONDO:0006488_MONDO:0006489,vaginal cancer,MONDO_grouped,disease,DISEASE_14179
14180,14180,14180,14180,14180,14180,14180,14180,MONDO:0010752,"VACTERL association, X-linked, with or without hydrocephalus",MONDO,disease,DISEASE_14180
14181,14181,14181,14181,14181,14181,14181,14181,MONDO:0859208,Hengel-Maroofian-Schols syndrome,MONDO,disease,DISEASE_14181
14182,14182,14182,14182,14182,14182,14182,14182,MONDO:0000660,akinetopsia,MONDO,disease,DISEASE_14182
14183,14183,14183,14183,14183,14183,14183,14183,MONDO:0003019,potassium deficiency disease,MONDO,disease,DISEASE_14183
14184,14184,14184,14184,14184,14184,14184,14184,MONDO:0004967_MONDO:0003541_MONDO:0000870_MONDO:0003538,acute lymphoblastic leukemia,MONDO_grouped,disease,DISEASE_14184
14185,14185,14185,14185,14185,14185,14185,14185,MONDO:0002473,cystic kidney disease,MONDO,disease,DISEASE_14185
14186,14186,14186,14186,14186,14186,14186,14186,MONDO:0014567,glutamate pyruvate transaminase 2 deficiency,MONDO,disease,DISEASE_14186
14187,14187,14187,14187,14187,14187,14187,14187,MONDO:0004220,endometrial endometrioid adenocarcinoma with spindled epithelial cells,MONDO,disease,DISEASE_14187
14188,14188,14188,14188,14188,14188,14188,14188,MONDO:0014158_MONDO:0013917_MONDO:0013916_MONDO:0009728_MONDO:0013718_MONDO:0013302_MONDO:0014374_MONDO:0011190_MONDO:0014537_MONDO:0013442_MONDO:0011456_MONDO:0014997_MONDO:0011752_MONDO:0013444_MONDO:0012680_MONDO:0019005,nephronophthisis,MONDO_grouped,disease,DISEASE_14188
14189,14189,14189,14189,14189,14189,14189,14189,MONDO:0008561,thumb deformity,MONDO,disease,DISEASE_14189
14190,14190,14190,14190,14190,14190,14190,14190,MONDO:0003723,blunt duct adenosis of breast,MONDO,disease,DISEASE_14190
14191,14191,14191,14191,14191,14191,14191,14191,MONDO:0013612_MONDO:0009269_MONDO:0054722_MONDO:0000127,geleophysic dysplasia,MONDO_grouped,disease,DISEASE_14191
14192,14192,14192,14192,14192,14192,14192,14192,MONDO:0004034,eye lymphoma,MONDO,disease,DISEASE_14192
14193,14193,14193,14193,14193,14193,14193,14193,MONDO:0012885_MONDO:0011342_MONDO:0010478_MONDO:0013870_MONDO:0100068_MONDO:0100587,SRD5A3-congenital disorder of glycosylation,MONDO_grouped,disease,DISEASE_14193
14194,14194,14194,14194,14194,14194,14194,14194,MONDO:0016717_MONDO:0022735,choroid plexus neoplasm,MONDO_grouped,disease,DISEASE_14194
14195,14195,14195,14195,14195,14195,14195,14195,MONDO:0016373,isolated facial myokymia,MONDO,disease,DISEASE_14195
14196,14196,14196,14196,14196,14196,14196,14196,MONDO:0001719_MONDO:0001720,gonococcal bursitis,MONDO_grouped,disease,DISEASE_14196
14197,14197,14197,14197,14197,14197,14197,14197,MONDO:8000024,"autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD",MONDO,disease,DISEASE_14197
14198,14198,14198,14198,14198,14198,14198,14198,MONDO:0002241,factor XIII deficiency,MONDO,disease,DISEASE_14198
14199,14199,14199,14199,14199,14199,14199,14199,MONDO:1010143,"incontinentia pigmenti, non-human animal",MONDO,disease,DISEASE_14199
14200,14200,14200,14200,14200,14200,14200,14200,MONDO:0015842,bicornuate uterus,MONDO,disease,DISEASE_14200
14201,14201,14201,14201,14201,14201,14201,14201,MONDO:0002680,chronic wasting disease,MONDO,disease,DISEASE_14201
14202,14202,14202,14202,14202,14202,14202,14202,MONDO:0042963,wandering spleen,MONDO,disease,DISEASE_14202
14203,14203,14203,14203,14203,14203,14203,14203,MONDO:0015402,mandibular arteriovenous malformation,MONDO,disease,DISEASE_14203
14204,14204,14204,14204,14204,14204,14204,14204,MONDO:1011810_MONDO:1012152,"megakaryoblastic leukemia, non-human animal",MONDO_grouped,disease,DISEASE_14204
14205,14205,14205,14205,14205,14205,14205,14205,MONDO:0004666_MONDO:0005895,metagonimiasis,MONDO_grouped,disease,DISEASE_14205
14206,14206,14206,14206,14206,14206,14206,14206,MONDO:1010669,"myeloperoxidase deficiency, dog",MONDO,disease,DISEASE_14206
14207,14207,14207,14207,14207,14207,14207,14207,MONDO:0015381,commissural lip fistula,MONDO,disease,DISEASE_14207
14208,14208,14208,14208,14208,14208,14208,14208,MONDO:1040017,intestinal fistula,MONDO,disease,DISEASE_14208
14209,14209,14209,14209,14209,14209,14209,14209,MONDO:1011228,"entropion, pig",MONDO,disease,DISEASE_14209
14210,14210,14210,14210,14210,14210,14210,14210,MONDO:0001105,renal hypertension,MONDO,disease,DISEASE_14210
14211,14211,14211,14211,14211,14211,14211,14211,MONDO:0004774,gonococcal iridocyclitis,MONDO,disease,DISEASE_14211
14212,14212,14212,14212,14212,14212,14212,14212,MONDO:0017887,renal cell carcinoma associated with neuroblastoma,MONDO,disease,DISEASE_14212
14213,14213,14213,14213,14213,14213,14213,14213,MONDO:0001512,intermittent proptosis,MONDO,disease,DISEASE_14213
14214,14214,14214,14214,14214,14214,14214,14214,MONDO:0044634,retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome,MONDO,disease,DISEASE_14214
14215,14215,14215,14215,14215,14215,14215,14215,MONDO:1011054,"polycystic kidney disease, domestic cat",MONDO,disease,DISEASE_14215
14216,14216,14216,14216,14216,14216,14216,14216,MONDO:0011603,GNE myopathy,MONDO,disease,DISEASE_14216
14217,14217,14217,14217,14217,14217,14217,14217,MONDO:0005385,vascular disorder,MONDO,disease,DISEASE_14217
14218,14218,14218,14218,14218,14218,14218,14218,MONDO:0017067_MONDO:0017073_MONDO:0017074,cervicothoracic spina bifida aperta,MONDO_grouped,disease,DISEASE_14218
14219,14219,14219,14219,14219,14219,14219,14219,MONDO:0011282,tumor suppressor gene on chromosome 11,MONDO,disease,DISEASE_14219
14220,14220,14220,14220,14220,14220,14220,14220,MONDO:0019238,inborn disorder of pyrimidine metabolism,MONDO,disease,DISEASE_14220
14221,14221,14221,14221,14221,14221,14221,14221,MONDO:0004672_MONDO:0005759,fasciolopsiasis,MONDO_grouped,disease,DISEASE_14221
14222,14222,14222,14222,14222,14222,14222,14222,MONDO:0011550,"fibromatosis, gingival, with hypertrichosis and intellectual disability",MONDO,disease,DISEASE_14222
14223,14223,14223,14223,14223,14223,14223,14223,MONDO:0007207,Böök syndrome,MONDO,disease,DISEASE_14223
14224,14224,14224,14224,14224,14224,14224,14224,MONDO:0014814_MONDO:0014088_MONDO:0011442_MONDO:0015609,advanced sleep phase syndrome,MONDO_grouped,disease,DISEASE_14224
14225,14225,14225,14225,14225,14225,14225,14225,MONDO:0006098,atypical lobular breast hyperplasia,MONDO,disease,DISEASE_14225
14226,14226,14226,14226,14226,14226,14226,14226,MONDO:0007547,epidermoid cysts,MONDO,disease,DISEASE_14226
14227,14227,14227,14227,14227,14227,14227,14227,MONDO:0002904,echolalia,MONDO,disease,DISEASE_14227
14228,14228,14228,14228,14228,14228,14228,14228,MONDO:0956992,posterior fossa group A ependymoma,MONDO,disease,DISEASE_14228
14229,14229,14229,14229,14229,14229,14229,14229,MONDO:0006883,malignant superior sulcus neoplasm,MONDO,disease,DISEASE_14229
14230,14230,14230,14230,14230,14230,14230,14230,MONDO:0013784_MONDO:1012392,neonatal-onset encephalopathy with rigidity and seizures,MONDO_grouped,disease,DISEASE_14230
14231,14231,14231,14231,14231,14231,14231,14231,MONDO:0700213,"trypanosomiasis, non-human animal",MONDO,disease,DISEASE_14231
14232,14232,14232,14232,14232,14232,14232,14232,MONDO:0011077,"microcephaly, corpus callosum dysgenesis, and cleft lip/palate",MONDO,disease,DISEASE_14232
14233,14233,14233,14233,14233,14233,14233,14233,MONDO:1010011,"dilated cardiomyopathy, non-human animal",MONDO,disease,DISEASE_14233
14234,14234,14234,14234,14234,14234,14234,14234,MONDO:0030537,"central hypoventilation syndrome, congenital, 2, and autonomic dysfunction",MONDO,disease,DISEASE_14234
14235,14235,14235,14235,14235,14235,14235,14235,MONDO:0007306,"Klippel-Feil syndrome 1, autosomal dominant",MONDO,disease,DISEASE_14235
14236,14236,14236,14236,14236,14236,14236,14236,MONDO:0014717,early-onset Lafora body disease,MONDO,disease,DISEASE_14236
14237,14237,14237,14237,14237,14237,14237,14237,MONDO:0006524,acrodermatitis chronica atrophicans,MONDO,disease,DISEASE_14237
14238,14238,14238,14238,14238,14238,14238,14238,MONDO:0005012,cutaneous melanoma,MONDO,disease,DISEASE_14238
14239,14239,14239,14239,14239,14239,14239,14239,MONDO:0009907,Prepapillary vascular loops,MONDO,disease,DISEASE_14239
14240,14240,14240,14240,14240,14240,14240,14240,MONDO:0800117,cutaneous botryomycosis,MONDO,disease,DISEASE_14240
14241,14241,14241,14241,14241,14241,14241,14241,MONDO:1011267_MONDO:1011268,"cone-rod dystrophy, IQCB1-related, black-footed cat",MONDO_grouped,disease,DISEASE_14241
14242,14242,14242,14242,14242,14242,14242,14242,MONDO:0006034,gastric adenosquamous carcinoma,MONDO,disease,DISEASE_14242
14243,14243,14243,14243,14243,14243,14243,14243,MONDO:0005919,placental insufficiency,MONDO,disease,DISEASE_14243
14244,14244,14244,14244,14244,14244,14244,14244,MONDO:1010710_MONDO:1010711,"trimethylaminuria (fishy taint), chicken",MONDO_grouped,disease,DISEASE_14244
14245,14245,14245,14245,14245,14245,14245,14245,MONDO:0020087,hereditary lipodystrophy,MONDO,disease,DISEASE_14245
14246,14246,14246,14246,14246,14246,14246,14246,MONDO:0957920,immunodeficiency 113 with autoimmunity and autoinflammation,MONDO,disease,DISEASE_14246
14247,14247,14247,14247,14247,14247,14247,14247,MONDO:0009252,essential fructosuria,MONDO,disease,DISEASE_14247
14248,14248,14248,14248,14248,14248,14248,14248,MONDO:0017589,follicular cholangitis and pancreatitis,MONDO,disease,DISEASE_14248
14249,14249,14249,14249,14249,14249,14249,14249,MONDO:0850339,posterior fossa ependymoma,MONDO,disease,DISEASE_14249
14250,14250,14250,14250,14250,14250,14250,14250,MONDO:1012490,"vertebral and spinal dysplasia, cattle",MONDO,disease,DISEASE_14250
14251,14251,14251,14251,14251,14251,14251,14251,MONDO:0005758,eunuchism,MONDO,disease,DISEASE_14251
14252,14252,14252,14252,14252,14252,14252,14252,MONDO:0044207_MONDO:0044208_MONDO:0009506,specific granule deficiency,MONDO_grouped,disease,DISEASE_14252
14253,14253,14253,14253,14253,14253,14253,14253,MONDO:0016080,congenital bronchobiliary fistula,MONDO,disease,DISEASE_14253
14254,14254,14254,14254,14254,14254,14254,14254,MONDO:0002515,hepatobiliary disorder,MONDO,disease,DISEASE_14254
14255,14255,14255,14255,14255,14255,14255,14255,MONDO:0001285,endometriosis of pelvic peritoneum,MONDO,disease,DISEASE_14255
14256,14256,14256,14256,14256,14256,14256,14256,MONDO:0006218,gallbladder biliary intraepithelial neoplasia,MONDO,disease,DISEASE_14256
14257,14257,14257,14257,14257,14257,14257,14257,MONDO:0020740_MONDO:0012806,ectodermal dysplasia and immunodeficiency,MONDO_grouped,disease,DISEASE_14257
14258,14258,14258,14258,14258,14258,14258,14258,MONDO:0016461,5q35 microduplication syndrome,MONDO,disease,DISEASE_14258
14259,14259,14259,14259,14259,14259,14259,14259,MONDO:0001161_MONDO:0002613,schizoid personality disorder,MONDO_grouped,disease,DISEASE_14259
14260,14260,14260,14260,14260,14260,14260,14260,MONDO:0003174,spinal cord astrocytoma,MONDO,disease,DISEASE_14260
14261,14261,14261,14261,14261,14261,14261,14261,MONDO:0016614,autosomal recessive ataxia due to PEX10 deficiency,MONDO,disease,DISEASE_14261
14262,14262,14262,14262,14262,14262,14262,14262,MONDO:0008499,short stature-wormian bones-dextrocardia syndrome,MONDO,disease,DISEASE_14262
14263,14263,14263,14263,14263,14263,14263,14263,MONDO:0014495,retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome,MONDO,disease,DISEASE_14263
14264,14264,14264,14264,14264,14264,14264,14264,MONDO:0024973,"pneumonia, atypical interstitial, of cattle",MONDO,disease,DISEASE_14264
14265,14265,14265,14265,14265,14265,14265,14265,MONDO:0022607,extraovarian Brenner tumor of the vagina,MONDO,disease,DISEASE_14265
14266,14266,14266,14266,14266,14266,14266,14266,MONDO:0004620,"Hodgkin's lymphoma, lymphocytic depletion",MONDO,disease,DISEASE_14266
14267,14267,14267,14267,14267,14267,14267,14267,MONDO:0000636,musculoskeletal system benign neoplasm,MONDO,disease,DISEASE_14267
14268,14268,14268,14268,14268,14268,14268,14268,MONDO:0020322,acute biphenotypic leukemia,MONDO,disease,DISEASE_14268
14269,14269,14269,14269,14269,14269,14269,14269,MONDO:0013600,insomnia,MONDO,disease,DISEASE_14269
14270,14270,14270,14270,14270,14270,14270,14270,MONDO:0008295,sporadic porphyria cutanea tarda,MONDO,disease,DISEASE_14270
14271,14271,14271,14271,14271,14271,14271,14271,MONDO:0002313,vernal conjunctivitis,MONDO,disease,DISEASE_14271
14272,14272,14272,14272,14272,14272,14272,14272,MONDO:0000587,"autoimmune disease of ear, nose and throat",MONDO,disease,DISEASE_14272
14273,14273,14273,14273,14273,14273,14273,14273,MONDO:0859139,blepharophimosis-impaired intellectual development syndrome,MONDO,disease,DISEASE_14273
14274,14274,14274,14274,14274,14274,14274,14274,MONDO:0001979,dumping syndrome,MONDO,disease,DISEASE_14274
14275,14275,14275,14275,14275,14275,14275,14275,MONDO:0004929,constant exophthalmos,MONDO,disease,DISEASE_14275
14276,14276,14276,14276,14276,14276,14276,14276,MONDO:0013720,complement component 4b deficiency,MONDO,disease,DISEASE_14276
14277,14277,14277,14277,14277,14277,14277,14277,MONDO:0002338,extratemporal epilepsy,MONDO,disease,DISEASE_14277
14278,14278,14278,14278,14278,14278,14278,14278,MONDO:0018856,lichen amyloidosis,MONDO,disease,DISEASE_14278
14279,14279,14279,14279,14279,14279,14279,14279,MONDO:0008151,gnathodiaphyseal dysplasia,MONDO,disease,DISEASE_14279
14280,14280,14280,14280,14280,14280,14280,14280,MONDO:0024553_MONDO:0013307_MONDO:0000863_MONDO:0010782,"myopathy, lactic acidosis, and sideroblastic anemia",MONDO_grouped,disease,DISEASE_14280
14281,14281,14281,14281,14281,14281,14281,14281,MONDO:0001782,mature cataract,MONDO,disease,DISEASE_14281
14282,14282,14282,14282,14282,14282,14282,14282,MONDO:0009448,iminoglycinuria,MONDO,disease,DISEASE_14282
14283,14283,14283,14283,14283,14283,14283,14283,MONDO:0008618,"mesomelic dwarfism, Reinhardt-Pfeiffer type",MONDO,disease,DISEASE_14283
14284,14284,14284,14284,14284,14284,14284,14284,MONDO:0001657,brain cancer,MONDO,disease,DISEASE_14284
14285,14285,14285,14285,14285,14285,14285,14285,MONDO:0850046,amniotic fluid embolism,MONDO,disease,DISEASE_14285
14286,14286,14286,14286,14286,14286,14286,14286,MONDO:0001868,primary angle-closure glaucoma,MONDO,disease,DISEASE_14286
14287,14287,14287,14287,14287,14287,14287,14287,MONDO:0023137,feigenbaum Bergeron syndrome,MONDO,disease,DISEASE_14287
14288,14288,14288,14288,14288,14288,14288,14288,MONDO:0017366_MONDO:0035540,hereditary pheochromocytoma-paraganglioma,MONDO_grouped,disease,DISEASE_14288
14289,14289,14289,14289,14289,14289,14289,14289,MONDO:1011685,"bleeding disorder, non-human animal",MONDO,disease,DISEASE_14289
14290,14290,14290,14290,14290,14290,14290,14290,MONDO:0030045,Liberfarb syndrome,MONDO,disease,DISEASE_14290
14291,14291,14291,14291,14291,14291,14291,14291,MONDO:0044204_MONDO:0044205_MONDO:0009833,Shwachman-Diamond syndrome,MONDO_grouped,disease,DISEASE_14291
14292,14292,14292,14292,14292,14292,14292,14292,MONDO:0012128_MONDO:0019443,"transposition of the great arteries, dextro-looped",MONDO_grouped,disease,DISEASE_14292
14293,14293,14293,14293,14293,14293,14293,14293,MONDO:0007625,focal epithelial hyperplasia of the oral mucosa,MONDO,disease,DISEASE_14293
14294,14294,14294,14294,14294,14294,14294,14294,MONDO:0015428,choroidal atrophy-alopecia syndrome,MONDO,disease,DISEASE_14294
14295,14295,14295,14295,14295,14295,14295,14295,MONDO:0859262,ACCES syndrome,MONDO,disease,DISEASE_14295
14296,14296,14296,14296,14296,14296,14296,14296,MONDO:0100538,dysplasminogenemia,MONDO,disease,DISEASE_14296
14297,14297,14297,14297,14297,14297,14297,14297,MONDO:0022602,brachydactyly small stature face anomalies,MONDO,disease,DISEASE_14297
14298,14298,14298,14298,14298,14298,14298,14298,MONDO:0007420,autosomal dominant deafness - onychodystrophy syndrome,MONDO,disease,DISEASE_14298
14299,14299,14299,14299,14299,14299,14299,14299,MONDO:0018463_MONDO:0010395_MONDO:0018464,mild phosphoribosylpyrophosphate synthetase superactivity,MONDO_grouped,disease,DISEASE_14299
14300,14300,14300,14300,14300,14300,14300,14300,MONDO:0002269,gastroenteritis,MONDO,disease,DISEASE_14300
14301,14301,14301,14301,14301,14301,14301,14301,MONDO:0005568,cholesterol embolism,MONDO,disease,DISEASE_14301
14302,14302,14302,14302,14302,14302,14302,14302,MONDO:0003685,retroperitoneal germ cell neoplasm,MONDO,disease,DISEASE_14302
14303,14303,14303,14303,14303,14303,14303,14303,MONDO:0010883,pectus excavatum-macrocephaly-dysplastic nails syndrome,MONDO,disease,DISEASE_14303
14304,14304,14304,14304,14304,14304,14304,14304,MONDO:0011039,"atrophia maculosa varioliformis cutis, familial",MONDO,disease,DISEASE_14304
14305,14305,14305,14305,14305,14305,14305,14305,MONDO:1011105_MONDO:1011106,"polycystic kidney disease, PKD2-related, domestic cat",MONDO_grouped,disease,DISEASE_14305
14306,14306,14306,14306,14306,14306,14306,14306,MONDO:0000257,acute diarrhea,MONDO,disease,DISEASE_14306
14307,14307,14307,14307,14307,14307,14307,14307,MONDO:0004827,esophagus squamous cell papilloma,MONDO,disease,DISEASE_14307
14308,14308,14308,14308,14308,14308,14308,14308,MONDO:0100549,focal nodular hyperplasia,MONDO,disease,DISEASE_14308
14309,14309,14309,14309,14309,14309,14309,14309,MONDO:0012105_MONDO:0015943,granulomatosis with polyangiitis,MONDO_grouped,disease,DISEASE_14309
14310,14310,14310,14310,14310,14310,14310,14310,MONDO:0018708,squamous cell carcinoma of the oral tongue,MONDO,disease,DISEASE_14310
14311,14311,14311,14311,14311,14311,14311,14311,MONDO:0020542,malignant Sertoli-Leydig cell tumor of ovary,MONDO,disease,DISEASE_14311
14312,14312,14312,14312,14312,14312,14312,14312,MONDO:0011083,trichodental syndrome,MONDO,disease,DISEASE_14312
14313,14313,14313,14313,14313,14313,14313,14313,MONDO:0010014,"craniometadiaphyseal dysplasia, wormian bone type",MONDO,disease,DISEASE_14313
14314,14314,14314,14314,14314,14314,14314,14314,MONDO:0016105_MONDO:0015923,acquired skeletal muscle disease,MONDO_grouped,disease,DISEASE_14314
14315,14315,14315,14315,14315,14315,14315,14315,MONDO:0015301,primary cutaneous amyloidosis,MONDO,disease,DISEASE_14315
14316,14316,14316,14316,14316,14316,14316,14316,MONDO:0004010,infiltrating renal pelvis/ureter urothelial carcinoma,MONDO,disease,DISEASE_14316
14317,14317,14317,14317,14317,14317,14317,14317,MONDO:0006049,papillary lung adenocarcinoma,MONDO,disease,DISEASE_14317
14318,14318,14318,14318,14318,14318,14318,14318,MONDO:0004853,gonococcal endophthalmia,MONDO,disease,DISEASE_14318
14319,14319,14319,14319,14319,14319,14319,14319,MONDO:0020749_MONDO:0020750_MONDO:0009092,polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy,MONDO_grouped,disease,DISEASE_14319
14320,14320,14320,14320,14320,14320,14320,14320,MONDO:0032793,O'Donnell-Luria-Rodan syndrome,MONDO,disease,DISEASE_14320
14321,14321,14321,14321,14321,14321,14321,14321,MONDO:0859166,"visceral leiomyopathy, African degenerative",MONDO,disease,DISEASE_14321
14322,14322,14322,14322,14322,14322,14322,14322,MONDO:0001952,parietal lobe cancer,MONDO,disease,DISEASE_14322
14323,14323,14323,14323,14323,14323,14323,14323,MONDO:0007369_MONDO:0019142,hereditary coproporphyria,MONDO_grouped,disease,DISEASE_14323
14324,14324,14324,14324,14324,14324,14324,14324,MONDO:0022937,deafness conductive stapedial ear malformation facial palsy,MONDO,disease,DISEASE_14324
14325,14325,14325,14325,14325,14325,14325,14325,MONDO:0013711,peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome,MONDO,disease,DISEASE_14325
14326,14326,14326,14326,14326,14326,14326,14326,MONDO:0010018,second metatarsal-metacarpal syndrome,MONDO,disease,DISEASE_14326
14327,14327,14327,14327,14327,14327,14327,14327,MONDO:0017280,demodicidosis,MONDO,disease,DISEASE_14327
14328,14328,14328,14328,14328,14328,14328,14328,MONDO:0010466_MONDO:0013563_MONDO:0014165_MONDO:0100247,multiple congenital anomalies-hypotonia-seizures syndrome,MONDO_grouped,disease,DISEASE_14328
14329,14329,14329,14329,14329,14329,14329,14329,MONDO:0022693,cerebral calcification cerebellar hypoplasia,MONDO,disease,DISEASE_14329
14330,14330,14330,14330,14330,14330,14330,14330,MONDO:1011632,"tetanic torticollar spasms, non-human animal",MONDO,disease,DISEASE_14330
14331,14331,14331,14331,14331,14331,14331,14331,MONDO:0054573,Lopes-Maciel-Rodan syndrome,MONDO,disease,DISEASE_14331
14332,14332,14332,14332,14332,14332,14332,14332,MONDO:0030897,Lessel-Kreienkamp syndrome,MONDO,disease,DISEASE_14332
14333,14333,14333,14333,14333,14333,14333,14333,MONDO:0020465,congenital eyelid retraction,MONDO,disease,DISEASE_14333
14334,14334,14334,14334,14334,14334,14334,14334,MONDO:0100040,FOXG1 disorder,MONDO,disease,DISEASE_14334
14335,14335,14335,14335,14335,14335,14335,14335,MONDO:1012005_MONDO:1012006_MONDO:1012007,"alloimmune hemolytic anemia of the newborn, dog",MONDO_grouped,disease,DISEASE_14335
14336,14336,14336,14336,14336,14336,14336,14336,MONDO:0023833,multifocal choroiditis,MONDO,disease,DISEASE_14336
14337,14337,14337,14337,14337,14337,14337,14337,MONDO:0003784,nasal cavity carcinoma in situ,MONDO,disease,DISEASE_14337
14338,14338,14338,14338,14338,14338,14338,14338,MONDO:0002848,skeletal muscle neoplasm,MONDO,disease,DISEASE_14338
14339,14339,14339,14339,14339,14339,14339,14339,MONDO:0015462,thin ribs-tubular bones-dysmorphism syndrome,MONDO,disease,DISEASE_14339
14340,14340,14340,14340,14340,14340,14340,14340,MONDO:0005719,Coronavinae infectious disease,MONDO,disease,DISEASE_14340
14341,14341,14341,14341,14341,14341,14341,14341,MONDO:0001326,dental pulp necrosis,MONDO,disease,DISEASE_14341
14342,14342,14342,14342,14342,14342,14342,14342,MONDO:0007949,Marshall syndrome,MONDO,disease,DISEASE_14342
14343,14343,14343,14343,14343,14343,14343,14343,MONDO:0012948,chromosome 6pter-p24 deletion syndrome,MONDO,disease,DISEASE_14343
14344,14344,14344,14344,14344,14344,14344,14344,MONDO:1010682,"AA amyloidosis, zebra finch",MONDO,disease,DISEASE_14344
14345,14345,14345,14345,14345,14345,14345,14345,MONDO:0008009,monilethrix,MONDO,disease,DISEASE_14345
14346,14346,14346,14346,14346,14346,14346,14346,MONDO:0013082,Hirschsprung disease-ganglioneuroblastoma syndrome,MONDO,disease,DISEASE_14346
14347,14347,14347,14347,14347,14347,14347,14347,MONDO:0006092,appendix villous adenoma,MONDO,disease,DISEASE_14347
14348,14348,14348,14348,14348,14348,14348,14348,MONDO:0003514_MONDO:0021282,malignant teratoma,MONDO_grouped,disease,DISEASE_14348
14349,14349,14349,14349,14349,14349,14349,14349,MONDO:0044797_MONDO:0044800,desmoplastic nevus,MONDO_grouped,disease,DISEASE_14349
14350,14350,14350,14350,14350,14350,14350,14350,MONDO:1010098_MONDO:0100557,TFAP2B-related congenital heart disease spectrum disorder,MONDO_grouped,disease,DISEASE_14350
14351,14351,14351,14351,14351,14351,14351,14351,MONDO:0005297_MONDO:0021960,urethritis,MONDO_grouped,disease,DISEASE_14351
14352,14352,14352,14352,14352,14352,14352,14352,MONDO:0013209_MONDO:0007027_MONDO:0957896,metabolic dysfunction-associated steatotic liver disease,MONDO_grouped,disease,DISEASE_14352
14353,14353,14353,14353,14353,14353,14353,14353,MONDO:0014906_MONDO:0011898,"Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;",MONDO_grouped,disease,DISEASE_14353
14354,14354,14354,14354,14354,14354,14354,14354,MONDO:1012979_MONDO:1011776,"inborn errors of metabolism, non-human animal",MONDO_grouped,disease,DISEASE_14354
14355,14355,14355,14355,14355,14355,14355,14355,MONDO:0008041,"myoclonic epilepsy, Hartung type",MONDO,disease,DISEASE_14355
14356,14356,14356,14356,14356,14356,14356,14356,MONDO:0043458,radiation injury,MONDO,disease,DISEASE_14356
14357,14357,14357,14357,14357,14357,14357,14357,MONDO:0000676,phonagnosia,MONDO,disease,DISEASE_14357
14358,14358,14358,14358,14358,14358,14358,14358,MONDO:1010734,"systemic lupus erythematosus, domestic cat",MONDO,disease,DISEASE_14358
14359,14359,14359,14359,14359,14359,14359,14359,MONDO:0003900,connective tissue disorder,MONDO,disease,DISEASE_14359
14360,14360,14360,14360,14360,14360,14360,14360,MONDO:0012073,ribose-5-P isomerase deficiency,MONDO,disease,DISEASE_14360
14361,14361,14361,14361,14361,14361,14361,14361,MONDO:0018897,primary cutaneous CD30+ T-cell lymphoproliferative disease,MONDO,disease,DISEASE_14361
14362,14362,14362,14362,14362,14362,14362,14362,MONDO:0013538,obsolete alpha-2-macroglobulin deficiency,MONDO,disease,DISEASE_14362
14363,14363,14363,14363,14363,14363,14363,14363,MONDO:0020490,mosaic trisomy 9,MONDO,disease,DISEASE_14363
14364,14364,14364,14364,14364,14364,14364,14364,MONDO:0017556_MONDO:0017557,"Madelung deformity, unilateral",MONDO_grouped,disease,DISEASE_14364
14365,14365,14365,14365,14365,14365,14365,14365,MONDO:0013408,FADD-related immunodeficiency,MONDO,disease,DISEASE_14365
14366,14366,14366,14366,14366,14366,14366,14366,MONDO:0021118,intestinal neoplasm,MONDO,disease,DISEASE_14366
14367,14367,14367,14367,14367,14367,14367,14367,MONDO:0004404,refractory precursor T-lymphoblastic lymphoma/leukemia,MONDO,disease,DISEASE_14367
14368,14368,14368,14368,14368,14368,14368,14368,MONDO:0030706_MONDO:0030708,Trichomonas cystitis,MONDO_grouped,disease,DISEASE_14368
14369,14369,14369,14369,14369,14369,14369,14369,MONDO:0016056,isolated congenital microcephaly,MONDO,disease,DISEASE_14369
14370,14370,14370,14370,14370,14370,14370,14370,MONDO:1011915,"diffuse cystic renal dysplasia and hepatic fibrosis, non-human animal",MONDO,disease,DISEASE_14370
14371,14371,14371,14371,14371,14371,14371,14371,MONDO:0008504,supravalvular aortic stenosis,MONDO,disease,DISEASE_14371
14372,14372,14372,14372,14372,14372,14372,14372,MONDO:0022011,bobble-head doll syndrome,MONDO,disease,DISEASE_14372
14373,14373,14373,14373,14373,14373,14373,14373,MONDO:0008489,"sternum, premature obliteration of sutures of",MONDO,disease,DISEASE_14373
14374,14374,14374,14374,14374,14374,14374,14374,MONDO:0006282_MONDO:1010964,lymphangiosarcoma,MONDO_grouped,disease,DISEASE_14374
14375,14375,14375,14375,14375,14375,14375,14375,MONDO:0004356,childhood multilocular cystic kidney neoplasm,MONDO,disease,DISEASE_14375
14376,14376,14376,14376,14376,14376,14376,14376,MONDO:0016682,giant cell glioblastoma,MONDO,disease,DISEASE_14376
14377,14377,14377,14377,14377,14377,14377,14377,MONDO:1011873_MONDO:1011893,"neuronal vacuolar disorder, non-human animal",MONDO_grouped,disease,DISEASE_14377
14378,14378,14378,14378,14378,14378,14378,14378,MONDO:0011064,"lethal chondrodysplasia, Seller type",MONDO,disease,DISEASE_14378
14379,14379,14379,14379,14379,14379,14379,14379,MONDO:0004064,iris melanoma,MONDO,disease,DISEASE_14379
14380,14380,14380,14380,14380,14380,14380,14380,MONDO:0006747,enterotoxemia,MONDO,disease,DISEASE_14380
14381,14381,14381,14381,14381,14381,14381,14381,MONDO:0023369,disorder of facial skeleton,MONDO,disease,DISEASE_14381
14382,14382,14382,14382,14382,14382,14382,14382,MONDO:0035408,furuncular myiasis due to Cordylobia rodhaini,MONDO,disease,DISEASE_14382
14383,14383,14383,14383,14383,14383,14383,14383,MONDO:0005715,congenital toxoplasmosis,MONDO,disease,DISEASE_14383
14384,14384,14384,14384,14384,14384,14384,14384,MONDO:0000859_MONDO:0017069_MONDO:0017062,spina bifida occulta,MONDO_grouped,disease,DISEASE_14384
14385,14385,14385,14385,14385,14385,14385,14385,MONDO:0009527,"lipase deficiency, combined",MONDO,disease,DISEASE_14385
14386,14386,14386,14386,14386,14386,14386,14386,MONDO:0003827_MONDO:0015698,transient hypogammaglobulinemia,MONDO_grouped,disease,DISEASE_14386
14387,14387,14387,14387,14387,14387,14387,14387,MONDO:0020803,obsolete bundle branch block,MONDO,disease,DISEASE_14387
14388,14388,14388,14388,14388,14388,14388,14388,MONDO:0060578,"neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures",MONDO,disease,DISEASE_14388
14389,14389,14389,14389,14389,14389,14389,14389,MONDO:0006085,angiolipoma,MONDO,disease,DISEASE_14389
14390,14390,14390,14390,14390,14390,14390,14390,MONDO:0005747_MONDO:0005986_MONDO:0100074,enterovirus infectious disease,MONDO_grouped,disease,DISEASE_14390
14391,14391,14391,14391,14391,14391,14391,14391,MONDO:0009144,Ebstein anomaly,MONDO,disease,DISEASE_14391
14392,14392,14392,14392,14392,14392,14392,14392,MONDO:0022694,cerebral calcifications opalescent teeth phosphaturia,MONDO,disease,DISEASE_14392
14393,14393,14393,14393,14393,14393,14393,14393,MONDO:0004584,maple bark strippers' lung,MONDO,disease,DISEASE_14393
14394,14394,14394,14394,14394,14394,14394,14394,MONDO:0004069_MONDO:0004689,inborn mitochondrial metabolism disorder,MONDO_grouped,disease,DISEASE_14394
14395,14395,14395,14395,14395,14395,14395,14395,MONDO:0004769,orbital pseudotumor,MONDO,disease,DISEASE_14395
14396,14396,14396,14396,14396,14396,14396,14396,MONDO:0014563,mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency,MONDO,disease,DISEASE_14396
14397,14397,14397,14397,14397,14397,14397,14397,MONDO:0035941,B-lymphoblastic leukemia/lymphoma with t(v;11q23.3),MONDO,disease,DISEASE_14397
14398,14398,14398,14398,14398,14398,14398,14398,MONDO:0035930,neu-laxova syndrome due to 3-phosphoserine phosphatase deficiency,MONDO,disease,DISEASE_14398
14399,14399,14399,14399,14399,14399,14399,14399,MONDO:0005351_MONDO:0005452_MONDO:0033926,anorexia nervosa,MONDO_grouped,disease,DISEASE_14399
14400,14400,14400,14400,14400,14400,14400,14400,MONDO:0700098,"neoplasm, non-human animal",MONDO,disease,DISEASE_14400
14401,14401,14401,14401,14401,14401,14401,14401,MONDO:0700204,"trichostrongyloidiasis, non-human animal",MONDO,disease,DISEASE_14401
14402,14402,14402,14402,14402,14402,14402,14402,MONDO:0014602,Hogue-Janssens syndrome 1,MONDO,disease,DISEASE_14402
14403,14403,14403,14403,14403,14403,14403,14403,MONDO:1010270,"alkaptonuria, non-human animal",MONDO,disease,DISEASE_14403
14404,14404,14404,14404,14404,14404,14404,14404,MONDO:0017205,primary oculocerebral lymphoma,MONDO,disease,DISEASE_14404
14405,14405,14405,14405,14405,14405,14405,14405,MONDO:0021339,carcinoma of hard palate,MONDO,disease,DISEASE_14405
14406,14406,14406,14406,14406,14406,14406,14406,MONDO:0001705,pure red-cell aplasia,MONDO,disease,DISEASE_14406
14407,14407,14407,14407,14407,14407,14407,14407,MONDO:0008040,transient myeloproliferative syndrome,MONDO,disease,DISEASE_14407
14408,14408,14408,14408,14408,14408,14408,14408,MONDO:0008399_MONDO:0012888_MONDO:0012889,"sarcoidosis, susceptibility to",MONDO_grouped,disease,DISEASE_14408
14409,14409,14409,14409,14409,14409,14409,14409,MONDO:0017699,"glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form",MONDO,disease,DISEASE_14409
14410,14410,14410,14410,14410,14410,14410,14410,MONDO:0034189,primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome,MONDO,disease,DISEASE_14410
14411,14411,14411,14411,14411,14411,14411,14411,MONDO:0040925,latent yaws,MONDO,disease,DISEASE_14411
14412,14412,14412,14412,14412,14412,14412,14412,MONDO:0030696,mitochondrial DNA depletion syndrome 20 (mngie type),MONDO,disease,DISEASE_14412
14413,14413,14413,14413,14413,14413,14413,14413,MONDO:0013818_MONDO:0024541_MONDO:0009105,trichohepatoenteric syndrome,MONDO_grouped,disease,DISEASE_14413
14414,14414,14414,14414,14414,14414,14414,14414,MONDO:0021690,obsolete congenital left ventricular aneurysm,MONDO,disease,DISEASE_14414
14415,14415,14415,14415,14415,14415,14415,14415,MONDO:0014541,motor developmental delay due to 14q32.2 paternally expressed gene defect,MONDO,disease,DISEASE_14415
14416,14416,14416,14416,14416,14416,14416,14416,MONDO:0012382_MONDO:0859362_MONDO:0011153_MONDO:0009734,"hyperinsulinemic hypoglycemia, familial",MONDO_grouped,disease,DISEASE_14416
14417,14417,14417,14417,14417,14417,14417,14417,MONDO:0021254,corpus uteri neoplasm,MONDO,disease,DISEASE_14417
14418,14418,14418,14418,14418,14418,14418,14418,MONDO:0024363,rapid eye movement sleep disorder,MONDO,disease,DISEASE_14418
14419,14419,14419,14419,14419,14419,14419,14419,MONDO:0017044,adult familial nephronophthisis-spastic quadriparesia syndrome,MONDO,disease,DISEASE_14419
14420,14420,14420,14420,14420,14420,14420,14420,MONDO:0019141,porokeratosis of Mibelli,MONDO,disease,DISEASE_14420
14421,14421,14421,14421,14421,14421,14421,14421,MONDO:0700113,"Anaplasmataceae infectious disease, non-human animal",MONDO,disease,DISEASE_14421
14422,14422,14422,14422,14422,14422,14422,14422,MONDO:0001904,polyneuropathy due to drug,MONDO,disease,DISEASE_14422
14423,14423,14423,14423,14423,14423,14423,14423,MONDO:0006668_MONDO:0043541_MONDO:0001690,bacterial conjunctivitis,MONDO_grouped,disease,DISEASE_14423
14424,14424,14424,14424,14424,14424,14424,14424,MONDO:1011451,"idiopathic pulmonary fibrosis, non-human animal",MONDO,disease,DISEASE_14424
14425,14425,14425,14425,14425,14425,14425,14425,MONDO:0008487,polycystic ovary syndrome,MONDO,disease,DISEASE_14425
14426,14426,14426,14426,14426,14426,14426,14426,MONDO:0020432_MONDO:0020433,ectasia of the right atrial appendage,MONDO_grouped,disease,DISEASE_14426
14427,14427,14427,14427,14427,14427,14427,14427,MONDO:0002650,scrotal carcinoma,MONDO,disease,DISEASE_14427
14428,14428,14428,14428,14428,14428,14428,14428,MONDO:0014764,spastic paraplegia-severe developmental delay-epilepsy syndrome,MONDO,disease,DISEASE_14428
14429,14429,14429,14429,14429,14429,14429,14429,MONDO:1012065,"autosomal dwarfism, chicken",MONDO,disease,DISEASE_14429
14430,14430,14430,14430,14430,14430,14430,14430,MONDO:0016377,Pitt-Hopkins-like syndrome,MONDO,disease,DISEASE_14430
14431,14431,14431,14431,14431,14431,14431,14431,MONDO:0015871,benign breast phyllodes tumor,MONDO,disease,DISEASE_14431
14432,14432,14432,14432,14432,14432,14432,14432,MONDO:0002612_MONDO:0005115,frontal lobe epilepsy,MONDO_grouped,disease,DISEASE_14432
14433,14433,14433,14433,14433,14433,14433,14433,MONDO:0005426,MRI defined brain infarct,MONDO,disease,DISEASE_14433
14434,14434,14434,14434,14434,14434,14434,14434,MONDO:0016445,familial anetoderma,MONDO,disease,DISEASE_14434
14435,14435,14435,14435,14435,14435,14435,14435,MONDO:0017345,Epstein-Barr virus-associated mesenchymal tumor,MONDO,disease,DISEASE_14435
14436,14436,14436,14436,14436,14436,14436,14436,MONDO:0041161,obsolete endometrial hyperplasia,MONDO,disease,DISEASE_14436
14437,14437,14437,14437,14437,14437,14437,14437,MONDO:0019146,inherited susceptibility to mycobacterial diseases,MONDO,disease,DISEASE_14437
14438,14438,14438,14438,14438,14438,14438,14438,MONDO:1010425,"Phelan-McDermid syndrome, crab-eating macaque",MONDO,disease,DISEASE_14438
14439,14439,14439,14439,14439,14439,14439,14439,MONDO:0004512_MONDO:0016746,meningeal melanomatosis,MONDO_grouped,disease,DISEASE_14439
14440,14440,14440,14440,14440,14440,14440,14440,MONDO:0021535,pancreatic neuroendocrine tumor G1,MONDO,disease,DISEASE_14440
14441,14441,14441,14441,14441,14441,14441,14441,MONDO:0015191,myopathic intestinal pseudoobstruction,MONDO,disease,DISEASE_14441
14442,14442,14442,14442,14442,14442,14442,14442,MONDO:0011842,GRN-related frontotemporal lobar degeneration with Tdp43 inclusions,MONDO,disease,DISEASE_14442
14443,14443,14443,14443,14443,14443,14443,14443,MONDO:0000554,endocervical adenocarcinoma,MONDO,disease,DISEASE_14443
14444,14444,14444,14444,14444,14444,14444,14444,MONDO:0023868,melanoma associated retinopathy,MONDO,disease,DISEASE_14444
14445,14445,14445,14445,14445,14445,14445,14445,MONDO:0017151,obsolete pulmonary arterial hypertension associated with connective tissue disease,MONDO,disease,DISEASE_14445
14446,14446,14446,14446,14446,14446,14446,14446,MONDO:1010543,"cystic fibrosis, domestic ferret",MONDO,disease,DISEASE_14446
14447,14447,14447,14447,14447,14447,14447,14447,MONDO:0009222,Gollop-Wolfgang complex,MONDO,disease,DISEASE_14447
14448,14448,14448,14448,14448,14448,14448,14448,MONDO:0010842,multiple cutaneous and mucosal venous malformations,MONDO,disease,DISEASE_14448
14449,14449,14449,14449,14449,14449,14449,14449,MONDO:1011572,"neuronal ceroid lipofuscinosis, domestic ferret",MONDO,disease,DISEASE_14449
14450,14450,14450,14450,14450,14450,14450,14450,MONDO:0025089,infectious bovine rhinotracheitis,MONDO,disease,DISEASE_14450
14451,14451,14451,14451,14451,14451,14451,14451,MONDO:0023059,Elliott ludman Teebi syndrome,MONDO,disease,DISEASE_14451
14452,14452,14452,14452,14452,14452,14452,14452,MONDO:0016730,gangliocytoma,MONDO,disease,DISEASE_14452
14453,14453,14453,14453,14453,14453,14453,14453,MONDO:0016907,partial deletion of the long arm of chromosome 8,MONDO,disease,DISEASE_14453
14454,14454,14454,14454,14454,14454,14454,14454,MONDO:1011913,"renal cysts, non-human animal",MONDO,disease,DISEASE_14454
14455,14455,14455,14455,14455,14455,14455,14455,MONDO:0002855,ectomesenchymoma,MONDO,disease,DISEASE_14455
14456,14456,14456,14456,14456,14456,14456,14456,MONDO:0859322_MONDO:0975830,"myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis",MONDO_grouped,disease,DISEASE_14456
14457,14457,14457,14457,14457,14457,14457,14457,MONDO:0004058,pancreatic cholera,MONDO,disease,DISEASE_14457
14458,14458,14458,14458,14458,14458,14458,14458,MONDO:0016563,progressive supranuclear palsy-corticobasal syndrome,MONDO,disease,DISEASE_14458
14459,14459,14459,14459,14459,14459,14459,14459,MONDO:0007599,"factor 9 and Factor XI, combined deficiency of",MONDO,disease,DISEASE_14459
14460,14460,14460,14460,14460,14460,14460,14460,MONDO:0010518,Wiskott-Aldrich syndrome,MONDO,disease,DISEASE_14460
14461,14461,14461,14461,14461,14461,14461,14461,MONDO:0014744,acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome,MONDO,disease,DISEASE_14461
14462,14462,14462,14462,14462,14462,14462,14462,MONDO:1011457,"glaucoma, non-human animal",MONDO,disease,DISEASE_14462
14463,14463,14463,14463,14463,14463,14463,14463,MONDO:0010191_MONDO:0013304_MONDO:0008668_MONDO:1011612_MONDO:1011615_MONDO:1011614_MONDO:0015629_MONDO:0015628_MONDO:0015630_MONDO:0015631_MONDO:1011611_MONDO:1011616_MONDO:1012640_MONDO:1012641,von Willebrand disease,MONDO_grouped,disease,DISEASE_14463
14464,14464,14464,14464,14464,14464,14464,14464,MONDO:0035452,mueller-weiss syndrome,MONDO,disease,DISEASE_14464
14465,14465,14465,14465,14465,14465,14465,14465,MONDO:0035459,idiopathic multidrug-resistant nephrotic syndrome,MONDO,disease,DISEASE_14465
14466,14466,14466,14466,14466,14466,14466,14466,MONDO:0004242,active peptic ulcer disease,MONDO,disease,DISEASE_14466
14467,14467,14467,14467,14467,14467,14467,14467,MONDO:0002201,vulvar trichoepithelioma,MONDO,disease,DISEASE_14467
14468,14468,14468,14468,14468,14468,14468,14468,MONDO:1012614,"membranoproliferative glomerulonephritis, CFH-related, pig",MONDO,disease,DISEASE_14468
14469,14469,14469,14469,14469,14469,14469,14469,MONDO:0018198,acute encephalopathy with biphasic seizures and late reduced diffusion,MONDO,disease,DISEASE_14469
14470,14470,14470,14470,14470,14470,14470,14470,MONDO:1011487,"complement component 3 deficiency, dog",MONDO,disease,DISEASE_14470
14471,14471,14471,14471,14471,14471,14471,14471,MONDO:0800064,osteogenesis imperfecta and a reduction of bone mineral density.,MONDO,disease,DISEASE_14471
14472,14472,14472,14472,14472,14472,14472,14472,MONDO:0004787,cervical mullerian papilloma,MONDO,disease,DISEASE_14472
14473,14473,14473,14473,14473,14473,14473,14473,MONDO:0018933,Mazabraud syndrome,MONDO,disease,DISEASE_14473
14474,14474,14474,14474,14474,14474,14474,14474,MONDO:0006307,mixed somatotroph-lactotroph pituitary gland adenoma,MONDO,disease,DISEASE_14474
14475,14475,14475,14475,14475,14475,14475,14475,MONDO:0006945,renal artery obstruction,MONDO,disease,DISEASE_14475
14476,14476,14476,14476,14476,14476,14476,14476,MONDO:0010665,Wilson-Turner syndrome,MONDO,disease,DISEASE_14476
14477,14477,14477,14477,14477,14477,14477,14477,MONDO:1010015,"hypertrophic cardiomyopathy, non-human animal",MONDO,disease,DISEASE_14477
14478,14478,14478,14478,14478,14478,14478,14478,MONDO:0019367,regional odontodysplasia,MONDO,disease,DISEASE_14478
14479,14479,14479,14479,14479,14479,14479,14479,MONDO:0019398,desmin-related myopathy with Mallory body-like inclusions,MONDO,disease,DISEASE_14479
14480,14480,14480,14480,14480,14480,14480,14480,MONDO:0005880,oesophagostomiasis,MONDO,disease,DISEASE_14480
14481,14481,14481,14481,14481,14481,14481,14481,MONDO:0025622,"Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1",MONDO,disease,DISEASE_14481
14482,14482,14482,14482,14482,14482,14482,14482,MONDO:0009101_MONDO:0011502_MONDO:0018105,Wolfram syndrome,MONDO_grouped,disease,DISEASE_14482
14483,14483,14483,14483,14483,14483,14483,14483,MONDO:1011712,"alloxan-diabetes, non-human animal",MONDO,disease,DISEASE_14483
14484,14484,14484,14484,14484,14484,14484,14484,MONDO:0011239,colobomatous macrophthalmia-microcornea syndrome,MONDO,disease,DISEASE_14484
14485,14485,14485,14485,14485,14485,14485,14485,MONDO:0957786,xerosis and growth failure with immune and pulmonary dysfunction syndrome,MONDO,disease,DISEASE_14485
14486,14486,14486,14486,14486,14486,14486,14486,MONDO:0003121_MONDO:0002919_MONDO:0002997,middle cranial fossa meningioma,MONDO_grouped,disease,DISEASE_14486
14487,14487,14487,14487,14487,14487,14487,14487,MONDO:0030028,"neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline",MONDO,disease,DISEASE_14487
14488,14488,14488,14488,14488,14488,14488,14488,MONDO:0021172,"Timothy syndrome, atypical type",MONDO,disease,DISEASE_14488
14489,14489,14489,14489,14489,14489,14489,14489,MONDO:0033853,congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome,MONDO,disease,DISEASE_14489
14490,14490,14490,14490,14490,14490,14490,14490,MONDO:0021058,neoplastic syndrome,MONDO,disease,DISEASE_14490
14491,14491,14491,14491,14491,14491,14491,14491,MONDO:0700169,canine cutaneous t-cell lymphoma,MONDO,disease,DISEASE_14491
14492,14492,14492,14492,14492,14492,14492,14492,MONDO:0011904_MONDO:0011593_MONDO:0014903_MONDO:0012965,"seizures, benign familial infantile",MONDO_grouped,disease,DISEASE_14492
14493,14493,14493,14493,14493,14493,14493,14493,MONDO:0010836_MONDO:0014426_MONDO:0012299_MONDO:0012754,nanophthalmos,MONDO_grouped,disease,DISEASE_14493
14494,14494,14494,14494,14494,14494,14494,14494,MONDO:1011655,"polled and multisystemic syndrome, non-human animal",MONDO,disease,DISEASE_14494
14495,14495,14495,14495,14495,14495,14495,14495,MONDO:0044878,adult germ cell tumor,MONDO,disease,DISEASE_14495
14496,14496,14496,14496,14496,14496,14496,14496,MONDO:0020560,atypical teratoid rhabdoid tumor,MONDO,disease,DISEASE_14496
14497,14497,14497,14497,14497,14497,14497,14497,MONDO:0013673,Wolfram-like syndrome,MONDO,disease,DISEASE_14497
14498,14498,14498,14498,14498,14498,14498,14498,MONDO:0009178_MONDO:0006543,epidermolysis bullosa dystrophica Neurotrophica,MONDO_grouped,disease,DISEASE_14498
14499,14499,14499,14499,14499,14499,14499,14499,MONDO:0044880,cystic tumor of the pancreas,MONDO,disease,DISEASE_14499
14500,14500,14500,14500,14500,14500,14500,14500,MONDO:0021096,papillary epithelial neoplasm,MONDO,disease,DISEASE_14500
14501,14501,14501,14501,14501,14501,14501,14501,MONDO:0006577,maxillary sinus cholesteatoma,MONDO,disease,DISEASE_14501
14502,14502,14502,14502,14502,14502,14502,14502,MONDO:0013472,fatal infantile hypertonic myofibrillar myopathy,MONDO,disease,DISEASE_14502
14503,14503,14503,14503,14503,14503,14503,14503,MONDO:0014516_MONDO:0009624_MONDO:0014592_MONDO:0000181,microcephaly and chorioretinopathy,MONDO_grouped,disease,DISEASE_14503
14504,14504,14504,14504,14504,14504,14504,14504,MONDO:0002602_MONDO:0003620_MONDO:0002714_MONDO:0024619_MONDO:0005071_MONDO:0044993,central nervous system disorder,MONDO_grouped,disease,DISEASE_14504
14505,14505,14505,14505,14505,14505,14505,14505,MONDO:0006537,conjunctival pigmentation,MONDO,disease,DISEASE_14505
14506,14506,14506,14506,14506,14506,14506,14506,MONDO:0009266_MONDO:0009267_MONDO:0009265_MONDO:0018150_MONDO:1011509_MONDO:1011507_MONDO:1011508,Gaucher disease,MONDO_grouped,disease,DISEASE_14506
14507,14507,14507,14507,14507,14507,14507,14507,MONDO:0044907,metastatic squamous cell carcinoma,MONDO,disease,DISEASE_14507
14508,14508,14508,14508,14508,14508,14508,14508,MONDO:0013063_MONDO:0011376_MONDO:0100234,"ventricular fibrillation, paroxysmal familial",MONDO_grouped,disease,DISEASE_14508
14509,14509,14509,14509,14509,14509,14509,14509,MONDO:0018957,pudendal neuralgia,MONDO,disease,DISEASE_14509
14510,14510,14510,14510,14510,14510,14510,14510,MONDO:0007893,Noonan syndrome with multiple lentigines,MONDO,disease,DISEASE_14510
14511,14511,14511,14511,14511,14511,14511,14511,MONDO:0011714,"partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome",MONDO,disease,DISEASE_14511
14512,14512,14512,14512,14512,14512,14512,14512,MONDO:0005275,lung disorder,MONDO,disease,DISEASE_14512
14513,14513,14513,14513,14513,14513,14513,14513,MONDO:0010865,pseudoaminopterin syndrome,MONDO,disease,DISEASE_14513
14514,14514,14514,14514,14514,14514,14514,14514,MONDO:0004255,Wolffian adnexal tumor,MONDO,disease,DISEASE_14514
14515,14515,14515,14515,14515,14515,14515,14515,MONDO:0002278,benign colon neoplasm,MONDO,disease,DISEASE_14515
14516,14516,14516,14516,14516,14516,14516,14516,MONDO:0007890,"lentiginosis, centrofacial neurodysraphic",MONDO,disease,DISEASE_14516
14517,14517,14517,14517,14517,14517,14517,14517,MONDO:0022559,benign angiitis of the central nervous system,MONDO,disease,DISEASE_14517
14518,14518,14518,14518,14518,14518,14518,14518,MONDO:0009075,Dandy-Walker malformation-postaxial polydactyly syndrome,MONDO,disease,DISEASE_14518
14519,14519,14519,14519,14519,14519,14519,14519,MONDO:0042913,Schrander-stumpel-Theunissen-Hulsmans syndrome,MONDO,disease,DISEASE_14519
14520,14520,14520,14520,14520,14520,14520,14520,MONDO:0009503,pyruvate dehydrogenase E3-binding protein deficiency,MONDO,disease,DISEASE_14520
14521,14521,14521,14521,14521,14521,14521,14521,MONDO:0008598,trichodysplasia-xeroderma syndrome,MONDO,disease,DISEASE_14521
14522,14522,14522,14522,14522,14522,14522,14522,MONDO:0016888,partial deletion of the short arm of chromosome 6,MONDO,disease,DISEASE_14522
14523,14523,14523,14523,14523,14523,14523,14523,MONDO:0016384,hypogonadotropic hypogonadism-frontoparietal alopecia syndrome,MONDO,disease,DISEASE_14523
14524,14524,14524,14524,14524,14524,14524,14524,MONDO:0100527,"dysplastic cortical hyperostosis, Kozlowski-Tsuruta type",MONDO,disease,DISEASE_14524
14525,14525,14525,14525,14525,14525,14525,14525,MONDO:0013422,type I complement component 8 deficiency,MONDO,disease,DISEASE_14525
14526,14526,14526,14526,14526,14526,14526,14526,MONDO:0100055_MONDO:0100060,intraosseous spindle cell rhabdomyosarcoma with TFCP2/NCOA2 rearrangements,MONDO_grouped,disease,DISEASE_14526
14527,14527,14527,14527,14527,14527,14527,14527,MONDO:1010052_MONDO:1011401_MONDO:1011402,"diabetes mellitus, non-human animal",MONDO_grouped,disease,DISEASE_14527
14528,14528,14528,14528,14528,14528,14528,14528,MONDO:0011950,infantile-onset autosomal recessive nonprogressive cerebellar ataxia,MONDO,disease,DISEASE_14528
14529,14529,14529,14529,14529,14529,14529,14529,MONDO:0004830,fasciitis,MONDO,disease,DISEASE_14529
14530,14530,14530,14530,14530,14530,14530,14530,MONDO:0001092,colon leiomyoma,MONDO,disease,DISEASE_14530
14531,14531,14531,14531,14531,14531,14531,14531,MONDO:0006042,meningeal tuberculosis,MONDO,disease,DISEASE_14531
14532,14532,14532,14532,14532,14532,14532,14532,MONDO:0016830_MONDO:0100496,Emery-Dreifuss muscular dystrophy,MONDO_grouped,disease,DISEASE_14532
14533,14533,14533,14533,14533,14533,14533,14533,MONDO:0015425,lethal recessive chondrodysplasia,MONDO,disease,DISEASE_14533
14534,14534,14534,14534,14534,14534,14534,14534,MONDO:0859186,Chopra-Amiel-Gordon syndrome,MONDO,disease,DISEASE_14534
14535,14535,14535,14535,14535,14535,14535,14535,MONDO:0019580,papular mucinosis of infancy,MONDO,disease,DISEASE_14535
14536,14536,14536,14536,14536,14536,14536,14536,MONDO:0100473,disorder of peptide and amine metabolism,MONDO,disease,DISEASE_14536
14537,14537,14537,14537,14537,14537,14537,14537,MONDO:1011505,"fibrocartilaginous embolic myelopathy, horse",MONDO,disease,DISEASE_14537
14538,14538,14538,14538,14538,14538,14538,14538,MONDO:0005661,babesiosis,MONDO,disease,DISEASE_14538
14539,14539,14539,14539,14539,14539,14539,14539,MONDO:0016297_MONDO:0016298,prelingual non-syndromic genetic hearing loss,MONDO_grouped,disease,DISEASE_14539
14540,14540,14540,14540,14540,14540,14540,14540,MONDO:0021340,intertrigo,MONDO,disease,DISEASE_14540
14541,14541,14541,14541,14541,14541,14541,14541,MONDO:0031014_MONDO:0850225,autoimmune gastritis,MONDO_grouped,disease,DISEASE_14541
14542,14542,14542,14542,14542,14542,14542,14542,MONDO:1011445,"fibrocartilaginous embolic myelopathy, non-human animal",MONDO,disease,DISEASE_14542
14543,14543,14543,14543,14543,14543,14543,14543,MONDO:0004828,lower urinary tract calculus,MONDO,disease,DISEASE_14543
14544,14544,14544,14544,14544,14544,14544,14544,MONDO:0021243,parotid gland neoplasm,MONDO,disease,DISEASE_14544
14545,14545,14545,14545,14545,14545,14545,14545,MONDO:0005854_MONDO:0016663,mixed connective tissue disease,MONDO_grouped,disease,DISEASE_14545
14546,14546,14546,14546,14546,14546,14546,14546,MONDO:0021124_MONDO:0005372,female infertility,MONDO_grouped,disease,DISEASE_14546
14547,14547,14547,14547,14547,14547,14547,14547,MONDO:0011106,facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome,MONDO,disease,DISEASE_14547
14548,14548,14548,14548,14548,14548,14548,14548,MONDO:0016370,Marchiafava-Bignami disease,MONDO,disease,DISEASE_14548
14549,14549,14549,14549,14549,14549,14549,14549,MONDO:1010948,"non-hodgkin lymphoma, dog",MONDO,disease,DISEASE_14549
14550,14550,14550,14550,14550,14550,14550,14550,MONDO:0032565,"ophthalmoplegia, external, with rib and vertebral anomalies",MONDO,disease,DISEASE_14550
14551,14551,14551,14551,14551,14551,14551,14551,MONDO:0001683,pancreatic mucinous ductal ectasia,MONDO,disease,DISEASE_14551
14552,14552,14552,14552,14552,14552,14552,14552,MONDO:0018643,susceptibility to localized juvenile periodontitis,MONDO,disease,DISEASE_14552
14553,14553,14553,14553,14553,14553,14553,14553,MONDO:0018663,regressive spondylometaphyseal dysplasia,MONDO,disease,DISEASE_14553
14554,14554,14554,14554,14554,14554,14554,14554,MONDO:0012992,pancreatic insufficiency-anemia-hyperostosis syndrome,MONDO,disease,DISEASE_14554
14555,14555,14555,14555,14555,14555,14555,14555,MONDO:0010140,isolated thyrotropin-releasing hormone deficiency,MONDO,disease,DISEASE_14555
14556,14556,14556,14556,14556,14556,14556,14556,MONDO:0020065,combined dystonia,MONDO,disease,DISEASE_14556
14557,14557,14557,14557,14557,14557,14557,14557,MONDO:0008763,Alstrom syndrome,MONDO,disease,DISEASE_14557
14558,14558,14558,14558,14558,14558,14558,14558,MONDO:0010638,keratosis follicularis-dwarfism-cerebral atrophy syndrome,MONDO,disease,DISEASE_14558
14559,14559,14559,14559,14559,14559,14559,14559,MONDO:0005036,gastric adenocarcinoma,MONDO,disease,DISEASE_14559
14560,14560,14560,14560,14560,14560,14560,14560,MONDO:0021067,mediastinal germ cell tumor,MONDO,disease,DISEASE_14560
14561,14561,14561,14561,14561,14561,14561,14561,MONDO:0800483,SF3B4-related acrofacial dysostosis,MONDO,disease,DISEASE_14561
14562,14562,14562,14562,14562,14562,14562,14562,MONDO:0016937,partial duplication of chromosome 19,MONDO,disease,DISEASE_14562
14563,14563,14563,14563,14563,14563,14563,14563,MONDO:0019426,X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome,MONDO,disease,DISEASE_14563
14564,14564,14564,14564,14564,14564,14564,14564,MONDO:0041447,metastatic malignant neoplasm in the colon,MONDO,disease,DISEASE_14564
14565,14565,14565,14565,14565,14565,14565,14565,MONDO:0009831,malignant pancreatic neoplasm,MONDO,disease,DISEASE_14565
14566,14566,14566,14566,14566,14566,14566,14566,MONDO:0037937,pyrimidine metabolism disease,MONDO,disease,DISEASE_14566
14567,14567,14567,14567,14567,14567,14567,14567,MONDO:0957271,"autoinflammatory disease, systemic, with vasculitis",MONDO,disease,DISEASE_14567
14568,14568,14568,14568,14568,14568,14568,14568,MONDO:0012195,arthrogryposis-severe scoliosis syndrome,MONDO,disease,DISEASE_14568
14569,14569,14569,14569,14569,14569,14569,14569,MONDO:0008808,aplasia cutis congenita-intestinal lymphangiectasia syndrome,MONDO,disease,DISEASE_14569
14570,14570,14570,14570,14570,14570,14570,14570,MONDO:0018725,corpus callosum agenesis-macrocephaly-hypertelorism syndrome,MONDO,disease,DISEASE_14570
14571,14571,14571,14571,14571,14571,14571,14571,MONDO:0032829,neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities,MONDO,disease,DISEASE_14571
14572,14572,14572,14572,14572,14572,14572,14572,MONDO:0016762,microcornea-corectopia-macular hypoplasia syndrome,MONDO,disease,DISEASE_14572
14573,14573,14573,14573,14573,14573,14573,14573,MONDO:0001739,purulent labyrinthitis,MONDO,disease,DISEASE_14573
14574,14574,14574,14574,14574,14574,14574,14574,MONDO:0006504,acquired metabolic disease,MONDO,disease,DISEASE_14574
14575,14575,14575,14575,14575,14575,14575,14575,MONDO:0010039,congenital heart defect-round face-developmental delay syndrome,MONDO,disease,DISEASE_14575
14576,14576,14576,14576,14576,14576,14576,14576,MONDO:0006196,endometrial serous adenocarcinoma,MONDO,disease,DISEASE_14576
14577,14577,14577,14577,14577,14577,14577,14577,MONDO:0014790,TMEM199-CDG,MONDO,disease,DISEASE_14577
14578,14578,14578,14578,14578,14578,14578,14578,MONDO:0020753,Orthocoronavirinae infectious disease,MONDO,disease,DISEASE_14578
14579,14579,14579,14579,14579,14579,14579,14579,MONDO:0007810,autosomal dominant ichthyosis vulgaris,MONDO,disease,DISEASE_14579
14580,14580,14580,14580,14580,14580,14580,14580,MONDO:0015883,"hidrotic ectodermal dysplasia, Halal type",MONDO,disease,DISEASE_14580
14581,14581,14581,14581,14581,14581,14581,14581,MONDO:0060640,"neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy",MONDO,disease,DISEASE_14581
14582,14582,14582,14582,14582,14582,14582,14582,MONDO:0006186,duodenal adenocarcinoma,MONDO,disease,DISEASE_14582
14583,14583,14583,14583,14583,14583,14583,14583,MONDO:0003329,ureteral obstruction,MONDO,disease,DISEASE_14583
14584,14584,14584,14584,14584,14584,14584,14584,MONDO:0060761,neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum,MONDO,disease,DISEASE_14584
14585,14585,14585,14585,14585,14585,14585,14585,MONDO:0001535,vagus nerve disorder,MONDO,disease,DISEASE_14585
14586,14586,14586,14586,14586,14586,14586,14586,MONDO:0008837,"ataxia, deafness, and cardiomyopathy",MONDO,disease,DISEASE_14586
14587,14587,14587,14587,14587,14587,14587,14587,MONDO:0000879,cutaneous candidiasis,MONDO,disease,DISEASE_14587
14588,14588,14588,14588,14588,14588,14588,14588,MONDO:1010660,"thrombocytopenia, domestic cat",MONDO,disease,DISEASE_14588
14589,14589,14589,14589,14589,14589,14589,14589,MONDO:0850417,tuberculous encephalopathy,MONDO,disease,DISEASE_14589
14590,14590,14590,14590,14590,14590,14590,14590,MONDO:0022454,angiosarcoma of the scalp,MONDO,disease,DISEASE_14590
14591,14591,14591,14591,14591,14591,14591,14591,MONDO:0850519,tetrahydrobiopterin (BH4)-deficient hyperphenylalaninemia,MONDO,disease,DISEASE_14591
14592,14592,14592,14592,14592,14592,14592,14592,MONDO:0044912,metastatic malignant neoplasm in the spinal cord,MONDO,disease,DISEASE_14592
14593,14593,14593,14593,14593,14593,14593,14593,MONDO:0044306,"neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination",MONDO,disease,DISEASE_14593
14594,14594,14594,14594,14594,14594,14594,14594,MONDO:0016548,megacystis-megaureter syndrome,MONDO,disease,DISEASE_14594
14595,14595,14595,14595,14595,14595,14595,14595,MONDO:0019560,lupus erythematosus tumidus,MONDO,disease,DISEASE_14595
14596,14596,14596,14596,14596,14596,14596,14596,MONDO:1011423,"complement component 6 deficiency, non-human animal",MONDO,disease,DISEASE_14596
14597,14597,14597,14597,14597,14597,14597,14597,MONDO:0043555,infantile diarrhea,MONDO,disease,DISEASE_14597
14598,14598,14598,14598,14598,14598,14598,14598,MONDO:1012044,"congenital cerebellar anomaly, pig",MONDO,disease,DISEASE_14598
14599,14599,14599,14599,14599,14599,14599,14599,MONDO:0006030_MONDO:0022103,chronic cystitis,MONDO_grouped,disease,DISEASE_14599
14600,14600,14600,14600,14600,14600,14600,14600,MONDO:0044685_MONDO:0031013,autoimmune/inflammatory optic neuropathy,MONDO_grouped,disease,DISEASE_14600
14601,14601,14601,14601,14601,14601,14601,14601,MONDO:0000747,obsolete umbilical hernia,MONDO,disease,DISEASE_14601
14602,14602,14602,14602,14602,14602,14602,14602,MONDO:0006567,kernicterus due to isoimmunization,MONDO,disease,DISEASE_14602
14603,14603,14603,14603,14603,14603,14603,14603,MONDO:0020729_MONDO:0030519_MONDO:0014840_MONDO:0030529_MONDO:0012987_MONDO:0013290_MONDO:0014083_MONDO:0859234_MONDO:0013287_MONDO:0013288_MONDO:0013289_MONDO:0011096,autosomal recessive agammaglobulinemia 1,MONDO_grouped,disease,DISEASE_14603
14604,14604,14604,14604,14604,14604,14604,14604,MONDO:0009579,Frank-Ter Haar syndrome,MONDO,disease,DISEASE_14604
14605,14605,14605,14605,14605,14605,14605,14605,MONDO:0859182,"Short stature, Dauber-Argente type",MONDO,disease,DISEASE_14605
14606,14606,14606,14606,14606,14606,14606,14606,MONDO:0016577,biliary atresia with splenic malformation syndrome,MONDO,disease,DISEASE_14606
14607,14607,14607,14607,14607,14607,14607,14607,MONDO:0023204,Fukuda-Miyanomae-Nakata syndrome,MONDO,disease,DISEASE_14607
14608,14608,14608,14608,14608,14608,14608,14608,MONDO:0005190,obsolete macroglobulinemia,MONDO,disease,DISEASE_14608
14609,14609,14609,14609,14609,14609,14609,14609,MONDO:1012299_MONDO:1012300,"displaced abomasum, cattle",MONDO_grouped,disease,DISEASE_14609
14610,14610,14610,14610,14610,14610,14610,14610,MONDO:0005542,acute coronary syndrome,MONDO,disease,DISEASE_14610
14611,14611,14611,14611,14611,14611,14611,14611,MONDO:0003654,childhood parosteal osteosarcoma,MONDO,disease,DISEASE_14611
14612,14612,14612,14612,14612,14612,14612,14612,MONDO:0032794_MONDO:0012525_MONDO:0013449_MONDO:0012990_MONDO:0013231_MONDO:0012723_MONDO:0011415_MONDO:0060650_MONDO:0013453_MONDO:0011458_MONDO:0013454_MONDO:0012056_MONDO:0013446_MONDO:0008764_MONDO:0013613_MONDO:0013457_MONDO:0014145_MONDO:0011473_MONDO:0008765_MONDO:0018998_MONDO:1011250,leber congenital amaurosis,MONDO_grouped,disease,DISEASE_14612
14613,14613,14613,14613,14613,14613,14613,14613,MONDO:0005979,thoracic outlet syndrome,MONDO,disease,DISEASE_14613
14614,14614,14614,14614,14614,14614,14614,14614,MONDO:0100459,azoospermia,MONDO,disease,DISEASE_14614
14615,14615,14615,14615,14615,14615,14615,14615,MONDO:0008057_MONDO:0011525,"Carney complex,",MONDO_grouped,disease,DISEASE_14615
14616,14616,14616,14616,14616,14616,14616,14616,MONDO:0010446,X-linked cone dysfunction syndrome with myopia,MONDO,disease,DISEASE_14616
14617,14617,14617,14617,14617,14617,14617,14617,MONDO:0002399,"tenosynovial giant cell tumor, localized type",MONDO,disease,DISEASE_14617
14618,14618,14618,14618,14618,14618,14618,14618,MONDO:0007883,"periodic fever, immunodeficiency, and thrombocytopenia syndrome",MONDO,disease,DISEASE_14618
14619,14619,14619,14619,14619,14619,14619,14619,MONDO:0851102,pulmonary artery disease,MONDO,disease,DISEASE_14619
14620,14620,14620,14620,14620,14620,14620,14620,MONDO:0001003,pneumoconiosis due to talc,MONDO,disease,DISEASE_14620
14621,14621,14621,14621,14621,14621,14621,14621,MONDO:0958303,childhood renal cell carcinoma with MiT translocations,MONDO,disease,DISEASE_14621
14622,14622,14622,14622,14622,14622,14622,14622,MONDO:0014686,"short stature, microcephaly, and endocrine dysfunction",MONDO,disease,DISEASE_14622
14623,14623,14623,14623,14623,14623,14623,14623,MONDO:0008848,atrioventricular dissociation,MONDO,disease,DISEASE_14623
14624,14624,14624,14624,14624,14624,14624,14624,MONDO:0013875,"3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome",MONDO,disease,DISEASE_14624
14625,14625,14625,14625,14625,14625,14625,14625,MONDO:0013540,deafness-lymphedema-leukemia syndrome,MONDO,disease,DISEASE_14625
14626,14626,14626,14626,14626,14626,14626,14626,MONDO:0018571,contractures-developmental delay-Pierre Robin syndrome,MONDO,disease,DISEASE_14626
14627,14627,14627,14627,14627,14627,14627,14627,MONDO:0011204,obsolete cerebellar degeneration-related autoantigen 3,MONDO,disease,DISEASE_14627
14628,14628,14628,14628,14628,14628,14628,14628,MONDO:0024357,drug induced central sleep apnea,MONDO,disease,DISEASE_14628
14629,14629,14629,14629,14629,14629,14629,14629,MONDO:0003274,thoracic cancer,MONDO,disease,DISEASE_14629
14630,14630,14630,14630,14630,14630,14630,14630,MONDO:0009036,"cardiocranial syndrome, Pfeiffer type",MONDO,disease,DISEASE_14630
14631,14631,14631,14631,14631,14631,14631,14631,MONDO:0030607_MONDO:0030606_MONDO:0031200,Bryant-Li-Bhoj neurodevelopmental syndrome,MONDO_grouped,disease,DISEASE_14631
14632,14632,14632,14632,14632,14632,14632,14632,MONDO:0010314,"polymicrogyria, bilateral perisylvian, X-linked",MONDO,disease,DISEASE_14632
14633,14633,14633,14633,14633,14633,14633,14633,MONDO:0019791,recessive mitochondrial ataxia syndrome,MONDO,disease,DISEASE_14633
14634,14634,14634,14634,14634,14634,14634,14634,MONDO:1011087_MONDO:1011088_MONDO:1011089_MONDO:1011090,"renal dysplasia, dog",MONDO_grouped,disease,DISEASE_14634
14635,14635,14635,14635,14635,14635,14635,14635,MONDO:0008912,cardiac septal defects with coarctation of the aorta,MONDO,disease,DISEASE_14635
14636,14636,14636,14636,14636,14636,14636,14636,MONDO:0009458_MONDO:0015708,Schimke immuno-osseous dysplasia,MONDO_grouped,disease,DISEASE_14636
14637,14637,14637,14637,14637,14637,14637,14637,MONDO:0019323,pemphigus erythematosus,MONDO,disease,DISEASE_14637
14638,14638,14638,14638,14638,14638,14638,14638,MONDO:0005537,perianal Crohn disease,MONDO,disease,DISEASE_14638
14639,14639,14639,14639,14639,14639,14639,14639,MONDO:0044714,mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome,MONDO,disease,DISEASE_14639
14640,14640,14640,14640,14640,14640,14640,14640,MONDO:0100351,POLD1-related polyposis and colorectal cancer syndrome,MONDO,disease,DISEASE_14640
14641,14641,14641,14641,14641,14641,14641,14641,MONDO:0012402,"opioid dependence, susceptibility to, 1",MONDO,disease,DISEASE_14641
14642,14642,14642,14642,14642,14642,14642,14642,MONDO:0018271,peripheral primitive neuroectodermal tumor,MONDO,disease,DISEASE_14642
14643,14643,14643,14643,14643,14643,14643,14643,MONDO:0007033,abducens nerve palsy,MONDO,disease,DISEASE_14643
14644,14644,14644,14644,14644,14644,14644,14644,MONDO:0002226,tuberculous oophoritis,MONDO,disease,DISEASE_14644
14645,14645,14645,14645,14645,14645,14645,14645,MONDO:0006409,signet ring cell gastric adenocarcinoma,MONDO,disease,DISEASE_14645
14646,14646,14646,14646,14646,14646,14646,14646,MONDO:0005881_MONDO:0004585,oligohydramnios,MONDO_grouped,disease,DISEASE_14646
14647,14647,14647,14647,14647,14647,14647,14647,MONDO:0002347,barbiturate dependence,MONDO,disease,DISEASE_14647
14648,14648,14648,14648,14648,14648,14648,14648,MONDO:0043771,radiodermatitis,MONDO,disease,DISEASE_14648
14649,14649,14649,14649,14649,14649,14649,14649,MONDO:0020785_MONDO:0020783_MONDO:0012016,capillary malformation-arteriovenous malformation,MONDO_grouped,disease,DISEASE_14649
14650,14650,14650,14650,14650,14650,14650,14650,MONDO:0000596,paraphilic disorder,MONDO,disease,DISEASE_14650
14651,14651,14651,14651,14651,14651,14651,14651,MONDO:0020153,cryptophthalmia,MONDO,disease,DISEASE_14651
14652,14652,14652,14652,14652,14652,14652,14652,MONDO:0019918,maternal uniparental disomy of chromosome 21,MONDO,disease,DISEASE_14652
14653,14653,14653,14653,14653,14653,14653,14653,MONDO:0100135,Dravet syndrome,MONDO,disease,DISEASE_14653
14654,14654,14654,14654,14654,14654,14654,14654,MONDO:1012506,"degenerative encephalopathy, dog",MONDO,disease,DISEASE_14654
14655,14655,14655,14655,14655,14655,14655,14655,MONDO:1012304,"hypocatalasia, domestic guinea pig",MONDO,disease,DISEASE_14655
14656,14656,14656,14656,14656,14656,14656,14656,MONDO:1012133,"immunoglobulin G deficiency, horse",MONDO,disease,DISEASE_14656
14657,14657,14657,14657,14657,14657,14657,14657,MONDO:0859318_MONDO:0859317_MONDO:0009917,"pseudohypoaldosteronism, type IB3, autosomal recessive",MONDO_grouped,disease,DISEASE_14657
14658,14658,14658,14658,14658,14658,14658,14658,MONDO:0012003_MONDO:0013269_MONDO:0011364_MONDO:0013489_MONDO:0010973_MONDO:0013386_MONDO:0009076_MONDO:0011708_MONDO:0012002_MONDO:0013365_MONDO:0014428_MONDO:0011568_MONDO:0012380_MONDO:0013978_MONDO:0011519_MONDO:0012442_MONDO:0011480_MONDO:0014675_MONDO:0014237_MONDO:0014740_MONDO:0013119_MONDO:0013210_MONDO:0011392_MONDO:0012670_MONDO:0013010_MONDO:0013471_MONDO:0011360_MONDO:0014739_MONDO:0011103_MONDO:0010860_MONDO:0011389_MONDO:0010807_MONDO:0012023_MONDO:0011350_MONDO:0010817_MONDO:0011058_MONDO:0012460_MONDO:0011832_MONDO:0013632_MONDO:0011767_MONDO:0011067_MONDO:0012452_MONDO:0012293_MONDO:0014293_MONDO:0013250_MONDO:0011625_MONDO:0013823_MONDO:0012602_MONDO:0011102_MONDO:0012060_MONDO:0012327_MONDO:0014853_MONDO:0013738_MONDO:0013985_MONDO:0013984_MONDO:0011226_MONDO:0013249_MONDO:0014854_MONDO:0012326_MONDO:0013826_MONDO:0011920_MONDO:0011279_MONDO:0013537_MONDO:0013305_MONDO:0968981_MONDO:0011192_MONDO:0011774_MONDO:0010915_MONDO:0011994_MONDO:0011351_MONDO:0012976_MONDO:0011074_MONDO:0012977_MONDO:0011991_MONDO:0013593_MONDO:0014594_MONDO:0014291_MONDO:0012974_MONDO:0012333_MONDO:0012030_MONDO:0011660_MONDO:0014603_MONDO:0012975_MONDO:0011657_MONDO:0012420_MONDO:0011286_MONDO:0012170_MONDO:0011761_MONDO:0014738_MONDO:0012376_MONDO:0012375_MONDO:0000912_MONDO:0012903_MONDO:0014363_MONDO:0012083_MONDO:0011912_MONDO:0013929_MONDO:0011159_MONDO:0012902_MONDO:0011032_MONDO:0010967_MONDO:0011602_MONDO:0010933_MONDO:0013114_MONDO:0011031_MONDO:0011673_MONDO:0011160_MONDO:0011553_MONDO:0014470_MONDO:0012485_MONDO:0012090_MONDO:0011762_MONDO:0014182_MONDO:0010965_MONDO:0010963_MONDO:0012370_MONDO:0012091_MONDO:0007424_MONDO:0012421_MONDO:0010986_MONDO:0013215_MONDO:0012273_MONDO:0012086_MONDO:0012445_MONDO:0011799_MONDO:0014283_MONDO:0012418_MONDO:0010987_MONDO:0012355_MONDO:0014469_MONDO:0013963_MONDO:0019587,autosomal recessive nonsyndromic hearing loss,MONDO_grouped,disease,DISEASE_14658
14659,14659,14659,14659,14659,14659,14659,14659,MONDO:0859283,"neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities",MONDO,disease,DISEASE_14659
14660,14660,14660,14660,14660,14660,14660,14660,MONDO:0005203,ischemia reperfusion injury,MONDO,disease,DISEASE_14660
14661,14661,14661,14661,14661,14661,14661,14661,MONDO:0009647,Morquio syndrome C,MONDO,disease,DISEASE_14661
14662,14662,14662,14662,14662,14662,14662,14662,MONDO:0014943,mitochondrial DNA depletion syndrome 15 (hepatocerebral type),MONDO,disease,DISEASE_14662
14663,14663,14663,14663,14663,14663,14663,14663,MONDO:0019391,Fanconi anemia,MONDO,disease,DISEASE_14663
14664,14664,14664,14664,14664,14664,14664,14664,MONDO:0003129,epithelial predominant pulmonary blastoma,MONDO,disease,DISEASE_14664
14665,14665,14665,14665,14665,14665,14665,14665,MONDO:1011279,"age-related macular degeneration, Rhesus monkey",MONDO,disease,DISEASE_14665
14666,14666,14666,14666,14666,14666,14666,14666,MONDO:0009378,hyper-beta-alaninemia,MONDO,disease,DISEASE_14666
14667,14667,14667,14667,14667,14667,14667,14667,MONDO:0022810,Combarros Calleja Leno syndrome,MONDO,disease,DISEASE_14667
14668,14668,14668,14668,14668,14668,14668,14668,MONDO:0021529,benign neoplasm of chest wall,MONDO,disease,DISEASE_14668
14669,14669,14669,14669,14669,14669,14669,14669,MONDO:0003634,proteinuria,MONDO,disease,DISEASE_14669
14670,14670,14670,14670,14670,14670,14670,14670,MONDO:0045056_MONDO:0020634,grade II meningioma,MONDO_grouped,disease,DISEASE_14670
14671,14671,14671,14671,14671,14671,14671,14671,MONDO:0043364,eosinophil peroxidase deficiency,MONDO,disease,DISEASE_14671
14672,14672,14672,14672,14672,14672,14672,14672,MONDO:0800330,"myoclonic epilepsy, juvenile, 2",MONDO,disease,DISEASE_14672
14673,14673,14673,14673,14673,14673,14673,14673,MONDO:0019076,circumscribed palmoplantar hypokeratosis,MONDO,disease,DISEASE_14673
14674,14674,14674,14674,14674,14674,14674,14674,MONDO:1011357,"serositis, non-human animal",MONDO,disease,DISEASE_14674
14675,14675,14675,14675,14675,14675,14675,14675,MONDO:0019086,carcinoma of esophagus,MONDO,disease,DISEASE_14675
14676,14676,14676,14676,14676,14676,14676,14676,MONDO:0002571,primary central nervous system lymphoma,MONDO,disease,DISEASE_14676
14677,14677,14677,14677,14677,14677,14677,14677,MONDO:0008004,familial mitral valve prolapse,MONDO,disease,DISEASE_14677
14678,14678,14678,14678,14678,14678,14678,14678,MONDO:0006525_MONDO:0002138,allergic contact dermatitis,MONDO_grouped,disease,DISEASE_14678
14679,14679,14679,14679,14679,14679,14679,14679,MONDO:0044334,connective and soft tissue neoplasm,MONDO,disease,DISEASE_14679
14680,14680,14680,14680,14680,14680,14680,14680,MONDO:0010587,"epidermodysplasia verruciformis, X-linked",MONDO,disease,DISEASE_14680
14681,14681,14681,14681,14681,14681,14681,14681,MONDO:0012224_MONDO:0012707_MONDO:0012226_MONDO:0011891_MONDO:0024566_MONDO:0011443_MONDO:0007367_MONDO:0000032_MONDO:0011231_MONDO:0012681_MONDO:0012972_MONDO:0800329_MONDO:0800354,"febrile seizures, familial",MONDO_grouped,disease,DISEASE_14681
14682,14682,14682,14682,14682,14682,14682,14682,MONDO:0004265,acute endometritis,MONDO,disease,DISEASE_14682
14683,14683,14683,14683,14683,14683,14683,14683,MONDO:0009392,"hyperopia, high",MONDO,disease,DISEASE_14683
14684,14684,14684,14684,14684,14684,14684,14684,MONDO:0007478,autosomal dominant Kenny-Caffey syndrome,MONDO,disease,DISEASE_14684
14685,14685,14685,14685,14685,14685,14685,14685,MONDO:0010096,tardive dyskinesia,MONDO,disease,DISEASE_14685
14686,14686,14686,14686,14686,14686,14686,14686,MONDO:0005526,tetanus,MONDO,disease,DISEASE_14686
14687,14687,14687,14687,14687,14687,14687,14687,MONDO:0021329,carcinoma of soft palate,MONDO,disease,DISEASE_14687
14688,14688,14688,14688,14688,14688,14688,14688,MONDO:0005544,hippocampal sclerosis of aging,MONDO,disease,DISEASE_14688
14689,14689,14689,14689,14689,14689,14689,14689,MONDO:0002523,cutaneous mucinosis,MONDO,disease,DISEASE_14689
14690,14690,14690,14690,14690,14690,14690,14690,MONDO:1012259,"spinal dysraphism, dog",MONDO,disease,DISEASE_14690
14691,14691,14691,14691,14691,14691,14691,14691,MONDO:0958185_MONDO:0958181_MONDO:0012172,mitochondrial trifunctional protein deficiency,MONDO_grouped,disease,DISEASE_14691
14692,14692,14692,14692,14692,14692,14692,14692,MONDO:0007227,Sillence syndrome,MONDO,disease,DISEASE_14692
14693,14693,14693,14693,14693,14693,14693,14693,MONDO:0850088,EGF-related primary hypomagnesemia with intellectual disability,MONDO,disease,DISEASE_14693
14694,14694,14694,14694,14694,14694,14694,14694,MONDO:0003513,gastric teratoma,MONDO,disease,DISEASE_14694
14695,14695,14695,14695,14695,14695,14695,14695,MONDO:0001999,primary pulmonary hypertension,MONDO,disease,DISEASE_14695
14696,14696,14696,14696,14696,14696,14696,14696,MONDO:0034121,NAD(P)HX dehydratase deficiency,MONDO,disease,DISEASE_14696
14697,14697,14697,14697,14697,14697,14697,14697,MONDO:0003651,macrotrabecular hepatoblastoma,MONDO,disease,DISEASE_14697
14698,14698,14698,14698,14698,14698,14698,14698,MONDO:1011489,"complement component 3 deficiency, rabbit",MONDO,disease,DISEASE_14698
14699,14699,14699,14699,14699,14699,14699,14699,MONDO:0007479,"dwarfism, Levi type",MONDO,disease,DISEASE_14699
14700,14700,14700,14700,14700,14700,14700,14700,MONDO:1011822,"squamous cell carcinoma of the digit, non-human animal",MONDO,disease,DISEASE_14700
14701,14701,14701,14701,14701,14701,14701,14701,MONDO:0019707,primary osteolysis,MONDO,disease,DISEASE_14701
14702,14702,14702,14702,14702,14702,14702,14702,MONDO:0009199,ethanolaminosis,MONDO,disease,DISEASE_14702
14703,14703,14703,14703,14703,14703,14703,14703,MONDO:0001919,cystoid macular retinal degeneration,MONDO,disease,DISEASE_14703
14704,14704,14704,14704,14704,14704,14704,14704,MONDO:0016106,progressive muscular dystrophy,MONDO,disease,DISEASE_14704
14705,14705,14705,14705,14705,14705,14705,14705,MONDO:0008288,popliteal cyst,MONDO,disease,DISEASE_14705
14706,14706,14706,14706,14706,14706,14706,14706,MONDO:0009870,pili torti,MONDO,disease,DISEASE_14706
14707,14707,14707,14707,14707,14707,14707,14707,MONDO:0001022,disuse amblyopia,MONDO,disease,DISEASE_14707
14708,14708,14708,14708,14708,14708,14708,14708,MONDO:0030341,"myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive",MONDO,disease,DISEASE_14708
14709,14709,14709,14709,14709,14709,14709,14709,MONDO:0016346,hydrocephalus-obesity-hypogonadism syndrome,MONDO,disease,DISEASE_14709
14710,14710,14710,14710,14710,14710,14710,14710,MONDO:0021294,carcinoma in situ of gastric cardia,MONDO,disease,DISEASE_14710
14711,14711,14711,14711,14711,14711,14711,14711,MONDO:0800468,SCN4A-related channelopathy,MONDO,disease,DISEASE_14711
14712,14712,14712,14712,14712,14712,14712,14712,MONDO:0004473_MONDO:0005753_MONDO:0041366,epiglottis cancer,MONDO_grouped,disease,DISEASE_14712
14713,14713,14713,14713,14713,14713,14713,14713,MONDO:0020460,acquired von willebrand syndrome,MONDO,disease,DISEASE_14713
14714,14714,14714,14714,14714,14714,14714,14714,MONDO:0007439,deoxyribose-5-phosphate aldolase deficiency,MONDO,disease,DISEASE_14714
14715,14715,14715,14715,14715,14715,14715,14715,MONDO:0002379_MONDO:0004099,cystic teratoma,MONDO_grouped,disease,DISEASE_14715
14716,14716,14716,14716,14716,14716,14716,14716,MONDO:0023186,Fraser Jequier Chen syndrome,MONDO,disease,DISEASE_14716
14717,14717,14717,14717,14717,14717,14717,14717,MONDO:0700152,canine hepatocellular carcinoma,MONDO,disease,DISEASE_14717
14718,14718,14718,14718,14718,14718,14718,14718,MONDO:0000924,compensatory emphysema,MONDO,disease,DISEASE_14718
14719,14719,14719,14719,14719,14719,14719,14719,MONDO:0024881,secondary malignant neoplasm,MONDO,disease,DISEASE_14719
14720,14720,14720,14720,14720,14720,14720,14720,MONDO:0000968,kidney lipoma,MONDO,disease,DISEASE_14720
14721,14721,14721,14721,14721,14721,14721,14721,MONDO:0020538,malignant dysgerminomatous germ cell tumor of ovary,MONDO,disease,DISEASE_14721
14722,14722,14722,14722,14722,14722,14722,14722,MONDO:0005815,pancreatic neuroendocrine neoplasm,MONDO,disease,DISEASE_14722
14723,14723,14723,14723,14723,14723,14723,14723,MONDO:0016243,hemoglobin E disease,MONDO,disease,DISEASE_14723
14724,14724,14724,14724,14724,14724,14724,14724,MONDO:1011453,"Legg-Calvé-Perthes disease, non-human animal",MONDO,disease,DISEASE_14724
14725,14725,14725,14725,14725,14725,14725,14725,MONDO:0008319_MONDO:0060729,"protoporphyria, erythropoietic",MONDO_grouped,disease,DISEASE_14725
14726,14726,14726,14726,14726,14726,14726,14726,MONDO:0013792,intracerebral hemorrhage,MONDO,disease,DISEASE_14726
14727,14727,14727,14727,14727,14727,14727,14727,MONDO:0019581,acral persistent papular mucinosis,MONDO,disease,DISEASE_14727
14728,14728,14728,14728,14728,14728,14728,14728,MONDO:0040678,infiltrating urothelial carcinoma,MONDO,disease,DISEASE_14728
14729,14729,14729,14729,14729,14729,14729,14729,MONDO:0043004,Weil's disease,MONDO,disease,DISEASE_14729
14730,14730,14730,14730,14730,14730,14730,14730,MONDO:0005678,bovine respiratory disease complex,MONDO,disease,DISEASE_14730
14731,14731,14731,14731,14731,14731,14731,14731,MONDO:0100353,HHV-7 infectious disease,MONDO,disease,DISEASE_14731
14732,14732,14732,14732,14732,14732,14732,14732,MONDO:0016291,"craniosynostosis, Herrmann-Opitz type",MONDO,disease,DISEASE_14732
14733,14733,14733,14733,14733,14733,14733,14733,MONDO:0011510,Bohring-Opitz syndrome,MONDO,disease,DISEASE_14733
14734,14734,14734,14734,14734,14734,14734,14734,MONDO:0012451_MONDO:0013260,"esophagitis, eosinophilic",MONDO_grouped,disease,DISEASE_14734
14735,14735,14735,14735,14735,14735,14735,14735,MONDO:0009603,3-hydroxyisobutyryl-CoA hydrolase deficiency,MONDO,disease,DISEASE_14735
14736,14736,14736,14736,14736,14736,14736,14736,MONDO:0001389_MONDO:0019825,congenital coronary artery anomaly,MONDO_grouped,disease,DISEASE_14736
14737,14737,14737,14737,14737,14737,14737,14737,MONDO:0006787,hidrocystoma,MONDO,disease,DISEASE_14737
14738,14738,14738,14738,14738,14738,14738,14738,MONDO:0015700,immunodeficiency due to a late component of complement deficiency,MONDO,disease,DISEASE_14738
14739,14739,14739,14739,14739,14739,14739,14739,MONDO:0005141_MONDO:0004649,Pseudomonas infection,MONDO_grouped,disease,DISEASE_14739
14740,14740,14740,14740,14740,14740,14740,14740,MONDO:0007376,fleck corneal dystrophy,MONDO,disease,DISEASE_14740
14741,14741,14741,14741,14741,14741,14741,14741,MONDO:0009680,congenital muscular dystrophy-infantile cataract-hypogonadism syndrome,MONDO,disease,DISEASE_14741
14742,14742,14742,14742,14742,14742,14742,14742,MONDO:0013485_MONDO:0012246_MONDO:0033480_MONDO:0011694_MONDO:0014867_MONDO:0012103_MONDO:0011819_MONDO:0030805_MONDO:0859334_MONDO:0008458_MONDO:0011781_MONDO:0008457_MONDO:0007574_MONDO:0011833_MONDO:0014626_MONDO:0033479_MONDO:0011834_MONDO:0012450_MONDO:0033482_MONDO:0008119_MONDO:0014776_MONDO:0012116_MONDO:0012449_MONDO:0007298_MONDO:0011529_MONDO:0013241_MONDO:0007296_MONDO:0011464_MONDO:0013594_MONDO:0011330_MONDO:0014417_MONDO:0014475_MONDO:0010847_MONDO:0013486_MONDO:0008654_MONDO:0011439_MONDO:0014410_MONDO:0032526_MONDO:0011540_MONDO:0012098_MONDO:0010848_MONDO:0033481_MONDO:0012247_MONDO:0016809_MONDO:0000437_MONDO:1012957_MONDO:0013029_MONDO:0975800,spinocerebellar ataxia,MONDO_grouped,disease,DISEASE_14742
14743,14743,14743,14743,14743,14743,14743,14743,MONDO:0015874,benign ductal tumor of breast,MONDO,disease,DISEASE_14743
14744,14744,14744,14744,14744,14744,14744,14744,MONDO:0019571,autosomal dominant cutis laxa,MONDO,disease,DISEASE_14744
14745,14745,14745,14745,14745,14745,14745,14745,MONDO:0850157,B-lymphoblastic leukemia/lymphoma with ETV6-RUNX1,MONDO,disease,DISEASE_14745
14746,14746,14746,14746,14746,14746,14746,14746,MONDO:0000344,Ross river fever,MONDO,disease,DISEASE_14746
14747,14747,14747,14747,14747,14747,14747,14747,MONDO:0007066,"adenosine triphosphatase deficiency, anemia due to",MONDO,disease,DISEASE_14747
14748,14748,14748,14748,14748,14748,14748,14748,MONDO:0005765_MONDO:0005779,foot and mouth disease,MONDO_grouped,disease,DISEASE_14748
14749,14749,14749,14749,14749,14749,14749,14749,MONDO:0009961,renal and mullerian duct hypoplasia,MONDO,disease,DISEASE_14749
14750,14750,14750,14750,14750,14750,14750,14750,MONDO:0011472,epidermolysis bullosa simplex due to plakophilin deficiency,MONDO,disease,DISEASE_14750
14751,14751,14751,14751,14751,14751,14751,14751,MONDO:0015064,"jejunal neuroendocrine tumor, well differentiated, low or intermediate grade",MONDO,disease,DISEASE_14751
14752,14752,14752,14752,14752,14752,14752,14752,MONDO:0014955_MONDO:0100444_MONDO:0100446_MONDO:0100437_MONDO:0800403,RCBTB1-related retinopathy,MONDO_grouped,disease,DISEASE_14752
14753,14753,14753,14753,14753,14753,14753,14753,MONDO:0008196,parastremmatic dwarfism,MONDO,disease,DISEASE_14753
14754,14754,14754,14754,14754,14754,14754,14754,MONDO:0100019,ECHS1-related paroxysmal dyskinesia,MONDO,disease,DISEASE_14754
14755,14755,14755,14755,14755,14755,14755,14755,MONDO:0014206,severe early-onset pulmonary alveolar proteinosis due to MARS deficiency,MONDO,disease,DISEASE_14755
14756,14756,14756,14756,14756,14756,14756,14756,MONDO:0001143,paralytic strabismus,MONDO,disease,DISEASE_14756
14757,14757,14757,14757,14757,14757,14757,14757,MONDO:0017409,fetal cytomegalovirus syndrome,MONDO,disease,DISEASE_14757
14758,14758,14758,14758,14758,14758,14758,14758,MONDO:0010408,syndactyly-telecanthus-anogenital and renal malformations syndrome,MONDO,disease,DISEASE_14758
14759,14759,14759,14759,14759,14759,14759,14759,MONDO:0007936,"macular dystrophy, fenestrated sheen type",MONDO,disease,DISEASE_14759
14760,14760,14760,14760,14760,14760,14760,14760,MONDO:0044710,lip and oral cavity squamous cell carcinoma,MONDO,disease,DISEASE_14760
14761,14761,14761,14761,14761,14761,14761,14761,MONDO:0006412,sinus histiocytosis with massive lymphadenopathy,MONDO,disease,DISEASE_14761
14762,14762,14762,14762,14762,14762,14762,14762,MONDO:0005174,acute hypotension,MONDO,disease,DISEASE_14762
14763,14763,14763,14763,14763,14763,14763,14763,MONDO:0018165,venous thoracic outlet syndrome,MONDO,disease,DISEASE_14763
14764,14764,14764,14764,14764,14764,14764,14764,MONDO:0019386,progressive rubella panencephalitis,MONDO,disease,DISEASE_14764
14765,14765,14765,14765,14765,14765,14765,14765,MONDO:0005734,dourine,MONDO,disease,DISEASE_14765
14766,14766,14766,14766,14766,14766,14766,14766,MONDO:0008008,MOMO syndrome,MONDO,disease,DISEASE_14766
14767,14767,14767,14767,14767,14767,14767,14767,MONDO:0032648,mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations,MONDO,disease,DISEASE_14767
14768,14768,14768,14768,14768,14768,14768,14768,MONDO:0006960_MONDO:0024333,sciatic neuropathy,MONDO_grouped,disease,DISEASE_14768
14769,14769,14769,14769,14769,14769,14769,14769,MONDO:0009428,obsolete childhood hypophosphatasia,MONDO,disease,DISEASE_14769
14770,14770,14770,14770,14770,14770,14770,14770,MONDO:0015392,nasal glial heterotopia,MONDO,disease,DISEASE_14770
14771,14771,14771,14771,14771,14771,14771,14771,MONDO:1011351_MONDO:1011340,"psychiatric disorder, non-human animal",MONDO_grouped,disease,DISEASE_14771
14772,14772,14772,14772,14772,14772,14772,14772,MONDO:0023726,mediastinal yolk sac tumor,MONDO,disease,DISEASE_14772
14773,14773,14773,14773,14773,14773,14773,14773,MONDO:0024422,auditory perceptual disorders,MONDO,disease,DISEASE_14773
14774,14774,14774,14774,14774,14774,14774,14774,MONDO:0035133,PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome,MONDO,disease,DISEASE_14774
14775,14775,14775,14775,14775,14775,14775,14775,MONDO:1010410,"epilepsy, white-tufted-ear marmoset",MONDO,disease,DISEASE_14775
14776,14776,14776,14776,14776,14776,14776,14776,MONDO:0003125,testicular sex cord-stromal neoplasm,MONDO,disease,DISEASE_14776
14777,14777,14777,14777,14777,14777,14777,14777,MONDO:0032764,Khan-Khan-Katsanis syndrome,MONDO,disease,DISEASE_14777
14778,14778,14778,14778,14778,14778,14778,14778,MONDO:0004280,asymmetric motor neuropathy,MONDO,disease,DISEASE_14778
14779,14779,14779,14779,14779,14779,14779,14779,MONDO:0020673,arterial occlusion,MONDO,disease,DISEASE_14779
14780,14780,14780,14780,14780,14780,14780,14780,MONDO:0017486,"radial hemimelia, unilateral",MONDO,disease,DISEASE_14780
14781,14781,14781,14781,14781,14781,14781,14781,MONDO:0700132_MONDO:1011814,"melanoma, non-human animal",MONDO_grouped,disease,DISEASE_14781
14782,14782,14782,14782,14782,14782,14782,14782,MONDO:0014218,severe dermatitis-multiple allergies-metabolic wasting syndrome,MONDO,disease,DISEASE_14782
14783,14783,14783,14783,14783,14783,14783,14783,MONDO:0016143,qualitative or quantitative defects of gamma-sarcoglycan,MONDO,disease,DISEASE_14783
14784,14784,14784,14784,14784,14784,14784,14784,MONDO:1012430,"necrosis of digits, dog",MONDO,disease,DISEASE_14784
14785,14785,14785,14785,14785,14785,14785,14785,MONDO:0003978,colon small cell neuroendocrine carcinoma,MONDO,disease,DISEASE_14785
14786,14786,14786,14786,14786,14786,14786,14786,MONDO:0019585,scleromyxedema without monoclonal gammopathy,MONDO,disease,DISEASE_14786
14787,14787,14787,14787,14787,14787,14787,14787,MONDO:0000927,asymptomatic neurosyphilis,MONDO,disease,DISEASE_14787
14788,14788,14788,14788,14788,14788,14788,14788,MONDO:0005767,gas gangrene,MONDO,disease,DISEASE_14788
14789,14789,14789,14789,14789,14789,14789,14789,MONDO:0019046,leukodystrophy,MONDO,disease,DISEASE_14789
14790,14790,14790,14790,14790,14790,14790,14790,MONDO:0001607,intrapelvic lymph node leukemic reticuloendotheliosis,MONDO,disease,DISEASE_14790
14791,14791,14791,14791,14791,14791,14791,14791,MONDO:0001620,louse-borne relapsing fever,MONDO,disease,DISEASE_14791
14792,14792,14792,14792,14792,14792,14792,14792,MONDO:1012283,"tremor syndrome with central axonopathy, dog",MONDO,disease,DISEASE_14792
14793,14793,14793,14793,14793,14793,14793,14793,MONDO:1012196,"ocular squamous cell carcinoma, horse",MONDO,disease,DISEASE_14793
14794,14794,14794,14794,14794,14794,14794,14794,MONDO:0004995_MONDO:0002100,cardiovascular disorder,MONDO_grouped,disease,DISEASE_14794
14795,14795,14795,14795,14795,14795,14795,14795,MONDO:0006698_MONDO:0006699,cholecystolithiasis,MONDO_grouped,disease,DISEASE_14795
14796,14796,14796,14796,14796,14796,14796,14796,MONDO:0008170,ovarian cancer,MONDO,disease,DISEASE_14796
14797,14797,14797,14797,14797,14797,14797,14797,MONDO:0010992,Ayme-Gripp syndrome,MONDO,disease,DISEASE_14797
14798,14798,14798,14798,14798,14798,14798,14798,MONDO:0001894,spinal cord sarcoma,MONDO,disease,DISEASE_14798
14799,14799,14799,14799,14799,14799,14799,14799,MONDO:0957497,disabling pansclerotic morphea of childhood,MONDO,disease,DISEASE_14799
14800,14800,14800,14800,14800,14800,14800,14800,MONDO:0005401,colonic neoplasm,MONDO,disease,DISEASE_14800
14801,14801,14801,14801,14801,14801,14801,14801,MONDO:0850200,T cell and NK cell immunodeficiency,MONDO,disease,DISEASE_14801
14802,14802,14802,14802,14802,14802,14802,14802,MONDO:0005683,brucellosis,MONDO,disease,DISEASE_14802
14803,14803,14803,14803,14803,14803,14803,14803,MONDO:0010929_MONDO:0014705_MONDO:0011481_MONDO:0044315_MONDO:0015469_MONDO:1011193,craniosynostosis,MONDO_grouped,disease,DISEASE_14803
14804,14804,14804,14804,14804,14804,14804,14804,MONDO:0011318,Tonoki syndrome,MONDO,disease,DISEASE_14804
14805,14805,14805,14805,14805,14805,14805,14805,MONDO:0011334,limb-mammary syndrome,MONDO,disease,DISEASE_14805
14806,14806,14806,14806,14806,14806,14806,14806,MONDO:0003126,breast hemangioma,MONDO,disease,DISEASE_14806
14807,14807,14807,14807,14807,14807,14807,14807,MONDO:0004159,pancreatic non-invasive mucinous cystadenocarcinoma,MONDO,disease,DISEASE_14807
14808,14808,14808,14808,14808,14808,14808,14808,MONDO:0018491,3-phosphoglycerate dehydrogenase deficiency,MONDO,disease,DISEASE_14808
14809,14809,14809,14809,14809,14809,14809,14809,MONDO:0020657,human papillomavirus-related squamous cell carcinoma,MONDO,disease,DISEASE_14809
14810,14810,14810,14810,14810,14810,14810,14810,MONDO:1012104,"Hodgkin disease, dog",MONDO,disease,DISEASE_14810
14811,14811,14811,14811,14811,14811,14811,14811,MONDO:0009275,neonatal hemochromatosis,MONDO,disease,DISEASE_14811
14812,14812,14812,14812,14812,14812,14812,14812,MONDO:0019626,isolated ankyloblepharon filiforme adnatum,MONDO,disease,DISEASE_14812
14813,14813,14813,14813,14813,14813,14813,14813,MONDO:1012710_MONDO:1012836_MONDO:1012843,"progressive retinal atrophy, SLC4A3-related, dog",MONDO_grouped,disease,DISEASE_14813
14814,14814,14814,14814,14814,14814,14814,14814,MONDO:0018923,22q11.2 deletion syndrome,MONDO,disease,DISEASE_14814
14815,14815,14815,14815,14815,14815,14815,14815,MONDO:0005074,papillary cystadenocarcinoma,MONDO,disease,DISEASE_14815
14816,14816,14816,14816,14816,14816,14816,14816,MONDO:0009541,"lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis",MONDO,disease,DISEASE_14816
14817,14817,14817,14817,14817,14817,14817,14817,MONDO:0022462,anophthalmia esophageal atresia cryptorchidism,MONDO,disease,DISEASE_14817
14818,14818,14818,14818,14818,14818,14818,14818,MONDO:1011145,"pulmonary agenesis, horse",MONDO,disease,DISEASE_14818
14819,14819,14819,14819,14819,14819,14819,14819,MONDO:0016972,partial duplication of the long arm of chromosome 22,MONDO,disease,DISEASE_14819
14820,14820,14820,14820,14820,14820,14820,14820,MONDO:0009279,triple-A syndrome,MONDO,disease,DISEASE_14820
14821,14821,14821,14821,14821,14821,14821,14821,MONDO:0015311,autism-facial port-wine stain syndrome,MONDO,disease,DISEASE_14821
14822,14822,14822,14822,14822,14822,14822,14822,MONDO:1012437,"fluoroquinolone-induced retinal degeneration, domestic cat",MONDO,disease,DISEASE_14822
14823,14823,14823,14823,14823,14823,14823,14823,MONDO:0006039,infectious colitis,MONDO,disease,DISEASE_14823
14824,14824,14824,14824,14824,14824,14824,14824,MONDO:1010537_MONDO:1010538_MONDO:1010539,"megacolon, pig",MONDO_grouped,disease,DISEASE_14824
14825,14825,14825,14825,14825,14825,14825,14825,MONDO:0006973,skin appendage carcinoma,MONDO,disease,DISEASE_14825
14826,14826,14826,14826,14826,14826,14826,14826,MONDO:0009062,cystic fibrosis-gastritis-megaloblastic anemia syndrome,MONDO,disease,DISEASE_14826
14827,14827,14827,14827,14827,14827,14827,14827,MONDO:0012570,body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency,MONDO,disease,DISEASE_14827
14828,14828,14828,14828,14828,14828,14828,14828,MONDO:0022321,2-methylacetoacetyl CoA thiolase deficiency,MONDO,disease,DISEASE_14828
14829,14829,14829,14829,14829,14829,14829,14829,MONDO:0006066,"acinar prostate adenocarcinoma, foamy gland variant",MONDO,disease,DISEASE_14829
14830,14830,14830,14830,14830,14830,14830,14830,MONDO:0859312,"neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities",MONDO,disease,DISEASE_14830
14831,14831,14831,14831,14831,14831,14831,14831,MONDO:1012980,"mucolipidosis, non-human animal",MONDO,disease,DISEASE_14831
14832,14832,14832,14832,14832,14832,14832,14832,MONDO:0008948,cerebrotendinous xanthomatosis,MONDO,disease,DISEASE_14832
14833,14833,14833,14833,14833,14833,14833,14833,MONDO:1011339,"obstetric disorder, non-human animal",MONDO,disease,DISEASE_14833
14834,14834,14834,14834,14834,14834,14834,14834,MONDO:0971141,localized pleural mesothelioma,MONDO,disease,DISEASE_14834
14835,14835,14835,14835,14835,14835,14835,14835,MONDO:0018945,McLeod neuroacanthocytosis syndrome,MONDO,disease,DISEASE_14835
14836,14836,14836,14836,14836,14836,14836,14836,MONDO:0017383,familial clubfoot due to PITX1 point mutation,MONDO,disease,DISEASE_14836
14837,14837,14837,14837,14837,14837,14837,14837,MONDO:0002212,pneumonic tularemia,MONDO,disease,DISEASE_14837
14838,14838,14838,14838,14838,14838,14838,14838,MONDO:0003308_MONDO:0971143,pleural mesothelioma,MONDO_grouped,disease,DISEASE_14838
14839,14839,14839,14839,14839,14839,14839,14839,MONDO:0800182,TEK-related primary glaucoma,MONDO,disease,DISEASE_14839
14840,14840,14840,14840,14840,14840,14840,14840,MONDO:0000894,mucinous bronchioloalveolar adenocarcinoma,MONDO,disease,DISEASE_14840
14841,14841,14841,14841,14841,14841,14841,14841,MONDO:0003641,central nervous system hematopoietic neoplasm,MONDO,disease,DISEASE_14841
14842,14842,14842,14842,14842,14842,14842,14842,MONDO:0014869,hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome,MONDO,disease,DISEASE_14842
14843,14843,14843,14843,14843,14843,14843,14843,MONDO:0700085,pentasomy,MONDO,disease,DISEASE_14843
14844,14844,14844,14844,14844,14844,14844,14844,MONDO:0016558,familial congenital mirror movements,MONDO,disease,DISEASE_14844
14845,14845,14845,14845,14845,14845,14845,14845,MONDO:0043543,iatrogenic disease,MONDO,disease,DISEASE_14845
14846,14846,14846,14846,14846,14846,14846,14846,MONDO:0800207,"neuropathy, small fiber",MONDO,disease,DISEASE_14846
14847,14847,14847,14847,14847,14847,14847,14847,MONDO:0007642,isolated agenesis of gallbladder,MONDO,disease,DISEASE_14847
14848,14848,14848,14848,14848,14848,14848,14848,MONDO:0002036,penile disorder,MONDO,disease,DISEASE_14848
14849,14849,14849,14849,14849,14849,14849,14849,MONDO:0017060_MONDO:0017061,open iniencephaly,MONDO_grouped,disease,DISEASE_14849
14850,14850,14850,14850,14850,14850,14850,14850,MONDO:0008880,Bowen syndrome of multiple malformations,MONDO,disease,DISEASE_14850
14851,14851,14851,14851,14851,14851,14851,14851,MONDO:0016012,diethylstilbestrol syndrome,MONDO,disease,DISEASE_14851
14852,14852,14852,14852,14852,14852,14852,14852,MONDO:0019662,"short rib-polydactyly syndrome, Majewski type",MONDO,disease,DISEASE_14852
14853,14853,14853,14853,14853,14853,14853,14853,MONDO:0003522,male orgasm disorder,MONDO,disease,DISEASE_14853
14854,14854,14854,14854,14854,14854,14854,14854,MONDO:1010123,"common variable immunodeficiency, non-human animal",MONDO,disease,DISEASE_14854
14855,14855,14855,14855,14855,14855,14855,14855,MONDO:0008149,"osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures",MONDO,disease,DISEASE_14855
14856,14856,14856,14856,14856,14856,14856,14856,MONDO:0957595,Ziegler-Huang syndrome,MONDO,disease,DISEASE_14856
14857,14857,14857,14857,14857,14857,14857,14857,MONDO:0008611,humerus trochlea aplasia,MONDO,disease,DISEASE_14857
14858,14858,14858,14858,14858,14858,14858,14858,MONDO:0020767,cauda equina syndrome with neurogenic bladder,MONDO,disease,DISEASE_14858
14859,14859,14859,14859,14859,14859,14859,14859,MONDO:0975797,"myelofibrosis, congenital, with anemia, neutropenia, developmental delay, and ocular abnormalities",MONDO,disease,DISEASE_14859
14860,14860,14860,14860,14860,14860,14860,14860,MONDO:0016318,progressive multifocal leukoencephalopathy,MONDO,disease,DISEASE_14860
14861,14861,14861,14861,14861,14861,14861,14861,MONDO:1012368,"linear IgA disease, dog",MONDO,disease,DISEASE_14861
14862,14862,14862,14862,14862,14862,14862,14862,MONDO:0018108,idiopathic disseminated cytomegalovirus infection,MONDO,disease,DISEASE_14862
14863,14863,14863,14863,14863,14863,14863,14863,MONDO:0001063,cardia cancer,MONDO,disease,DISEASE_14863
14864,14864,14864,14864,14864,14864,14864,14864,MONDO:0000473,arterial disorder,MONDO,disease,DISEASE_14864
14865,14865,14865,14865,14865,14865,14865,14865,MONDO:1012356,"growth-hormone-receptor deficiency dwarfism, cattle",MONDO,disease,DISEASE_14865
14866,14866,14866,14866,14866,14866,14866,14866,MONDO:0004311,carcinoma of Cowper glands,MONDO,disease,DISEASE_14866
14867,14867,14867,14867,14867,14867,14867,14867,MONDO:1011992_MONDO:1012432,"congenital keratoconjunctivitis sicca and ichthyosiform dermatosis, non-human animal",MONDO_grouped,disease,DISEASE_14867
14868,14868,14868,14868,14868,14868,14868,14868,MONDO:0012873,"Ehlers-Danlos syndrome, spondylocheirodysplastic type",MONDO,disease,DISEASE_14868
14869,14869,14869,14869,14869,14869,14869,14869,MONDO:0007488,Lewy body dementia,MONDO,disease,DISEASE_14869
14870,14870,14870,14870,14870,14870,14870,14870,MONDO:0000670_MONDO:0001385,cortical deafness,MONDO_grouped,disease,DISEASE_14870
14871,14871,14871,14871,14871,14871,14871,14871,MONDO:0014561_MONDO:0009611_MONDO:0012435_MONDO:0009610_MONDO:0009787_MONDO:0044723_MONDO:0044724_MONDO:0859237_MONDO:0017359,3-methylglutaconic aciduria,MONDO_grouped,disease,DISEASE_14871
14872,14872,14872,14872,14872,14872,14872,14872,MONDO:0020442,left superior vena cava persisting to left-sided atrium,MONDO,disease,DISEASE_14872
14873,14873,14873,14873,14873,14873,14873,14873,MONDO:0006843,macular holes,MONDO,disease,DISEASE_14873
14874,14874,14874,14874,14874,14874,14874,14874,MONDO:0970957,terminal extramedullary conus spinal cord lipoma,MONDO,disease,DISEASE_14874
14875,14875,14875,14875,14875,14875,14875,14875,MONDO:1012947,"ametapodia, chicken",MONDO,disease,DISEASE_14875
14876,14876,14876,14876,14876,14876,14876,14876,MONDO:0003568,disorder of optic chiasm,MONDO,disease,DISEASE_14876
14877,14877,14877,14877,14877,14877,14877,14877,MONDO:0003967_MONDO:0003968,synchronous multifocal osteogenic sarcoma,MONDO_grouped,disease,DISEASE_14877
14878,14878,14878,14878,14878,14878,14878,14878,MONDO:0019625_MONDO:0850095,familial thoracic aortic aneurysm and aortic dissection,MONDO_grouped,disease,DISEASE_14878
14879,14879,14879,14879,14879,14879,14879,14879,MONDO:0003210,intrahepatic cholangiocarcinoma,MONDO,disease,DISEASE_14879
14880,14880,14880,14880,14880,14880,14880,14880,MONDO:0030862_MONDO:0030859_MONDO:0800103_MONDO:0100349,COACH syndrome,MONDO_grouped,disease,DISEASE_14880
14881,14881,14881,14881,14881,14881,14881,14881,MONDO:0017346,Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly,MONDO,disease,DISEASE_14881
14882,14882,14882,14882,14882,14882,14882,14882,MONDO:0005634,acute hemorrhagic conjunctivitis,MONDO,disease,DISEASE_14882
14883,14883,14883,14883,14883,14883,14883,14883,MONDO:0002366,autonomic nervous system neoplasm,MONDO,disease,DISEASE_14883
14884,14884,14884,14884,14884,14884,14884,14884,MONDO:0011685,"polysubstance abuse, susceptibility to",MONDO,disease,DISEASE_14884
14885,14885,14885,14885,14885,14885,14885,14885,MONDO:0020408,complete atrioventricular canal-tetralogy of fallot syndrome,MONDO,disease,DISEASE_14885
14886,14886,14886,14886,14886,14886,14886,14886,MONDO:0021123,Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone,MONDO,disease,DISEASE_14886
14887,14887,14887,14887,14887,14887,14887,14887,MONDO:1012757,"cerebellar hypoplasia, VLDLR-associated, dog",MONDO,disease,DISEASE_14887
14888,14888,14888,14888,14888,14888,14888,14888,MONDO:0032780,"hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities",MONDO,disease,DISEASE_14888
14889,14889,14889,14889,14889,14889,14889,14889,MONDO:0006112,bladder inflammatory myofibroblastic tumor,MONDO,disease,DISEASE_14889
14890,14890,14890,14890,14890,14890,14890,14890,MONDO:0005536,pancolitis,MONDO,disease,DISEASE_14890
14891,14891,14891,14891,14891,14891,14891,14891,MONDO:0018253,intellectual disability-facial dysmorphism-hand anomalies syndrome,MONDO,disease,DISEASE_14891
14892,14892,14892,14892,14892,14892,14892,14892,MONDO:0032786_MONDO:0014143_MONDO:0030679_MONDO:0008104_MONDO:0012690_MONDO:0013186_MONDO:0014691_MONDO:0033669_MONDO:0014693_MONDO:0032839_MONDO:0011531_MONDO:0012547_MONDO:0013379_MONDO:0012371_MONDO:0018997,Noonan syndrome,MONDO_grouped,disease,DISEASE_14892
14893,14893,14893,14893,14893,14893,14893,14893,MONDO:0013601,gluthathione peroxidase deficiency,MONDO,disease,DISEASE_14893
14894,14894,14894,14894,14894,14894,14894,14894,MONDO:0004128,lung occult large cell carcinoma,MONDO,disease,DISEASE_14894
14895,14895,14895,14895,14895,14895,14895,14895,MONDO:0010150,head and neck squamous cell carcinoma,MONDO,disease,DISEASE_14895
14896,14896,14896,14896,14896,14896,14896,14896,MONDO:0002843,fungal gastritis,MONDO,disease,DISEASE_14896
14897,14897,14897,14897,14897,14897,14897,14897,MONDO:0001009,solitary cyst of breast,MONDO,disease,DISEASE_14897
14898,14898,14898,14898,14898,14898,14898,14898,MONDO:0020348_MONDO:0020349,acute motor and sensory axonal neuropathy,MONDO_grouped,disease,DISEASE_14898
14899,14899,14899,14899,14899,14899,14899,14899,MONDO:1012880,"motor neuron disease, TMCO6-related, sheep",MONDO,disease,DISEASE_14899
14900,14900,14900,14900,14900,14900,14900,14900,MONDO:0003497,renal pelvis squamous cell carcinoma,MONDO,disease,DISEASE_14900
14901,14901,14901,14901,14901,14901,14901,14901,MONDO:1010818,"polydactyly, Western roe deer",MONDO,disease,DISEASE_14901
14902,14902,14902,14902,14902,14902,14902,14902,MONDO:0006519,rectal cancer,MONDO,disease,DISEASE_14902
14903,14903,14903,14903,14903,14903,14903,14903,MONDO:0006745,endometrioid stromal sarcoma,MONDO,disease,DISEASE_14903
14904,14904,14904,14904,14904,14904,14904,14904,MONDO:0006356,parotid gland adenoid cystic carcinoma,MONDO,disease,DISEASE_14904
14905,14905,14905,14905,14905,14905,14905,14905,MONDO:0019228_MONDO:0019237,inborn disorder of histidine metabolism,MONDO_grouped,disease,DISEASE_14905
14906,14906,14906,14906,14906,14906,14906,14906,MONDO:0700230,GPR143-related foveal hypoplasia,MONDO,disease,DISEASE_14906
14907,14907,14907,14907,14907,14907,14907,14907,MONDO:0018767_MONDO:0100041,severe primary trimethylaminuria,MONDO_grouped,disease,DISEASE_14907
14908,14908,14908,14908,14908,14908,14908,14908,MONDO:0015403_MONDO:0015404_MONDO:0018716,non-involuting congenital hemangioma,MONDO_grouped,disease,DISEASE_14908
14909,14909,14909,14909,14909,14909,14909,14909,MONDO:0016689,gemistocytic astrocytoma,MONDO,disease,DISEASE_14909
14910,14910,14910,14910,14910,14910,14910,14910,MONDO:0013477_MONDO:0013200_MONDO:0013195_MONDO:0013369_MONDO:0013475_MONDO:0013852_MONDO:0013474_MONDO:0013197_MONDO:0011843_MONDO:0014883_MONDO:0012112_MONDO:0007266_MONDO:0012799_MONDO:0008647_MONDO:0013455_MONDO:0007267_MONDO:0007268_MONDO:0013412_MONDO:0012111_MONDO:0012804_MONDO:0010946_MONDO:0005045_MONDO:1010460_MONDO:0013476_MONDO:1010458_MONDO:1010462,hypertrophic cardiomyopathy,MONDO_grouped,disease,DISEASE_14910
14911,14911,14911,14911,14911,14911,14911,14911,MONDO:0060562,"encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities",MONDO,disease,DISEASE_14911
14912,14912,14912,14912,14912,14912,14912,14912,MONDO:0009435,"hypospadias-intellectual disability, Goldblatt type syndrome",MONDO,disease,DISEASE_14912
14913,14913,14913,14913,14913,14913,14913,14913,MONDO:0021335,carcinoma of duodenum,MONDO,disease,DISEASE_14913
14914,14914,14914,14914,14914,14914,14914,14914,MONDO:0018714,primary intralymphatic angioendothelioma,MONDO,disease,DISEASE_14914
14915,14915,14915,14915,14915,14915,14915,14915,MONDO:0005789_MONDO:0005344_MONDO:0005788_MONDO:0005790,hepatitis D virus infection,MONDO_grouped,disease,DISEASE_14915
14916,14916,14916,14916,14916,14916,14916,14916,MONDO:0001601,Plasmodium ovale malaria,MONDO,disease,DISEASE_14916
14917,14917,14917,14917,14917,14917,14917,14917,MONDO:0021368,neoplasm of major salivary gland,MONDO,disease,DISEASE_14917
14918,14918,14918,14918,14918,14918,14918,14918,MONDO:0006276,lung inflammatory myofibroblastic tumor,MONDO,disease,DISEASE_14918
14919,14919,14919,14919,14919,14919,14919,14919,MONDO:0800142,chronic mucocutaneous candidiasis and connective tissue disease due to JNK1 haploinsufficiency,MONDO,disease,DISEASE_14919
14920,14920,14920,14920,14920,14920,14920,14920,MONDO:0010263,Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome,MONDO,disease,DISEASE_14920
14921,14921,14921,14921,14921,14921,14921,14921,MONDO:0017902,autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency,MONDO,disease,DISEASE_14921
14922,14922,14922,14922,14922,14922,14922,14922,MONDO:0011178,infantile convulsions and choreoathetosis,MONDO,disease,DISEASE_14922
14923,14923,14923,14923,14923,14923,14923,14923,MONDO:0019538,Gaisbock syndrome,MONDO,disease,DISEASE_14923
14924,14924,14924,14924,14924,14924,14924,14924,MONDO:1010496_MONDO:1010497,"patent ductus venosus, gray wolf",MONDO_grouped,disease,DISEASE_14924
14925,14925,14925,14925,14925,14925,14925,14925,MONDO:0004037,retinal edema,MONDO,disease,DISEASE_14925
14926,14926,14926,14926,14926,14926,14926,14926,MONDO:0009140,Silverman-Handmaker type dyssegmental dysplasia,MONDO,disease,DISEASE_14926
14927,14927,14927,14927,14927,14927,14927,14927,MONDO:0007907,lipoma of the conjunctiva,MONDO,disease,DISEASE_14927
14928,14928,14928,14928,14928,14928,14928,14928,MONDO:0008911,"cardiac lipidosis, familial",MONDO,disease,DISEASE_14928
14929,14929,14929,14929,14929,14929,14929,14929,MONDO:0021180,acquired xanthinuria,MONDO,disease,DISEASE_14929
14930,14930,14930,14930,14930,14930,14930,14930,MONDO:0007176,helicoid peripapillary chorioretinal degeneration,MONDO,disease,DISEASE_14930
14931,14931,14931,14931,14931,14931,14931,14931,MONDO:0007131,anonychia with flexural pigmentation,MONDO,disease,DISEASE_14931
14932,14932,14932,14932,14932,14932,14932,14932,MONDO:0008559_MONDO:0008560,thrombophilia due to thrombin defect,MONDO_grouped,disease,DISEASE_14932
14933,14933,14933,14933,14933,14933,14933,14933,MONDO:0015459,nasopharyngeal carcinoma,MONDO,disease,DISEASE_14933
14934,14934,14934,14934,14934,14934,14934,14934,MONDO:0001799,localized anterior staphyloma,MONDO,disease,DISEASE_14934
14935,14935,14935,14935,14935,14935,14935,14935,MONDO:0001988,external pathological resorption,MONDO,disease,DISEASE_14935
14936,14936,14936,14936,14936,14936,14936,14936,MONDO:0003345,hilar cholangiocarcinoma,MONDO,disease,DISEASE_14936
14937,14937,14937,14937,14937,14937,14937,14937,MONDO:0957196,"diffuse midline glioma, H3 K27M-mutant",MONDO,disease,DISEASE_14937
14938,14938,14938,14938,14938,14938,14938,14938,MONDO:0013128_MONDO:0008073_MONDO:0014891_MONDO:0013643_MONDO:0000608,familial juvenile hyperuricemic nephropathy,MONDO_grouped,disease,DISEASE_14938
14939,14939,14939,14939,14939,14939,14939,14939,MONDO:0023809,Milner-Khallouf-Gibson syndrome,MONDO,disease,DISEASE_14939
14940,14940,14940,14940,14940,14940,14940,14940,MONDO:1012760,"cholesterol deficiency, APOB-related, cattle",MONDO,disease,DISEASE_14940
14941,14941,14941,14941,14941,14941,14941,14941,MONDO:0002314_MONDO:0004811,chronic conjunctivitis,MONDO_grouped,disease,DISEASE_14941
14942,14942,14942,14942,14942,14942,14942,14942,MONDO:0005675,border disease,MONDO,disease,DISEASE_14942
14943,14943,14943,14943,14943,14943,14943,14943,MONDO:0016516,Kenny-Caffey syndrome,MONDO,disease,DISEASE_14943
14944,14944,14944,14944,14944,14944,14944,14944,MONDO:0008287,Greig cephalopolysyndactyly syndrome,MONDO,disease,DISEASE_14944
14945,14945,14945,14945,14945,14945,14945,14945,MONDO:0004926_MONDO:0001610_MONDO:0004812_MONDO:0004925_MONDO:1011289,dacryocystitis,MONDO_grouped,disease,DISEASE_14945
14946,14946,14946,14946,14946,14946,14946,14946,MONDO:0003452,cochlear disorder,MONDO,disease,DISEASE_14946
14947,14947,14947,14947,14947,14947,14947,14947,MONDO:0000677,semantic agnosia,MONDO,disease,DISEASE_14947
14948,14948,14948,14948,14948,14948,14948,14948,MONDO:0019128,mullerian aplasia,MONDO,disease,DISEASE_14948
14949,14949,14949,14949,14949,14949,14949,14949,MONDO:0043183,podder-tolmie syndrome,MONDO,disease,DISEASE_14949
14950,14950,14950,14950,14950,14950,14950,14950,MONDO:0011071,hereditary thrombocytopenia and hematologic cancer predisposition syndrome,MONDO,disease,DISEASE_14950
14951,14951,14951,14951,14951,14951,14951,14951,MONDO:0004323,muscular atrophy,MONDO,disease,DISEASE_14951
14952,14952,14952,14952,14952,14952,14952,14952,MONDO:0011724,encephalopathy due to GLUT1 deficiency,MONDO,disease,DISEASE_14952
14953,14953,14953,14953,14953,14953,14953,14953,MONDO:0016509,microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome,MONDO,disease,DISEASE_14953
14954,14954,14954,14954,14954,14954,14954,14954,MONDO:0006905,pigmented spindle cell nevus,MONDO,disease,DISEASE_14954
14955,14955,14955,14955,14955,14955,14955,14955,MONDO:0016156,qualitative or quantitative defects of FKRP,MONDO,disease,DISEASE_14955
14956,14956,14956,14956,14956,14956,14956,14956,MONDO:0020491,subcortical band heterotopia,MONDO,disease,DISEASE_14956
14957,14957,14957,14957,14957,14957,14957,14957,MONDO:1011941_MONDO:1012971,"Ancon dwarfism, non-human animal",MONDO_grouped,disease,DISEASE_14957
14958,14958,14958,14958,14958,14958,14958,14958,MONDO:0036976,benign epithelial neoplasm,MONDO,disease,DISEASE_14958
14959,14959,14959,14959,14959,14959,14959,14959,MONDO:0001492,kyphoscoliotic heart disease,MONDO,disease,DISEASE_14959
14960,14960,14960,14960,14960,14960,14960,14960,MONDO:0017775,melioidosis,MONDO,disease,DISEASE_14960
14961,14961,14961,14961,14961,14961,14961,14961,MONDO:0010356,nephrogenic syndrome of inappropriate antidiuresis,MONDO,disease,DISEASE_14961
14962,14962,14962,14962,14962,14962,14962,14962,MONDO:0971066,megaloblastic anemia-immunodeficiency due to folate transporter 1 deficiency,MONDO,disease,DISEASE_14962
14963,14963,14963,14963,14963,14963,14963,14963,MONDO:0007461,short stature-valvular heart disease-characteristic facies syndrome,MONDO,disease,DISEASE_14963
14964,14964,14964,14964,14964,14964,14964,14964,MONDO:0005021,dilated cardiomyopathy,MONDO,disease,DISEASE_14964
14965,14965,14965,14965,14965,14965,14965,14965,MONDO:0023541,Kasznica-Carlson-Coppedge syndrome,MONDO,disease,DISEASE_14965
14966,14966,14966,14966,14966,14966,14966,14966,MONDO:0024355,respiratory tract infectious disorder,MONDO,disease,DISEASE_14966
14967,14967,14967,14967,14967,14967,14967,14967,MONDO:0018362,persistent idiopathic facial pain,MONDO,disease,DISEASE_14967
14968,14968,14968,14968,14968,14968,14968,14968,MONDO:1011027,"sensory neuropathy, RETREG1-related, dog",MONDO,disease,DISEASE_14968
14969,14969,14969,14969,14969,14969,14969,14969,MONDO:0019284,inherited isolated nail anomaly,MONDO,disease,DISEASE_14969
14970,14970,14970,14970,14970,14970,14970,14970,MONDO:1012002,"vitreous degeneration, non-human animal",MONDO,disease,DISEASE_14970
14971,14971,14971,14971,14971,14971,14971,14971,MONDO:0017335,microtriplication 11q24.1,MONDO,disease,DISEASE_14971
14972,14972,14972,14972,14972,14972,14972,14972,MONDO:0004860_MONDO:0044137,vitreous disorder,MONDO_grouped,disease,DISEASE_14972
14973,14973,14973,14973,14973,14973,14973,14973,MONDO:1012694_MONDO:1012777,"dwarfism, PRKG2-related, dog",MONDO_grouped,disease,DISEASE_14973
14974,14974,14974,14974,14974,14974,14974,14974,MONDO:1011923,"respiratory distress syndrome, non-human animal",MONDO,disease,DISEASE_14974
14975,14975,14975,14975,14975,14975,14975,14975,MONDO:0043878,hereditary optic atrophy,MONDO,disease,DISEASE_14975
14976,14976,14976,14976,14976,14976,14976,14976,MONDO:0024686,"tenosynovial giant cell tumor, diffuse type",MONDO,disease,DISEASE_14976
14977,14977,14977,14977,14977,14977,14977,14977,MONDO:0015387,nasolacrimal duct cyst,MONDO,disease,DISEASE_14977
14978,14978,14978,14978,14978,14978,14978,14978,MONDO:1012345,"comedo syndrome, dog",MONDO,disease,DISEASE_14978
14979,14979,14979,14979,14979,14979,14979,14979,MONDO:0008304,premature chromatid separation trait,MONDO,disease,DISEASE_14979
14980,14980,14980,14980,14980,14980,14980,14980,MONDO:0018061,trichodermodysplasia-dental alterations syndrome,MONDO,disease,DISEASE_14980
14981,14981,14981,14981,14981,14981,14981,14981,MONDO:0013074,encephalocraniocutaneous lipomatosis,MONDO,disease,DISEASE_14981
14982,14982,14982,14982,14982,14982,14982,14982,MONDO:0008700,acheiropody,MONDO,disease,DISEASE_14982
14983,14983,14983,14983,14983,14983,14983,14983,MONDO:0006368,phosphaturic mesenchymal tumor,MONDO,disease,DISEASE_14983
14984,14984,14984,14984,14984,14984,14984,14984,MONDO:0001470,anal margin squamous cell carcinoma,MONDO,disease,DISEASE_14984
14985,14985,14985,14985,14985,14985,14985,14985,MONDO:0005618_MONDO:0005451_MONDO:0003265_MONDO:0002104,anxiety disorder,MONDO_grouped,disease,DISEASE_14985
14986,14986,14986,14986,14986,14986,14986,14986,MONDO:0032931,"pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal",MONDO,disease,DISEASE_14986
14987,14987,14987,14987,14987,14987,14987,14987,MONDO:1010122,trichrome vitiligo,MONDO,disease,DISEASE_14987
14988,14988,14988,14988,14988,14988,14988,14988,MONDO:0014458,Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young,MONDO,disease,DISEASE_14988
14989,14989,14989,14989,14989,14989,14989,14989,MONDO:0019565,hereditary von Willebrand disease,MONDO,disease,DISEASE_14989
14990,14990,14990,14990,14990,14990,14990,14990,MONDO:0100525,TCF7L2-related neurodevelopmental disorder,MONDO,disease,DISEASE_14990
14991,14991,14991,14991,14991,14991,14991,14991,MONDO:1010542_MONDO:1012367,"protein-losing enteropathy, dog",MONDO_grouped,disease,DISEASE_14991
14992,14992,14992,14992,14992,14992,14992,14992,MONDO:0006731,drug-induced akathisia,MONDO,disease,DISEASE_14992
14993,14993,14993,14993,14993,14993,14993,14993,MONDO:1012136,"inborn error of hepatic metabolism, dog",MONDO,disease,DISEASE_14993
14994,14994,14994,14994,14994,14994,14994,14994,MONDO:0008913_MONDO:0031323,"cardiac valvular defect, developmental",MONDO_grouped,disease,DISEASE_14994
14995,14995,14995,14995,14995,14995,14995,14995,MONDO:0044347,erythrocyte disorder,MONDO,disease,DISEASE_14995
14996,14996,14996,14996,14996,14996,14996,14996,MONDO:0015193_MONDO:0018221,hydrops fetalis,MONDO_grouped,disease,DISEASE_14996
14997,14997,14997,14997,14997,14997,14997,14997,MONDO:0005473_MONDO:0021895,temporomandibular joint disorder,MONDO_grouped,disease,DISEASE_14997
14998,14998,14998,14998,14998,14998,14998,14998,MONDO:0008901,Tel Hashomer camptodactyly syndrome,MONDO,disease,DISEASE_14998
14999,14999,14999,14999,14999,14999,14999,14999,MONDO:0023015,duodenal atresia tetralogy of fallot,MONDO,disease,DISEASE_14999
15000,15000,15000,15000,15000,15000,15000,15000,MONDO:0009072,Dandy-Walker syndrome,MONDO,disease,DISEASE_15000
15001,15001,15001,15001,15001,15001,15001,15001,MONDO:0000591,intrinsic cardiomyopathy,MONDO,disease,DISEASE_15001
15002,15002,15002,15002,15002,15002,15002,15002,MONDO:0024327,chronic renal failure syndrome,MONDO,disease,DISEASE_15002
15003,15003,15003,15003,15003,15003,15003,15003,MONDO:0700261,ADAR-related type 1 interferonopathy,MONDO,disease,DISEASE_15003
15004,15004,15004,15004,15004,15004,15004,15004,MONDO:0859383,ichthyosis hystrix,MONDO,disease,DISEASE_15004
15005,15005,15005,15005,15005,15005,15005,15005,MONDO:0017846_MONDO:0015087_MONDO:0017847,autosomal dominant spastic ataxia,MONDO_grouped,disease,DISEASE_15005
15006,15006,15006,15006,15006,15006,15006,15006,MONDO:0002087,peritoneum cancer,MONDO,disease,DISEASE_15006
15007,15007,15007,15007,15007,15007,15007,15007,MONDO:0017050,intraocular medulloepithelioma,MONDO,disease,DISEASE_15007
15008,15008,15008,15008,15008,15008,15008,15008,MONDO:1012465,"idiopathic congenital chondrodystrophy, cattle",MONDO,disease,DISEASE_15008
15009,15009,15009,15009,15009,15009,15009,15009,MONDO:0009228,gingival fibromatosis-facial dysmorphism syndrome,MONDO,disease,DISEASE_15009
15010,15010,15010,15010,15010,15010,15010,15010,MONDO:0013456,constitutional megaloblastic anemia with severe neurologic disease,MONDO,disease,DISEASE_15010
15011,15011,15011,15011,15011,15011,15011,15011,MONDO:0009865,glycogen storage disease due to phosphoglycerate mutase deficiency,MONDO,disease,DISEASE_15011
15012,15012,15012,15012,15012,15012,15012,15012,MONDO:0008864,Biemond syndrome type 2,MONDO,disease,DISEASE_15012
15013,15013,15013,15013,15013,15013,15013,15013,MONDO:0003956,Baastrup syndrome,MONDO,disease,DISEASE_15013
15014,15014,15014,15014,15014,15014,15014,15014,MONDO:0011518,Wiedemann-Steiner syndrome,MONDO,disease,DISEASE_15014
15015,15015,15015,15015,15015,15015,15015,15015,MONDO:0002677_MONDO:0700191_MONDO:0002676,conventional fibrosarcoma,MONDO_grouped,disease,DISEASE_15015
15016,15016,15016,15016,15016,15016,15016,15016,MONDO:0007051,acromegaloid facial appearance syndrome,MONDO,disease,DISEASE_15016
15017,15017,15017,15017,15017,15017,15017,15017,MONDO:0021312,malignant tumor of adrenal cortex,MONDO,disease,DISEASE_15017
15018,15018,15018,15018,15018,15018,15018,15018,MONDO:0007775,"hypersecretion of adrenal androgens, familial",MONDO,disease,DISEASE_15018
15019,15019,15019,15019,15019,15019,15019,15019,MONDO:0800041,MELAS syndrome caused by mutation in MTTS2,MONDO,disease,DISEASE_15019
15020,15020,15020,15020,15020,15020,15020,15020,MONDO:0035018,frontonasal dysplasia-bifid nose-upper limb anomalies syndrome,MONDO,disease,DISEASE_15020
15021,15021,15021,15021,15021,15021,15021,15021,MONDO:0005085,pterygium,MONDO,disease,DISEASE_15021
15022,15022,15022,15022,15022,15022,15022,15022,MONDO:0008262,Poland syndrome,MONDO,disease,DISEASE_15022
15023,15023,15023,15023,15023,15023,15023,15023,MONDO:0003495,ovarian squamous cell neoplasm,MONDO,disease,DISEASE_15023
15024,15024,15024,15024,15024,15024,15024,15024,MONDO:0019465,nodal marginal zone B-cell lymphoma,MONDO,disease,DISEASE_15024
15025,15025,15025,15025,15025,15025,15025,15025,MONDO:0800390,chemotherapy-induced toxicity,MONDO,disease,DISEASE_15025
15026,15026,15026,15026,15026,15026,15026,15026,MONDO:0019464,heavy chain disease,MONDO,disease,DISEASE_15026
15027,15027,15027,15027,15027,15027,15027,15027,MONDO:0011909_MONDO:0010549_MONDO:0014074_MONDO:0010479_MONDO:0957273_MONDO:0036484_MONDO:0013758_MONDO:0011674_MONDO:0012012_MONDO:0018778,Charcot-Marie-Tooth disease dominant intermediate,MONDO_grouped,disease,DISEASE_15027
15028,15028,15028,15028,15028,15028,15028,15028,MONDO:0022311,cote katsantoni syndrome,MONDO,disease,DISEASE_15028
15029,15029,15029,15029,15029,15029,15029,15029,MONDO:0022634,camptodactyly vertebral fusion,MONDO,disease,DISEASE_15029
15030,15030,15030,15030,15030,15030,15030,15030,MONDO:0004463,cellular phase chronic idiopathic myelofibrosis,MONDO,disease,DISEASE_15030
15031,15031,15031,15031,15031,15031,15031,15031,MONDO:1012642_MONDO:1012643_MONDO:1012644,"von Willebrand disease III, dog",MONDO_grouped,disease,DISEASE_15031
15032,15032,15032,15032,15032,15032,15032,15032,MONDO:0700249_MONDO:0958184,epidermolytic hyperkeratosis,MONDO_grouped,disease,DISEASE_15032
15033,15033,15033,15033,15033,15033,15033,15033,MONDO:0005963,sparganosis,MONDO,disease,DISEASE_15033
15034,15034,15034,15034,15034,15034,15034,15034,MONDO:0005874,neuroschistosomiasis,MONDO,disease,DISEASE_15034
15035,15035,15035,15035,15035,15035,15035,15035,MONDO:0004556,carcinoma arising in nasal papillomatosis,MONDO,disease,DISEASE_15035
15036,15036,15036,15036,15036,15036,15036,15036,MONDO:0014089,corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome,MONDO,disease,DISEASE_15036
15037,15037,15037,15037,15037,15037,15037,15037,MONDO:0004244,proximal-type epithelioid sarcoma,MONDO,disease,DISEASE_15037
15038,15038,15038,15038,15038,15038,15038,15038,MONDO:1011697,"hemophagocytic syndrome, non-human animal",MONDO,disease,DISEASE_15038
15039,15039,15039,15039,15039,15039,15039,15039,MONDO:0011046,"short stature, Brussels type",MONDO,disease,DISEASE_15039
15040,15040,15040,15040,15040,15040,15040,15040,MONDO:0060627_MONDO:0040500_MONDO:0060724_MONDO:0032824_MONDO:0029140_MONDO:0859271,glycosylphosphatidylinositol biosynthesis defect,MONDO_grouped,disease,DISEASE_15040
15041,15041,15041,15041,15041,15041,15041,15041,MONDO:0010354,Allan-Herndon-Dudley syndrome,MONDO,disease,DISEASE_15041
15042,15042,15042,15042,15042,15042,15042,15042,MONDO:0859266,"neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy",MONDO,disease,DISEASE_15042
15043,15043,15043,15043,15043,15043,15043,15043,MONDO:0013949_MONDO:0013948_MONDO:0013951_MONDO:0013952_MONDO:0013930_MONDO:0013942_MONDO:0008953_MONDO:0013936_MONDO:0013927_MONDO:0008954_MONDO:0013938_MONDO:0013932,peroxisome biogenesis disorder 11A (Zellweger),MONDO_grouped,disease,DISEASE_15043
15044,15044,15044,15044,15044,15044,15044,15044,MONDO:0013797,chromosome 17q12 deletion syndrome,MONDO,disease,DISEASE_15044
15045,15045,15045,15045,15045,15045,15045,15045,MONDO:0016385,hypogonadism-mitral valve prolapse-intellectual disability syndrome,MONDO,disease,DISEASE_15045
15046,15046,15046,15046,15046,15046,15046,15046,MONDO:0018680,cutaneous pseudolymphoma,MONDO,disease,DISEASE_15046
15047,15047,15047,15047,15047,15047,15047,15047,MONDO:0014865,autosomal recessive severe congenital neutropenia due to CSF3R deficiency,MONDO,disease,DISEASE_15047
15048,15048,15048,15048,15048,15048,15048,15048,MONDO:0019742,late-onset nephronophthisis,MONDO,disease,DISEASE_15048
15049,15049,15049,15049,15049,15049,15049,15049,MONDO:0016528,limb body wall complex,MONDO,disease,DISEASE_15049
15050,15050,15050,15050,15050,15050,15050,15050,MONDO:0007091,amelia and terminal transverse hemimelia,MONDO,disease,DISEASE_15050
15051,15051,15051,15051,15051,15051,15051,15051,MONDO:0021666,ear infection,MONDO,disease,DISEASE_15051
15052,15052,15052,15052,15052,15052,15052,15052,MONDO:0022876,Cortes Lacassie syndrome,MONDO,disease,DISEASE_15052
15053,15053,15053,15053,15053,15053,15053,15053,MONDO:1011749,"linear IgA disease, non-human animal",MONDO,disease,DISEASE_15053
15054,15054,15054,15054,15054,15054,15054,15054,MONDO:1010761_MONDO:1010762,"protoporphyria, chicken",MONDO_grouped,disease,DISEASE_15054
15055,15055,15055,15055,15055,15055,15055,15055,MONDO:0021632,primary brain neoplasm,MONDO,disease,DISEASE_15055
15056,15056,15056,15056,15056,15056,15056,15056,MONDO:0030487_MONDO:0009593_MONDO:0012713,"spondylometaphyseal dysplasia, pagnamenta type",MONDO_grouped,disease,DISEASE_15056
15057,15057,15057,15057,15057,15057,15057,15057,MONDO:0012160,spondylometaphyseal dysplasia-cone-rod dystrophy syndrome,MONDO,disease,DISEASE_15057
15058,15058,15058,15058,15058,15058,15058,15058,MONDO:0007834,islet cell adenomatosis,MONDO,disease,DISEASE_15058
15059,15059,15059,15059,15059,15059,15059,15059,MONDO:0004296,cervical lymphoepithelioma-like carcinoma,MONDO,disease,DISEASE_15059
15060,15060,15060,15060,15060,15060,15060,15060,MONDO:0850312_MONDO:0016690,anaplastic pleomorphic xanthoastrocytoma,MONDO_grouped,disease,DISEASE_15060
15061,15061,15061,15061,15061,15061,15061,15061,MONDO:0013894,short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome,MONDO,disease,DISEASE_15061
15062,15062,15062,15062,15062,15062,15062,15062,MONDO:0019148,Wolman disease,MONDO,disease,DISEASE_15062
15063,15063,15063,15063,15063,15063,15063,15063,MONDO:0009888,"polycystic kidney, cataract, and congenital blindness",MONDO,disease,DISEASE_15063
15064,15064,15064,15064,15064,15064,15064,15064,MONDO:0017879,hantavirus pulmonary syndrome,MONDO,disease,DISEASE_15064
15065,15065,15065,15065,15065,15065,15065,15065,MONDO:0850049,painful legs and moving toes syndrome,MONDO,disease,DISEASE_15065
15066,15066,15066,15066,15066,15066,15066,15066,MONDO:0018184,gastric linitis plastica,MONDO,disease,DISEASE_15066
15067,15067,15067,15067,15067,15067,15067,15067,MONDO:0002939,skin pigmented basal cell carcinoma,MONDO,disease,DISEASE_15067
15068,15068,15068,15068,15068,15068,15068,15068,MONDO:1012390,"sensory ataxic neuropathy, dog",MONDO,disease,DISEASE_15068
15069,15069,15069,15069,15069,15069,15069,15069,MONDO:0008338,"contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A",MONDO,disease,DISEASE_15069
15070,15070,15070,15070,15070,15070,15070,15070,MONDO:0045017,cholesterol biosynthetic process disease,MONDO,disease,DISEASE_15070
15071,15071,15071,15071,15071,15071,15071,15071,MONDO:0035775,CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome,MONDO,disease,DISEASE_15071
15072,15072,15072,15072,15072,15072,15072,15072,MONDO:0700013,chromosome 6 disorder,MONDO,disease,DISEASE_15072
15073,15073,15073,15073,15073,15073,15073,15073,MONDO:1011543_MONDO:1011544_MONDO:1012103,"idiopathic pulmonary fibrosis, dog",MONDO_grouped,disease,DISEASE_15073
15074,15074,15074,15074,15074,15074,15074,15074,MONDO:0017939_MONDO:0018948,classic multiminicore myopathy,MONDO_grouped,disease,DISEASE_15074
15075,15075,15075,15075,15075,15075,15075,15075,MONDO:0007447,autosomal dominant vibratory urticaria,MONDO,disease,DISEASE_15075
15076,15076,15076,15076,15076,15076,15076,15076,MONDO:0007804,Pallister-Hall syndrome,MONDO,disease,DISEASE_15076
15077,15077,15077,15077,15077,15077,15077,15077,MONDO:0100202_MONDO:0100206,"lumbar disk herniation, susceptibility to",MONDO_grouped,disease,DISEASE_15077
15078,15078,15078,15078,15078,15078,15078,15078,MONDO:0017561,congenital genu flexum,MONDO,disease,DISEASE_15078
15079,15079,15079,15079,15079,15079,15079,15079,MONDO:0010275_MONDO:0008473,"spondyloepimetaphyseal dysplasia, Bieganski type",MONDO_grouped,disease,DISEASE_15079
15080,15080,15080,15080,15080,15080,15080,15080,MONDO:0017221_MONDO:0017223_MONDO:0017222_MONDO:0017226,"Pelizaeus-Merzbacher disease, connatal form",MONDO_grouped,disease,DISEASE_15080
15081,15081,15081,15081,15081,15081,15081,15081,MONDO:0000282,Whitewater Arroyo hemorrhagic fever,MONDO,disease,DISEASE_15081
15082,15082,15082,15082,15082,15082,15082,15082,MONDO:0009355,Hooft disease,MONDO,disease,DISEASE_15082
15083,15083,15083,15083,15083,15083,15083,15083,MONDO:0003550,esophageal adenosquamous carcinoma,MONDO,disease,DISEASE_15083
15084,15084,15084,15084,15084,15084,15084,15084,MONDO:0002194,vestibular papilloma,MONDO,disease,DISEASE_15084
15085,15085,15085,15085,15085,15085,15085,15085,MONDO:0009807_MONDO:0005380_MONDO:0005166_MONDO:0001068_MONDO:0045053_MONDO:0009808,osteosarcoma,MONDO_grouped,disease,DISEASE_15085
15086,15086,15086,15086,15086,15086,15086,15086,MONDO:1012472,"horn cancer, zebu cattle",MONDO,disease,DISEASE_15086
15087,15087,15087,15087,15087,15087,15087,15087,MONDO:0010971,infundibulopelvic stenosis-multicystic kidney syndrome,MONDO,disease,DISEASE_15087
15088,15088,15088,15088,15088,15088,15088,15088,MONDO:0002693,lateral sinus thrombosis,MONDO,disease,DISEASE_15088
15089,15089,15089,15089,15089,15089,15089,15089,MONDO:1012579,"oculocutaneous albinism, non-human animal",MONDO,disease,DISEASE_15089
15090,15090,15090,15090,15090,15090,15090,15090,MONDO:1012625,"X-linked paralytic tremor, PLP1-related, rabbit",MONDO,disease,DISEASE_15090
15091,15091,15091,15091,15091,15091,15091,15091,MONDO:0002569,gastric dilatation,MONDO,disease,DISEASE_15091
15092,15092,15092,15092,15092,15092,15092,15092,MONDO:0004412,malignant spiradenoma,MONDO,disease,DISEASE_15092
15093,15093,15093,15093,15093,15093,15093,15093,MONDO:0958130,Greig cephalopolysyndactyly-contiguous gene syndrome,MONDO,disease,DISEASE_15093
15094,15094,15094,15094,15094,15094,15094,15094,MONDO:0005921_MONDO:0001943,Plasmodium vivax malaria,MONDO_grouped,disease,DISEASE_15094
15095,15095,15095,15095,15095,15095,15095,15095,MONDO:0022839,congenital human immunodeficiency virus,MONDO,disease,DISEASE_15095
15096,15096,15096,15096,15096,15096,15096,15096,MONDO:0850468,BN2 diffuse large B-cell lymphoma,MONDO,disease,DISEASE_15096
15097,15097,15097,15097,15097,15097,15097,15097,MONDO:0007566,multiple self-healing squamous epithelioma,MONDO,disease,DISEASE_15097
15098,15098,15098,15098,15098,15098,15098,15098,MONDO:0001321,obsolete scleral staphyloma,MONDO,disease,DISEASE_15098
15099,15099,15099,15099,15099,15099,15099,15099,MONDO:0005441,otitis media,MONDO,disease,DISEASE_15099
15100,15100,15100,15100,15100,15100,15100,15100,MONDO:0958353,intermediate collagen VI-related muscular dystrophy,MONDO,disease,DISEASE_15100
15101,15101,15101,15101,15101,15101,15101,15101,MONDO:0011055,distal monosomy 10p,MONDO,disease,DISEASE_15101
15102,15102,15102,15102,15102,15102,15102,15102,MONDO:0008141,"ossicular malformations, familial",MONDO,disease,DISEASE_15102
15103,15103,15103,15103,15103,15103,15103,15103,MONDO:0019474,hepatosplenic T-cell lymphoma,MONDO,disease,DISEASE_15103
15104,15104,15104,15104,15104,15104,15104,15104,MONDO:0000321,typhoidal tularemia,MONDO,disease,DISEASE_15104
15105,15105,15105,15105,15105,15105,15105,15105,MONDO:0005797,HIV wasting syndrome,MONDO,disease,DISEASE_15105
15106,15106,15106,15106,15106,15106,15106,15106,MONDO:0018476,dystonia-aphonia syndrome,MONDO,disease,DISEASE_15106
15107,15107,15107,15107,15107,15107,15107,15107,MONDO:0005320,tibia fracture,MONDO,disease,DISEASE_15107
15108,15108,15108,15108,15108,15108,15108,15108,MONDO:1010323,"entropion, non-human animal",MONDO,disease,DISEASE_15108
15109,15109,15109,15109,15109,15109,15109,15109,MONDO:0004893,hypertropia,MONDO,disease,DISEASE_15109
15110,15110,15110,15110,15110,15110,15110,15110,MONDO:0012541,"deafness with labyrinthine aplasia, microtia, and microdontia",MONDO,disease,DISEASE_15110
15111,15111,15111,15111,15111,15111,15111,15111,MONDO:0019967,Kienbock disease,MONDO,disease,DISEASE_15111
15112,15112,15112,15112,15112,15112,15112,15112,MONDO:0800408,urogenital adysplasia,MONDO,disease,DISEASE_15112
15113,15113,15113,15113,15113,15113,15113,15113,MONDO:0011925,congenital merosin-deficient muscular dystrophy 1A,MONDO,disease,DISEASE_15113
15114,15114,15114,15114,15114,15114,15114,15114,MONDO:0859247,neurocardiofaciodigital syndrome,MONDO,disease,DISEASE_15114
15115,15115,15115,15115,15115,15115,15115,15115,MONDO:0003001,seminoma,MONDO,disease,DISEASE_15115
15116,15116,15116,15116,15116,15116,15116,15116,MONDO:1012004,"osseous choristoma of the ciliary body, non-human animal",MONDO,disease,DISEASE_15116
15117,15117,15117,15117,15117,15117,15117,15117,MONDO:0001833,lacrimal duct obstruction,MONDO,disease,DISEASE_15117
15118,15118,15118,15118,15118,15118,15118,15118,MONDO:0018967,short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia,MONDO,disease,DISEASE_15118
15119,15119,15119,15119,15119,15119,15119,15119,MONDO:0012033,bradyopsia,MONDO,disease,DISEASE_15119
15120,15120,15120,15120,15120,15120,15120,15120,MONDO:0004271,pregnancy adenoma,MONDO,disease,DISEASE_15120
15121,15121,15121,15121,15121,15121,15121,15121,MONDO:0016622,Melhem-Fahl syndrome,MONDO,disease,DISEASE_15121
15122,15122,15122,15122,15122,15122,15122,15122,MONDO:0021043,mixed neoplasm,MONDO,disease,DISEASE_15122
15123,15123,15123,15123,15123,15123,15123,15123,MONDO:0012283,"cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss",MONDO,disease,DISEASE_15123
15124,15124,15124,15124,15124,15124,15124,15124,MONDO:0008743,Stimmler syndrome,MONDO,disease,DISEASE_15124
15125,15125,15125,15125,15125,15125,15125,15125,MONDO:0005197,thymus neoplasm,MONDO,disease,DISEASE_15125
15126,15126,15126,15126,15126,15126,15126,15126,MONDO:0005404,myalgic encephalomeyelitis/chronic fatigue syndrome,MONDO,disease,DISEASE_15126
15127,15127,15127,15127,15127,15127,15127,15127,MONDO:0021183,HTLV-2 infection,MONDO,disease,DISEASE_15127
15128,15128,15128,15128,15128,15128,15128,15128,MONDO:1012769,"cancer, TP53-related, pig",MONDO,disease,DISEASE_15128
15129,15129,15129,15129,15129,15129,15129,15129,MONDO:0012519,Rubinstein-Taybi syndrome due to 16p13.3 microdeletion,MONDO,disease,DISEASE_15129
15130,15130,15130,15130,15130,15130,15130,15130,MONDO:0000919,ampulla of vater cancer,MONDO,disease,DISEASE_15130
15131,15131,15131,15131,15131,15131,15131,15131,MONDO:0005692,cat-scratch disease,MONDO,disease,DISEASE_15131
15132,15132,15132,15132,15132,15132,15132,15132,MONDO:0958119,embryonal tumor with multilayered rosettes,MONDO,disease,DISEASE_15132
15133,15133,15133,15133,15133,15133,15133,15133,MONDO:1011323,"idiopathic disease, non-human animal",MONDO,disease,DISEASE_15133
15134,15134,15134,15134,15134,15134,15134,15134,MONDO:0020446_MONDO:0020447,coronary sinus stenosis,MONDO_grouped,disease,DISEASE_15134
15135,15135,15135,15135,15135,15135,15135,15135,MONDO:0024543_MONDO:0013605_MONDO:0009242,brittle cornea syndrome,MONDO_grouped,disease,DISEASE_15135
15136,15136,15136,15136,15136,15136,15136,15136,MONDO:0005674,bone giant cell tumor,MONDO,disease,DISEASE_15136
15137,15137,15137,15137,15137,15137,15137,15137,MONDO:0013806,familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome,MONDO,disease,DISEASE_15137
15138,15138,15138,15138,15138,15138,15138,15138,MONDO:0008588,hereditary geniospasm,MONDO,disease,DISEASE_15138
15139,15139,15139,15139,15139,15139,15139,15139,MONDO:0011332,"Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin",MONDO,disease,DISEASE_15139
15140,15140,15140,15140,15140,15140,15140,15140,MONDO:0006386,primary peritoneal serous adenocarcinoma,MONDO,disease,DISEASE_15140
15141,15141,15141,15141,15141,15141,15141,15141,MONDO:0800498,childhood-onset genetic generalized epilepsy syndrome,MONDO,disease,DISEASE_15141
15142,15142,15142,15142,15142,15142,15142,15142,MONDO:0004079,lung mucous gland adenoma,MONDO,disease,DISEASE_15142
15143,15143,15143,15143,15143,15143,15143,15143,MONDO:0016976,well-differentiated thymic neuroendocrine carcinoma,MONDO,disease,DISEASE_15143
15144,15144,15144,15144,15144,15144,15144,15144,MONDO:0021327,carcinoma of urethra,MONDO,disease,DISEASE_15144
15145,15145,15145,15145,15145,15145,15145,15145,MONDO:0016392,cerebellar hypoplasia-tapetoretinal degeneration syndrome,MONDO,disease,DISEASE_15145
15146,15146,15146,15146,15146,15146,15146,15146,MONDO:0005304,biliary tract neoplasm,MONDO,disease,DISEASE_15146
15147,15147,15147,15147,15147,15147,15147,15147,MONDO:0700112_MONDO:0014762_MONDO:0013403_MONDO:0013887_MONDO:0859222_MONDO:0014967_MONDO:0011546_MONDO:0011659,"heterotaxy, visceral, 5, autosomal",MONDO_grouped,disease,DISEASE_15147
15148,15148,15148,15148,15148,15148,15148,15148,MONDO:0012473,"right pulmonary artery, anomalous origin of, familial",MONDO,disease,DISEASE_15148
15149,15149,15149,15149,15149,15149,15149,15149,MONDO:0800378,"17,20-lyase deficiency, isolated",MONDO,disease,DISEASE_15149
15150,15150,15150,15150,15150,15150,15150,15150,MONDO:0001511,thyrotoxic exophthalmos,MONDO,disease,DISEASE_15150
15151,15151,15151,15151,15151,15151,15151,15151,MONDO:0021581,connective tissue neoplasm,MONDO,disease,DISEASE_15151
15152,15152,15152,15152,15152,15152,15152,15152,MONDO:0002415,bone carcinoma,MONDO,disease,DISEASE_15152
15153,15153,15153,15153,15153,15153,15153,15153,MONDO:0700143_MONDO:0700160,canine mammary carcinoma,MONDO_grouped,disease,DISEASE_15153
15154,15154,15154,15154,15154,15154,15154,15154,MONDO:0958333,"thrombocytopenia 13, syndromic",MONDO,disease,DISEASE_15154
15155,15155,15155,15155,15155,15155,15155,15155,MONDO:0009327,"heart, malformation of",MONDO,disease,DISEASE_15155
15156,15156,15156,15156,15156,15156,15156,15156,MONDO:0004985_MONDO:0000693_MONDO:0024613_MONDO:0001866,bipolar disorder,MONDO_grouped,disease,DISEASE_15156
15157,15157,15157,15157,15157,15157,15157,15157,MONDO:1012091,"gastric dilatation volvulus syndrome, dog",MONDO,disease,DISEASE_15157
15158,15158,15158,15158,15158,15158,15158,15158,MONDO:0010922,Satoyoshi syndrome,MONDO,disease,DISEASE_15158
15159,15159,15159,15159,15159,15159,15159,15159,MONDO:0009666,holocarboxylase synthetase deficiency,MONDO,disease,DISEASE_15159
15160,15160,15160,15160,15160,15160,15160,15160,MONDO:0022889,craniostenosis with congenital heart disease intellectual disability,MONDO,disease,DISEASE_15160
15161,15161,15161,15161,15161,15161,15161,15161,MONDO:0016698,ependymoma,MONDO,disease,DISEASE_15161
15162,15162,15162,15162,15162,15162,15162,15162,MONDO:0001521,intermittent explosive disorder,MONDO,disease,DISEASE_15162
15163,15163,15163,15163,15163,15163,15163,15163,MONDO:0019870,distal trisomy 1p36,MONDO,disease,DISEASE_15163
15164,15164,15164,15164,15164,15164,15164,15164,MONDO:0019963,bronchial endocrine tumor,MONDO,disease,DISEASE_15164
15165,15165,15165,15165,15165,15165,15165,15165,MONDO:0002544_MONDO:0016695_MONDO:0002543_MONDO:0002540_MONDO:0002541,brain oligodendroglioma,MONDO_grouped,disease,DISEASE_15165
15166,15166,15166,15166,15166,15166,15166,15166,MONDO:0031084,"amelogenesis imperfecta, IIa 1K",MONDO,disease,DISEASE_15166
15167,15167,15167,15167,15167,15167,15167,15167,MONDO:0958323,neurodevelopmental disorder with early-onset parkinsonism and behavioral abnormalities,MONDO,disease,DISEASE_15167
15168,15168,15168,15168,15168,15168,15168,15168,MONDO:0016723,pineocytoma,MONDO,disease,DISEASE_15168
15169,15169,15169,15169,15169,15169,15169,15169,MONDO:0041114,peripheral ischemia,MONDO,disease,DISEASE_15169
15170,15170,15170,15170,15170,15170,15170,15170,MONDO:0001021,ametropic amblyopia,MONDO,disease,DISEASE_15170
15171,15171,15171,15171,15171,15171,15171,15171,MONDO:1011944,"multiple exostoses, non-human animal",MONDO,disease,DISEASE_15171
15172,15172,15172,15172,15172,15172,15172,15172,MONDO:0023071,enterovirus antenatal infection,MONDO,disease,DISEASE_15172
15173,15173,15173,15173,15173,15173,15173,15173,MONDO:0013028,adenosine monophosphate deaminase deficiency,MONDO,disease,DISEASE_15173
15174,15174,15174,15174,15174,15174,15174,15174,MONDO:0030894,"AMED syndrome, digenic",MONDO,disease,DISEASE_15174
15175,15175,15175,15175,15175,15175,15175,15175,MONDO:0018332,"multiple acyl-CoA dehydrogenase deficiency, severe neonatal type",MONDO,disease,DISEASE_15175
15176,15176,15176,15176,15176,15176,15176,15176,MONDO:0001478,anisometropia,MONDO,disease,DISEASE_15176
15177,15177,15177,15177,15177,15177,15177,15177,MONDO:0003331_MONDO:0002372_MONDO:0003281_MONDO:0003851_MONDO:0003852,ovarian monodermal teratoma,MONDO_grouped,disease,DISEASE_15177
15178,15178,15178,15178,15178,15178,15178,15178,MONDO:0100116,Middle East respiratory syndrome,MONDO,disease,DISEASE_15178
15179,15179,15179,15179,15179,15179,15179,15179,MONDO:1012918,"ataxia, HACE1-related, dog",MONDO,disease,DISEASE_15179
15180,15180,15180,15180,15180,15180,15180,15180,MONDO:0009442,ichthyosis congenita with biliary atresia,MONDO,disease,DISEASE_15180
15181,15181,15181,15181,15181,15181,15181,15181,MONDO:0002706,cervix endometriosis,MONDO,disease,DISEASE_15181
15182,15182,15182,15182,15182,15182,15182,15182,MONDO:0012202,"malaria, mild, susceptibility to",MONDO,disease,DISEASE_15182
15183,15183,15183,15183,15183,15183,15183,15183,MONDO:0010081,"subaortic stenosis, membranous",MONDO,disease,DISEASE_15183
15184,15184,15184,15184,15184,15184,15184,15184,MONDO:0017790,gastric adenocarcinoma and proximal polyposis of the stomach,MONDO,disease,DISEASE_15184
15185,15185,15185,15185,15185,15185,15185,15185,MONDO:0011129_MONDO:0009277_MONDO:0005041_MONDO:1011510_MONDO:1011512_MONDO:1011514_MONDO:1011516,glaucoma,MONDO_grouped,disease,DISEASE_15185
15186,15186,15186,15186,15186,15186,15186,15186,MONDO:0001154,Siberian tick typhus,MONDO,disease,DISEASE_15186
15187,15187,15187,15187,15187,15187,15187,15187,MONDO:0007725,hereditary progressive mucinous histiocytosis,MONDO,disease,DISEASE_15187
15188,15188,15188,15188,15188,15188,15188,15188,MONDO:0016863,Okihiro syndrome due to 20q13 microdeletion,MONDO,disease,DISEASE_15188
15189,15189,15189,15189,15189,15189,15189,15189,MONDO:0100198,Mendelian encephalopathy,MONDO,disease,DISEASE_15189
15190,15190,15190,15190,15190,15190,15190,15190,MONDO:0009990,Revesz syndrome,MONDO,disease,DISEASE_15190
15191,15191,15191,15191,15191,15191,15191,15191,MONDO:0003032,superior vena cava angiosarcoma,MONDO,disease,DISEASE_15191
15192,15192,15192,15192,15192,15192,15192,15192,MONDO:0008358,radial ray hypoplasia-choanal atresia syndrome,MONDO,disease,DISEASE_15192
15193,15193,15193,15193,15193,15193,15193,15193,MONDO:0008970,chondrodysplasia Blomstrand type,MONDO,disease,DISEASE_15193
15194,15194,15194,15194,15194,15194,15194,15194,MONDO:0021851,alopecia universalis onychodystrophy vitiligo,MONDO,disease,DISEASE_15194
15195,15195,15195,15195,15195,15195,15195,15195,MONDO:0016902,partial deletion of the long arm of chromosome 3,MONDO,disease,DISEASE_15195
15196,15196,15196,15196,15196,15196,15196,15196,MONDO:0017584,Sagliker syndrome,MONDO,disease,DISEASE_15196
15197,15197,15197,15197,15197,15197,15197,15197,MONDO:0002073,malignant pineal area germ cell neoplasm,MONDO,disease,DISEASE_15197
15198,15198,15198,15198,15198,15198,15198,15198,MONDO:0015344,idiopathic acute transverse myelitis,MONDO,disease,DISEASE_15198
15199,15199,15199,15199,15199,15199,15199,15199,MONDO:0013423,immunodeficiency due to MASP-2 deficiency,MONDO,disease,DISEASE_15199
15200,15200,15200,15200,15200,15200,15200,15200,MONDO:0004110,refractory hairy cell leukemia,MONDO,disease,DISEASE_15200
15201,15201,15201,15201,15201,15201,15201,15201,MONDO:0043762,tubal pregnancy,MONDO,disease,DISEASE_15201
15202,15202,15202,15202,15202,15202,15202,15202,MONDO:0001406,peripheral nervous system neoplasm,MONDO,disease,DISEASE_15202
15203,15203,15203,15203,15203,15203,15203,15203,MONDO:1010639,"factor XII deficiency, dog",MONDO,disease,DISEASE_15203
15204,15204,15204,15204,15204,15204,15204,15204,MONDO:1011631,"stringhalt, non-human animal",MONDO,disease,DISEASE_15204
15205,15205,15205,15205,15205,15205,15205,15205,MONDO:0019322,pemphigus vegetans,MONDO,disease,DISEASE_15205
15206,15206,15206,15206,15206,15206,15206,15206,MONDO:0003790,prostatic urethra urothelial carcinoma,MONDO,disease,DISEASE_15206
15207,15207,15207,15207,15207,15207,15207,15207,MONDO:0023605,Laugier-Hunziker syndrome,MONDO,disease,DISEASE_15207
15208,15208,15208,15208,15208,15208,15208,15208,MONDO:0000303,conidiobolomycosis,MONDO,disease,DISEASE_15208
15209,15209,15209,15209,15209,15209,15209,15209,MONDO:0032843,oculopharyngeal myopathy with leukoencephalopathy 1,MONDO,disease,DISEASE_15209
15210,15210,15210,15210,15210,15210,15210,15210,MONDO:0007210,"Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay",MONDO,disease,DISEASE_15210
15211,15211,15211,15211,15211,15211,15211,15211,MONDO:1010790,"focal nonepidermolytic palmoplantar keratoderma, KRT16-related, dog",MONDO,disease,DISEASE_15211
15212,15212,15212,15212,15212,15212,15212,15212,MONDO:0011466,"distal myopathy, Welander type",MONDO,disease,DISEASE_15212
15213,15213,15213,15213,15213,15213,15213,15213,MONDO:0016417,congenital ichthyosis-microcephalus-tetraplegia syndrome,MONDO,disease,DISEASE_15213
15214,15214,15214,15214,15214,15214,15214,15214,MONDO:0018017,goblet cell carcinoma,MONDO,disease,DISEASE_15214
15215,15215,15215,15215,15215,15215,15215,15215,MONDO:0020589,cardiac germ cell tumor,MONDO,disease,DISEASE_15215
15216,15216,15216,15216,15216,15216,15216,15216,MONDO:0008343,pulmonary atresia with ventricular septal defect,MONDO,disease,DISEASE_15216
15217,15217,15217,15217,15217,15217,15217,15217,MONDO:0004622,chronic intestinal vascular insufficiency,MONDO,disease,DISEASE_15217
15218,15218,15218,15218,15218,15218,15218,15218,MONDO:0011022,Potocki-Shaffer syndrome,MONDO,disease,DISEASE_15218
15219,15219,15219,15219,15219,15219,15219,15219,MONDO:0017749,disorder of multiple glycosylation,MONDO,disease,DISEASE_15219
15220,15220,15220,15220,15220,15220,15220,15220,MONDO:0002952,follicular basal cell carcinoma,MONDO,disease,DISEASE_15220
15221,15221,15221,15221,15221,15221,15221,15221,MONDO:0007413,Cyprus facial-neuromusculoskeletal syndrome,MONDO,disease,DISEASE_15221
15222,15222,15222,15222,15222,15222,15222,15222,MONDO:0800037,MELAS syndrome caused by mutation in MTTS1,MONDO,disease,DISEASE_15222
15223,15223,15223,15223,15223,15223,15223,15223,MONDO:0010383_MONDO:0023178_MONDO:0023179_MONDO:0023180,fragile X syndrome,MONDO_grouped,disease,DISEASE_15223
15224,15224,15224,15224,15224,15224,15224,15224,MONDO:1011768,"bone spavin, non-human animal",MONDO,disease,DISEASE_15224
15225,15225,15225,15225,15225,15225,15225,15225,MONDO:1012976,"hyperkeratosis, non-human animal",MONDO,disease,DISEASE_15225
15226,15226,15226,15226,15226,15226,15226,15226,MONDO:0016369_MONDO:0970950_MONDO:0016368_MONDO:0014347_MONDO:0010002,Rothmund-Thomson syndrome,MONDO_grouped,disease,DISEASE_15226
15227,15227,15227,15227,15227,15227,15227,15227,MONDO:0014497,polyendocrine-polyneuropathy syndrome,MONDO,disease,DISEASE_15227
15228,15228,15228,15228,15228,15228,15228,15228,MONDO:0010805,bladder exstrophy,MONDO,disease,DISEASE_15228
15229,15229,15229,15229,15229,15229,15229,15229,MONDO:0003860,cerebellopontine angle meningioma,MONDO,disease,DISEASE_15229
15230,15230,15230,15230,15230,15230,15230,15230,MONDO:0018282,qualitative or quantitative defects of alpha-dystroglycan,MONDO,disease,DISEASE_15230
15231,15231,15231,15231,15231,15231,15231,15231,MONDO:0019471,adult T-cell leukemia/lymphoma,MONDO,disease,DISEASE_15231
15232,15232,15232,15232,15232,15232,15232,15232,MONDO:0007234,branchial myoclonus with spastic paraparesis and cerebellar ataxia,MONDO,disease,DISEASE_15232
15233,15233,15233,15233,15233,15233,15233,15233,MONDO:0032930_MONDO:0030051,intellectual developmental disorder with poor growth and with or without seizures or ataxia,MONDO_grouped,disease,DISEASE_15233
15234,15234,15234,15234,15234,15234,15234,15234,MONDO:0011029,myeloid tumor suppressor,MONDO,disease,DISEASE_15234
15235,15235,15235,15235,15235,15235,15235,15235,MONDO:1012967,"liver disorder, non-human animal",MONDO,disease,DISEASE_15235
15236,15236,15236,15236,15236,15236,15236,15236,MONDO:0003111,gastric neuroendocrine neoplasm,MONDO,disease,DISEASE_15236
15237,15237,15237,15237,15237,15237,15237,15237,MONDO:1012924,"cataract, FYCO1-related, dog",MONDO,disease,DISEASE_15237
15238,15238,15238,15238,15238,15238,15238,15238,MONDO:0018216,Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome,MONDO,disease,DISEASE_15238
15239,15239,15239,15239,15239,15239,15239,15239,MONDO:0005625,cerebral malaria,MONDO,disease,DISEASE_15239
15240,15240,15240,15240,15240,15240,15240,15240,MONDO:0000698,gamma-amino butyric acid metabolism disorder,MONDO,disease,DISEASE_15240
15241,15241,15241,15241,15241,15241,15241,15241,MONDO:0003941,classic variant of chromophobe renal cell carcinoma,MONDO,disease,DISEASE_15241
15242,15242,15242,15242,15242,15242,15242,15242,MONDO:0006939,pyelonephritis,MONDO,disease,DISEASE_15242
15243,15243,15243,15243,15243,15243,15243,15243,MONDO:1012321,"pseudocholinesterase deficiency, horse",MONDO,disease,DISEASE_15243
15244,15244,15244,15244,15244,15244,15244,15244,MONDO:0010999,fallot complex-intellectual disability-growth delay syndrome,MONDO,disease,DISEASE_15244
15245,15245,15245,15245,15245,15245,15245,15245,MONDO:0700130,partial segmental duplication,MONDO,disease,DISEASE_15245
15246,15246,15246,15246,15246,15246,15246,15246,MONDO:0010825,atrioventricular defect-blepharophimosis-radial and anal defect syndrome,MONDO,disease,DISEASE_15246
15247,15247,15247,15247,15247,15247,15247,15247,MONDO:0013840,encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome,MONDO,disease,DISEASE_15247
15248,15248,15248,15248,15248,15248,15248,15248,MONDO:0007130_MONDO:0017705_MONDO:0020295_MONDO:0020453,congenital total pulmonary venous return anomaly,MONDO_grouped,disease,DISEASE_15248
15249,15249,15249,15249,15249,15249,15249,15249,MONDO:0009955,rapadilino syndrome,MONDO,disease,DISEASE_15249
15250,15250,15250,15250,15250,15250,15250,15250,MONDO:0958095,"Nodal T-follicular helper cell lymphoma, follicular type",MONDO,disease,DISEASE_15250
15251,15251,15251,15251,15251,15251,15251,15251,MONDO:0008327,exfoliation syndrome,MONDO,disease,DISEASE_15251
15252,15252,15252,15252,15252,15252,15252,15252,MONDO:0015104_MONDO:1010706_MONDO:1010707,porphyria cutanea tarda,MONDO_grouped,disease,DISEASE_15252
15253,15253,15253,15253,15253,15253,15253,15253,MONDO:0009296_MONDO:0045010,glycoprotein storage disease,MONDO_grouped,disease,DISEASE_15253
15254,15254,15254,15254,15254,15254,15254,15254,MONDO:0025293,poult enteritis mortality syndrome,MONDO,disease,DISEASE_15254
15255,15255,15255,15255,15255,15255,15255,15255,MONDO:1011576,"neuronal ceroid lipofuscinosis, peach-faced lovebird",MONDO,disease,DISEASE_15255
15256,15256,15256,15256,15256,15256,15256,15256,MONDO:0006941,rat-bite fever,MONDO,disease,DISEASE_15256
15257,15257,15257,15257,15257,15257,15257,15257,MONDO:1010229,"dysautonomia, non-human animal",MONDO,disease,DISEASE_15257
15258,15258,15258,15258,15258,15258,15258,15258,MONDO:0859221,Yoon-Bellen neurodevelopmental syndrome,MONDO,disease,DISEASE_15258
15259,15259,15259,15259,15259,15259,15259,15259,MONDO:0013238,chromosome 17q23.1-q23.2 deletion syndrome,MONDO,disease,DISEASE_15259
15260,15260,15260,15260,15260,15260,15260,15260,MONDO:0002979,papillary squamous carcinoma,MONDO,disease,DISEASE_15260
15261,15261,15261,15261,15261,15261,15261,15261,MONDO:1011358,"skin appendage disorder, non-human animal",MONDO,disease,DISEASE_15261
15262,15262,15262,15262,15262,15262,15262,15262,MONDO:0859375,"developmental delay with hypotonia, myopathy, and brain abnormalities",MONDO,disease,DISEASE_15262
15263,15263,15263,15263,15263,15263,15263,15263,MONDO:0019255,sphingolipidosis,MONDO,disease,DISEASE_15263
15264,15264,15264,15264,15264,15264,15264,15264,MONDO:0019606_MONDO:0005576,simple cryoglobulinemia,MONDO_grouped,disease,DISEASE_15264
15265,15265,15265,15265,15265,15265,15265,15265,MONDO:0975755,eccrine angiomatous hamartoma,MONDO,disease,DISEASE_15265
15266,15266,15266,15266,15266,15266,15266,15266,MONDO:0003433,water-clear cell adenoma,MONDO,disease,DISEASE_15266
15267,15267,15267,15267,15267,15267,15267,15267,MONDO:1012366,"melanoblastoma, pig",MONDO,disease,DISEASE_15267
15268,15268,15268,15268,15268,15268,15268,15268,MONDO:1011721,"subclinical hypomagnesemia, non-human animal",MONDO,disease,DISEASE_15268
15269,15269,15269,15269,15269,15269,15269,15269,MONDO:0001611,phlegmonous dacryocystitis,MONDO,disease,DISEASE_15269
15270,15270,15270,15270,15270,15270,15270,15270,MONDO:1011360,"syndromic disease, non-human animal",MONDO,disease,DISEASE_15270
15271,15271,15271,15271,15271,15271,15271,15271,MONDO:0004705,liver solitary fibrous tumor,MONDO,disease,DISEASE_15271
15272,15272,15272,15272,15272,15272,15272,15272,MONDO:0017564_MONDO:0017565_MONDO:0017566_MONDO:0017567,"macrodactyly of fingers, unilateral",MONDO_grouped,disease,DISEASE_15272
15273,15273,15273,15273,15273,15273,15273,15273,MONDO:0001806,vaginal squamous tumor,MONDO,disease,DISEASE_15273
15274,15274,15274,15274,15274,15274,15274,15274,MONDO:0025066,"epidermitis, exudative, of swine",MONDO,disease,DISEASE_15274
15275,15275,15275,15275,15275,15275,15275,15275,MONDO:0012407,pyridoxal phosphate-responsive seizures,MONDO,disease,DISEASE_15275
15276,15276,15276,15276,15276,15276,15276,15276,MONDO:0006759,femoral neuropathy,MONDO,disease,DISEASE_15276
15277,15277,15277,15277,15277,15277,15277,15277,MONDO:0035940,B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2),MONDO,disease,DISEASE_15277
15278,15278,15278,15278,15278,15278,15278,15278,MONDO:0020493,Haddad syndrome,MONDO,disease,DISEASE_15278
15279,15279,15279,15279,15279,15279,15279,15279,MONDO:0009400_MONDO:0009401_MONDO:0007752_MONDO:0023419,hyperprolinemia,MONDO_grouped,disease,DISEASE_15279
15280,15280,15280,15280,15280,15280,15280,15280,MONDO:0956990_MONDO:0956991,"supratentorial ependymoma, ZFTA fusion–positive",MONDO_grouped,disease,DISEASE_15280
15281,15281,15281,15281,15281,15281,15281,15281,MONDO:0007118,isolated anhidrosis with normal sweat glands,MONDO,disease,DISEASE_15281
15282,15282,15282,15282,15282,15282,15282,15282,MONDO:0005449,conduction system disorder,MONDO,disease,DISEASE_15282
15283,15283,15283,15283,15283,15283,15283,15283,MONDO:0003460_MONDO:0003693,clear cell adenofibroma,MONDO_grouped,disease,DISEASE_15283
15284,15284,15284,15284,15284,15284,15284,15284,MONDO:0002671,signet ring cell breast carcinoma,MONDO,disease,DISEASE_15284
15285,15285,15285,15285,15285,15285,15285,15285,MONDO:0005546,fibromyalgia,MONDO,disease,DISEASE_15285
15286,15286,15286,15286,15286,15286,15286,15286,MONDO:0006922,Anaplasmataceae infectious disease,MONDO,disease,DISEASE_15286
15287,15287,15287,15287,15287,15287,15287,15287,MONDO:0100457,"achalasia, familial esophageal",MONDO,disease,DISEASE_15287
15288,15288,15288,15288,15288,15288,15288,15288,MONDO:1012633,"XX difference of sexual development, dog",MONDO,disease,DISEASE_15288
15289,15289,15289,15289,15289,15289,15289,15289,MONDO:0017349,myopericytoma,MONDO,disease,DISEASE_15289
15290,15290,15290,15290,15290,15290,15290,15290,MONDO:0700053_MONDO:0700049_MONDO:0700050,"viral infectious disease, non-human animal",MONDO_grouped,disease,DISEASE_15290
15291,15291,15291,15291,15291,15291,15291,15291,MONDO:0850197,medulloblastoma SHH activated,MONDO,disease,DISEASE_15291
15292,15292,15292,15292,15292,15292,15292,15292,MONDO:1011718,"Kurosawa and Kusanagi hypercholesterolaemia, non-human animal",MONDO,disease,DISEASE_15292
15293,15293,15293,15293,15293,15293,15293,15293,MONDO:0003437,occult small cell lung carcinoma,MONDO,disease,DISEASE_15293
15294,15294,15294,15294,15294,15294,15294,15294,MONDO:0000913_MONDO:0012981_MONDO:0012985_MONDO:0010053_MONDO:0008447_MONDO:0019350_MONDO:0000094,hereditary spherocytosis,MONDO_grouped,disease,DISEASE_15294
15295,15295,15295,15295,15295,15295,15295,15295,MONDO:0019397,unknown leukodystrophy,MONDO,disease,DISEASE_15295
15296,15296,15296,15296,15296,15296,15296,15296,MONDO:0032645,trichohepatoneurodevelopmental syndrome,MONDO,disease,DISEASE_15296
15297,15297,15297,15297,15297,15297,15297,15297,MONDO:0012192,permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome,MONDO,disease,DISEASE_15297
15298,15298,15298,15298,15298,15298,15298,15298,MONDO:0018117,"disorder of phospholipids, sphingolipids and fatty acids biosynthesis",MONDO,disease,DISEASE_15298
15299,15299,15299,15299,15299,15299,15299,15299,MONDO:0002518,gallbladder papillary neoplasm,MONDO,disease,DISEASE_15299
15300,15300,15300,15300,15300,15300,15300,15300,MONDO:1012828_MONDO:1012841,"muscular dystrophy, ANO5-related, rabbit",MONDO_grouped,disease,DISEASE_15300
15301,15301,15301,15301,15301,15301,15301,15301,MONDO:0859515,"congenital myopathy 10b, mild variant",MONDO,disease,DISEASE_15301
15302,15302,15302,15302,15302,15302,15302,15302,MONDO:0000827,salmonellosis,MONDO,disease,DISEASE_15302
15303,15303,15303,15303,15303,15303,15303,15303,MONDO:0800132,autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency,MONDO,disease,DISEASE_15303
15304,15304,15304,15304,15304,15304,15304,15304,MONDO:0011411,Chudley-McCullough syndrome,MONDO,disease,DISEASE_15304
15305,15305,15305,15305,15305,15305,15305,15305,MONDO:0020806,sinoatrial block,MONDO,disease,DISEASE_15305
15306,15306,15306,15306,15306,15306,15306,15306,MONDO:0015454,multiple carboxylase deficiency,MONDO,disease,DISEASE_15306
15307,15307,15307,15307,15307,15307,15307,15307,MONDO:0008199_MONDO:0017279_MONDO:0000828,late-onset Parkinson disease,MONDO_grouped,disease,DISEASE_15307
15308,15308,15308,15308,15308,15308,15308,15308,MONDO:0001609,agranulocytosis,MONDO,disease,DISEASE_15308
15309,15309,15309,15309,15309,15309,15309,15309,MONDO:0005856,Mononegavirales infectious disease,MONDO,disease,DISEASE_15309
15310,15310,15310,15310,15310,15310,15310,15310,MONDO:0024661,tubulovillous adenoma,MONDO,disease,DISEASE_15310
15311,15311,15311,15311,15311,15311,15311,15311,MONDO:0800158,inborn disorder of glutamate/glutamine and aspartate/asparagine metabolism,MONDO,disease,DISEASE_15311
15312,15312,15312,15312,15312,15312,15312,15312,MONDO:0019728_MONDO:0019730,heavy chain deposition disease,MONDO_grouped,disease,DISEASE_15312
15313,15313,15313,15313,15313,15313,15313,15313,MONDO:0020440,persistent left superior vena cava connecting to the left-sided atrium,MONDO,disease,DISEASE_15313
15314,15314,15314,15314,15314,15314,15314,15314,MONDO:0033619,"myopathy, epilepsy, and progressive cerebral atrophy",MONDO,disease,DISEASE_15314
15315,15315,15315,15315,15315,15315,15315,15315,MONDO:1011859,"spastic paresis, non-human animal",MONDO,disease,DISEASE_15315
15316,15316,15316,15316,15316,15316,15316,15316,MONDO:0000675,pain agnosia,MONDO,disease,DISEASE_15316
15317,15317,15317,15317,15317,15317,15317,15317,MONDO:1012235,"renal disease, dog",MONDO,disease,DISEASE_15317
15318,15318,15318,15318,15318,15318,15318,15318,MONDO:0009882,"plasma clot retraction factor, deficiency of",MONDO,disease,DISEASE_15318
15319,15319,15319,15319,15319,15319,15319,15319,MONDO:0018109,fulminant viral hepatitis,MONDO,disease,DISEASE_15319
15320,15320,15320,15320,15320,15320,15320,15320,MONDO:0006199,endometrial undifferentiated carcinoma,MONDO,disease,DISEASE_15320
15321,15321,15321,15321,15321,15321,15321,15321,MONDO:0006811_MONDO:0018624,intracranial hypotension,MONDO_grouped,disease,DISEASE_15321
15322,15322,15322,15322,15322,15322,15322,15322,MONDO:0012205,autosomal dominant striatal neurodegeneration type 1,MONDO,disease,DISEASE_15322
15323,15323,15323,15323,15323,15323,15323,15323,MONDO:0012669,Legius syndrome,MONDO,disease,DISEASE_15323
15324,15324,15324,15324,15324,15324,15324,15324,MONDO:0007396,"dysostosis, Stanescu type",MONDO,disease,DISEASE_15324
15325,15325,15325,15325,15325,15325,15325,15325,MONDO:0010608,Hhhh syndrome,MONDO,disease,DISEASE_15325
15326,15326,15326,15326,15326,15326,15326,15326,MONDO:0002625,Ewing sarcoma of bone,MONDO,disease,DISEASE_15326
15327,15327,15327,15327,15327,15327,15327,15327,MONDO:0044318,intellectual developmental disorder with gastrointestinal difficulties and high pain threshold,MONDO,disease,DISEASE_15327
15328,15328,15328,15328,15328,15328,15328,15328,MONDO:0001199,dislocation of ear ossicle,MONDO,disease,DISEASE_15328
15329,15329,15329,15329,15329,15329,15329,15329,MONDO:0007859,"palmoplantar keratoderma i, striate, focal, or diffuse",MONDO,disease,DISEASE_15329
15330,15330,15330,15330,15330,15330,15330,15330,MONDO:0019120,pili bifurcati,MONDO,disease,DISEASE_15330
15331,15331,15331,15331,15331,15331,15331,15331,MONDO:0018048,heparin-induced thrombocytopenia,MONDO,disease,DISEASE_15331
15332,15332,15332,15332,15332,15332,15332,15332,MONDO:0019726_MONDO:0019727,type II mixed cryoglobulinemia,MONDO_grouped,disease,DISEASE_15332
15333,15333,15333,15333,15333,15333,15333,15333,MONDO:1010961,"prostate cancer, dog",MONDO,disease,DISEASE_15333
15334,15334,15334,15334,15334,15334,15334,15334,MONDO:0006414_MONDO:0005089_MONDO:0004309,skin sarcoma,MONDO_grouped,disease,DISEASE_15334
15335,15335,15335,15335,15335,15335,15335,15335,MONDO:0700155,canine thyroid adenocarcinoma,MONDO,disease,DISEASE_15335
15336,15336,15336,15336,15336,15336,15336,15336,MONDO:0018086,ulerythema ophryogenesis,MONDO,disease,DISEASE_15336
15337,15337,15337,15337,15337,15337,15337,15337,MONDO:0007847,keloid formation,MONDO,disease,DISEASE_15337
15338,15338,15338,15338,15338,15338,15338,15338,MONDO:0009227_MONDO:0014122,"myofibromatosis, infantile",MONDO_grouped,disease,DISEASE_15338
15339,15339,15339,15339,15339,15339,15339,15339,MONDO:0012373,"ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features",MONDO,disease,DISEASE_15339
15340,15340,15340,15340,15340,15340,15340,15340,MONDO:0044889,high grade B-cell lymphoma,MONDO,disease,DISEASE_15340
15341,15341,15341,15341,15341,15341,15341,15341,MONDO:0035879,granuloma faciale,MONDO,disease,DISEASE_15341
15342,15342,15342,15342,15342,15342,15342,15342,MONDO:0006793,hyperpituitarism,MONDO,disease,DISEASE_15342
15343,15343,15343,15343,15343,15343,15343,15343,MONDO:0030060,neurodevelopmental disorder with language impairment and behavioral abnormalities,MONDO,disease,DISEASE_15343
15344,15344,15344,15344,15344,15344,15344,15344,MONDO:0017291,reversible cerebral vasoconstriction syndrome,MONDO,disease,DISEASE_15344
15345,15345,15345,15345,15345,15345,15345,15345,MONDO:0006435,submandibular gland adenocarcinoma,MONDO,disease,DISEASE_15345
15346,15346,15346,15346,15346,15346,15346,15346,MONDO:0018826,Lewis-Sumner syndrome,MONDO,disease,DISEASE_15346
15347,15347,15347,15347,15347,15347,15347,15347,MONDO:0032773,uridine-cytidineuria,MONDO,disease,DISEASE_15347
15348,15348,15348,15348,15348,15348,15348,15348,MONDO:0014931,Alazami-Yuan syndrome,MONDO,disease,DISEASE_15348
15349,15349,15349,15349,15349,15349,15349,15349,MONDO:0012613_MONDO:0030912_MONDO:0013785_MONDO:0014580_MONDO:0014354_MONDO:0030918_MONDO:0020846_MONDO:0014348_MONDO:0013651_MONDO:0013694_MONDO:0012612_MONDO:0012614_MONDO:0014649_MONDO:0014357_MONDO:0014815_MONDO:0012615_MONDO:0012619_MONDO:0012618_MONDO:0044313_MONDO:0013581_MONDO:0030916_MONDO:0014499_MONDO:0020847_MONDO:0030913_MONDO:0013266_MONDO:0012617_MONDO:0014759_MONDO:0013819_MONDO:0014930_MONDO:0014842_MONDO:0013805_MONDO:0015020_MONDO:0013173_MONDO:0013509_MONDO:0013704_MONDO:0012869_MONDO:0013528_MONDO:0014524_MONDO:0013705_MONDO:0014855_MONDO:0013703_MONDO:0032605_MONDO:0009580_MONDO:0014617_MONDO:0014996_MONDO:0013629_MONDO:0014599_MONDO:0013702_MONDO:0013820_MONDO:0013706_MONDO:0013707_MONDO:0014858_MONDO:0013821_MONDO:0013709_MONDO:0030922_MONDO:0013708_MONDO:0014699_MONDO:0030910_MONDO:0014409_MONDO:0013656_MONDO:0012623_MONDO:0012037_MONDO:0007974_MONDO:0013655_MONDO:0030911_MONDO:0054861_MONDO:0014678_MONDO:0013657_MONDO:0030917_MONDO:0020850_MONDO:0013658_MONDO:0014482_MONDO:0014486_MONDO:0013697_MONDO:0014876_MONDO:0030920_MONDO:0030919_MONDO:0030915_MONDO:0014430_MONDO:0054837_MONDO:0012946_MONDO:0014962_MONDO:0012960_MONDO:0011828_MONDO:0012947_MONDO:0014832_MONDO:0100172,"intellectual disability, autosomal recessive",MONDO_grouped,disease,DISEASE_15349
15350,15350,15350,15350,15350,15350,15350,15350,MONDO:0019130,tubular renal disease-cardiomyopathy syndrome,MONDO,disease,DISEASE_15350
15351,15351,15351,15351,15351,15351,15351,15351,MONDO:0008995,Yunis-Varon syndrome,MONDO,disease,DISEASE_15351
15352,15352,15352,15352,15352,15352,15352,15352,MONDO:0007671,fibronectin glomerulopathy,MONDO,disease,DISEASE_15352
15353,15353,15353,15353,15353,15353,15353,15353,MONDO:0019209,Japanese encephalitis,MONDO,disease,DISEASE_15353
15354,15354,15354,15354,15354,15354,15354,15354,MONDO:0016927,partial duplication of chromosome 6,MONDO,disease,DISEASE_15354
15355,15355,15355,15355,15355,15355,15355,15355,MONDO:0100225,collagen 6-related myopathy,MONDO,disease,DISEASE_15355
15356,15356,15356,15356,15356,15356,15356,15356,MONDO:0007718,"hepatic adenomas, familial",MONDO,disease,DISEASE_15356
15357,15357,15357,15357,15357,15357,15357,15357,MONDO:0015240,digitotalar dysmorphism,MONDO,disease,DISEASE_15357
15358,15358,15358,15358,15358,15358,15358,15358,MONDO:0009836,"pancreatitis, sclerosing cholangitis, and sicca complex",MONDO,disease,DISEASE_15358
15359,15359,15359,15359,15359,15359,15359,15359,MONDO:0032916,Imagawa-Matsumoto syndrome,MONDO,disease,DISEASE_15359
15360,15360,15360,15360,15360,15360,15360,15360,MONDO:0011734,Cardioneuromyopathy with hyaline masses and nemaline rods,MONDO,disease,DISEASE_15360
15361,15361,15361,15361,15361,15361,15361,15361,MONDO:0040503_MONDO:0054740_MONDO:0007339,blepharocheilodontic syndrome,MONDO_grouped,disease,DISEASE_15361
15362,15362,15362,15362,15362,15362,15362,15362,MONDO:0009910,Wiedemann-Rautenstrauch syndrome,MONDO,disease,DISEASE_15362
15363,15363,15363,15363,15363,15363,15363,15363,MONDO:0007171_MONDO:0014329_MONDO:0015281,atrial standstill,MONDO_grouped,disease,DISEASE_15363
15364,15364,15364,15364,15364,15364,15364,15364,MONDO:0008023,muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome,MONDO,disease,DISEASE_15364
15365,15365,15365,15365,15365,15365,15365,15365,MONDO:0019428,fried syndrome,MONDO,disease,DISEASE_15365
15366,15366,15366,15366,15366,15366,15366,15366,MONDO:1011016_MONDO:1011015_MONDO:1011017_MONDO:1012045_MONDO:1012046_MONDO:1012047_MONDO:1012048_MONDO:1012049_MONDO:1012550,"cerebellar degeneration, dog",MONDO_grouped,disease,DISEASE_15366
15367,15367,15367,15367,15367,15367,15367,15367,MONDO:0006649,anterior ischemic optic neuropathy,MONDO,disease,DISEASE_15367
15368,15368,15368,15368,15368,15368,15368,15368,MONDO:0002974,cervical cancer,MONDO,disease,DISEASE_15368
15369,15369,15369,15369,15369,15369,15369,15369,MONDO:0012456_MONDO:0000365,congenital primary aphakia,MONDO_grouped,disease,DISEASE_15369
15370,15370,15370,15370,15370,15370,15370,15370,MONDO:0007150,arcus senilis,MONDO,disease,DISEASE_15370
15371,15371,15371,15371,15371,15371,15371,15371,MONDO:1011607,"vestibular disease, Sumatran tiger",MONDO,disease,DISEASE_15371
15372,15372,15372,15372,15372,15372,15372,15372,MONDO:1012285,"ventricular arrhythmias and sudden death, dog",MONDO,disease,DISEASE_15372
15373,15373,15373,15373,15373,15373,15373,15373,MONDO:1011661,"esophageal motility disorder, non-human animal",MONDO,disease,DISEASE_15373
15374,15374,15374,15374,15374,15374,15374,15374,MONDO:0019542_MONDO:0002492,acute liver failure,MONDO_grouped,disease,DISEASE_15374
15375,15375,15375,15375,15375,15375,15375,15375,MONDO:0019434,systemic-onset juvenile idiopathic arthritis,MONDO,disease,DISEASE_15375
15376,15376,15376,15376,15376,15376,15376,15376,MONDO:0002989_MONDO:0006717_MONDO:0002990,benign fibrous histiocytoma,MONDO_grouped,disease,DISEASE_15376
15377,15377,15377,15377,15377,15377,15377,15377,MONDO:1011271,"Peters anomaly, snow leopard",MONDO,disease,DISEASE_15377
15378,15378,15378,15378,15378,15378,15378,15378,MONDO:0006506,congenital nonspherocytic hemolytic anemia,MONDO,disease,DISEASE_15378
15379,15379,15379,15379,15379,15379,15379,15379,MONDO:0007070,adiposis dolorosa,MONDO,disease,DISEASE_15379
15380,15380,15380,15380,15380,15380,15380,15380,MONDO:0044345,Schistosoma mansoni infectious disease,MONDO,disease,DISEASE_15380
15381,15381,15381,15381,15381,15381,15381,15381,MONDO:0017235,familial omphalocele syndrome with facial dysmorphism,MONDO,disease,DISEASE_15381
15382,15382,15382,15382,15382,15382,15382,15382,MONDO:0011618,liver fibrocystic disease and polydactyly,MONDO,disease,DISEASE_15382
15383,15383,15383,15383,15383,15383,15383,15383,MONDO:0006589_MONDO:0100505,occupational dermatitis,MONDO_grouped,disease,DISEASE_15383
15384,15384,15384,15384,15384,15384,15384,15384,MONDO:0010200,Wilson disease,MONDO,disease,DISEASE_15384
15385,15385,15385,15385,15385,15385,15385,15385,MONDO:0005936,recurrent pneumonia,MONDO,disease,DISEASE_15385
15386,15386,15386,15386,15386,15386,15386,15386,MONDO:0009060,cystic disease of lung,MONDO,disease,DISEASE_15386
15387,15387,15387,15387,15387,15387,15387,15387,MONDO:0012350,complement factor H deficiency,MONDO,disease,DISEASE_15387
15388,15388,15388,15388,15388,15388,15388,15388,MONDO:0013700,pancreatic triacylglycerol lipase deficiency,MONDO,disease,DISEASE_15388
15389,15389,15389,15389,15389,15389,15389,15389,MONDO:0043087,thickened earlobes with conductive deafness from incus-stapes abnormalities,MONDO,disease,DISEASE_15389
15390,15390,15390,15390,15390,15390,15390,15390,MONDO:0015739_MONDO:0015738,adult-onset nemaline myopathy,MONDO_grouped,disease,DISEASE_15390
15391,15391,15391,15391,15391,15391,15391,15391,MONDO:1011597,"severe combined immunodeficiency disease, horse",MONDO,disease,DISEASE_15391
15392,15392,15392,15392,15392,15392,15392,15392,MONDO:0017077,myelocystocele,MONDO,disease,DISEASE_15392
15393,15393,15393,15393,15393,15393,15393,15393,MONDO:0003140_MONDO:0030700,immune-complex glomerulonephritis,MONDO_grouped,disease,DISEASE_15393
15394,15394,15394,15394,15394,15394,15394,15394,MONDO:0010952,hereditary hyperferritinemia with congenital cataracts,MONDO,disease,DISEASE_15394
15395,15395,15395,15395,15395,15395,15395,15395,MONDO:0020693,glycogen storage disease due to liver phosphorylase kinase deficiency,MONDO,disease,DISEASE_15395
15396,15396,15396,15396,15396,15396,15396,15396,MONDO:0100129,intracranial arachoid cyst,MONDO,disease,DISEASE_15396
15397,15397,15397,15397,15397,15397,15397,15397,MONDO:0001110_MONDO:0003529,chronic pyelonephritis,MONDO_grouped,disease,DISEASE_15397
15398,15398,15398,15398,15398,15398,15398,15398,MONDO:0100420_MONDO:0100425,"acute myeloid leukemia, WT1 gene mutation",MONDO_grouped,disease,DISEASE_15398
15399,15399,15399,15399,15399,15399,15399,15399,MONDO:0001405,dermatophytosis of groin and perianal area,MONDO,disease,DISEASE_15399
15400,15400,15400,15400,15400,15400,15400,15400,MONDO:0001532,capillariasis,MONDO,disease,DISEASE_15400
15401,15401,15401,15401,15401,15401,15401,15401,MONDO:0002457,Treacher-Collins syndrome,MONDO,disease,DISEASE_15401
15402,15402,15402,15402,15402,15402,15402,15402,MONDO:0004188,iris spindle cell melanoma,MONDO,disease,DISEASE_15402
15403,15403,15403,15403,15403,15403,15403,15403,MONDO:0005295,intermittent vascular claudication,MONDO,disease,DISEASE_15403
15404,15404,15404,15404,15404,15404,15404,15404,MONDO:0009522,Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome,MONDO,disease,DISEASE_15404
15405,15405,15405,15405,15405,15405,15405,15405,MONDO:0017196,osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome,MONDO,disease,DISEASE_15405
15406,15406,15406,15406,15406,15406,15406,15406,MONDO:0019478,adult nodular lymphocyte predominant Hodgkin lymphoma,MONDO,disease,DISEASE_15406
15407,15407,15407,15407,15407,15407,15407,15407,MONDO:0008440,spastic paraplegia-nephritis-deafness syndrome,MONDO,disease,DISEASE_15407
15408,15408,15408,15408,15408,15408,15408,15408,MONDO:0010057,"spinal muscular atrophy, Ryukyuan type",MONDO,disease,DISEASE_15408
15409,15409,15409,15409,15409,15409,15409,15409,MONDO:0016847,trisomy 1q,MONDO,disease,DISEASE_15409
15410,15410,15410,15410,15410,15410,15410,15410,MONDO:0013772,Huppke-Brendel syndrome,MONDO,disease,DISEASE_15410
15411,15411,15411,15411,15411,15411,15411,15411,MONDO:1012273_MONDO:1012274,"thrombopathia, dog",MONDO_grouped,disease,DISEASE_15411
15412,15412,15412,15412,15412,15412,15412,15412,MONDO:1011554,"ligneous membranitis, dog",MONDO,disease,DISEASE_15412
15413,15413,15413,15413,15413,15413,15413,15413,MONDO:0044212_MONDO:0044213,chronic idiopathic urticaria,MONDO_grouped,disease,DISEASE_15413
15414,15414,15414,15414,15414,15414,15414,15414,MONDO:0005448,hepatitis C induced liver cirrhosis,MONDO,disease,DISEASE_15414
15415,15415,15415,15415,15415,15415,15415,15415,MONDO:0003208,breast secretory carcinoma,MONDO,disease,DISEASE_15415
15416,15416,15416,15416,15416,15416,15416,15416,MONDO:0014422_MONDO:0012573_MONDO:0010755_MONDO:0008653_MONDO:0013356_MONDO:0006007_MONDO:0013682_MONDO:0013683_MONDO:0013684_MONDO:0014161,vesicoureteral reflux,MONDO_grouped,disease,DISEASE_15416
15417,15417,15417,15417,15417,15417,15417,15417,MONDO:0043735,osteoradionecrosis,MONDO,disease,DISEASE_15417
15418,15418,15418,15418,15418,15418,15418,15418,MONDO:0016497,paraparetic variant of Guillain-Barre syndrome,MONDO,disease,DISEASE_15418
15419,15419,15419,15419,15419,15419,15419,15419,MONDO:0006336,ovarian endometrioid adenocarcinoma with squamous differentiation,MONDO,disease,DISEASE_15419
15420,15420,15420,15420,15420,15420,15420,15420,MONDO:0013787,"psychomotor retardation, epilepsy, and craniofacial dysmorphism",MONDO,disease,DISEASE_15420
15421,15421,15421,15421,15421,15421,15421,15421,MONDO:0003983,synchronous bilateral breast carcinoma,MONDO,disease,DISEASE_15421
15422,15422,15422,15422,15422,15422,15422,15422,MONDO:0007469,double nail for fifth toe,MONDO,disease,DISEASE_15422
15423,15423,15423,15423,15423,15423,15423,15423,MONDO:1012523,"sudden acquired retinal degeneration syndrome, dog",MONDO,disease,DISEASE_15423
15424,15424,15424,15424,15424,15424,15424,15424,MONDO:1011815,"renal cystadenocarcinoma and nodular dermatofibrosis, non-human animal",MONDO,disease,DISEASE_15424
15425,15425,15425,15425,15425,15425,15425,15425,MONDO:0009195,erythema of acral regions,MONDO,disease,DISEASE_15425
15426,15426,15426,15426,15426,15426,15426,15426,MONDO:0033839,osteoradionecrosis of the mandible,MONDO,disease,DISEASE_15426
15427,15427,15427,15427,15427,15427,15427,15427,MONDO:0008875,blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome,MONDO,disease,DISEASE_15427
15428,15428,15428,15428,15428,15428,15428,15428,MONDO:1012554,"atypical myopathy, horse",MONDO,disease,DISEASE_15428
15429,15429,15429,15429,15429,15429,15429,15429,MONDO:0007989,congenital microcoria,MONDO,disease,DISEASE_15429
15430,15430,15430,15430,15430,15430,15430,15430,MONDO:0020658,infiltrating ureter transitional cell carcinoma,MONDO,disease,DISEASE_15430
15431,15431,15431,15431,15431,15431,15431,15431,MONDO:1012124,"hypotrophic axonopathy, Japanese quail",MONDO,disease,DISEASE_15431
15432,15432,15432,15432,15432,15432,15432,15432,MONDO:0001303,abnormal pupillary function,MONDO,disease,DISEASE_15432
15433,15433,15433,15433,15433,15433,15433,15433,MONDO:0005803,hyperinsulinemic hypoglycemia,MONDO,disease,DISEASE_15433
15434,15434,15434,15434,15434,15434,15434,15434,MONDO:0001138_MONDO:0024310,angiodysplasia of intestine,MONDO_grouped,disease,DISEASE_15434
15435,15435,15435,15435,15435,15435,15435,15435,MONDO:0023297,guttate psoriasis,MONDO,disease,DISEASE_15435
15436,15436,15436,15436,15436,15436,15436,15436,MONDO:0021941,infection by Trypanosoma rhodesiense,MONDO,disease,DISEASE_15436
15437,15437,15437,15437,15437,15437,15437,15437,MONDO:0007372,"cornea plana 1, autosomal dominant",MONDO,disease,DISEASE_15437
15438,15438,15438,15438,15438,15438,15438,15438,MONDO:0004696,larynx carcinoma in situ,MONDO,disease,DISEASE_15438
15439,15439,15439,15439,15439,15439,15439,15439,MONDO:0957466,primary tuberculosis of the digestive system,MONDO,disease,DISEASE_15439
15440,15440,15440,15440,15440,15440,15440,15440,MONDO:0008687,Woronets trait,MONDO,disease,DISEASE_15440
15441,15441,15441,15441,15441,15441,15441,15441,MONDO:0005626,epithelial neoplasm,MONDO,disease,DISEASE_15441
15442,15442,15442,15442,15442,15442,15442,15442,MONDO:0958266,immune-mediated scleritis,MONDO,disease,DISEASE_15442
15443,15443,15443,15443,15443,15443,15443,15443,MONDO:1011753,"juvenile with age-dependent emphysema hypotrichosis, non-human animal",MONDO,disease,DISEASE_15443
15444,15444,15444,15444,15444,15444,15444,15444,MONDO:0010221,CHIME syndrome,MONDO,disease,DISEASE_15444
15445,15445,15445,15445,15445,15445,15445,15445,MONDO:0004460,thyroid gland fetal adenoma,MONDO,disease,DISEASE_15445
15446,15446,15446,15446,15446,15446,15446,15446,MONDO:0007062,"adactylia, unilateral",MONDO,disease,DISEASE_15446
15447,15447,15447,15447,15447,15447,15447,15447,MONDO:0002131,jaw cancer,MONDO,disease,DISEASE_15447
15448,15448,15448,15448,15448,15448,15448,15448,MONDO:0800456,SYNCRIP-related neurodevelopmental disorder,MONDO,disease,DISEASE_15448
15449,15449,15449,15449,15449,15449,15449,15449,MONDO:0009129,"dwarfism, proportionate, with hip dislocation",MONDO,disease,DISEASE_15449
15450,15450,15450,15450,15450,15450,15450,15450,MONDO:0021525,benign neoplasm of corpus uteri,MONDO,disease,DISEASE_15450
15451,15451,15451,15451,15451,15451,15451,15451,MONDO:0016884,partial deletion of the short arm of chromosome 2,MONDO,disease,DISEASE_15451
15452,15452,15452,15452,15452,15452,15452,15452,MONDO:0859230,Kury-Isidor syndrome,MONDO,disease,DISEASE_15452
15453,15453,15453,15453,15453,15453,15453,15453,MONDO:0020066_MONDO:1011493_MONDO:1011497_MONDO:1011495_MONDO:0020521_MONDO:0020522_MONDO:1011496,Ehlers-Danlos syndrome,MONDO_grouped,disease,DISEASE_15453
15454,15454,15454,15454,15454,15454,15454,15454,MONDO:0003564,localized pulmonary fibrosis,MONDO,disease,DISEASE_15454
15455,15455,15455,15455,15455,15455,15455,15455,MONDO:0005527_MONDO:0043512,toxic encephalopathy,MONDO_grouped,disease,DISEASE_15455
15456,15456,15456,15456,15456,15456,15456,15456,MONDO:1010299_MONDO:1011972,"osteochondrosis, non-human animal",MONDO_grouped,disease,DISEASE_15456
15457,15457,15457,15457,15457,15457,15457,15457,MONDO:0000520,parietal lobe ependymal tumor,MONDO,disease,DISEASE_15457
15458,15458,15458,15458,15458,15458,15458,15458,MONDO:0001079,pancreatic steatorrhea,MONDO,disease,DISEASE_15458
15459,15459,15459,15459,15459,15459,15459,15459,MONDO:0008257,"platelet responsiveness to adrenaline, depressed",MONDO,disease,DISEASE_15459
15460,15460,15460,15460,15460,15460,15460,15460,MONDO:0024544_MONDO:0014709_MONDO:0100229,obsolete Heimler syndrome,MONDO_grouped,disease,DISEASE_15460
15461,15461,15461,15461,15461,15461,15461,15461,MONDO:0019500_MONDO:0003668,extragonadal teratoma,MONDO_grouped,disease,DISEASE_15461
15462,15462,15462,15462,15462,15462,15462,15462,MONDO:0022755,chromosome 18 mosaic monosomy,MONDO,disease,DISEASE_15462
15463,15463,15463,15463,15463,15463,15463,15463,MONDO:0018513,squamous cell carcinoma of colon,MONDO,disease,DISEASE_15463
15464,15464,15464,15464,15464,15464,15464,15464,MONDO:1010516,"Jacobsen syndrome, cattle",MONDO,disease,DISEASE_15464
15465,15465,15465,15465,15465,15465,15465,15465,MONDO:0009658_MONDO:0011093_MONDO:0009662_MONDO:0009656_MONDO:0009657_MONDO:0009661_MONDO:0030524_MONDO:0009659_MONDO:0009655_MONDO:0010674_MONDO:0009660_MONDO:0015012_MONDO:0018937_MONDO:0018938_MONDO:0001586_MONDO:0019249_MONDO:1012617,mucopolysaccharidosis,MONDO_grouped,disease,DISEASE_15465
15466,15466,15466,15466,15466,15466,15466,15466,MONDO:0030702,autoimmune atherosclerosis,MONDO,disease,DISEASE_15466
15467,15467,15467,15467,15467,15467,15467,15467,MONDO:0016869,partial deletion of chromosome 4,MONDO,disease,DISEASE_15467
15468,15468,15468,15468,15468,15468,15468,15468,MONDO:1010804,"hyperostosis, pig",MONDO,disease,DISEASE_15468
15469,15469,15469,15469,15469,15469,15469,15469,MONDO:0009452,Vici syndrome,MONDO,disease,DISEASE_15469
15470,15470,15470,15470,15470,15470,15470,15470,MONDO:0006056,squamous cell breast carcinoma,MONDO,disease,DISEASE_15470
15471,15471,15471,15471,15471,15471,15471,15471,MONDO:0009191,Lowry-Wood syndrome,MONDO,disease,DISEASE_15471
15472,15472,15472,15472,15472,15472,15472,15472,MONDO:0016147,qualitative or quantitative defects of dystrophin,MONDO,disease,DISEASE_15472
15473,15473,15473,15473,15473,15473,15473,15473,MONDO:0006981,subacute bacterial endocarditis,MONDO,disease,DISEASE_15473
15474,15474,15474,15474,15474,15474,15474,15474,MONDO:0021533,intestinal neuroendocrine tumor G1,MONDO,disease,DISEASE_15474
15475,15475,15475,15475,15475,15475,15475,15475,MONDO:0009324,Hartnup disease,MONDO,disease,DISEASE_15475
15476,15476,15476,15476,15476,15476,15476,15476,MONDO:0006027,breast synovial sarcoma,MONDO,disease,DISEASE_15476
15477,15477,15477,15477,15477,15477,15477,15477,MONDO:0014286_MONDO:0014671_MONDO:0013381_MONDO:0011002_MONDO:0013634_MONDO:0010688_MONDO:0019551_MONDO:0009751,"neuropathy, hereditary sensory,",MONDO_grouped,disease,DISEASE_15477
15478,15478,15478,15478,15478,15478,15478,15478,MONDO:0032600,Snijders Blok-Campeau syndrome,MONDO,disease,DISEASE_15478
15479,15479,15479,15479,15479,15479,15479,15479,MONDO:0008716,acrogeria,MONDO,disease,DISEASE_15479
15480,15480,15480,15480,15480,15480,15480,15480,MONDO:0013208,cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome,MONDO,disease,DISEASE_15480
15481,15481,15481,15481,15481,15481,15481,15481,MONDO:0001554_MONDO:0001553,phacogenic glaucoma,MONDO_grouped,disease,DISEASE_15481
15482,15482,15482,15482,15482,15482,15482,15482,MONDO:1011715,"pseudocholinesterase deficiency, non-human animal",MONDO,disease,DISEASE_15482
15483,15483,15483,15483,15483,15483,15483,15483,MONDO:0006312,myofibroma,MONDO,disease,DISEASE_15483
15484,15484,15484,15484,15484,15484,15484,15484,MONDO:0011090,isolated hereditary congenital facial paralysis,MONDO,disease,DISEASE_15484
15485,15485,15485,15485,15485,15485,15485,15485,MONDO:0004669_MONDO:0001142,salivary gland cancer,MONDO_grouped,disease,DISEASE_15485
15486,15486,15486,15486,15486,15486,15486,15486,MONDO:0017341,virus associated tumor,MONDO,disease,DISEASE_15486
15487,15487,15487,15487,15487,15487,15487,15487,MONDO:0008372,retinal aplasia,MONDO,disease,DISEASE_15487
15488,15488,15488,15488,15488,15488,15488,15488,MONDO:0020545,staphylococcal toxic-shock syndrome,MONDO,disease,DISEASE_15488
15489,15489,15489,15489,15489,15489,15489,15489,MONDO:0011315,Osebold skeletal dysplasia/osteolysis syndrome,MONDO,disease,DISEASE_15489
15490,15490,15490,15490,15490,15490,15490,15490,MONDO:0021209,heart neoplasm,MONDO,disease,DISEASE_15490
15491,15491,15491,15491,15491,15491,15491,15491,MONDO:0008459,spinocerebellar atrophy with pupillary paralysis,MONDO,disease,DISEASE_15491
15492,15492,15492,15492,15492,15492,15492,15492,MONDO:1011052,"polycystic kidney disease, crab-eating macaque",MONDO,disease,DISEASE_15492
15493,15493,15493,15493,15493,15493,15493,15493,MONDO:0016240,hemimelia,MONDO,disease,DISEASE_15493
15494,15494,15494,15494,15494,15494,15494,15494,MONDO:0030986,"blistering, acantholytic, of oral and laryngeal mucosa",MONDO,disease,DISEASE_15494
15495,15495,15495,15495,15495,15495,15495,15495,MONDO:0004211,L-cell glucagon-like peptide-producing neuroendocrine tumor,MONDO,disease,DISEASE_15495
15496,15496,15496,15496,15496,15496,15496,15496,MONDO:1010619,"omphalocele, domestic cat",MONDO,disease,DISEASE_15496
15497,15497,15497,15497,15497,15497,15497,15497,MONDO:0006607_MONDO:0037735,sebaceous gland disorder,MONDO_grouped,disease,DISEASE_15497
15498,15498,15498,15498,15498,15498,15498,15498,MONDO:0009740,neurofaciodigitorenal syndrome,MONDO,disease,DISEASE_15498
15499,15499,15499,15499,15499,15499,15499,15499,MONDO:0004238,petrous apex meningioma,MONDO,disease,DISEASE_15499
15500,15500,15500,15500,15500,15500,15500,15500,MONDO:0017811,severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion,MONDO,disease,DISEASE_15500
15501,15501,15501,15501,15501,15501,15501,15501,MONDO:0010588,"exudative vitreoretinopathy 2, X-linked",MONDO,disease,DISEASE_15501
15502,15502,15502,15502,15502,15502,15502,15502,MONDO:1012412_MONDO:1012649,"type 2 polysaccharide storage myopathy, horse",MONDO_grouped,disease,DISEASE_15502
15503,15503,15503,15503,15503,15503,15503,15503,MONDO:0018177_MONDO:0000460,glioblastoma,MONDO_grouped,disease,DISEASE_15503
15504,15504,15504,15504,15504,15504,15504,15504,MONDO:0004816,refractory plasma cell neoplasm,MONDO,disease,DISEASE_15504
15505,15505,15505,15505,15505,15505,15505,15505,MONDO:0016433,dysmorphism-short stature-deafness-disorder of sex development syndrome,MONDO,disease,DISEASE_15505
15506,15506,15506,15506,15506,15506,15506,15506,MONDO:0003930,non-invasive bladder urothelial carcinoma,MONDO,disease,DISEASE_15506
15507,15507,15507,15507,15507,15507,15507,15507,MONDO:0001805,female breast central part cancer,MONDO,disease,DISEASE_15507
15508,15508,15508,15508,15508,15508,15508,15508,MONDO:1012560,"dysplastic gangliocytoma of the cerebellum, domestic cat",MONDO,disease,DISEASE_15508
15509,15509,15509,15509,15509,15509,15509,15509,MONDO:0015487,fatal infantile encephalocardiomyopathy,MONDO,disease,DISEASE_15509
15510,15510,15510,15510,15510,15510,15510,15510,MONDO:0009840,Partington-Anderson syndrome,MONDO,disease,DISEASE_15510
15511,15511,15511,15511,15511,15511,15511,15511,MONDO:1012818_MONDO:1012819_MONDO:1012820,"hypotrichosis, HR-related, domestic cat",MONDO_grouped,disease,DISEASE_15511
15512,15512,15512,15512,15512,15512,15512,15512,MONDO:0021049,vulvar neoplasm,MONDO,disease,DISEASE_15512
15513,15513,15513,15513,15513,15513,15513,15513,MONDO:0020340,bilateral perisylvian polymicrogyria,MONDO,disease,DISEASE_15513
15514,15514,15514,15514,15514,15514,15514,15514,MONDO:0017107_MONDO:0017108_MONDO:0017109,isolated cerebellar vermis agenesis,MONDO_grouped,disease,DISEASE_15514
15515,15515,15515,15515,15515,15515,15515,15515,MONDO:1011255_MONDO:1011262,"congenital stationary night blindness, TRPM1-related, horse",MONDO_grouped,disease,DISEASE_15515
15516,15516,15516,15516,15516,15516,15516,15516,MONDO:0013493,acetyl-coa carboxylase deficiency,MONDO,disease,DISEASE_15516
15517,15517,15517,15517,15517,15517,15517,15517,MONDO:1011108_MONDO:1011109_MONDO:1011111_MONDO:1011112_MONDO:1011115_MONDO:1011116_MONDO:1011117,"cryptorchidism, dog",MONDO_grouped,disease,DISEASE_15517
15518,15518,15518,15518,15518,15518,15518,15518,MONDO:0700031,mosaic trisomy 18,MONDO,disease,DISEASE_15518
15519,15519,15519,15519,15519,15519,15519,15519,MONDO:0018079,thymic epithelial neoplasm,MONDO,disease,DISEASE_15519
15520,15520,15520,15520,15520,15520,15520,15520,MONDO:0014553,Tenorio syndrome,MONDO,disease,DISEASE_15520
15521,15521,15521,15521,15521,15521,15521,15521,MONDO:0009055,cutis marmorata telangiectatica congenita,MONDO,disease,DISEASE_15521
15522,15522,15522,15522,15522,15522,15522,15522,MONDO:0043777,rhinophyma,MONDO,disease,DISEASE_15522
15523,15523,15523,15523,15523,15523,15523,15523,MONDO:0019024,mast cell sarcoma,MONDO,disease,DISEASE_15523
15524,15524,15524,15524,15524,15524,15524,15524,MONDO:0013722,hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism,MONDO,disease,DISEASE_15524
15525,15525,15525,15525,15525,15525,15525,15525,MONDO:0044646,early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome,MONDO,disease,DISEASE_15525
15526,15526,15526,15526,15526,15526,15526,15526,MONDO:1012396,"reactive perforating collagenosis, domestic cat",MONDO,disease,DISEASE_15526
15527,15527,15527,15527,15527,15527,15527,15527,MONDO:0971043,"neurodevelopmental disorder with hypotonia, feeding difficulties, facial dysmorphism, and brain abnormalities",MONDO,disease,DISEASE_15527
15528,15528,15528,15528,15528,15528,15528,15528,MONDO:0016041,congenital microgastria,MONDO,disease,DISEASE_15528
15529,15529,15529,15529,15529,15529,15529,15529,MONDO:0006641,afferent loop syndrome,MONDO,disease,DISEASE_15529
15530,15530,15530,15530,15530,15530,15530,15530,MONDO:0018661,Zika virus infectious disease,MONDO,disease,DISEASE_15530
15531,15531,15531,15531,15531,15531,15531,15531,MONDO:0004713,lower gum cancer,MONDO,disease,DISEASE_15531
15532,15532,15532,15532,15532,15532,15532,15532,MONDO:0005057,large cell neuroendocrine carcinoma,MONDO,disease,DISEASE_15532
15533,15533,15533,15533,15533,15533,15533,15533,MONDO:0021750,pyonephrosis,MONDO,disease,DISEASE_15533
15534,15534,15534,15534,15534,15534,15534,15534,MONDO:0022919,cytokine receptor deficiency,MONDO,disease,DISEASE_15534
15535,15535,15535,15535,15535,15535,15535,15535,MONDO:0957871_MONDO:0957870_MONDO:0957873_MONDO:0957872_MONDO:0020507_MONDO:0800448,leukoencephalopathy with vanishing white matter,MONDO_grouped,disease,DISEASE_15535
15536,15536,15536,15536,15536,15536,15536,15536,MONDO:1010091,"microtia, non-human animal",MONDO,disease,DISEASE_15536
15537,15537,15537,15537,15537,15537,15537,15537,MONDO:0000330,endemic typhus,MONDO,disease,DISEASE_15537
15538,15538,15538,15538,15538,15538,15538,15538,MONDO:0022337,AIDS dysmorphic syndrome,MONDO,disease,DISEASE_15538
15539,15539,15539,15539,15539,15539,15539,15539,MONDO:0958138,early-onset immune dysregulation due to DOCK11 complete deficiency,MONDO,disease,DISEASE_15539
15540,15540,15540,15540,15540,15540,15540,15540,MONDO:0003607,neuritis of upper limb,MONDO,disease,DISEASE_15540
15541,15541,15541,15541,15541,15541,15541,15541,MONDO:0001240,neonatal anemia,MONDO,disease,DISEASE_15541
15542,15542,15542,15542,15542,15542,15542,15542,MONDO:0017708,mevalonate kinase deficiency,MONDO,disease,DISEASE_15542
15543,15543,15543,15543,15543,15543,15543,15543,MONDO:0041261,disorder of acid-base balance,MONDO,disease,DISEASE_15543
15544,15544,15544,15544,15544,15544,15544,15544,MONDO:0971077,episodic memory defect leukoencephalopathy,MONDO,disease,DISEASE_15544
15545,15545,15545,15545,15545,15545,15545,15545,MONDO:0001547,atrophic nonflaccid tympanic membrane,MONDO,disease,DISEASE_15545
15546,15546,15546,15546,15546,15546,15546,15546,MONDO:0004681,learning disability,MONDO,disease,DISEASE_15546
15547,15547,15547,15547,15547,15547,15547,15547,MONDO:0016447,white fibrous papulosis of the neck,MONDO,disease,DISEASE_15547
15548,15548,15548,15548,15548,15548,15548,15548,MONDO:0021343,carcinoma of floor of mouth,MONDO,disease,DISEASE_15548
15549,15549,15549,15549,15549,15549,15549,15549,MONDO:0017919,exstrophy-epispadias complex,MONDO,disease,DISEASE_15549
15550,15550,15550,15550,15550,15550,15550,15550,MONDO:1012033,"brachycephalic airway obstruction syndrome, domestic cat",MONDO,disease,DISEASE_15550
15551,15551,15551,15551,15551,15551,15551,15551,MONDO:0019665_MONDO:0008274_MONDO:0043168,monostotic fibrous dysplasia,MONDO_grouped,disease,DISEASE_15551
15552,15552,15552,15552,15552,15552,15552,15552,MONDO:0009513,laryngo-onycho-cutaneous syndrome,MONDO,disease,DISEASE_15552
15553,15553,15553,15553,15553,15553,15553,15553,MONDO:0006355,parotid gland acinic cell carcinoma,MONDO,disease,DISEASE_15553
15554,15554,15554,15554,15554,15554,15554,15554,MONDO:0005581,AVL induced bursal lymphoma,MONDO,disease,DISEASE_15554
15555,15555,15555,15555,15555,15555,15555,15555,MONDO:0971128,multiple evanescent white dot syndrome,MONDO,disease,DISEASE_15555
15556,15556,15556,15556,15556,15556,15556,15556,MONDO:0009218,Farber lipogranulomatosis,MONDO,disease,DISEASE_15556
15557,15557,15557,15557,15557,15557,15557,15557,MONDO:0014221,triosephosphate isomerase deficiency,MONDO,disease,DISEASE_15557
15558,15558,15558,15558,15558,15558,15558,15558,MONDO:0003561,malignant giant cell tumor of soft parts,MONDO,disease,DISEASE_15558
15559,15559,15559,15559,15559,15559,15559,15559,MONDO:0020415,Kommerell diverticulum,MONDO,disease,DISEASE_15559
15560,15560,15560,15560,15560,15560,15560,15560,MONDO:0000063,obsolete molybdenum cofactor deficiency,MONDO,disease,DISEASE_15560
15561,15561,15561,15561,15561,15561,15561,15561,MONDO:0021650,uterine corpus neuroendocrine neoplasm,MONDO,disease,DISEASE_15561
15562,15562,15562,15562,15562,15562,15562,15562,MONDO:0009201,"facial abnormalities, kyphoscoliosis, and intellectual disability",MONDO,disease,DISEASE_15562
15563,15563,15563,15563,15563,15563,15563,15563,MONDO:0032781,"congenital hypotonia, epilepsy, developmental delay, and digital anomalies",MONDO,disease,DISEASE_15563
15564,15564,15564,15564,15564,15564,15564,15564,MONDO:0001371,protein-energy malnutrition,MONDO,disease,DISEASE_15564
15565,15565,15565,15565,15565,15565,15565,15565,MONDO:0012596,PSAT deficiency,MONDO,disease,DISEASE_15565
15566,15566,15566,15566,15566,15566,15566,15566,MONDO:0009025,apparent mineralocorticoid excess,MONDO,disease,DISEASE_15566
15567,15567,15567,15567,15567,15567,15567,15567,MONDO:0009946,hemolytic anemia due to pyrimidine 5' nucleotidase deficiency,MONDO,disease,DISEASE_15567
15568,15568,15568,15568,15568,15568,15568,15568,MONDO:0017084,leptomyelolipoma,MONDO,disease,DISEASE_15568
15569,15569,15569,15569,15569,15569,15569,15569,MONDO:0020794,colorectal medullary carcinoma,MONDO,disease,DISEASE_15569
15570,15570,15570,15570,15570,15570,15570,15570,MONDO:0020543,"theca steroid-producing cell malignant tumor of ovary, not further specified",MONDO,disease,DISEASE_15570
15571,15571,15571,15571,15571,15571,15571,15571,MONDO:0018471,generalized eruptive keratoacanthoma,MONDO,disease,DISEASE_15571
15572,15572,15572,15572,15572,15572,15572,15572,MONDO:0019803,angioma serpiginosum,MONDO,disease,DISEASE_15572
15573,15573,15573,15573,15573,15573,15573,15573,MONDO:0003726_MONDO:0004273,apocrine adenosis of breast,MONDO_grouped,disease,DISEASE_15573
15574,15574,15574,15574,15574,15574,15574,15574,MONDO:0012582,interstitial lung disease due to ABCA3 deficiency,MONDO,disease,DISEASE_15574
15575,15575,15575,15575,15575,15575,15575,15575,MONDO:0020665,high grade malignant neoplasm,MONDO,disease,DISEASE_15575
15576,15576,15576,15576,15576,15576,15576,15576,MONDO:0012732,"tremor, hereditary essential, and idiopathic normal pressure hydrocephalus",MONDO,disease,DISEASE_15576
15577,15577,15577,15577,15577,15577,15577,15577,MONDO:0012416,Devriendt syndrome,MONDO,disease,DISEASE_15577
15578,15578,15578,15578,15578,15578,15578,15578,MONDO:0002644,idiopathic granulomatous myositis,MONDO,disease,DISEASE_15578
15579,15579,15579,15579,15579,15579,15579,15579,MONDO:0002298_MONDO:0024323_MONDO:0024325,cutaneous glomangioma,MONDO_grouped,disease,DISEASE_15579
15580,15580,15580,15580,15580,15580,15580,15580,MONDO:0017747,disorder of fucoglycosan synthesis,MONDO,disease,DISEASE_15580
15581,15581,15581,15581,15581,15581,15581,15581,MONDO:0012687,familial cavitary optic disk anomaly,MONDO,disease,DISEASE_15581
15582,15582,15582,15582,15582,15582,15582,15582,MONDO:0008986,circumvallate placenta syndrome,MONDO,disease,DISEASE_15582
15583,15583,15583,15583,15583,15583,15583,15583,MONDO:0005509_MONDO:0002637,histiocytoma,MONDO_grouped,disease,DISEASE_15583
15584,15584,15584,15584,15584,15584,15584,15584,MONDO:0034021,spondylodysplastic Ehlers-Danlos syndrome,MONDO,disease,DISEASE_15584
15585,15585,15585,15585,15585,15585,15585,15585,MONDO:0020656,human papillomavirus-related penile squamous cell carcinoma,MONDO,disease,DISEASE_15585
15586,15586,15586,15586,15586,15586,15586,15586,MONDO:0010528,anosmia,MONDO,disease,DISEASE_15586
15587,15587,15587,15587,15587,15587,15587,15587,MONDO:0010578,deafness dystonia syndrome,MONDO,disease,DISEASE_15587
15588,15588,15588,15588,15588,15588,15588,15588,MONDO:0005364,Graves disease,MONDO,disease,DISEASE_15588
15589,15589,15589,15589,15589,15589,15589,15589,MONDO:0015978,functional neutrophil defect,MONDO,disease,DISEASE_15589
15590,15590,15590,15590,15590,15590,15590,15590,MONDO:1012458,"hemangiosarcoma, orange-winged Amazon parrot",MONDO,disease,DISEASE_15590
15591,15591,15591,15591,15591,15591,15591,15591,MONDO:0010541,X-linked calvarial hyperostosis,MONDO,disease,DISEASE_15591
15592,15592,15592,15592,15592,15592,15592,15592,MONDO:0019316,maculopapular cutaneous mastocytosis,MONDO,disease,DISEASE_15592
15593,15593,15593,15593,15593,15593,15593,15593,MONDO:0002755,solitary osseous plasmacytoma,MONDO,disease,DISEASE_15593
15594,15594,15594,15594,15594,15594,15594,15594,MONDO:0000709,Crohn ileitis,MONDO,disease,DISEASE_15594
15595,15595,15595,15595,15595,15595,15595,15595,MONDO:0001032,Mooren ulcer,MONDO,disease,DISEASE_15595
15596,15596,15596,15596,15596,15596,15596,15596,MONDO:0021824,"adult progressive spinal muscular atrophy, Aran Duchenne type",MONDO,disease,DISEASE_15596
15597,15597,15597,15597,15597,15597,15597,15597,MONDO:0017317_MONDO:0017318,phakomatosis pigmentokeratotica,MONDO_grouped,disease,DISEASE_15597
15598,15598,15598,15598,15598,15598,15598,15598,MONDO:0018755,scorpion envenomation,MONDO,disease,DISEASE_15598
15599,15599,15599,15599,15599,15599,15599,15599,MONDO:0018341,3q27.3 microdeletion syndrome,MONDO,disease,DISEASE_15599
15600,15600,15600,15600,15600,15600,15600,15600,MONDO:0004744,borderline glaucoma,MONDO,disease,DISEASE_15600
15601,15601,15601,15601,15601,15601,15601,15601,MONDO:0017837,multiple sclerosis-ichthyosis-factor VIII deficiency syndrome,MONDO,disease,DISEASE_15601
15602,15602,15602,15602,15602,15602,15602,15602,MONDO:0044740,salivary gland squamous cell carcinoma,MONDO,disease,DISEASE_15602
15603,15603,15603,15603,15603,15603,15603,15603,MONDO:0001258_MONDO:0001631_MONDO:1040011,vertebral artery occlusion,MONDO_grouped,disease,DISEASE_15603
15604,15604,15604,15604,15604,15604,15604,15604,MONDO:0001244,vitamin K deficiency hemorrhagic disease,MONDO,disease,DISEASE_15604
15605,15605,15605,15605,15605,15605,15605,15605,MONDO:0002163,thymus lipoma,MONDO,disease,DISEASE_15605
15606,15606,15606,15606,15606,15606,15606,15606,MONDO:0007259,craniofaciofrontodigital syndrome,MONDO,disease,DISEASE_15606
15607,15607,15607,15607,15607,15607,15607,15607,MONDO:0017843,congenital pulmonary sequestration,MONDO,disease,DISEASE_15607
15608,15608,15608,15608,15608,15608,15608,15608,MONDO:0100047_MONDO:0011556_MONDO:0013876_MONDO:0013101_MONDO:0013102_MONDO:0013104_MONDO:0013105_MONDO:0013106,"basal cell carcinoma, susceptibility to",MONDO_grouped,disease,DISEASE_15608
15609,15609,15609,15609,15609,15609,15609,15609,MONDO:0011227,short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome,MONDO,disease,DISEASE_15609
15610,15610,15610,15610,15610,15610,15610,15610,MONDO:0023099,FRAXD syndrome,MONDO,disease,DISEASE_15610
15611,15611,15611,15611,15611,15611,15611,15611,MONDO:0017904,steroid dehydrogenase deficiency-dental anomalies syndrome,MONDO,disease,DISEASE_15611
15612,15612,15612,15612,15612,15612,15612,15612,MONDO:0007663,glaucoma with elevated episcleral venous pressure,MONDO,disease,DISEASE_15612
15613,15613,15613,15613,15613,15613,15613,15613,MONDO:0005167,fibroma,MONDO,disease,DISEASE_15613
15614,15614,15614,15614,15614,15614,15614,15614,MONDO:0024418,muscular fibrosis multifocal obstructed vessels,MONDO,disease,DISEASE_15614
15615,15615,15615,15615,15615,15615,15615,15615,MONDO:0010029_MONDO:1010624,situs inversus,MONDO_grouped,disease,DISEASE_15615
15616,15616,15616,15616,15616,15616,15616,15616,MONDO:0000981,Histoplasma pericarditis,MONDO,disease,DISEASE_15616
15617,15617,15617,15617,15617,15617,15617,15617,MONDO:0003982,bilateral breast carcinoma,MONDO,disease,DISEASE_15617
15618,15618,15618,15618,15618,15618,15618,15618,MONDO:1012646,"autosomal dominant nephritis, dog",MONDO,disease,DISEASE_15618
15619,15619,15619,15619,15619,15619,15619,15619,MONDO:0024953,"lameness, non-human animal",MONDO,disease,DISEASE_15619
15620,15620,15620,15620,15620,15620,15620,15620,MONDO:0004612,malignant histiocytosis,MONDO,disease,DISEASE_15620
15621,15621,15621,15621,15621,15621,15621,15621,MONDO:0006091,appendix neuroendocrine tumor G1,MONDO,disease,DISEASE_15621
15622,15622,15622,15622,15622,15622,15622,15622,MONDO:0017357,transient hyperammonemia of the newborn,MONDO,disease,DISEASE_15622
15623,15623,15623,15623,15623,15623,15623,15623,MONDO:0009281,glutaryl-CoA dehydrogenase deficiency,MONDO,disease,DISEASE_15623
15624,15624,15624,15624,15624,15624,15624,15624,MONDO:0014487,congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome,MONDO,disease,DISEASE_15624
15625,15625,15625,15625,15625,15625,15625,15625,MONDO:0018800,Kallmann syndrome,MONDO,disease,DISEASE_15625
15626,15626,15626,15626,15626,15626,15626,15626,MONDO:0023084,epiphyseal dysplasia dysmorphism camptodactyly,MONDO,disease,DISEASE_15626
15627,15627,15627,15627,15627,15627,15627,15627,MONDO:0006173,conjunctival squamous cell carcinoma,MONDO,disease,DISEASE_15627
15628,15628,15628,15628,15628,15628,15628,15628,MONDO:0001994,sphenoidal sinus cancer,MONDO,disease,DISEASE_15628
15629,15629,15629,15629,15629,15629,15629,15629,MONDO:0005092,signet ring cell carcinoma,MONDO,disease,DISEASE_15629
15630,15630,15630,15630,15630,15630,15630,15630,MONDO:0025506,porcine postweaning multisystemic wasting syndrome,MONDO,disease,DISEASE_15630
15631,15631,15631,15631,15631,15631,15631,15631,MONDO:0042960,Sackey-Sakati-Aur syndrome,MONDO,disease,DISEASE_15631
15632,15632,15632,15632,15632,15632,15632,15632,MONDO:0011349,"osteoma of cranial vault, familial",MONDO,disease,DISEASE_15632
15633,15633,15633,15633,15633,15633,15633,15633,MONDO:0859249,parenti-mignot neurodevelopmental syndrome,MONDO,disease,DISEASE_15633
15634,15634,15634,15634,15634,15634,15634,15634,MONDO:0014391,severe combined immunodeficiency due to CTPS1 deficiency,MONDO,disease,DISEASE_15634
15635,15635,15635,15635,15635,15635,15635,15635,MONDO:0014483,retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies,MONDO,disease,DISEASE_15635
15636,15636,15636,15636,15636,15636,15636,15636,MONDO:0007346,cochleosaccular degeneration-cataract syndrome,MONDO,disease,DISEASE_15636
15637,15637,15637,15637,15637,15637,15637,15637,MONDO:0024626_MONDO:0024632,defective phagocytic cell engulfment,MONDO_grouped,disease,DISEASE_15637
15638,15638,15638,15638,15638,15638,15638,15638,MONDO:0060596_MONDO:0032855_MONDO:0044319_MONDO:0032820_MONDO:0060763,neurodevelopmental disorder with dysmorphic facies and distal limb anomalies,MONDO_grouped,disease,DISEASE_15638
15639,15639,15639,15639,15639,15639,15639,15639,MONDO:0016146_MONDO:0100153,caveolinopathy,MONDO_grouped,disease,DISEASE_15639
15640,15640,15640,15640,15640,15640,15640,15640,MONDO:0013960,sinoatrial node dysfunction and deafness,MONDO,disease,DISEASE_15640
15641,15641,15641,15641,15641,15641,15641,15641,MONDO:0016961,partial duplication of the long arm of chromosome 10,MONDO,disease,DISEASE_15641
15642,15642,15642,15642,15642,15642,15642,15642,MONDO:1012847,"cerebral dysgenesis, PEA15 related, domestic cat",MONDO,disease,DISEASE_15642
15643,15643,15643,15643,15643,15643,15643,15643,MONDO:0004324,testicular fibroma,MONDO,disease,DISEASE_15643
15644,15644,15644,15644,15644,15644,15644,15644,MONDO:0800176,black widow spider envenomation,MONDO,disease,DISEASE_15644
15645,15645,15645,15645,15645,15645,15645,15645,MONDO:0013812_MONDO:0009470,Baraitser-winter syndrome,MONDO_grouped,disease,DISEASE_15645
15646,15646,15646,15646,15646,15646,15646,15646,MONDO:0004151,spinal meninges cancer,MONDO,disease,DISEASE_15646
15647,15647,15647,15647,15647,15647,15647,15647,MONDO:0008888,Williams-Campbell syndrome,MONDO,disease,DISEASE_15647
15648,15648,15648,15648,15648,15648,15648,15648,MONDO:0958123,isolated pulmonary artery sling,MONDO,disease,DISEASE_15648
15649,15649,15649,15649,15649,15649,15649,15649,MONDO:0016960,partial trisomy of the long arm of chromosome 9,MONDO,disease,DISEASE_15649
15650,15650,15650,15650,15650,15650,15650,15650,MONDO:0001332,palindromic rheumatism,MONDO,disease,DISEASE_15650
15651,15651,15651,15651,15651,15651,15651,15651,MONDO:0002447,endometrial carcinoma,MONDO,disease,DISEASE_15651
15652,15652,15652,15652,15652,15652,15652,15652,MONDO:0009621,microcephaly-cervical spine fusion anomalies syndrome,MONDO,disease,DISEASE_15652
15653,15653,15653,15653,15653,15653,15653,15653,MONDO:0017229,distal monosomy 12p,MONDO,disease,DISEASE_15653
15654,15654,15654,15654,15654,15654,15654,15654,MONDO:0032679_MONDO:0859323_MONDO:0030020_MONDO:0033569_MONDO:0030017_MONDO:0033570_MONDO:0859228_MONDO:0030378_MONDO:0030311_MONDO:0014269_MONDO:0030006_MONDO:0054741_MONDO:0859337_MONDO:0033631_MONDO:0054742_MONDO:0033534_MONDO:0033533_MONDO:0030543_MONDO:0014775_MONDO:0014781_MONDO:0032726_MONDO:0032712_MONDO:0054654_MONDO:0033537_MONDO:0030007_MONDO:0030008_MONDO:0054677_MONDO:0020727_MONDO:0054781_MONDO:0957537_MONDO:0957992_MONDO:0033566_MONDO:0000732,combined oxidative phosphorylation deficiency,MONDO_grouped,disease,DISEASE_15654
15655,15655,15655,15655,15655,15655,15655,15655,MONDO:0007669,renal cysts and diabetes syndrome,MONDO,disease,DISEASE_15655
15656,15656,15656,15656,15656,15656,15656,15656,MONDO:0001263,histoplasmosis retinitis,MONDO,disease,DISEASE_15656
15657,15657,15657,15657,15657,15657,15657,15657,MONDO:0004382,laryngeal disorder,MONDO,disease,DISEASE_15657
15658,15658,15658,15658,15658,15658,15658,15658,MONDO:0015085,bathing suit ichthyosis,MONDO,disease,DISEASE_15658
15659,15659,15659,15659,15659,15659,15659,15659,MONDO:0042487,uterine cervix carcinoma in situ,MONDO,disease,DISEASE_15659
15660,15660,15660,15660,15660,15660,15660,15660,MONDO:0043135,microcephaly microphthalmos blindness,MONDO,disease,DISEASE_15660
15661,15661,15661,15661,15661,15661,15661,15661,MONDO:1012389,"exercise-induced collapse, dog",MONDO,disease,DISEASE_15661
15662,15662,15662,15662,15662,15662,15662,15662,MONDO:0015082,alopecia antibody deficiency,MONDO,disease,DISEASE_15662
15663,15663,15663,15663,15663,15663,15663,15663,MONDO:0010981,absent tibia-polydactyly-arachnoid cyst syndrome,MONDO,disease,DISEASE_15663
15664,15664,15664,15664,15664,15664,15664,15664,MONDO:0012061,familial sick sinus syndrome,MONDO,disease,DISEASE_15664
15665,15665,15665,15665,15665,15665,15665,15665,MONDO:0016419,hereditary breast carcinoma,MONDO,disease,DISEASE_15665
15666,15666,15666,15666,15666,15666,15666,15666,MONDO:0009971,respiratory distress syndrome in premature infants,MONDO,disease,DISEASE_15666
15667,15667,15667,15667,15667,15667,15667,15667,MONDO:0030947,"neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities",MONDO,disease,DISEASE_15667
15668,15668,15668,15668,15668,15668,15668,15668,MONDO:0006625,altitude sickness,MONDO,disease,DISEASE_15668
15669,15669,15669,15669,15669,15669,15669,15669,MONDO:0001093,colonic lymphangioma,MONDO,disease,DISEASE_15669
15670,15670,15670,15670,15670,15670,15670,15670,MONDO:0001187_MONDO:0006026_MONDO:0004272,urinary bladder cancer,MONDO_grouped,disease,DISEASE_15670
15671,15671,15671,15671,15671,15671,15671,15671,MONDO:0010519,alpha thalassemia-X-linked intellectual disability syndrome,MONDO,disease,DISEASE_15671
15672,15672,15672,15672,15672,15672,15672,15672,MONDO:0013364,Rubinstein-Taybi syndrome due to EP300 haploinsufficiency,MONDO,disease,DISEASE_15672
15673,15673,15673,15673,15673,15673,15673,15673,MONDO:0001361,spontaneous ocular nystagmus,MONDO,disease,DISEASE_15673
15674,15674,15674,15674,15674,15674,15674,15674,MONDO:1010083,"Scott Syndrome, non-human animal",MONDO,disease,DISEASE_15674
15675,15675,15675,15675,15675,15675,15675,15675,MONDO:0004413,cervical non-keratinizing squamous cell carcinoma,MONDO,disease,DISEASE_15675
15676,15676,15676,15676,15676,15676,15676,15676,MONDO:0021636,astrocytic tumor,MONDO,disease,DISEASE_15676
15677,15677,15677,15677,15677,15677,15677,15677,MONDO:0032787,holoprosencephaly 12 with or without pancreatic agenesis,MONDO,disease,DISEASE_15677
15678,15678,15678,15678,15678,15678,15678,15678,MONDO:1012459,"hemangiosarcoma, African hunting dog",MONDO,disease,DISEASE_15678
15679,15679,15679,15679,15679,15679,15679,15679,MONDO:0018045,Hoyeraal-Hreidarsson syndrome,MONDO,disease,DISEASE_15679
15680,15680,15680,15680,15680,15680,15680,15680,MONDO:0060455,X-linked congenital hemolytic anemia,MONDO,disease,DISEASE_15680
15681,15681,15681,15681,15681,15681,15681,15681,MONDO:0022609,bronchial adenomas/carcinoids childhood,MONDO,disease,DISEASE_15681
15682,15682,15682,15682,15682,15682,15682,15682,MONDO:0001027,gonococcal seminal vesiculitis,MONDO,disease,DISEASE_15682
15683,15683,15683,15683,15683,15683,15683,15683,MONDO:0024480,dermatosis of eyelid,MONDO,disease,DISEASE_15683
15684,15684,15684,15684,15684,15684,15684,15684,MONDO:0007115,"angioma serpiginosum, autosomal dominant",MONDO,disease,DISEASE_15684
15685,15685,15685,15685,15685,15685,15685,15685,MONDO:0012423,MORM syndrome,MONDO,disease,DISEASE_15685
15686,15686,15686,15686,15686,15686,15686,15686,MONDO:0009768,"oculodentodigital dysplasia, autosomal recessive",MONDO,disease,DISEASE_15686
15687,15687,15687,15687,15687,15687,15687,15687,MONDO:0023043,ectodermal dysplasia alopecia preaxial polydactyly,MONDO,disease,DISEASE_15687
15688,15688,15688,15688,15688,15688,15688,15688,MONDO:0002485,breast neuroendocrine neoplasm,MONDO,disease,DISEASE_15688
15689,15689,15689,15689,15689,15689,15689,15689,MONDO:0006481,ureter carcinoma,MONDO,disease,DISEASE_15689
15690,15690,15690,15690,15690,15690,15690,15690,MONDO:1012261,"stringhalt, horse",MONDO,disease,DISEASE_15690
15691,15691,15691,15691,15691,15691,15691,15691,MONDO:0015804,infant botulism,MONDO,disease,DISEASE_15691
15692,15692,15692,15692,15692,15692,15692,15692,MONDO:0002772_MONDO:0850302,intraventricular meningioma,MONDO_grouped,disease,DISEASE_15692
15693,15693,15693,15693,15693,15693,15693,15693,MONDO:0000497,pyometritis,MONDO,disease,DISEASE_15693
15694,15694,15694,15694,15694,15694,15694,15694,MONDO:0700122,PBRM1-related BAFopathy,MONDO,disease,DISEASE_15694
15695,15695,15695,15695,15695,15695,15695,15695,MONDO:0007552_MONDO:0011398_MONDO:1012068_MONDO:1012070_MONDO:1012071_MONDO:1012072,pretibial dystrophic epidermolysis bullosa,MONDO_grouped,disease,DISEASE_15695
15696,15696,15696,15696,15696,15696,15696,15696,MONDO:0033304,"nonsyndromic deafness, Y-linked",MONDO,disease,DISEASE_15696
15697,15697,15697,15697,15697,15697,15697,15697,MONDO:0026763,"holoprosencephaly 13, X-linked",MONDO,disease,DISEASE_15697
15698,15698,15698,15698,15698,15698,15698,15698,MONDO:0004359,delusional disorder,MONDO,disease,DISEASE_15698
15699,15699,15699,15699,15699,15699,15699,15699,MONDO:0019568_MONDO:0019567_MONDO:0007522,"Ehlers-Danlos syndrome, classic type",MONDO_grouped,disease,DISEASE_15699
15700,15700,15700,15700,15700,15700,15700,15700,MONDO:0010331_MONDO:0011817_MONDO:0012009_MONDO:0012010_MONDO:0012147_MONDO:0012585_MONDO:0012628_MONDO:0012788_MONDO:0013765_MONDO:0800425,"coronary heart disease, susceptibility to",MONDO_grouped,disease,DISEASE_15700
15701,15701,15701,15701,15701,15701,15701,15701,MONDO:0000409,chorioamnionitis,MONDO,disease,DISEASE_15701
15702,15702,15702,15702,15702,15702,15702,15702,MONDO:0019103,benign exophthalmos syndrome,MONDO,disease,DISEASE_15702
15703,15703,15703,15703,15703,15703,15703,15703,MONDO:0004659,eye carcinoma in situ,MONDO,disease,DISEASE_15703
15704,15704,15704,15704,15704,15704,15704,15704,MONDO:0011730,fumaric aciduria,MONDO,disease,DISEASE_15704
15705,15705,15705,15705,15705,15705,15705,15705,MONDO:0014984,"lung disease, immunodeficiency, and chromosome breakage syndrome;",MONDO,disease,DISEASE_15705
15706,15706,15706,15706,15706,15706,15706,15706,MONDO:0019498,tungiasis,MONDO,disease,DISEASE_15706
15707,15707,15707,15707,15707,15707,15707,15707,MONDO:1012346_MONDO:1012347,"facial eczema, cattle",MONDO_grouped,disease,DISEASE_15707
15708,15708,15708,15708,15708,15708,15708,15708,MONDO:0007169,atherosclerosis susceptibility,MONDO,disease,DISEASE_15708
15709,15709,15709,15709,15709,15709,15709,15709,MONDO:0800120,Mac-Leod-Swyer-James-Syndrome,MONDO,disease,DISEASE_15709
15710,15710,15710,15710,15710,15710,15710,15710,MONDO:0003612,uterine ligament cancer,MONDO,disease,DISEASE_15710
15711,15711,15711,15711,15711,15711,15711,15711,MONDO:1011492,"Ehlers-Danlos syndrome, American mink",MONDO,disease,DISEASE_15711
15712,15712,15712,15712,15712,15712,15712,15712,MONDO:0004627_MONDO:0000920_MONDO:0002866,duodenitis,MONDO_grouped,disease,DISEASE_15712
15713,15713,15713,15713,15713,15713,15713,15713,MONDO:0009849,hyperimmunoglobulinemia D with periodic fever,MONDO,disease,DISEASE_15713
15714,15714,15714,15714,15714,15714,15714,15714,MONDO:0011399_MONDO:0100563_MONDO:0100565,alpha thalassemia spectrum,MONDO_grouped,disease,DISEASE_15714
15715,15715,15715,15715,15715,15715,15715,15715,MONDO:0008506,symphalangism of toes,MONDO,disease,DISEASE_15715
15716,15716,15716,15716,15716,15716,15716,15716,MONDO:0800183,PAX6-related ocular dysgenesis,MONDO,disease,DISEASE_15716
15717,15717,15717,15717,15717,15717,15717,15717,MONDO:0010225_MONDO:0010359_MONDO:0015612,Dent disease,MONDO_grouped,disease,DISEASE_15717
15718,15718,15718,15718,15718,15718,15718,15718,MONDO:0020838,anterior nasal diphtheria,MONDO,disease,DISEASE_15718
15719,15719,15719,15719,15719,15719,15719,15719,MONDO:0008250_MONDO:0010615_MONDO:0032569_MONDO:0009876_MONDO:0032567_MONDO:0013006,isolated growth hormone deficiency,MONDO_grouped,disease,DISEASE_15719
15720,15720,15720,15720,15720,15720,15720,15720,MONDO:0100002,food protein-induced allergic proctocolitis,MONDO,disease,DISEASE_15720
15721,15721,15721,15721,15721,15721,15721,15721,MONDO:0011375,brittle bone disorder,MONDO,disease,DISEASE_15721
15722,15722,15722,15722,15722,15722,15722,15722,MONDO:0859176,neurodevelopmental disorder with motor and speech delay and behavioral abnormalities,MONDO,disease,DISEASE_15722
15723,15723,15723,15723,15723,15723,15723,15723,MONDO:0002477,prostate neuroendocrine neoplasm,MONDO,disease,DISEASE_15723
15724,15724,15724,15724,15724,15724,15724,15724,MONDO:0005528,inborn vitamin metabolic disorder,MONDO,disease,DISEASE_15724
15725,15725,15725,15725,15725,15725,15725,15725,MONDO:0100524,ASAH1-related sphingolipidosis,MONDO,disease,DISEASE_15725
15726,15726,15726,15726,15726,15726,15726,15726,MONDO:0011728,benign essential blepharospasm,MONDO,disease,DISEASE_15726
15727,15727,15727,15727,15727,15727,15727,15727,MONDO:0007934,benign concentric annular macular dystrophy,MONDO,disease,DISEASE_15727
15728,15728,15728,15728,15728,15728,15728,15728,MONDO:0016503,congenital erosive and vesicular dermatosis,MONDO,disease,DISEASE_15728
15729,15729,15729,15729,15729,15729,15729,15729,MONDO:1040005_MONDO:1040006,PRPF19-related neurodevelopmental disorder,MONDO_grouped,disease,DISEASE_15729
15730,15730,15730,15730,15730,15730,15730,15730,MONDO:0011358,"blue nevi, familial multiple",MONDO,disease,DISEASE_15730
15731,15731,15731,15731,15731,15731,15731,15731,MONDO:1012217_MONDO:1012218,"polyarthritis, dog",MONDO_grouped,disease,DISEASE_15731
15732,15732,15732,15732,15732,15732,15732,15732,MONDO:0800397_MONDO:0800398,GRM6-related retinopathy,MONDO_grouped,disease,DISEASE_15732
15733,15733,15733,15733,15733,15733,15733,15733,MONDO:0003843,cerebral hemisphere lipoma,MONDO,disease,DISEASE_15733
15734,15734,15734,15734,15734,15734,15734,15734,MONDO:0019562,localized scleroderma,MONDO,disease,DISEASE_15734
15735,15735,15735,15735,15735,15735,15735,15735,MONDO:0957229,hatipoglu immunodeficiency syndrome,MONDO,disease,DISEASE_15735
15736,15736,15736,15736,15736,15736,15736,15736,MONDO:0008445,delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome,MONDO,disease,DISEASE_15736
15737,15737,15737,15737,15737,15737,15737,15737,MONDO:0003594,mixed liposarcoma,MONDO,disease,DISEASE_15737
15738,15738,15738,15738,15738,15738,15738,15738,MONDO:0004707,anal canal carcinoma in situ,MONDO,disease,DISEASE_15738
15739,15739,15739,15739,15739,15739,15739,15739,MONDO:0001964,chronic tubotympanic suppurative otitis media,MONDO,disease,DISEASE_15739
15740,15740,15740,15740,15740,15740,15740,15740,MONDO:0006006,verrucous carcinoma,MONDO,disease,DISEASE_15740
15741,15741,15741,15741,15741,15741,15741,15741,MONDO:1011301_MONDO:1012970,"auditory system disorder, non-human animal",MONDO_grouped,disease,DISEASE_15741
15742,15742,15742,15742,15742,15742,15742,15742,MONDO:0005188,iatrogenic Kaposi's sarcoma,MONDO,disease,DISEASE_15742
15743,15743,15743,15743,15743,15743,15743,15743,MONDO:0003788,childhood embryonal testis carcinoma,MONDO,disease,DISEASE_15743
15744,15744,15744,15744,15744,15744,15744,15744,MONDO:0011235,pelvic dysplasia-arthrogryposis of lower limbs syndrome,MONDO,disease,DISEASE_15744
15745,15745,15745,15745,15745,15745,15745,15745,MONDO:0017858,acute erythroid leukemia,MONDO,disease,DISEASE_15745
15746,15746,15746,15746,15746,15746,15746,15746,MONDO:0100403_MONDO:0100418_MONDO:0100419,"acute myeloid leukemia, loss of chromosome 17p",MONDO_grouped,disease,DISEASE_15746
15747,15747,15747,15747,15747,15747,15747,15747,MONDO:1010408,"epilepsy, Mongolian gerbil",MONDO,disease,DISEASE_15747
15748,15748,15748,15748,15748,15748,15748,15748,MONDO:0001288,endometriosis of rectovaginal septum and vagina,MONDO,disease,DISEASE_15748
15749,15749,15749,15749,15749,15749,15749,15749,MONDO:0034987,intraductal tubulopapillary neoplasm of pancreas,MONDO,disease,DISEASE_15749
15750,15750,15750,15750,15750,15750,15750,15750,MONDO:0019789,cytophagic histiocytic panniculitis,MONDO,disease,DISEASE_15750
15751,15751,15751,15751,15751,15751,15751,15751,MONDO:0016330,non-familial hypertrophic cardiomyopathy,MONDO,disease,DISEASE_15751
15752,15752,15752,15752,15752,15752,15752,15752,MONDO:1012344,"familial convulsions and ataxia, cattle",MONDO,disease,DISEASE_15752
15753,15753,15753,15753,15753,15753,15753,15753,MONDO:0008594,familial multiple discoid fibromas,MONDO,disease,DISEASE_15753
15754,15754,15754,15754,15754,15754,15754,15754,MONDO:0024337,urothelial neoplasm,MONDO,disease,DISEASE_15754
15755,15755,15755,15755,15755,15755,15755,15755,MONDO:0009082,high myopia-sensorineural deafness syndrome,MONDO,disease,DISEASE_15755
15756,15756,15756,15756,15756,15756,15756,15756,MONDO:0011758,Hurler syndrome,MONDO,disease,DISEASE_15756
15757,15757,15757,15757,15757,15757,15757,15757,MONDO:0004062_MONDO:0004063_MONDO:0004065_MONDO:0004066,intermediate cell type uveal melanoma,MONDO_grouped,disease,DISEASE_15757
15758,15758,15758,15758,15758,15758,15758,15758,MONDO:0014936,ZTTK syndrome,MONDO,disease,DISEASE_15758
15759,15759,15759,15759,15759,15759,15759,15759,MONDO:0017283,DeSanto-Shinawi Syndrome due to 10p11.21p12.31 microdeletion,MONDO,disease,DISEASE_15759
15760,15760,15760,15760,15760,15760,15760,15760,MONDO:0002631_MONDO:0002628,conventional osteosarcoma,MONDO_grouped,disease,DISEASE_15760
15761,15761,15761,15761,15761,15761,15761,15761,MONDO:0015944,axial mesodermal dysplasia spectrum,MONDO,disease,DISEASE_15761
15762,15762,15762,15762,15762,15762,15762,15762,MONDO:0012108,"spondyloepimetaphyseal dysplasia, matrilin-3 type",MONDO,disease,DISEASE_15762
15763,15763,15763,15763,15763,15763,15763,15763,MONDO:0021232,pineal body neoplasm,MONDO,disease,DISEASE_15763
15764,15764,15764,15764,15764,15764,15764,15764,MONDO:0001229,small intestine diverticulitis,MONDO,disease,DISEASE_15764
15765,15765,15765,15765,15765,15765,15765,15765,MONDO:0005632,acute chest syndrome,MONDO,disease,DISEASE_15765
15766,15766,15766,15766,15766,15766,15766,15766,MONDO:0003078,extraocular retinoblastoma,MONDO,disease,DISEASE_15766
15767,15767,15767,15767,15767,15767,15767,15767,MONDO:0003739,selective immunoglobulin deficiency disease,MONDO,disease,DISEASE_15767
15768,15768,15768,15768,15768,15768,15768,15768,MONDO:0012368,aminoacylase 1 deficiency,MONDO,disease,DISEASE_15768
15769,15769,15769,15769,15769,15769,15769,15769,MONDO:0020588,lung PEComa,MONDO,disease,DISEASE_15769
15770,15770,15770,15770,15770,15770,15770,15770,MONDO:0001552,dyscalculia,MONDO,disease,DISEASE_15770
15771,15771,15771,15771,15771,15771,15771,15771,MONDO:0011698,glycine N-methyltransferase deficiency,MONDO,disease,DISEASE_15771
15772,15772,15772,15772,15772,15772,15772,15772,MONDO:0008699,achalasia microcephaly syndrome,MONDO,disease,DISEASE_15772
15773,15773,15773,15773,15773,15773,15773,15773,MONDO:0001447,detrusor sphincter dyssynergia,MONDO,disease,DISEASE_15773
15774,15774,15774,15774,15774,15774,15774,15774,MONDO:0005065,mesothelioma,MONDO,disease,DISEASE_15774
15775,15775,15775,15775,15775,15775,15775,15775,MONDO:0009236,Kandori fleck retina,MONDO,disease,DISEASE_15775
15776,15776,15776,15776,15776,15776,15776,15776,MONDO:0020788_MONDO:0020787_MONDO:0014631,"hypomagnesemia, seizures, and intellectual disability",MONDO_grouped,disease,DISEASE_15776
15777,15777,15777,15777,15777,15777,15777,15777,MONDO:0017396,toxic dermatosis,MONDO,disease,DISEASE_15777
15778,15778,15778,15778,15778,15778,15778,15778,MONDO:0003177,prostate adenoid cystic carcinoma,MONDO,disease,DISEASE_15778
15779,15779,15779,15779,15779,15779,15779,15779,MONDO:0007073,Hypoglossia-hypodactyly syndrome,MONDO,disease,DISEASE_15779
15780,15780,15780,15780,15780,15780,15780,15780,MONDO:0011405,poikiloderma with neutropenia,MONDO,disease,DISEASE_15780
15781,15781,15781,15781,15781,15781,15781,15781,MONDO:0012764,RIDDLE syndrome,MONDO,disease,DISEASE_15781
15782,15782,15782,15782,15782,15782,15782,15782,MONDO:0016735,papillary glioneuronal tumor,MONDO,disease,DISEASE_15782
15783,15783,15783,15783,15783,15783,15783,15783,MONDO:0035639_MONDO:0035642,mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2),MONDO_grouped,disease,DISEASE_15783
15784,15784,15784,15784,15784,15784,15784,15784,MONDO:0002072,melanotic neuroectodermal tumor,MONDO,disease,DISEASE_15784
15785,15785,15785,15785,15785,15785,15785,15785,MONDO:0003246,sclerosing hepatic carcinoma,MONDO,disease,DISEASE_15785
15786,15786,15786,15786,15786,15786,15786,15786,MONDO:0015386,epignathus,MONDO,disease,DISEASE_15786
15787,15787,15787,15787,15787,15787,15787,15787,MONDO:0100174,"age related macular degeneration, susceptibility to",MONDO,disease,DISEASE_15787
15788,15788,15788,15788,15788,15788,15788,15788,MONDO:0009574,megalencephaly with dysmyelination,MONDO,disease,DISEASE_15788
15789,15789,15789,15789,15789,15789,15789,15789,MONDO:0030030,Nizon-Isidor syndrome,MONDO,disease,DISEASE_15789
15790,15790,15790,15790,15790,15790,15790,15790,MONDO:0000758,bacillary angiomatosis,MONDO,disease,DISEASE_15790
15791,15791,15791,15791,15791,15791,15791,15791,MONDO:0015882,obsolete rare tumor of pancreas,MONDO,disease,DISEASE_15791
15792,15792,15792,15792,15792,15792,15792,15792,MONDO:0045072,ectopic hormone secretion syndrome associated with neoplasia,MONDO,disease,DISEASE_15792
15793,15793,15793,15793,15793,15793,15793,15793,MONDO:0030852,"neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities",MONDO,disease,DISEASE_15793
15794,15794,15794,15794,15794,15794,15794,15794,MONDO:0012219,"spondyloepiphyseal dysplasia tarda, autosomal recessive, Leroy-Spranger type",MONDO,disease,DISEASE_15794
15795,15795,15795,15795,15795,15795,15795,15795,MONDO:0008755,Moynahan syndrome,MONDO,disease,DISEASE_15795
15796,15796,15796,15796,15796,15796,15796,15796,MONDO:0700012,chromosome 5 disorder,MONDO,disease,DISEASE_15796
15797,15797,15797,15797,15797,15797,15797,15797,MONDO:0002422,adamantinoma,MONDO,disease,DISEASE_15797
15798,15798,15798,15798,15798,15798,15798,15798,MONDO:0004200,superficial urinary bladder carcinoma,MONDO,disease,DISEASE_15798
15799,15799,15799,15799,15799,15799,15799,15799,MONDO:0006526,allergic urticaria,MONDO,disease,DISEASE_15799
15800,15800,15800,15800,15800,15800,15800,15800,MONDO:0006122,calcifying nested epithelial stromal tumor of the liver,MONDO,disease,DISEASE_15800
15801,15801,15801,15801,15801,15801,15801,15801,MONDO:0017275,spastic paraplegia-facial-cutaneous lesions syndrome,MONDO,disease,DISEASE_15801
15802,15802,15802,15802,15802,15802,15802,15802,MONDO:0032733,"global developmental delay, progressive ataxia, and elevated glutamine",MONDO,disease,DISEASE_15802
15803,15803,15803,15803,15803,15803,15803,15803,MONDO:0000496,hemorrhagic cystitis,MONDO,disease,DISEASE_15803
15804,15804,15804,15804,15804,15804,15804,15804,MONDO:0021528,benign neoplasm of male breast,MONDO,disease,DISEASE_15804
15805,15805,15805,15805,15805,15805,15805,15805,MONDO:1011785,"lethal multi-organ developmental dysplasia, non-human animal",MONDO,disease,DISEASE_15805
15806,15806,15806,15806,15806,15806,15806,15806,MONDO:1012864,"encephalopathy, ASPA-related, domestic cat",MONDO,disease,DISEASE_15806
15807,15807,15807,15807,15807,15807,15807,15807,MONDO:0009618,microcephaly-cardiomyopathy syndrome,MONDO,disease,DISEASE_15807
15808,15808,15808,15808,15808,15808,15808,15808,MONDO:0008756,alopecia - intellectual disability syndrome,MONDO,disease,DISEASE_15808
15809,15809,15809,15809,15809,15809,15809,15809,MONDO:0000963,esophageal lipoma,MONDO,disease,DISEASE_15809
15810,15810,15810,15810,15810,15810,15810,15810,MONDO:0008152,multicentric carpo-tarsal osteolysis with or without nephropathy,MONDO,disease,DISEASE_15810
15811,15811,15811,15811,15811,15811,15811,15811,MONDO:0009021,Toriello-Carey syndrome,MONDO,disease,DISEASE_15811
15812,15812,15812,15812,15812,15812,15812,15812,MONDO:0022057,calcifying epithelial odontogenic tumor,MONDO,disease,DISEASE_15812
15813,15813,15813,15813,15813,15813,15813,15813,MONDO:0014969,isolated sedoheptulokinase deficiency,MONDO,disease,DISEASE_15813
15814,15814,15814,15814,15814,15814,15814,15814,MONDO:0017928,9p13 microdeletion syndrome,MONDO,disease,DISEASE_15814
15815,15815,15815,15815,15815,15815,15815,15815,MONDO:0859215,"dystonia, early-onset, and/or spastic paraplegia",MONDO,disease,DISEASE_15815
15816,15816,15816,15816,15816,15816,15816,15816,MONDO:0020511_MONDO:0000814_MONDO:0000871_MONDO:0000872_MONDO:0003539_MONDO:0020512,precursor B-cell acute lymphoblastic leukemia,MONDO_grouped,disease,DISEASE_15816
15817,15817,15817,15817,15817,15817,15817,15817,MONDO:0020635,anaplastic meningioma,MONDO,disease,DISEASE_15817
15818,15818,15818,15818,15818,15818,15818,15818,MONDO:0044092,collagenous sprue,MONDO,disease,DISEASE_15818
15819,15819,15819,15819,15819,15819,15819,15819,MONDO:0017157,pulmonary hypertension owing to lung disease and/or hypoxia,MONDO,disease,DISEASE_15819
15820,15820,15820,15820,15820,15820,15820,15820,MONDO:0025483,"mammary neoplasms, animal",MONDO,disease,DISEASE_15820
15821,15821,15821,15821,15821,15821,15821,15821,MONDO:0017210_MONDO:0017634_MONDO:0017209,infectious anterior uveitis,MONDO_grouped,disease,DISEASE_15821
15822,15822,15822,15822,15822,15822,15822,15822,MONDO:0010803,Eiken syndrome,MONDO,disease,DISEASE_15822
15823,15823,15823,15823,15823,15823,15823,15823,MONDO:0032828,"spastic tetraplegia and axial hypotonia, progressive",MONDO,disease,DISEASE_15823
15824,15824,15824,15824,15824,15824,15824,15824,MONDO:0000532,lung combined type small cell adenocarcinoma,MONDO,disease,DISEASE_15824
15825,15825,15825,15825,15825,15825,15825,15825,MONDO:0001156,borderline personality disorder,MONDO,disease,DISEASE_15825
15826,15826,15826,15826,15826,15826,15826,15826,MONDO:0014466_MONDO:0009736_MONDO:0000179,Neu-Laxova syndrome,MONDO_grouped,disease,DISEASE_15826
15827,15827,15827,15827,15827,15827,15827,15827,MONDO:0008090,cyclic hematopoiesis,MONDO,disease,DISEASE_15827
15828,15828,15828,15828,15828,15828,15828,15828,MONDO:1012910,"spinocerebellar ataxia, ATXN3-related, white-tufted-ear marmoset",MONDO,disease,DISEASE_15828
15829,15829,15829,15829,15829,15829,15829,15829,MONDO:0004194,ovarian stromal hyperthecosis,MONDO,disease,DISEASE_15829
15830,15830,15830,15830,15830,15830,15830,15830,MONDO:0001920_MONDO:0001031,chronic purulent otitis media,MONDO_grouped,disease,DISEASE_15830
15831,15831,15831,15831,15831,15831,15831,15831,MONDO:1010555,"spina bifida, snow leopard",MONDO,disease,DISEASE_15831
15832,15832,15832,15832,15832,15832,15832,15832,MONDO:0022908,cutis gyratum acanthosis nigricans craniosynostosis,MONDO,disease,DISEASE_15832
15833,15833,15833,15833,15833,15833,15833,15833,MONDO:0002577,extrahepatic bile duct rhabdomyosarcoma,MONDO,disease,DISEASE_15833
15834,15834,15834,15834,15834,15834,15834,15834,MONDO:0017453,fetal parvovirus syndrome,MONDO,disease,DISEASE_15834
15835,15835,15835,15835,15835,15835,15835,15835,MONDO:0011212,"sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth",MONDO,disease,DISEASE_15835
15836,15836,15836,15836,15836,15836,15836,15836,MONDO:0003413,hair follicle neoplasm,MONDO,disease,DISEASE_15836
15837,15837,15837,15837,15837,15837,15837,15837,MONDO:1012438,"sebaceous gland dysplasia, domestic cat",MONDO,disease,DISEASE_15837
15838,15838,15838,15838,15838,15838,15838,15838,MONDO:0019857,congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies,MONDO,disease,DISEASE_15838
15839,15839,15839,15839,15839,15839,15839,15839,MONDO:0008840_MONDO:1011028,ataxia telangiectasia,MONDO_grouped,disease,DISEASE_15839
15840,15840,15840,15840,15840,15840,15840,15840,MONDO:0020797,decompression sickness,MONDO,disease,DISEASE_15840
15841,15841,15841,15841,15841,15841,15841,15841,MONDO:0022481,APO A-i deficiency,MONDO,disease,DISEASE_15841
15842,15842,15842,15842,15842,15842,15842,15842,MONDO:0016383,nephrogenic diabetes insipidus,MONDO,disease,DISEASE_15842
15843,15843,15843,15843,15843,15843,15843,15843,MONDO:0005249,pneumonia,MONDO,disease,DISEASE_15843
15844,15844,15844,15844,15844,15844,15844,15844,MONDO:0010649,isolated congenital megalocornea,MONDO,disease,DISEASE_15844
15845,15845,15845,15845,15845,15845,15845,15845,MONDO:0015941,epiphyseal dysplasia-hearing loss-dysmorphism syndrome,MONDO,disease,DISEASE_15845
15846,15846,15846,15846,15846,15846,15846,15846,MONDO:0020830,diaphragmitis,MONDO,disease,DISEASE_15846
15847,15847,15847,15847,15847,15847,15847,15847,MONDO:0007000,Treponema infectious disease,MONDO,disease,DISEASE_15847
15848,15848,15848,15848,15848,15848,15848,15848,MONDO:0006658,arteriolosclerosis,MONDO,disease,DISEASE_15848
15849,15849,15849,15849,15849,15849,15849,15849,MONDO:0004862,vitreous abscess,MONDO,disease,DISEASE_15849
15850,15850,15850,15850,15850,15850,15850,15850,MONDO:0021491,benign neoplasm of gum,MONDO,disease,DISEASE_15850
15851,15851,15851,15851,15851,15851,15851,15851,MONDO:0007476,familial Dupuytren contracture,MONDO,disease,DISEASE_15851
15852,15852,15852,15852,15852,15852,15852,15852,MONDO:0010317,"intellectual disability, X-linked, with or without seizures, arx-related",MONDO,disease,DISEASE_15852
15853,15853,15853,15853,15853,15853,15853,15853,MONDO:0014994,"global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies",MONDO,disease,DISEASE_15853
15854,15854,15854,15854,15854,15854,15854,15854,MONDO:0015294,nephrogenic systemic fibrosis,MONDO,disease,DISEASE_15854
15855,15855,15855,15855,15855,15855,15855,15855,MONDO:0019943,hereditary continuous muscle fiber activity,MONDO,disease,DISEASE_15855
15856,15856,15856,15856,15856,15856,15856,15856,MONDO:0018298,multicentric osteolysis-nodulosis-arthropathy spectrum,MONDO,disease,DISEASE_15856
15857,15857,15857,15857,15857,15857,15857,15857,MONDO:0016372_MONDO:0002639_MONDO:0002781_MONDO:0004279,glossopharyngeal neuralgia,MONDO_grouped,disease,DISEASE_15857
15858,15858,15858,15858,15858,15858,15858,15858,MONDO:0013681,alpha-methylacyl-CoA racemase deficiency,MONDO,disease,DISEASE_15858
15859,15859,15859,15859,15859,15859,15859,15859,MONDO:0958150,Borrelia miyamotoi disease,MONDO,disease,DISEASE_15859
15860,15860,15860,15860,15860,15860,15860,15860,MONDO:0958006_MONDO:0032885_MONDO:0011198_MONDO:0013014,"spondyloepimetaphyseal dysplasia, Guo-Campeau type",MONDO_grouped,disease,DISEASE_15860
15861,15861,15861,15861,15861,15861,15861,15861,MONDO:0001870,acute poststreptococcal glomerulonephritis,MONDO,disease,DISEASE_15861
15862,15862,15862,15862,15862,15862,15862,15862,MONDO:0019964,thymic neuroendocrine tumor,MONDO,disease,DISEASE_15862
15863,15863,15863,15863,15863,15863,15863,15863,MONDO:0007460,"discrimination, Two-point, reduction 1N",MONDO,disease,DISEASE_15863
15864,15864,15864,15864,15864,15864,15864,15864,MONDO:0005901,pasteurellosis,MONDO,disease,DISEASE_15864
15865,15865,15865,15865,15865,15865,15865,15865,MONDO:0003865,acral lentiginous melanoma,MONDO,disease,DISEASE_15865
15866,15866,15866,15866,15866,15866,15866,15866,MONDO:0009042,craniotelencephalic dysplasia,MONDO,disease,DISEASE_15866
15867,15867,15867,15867,15867,15867,15867,15867,MONDO:0013252,Warsaw breakage syndrome,MONDO,disease,DISEASE_15867
15868,15868,15868,15868,15868,15868,15868,15868,MONDO:0016986,congenital smooth muscle hamartoma,MONDO,disease,DISEASE_15868
15869,15869,15869,15869,15869,15869,15869,15869,MONDO:0016831_MONDO:0019319,linear verrucous nevus syndrome,MONDO_grouped,disease,DISEASE_15869
15870,15870,15870,15870,15870,15870,15870,15870,MONDO:0004219,polyvesicular vitelline pattern testicular yolk sac tumor,MONDO,disease,DISEASE_15870
15871,15871,15871,15871,15871,15871,15871,15871,MONDO:0001055,conjunctival pterygium,MONDO,disease,DISEASE_15871
15872,15872,15872,15872,15872,15872,15872,15872,MONDO:0010516,"midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis",MONDO,disease,DISEASE_15872
15873,15873,15873,15873,15873,15873,15873,15873,MONDO:0008605,"triphalangeal thumb, Nonopposable",MONDO,disease,DISEASE_15873
15874,15874,15874,15874,15874,15874,15874,15874,MONDO:0011124,spondyloepimetaphyseal dysplasia-abnormal dentition syndrome,MONDO,disease,DISEASE_15874
15875,15875,15875,15875,15875,15875,15875,15875,MONDO:0017281,renal caliceal diverticuli-deafness syndrome,MONDO,disease,DISEASE_15875
15876,15876,15876,15876,15876,15876,15876,15876,MONDO:0017999,fatty acid hydroxylase-associated neurodegeneration,MONDO,disease,DISEASE_15876
15877,15877,15877,15877,15877,15877,15877,15877,MONDO:0020920_MONDO:0006753_MONDO:8000002,escherichia coli infection,MONDO_grouped,disease,DISEASE_15877
15878,15878,15878,15878,15878,15878,15878,15878,MONDO:0019144,hereditary thrombophilia due to congenital protein S deficiency,MONDO,disease,DISEASE_15878
15879,15879,15879,15879,15879,15879,15879,15879,MONDO:0013517,beta-thalassemia HBB/LCRB,MONDO,disease,DISEASE_15879
15880,15880,15880,15880,15880,15880,15880,15880,MONDO:0005214,vulva sarcoma,MONDO,disease,DISEASE_15880
15881,15881,15881,15881,15881,15881,15881,15881,MONDO:0021627,eyelid capillary hemangioma,MONDO,disease,DISEASE_15881
15882,15882,15882,15882,15882,15882,15882,15882,MONDO:0015562,distal monosomy 17q,MONDO,disease,DISEASE_15882
15883,15883,15883,15883,15883,15883,15883,15883,MONDO:0003604,functioning pituitary gland neoplasm,MONDO,disease,DISEASE_15883
15884,15884,15884,15884,15884,15884,15884,15884,MONDO:0006116,breast carcinoma by gene expression profile,MONDO,disease,DISEASE_15884
15885,15885,15885,15885,15885,15885,15885,15885,MONDO:0043162,pagon stephan syndrome,MONDO,disease,DISEASE_15885
15886,15886,15886,15886,15886,15886,15886,15886,MONDO:0006128,central nervous system anaplastic large cell lymphoma,MONDO,disease,DISEASE_15886
15887,15887,15887,15887,15887,15887,15887,15887,MONDO:0017785,PENS syndrome,MONDO,disease,DISEASE_15887
15888,15888,15888,15888,15888,15888,15888,15888,MONDO:1012154,"megaesophagus, domestic ferret",MONDO,disease,DISEASE_15888
15889,15889,15889,15889,15889,15889,15889,15889,MONDO:0006888,paraneoplastic polyneuropathy,MONDO,disease,DISEASE_15889
15890,15890,15890,15890,15890,15890,15890,15890,MONDO:1012184,"navicular disease, horse",MONDO,disease,DISEASE_15890
15891,15891,15891,15891,15891,15891,15891,15891,MONDO:0017975,sex chromosome disorder of sex development,MONDO,disease,DISEASE_15891
15892,15892,15892,15892,15892,15892,15892,15892,MONDO:0020333,aggressive systemic mastocytosis,MONDO,disease,DISEASE_15892
15893,15893,15893,15893,15893,15893,15893,15893,MONDO:0014017_MONDO:0032568_MONDO:0859281,intellectual developmental disorder with autism and macrocephaly,MONDO_grouped,disease,DISEASE_15893
15894,15894,15894,15894,15894,15894,15894,15894,MONDO:0001357_MONDO:0000387,hypochromic anemia,MONDO_grouped,disease,DISEASE_15894
15895,15895,15895,15895,15895,15895,15895,15895,MONDO:1010723,"glucocorticoid resistance, dog",MONDO,disease,DISEASE_15895
15896,15896,15896,15896,15896,15896,15896,15896,MONDO:0008859,"berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification",MONDO,disease,DISEASE_15896
15897,15897,15897,15897,15897,15897,15897,15897,MONDO:0011258_MONDO:0007360_MONDO:0012025_MONDO:0018878,branchiootic syndrome,MONDO_grouped,disease,DISEASE_15897
15898,15898,15898,15898,15898,15898,15898,15898,MONDO:0003756,ovarian mucinous neoplasm,MONDO,disease,DISEASE_15898
15899,15899,15899,15899,15899,15899,15899,15899,MONDO:0030057,"neurodevelopmental, jaw, eye, and digital syndrome",MONDO,disease,DISEASE_15899
15900,15900,15900,15900,15900,15900,15900,15900,MONDO:0009790,Opticocochleodentate degeneration,MONDO,disease,DISEASE_15900
15901,15901,15901,15901,15901,15901,15901,15901,MONDO:0010976_MONDO:0030535_MONDO:0014014,"epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive",MONDO_grouped,disease,DISEASE_15901
15902,15902,15902,15902,15902,15902,15902,15902,MONDO:0007370,"coracoclavicular joint, anomalous",MONDO,disease,DISEASE_15902
15903,15903,15903,15903,15903,15903,15903,15903,MONDO:0001434,inflammatory spondylopathy,MONDO,disease,DISEASE_15903
15904,15904,15904,15904,15904,15904,15904,15904,MONDO:0024540_MONDO:0012871_MONDO:0002441,Jervell and Lange-Nielsen syndrome,MONDO_grouped,disease,DISEASE_15904
15905,15905,15905,15905,15905,15905,15905,15905,MONDO:0002551,c-P angle neurinoma,MONDO,disease,DISEASE_15905
15906,15906,15906,15906,15906,15906,15906,15906,MONDO:0013366_MONDO:0012349_MONDO:0014694_MONDO:0020692_MONDO:0012097_MONDO:1011204,"spondylocostal dysostosis 4, autosomal recessive",MONDO_grouped,disease,DISEASE_15906
15907,15907,15907,15907,15907,15907,15907,15907,MONDO:0009501,metabolic myopathy due to lactate transporter defect,MONDO,disease,DISEASE_15907
15908,15908,15908,15908,15908,15908,15908,15908,MONDO:0100514,familial ovarian carcinoma,MONDO,disease,DISEASE_15908
15909,15909,15909,15909,15909,15909,15909,15909,MONDO:0024945_MONDO:1011778,"hepatitis, non-human animal",MONDO_grouped,disease,DISEASE_15909
15910,15910,15910,15910,15910,15910,15910,15910,MONDO:0012436,neonatal diabetes mellitus with congenital hypothyroidism,MONDO,disease,DISEASE_15910
15911,15911,15911,15911,15911,15911,15911,15911,MONDO:0013869,adenine phosphoribosyltransferase deficiency,MONDO,disease,DISEASE_15911
15912,15912,15912,15912,15912,15912,15912,15912,MONDO:0015744,distal trisomy 19q,MONDO,disease,DISEASE_15912
15913,15913,15913,15913,15913,15913,15913,15913,MONDO:0008815,argininosuccinic aciduria,MONDO,disease,DISEASE_15913
15914,15914,15914,15914,15914,15914,15914,15914,MONDO:1012456,"multiple autoimmune diseases syndrome, dog",MONDO,disease,DISEASE_15914
15915,15915,15915,15915,15915,15915,15915,15915,MONDO:0008543,tetralogy of fallot and glaucoma,MONDO,disease,DISEASE_15915
15916,15916,15916,15916,15916,15916,15916,15916,MONDO:0006327,ocular sebaceous carcinoma,MONDO,disease,DISEASE_15916
15917,15917,15917,15917,15917,15917,15917,15917,MONDO:0024650,drug-induced osteoporosis,MONDO,disease,DISEASE_15917
15918,15918,15918,15918,15918,15918,15918,15918,MONDO:0007606,fibrodysplasia ossificans progressiva,MONDO,disease,DISEASE_15918
15919,15919,15919,15919,15919,15919,15919,15919,MONDO:0009622,Jawad syndrome,MONDO,disease,DISEASE_15919
15920,15920,15920,15920,15920,15920,15920,15920,MONDO:0060532,congenital heart defects and skeletal malformations syndrome,MONDO,disease,DISEASE_15920
15921,15921,15921,15921,15921,15921,15921,15921,MONDO:0007035,acanthosis nigricans,MONDO,disease,DISEASE_15921
15922,15922,15922,15922,15922,15922,15922,15922,MONDO:0014184_MONDO:0011710_MONDO:0011711_MONDO:0000724_MONDO:0011780_MONDO:0012917,specific language impairment,MONDO_grouped,disease,DISEASE_15922
15923,15923,15923,15923,15923,15923,15923,15923,MONDO:0009878_MONDO:0024464_MONDO:0013518,"pituitary hormone deficiency, combined",MONDO_grouped,disease,DISEASE_15923
15924,15924,15924,15924,15924,15924,15924,15924,MONDO:0007841,coxopodopatellar syndrome,MONDO,disease,DISEASE_15924
15925,15925,15925,15925,15925,15925,15925,15925,MONDO:1011194_MONDO:1011195,"osteochondrodysplasia, dog",MONDO_grouped,disease,DISEASE_15925
15926,15926,15926,15926,15926,15926,15926,15926,MONDO:0100492,Bonnevie-Ullrich syndrome,MONDO,disease,DISEASE_15926
15927,15927,15927,15927,15927,15927,15927,15927,MONDO:0044651,early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome,MONDO,disease,DISEASE_15927
15928,15928,15928,15928,15928,15928,15928,15928,MONDO:0010089,isolated sulfite oxidase deficiency,MONDO,disease,DISEASE_15928
15929,15929,15929,15929,15929,15929,15929,15929,MONDO:0032681,"encephalopathy, progressive, early-onset, with episodic rhabdomyolysis",MONDO,disease,DISEASE_15929
15930,15930,15930,15930,15930,15930,15930,15930,MONDO:0043549,crush syndrome,MONDO,disease,DISEASE_15930
15931,15931,15931,15931,15931,15931,15931,15931,MONDO:0007691,"Guillain-Barre syndrome, familial",MONDO,disease,DISEASE_15931
15932,15932,15932,15932,15932,15932,15932,15932,MONDO:0017339,exfoliative ichthyosis,MONDO,disease,DISEASE_15932
15933,15933,15933,15933,15933,15933,15933,15933,MONDO:0016547,Beckwith-Wiedemann syndrome due to NSD1 mutation,MONDO,disease,DISEASE_15933
15934,15934,15934,15934,15934,15934,15934,15934,MONDO:0010885,angiokeratoma corporis diffusum with arteriovenous fistulas,MONDO,disease,DISEASE_15934
15935,15935,15935,15935,15935,15935,15935,15935,MONDO:0006925_MONDO:0006765,Fusobacteriaceae infectious disease,MONDO_grouped,disease,DISEASE_15935
15936,15936,15936,15936,15936,15936,15936,15936,MONDO:0001514,prolapse of urethra,MONDO,disease,DISEASE_15936
15937,15937,15937,15937,15937,15937,15937,15937,MONDO:0020738_MONDO:0007990,multiple benign circumferential skin creases on limbs 1,MONDO_grouped,disease,DISEASE_15937
15938,15938,15938,15938,15938,15938,15938,15938,MONDO:0007334,autosomal dominant popliteal pterygium syndrome,MONDO,disease,DISEASE_15938
15939,15939,15939,15939,15939,15939,15939,15939,MONDO:1010623,"situs inversus, horse",MONDO,disease,DISEASE_15939
15940,15940,15940,15940,15940,15940,15940,15940,MONDO:0000592,specific developmental disorder,MONDO,disease,DISEASE_15940
15941,15941,15941,15941,15941,15941,15941,15941,MONDO:1011835,"congenital cerebellar anomaly, non-human animal",MONDO,disease,DISEASE_15941
15942,15942,15942,15942,15942,15942,15942,15942,MONDO:0014995,"neurodevelopmental disorder with hypotonia, seizures, and absent language",MONDO,disease,DISEASE_15942
15943,15943,15943,15943,15943,15943,15943,15943,MONDO:0032779,neurodevelopmental disorder with microcephaly and structural brain anomalies,MONDO,disease,DISEASE_15943
15944,15944,15944,15944,15944,15944,15944,15944,MONDO:0060510,Cohen-Gibson syndrome,MONDO,disease,DISEASE_15944
15945,15945,15945,15945,15945,15945,15945,15945,MONDO:0700141_MONDO:0700168,canine melanoma,MONDO_grouped,disease,DISEASE_15945
15946,15946,15946,15946,15946,15946,15946,15946,MONDO:0008217,pelvis-shoulder dysplasia,MONDO,disease,DISEASE_15946
15947,15947,15947,15947,15947,15947,15947,15947,MONDO:0004725,rectum carcinoma in situ,MONDO,disease,DISEASE_15947
15948,15948,15948,15948,15948,15948,15948,15948,MONDO:0016872,partial deletion of chromosome 7,MONDO,disease,DISEASE_15948
15949,15949,15949,15949,15949,15949,15949,15949,MONDO:1010526_MONDO:1010525_MONDO:1010530_MONDO:1010527_MONDO:1010528_MONDO:1010529_MONDO:1010531_MONDO:1010532,"cleft palate, dog",MONDO_grouped,disease,DISEASE_15949
15950,15950,15950,15950,15950,15950,15950,15950,MONDO:0020782,chronic gingivitis,MONDO,disease,DISEASE_15950
15951,15951,15951,15951,15951,15951,15951,15951,MONDO:1012693,"melanoma-bearing Libechov minipig, pig",MONDO,disease,DISEASE_15951
15952,15952,15952,15952,15952,15952,15952,15952,MONDO:0004962,stage II endometrioid carcinoma,MONDO,disease,DISEASE_15952
15953,15953,15953,15953,15953,15953,15953,15953,MONDO:0014137_MONDO:0008302,"precocious puberty, central",MONDO_grouped,disease,DISEASE_15953
15954,15954,15954,15954,15954,15954,15954,15954,MONDO:0019480,Langerhans cell sarcoma,MONDO,disease,DISEASE_15954
15955,15955,15955,15955,15955,15955,15955,15955,MONDO:0060589,"facial palsy, congenital, with ptosis and velopharyngeal dysfunction",MONDO,disease,DISEASE_15955
15956,15956,15956,15956,15956,15956,15956,15956,MONDO:0016657,8p11.2 deletion syndrome,MONDO,disease,DISEASE_15956
15957,15957,15957,15957,15957,15957,15957,15957,MONDO:0013543,trypsinogen deficiency,MONDO,disease,DISEASE_15957
15958,15958,15958,15958,15958,15958,15958,15958,MONDO:0018525,solid pseudopapillary carcinoma of pancreas,MONDO,disease,DISEASE_15958
15959,15959,15959,15959,15959,15959,15959,15959,MONDO:0020494,oculootodental syndrome,MONDO,disease,DISEASE_15959
15960,15960,15960,15960,15960,15960,15960,15960,MONDO:0011206,ventriculomegaly with defects of the radius and kidney,MONDO,disease,DISEASE_15960
15961,15961,15961,15961,15961,15961,15961,15961,MONDO:1012369,"renal cystadenocarcinoma and nodular dermatofibrosis, dog",MONDO,disease,DISEASE_15961
15962,15962,15962,15962,15962,15962,15962,15962,MONDO:0043257,pemphigus and fogo selvagem,MONDO,disease,DISEASE_15962
15963,15963,15963,15963,15963,15963,15963,15963,MONDO:0021301,adenoma of nipple,MONDO,disease,DISEASE_15963
15964,15964,15964,15964,15964,15964,15964,15964,MONDO:0022989,diomedi bernardi placidi syndrome,MONDO,disease,DISEASE_15964
15965,15965,15965,15965,15965,15965,15965,15965,MONDO:0009229,hyaline fibromatosis syndrome,MONDO,disease,DISEASE_15965
15966,15966,15966,15966,15966,15966,15966,15966,MONDO:0014512,PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation,MONDO,disease,DISEASE_15966
15967,15967,15967,15967,15967,15967,15967,15967,MONDO:0005910,phagocyte bactericidal dysfunction,MONDO,disease,DISEASE_15967
15968,15968,15968,15968,15968,15968,15968,15968,MONDO:0007761,obsolete hyperlipoproteinemia type IV,MONDO,disease,DISEASE_15968
15969,15969,15969,15969,15969,15969,15969,15969,MONDO:0009613,"methylmalonic aciduria, cblA type",MONDO,disease,DISEASE_15969
15970,15970,15970,15970,15970,15970,15970,15970,MONDO:0043176,phosphoribosylpyrophosphate synthetase deficiency,MONDO,disease,DISEASE_15970
15971,15971,15971,15971,15971,15971,15971,15971,MONDO:0019466,lymphomatoid granulomatosis,MONDO,disease,DISEASE_15971
15972,15972,15972,15972,15972,15972,15972,15972,MONDO:0020688,spinal cord ischemia,MONDO,disease,DISEASE_15972
15973,15973,15973,15973,15973,15973,15973,15973,MONDO:0008587,tracheobronchopathia osteochondroplastica,MONDO,disease,DISEASE_15973
15974,15974,15974,15974,15974,15974,15974,15974,MONDO:1011900,"hypopigmentation and deafness, non-human animal",MONDO,disease,DISEASE_15974
15975,15975,15975,15975,15975,15975,15975,15975,MONDO:0021192_MONDO:0006328,odontogenic neoplasm,MONDO_grouped,disease,DISEASE_15975
15976,15976,15976,15976,15976,15976,15976,15976,MONDO:0011678,homozygous 11P15-p14 deletion syndrome,MONDO,disease,DISEASE_15976
15977,15977,15977,15977,15977,15977,15977,15977,MONDO:0858997,cancer of unknown primary site,MONDO,disease,DISEASE_15977
15978,15978,15978,15978,15978,15978,15978,15978,MONDO:0007646,Gamstorp-Wohlfart syndrome,MONDO,disease,DISEASE_15978
15979,15979,15979,15979,15979,15979,15979,15979,MONDO:0100532,"blepharospasm, benign essential, susceptibility to",MONDO,disease,DISEASE_15979
15980,15980,15980,15980,15980,15980,15980,15980,MONDO:0013621,LAMB2-related infantile-onset nephrotic syndrome,MONDO,disease,DISEASE_15980
15981,15981,15981,15981,15981,15981,15981,15981,MONDO:0800138,multisystem autoimmune disease due to IKAROS gain of function,MONDO,disease,DISEASE_15981
15982,15982,15982,15982,15982,15982,15982,15982,MONDO:1011930,"recurrent airway obstruction, non-human animal",MONDO,disease,DISEASE_15982
15983,15983,15983,15983,15983,15983,15983,15983,MONDO:0009764,"ocular motor apraxia, Cogan type",MONDO,disease,DISEASE_15983
15984,15984,15984,15984,15984,15984,15984,15984,MONDO:0001591,senile entropion,MONDO,disease,DISEASE_15984
15985,15985,15985,15985,15985,15985,15985,15985,MONDO:0019308,junctional epidermolysis bullosa inversa,MONDO,disease,DISEASE_15985
15986,15986,15986,15986,15986,15986,15986,15986,MONDO:0018242,autoimmune hypoparathyroidism,MONDO,disease,DISEASE_15986
15987,15987,15987,15987,15987,15987,15987,15987,MONDO:0009857_MONDO:0022971,persistent Mullerian duct syndrome,MONDO_grouped,disease,DISEASE_15987
15988,15988,15988,15988,15988,15988,15988,15988,MONDO:0012310,"fibrosis of extraocular muscles, congenital, with synergistic divergence",MONDO,disease,DISEASE_15988
15989,15989,15989,15989,15989,15989,15989,15989,MONDO:0023062,encephalocele anencephaly,MONDO,disease,DISEASE_15989
15990,15990,15990,15990,15990,15990,15990,15990,MONDO:0100360_MONDO:0100361_MONDO:0100362,herpes simplex type 2 infectious disease,MONDO_grouped,disease,DISEASE_15990
15991,15991,15991,15991,15991,15991,15991,15991,MONDO:0021373,neoplasm of parietal lobe,MONDO,disease,DISEASE_15991
15992,15992,15992,15992,15992,15992,15992,15992,MONDO:0019119,muscular channelopathy,MONDO,disease,DISEASE_15992
15993,15993,15993,15993,15993,15993,15993,15993,MONDO:0021669_MONDO:0021674_MONDO:0021673_MONDO:0021677,post-infectious disorder,MONDO_grouped,disease,DISEASE_15993
15994,15994,15994,15994,15994,15994,15994,15994,MONDO:0041526,pregnancy disorder with abortive outcome,MONDO,disease,DISEASE_15994
15995,15995,15995,15995,15995,15995,15995,15995,MONDO:0859361,neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia,MONDO,disease,DISEASE_15995
15996,15996,15996,15996,15996,15996,15996,15996,MONDO:0015079,multiple polyglandular tumor,MONDO,disease,DISEASE_15996
15997,15997,15997,15997,15997,15997,15997,15997,MONDO:0005417_MONDO:0100114,wet macular degeneration,MONDO_grouped,disease,DISEASE_15997
15998,15998,15998,15998,15998,15998,15998,15998,MONDO:0004927,dacryocystocele,MONDO,disease,DISEASE_15998
15999,15999,15999,15999,15999,15999,15999,15999,MONDO:0100288,enhanced S-cone syndrome,MONDO,disease,DISEASE_15999
16000,16000,16000,16000,16000,16000,16000,16000,MONDO:0005139,morbid obesity,MONDO,disease,DISEASE_16000
16001,16001,16001,16001,16001,16001,16001,16001,MONDO:1011230,"entropion, goat",MONDO,disease,DISEASE_16001
16002,16002,16002,16002,16002,16002,16002,16002,MONDO:1012507_MONDO:1012508,"Guillain-Barr-like polyradiculoneuropathy, dog",MONDO_grouped,disease,DISEASE_16002
16003,16003,16003,16003,16003,16003,16003,16003,MONDO:0975801,"encephalopathy, acute transient",MONDO,disease,DISEASE_16003
16004,16004,16004,16004,16004,16004,16004,16004,MONDO:0002038,head and neck carcinoma,MONDO,disease,DISEASE_16004
16005,16005,16005,16005,16005,16005,16005,16005,MONDO:0020338,adult pure red cell aplasia,MONDO,disease,DISEASE_16005
16006,16006,16006,16006,16006,16006,16006,16006,MONDO:0021303,adenoma of small intestine,MONDO,disease,DISEASE_16006
16007,16007,16007,16007,16007,16007,16007,16007,MONDO:0010741,"tooth agenesis, selective, X-linked, 1",MONDO,disease,DISEASE_16007
16008,16008,16008,16008,16008,16008,16008,16008,MONDO:0100299,PAX5-related B lymphopenia and autism spectrum disorder,MONDO,disease,DISEASE_16008
16009,16009,16009,16009,16009,16009,16009,16009,MONDO:0002822,trabecular adenocarcinoma,MONDO,disease,DISEASE_16009
16010,16010,16010,16010,16010,16010,16010,16010,MONDO:1010749,"Ehlers-Danlos syndrome, dermatosparaxis type, ADAMTS2-related, sheep",MONDO,disease,DISEASE_16010
16011,16011,16011,16011,16011,16011,16011,16011,MONDO:0006300,medullomyoblastoma with myogenic differentiation,MONDO,disease,DISEASE_16011
16012,16012,16012,16012,16012,16012,16012,16012,MONDO:0008280,Peutz-Jeghers syndrome,MONDO,disease,DISEASE_16012
16013,16013,16013,16013,16013,16013,16013,16013,MONDO:0001724,supraglottis cancer,MONDO,disease,DISEASE_16013
16014,16014,16014,16014,16014,16014,16014,16014,MONDO:0010797,Pearson syndrome,MONDO,disease,DISEASE_16014
16015,16015,16015,16015,16015,16015,16015,16015,MONDO:0021089,peripheral nervous system cancer,MONDO,disease,DISEASE_16015
16016,16016,16016,16016,16016,16016,16016,16016,MONDO:0001269,scleral disorder,MONDO,disease,DISEASE_16016
16017,16017,16017,16017,16017,16017,16017,16017,MONDO:0018479_MONDO:1010564,congenital adrenal hyperplasia,MONDO_grouped,disease,DISEASE_16017
16018,16018,16018,16018,16018,16018,16018,16018,MONDO:1012621,"congenital myasthenic syndrome, CHRNE-related, cattle",MONDO,disease,DISEASE_16018
16019,16019,16019,16019,16019,16019,16019,16019,MONDO:1011285_MONDO:1012673_MONDO:1012806_MONDO:1012873,"syndromic retinal atrophy, BBS2-related, dog",MONDO_grouped,disease,DISEASE_16019
16020,16020,16020,16020,16020,16020,16020,16020,MONDO:0014070_MONDO:0018264_MONDO:0008745_MONDO:0011749_MONDO:0011683_MONDO:0008746_MONDO:0014127_MONDO:0008747_MONDO:0030899_MONDO:0018135_MONDO:0018910,oculocutaneous albinism,MONDO_grouped,disease,DISEASE_16020
16021,16021,16021,16021,16021,16021,16021,16021,MONDO:0014811,"cerebellar atrophy, visual impairment, and psychomotor retardation;",MONDO,disease,DISEASE_16021
16022,16022,16022,16022,16022,16022,16022,16022,MONDO:0014888,MIRAGE syndrome,MONDO,disease,DISEASE_16022
16023,16023,16023,16023,16023,16023,16023,16023,MONDO:0003964_MONDO:0021929_MONDO:1010920_MONDO:1010921,myositis ossificans,MONDO_grouped,disease,DISEASE_16023
16024,16024,16024,16024,16024,16024,16024,16024,MONDO:0013550,distal myopathy with posterior leg and anterior hand involvement,MONDO,disease,DISEASE_16024
16025,16025,16025,16025,16025,16025,16025,16025,MONDO:0011115,spastic paraplegia and Evans syndrome,MONDO,disease,DISEASE_16025
16026,16026,16026,16026,16026,16026,16026,16026,MONDO:0004920,hydrocele,MONDO,disease,DISEASE_16026
16027,16027,16027,16027,16027,16027,16027,16027,MONDO:0005040,germ cell tumor,MONDO,disease,DISEASE_16027
16028,16028,16028,16028,16028,16028,16028,16028,MONDO:1012145_MONDO:1012146_MONDO:1012147_MONDO:1012148,"malignant hyperthermia, dog",MONDO_grouped,disease,DISEASE_16028
16029,16029,16029,16029,16029,16029,16029,16029,MONDO:0004564,thyroid malformation,MONDO,disease,DISEASE_16029
16030,16030,16030,16030,16030,16030,16030,16030,MONDO:0030042,"proteinuria, chronic benign",MONDO,disease,DISEASE_16030
16031,16031,16031,16031,16031,16031,16031,16031,MONDO:0015072,liver neuroendocrine carcinoma,MONDO,disease,DISEASE_16031
16032,16032,16032,16032,16032,16032,16032,16032,MONDO:0011621,acropectoral syndrome,MONDO,disease,DISEASE_16032
16033,16033,16033,16033,16033,16033,16033,16033,MONDO:0000544,mucosal melanoma,MONDO,disease,DISEASE_16033
16034,16034,16034,16034,16034,16034,16034,16034,MONDO:0006670_MONDO:0021108_MONDO:0007015_MONDO:0006764_MONDO:0006836,bacterial meningitis,MONDO_grouped,disease,DISEASE_16034
16035,16035,16035,16035,16035,16035,16035,16035,MONDO:0100363_MONDO:0100364,genital herpes simplex type 2 infectious disorder,MONDO_grouped,disease,DISEASE_16035
16036,16036,16036,16036,16036,16036,16036,16036,MONDO:0019056_MONDO:0043218_MONDO:0005559_MONDO:0020124,neuromuscular disease,MONDO_grouped,disease,DISEASE_16036
16037,16037,16037,16037,16037,16037,16037,16037,MONDO:0019926,X small rings,MONDO,disease,DISEASE_16037
16038,16038,16038,16038,16038,16038,16038,16038,MONDO:0005769,geniculate herpes zoster,MONDO,disease,DISEASE_16038
16039,16039,16039,16039,16039,16039,16039,16039,MONDO:1011447,"Waardenburg syndrome, non-human animal",MONDO,disease,DISEASE_16039
16040,16040,16040,16040,16040,16040,16040,16040,MONDO:0007594,factor 5 excess with spontaneous thrombosis,MONDO,disease,DISEASE_16040
16041,16041,16041,16041,16041,16041,16041,16041,MONDO:0006107,benign thyroid gland neoplasm,MONDO,disease,DISEASE_16041
16042,16042,16042,16042,16042,16042,16042,16042,MONDO:0100558,RNU4ATAC spectrum disorder,MONDO,disease,DISEASE_16042
16043,16043,16043,16043,16043,16043,16043,16043,MONDO:0004178,"testicular yolk sac tumor, endodermal sinus pattern",MONDO,disease,DISEASE_16043
16044,16044,16044,16044,16044,16044,16044,16044,MONDO:0012839,pyogenic bacterial infections due to MyD88 deficiency,MONDO,disease,DISEASE_16044
16045,16045,16045,16045,16045,16045,16045,16045,MONDO:0007924,Bannayan-Riley-Ruvalcaba syndrome,MONDO,disease,DISEASE_16045
16046,16046,16046,16046,16046,16046,16046,16046,MONDO:0100289,Goldmann-Favre syndrome,MONDO,disease,DISEASE_16046
16047,16047,16047,16047,16047,16047,16047,16047,MONDO:0006660,arthus reaction,MONDO,disease,DISEASE_16047
16048,16048,16048,16048,16048,16048,16048,16048,MONDO:0001363,blind hypertensive eye,MONDO,disease,DISEASE_16048
16049,16049,16049,16049,16049,16049,16049,16049,MONDO:0009984,late-adult onset retinitis pigmentosa,MONDO,disease,DISEASE_16049
16050,16050,16050,16050,16050,16050,16050,16050,MONDO:0007654,"genu valgum, st. Helena familial",MONDO,disease,DISEASE_16050
16051,16051,16051,16051,16051,16051,16051,16051,MONDO:0030712_MONDO:0030134_MONDO:0023671_MONDO:0020793_MONDO:0025193,oculopharyngodistal myopathy,MONDO_grouped,disease,DISEASE_16051
16052,16052,16052,16052,16052,16052,16052,16052,MONDO:0016159,Gemignani syndrome,MONDO,disease,DISEASE_16052
16053,16053,16053,16053,16053,16053,16053,16053,MONDO:0022089,Carnevale hernandez castillo syndrome,MONDO,disease,DISEASE_16053
16054,16054,16054,16054,16054,16054,16054,16054,MONDO:0002815,acute myocarditis,MONDO,disease,DISEASE_16054
16055,16055,16055,16055,16055,16055,16055,16055,MONDO:0024570_MONDO:0007767_MONDO:0001741_MONDO:0005333_MONDO:0012406_MONDO:1010591_MONDO:1010593,hyperparathyroidism,MONDO_grouped,disease,DISEASE_16055
16056,16056,16056,16056,16056,16056,16056,16056,MONDO:0007774,hyperreflexia,MONDO,disease,DISEASE_16056
16057,16057,16057,16057,16057,16057,16057,16057,MONDO:0002548,cellular schwannoma,MONDO,disease,DISEASE_16057
16058,16058,16058,16058,16058,16058,16058,16058,MONDO:0002549,schwannoma of twelfth cranial nerve,MONDO,disease,DISEASE_16058
16059,16059,16059,16059,16059,16059,16059,16059,MONDO:1010703,"glycogen storage disease, PYGM-related, cattle",MONDO,disease,DISEASE_16059
16060,16060,16060,16060,16060,16060,16060,16060,MONDO:0001518,spastic entropion,MONDO,disease,DISEASE_16060
16061,16061,16061,16061,16061,16061,16061,16061,MONDO:0005662,balantidiasis,MONDO,disease,DISEASE_16061
16062,16062,16062,16062,16062,16062,16062,16062,MONDO:0007203,blue rubber bleb nevus,MONDO,disease,DISEASE_16062
16063,16063,16063,16063,16063,16063,16063,16063,MONDO:0010749,trigonocephaly-short stature-developmental delay syndrome,MONDO,disease,DISEASE_16063
16064,16064,16064,16064,16064,16064,16064,16064,MONDO:0018991,hepatoportal sclerosis,MONDO,disease,DISEASE_16064
16065,16065,16065,16065,16065,16065,16065,16065,MONDO:0021367,"leukemia, myeloid, accelerated-phase",MONDO,disease,DISEASE_16065
16066,16066,16066,16066,16066,16066,16066,16066,MONDO:0006992,syphilitic aortitis,MONDO,disease,DISEASE_16066
16067,16067,16067,16067,16067,16067,16067,16067,MONDO:0001113,Fiedler's myocarditis,MONDO,disease,DISEASE_16067
16068,16068,16068,16068,16068,16068,16068,16068,MONDO:0017602,ALK-positive anaplastic large cell lymphoma,MONDO,disease,DISEASE_16068
16069,16069,16069,16069,16069,16069,16069,16069,MONDO:0003934,breast apocrine carcinoma,MONDO,disease,DISEASE_16069
16070,16070,16070,16070,16070,16070,16070,16070,MONDO:0003401,central nervous system endodermal sinus tumor,MONDO,disease,DISEASE_16070
16071,16071,16071,16071,16071,16071,16071,16071,MONDO:0850054,hemophilia B leyden,MONDO,disease,DISEASE_16071
16072,16072,16072,16072,16072,16072,16072,16072,MONDO:0008752_MONDO:0018210_MONDO:0018209_MONDO:1011014,Alexander disease,MONDO_grouped,disease,DISEASE_16072
16073,16073,16073,16073,16073,16073,16073,16073,MONDO:0000524,mixed extragonadal germ cell cancer,MONDO,disease,DISEASE_16073
16074,16074,16074,16074,16074,16074,16074,16074,MONDO:0001437_MONDO:0018483,pulmonary alveolar proteinosis,MONDO_grouped,disease,DISEASE_16074
16075,16075,16075,16075,16075,16075,16075,16075,MONDO:0007013,vasculogenic impotence,MONDO,disease,DISEASE_16075
16076,16076,16076,16076,16076,16076,16076,16076,MONDO:0020574,central nervous system nongerminomatous germ cell tumor,MONDO,disease,DISEASE_16076
16077,16077,16077,16077,16077,16077,16077,16077,MONDO:0005642,atopic conjunctivitis,MONDO,disease,DISEASE_16077
16078,16078,16078,16078,16078,16078,16078,16078,MONDO:0008388,ringed hair disease,MONDO,disease,DISEASE_16078
16079,16079,16079,16079,16079,16079,16079,16079,MONDO:1010807,"polydactyly, springbok",MONDO,disease,DISEASE_16079
16080,16080,16080,16080,16080,16080,16080,16080,MONDO:0021505,benign neoplasm of endocardium,MONDO,disease,DISEASE_16080
16081,16081,16081,16081,16081,16081,16081,16081,MONDO:0022758,"chromosome 22, monosome mosaic",MONDO,disease,DISEASE_16081
16082,16082,16082,16082,16082,16082,16082,16082,MONDO:0012290,CEDNIK syndrome,MONDO,disease,DISEASE_16082
16083,16083,16083,16083,16083,16083,16083,16083,MONDO:0016049,"congenital myopathy, Paradas type",MONDO,disease,DISEASE_16083
16084,16084,16084,16084,16084,16084,16084,16084,MONDO:0018008,idiopathic giant cell myocarditis,MONDO,disease,DISEASE_16084
16085,16085,16085,16085,16085,16085,16085,16085,MONDO:0030978,"ENDOVE syndrome, limb-only type",MONDO,disease,DISEASE_16085
16086,16086,16086,16086,16086,16086,16086,16086,MONDO:0024990,swine disease,MONDO,disease,DISEASE_16086
16087,16087,16087,16087,16087,16087,16087,16087,MONDO:0027676_MONDO:0032646_MONDO:0012561_MONDO:0019719,congenital anomalies of kidney and urinary tract,MONDO_grouped,disease,DISEASE_16087
16088,16088,16088,16088,16088,16088,16088,16088,MONDO:0000771_MONDO:0004784,allergic respiratory disease,MONDO_grouped,disease,DISEASE_16088
16089,16089,16089,16089,16089,16089,16089,16089,MONDO:0030676_MONDO:0013150,"parkinsonism-dystonia 3, childhood-onset",MONDO_grouped,disease,DISEASE_16089
16090,16090,16090,16090,16090,16090,16090,16090,MONDO:0006362_MONDO:0971145,peritoneal mesothelioma,MONDO_grouped,disease,DISEASE_16090
16091,16091,16091,16091,16091,16091,16091,16091,MONDO:0007723_MONDO:0010834_MONDO:0013383_MONDO:0010833_MONDO:0013384_MONDO:0100179_MONDO:0011741_MONDO:0011742_MONDO:0012042_MONDO:0012710,"Hirschsprung disease, susceptibility to",MONDO_grouped,disease,DISEASE_16091
16092,16092,16092,16092,16092,16092,16092,16092,MONDO:0013237,"susceptibility to mononeuropathy of the median nerve, mild",MONDO,disease,DISEASE_16092
16093,16093,16093,16093,16093,16093,16093,16093,MONDO:0009249_MONDO:0021759,hereditary fructose intolerance,MONDO_grouped,disease,DISEASE_16093
16094,16094,16094,16094,16094,16094,16094,16094,MONDO:0016038,calcified aponeurotic fibroma,MONDO,disease,DISEASE_16094
16095,16095,16095,16095,16095,16095,16095,16095,MONDO:1012318,"nodular dermatofibrosis and kidney disease, dog",MONDO,disease,DISEASE_16095
16096,16096,16096,16096,16096,16096,16096,16096,MONDO:0043108,infantile striato thalamic degeneration,MONDO,disease,DISEASE_16096
16097,16097,16097,16097,16097,16097,16097,16097,MONDO:0003158_MONDO:0003990,malignant myoepithelioma,MONDO_grouped,disease,DISEASE_16097
16098,16098,16098,16098,16098,16098,16098,16098,MONDO:0013574,cutis laxa - Marfanoid syndrome,MONDO,disease,DISEASE_16098
16099,16099,16099,16099,16099,16099,16099,16099,MONDO:0003837,TSH producing pituitary tumor,MONDO,disease,DISEASE_16099
16100,16100,16100,16100,16100,16100,16100,16100,MONDO:0002929,pulmonary immaturity,MONDO,disease,DISEASE_16100
16101,16101,16101,16101,16101,16101,16101,16101,MONDO:0001404,ecthyma,MONDO,disease,DISEASE_16101
16102,16102,16102,16102,16102,16102,16102,16102,MONDO:0005517,pharynx cancer,MONDO,disease,DISEASE_16102
16103,16103,16103,16103,16103,16103,16103,16103,MONDO:0011224,monomelic amyotrophy,MONDO,disease,DISEASE_16103
16104,16104,16104,16104,16104,16104,16104,16104,MONDO:0001469,cascade stomach,MONDO,disease,DISEASE_16104
16105,16105,16105,16105,16105,16105,16105,16105,MONDO:0007474,duodenal ulcer due to antral G-cell hyperfunction,MONDO,disease,DISEASE_16105
16106,16106,16106,16106,16106,16106,16106,16106,MONDO:0004054,acute canaliculitis,MONDO,disease,DISEASE_16106
16107,16107,16107,16107,16107,16107,16107,16107,MONDO:1012455,"ocular melanosis, dog",MONDO,disease,DISEASE_16107
16108,16108,16108,16108,16108,16108,16108,16108,MONDO:0012385,"metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands",MONDO,disease,DISEASE_16108
16109,16109,16109,16109,16109,16109,16109,16109,MONDO:1010192_MONDO:1011807,"central core myopathy, non-human animal",MONDO_grouped,disease,DISEASE_16109
16110,16110,16110,16110,16110,16110,16110,16110,MONDO:0016203,hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency,MONDO,disease,DISEASE_16110
16111,16111,16111,16111,16111,16111,16111,16111,MONDO:0008233,pheochromocytoma,MONDO,disease,DISEASE_16111
16112,16112,16112,16112,16112,16112,16112,16112,MONDO:0008610_MONDO:0010565,blue color blindness,MONDO_grouped,disease,DISEASE_16112
16113,16113,16113,16113,16113,16113,16113,16113,MONDO:0012165,BNAR syndrome,MONDO,disease,DISEASE_16113
16114,16114,16114,16114,16114,16114,16114,16114,MONDO:0021473,benign neoplasm of epididymis,MONDO,disease,DISEASE_16114
16115,16115,16115,16115,16115,16115,16115,16115,MONDO:0016216,adult hepatocellular carcinoma,MONDO,disease,DISEASE_16115
16116,16116,16116,16116,16116,16116,16116,16116,MONDO:0002381_MONDO:0021110_MONDO:0005524,sweat gland neoplasm,MONDO_grouped,disease,DISEASE_16116
16117,16117,16117,16117,16117,16117,16117,16117,MONDO:0002250,basilar artery insufficiency,MONDO,disease,DISEASE_16117
16118,16118,16118,16118,16118,16118,16118,16118,MONDO:0060759,"neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures",MONDO,disease,DISEASE_16118
16119,16119,16119,16119,16119,16119,16119,16119,MONDO:0017714,acyl-CoA dehydrogenase deficiency,MONDO,disease,DISEASE_16119
16120,16120,16120,16120,16120,16120,16120,16120,MONDO:0006248,hydatidiform mole,MONDO,disease,DISEASE_16120
16121,16121,16121,16121,16121,16121,16121,16121,MONDO:0005687,Caliciviridae infectious disease,MONDO,disease,DISEASE_16121
16122,16122,16122,16122,16122,16122,16122,16122,MONDO:0035663_MONDO:0035664_MONDO:0035665,neuromyelitis optica spectrum disorder with anti-AQP4 antibodies,MONDO_grouped,disease,DISEASE_16122
16123,16123,16123,16123,16123,16123,16123,16123,MONDO:0003507,choriocarcinoma of ovary,MONDO,disease,DISEASE_16123
16124,16124,16124,16124,16124,16124,16124,16124,MONDO:1011723,"mitochondrial fission encephalopathy, non-human animal",MONDO,disease,DISEASE_16124
16125,16125,16125,16125,16125,16125,16125,16125,MONDO:0019040,chromosomal disorder,MONDO,disease,DISEASE_16125
16126,16126,16126,16126,16126,16126,16126,16126,MONDO:0001752,alveolar periostitis,MONDO,disease,DISEASE_16126
16127,16127,16127,16127,16127,16127,16127,16127,MONDO:0006292,malignant mesothelioma,MONDO,disease,DISEASE_16127
16128,16128,16128,16128,16128,16128,16128,16128,MONDO:0002697_MONDO:0020540,ovarian gonadoblastoma,MONDO_grouped,disease,DISEASE_16128
16129,16129,16129,16129,16129,16129,16129,16129,MONDO:0800467,dyskeratosis congenita and related telomere biology disorder,MONDO,disease,DISEASE_16129
16130,16130,16130,16130,16130,16130,16130,16130,MONDO:0000251_MONDO:0044762_MONDO:0044763,diarrheal disease secondary to altered bowel motility,MONDO_grouped,disease,DISEASE_16130
16131,16131,16131,16131,16131,16131,16131,16131,MONDO:0001164_MONDO:0002411,antisocial personality disorder,MONDO_grouped,disease,DISEASE_16131
16132,16132,16132,16132,16132,16132,16132,16132,MONDO:0003397,gingival hypertrophy,MONDO,disease,DISEASE_16132
16133,16133,16133,16133,16133,16133,16133,16133,MONDO:0011037,"renal dysplasia, cystic, susceptibility to",MONDO,disease,DISEASE_16133
16134,16134,16134,16134,16134,16134,16134,16134,MONDO:0010149,transcobalamin II deficiency,MONDO,disease,DISEASE_16134
16135,16135,16135,16135,16135,16135,16135,16135,MONDO:0003254,cardiac granular cell neoplasm,MONDO,disease,DISEASE_16135
16136,16136,16136,16136,16136,16136,16136,16136,MONDO:0001294,Horner syndrome,MONDO,disease,DISEASE_16136
16137,16137,16137,16137,16137,16137,16137,16137,MONDO:0001729,active cochlear Meniere disease,MONDO,disease,DISEASE_16137
16138,16138,16138,16138,16138,16138,16138,16138,MONDO:0000465,atrioventricular block,MONDO,disease,DISEASE_16138
16139,16139,16139,16139,16139,16139,16139,16139,MONDO:0017505,"apodia, bilateral",MONDO,disease,DISEASE_16139
16140,16140,16140,16140,16140,16140,16140,16140,MONDO:0001200_MONDO:0100078,secondary hypertension,MONDO_grouped,disease,DISEASE_16140
16141,16141,16141,16141,16141,16141,16141,16141,MONDO:0014233,early-onset Parkinson disease 20,MONDO,disease,DISEASE_16141
16142,16142,16142,16142,16142,16142,16142,16142,MONDO:0014648,Al-Raqad syndrome,MONDO,disease,DISEASE_16142
16143,16143,16143,16143,16143,16143,16143,16143,MONDO:0021758,acquired agranulocytosis,MONDO,disease,DISEASE_16143
16144,16144,16144,16144,16144,16144,16144,16144,MONDO:0017621,congenital sucrase-isomaltase deficiency with starch and lactose intolerance,MONDO,disease,DISEASE_16144
16145,16145,16145,16145,16145,16145,16145,16145,MONDO:0020430,cor triatriatum sinister,MONDO,disease,DISEASE_16145
16146,16146,16146,16146,16146,16146,16146,16146,MONDO:0003785,leukopenia,MONDO,disease,DISEASE_16146
16147,16147,16147,16147,16147,16147,16147,16147,MONDO:0002758,vulva verrucous carcinoma,MONDO,disease,DISEASE_16147
16148,16148,16148,16148,16148,16148,16148,16148,MONDO:0007935,cystoid macular edema,MONDO,disease,DISEASE_16148
16149,16149,16149,16149,16149,16149,16149,16149,MONDO:0018640,secondary vasculitis,MONDO,disease,DISEASE_16149
16150,16150,16150,16150,16150,16150,16150,16150,MONDO:0024873,clitoral carcinoma,MONDO,disease,DISEASE_16150
16151,16151,16151,16151,16151,16151,16151,16151,MONDO:0022777,cleft lip palate dysmorphism kumar type,MONDO,disease,DISEASE_16151
16152,16152,16152,16152,16152,16152,16152,16152,MONDO:0016522,Kousseff syndrome,MONDO,disease,DISEASE_16152
16153,16153,16153,16153,16153,16153,16153,16153,MONDO:0013867_MONDO:0024537,Brown-Vialetto-van Laere syndrome,MONDO_grouped,disease,DISEASE_16153
16154,16154,16154,16154,16154,16154,16154,16154,MONDO:1010551,"patent urachus, domestic cat",MONDO,disease,DISEASE_16154
16155,16155,16155,16155,16155,16155,16155,16155,MONDO:0100090_MONDO:0100097,congenital alveolar dysplasia due to FGF10,MONDO_grouped,disease,DISEASE_16155
16156,16156,16156,16156,16156,16156,16156,16156,MONDO:0015724,non-distal trisomy 13q,MONDO,disease,DISEASE_16156
16157,16157,16157,16157,16157,16157,16157,16157,MONDO:0009517,Donohue syndrome,MONDO,disease,DISEASE_16157
16158,16158,16158,16158,16158,16158,16158,16158,MONDO:0013279_MONDO:0013370_MONDO:0013062_MONDO:0013372_MONDO:0100316_MONDO:0014550_MONDO:0012737_MONDO:0012736_MONDO:0011377_MONDO:0032915_MONDO:0012738_MONDO:0032756_MONDO:0014548_MONDO:0013367_MONDO:0002442_MONDO:0800323,long QT syndrome,MONDO_grouped,disease,DISEASE_16158
16159,16159,16159,16159,16159,16159,16159,16159,MONDO:0044791,combined hepatocellular carcinoma and cholangiocarcinoma,MONDO,disease,DISEASE_16159
16160,16160,16160,16160,16160,16160,16160,16160,MONDO:0008246,pigmented paravenous retinochoroidal atrophy,MONDO,disease,DISEASE_16160
16161,16161,16161,16161,16161,16161,16161,16161,MONDO:0009330,"hemangiopericytoma, malignant",MONDO,disease,DISEASE_16161
16162,16162,16162,16162,16162,16162,16162,16162,MONDO:0015666,familial idiopathic dilatation of the right atrium,MONDO,disease,DISEASE_16162
16163,16163,16163,16163,16163,16163,16163,16163,MONDO:0017304,ocular albinism,MONDO,disease,DISEASE_16163
16164,16164,16164,16164,16164,16164,16164,16164,MONDO:0009371,3-hydroxyisobutyric aciduria,MONDO,disease,DISEASE_16164
16165,16165,16165,16165,16165,16165,16165,16165,MONDO:0003009_MONDO:0015900,hyperaldosteronism,MONDO_grouped,disease,DISEASE_16165
16166,16166,16166,16166,16166,16166,16166,16166,MONDO:0010691,Norrie disease,MONDO,disease,DISEASE_16166
16167,16167,16167,16167,16167,16167,16167,16167,MONDO:0007445,dermatopathia pigmentosa reticularis,MONDO,disease,DISEASE_16167
16168,16168,16168,16168,16168,16168,16168,16168,MONDO:0008018,Muir-Torre syndrome,MONDO,disease,DISEASE_16168
16169,16169,16169,16169,16169,16169,16169,16169,MONDO:1010554,"patent urachus, sheep",MONDO,disease,DISEASE_16169
16170,16170,16170,16170,16170,16170,16170,16170,MONDO:1011004,"leukodystrophy, American mink",MONDO,disease,DISEASE_16170
16171,16171,16171,16171,16171,16171,16171,16171,MONDO:0003187,Bartholin gland adenoid cystic carcinoma,MONDO,disease,DISEASE_16171
16172,16172,16172,16172,16172,16172,16172,16172,MONDO:0009121,von Voss-Cherstvoy syndrome,MONDO,disease,DISEASE_16172
16173,16173,16173,16173,16173,16173,16173,16173,MONDO:0007022,xanthogranulomatous pyelonephritis,MONDO,disease,DISEASE_16173
16174,16174,16174,16174,16174,16174,16174,16174,MONDO:0009210,congenital factor V deficiency,MONDO,disease,DISEASE_16174
16175,16175,16175,16175,16175,16175,16175,16175,MONDO:0009606,methemoglobinemia due to deficiency of methemoglobin reductase,MONDO,disease,DISEASE_16175
16176,16176,16176,16176,16176,16176,16176,16176,MONDO:0100216,DICER1-related tumor predisposition,MONDO,disease,DISEASE_16176
16177,16177,16177,16177,16177,16177,16177,16177,MONDO:0004971,adenoid cystic carcinoma,MONDO,disease,DISEASE_16177
16178,16178,16178,16178,16178,16178,16178,16178,MONDO:0004092,thymic basaloid carcinoma,MONDO,disease,DISEASE_16178
16179,16179,16179,16179,16179,16179,16179,16179,MONDO:0006151,colon dysplasia,MONDO,disease,DISEASE_16179
16180,16180,16180,16180,16180,16180,16180,16180,MONDO:0006874,obstructive jaundice,MONDO,disease,DISEASE_16180
16181,16181,16181,16181,16181,16181,16181,16181,MONDO:0043209,albinism,MONDO,disease,DISEASE_16181
16182,16182,16182,16182,16182,16182,16182,16182,MONDO:0010028,sialuria,MONDO,disease,DISEASE_16182
16183,16183,16183,16183,16183,16183,16183,16183,MONDO:0019212,disseminated superficial actinic porokeratosis,MONDO,disease,DISEASE_16183
16184,16184,16184,16184,16184,16184,16184,16184,MONDO:0859191,"biliary, renal, neurologic, and skeletal syndrome",MONDO,disease,DISEASE_16184
16185,16185,16185,16185,16185,16185,16185,16185,MONDO:0005207,choriocarcinoma,MONDO,disease,DISEASE_16185
16186,16186,16186,16186,16186,16186,16186,16186,MONDO:0006493,Warthin tumor,MONDO,disease,DISEASE_16186
16187,16187,16187,16187,16187,16187,16187,16187,MONDO:0001653,prepuce cancer,MONDO,disease,DISEASE_16187
16188,16188,16188,16188,16188,16188,16188,16188,MONDO:0015803,wound botulism,MONDO,disease,DISEASE_16188
16189,16189,16189,16189,16189,16189,16189,16189,MONDO:0700038,TDP-43 proteinopathy,MONDO,disease,DISEASE_16189
16190,16190,16190,16190,16190,16190,16190,16190,MONDO:1011988_MONDO:1011887,"retinal and skeletal dysplasia, non-human animal",MONDO_grouped,disease,DISEASE_16190
16191,16191,16191,16191,16191,16191,16191,16191,MONDO:0000627,benign endocrine neoplasm,MONDO,disease,DISEASE_16191
16192,16192,16192,16192,16192,16192,16192,16192,MONDO:0011713,melanoma-pancreatic cancer syndrome,MONDO,disease,DISEASE_16192
16193,16193,16193,16193,16193,16193,16193,16193,MONDO:0002377,breast intracanalicular fibroadenoma,MONDO,disease,DISEASE_16193
16194,16194,16194,16194,16194,16194,16194,16194,MONDO:0016188,qualitative or quantitative defects of alphaB-cristallin,MONDO,disease,DISEASE_16194
16195,16195,16195,16195,16195,16195,16195,16195,MONDO:0800460,ASAH1-related disorders,MONDO,disease,DISEASE_16195
16196,16196,16196,16196,16196,16196,16196,16196,MONDO:0015720_MONDO:0015716_MONDO:0015717_MONDO:0015721,moderately severe hemophilia,MONDO_grouped,disease,DISEASE_16196
16197,16197,16197,16197,16197,16197,16197,16197,MONDO:0000363,gummatous syphilis,MONDO,disease,DISEASE_16197
16198,16198,16198,16198,16198,16198,16198,16198,MONDO:0017310,Marfan and Marfan-related disorder,MONDO,disease,DISEASE_16198
16199,16199,16199,16199,16199,16199,16199,16199,MONDO:1010680,"AA amyloidosis, cheetah",MONDO,disease,DISEASE_16199
16200,16200,16200,16200,16200,16200,16200,16200,MONDO:0007423,"deafness, mid-tone neural",MONDO,disease,DISEASE_16200
16201,16201,16201,16201,16201,16201,16201,16201,MONDO:0008058,cylindrical spirals myopathy,MONDO,disease,DISEASE_16201
16202,16202,16202,16202,16202,16202,16202,16202,MONDO:0024564_MONDO:0015026_MONDO:0957264,cerebroretinal microangiopathy with calcifications and cysts,MONDO_grouped,disease,DISEASE_16202
16203,16203,16203,16203,16203,16203,16203,16203,MONDO:0008234_MONDO:0008082_MONDO:0012552_MONDO:0007540_MONDO:0019003_MONDO:0017169,multiple endocrine neoplasia,MONDO_grouped,disease,DISEASE_16203
16204,16204,16204,16204,16204,16204,16204,16204,MONDO:0005033,ganglioneuroma,MONDO,disease,DISEASE_16204
16205,16205,16205,16205,16205,16205,16205,16205,MONDO:0958104,digenic Alport syndrome,MONDO,disease,DISEASE_16205
16206,16206,16206,16206,16206,16206,16206,16206,MONDO:0043230,ciguatera fish poisoning,MONDO,disease,DISEASE_16206
16207,16207,16207,16207,16207,16207,16207,16207,MONDO:0004329,pancreatic intraductal papillary-mucinous neoplasm with high grade dysplasia,MONDO,disease,DISEASE_16207
16208,16208,16208,16208,16208,16208,16208,16208,MONDO:0017668,intellectual disability-short stature-hypertelorism syndrome,MONDO,disease,DISEASE_16208
16209,16209,16209,16209,16209,16209,16209,16209,MONDO:0021641,Bunyaviridae infectious disease,MONDO,disease,DISEASE_16209
16210,16210,16210,16210,16210,16210,16210,16210,MONDO:0015372,autosomal dominant macrothrombocytopenia,MONDO,disease,DISEASE_16210
16211,16211,16211,16211,16211,16211,16211,16211,MONDO:0011384_MONDO:0011440_MONDO:0011815_MONDO:0012109_MONDO:0012458_MONDO:0012459_MONDO:0012587_MONDO:0012599,"hypertension, essential, susceptibility to",MONDO_grouped,disease,DISEASE_16211
16212,16212,16212,16212,16212,16212,16212,16212,MONDO:0850092,post-cardiac arrest syndrome,MONDO,disease,DISEASE_16212
16213,16213,16213,16213,16213,16213,16213,16213,MONDO:0018806,primary intrahepatic lithiasis,MONDO,disease,DISEASE_16213
16214,16214,16214,16214,16214,16214,16214,16214,MONDO:0005691_MONDO:0005927,cardiovirus infectious disease,MONDO_grouped,disease,DISEASE_16214
16215,16215,16215,16215,16215,16215,16215,16215,MONDO:0006999,tooth disorder,MONDO,disease,DISEASE_16215
16216,16216,16216,16216,16216,16216,16216,16216,MONDO:0018965,Alport syndrome,MONDO,disease,DISEASE_16216
16217,16217,16217,16217,16217,16217,16217,16217,MONDO:0019838,adenohypophysitis,MONDO,disease,DISEASE_16217
16218,16218,16218,16218,16218,16218,16218,16218,MONDO:0012174,peripheral cone dystrophy,MONDO,disease,DISEASE_16218
16219,16219,16219,16219,16219,16219,16219,16219,MONDO:0016005,indomethacin embryofetopathy,MONDO,disease,DISEASE_16219
16220,16220,16220,16220,16220,16220,16220,16220,MONDO:0015808,folliculotropic mycosis fungoides,MONDO,disease,DISEASE_16220
16221,16221,16221,16221,16221,16221,16221,16221,MONDO:0005132_MONDO:0024354_MONDO:0000878,cytomegalovirus infection,MONDO_grouped,disease,DISEASE_16221
16222,16222,16222,16222,16222,16222,16222,16222,MONDO:1011217,"coloboma, llama",MONDO,disease,DISEASE_16222
16223,16223,16223,16223,16223,16223,16223,16223,MONDO:0005013,dedifferentiated chondrosarcoma,MONDO,disease,DISEASE_16223
16224,16224,16224,16224,16224,16224,16224,16224,MONDO:1012248_MONDO:1012249,"sarcoid, ass",MONDO_grouped,disease,DISEASE_16224
16225,16225,16225,16225,16225,16225,16225,16225,MONDO:1012162,"congenital melanoma, pig",MONDO,disease,DISEASE_16225
16226,16226,16226,16226,16226,16226,16226,16226,MONDO:1012194,"occipital dysplasia, dog",MONDO,disease,DISEASE_16226
16227,16227,16227,16227,16227,16227,16227,16227,MONDO:0008707,acro-renal-mandibular syndrome,MONDO,disease,DISEASE_16227
16228,16228,16228,16228,16228,16228,16228,16228,MONDO:0012270,Tukel syndrome,MONDO,disease,DISEASE_16228
16229,16229,16229,16229,16229,16229,16229,16229,MONDO:0020937,"contractures, pterygia, and variable skeletal fusions syndrome",MONDO,disease,DISEASE_16229
16230,16230,16230,16230,16230,16230,16230,16230,MONDO:0010121,thrombocytopenia-absent radius syndrome,MONDO,disease,DISEASE_16230
16231,16231,16231,16231,16231,16231,16231,16231,MONDO:0002790,seminal vesicle tumor,MONDO,disease,DISEASE_16231
16232,16232,16232,16232,16232,16232,16232,16232,MONDO:0017070,total spina bifida cystica,MONDO,disease,DISEASE_16232
16233,16233,16233,16233,16233,16233,16233,16233,MONDO:0017882,Omsk hemorrhagic fever,MONDO,disease,DISEASE_16233
16234,16234,16234,16234,16234,16234,16234,16234,MONDO:0002095,vascular cancer,MONDO,disease,DISEASE_16234
16235,16235,16235,16235,16235,16235,16235,16235,MONDO:0003357_MONDO:0004206_MONDO:0004207,lung leiomyosarcoma,MONDO_grouped,disease,DISEASE_16235
16236,16236,16236,16236,16236,16236,16236,16236,MONDO:0004795_MONDO:0001051,otitis externa,MONDO_grouped,disease,DISEASE_16236
16237,16237,16237,16237,16237,16237,16237,16237,MONDO:0003163,cauda equina intradural extramedullary astrocytoma,MONDO,disease,DISEASE_16237
16238,16238,16238,16238,16238,16238,16238,16238,MONDO:0018050,tibial aplasia-ectrodactyly syndrome,MONDO,disease,DISEASE_16238
16239,16239,16239,16239,16239,16239,16239,16239,MONDO:0010770,"ubiquitin-activating enzyme, Y-linked",MONDO,disease,DISEASE_16239
16240,16240,16240,16240,16240,16240,16240,16240,MONDO:0018595,single-organ polyarteritis nodosa,MONDO,disease,DISEASE_16240
16241,16241,16241,16241,16241,16241,16241,16241,MONDO:0006374,placental choriocarcinoma,MONDO,disease,DISEASE_16241
16242,16242,16242,16242,16242,16242,16242,16242,MONDO:0800459,noxacusis,MONDO,disease,DISEASE_16242
16243,16243,16243,16243,16243,16243,16243,16243,MONDO:0006078,AIDS-related primary central nervous system lymphoma,MONDO,disease,DISEASE_16243
16244,16244,16244,16244,16244,16244,16244,16244,MONDO:0011017,Naxos disease,MONDO,disease,DISEASE_16244
16245,16245,16245,16245,16245,16245,16245,16245,MONDO:0004262,breast myoepitheliosis,MONDO,disease,DISEASE_16245
16246,16246,16246,16246,16246,16246,16246,16246,MONDO:0016581,conotruncal heart malformations,MONDO,disease,DISEASE_16246
16247,16247,16247,16247,16247,16247,16247,16247,MONDO:0035350,letrozole toxicity,MONDO,disease,DISEASE_16247
16248,16248,16248,16248,16248,16248,16248,16248,MONDO:0018955,recurrent respiratory papillomatosis,MONDO,disease,DISEASE_16248
16249,16249,16249,16249,16249,16249,16249,16249,MONDO:1011926,"shivers, non-human animal",MONDO,disease,DISEASE_16249
16250,16250,16250,16250,16250,16250,16250,16250,MONDO:0009909,progesterone resistance,MONDO,disease,DISEASE_16250
16251,16251,16251,16251,16251,16251,16251,16251,MONDO:0020390,pulmonary artery coming from patent ductus arteriosus,MONDO,disease,DISEASE_16251
16252,16252,16252,16252,16252,16252,16252,16252,MONDO:0017942,Hendra virus infection,MONDO,disease,DISEASE_16252
16253,16253,16253,16253,16253,16253,16253,16253,MONDO:0018581,progressive encephalomyelitis with rigidity and myoclonus,MONDO,disease,DISEASE_16253
16254,16254,16254,16254,16254,16254,16254,16254,MONDO:0015595,posttransplant acute limbic encephalitis,MONDO,disease,DISEASE_16254
16255,16255,16255,16255,16255,16255,16255,16255,MONDO:0017685,"vitamin B12-responsive methylmalonic acidemia, type cblDv2",MONDO,disease,DISEASE_16255
16256,16256,16256,16256,16256,16256,16256,16256,MONDO:0001918,epiphora due to excess lacrimation,MONDO,disease,DISEASE_16256
16257,16257,16257,16257,16257,16257,16257,16257,MONDO:1011831_MONDO:1011832_MONDO:1011847_MONDO:1011865_MONDO:1011882,"distal axonopathy, non-human animal",MONDO_grouped,disease,DISEASE_16257
16258,16258,16258,16258,16258,16258,16258,16258,MONDO:0013967_MONDO:0013945_MONDO:0013950_MONDO:0009959_MONDO:0054549_MONDO:0013943_MONDO:0013931_MONDO:0011101_MONDO:0008736_MONDO:0013937_MONDO:0013933_MONDO:0013939_MONDO:0019234,peroxisome biogenesis disorder,MONDO_grouped,disease,DISEASE_16258
16259,16259,16259,16259,16259,16259,16259,16259,MONDO:0015282,cardiomyopathy-cataract-hip spine disease syndrome,MONDO,disease,DISEASE_16259
16260,16260,16260,16260,16260,16260,16260,16260,MONDO:0850388,"childhood supratentorial embryonal tumor with multilayered rosettes, C19MC-altered",MONDO,disease,DISEASE_16260
16261,16261,16261,16261,16261,16261,16261,16261,MONDO:0036511,childhood malignant kidney neoplasm,MONDO,disease,DISEASE_16261
16262,16262,16262,16262,16262,16262,16262,16262,MONDO:0004651,smallpox,MONDO,disease,DISEASE_16262
16263,16263,16263,16263,16263,16263,16263,16263,MONDO:0018053,trichothiodystrophy,MONDO,disease,DISEASE_16263
16264,16264,16264,16264,16264,16264,16264,16264,MONDO:0001519,entropion,MONDO,disease,DISEASE_16264
16265,16265,16265,16265,16265,16265,16265,16265,MONDO:0009498,lethal Kniest-like dysplasia,MONDO,disease,DISEASE_16265
16266,16266,16266,16266,16266,16266,16266,16266,MONDO:0008087,hereditary neuropathy with liability to pressure palsies,MONDO,disease,DISEASE_16266
16267,16267,16267,16267,16267,16267,16267,16267,MONDO:0029131,"peripheral neuropathy, autosomal recessive, with or without impaired intellectual development",MONDO,disease,DISEASE_16267
16268,16268,16268,16268,16268,16268,16268,16268,MONDO:0043452,"chromosome 8, trisomy",MONDO,disease,DISEASE_16268
16269,16269,16269,16269,16269,16269,16269,16269,MONDO:0035944,B-lymphoblastic leukemia/lymphoma with hypodiploidy,MONDO,disease,DISEASE_16269
16270,16270,16270,16270,16270,16270,16270,16270,MONDO:0014714,progressive microcephaly-seizures-cortical blindness-developmental delay syndrome,MONDO,disease,DISEASE_16270
16271,16271,16271,16271,16271,16271,16271,16271,MONDO:0002722,olfactory nerve neoplasm,MONDO,disease,DISEASE_16271
16272,16272,16272,16272,16272,16272,16272,16272,MONDO:0003399,pineal region yolk sac tumor,MONDO,disease,DISEASE_16272
16273,16273,16273,16273,16273,16273,16273,16273,MONDO:0010485,X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome,MONDO,disease,DISEASE_16273
16274,16274,16274,16274,16274,16274,16274,16274,MONDO:0012872,"thrombophilia, familial, due to decreased release of tissue plasminogen activator",MONDO,disease,DISEASE_16274
16275,16275,16275,16275,16275,16275,16275,16275,MONDO:0021271,villous adenoma of colon,MONDO,disease,DISEASE_16275
16276,16276,16276,16276,16276,16276,16276,16276,MONDO:0036193,parkinsonism with polyneuropathy,MONDO,disease,DISEASE_16276
16277,16277,16277,16277,16277,16277,16277,16277,MONDO:0700079,hormone receptor-positive breast cancer,MONDO,disease,DISEASE_16277
16278,16278,16278,16278,16278,16278,16278,16278,MONDO:0007470,calvarial doughnut lesions-bone fragility syndrome,MONDO,disease,DISEASE_16278
16279,16279,16279,16279,16279,16279,16279,16279,MONDO:0021652,diffuse type adenocarcinoma,MONDO,disease,DISEASE_16279
16280,16280,16280,16280,16280,16280,16280,16280,MONDO:0007123,ankyloblepharon filiforme adnatum-cleft palate syndrome,MONDO,disease,DISEASE_16280
16281,16281,16281,16281,16281,16281,16281,16281,MONDO:0958071,Hao-Fountain syndrome due to USP7 mutation,MONDO,disease,DISEASE_16281
16282,16282,16282,16282,16282,16282,16282,16282,MONDO:0003403,testicular non-seminomatous germ cell cancer,MONDO,disease,DISEASE_16282
16283,16283,16283,16283,16283,16283,16283,16283,MONDO:0006862,myofascial pain syndrome,MONDO,disease,DISEASE_16283
16284,16284,16284,16284,16284,16284,16284,16284,MONDO:0002098,facial nerve disorder,MONDO,disease,DISEASE_16284
16285,16285,16285,16285,16285,16285,16285,16285,MONDO:0019269,ichthyosis,MONDO,disease,DISEASE_16285
16286,16286,16286,16286,16286,16286,16286,16286,MONDO:0004020,mediastinal gray zone lymphoma,MONDO,disease,DISEASE_16286
16287,16287,16287,16287,16287,16287,16287,16287,MONDO:0003098,mediastinal neural neoplasm,MONDO,disease,DISEASE_16287
16288,16288,16288,16288,16288,16288,16288,16288,MONDO:0009393,ornithine translocase deficiency,MONDO,disease,DISEASE_16288
16289,16289,16289,16289,16289,16289,16289,16289,MONDO:0018737,catastrophic antiphospholipid syndrome,MONDO,disease,DISEASE_16289
16290,16290,16290,16290,16290,16290,16290,16290,MONDO:0002946,gynatresia,MONDO,disease,DISEASE_16290
16291,16291,16291,16291,16291,16291,16291,16291,MONDO:0022552,Bazopoulou Kyrkanidou syndrome,MONDO,disease,DISEASE_16291
16292,16292,16292,16292,16292,16292,16292,16292,MONDO:1012195,"ocular squamous cell carcinoma, domestic cat",MONDO,disease,DISEASE_16292
16293,16293,16293,16293,16293,16293,16293,16293,MONDO:0017190_MONDO:0017191,sporadic pheochromocytoma/secreting paraganglioma,MONDO_grouped,disease,DISEASE_16293
16294,16294,16294,16294,16294,16294,16294,16294,MONDO:0009502,pyruvate dehydrogenase E2 deficiency,MONDO,disease,DISEASE_16294
16295,16295,16295,16295,16295,16295,16295,16295,MONDO:0001896,obstructive hydrocephalus,MONDO,disease,DISEASE_16295
16296,16296,16296,16296,16296,16296,16296,16296,MONDO:0003769,herpetic gastritis,MONDO,disease,DISEASE_16296
16297,16297,16297,16297,16297,16297,16297,16297,MONDO:0007228,brachymesomelia-renal syndrome,MONDO,disease,DISEASE_16297
16298,16298,16298,16298,16298,16298,16298,16298,MONDO:0007784,selective pituitary resistance to thyroid hormone,MONDO,disease,DISEASE_16298
16299,16299,16299,16299,16299,16299,16299,16299,MONDO:0021220,eye neoplasm,MONDO,disease,DISEASE_16299
16300,16300,16300,16300,16300,16300,16300,16300,MONDO:0859213,"congenital heart defects, multiple types, 8, with or without heterotaxy",MONDO,disease,DISEASE_16300
16301,16301,16301,16301,16301,16301,16301,16301,MONDO:0007875,Larsen syndrome,MONDO,disease,DISEASE_16301
16302,16302,16302,16302,16302,16302,16302,16302,MONDO:0016386,hypogonadotropic hypogonadism-retinitis pigmentosa syndrome,MONDO,disease,DISEASE_16302
16303,16303,16303,16303,16303,16303,16303,16303,MONDO:0024386,"large cell lung carcinoma, clear cell variant",MONDO,disease,DISEASE_16303
16304,16304,16304,16304,16304,16304,16304,16304,MONDO:0003096_MONDO:0002323_MONDO:0003643,deep hemangioma,MONDO_grouped,disease,DISEASE_16304
16305,16305,16305,16305,16305,16305,16305,16305,MONDO:0005698,cervical incompetence,MONDO,disease,DISEASE_16305
16306,16306,16306,16306,16306,16306,16306,16306,MONDO:0012853,Fontaine progeroid syndrome,MONDO,disease,DISEASE_16306
16307,16307,16307,16307,16307,16307,16307,16307,MONDO:1011435,"Becker type muscular dystrophy, non-human animal",MONDO,disease,DISEASE_16307
16308,16308,16308,16308,16308,16308,16308,16308,MONDO:0011810,horizontal gaze palsy with progressive scoliosis,MONDO,disease,DISEASE_16308
16309,16309,16309,16309,16309,16309,16309,16309,MONDO:1010130,"hypertrichosis, non-human animal",MONDO,disease,DISEASE_16309
16310,16310,16310,16310,16310,16310,16310,16310,MONDO:0015313,"choanal atresia, bilateral",MONDO,disease,DISEASE_16310
16311,16311,16311,16311,16311,16311,16311,16311,MONDO:0007996,"microphthalmia, isolated, with corectopia",MONDO,disease,DISEASE_16311
16312,16312,16312,16312,16312,16312,16312,16312,MONDO:0005819,laryngeal tuberculosis,MONDO,disease,DISEASE_16312
16313,16313,16313,16313,16313,16313,16313,16313,MONDO:0018840,isolated congenital hepatic fibrosis,MONDO,disease,DISEASE_16313
16314,16314,16314,16314,16314,16314,16314,16314,MONDO:1012336,"reduced glutathione deficiency due to amino-acid transport defect, sheep",MONDO,disease,DISEASE_16314
16315,16315,16315,16315,16315,16315,16315,16315,MONDO:0003113_MONDO:0015935_MONDO:0018201,extragonadal germ cell cancer,MONDO_grouped,disease,DISEASE_16315
16316,16316,16316,16316,16316,16316,16316,16316,MONDO:0003740_MONDO:0003748,AIDS phobia,MONDO_grouped,disease,DISEASE_16316
16317,16317,16317,16317,16317,16317,16317,16317,MONDO:0020530,Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency,MONDO,disease,DISEASE_16317
16318,16318,16318,16318,16318,16318,16318,16318,MONDO:0100342_MONDO:0850125,malignant glioma,MONDO_grouped,disease,DISEASE_16318
16319,16319,16319,16319,16319,16319,16319,16319,MONDO:0000308_MONDO:0000256,primary systemic mycosis,MONDO_grouped,disease,DISEASE_16319
16320,16320,16320,16320,16320,16320,16320,16320,MONDO:0002420,tic disorder,MONDO,disease,DISEASE_16320
16321,16321,16321,16321,16321,16321,16321,16321,MONDO:0001557,olecranon bursitis,MONDO,disease,DISEASE_16321
16322,16322,16322,16322,16322,16322,16322,16322,MONDO:0005506,eccrine sweat gland cancer,MONDO,disease,DISEASE_16322
16323,16323,16323,16323,16323,16323,16323,16323,MONDO:0012629_MONDO:0700089_MONDO:0700088,paroxysmal nonkinesigenic dyskinesia,MONDO_grouped,disease,DISEASE_16323
16324,16324,16324,16324,16324,16324,16324,16324,MONDO:0022545,Barnicoat Baraitser syndrome,MONDO,disease,DISEASE_16324
16325,16325,16325,16325,16325,16325,16325,16325,MONDO:0006470,tonsillar squamous cell carcinoma,MONDO,disease,DISEASE_16325
16326,16326,16326,16326,16326,16326,16326,16326,MONDO:0006876,ocular tuberculosis,MONDO,disease,DISEASE_16326
16327,16327,16327,16327,16327,16327,16327,16327,MONDO:0044879,pancreatic mucinous-cystic neoplasm,MONDO,disease,DISEASE_16327
16328,16328,16328,16328,16328,16328,16328,16328,MONDO:1010159,"split hand, non-human animal",MONDO,disease,DISEASE_16328
16329,16329,16329,16329,16329,16329,16329,16329,MONDO:0004566,postgastrectomy syndrome,MONDO,disease,DISEASE_16329
16330,16330,16330,16330,16330,16330,16330,16330,MONDO:0004856,rosacea conjunctivitis,MONDO,disease,DISEASE_16330
16331,16331,16331,16331,16331,16331,16331,16331,MONDO:0031028,developmental and epileptic encephalopathy 105 with hypopituitarism,MONDO,disease,DISEASE_16331
16332,16332,16332,16332,16332,16332,16332,16332,MONDO:0020639,monosomy,MONDO,disease,DISEASE_16332
16333,16333,16333,16333,16333,16333,16333,16333,MONDO:0008775,"Amobarbital, deficient N-hydroxylation of",MONDO,disease,DISEASE_16333
16334,16334,16334,16334,16334,16334,16334,16334,MONDO:0970951,El Hayek-Chahrour neurodevelopmental disorder,MONDO,disease,DISEASE_16334
16335,16335,16335,16335,16335,16335,16335,16335,MONDO:0017337,inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency,MONDO,disease,DISEASE_16335
16336,16336,16336,16336,16336,16336,16336,16336,MONDO:0030827_MONDO:0800047,"macrothrombocytopenia, isolated, 2, autosomal dominant",MONDO_grouped,disease,DISEASE_16336
16337,16337,16337,16337,16337,16337,16337,16337,MONDO:0014181_MONDO:0027694_MONDO:0011632_MONDO:0012945_MONDO:0013891_MONDO:0011196_MONDO:0013264_MONDO:0013715_MONDO:0012790_MONDO:0011951_MONDO:0010459_MONDO:0014531_MONDO:0014223_MONDO:0007103_MONDO:0012077_MONDO:0011691_MONDO:0957538_MONDO:0012753_MONDO:0011223_MONDO:0004976_MONDO:0005145_MONDO:0011952,amyotrophic lateral sclerosis,MONDO_grouped,disease,DISEASE_16337
16338,16338,16338,16338,16338,16338,16338,16338,MONDO:0018007,mosaic genome-wide paternal uniparental disomy,MONDO,disease,DISEASE_16338
16339,16339,16339,16339,16339,16339,16339,16339,MONDO:0001484,paranoid schizophrenia,MONDO,disease,DISEASE_16339
16340,16340,16340,16340,16340,16340,16340,16340,MONDO:0017440_MONDO:0017482_MONDO:0017483,humeral agenesis/hypoplasia,MONDO_grouped,disease,DISEASE_16340
16341,16341,16341,16341,16341,16341,16341,16341,MONDO:0056816,vulvar neuroendocrine carcinoma,MONDO,disease,DISEASE_16341
16342,16342,16342,16342,16342,16342,16342,16342,MONDO:1011649,"persistent right aortic arch with subclavian artery and ligamentum arteriosum, non-human animal",MONDO,disease,DISEASE_16342
16343,16343,16343,16343,16343,16343,16343,16343,MONDO:0007045,"acrofacial dysostosis, Catania type",MONDO,disease,DISEASE_16343
16344,16344,16344,16344,16344,16344,16344,16344,MONDO:0024358,complex sleep apnea,MONDO,disease,DISEASE_16344
16345,16345,16345,16345,16345,16345,16345,16345,MONDO:1012270_MONDO:1012271_MONDO:1012272,"thrombasthenia, dog",MONDO_grouped,disease,DISEASE_16345
16346,16346,16346,16346,16346,16346,16346,16346,MONDO:0016301,congenitally corrected transposition of the great arteries,MONDO,disease,DISEASE_16346
16347,16347,16347,16347,16347,16347,16347,16347,MONDO:1010079,"prekallikrein deficiency, non-human animal",MONDO,disease,DISEASE_16347
16348,16348,16348,16348,16348,16348,16348,16348,MONDO:0008115_MONDO:0013691_MONDO:0015267,Feingold syndrome,MONDO_grouped,disease,DISEASE_16348
16349,16349,16349,16349,16349,16349,16349,16349,MONDO:0043349,intravascular papillary endothelial hyperplasia,MONDO,disease,DISEASE_16349
16350,16350,16350,16350,16350,16350,16350,16350,MONDO:0002266,malt worker's lung,MONDO,disease,DISEASE_16350
16351,16351,16351,16351,16351,16351,16351,16351,MONDO:0006353_MONDO:0003923_MONDO:0004327_MONDO:0004457_MONDO:0003752,paranasal sinus Schneiderian papilloma,MONDO_grouped,disease,DISEASE_16351
16352,16352,16352,16352,16352,16352,16352,16352,MONDO:0859189,"muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome",MONDO,disease,DISEASE_16352
16353,16353,16353,16353,16353,16353,16353,16353,MONDO:0045058_MONDO:0006068_MONDO:0006069,ACTH-producing pituitary gland neoplasm,MONDO_grouped,disease,DISEASE_16353
16354,16354,16354,16354,16354,16354,16354,16354,MONDO:0017818,lethal arteriopathy syndrome due to fibulin-4 deficiency,MONDO,disease,DISEASE_16354
16355,16355,16355,16355,16355,16355,16355,16355,MONDO:0022770,circumscribed cutaneous aplasia of the vertex,MONDO,disease,DISEASE_16355
16356,16356,16356,16356,16356,16356,16356,16356,MONDO:0003304,plexiform neurofibroma,MONDO,disease,DISEASE_16356
16357,16357,16357,16357,16357,16357,16357,16357,MONDO:0015203,coronary artery congenital malformation,MONDO,disease,DISEASE_16357
16358,16358,16358,16358,16358,16358,16358,16358,MONDO:0035819,cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome,MONDO,disease,DISEASE_16358
16359,16359,16359,16359,16359,16359,16359,16359,MONDO:0001673,diarrheal disease,MONDO,disease,DISEASE_16359
16360,16360,16360,16360,16360,16360,16360,16360,MONDO:0041186,Rowell syndrome,MONDO,disease,DISEASE_16360
16361,16361,16361,16361,16361,16361,16361,16361,MONDO:0001372,bladder neck cancer,MONDO,disease,DISEASE_16361
16362,16362,16362,16362,16362,16362,16362,16362,MONDO:0018133,attenuated Chédiak-Higashi syndrome,MONDO,disease,DISEASE_16362
16363,16363,16363,16363,16363,16363,16363,16363,MONDO:0024572,immunodeficiency-related disorder,MONDO,disease,DISEASE_16363
16364,16364,16364,16364,16364,16364,16364,16364,MONDO:0013564,anhaptoglobinemia,MONDO,disease,DISEASE_16364
16365,16365,16365,16365,16365,16365,16365,16365,MONDO:0013421,type II complement component 8 deficiency,MONDO,disease,DISEASE_16365
16366,16366,16366,16366,16366,16366,16366,16366,MONDO:0020370,Cogan-Reese syndrome,MONDO,disease,DISEASE_16366
16367,16367,16367,16367,16367,16367,16367,16367,MONDO:0032888,neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies,MONDO,disease,DISEASE_16367
16368,16368,16368,16368,16368,16368,16368,16368,MONDO:0009366,normal pressure hydrocephalus,MONDO,disease,DISEASE_16368
16369,16369,16369,16369,16369,16369,16369,16369,MONDO:0008689,dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema,MONDO,disease,DISEASE_16369
16370,16370,16370,16370,16370,16370,16370,16370,MONDO:0018870,arterial calcification of infancy,MONDO,disease,DISEASE_16370
16371,16371,16371,16371,16371,16371,16371,16371,MONDO:0020501,Crimean-Congo hemorrhagic fever,MONDO,disease,DISEASE_16371
16372,16372,16372,16372,16372,16372,16372,16372,MONDO:0001203,prolapse of lacrimal gland,MONDO,disease,DISEASE_16372
16373,16373,16373,16373,16373,16373,16373,16373,MONDO:0005254,symptomatic heart failure,MONDO,disease,DISEASE_16373
16374,16374,16374,16374,16374,16374,16374,16374,MONDO:0010099,Tay-Sachs disease AB variant,MONDO,disease,DISEASE_16374
16375,16375,16375,16375,16375,16375,16375,16375,MONDO:0011345,"facial dysmorphism, selective tooth agenesis, and choroid calcification",MONDO,disease,DISEASE_16375
16376,16376,16376,16376,16376,16376,16376,16376,MONDO:0043320,piriformis syndrome,MONDO,disease,DISEASE_16376
16377,16377,16377,16377,16377,16377,16377,16377,MONDO:0100241_MONDO:0004680,inherited thrombocytopenia,MONDO_grouped,disease,DISEASE_16377
16378,16378,16378,16378,16378,16378,16378,16378,MONDO:0013041,atypical hemolytic-uremic syndrome with I factor anomaly,MONDO,disease,DISEASE_16378
16379,16379,16379,16379,16379,16379,16379,16379,MONDO:0011786_MONDO:0005324_MONDO:0024332_MONDO:1011130,allergic rhinitis,MONDO_grouped,disease,DISEASE_16379
16380,16380,16380,16380,16380,16380,16380,16380,MONDO:0009858,Pfeiffer-Palm-Teller syndrome,MONDO,disease,DISEASE_16380
16381,16381,16381,16381,16381,16381,16381,16381,MONDO:0021475,benign neoplasm of nasal cavity,MONDO,disease,DISEASE_16381
16382,16382,16382,16382,16382,16382,16382,16382,MONDO:0022177,chromosome 13q trisomy,MONDO,disease,DISEASE_16382
16383,16383,16383,16383,16383,16383,16383,16383,MONDO:0033969,inflammatory bowel disease-recurrent sinopulmonary infections syndrome,MONDO,disease,DISEASE_16383
16384,16384,16384,16384,16384,16384,16384,16384,MONDO:0043459,radiation-induced disorder,MONDO,disease,DISEASE_16384
16385,16385,16385,16385,16385,16385,16385,16385,MONDO:0002039,cognitive disorder,MONDO,disease,DISEASE_16385
16386,16386,16386,16386,16386,16386,16386,16386,MONDO:0007404,Cri-du-chat syndrome,MONDO,disease,DISEASE_16386
16387,16387,16387,16387,16387,16387,16387,16387,MONDO:0012110,growth delay due to insulin-like growth factor type 1 deficiency,MONDO,disease,DISEASE_16387
16388,16388,16388,16388,16388,16388,16388,16388,MONDO:0800146,"agammaglobulinemia, autosomal recessive, due to BOB1 deficiency",MONDO,disease,DISEASE_16388
16389,16389,16389,16389,16389,16389,16389,16389,MONDO:0013270,"obsolete Rett syndrome, congenital variant",MONDO,disease,DISEASE_16389
16390,16390,16390,16390,16390,16390,16390,16390,MONDO:0005187,human herpesvirus 8 infection,MONDO,disease,DISEASE_16390
16391,16391,16391,16391,16391,16391,16391,16391,MONDO:0005157,lymphoid neoplasm,MONDO,disease,DISEASE_16391
16392,16392,16392,16392,16392,16392,16392,16392,MONDO:0003906,"ovarian yolk sac tumor, hepatoid pattern",MONDO,disease,DISEASE_16392
16393,16393,16393,16393,16393,16393,16393,16393,MONDO:0004919,infected hydrocele,MONDO,disease,DISEASE_16393
16394,16394,16394,16394,16394,16394,16394,16394,MONDO:0005235,smoldering plasma cell myeloma,MONDO,disease,DISEASE_16394
16395,16395,16395,16395,16395,16395,16395,16395,MONDO:0020646,ocular adnexal lymphoma,MONDO,disease,DISEASE_16395
16396,16396,16396,16396,16396,16396,16396,16396,MONDO:0000681,tactile agnosia,MONDO,disease,DISEASE_16396
16397,16397,16397,16397,16397,16397,16397,16397,MONDO:1010896,"sphingomyelin lipidosis, raccoon",MONDO,disease,DISEASE_16397
16398,16398,16398,16398,16398,16398,16398,16398,MONDO:0030604,cystic partially differentiated nephroblastoma,MONDO,disease,DISEASE_16398
16399,16399,16399,16399,16399,16399,16399,16399,MONDO:0400002,calcium-alkali syndrome,MONDO,disease,DISEASE_16399
16400,16400,16400,16400,16400,16400,16400,16400,MONDO:0023023,neonatal dacryocystitis,MONDO,disease,DISEASE_16400
16401,16401,16401,16401,16401,16401,16401,16401,MONDO:0700080,EPHB4-associated vascular malformation spectrum,MONDO,disease,DISEASE_16401
16402,16402,16402,16402,16402,16402,16402,16402,MONDO:0013873,IMAGe syndrome,MONDO,disease,DISEASE_16402
16403,16403,16403,16403,16403,16403,16403,16403,MONDO:0005063,medullary breast carcinoma,MONDO,disease,DISEASE_16403
16404,16404,16404,16404,16404,16404,16404,16404,MONDO:0019801_MONDO:0015128_MONDO:0043370_MONDO:0100315,acute adrenal insufficiency,MONDO_grouped,disease,DISEASE_16404
16405,16405,16405,16405,16405,16405,16405,16405,MONDO:0018777,autosomal dominant preaxial polydactyly-upperback hypertrichosis syndrome,MONDO,disease,DISEASE_16405
16406,16406,16406,16406,16406,16406,16406,16406,MONDO:1012445,"juvenile idiopathic epilepsy, horse",MONDO,disease,DISEASE_16406
16407,16407,16407,16407,16407,16407,16407,16407,MONDO:0009590,metachromatic leukodystrophy due to saposin B deficiency,MONDO,disease,DISEASE_16407
16408,16408,16408,16408,16408,16408,16408,16408,MONDO:0958115,autosomal recessive combined immunodeficiency due to complete IL6ST deficiency,MONDO,disease,DISEASE_16408
16409,16409,16409,16409,16409,16409,16409,16409,MONDO:0017686,inborn aminoacylase deficiency,MONDO,disease,DISEASE_16409
16410,16410,16410,16410,16410,16410,16410,16410,MONDO:0005820,Lassa fever,MONDO,disease,DISEASE_16410
16411,16411,16411,16411,16411,16411,16411,16411,MONDO:0016207,phacoanaphylactic uveitis,MONDO,disease,DISEASE_16411
16412,16412,16412,16412,16412,16412,16412,16412,MONDO:0023124,familial pulmonary arterial hypertension leucopenia and atrial septal defect,MONDO,disease,DISEASE_16412
16413,16413,16413,16413,16413,16413,16413,16413,MONDO:0001414,osteopoikilosis,MONDO,disease,DISEASE_16413
16414,16414,16414,16414,16414,16414,16414,16414,MONDO:0000895,nonmucinous bronchioloalveolar adenocarcinoma,MONDO,disease,DISEASE_16414
16415,16415,16415,16415,16415,16415,16415,16415,MONDO:0030046,neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity,MONDO,disease,DISEASE_16415
16416,16416,16416,16416,16416,16416,16416,16416,MONDO:0100273,glyceronephosphate O-acyltransferase deficiency,MONDO,disease,DISEASE_16416
16417,16417,16417,16417,16417,16417,16417,16417,MONDO:0016786,partial hydatidiform mole,MONDO,disease,DISEASE_16417
16418,16418,16418,16418,16418,16418,16418,16418,MONDO:0018197,"mitochondrial DNA depletion syndrome, hepatocerebrorenal form",MONDO,disease,DISEASE_16418
16419,16419,16419,16419,16419,16419,16419,16419,MONDO:0019355,adult-onset Still disease,MONDO,disease,DISEASE_16419
16420,16420,16420,16420,16420,16420,16420,16420,MONDO:0018465,insulin autoimmune syndrome,MONDO,disease,DISEASE_16420
16421,16421,16421,16421,16421,16421,16421,16421,MONDO:0015427_MONDO:1010422_MONDO:1010423,paroxysmal dyskinesia,MONDO_grouped,disease,DISEASE_16421
16422,16422,16422,16422,16422,16422,16422,16422,MONDO:0009205,faciocardiorenal syndrome,MONDO,disease,DISEASE_16422
16423,16423,16423,16423,16423,16423,16423,16423,MONDO:0042498,Ruzicka-Goerz-Anton syndrome,MONDO,disease,DISEASE_16423
16424,16424,16424,16424,16424,16424,16424,16424,MONDO:0018805,bile duct cyst,MONDO,disease,DISEASE_16424
16425,16425,16425,16425,16425,16425,16425,16425,MONDO:0100291,early T cell progenitor acute lymphoblastic leukemia,MONDO,disease,DISEASE_16425
16426,16426,16426,16426,16426,16426,16426,16426,MONDO:0044787,nasal cavity and paranasal sinus squamous cell carcinoma,MONDO,disease,DISEASE_16426
16427,16427,16427,16427,16427,16427,16427,16427,MONDO:0017795_MONDO:0000513_MONDO:0006079,ameloblastoma,MONDO_grouped,disease,DISEASE_16427
16428,16428,16428,16428,16428,16428,16428,16428,MONDO:0000726_MONDO:0005488_MONDO:0100076,idiopathic scoliosis,MONDO_grouped,disease,DISEASE_16428
16429,16429,16429,16429,16429,16429,16429,16429,MONDO:0044887,central nervous system non-hodgkin lymphoma,MONDO,disease,DISEASE_16429
16430,16430,16430,16430,16430,16430,16430,16430,MONDO:0009348,classic Hodgkin lymphoma,MONDO,disease,DISEASE_16430
16431,16431,16431,16431,16431,16431,16431,16431,MONDO:0006407,sarcomatoid mesothelioma,MONDO,disease,DISEASE_16431
16432,16432,16432,16432,16432,16432,16432,16432,MONDO:0006679,bladder neck obstruction,MONDO,disease,DISEASE_16432
16433,16433,16433,16433,16433,16433,16433,16433,MONDO:0012564,Polyosteolysis-hyperostosis syndrome,MONDO,disease,DISEASE_16433
16434,16434,16434,16434,16434,16434,16434,16434,MONDO:0005896,Paramyxoviridae infectious disease,MONDO,disease,DISEASE_16434
16435,16435,16435,16435,16435,16435,16435,16435,MONDO:1012444,"polled and multisystemic syndrome, cattle",MONDO,disease,DISEASE_16435
16436,16436,16436,16436,16436,16436,16436,16436,MONDO:0041095,malignant otitis externa caused by Pseudomonas aeruginosa,MONDO,disease,DISEASE_16436
16437,16437,16437,16437,16437,16437,16437,16437,MONDO:1012895,"thrombocytopenia, TUBB1-related, dog",MONDO,disease,DISEASE_16437
16438,16438,16438,16438,16438,16438,16438,16438,MONDO:0008460,splenogonadal fusion-limb defects-micrognathia syndrome,MONDO,disease,DISEASE_16438
16439,16439,16439,16439,16439,16439,16439,16439,MONDO:0016840,trisomy 17p,MONDO,disease,DISEASE_16439
16440,16440,16440,16440,16440,16440,16440,16440,MONDO:0004781_MONDO:0003672_MONDO:0003678,acute myocardial infarction,MONDO_grouped,disease,DISEASE_16440
16441,16441,16441,16441,16441,16441,16441,16441,MONDO:0100167,"pulmonary disease, chronic obstructive, susceptibility to",MONDO,disease,DISEASE_16441
16442,16442,16442,16442,16442,16442,16442,16442,MONDO:1011748,"urticaria pigmentosa, non-human animal",MONDO,disease,DISEASE_16442
16443,16443,16443,16443,16443,16443,16443,16443,MONDO:0958354_MONDO:0968990_MONDO:0968991,genetic central precocious puberty in female,MONDO_grouped,disease,DISEASE_16443
16444,16444,16444,16444,16444,16444,16444,16444,MONDO:0007289,cataract 13 with adult I phenotype,MONDO,disease,DISEASE_16444
16445,16445,16445,16445,16445,16445,16445,16445,MONDO:0859350,"neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies",MONDO,disease,DISEASE_16445
16446,16446,16446,16446,16446,16446,16446,16446,MONDO:0002993_MONDO:0024638,pancreatic somatostatinoma,MONDO_grouped,disease,DISEASE_16446
16447,16447,16447,16447,16447,16447,16447,16447,MONDO:1011306_MONDO:1012982,"cardiovascular disorder, non-human animal",MONDO_grouped,disease,DISEASE_16447
16448,16448,16448,16448,16448,16448,16448,16448,MONDO:1011698,"reduced glutathione deficiency due to amino-acid transport defect, non-human animal",MONDO,disease,DISEASE_16448
16449,16449,16449,16449,16449,16449,16449,16449,MONDO:0024560,PDA1,MONDO,disease,DISEASE_16449
16450,16450,16450,16450,16450,16450,16450,16450,MONDO:1011699,"reduced glutathione deficiency, non-human animal",MONDO,disease,DISEASE_16450
16451,16451,16451,16451,16451,16451,16451,16451,MONDO:0859253,"osteoporosis, childhood- or juvenile-onset, with developmental delay",MONDO,disease,DISEASE_16451
16452,16452,16452,16452,16452,16452,16452,16452,MONDO:0007499,ear folding,MONDO,disease,DISEASE_16452
16453,16453,16453,16453,16453,16453,16453,16453,MONDO:0013467,immunodeficiency due to ficolin3 deficiency,MONDO,disease,DISEASE_16453
16454,16454,16454,16454,16454,16454,16454,16454,MONDO:0002811,main bronchus cancer,MONDO,disease,DISEASE_16454
16455,16455,16455,16455,16455,16455,16455,16455,MONDO:0005971,staphyloenterotoxemia,MONDO,disease,DISEASE_16455
16456,16456,16456,16456,16456,16456,16456,16456,MONDO:0005037,gastric intestinal type adenocarcinoma,MONDO,disease,DISEASE_16456
16457,16457,16457,16457,16457,16457,16457,16457,MONDO:0000550,extra-adrenal sympathetic paraganglioma,MONDO,disease,DISEASE_16457
16458,16458,16458,16458,16458,16458,16458,16458,MONDO:0005144,familial amyotrophic lateral sclerosis,MONDO,disease,DISEASE_16458
16459,16459,16459,16459,16459,16459,16459,16459,MONDO:0859517,"congenital myopathy 2b, severe infantile, autosomal recessive",MONDO,disease,DISEASE_16459
16460,16460,16460,16460,16460,16460,16460,16460,MONDO:0004440,pineal region meningioma,MONDO,disease,DISEASE_16460
16461,16461,16461,16461,16461,16461,16461,16461,MONDO:0004108,diaphragma sellae meningioma,MONDO,disease,DISEASE_16461
16462,16462,16462,16462,16462,16462,16462,16462,MONDO:0010306_MONDO:0010655_MONDO:0019420_MONDO:0019421,"X-linked intellectual disability, Cabezas type",MONDO_grouped,disease,DISEASE_16462
16463,16463,16463,16463,16463,16463,16463,16463,MONDO:0018268,Medich giant platelet syndrome,MONDO,disease,DISEASE_16463
16464,16464,16464,16464,16464,16464,16464,16464,MONDO:0031646,Braddock-Carey syndrome,MONDO,disease,DISEASE_16464
16465,16465,16465,16465,16465,16465,16465,16465,MONDO:0017590,carcinoma of the ampulla of vater,MONDO,disease,DISEASE_16465
16466,16466,16466,16466,16466,16466,16466,16466,MONDO:0018746,mucous membrane pemphigoid,MONDO,disease,DISEASE_16466
16467,16467,16467,16467,16467,16467,16467,16467,MONDO:0015019,Yao syndrome,MONDO,disease,DISEASE_16467
16468,16468,16468,16468,16468,16468,16468,16468,MONDO:0011135,"superior transverse scapular ligament, calcification of, familial",MONDO,disease,DISEASE_16468
16469,16469,16469,16469,16469,16469,16469,16469,MONDO:0011155,vacuolar Neuromyopathy,MONDO,disease,DISEASE_16469
16470,16470,16470,16470,16470,16470,16470,16470,MONDO:0002317,central nervous system origin vertigo,MONDO,disease,DISEASE_16470
16471,16471,16471,16471,16471,16471,16471,16471,MONDO:1011412,"methemoglobinemia, non-human animal",MONDO,disease,DISEASE_16471
16472,16472,16472,16472,16472,16472,16472,16472,MONDO:0700173,horse sarcoid,MONDO,disease,DISEASE_16472
16473,16473,16473,16473,16473,16473,16473,16473,MONDO:0100517,PSAP-related sphingolipidosis,MONDO,disease,DISEASE_16473
16474,16474,16474,16474,16474,16474,16474,16474,MONDO:0014552,lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome,MONDO,disease,DISEASE_16474
16475,16475,16475,16475,16475,16475,16475,16475,MONDO:0006450,therapy-related myeloid neoplasm,MONDO,disease,DISEASE_16475
16476,16476,16476,16476,16476,16476,16476,16476,MONDO:0004645,cheek mucosa cancer,MONDO,disease,DISEASE_16476
16477,16477,16477,16477,16477,16477,16477,16477,MONDO:0016010,vitamin K-antagonist embryofetopathy,MONDO,disease,DISEASE_16477
16478,16478,16478,16478,16478,16478,16478,16478,MONDO:0017781,12p12.1 microdeletion syndrome,MONDO,disease,DISEASE_16478
16479,16479,16479,16479,16479,16479,16479,16479,MONDO:0850281,mammary analog secretory carcinoma,MONDO,disease,DISEASE_16479
16480,16480,16480,16480,16480,16480,16480,16480,MONDO:0007944_MONDO:0009558_MONDO:0013385_MONDO:0030067,Treacher Collins syndrome,MONDO_grouped,disease,DISEASE_16480
16481,16481,16481,16481,16481,16481,16481,16481,MONDO:0001160,dissociative disorder,MONDO,disease,DISEASE_16481
16482,16482,16482,16482,16482,16482,16482,16482,MONDO:0010798,proximal tubulopathy-diabetes mellitus-cerebellar ataxia syndrome,MONDO,disease,DISEASE_16482
16483,16483,16483,16483,16483,16483,16483,16483,MONDO:0100567,hereditary angioedema with normal C1Inh,MONDO,disease,DISEASE_16483
16484,16484,16484,16484,16484,16484,16484,16484,MONDO:0019188,Rubinstein-Taybi syndrome,MONDO,disease,DISEASE_16484
16485,16485,16485,16485,16485,16485,16485,16485,MONDO:0007603,Felty syndrome,MONDO,disease,DISEASE_16485
16486,16486,16486,16486,16486,16486,16486,16486,MONDO:0012986,bilateral parasagittal parieto-occipital polymicrogyria,MONDO,disease,DISEASE_16486
16487,16487,16487,16487,16487,16487,16487,16487,MONDO:0007785,"hyperthyroxinemia, dystransthyretinemic",MONDO,disease,DISEASE_16487
16488,16488,16488,16488,16488,16488,16488,16488,MONDO:0033169,curariform drugs toxicity,MONDO,disease,DISEASE_16488
16489,16489,16489,16489,16489,16489,16489,16489,MONDO:0011209,progeroid facial appearance with hand anomalies,MONDO,disease,DISEASE_16489
16490,16490,16490,16490,16490,16490,16490,16490,MONDO:0017462_MONDO:0017463_MONDO:0017464_MONDO:0017465_MONDO:0017466,congenital pseudoarthrosis of the tibia,MONDO_grouped,disease,DISEASE_16490
16491,16491,16491,16491,16491,16491,16491,16491,MONDO:0021631,brain astrocytoma,MONDO,disease,DISEASE_16491
16492,16492,16492,16492,16492,16492,16492,16492,MONDO:0011449,Salla disease,MONDO,disease,DISEASE_16492
16493,16493,16493,16493,16493,16493,16493,16493,MONDO:0019536,Shiga toxin-associated hemolytic uremic syndrome,MONDO,disease,DISEASE_16493
16494,16494,16494,16494,16494,16494,16494,16494,MONDO:0020741,pyridoxine-dependent epilepsy caused by ALDH7A1 mutant,MONDO,disease,DISEASE_16494
16495,16495,16495,16495,16495,16495,16495,16495,MONDO:0100434,chronic mountain sickness,MONDO,disease,DISEASE_16495
16496,16496,16496,16496,16496,16496,16496,16496,MONDO:0859371,"rhabdomyolysis, susceptibility to, 1",MONDO,disease,DISEASE_16496
16497,16497,16497,16497,16497,16497,16497,16497,MONDO:0007375,epithelial basement membrane dystrophy,MONDO,disease,DISEASE_16497
16498,16498,16498,16498,16498,16498,16498,16498,MONDO:0004039,papillary extrahepatic bile duct adenocarcinoma,MONDO,disease,DISEASE_16498
16499,16499,16499,16499,16499,16499,16499,16499,MONDO:0022795,deficiency of coenzyme q cytochrome c reductase,MONDO,disease,DISEASE_16499
16500,16500,16500,16500,16500,16500,16500,16500,MONDO:0011783_MONDO:0011969_MONDO:0014270_MONDO:0012117_MONDO:0011291_MONDO:0011933_MONDO:0011772_MONDO:0013810_MONDO:0012635_MONDO:0013325_MONDO:0010490_MONDO:0012118_MONDO:0010998_MONDO:0013349_MONDO:0013281_MONDO:0100586_MONDO:0100559_MONDO:0100589,ALG12-congenital disorder of glycosylation,MONDO_grouped,disease,DISEASE_16500
16501,16501,16501,16501,16501,16501,16501,16501,MONDO:1011960,"rupture of the cranial cruciate ligament, non-human animal",MONDO,disease,DISEASE_16501
16502,16502,16502,16502,16502,16502,16502,16502,MONDO:0006429,splenic hodgkin lymphoma,MONDO,disease,DISEASE_16502
16503,16503,16503,16503,16503,16503,16503,16503,MONDO:1011455,"arthrogryposis multiplex congenita, non-human animal",MONDO,disease,DISEASE_16503
16504,16504,16504,16504,16504,16504,16504,16504,MONDO:0023006,doxorubicin induced cardiomyopathy,MONDO,disease,DISEASE_16504
16505,16505,16505,16505,16505,16505,16505,16505,MONDO:0007421,deafness-ear malformation-facial palsy syndrome,MONDO,disease,DISEASE_16505
16506,16506,16506,16506,16506,16506,16506,16506,MONDO:0003510,malignant testicular germ cell tumor,MONDO,disease,DISEASE_16506
16507,16507,16507,16507,16507,16507,16507,16507,MONDO:0012759_MONDO:0008898_MONDO:0008899_MONDO:0000111,"camptodactyly syndrome, Guadalajara",MONDO_grouped,disease,DISEASE_16507
16508,16508,16508,16508,16508,16508,16508,16508,MONDO:0958279,megalencephaly-polydactyly syndrome,MONDO,disease,DISEASE_16508
16509,16509,16509,16509,16509,16509,16509,16509,MONDO:0034142,pancreatic agenesis-holoprosencephaly syndrome,MONDO,disease,DISEASE_16509
16510,16510,16510,16510,16510,16510,16510,16510,MONDO:0004209,cerebral primitive neuroectodermal tumor,MONDO,disease,DISEASE_16510
16511,16511,16511,16511,16511,16511,16511,16511,MONDO:0001215,allescheriosis,MONDO,disease,DISEASE_16511
16512,16512,16512,16512,16512,16512,16512,16512,MONDO:0007744,cholesterol-ester transfer protein deficiency,MONDO,disease,DISEASE_16512
16513,16513,16513,16513,16513,16513,16513,16513,MONDO:0003319,scrotum neoplasm,MONDO,disease,DISEASE_16513
16514,16514,16514,16514,16514,16514,16514,16514,MONDO:0008697,obsolete acetophenetidin sensitivity,MONDO,disease,DISEASE_16514
16515,16515,16515,16515,16515,16515,16515,16515,MONDO:0009491,Haim-Munk syndrome,MONDO,disease,DISEASE_16515
16516,16516,16516,16516,16516,16516,16516,16516,MONDO:0015262,brachyolmia,MONDO,disease,DISEASE_16516
16517,16517,16517,16517,16517,16517,16517,16517,MONDO:0011501,wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia,MONDO,disease,DISEASE_16517
16518,16518,16518,16518,16518,16518,16518,16518,MONDO:0003470,cellular ependymoma,MONDO,disease,DISEASE_16518
16519,16519,16519,16519,16519,16519,16519,16519,MONDO:0018112,obsolete isolated scaphocephaly,MONDO,disease,DISEASE_16519
16520,16520,16520,16520,16520,16520,16520,16520,MONDO:0009238,hereditary folate malabsorption,MONDO,disease,DISEASE_16520
16521,16521,16521,16521,16521,16521,16521,16521,MONDO:0010515,Meester-Loeys syndrome,MONDO,disease,DISEASE_16521
16522,16522,16522,16522,16522,16522,16522,16522,MONDO:0043071,Zazam Sheriff Phillips syndrome,MONDO,disease,DISEASE_16522
16523,16523,16523,16523,16523,16523,16523,16523,MONDO:0022022,bowenoid papulosis,MONDO,disease,DISEASE_16523
16524,16524,16524,16524,16524,16524,16524,16524,MONDO:0002078,heart septal defect,MONDO,disease,DISEASE_16524
16525,16525,16525,16525,16525,16525,16525,16525,MONDO:0013333,odontoid hypoplasia,MONDO,disease,DISEASE_16525
16526,16526,16526,16526,16526,16526,16526,16526,MONDO:0019399,Isaac syndrome,MONDO,disease,DISEASE_16526
16527,16527,16527,16527,16527,16527,16527,16527,MONDO:0013535,hydroxyacyl glutathione hydrolase deficiency,MONDO,disease,DISEASE_16527
16528,16528,16528,16528,16528,16528,16528,16528,MONDO:0035450,aprosencephaly,MONDO,disease,DISEASE_16528
16529,16529,16529,16529,16529,16529,16529,16529,MONDO:1010501,"Budd-chiari syndrome, dog",MONDO,disease,DISEASE_16529
16530,16530,16530,16530,16530,16530,16530,16530,MONDO:1011315,"disorder of orbital region, non-human animal",MONDO,disease,DISEASE_16530
16531,16531,16531,16531,16531,16531,16531,16531,MONDO:0004114,urinary bladder small cell neuroendocrine carcinoma,MONDO,disease,DISEASE_16531
16532,16532,16532,16532,16532,16532,16532,16532,MONDO:0025491,feline infectious peritonitis,MONDO,disease,DISEASE_16532
16533,16533,16533,16533,16533,16533,16533,16533,MONDO:0004080,glottis squamous cell carcinoma,MONDO,disease,DISEASE_16533
16534,16534,16534,16534,16534,16534,16534,16534,MONDO:0005609,herpes zoster,MONDO,disease,DISEASE_16534
16535,16535,16535,16535,16535,16535,16535,16535,MONDO:1011102_MONDO:1011103_MONDO:1011104,"renal agenesis, dog",MONDO_grouped,disease,DISEASE_16535
16536,16536,16536,16536,16536,16536,16536,16536,MONDO:0009268,Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,MONDO,disease,DISEASE_16536
16537,16537,16537,16537,16537,16537,16537,16537,MONDO:0007871,familial congenital nasolacrimal duct obstruction,MONDO,disease,DISEASE_16537
16538,16538,16538,16538,16538,16538,16538,16538,MONDO:0017579,Baraitser-Winter cerebrofrontofacial syndrome,MONDO,disease,DISEASE_16538
16539,16539,16539,16539,16539,16539,16539,16539,MONDO:0019892,distal monosomy 7p,MONDO,disease,DISEASE_16539
16540,16540,16540,16540,16540,16540,16540,16540,MONDO:0018001,inverse Klippel-Trenaunay syndrome,MONDO,disease,DISEASE_16540
16541,16541,16541,16541,16541,16541,16541,16541,MONDO:0018846_MONDO:0017967,penile agenesis,MONDO_grouped,disease,DISEASE_16541
16542,16542,16542,16542,16542,16542,16542,16542,MONDO:0023682,tympanic paraganglioma,MONDO,disease,DISEASE_16542
16543,16543,16543,16543,16543,16543,16543,16543,MONDO:0021353,tumor of uterus,MONDO,disease,DISEASE_16543
16544,16544,16544,16544,16544,16544,16544,16544,MONDO:0006855,mesenteric vascular occlusion,MONDO,disease,DISEASE_16544
16545,16545,16545,16545,16545,16545,16545,16545,MONDO:0001481,femoral vein thrombophlebitis,MONDO,disease,DISEASE_16545
16546,16546,16546,16546,16546,16546,16546,16546,MONDO:0015051,tubular duplication of the esophagus,MONDO,disease,DISEASE_16546
16547,16547,16547,16547,16547,16547,16547,16547,MONDO:0013254,"microcephaly, seizures, and developmental delay",MONDO,disease,DISEASE_16547
16548,16548,16548,16548,16548,16548,16548,16548,MONDO:0001636,mechanical entropion,MONDO,disease,DISEASE_16548
16549,16549,16549,16549,16549,16549,16549,16549,MONDO:0041259,diphtheritic myocarditis,MONDO,disease,DISEASE_16549
16550,16550,16550,16550,16550,16550,16550,16550,MONDO:0859172,"hemolytic disease of fetus and newborn, RH-induced",MONDO,disease,DISEASE_16550
16551,16551,16551,16551,16551,16551,16551,16551,MONDO:0015345,perioral myoclonia with absences,MONDO,disease,DISEASE_16551
16552,16552,16552,16552,16552,16552,16552,16552,MONDO:0023149,infection due to clostridium perfringens,MONDO,disease,DISEASE_16552
16553,16553,16553,16553,16553,16553,16553,16553,MONDO:1010076,"hypereosinophilic syndrome, non-human animal",MONDO,disease,DISEASE_16553
16554,16554,16554,16554,16554,16554,16554,16554,MONDO:0859146,"growth restriction, hypoplastic kidneys, alopecia, and distinctive facies",MONDO,disease,DISEASE_16554
16555,16555,16555,16555,16555,16555,16555,16555,MONDO:0004708,esophagus carcinoma in situ,MONDO,disease,DISEASE_16555
16556,16556,16556,16556,16556,16556,16556,16556,MONDO:0010207,wooly hair-hypotrichosis-everted lower lip-outstanding ears syndrome,MONDO,disease,DISEASE_16556
16557,16557,16557,16557,16557,16557,16557,16557,MONDO:0060527,maleylacetoacetate isomerase deficiency,MONDO,disease,DISEASE_16557
16558,16558,16558,16558,16558,16558,16558,16558,MONDO:0958274,benign atrophic papulosis,MONDO,disease,DISEASE_16558
16559,16559,16559,16559,16559,16559,16559,16559,MONDO:0100584,SNUPN-related muscular dystrophy with or without multi-system involvement,MONDO,disease,DISEASE_16559
16560,16560,16560,16560,16560,16560,16560,16560,MONDO:0005005,clear cell renal carcinoma,MONDO,disease,DISEASE_16560
16561,16561,16561,16561,16561,16561,16561,16561,MONDO:0005710,composite lymphoma,MONDO,disease,DISEASE_16561
16562,16562,16562,16562,16562,16562,16562,16562,MONDO:0001947,suppurative thyroiditis,MONDO,disease,DISEASE_16562
16563,16563,16563,16563,16563,16563,16563,16563,MONDO:0010872,"parotid salivary glands, polycystic dysgenetic disease of",MONDO,disease,DISEASE_16563
16564,16564,16564,16564,16564,16564,16564,16564,MONDO:0016608,megalencephaly,MONDO,disease,DISEASE_16564
16565,16565,16565,16565,16565,16565,16565,16565,MONDO:0015557,Smouldering systemic mastocytosis,MONDO,disease,DISEASE_16565
16566,16566,16566,16566,16566,16566,16566,16566,MONDO:0800500,childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy,MONDO,disease,DISEASE_16566
16567,16567,16567,16567,16567,16567,16567,16567,MONDO:0020473,dappled diaphyseal dysplasia,MONDO,disease,DISEASE_16567
16568,16568,16568,16568,16568,16568,16568,16568,MONDO:0018446,autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome,MONDO,disease,DISEASE_16568
16569,16569,16569,16569,16569,16569,16569,16569,MONDO:0011373,"urinary tract infections, recurrent, susceptibility to",MONDO,disease,DISEASE_16569
16570,16570,16570,16570,16570,16570,16570,16570,MONDO:0022734,chorioretinopathy dominant form microcephaly,MONDO,disease,DISEASE_16570
16571,16571,16571,16571,16571,16571,16571,16571,MONDO:0043154,neonatal ovarian cyst,MONDO,disease,DISEASE_16571
16572,16572,16572,16572,16572,16572,16572,16572,MONDO:0018536,adenocarcinoma of gallbladder and extrahepatic biliary tract,MONDO,disease,DISEASE_16572
16573,16573,16573,16573,16573,16573,16573,16573,MONDO:0007910,lipoprotein types--Lt system,MONDO,disease,DISEASE_16573
16574,16574,16574,16574,16574,16574,16574,16574,MONDO:0022803,coloboma porencephaly hydronephrosis,MONDO,disease,DISEASE_16574
16575,16575,16575,16575,16575,16575,16575,16575,MONDO:0043009,hereditary lethal multiple congenital anomalies/dysmorphic syndrome,MONDO,disease,DISEASE_16575
16576,16576,16576,16576,16576,16576,16576,16576,MONDO:0005511,janus kinase-3 deficiency,MONDO,disease,DISEASE_16576
16577,16577,16577,16577,16577,16577,16577,16577,MONDO:0020400,congenital supravalvular mitral ring,MONDO,disease,DISEASE_16577
16578,16578,16578,16578,16578,16578,16578,16578,MONDO:0019586,X-linked nonsyndromic hearing loss,MONDO,disease,DISEASE_16578
16579,16579,16579,16579,16579,16579,16579,16579,MONDO:0018089_MONDO:0018090,double outlet right ventricle,MONDO_grouped,disease,DISEASE_16579
16580,16580,16580,16580,16580,16580,16580,16580,MONDO:1012966,"congenital disorder of glycosylation, non-human animal",MONDO,disease,DISEASE_16580
16581,16581,16581,16581,16581,16581,16581,16581,MONDO:0016192,qualitative or quantitative defects of telethonin,MONDO,disease,DISEASE_16581
16582,16582,16582,16582,16582,16582,16582,16582,MONDO:0015264,cryptogenic organizing pneumonia,MONDO,disease,DISEASE_16582
16583,16583,16583,16583,16583,16583,16583,16583,MONDO:0014327_MONDO:0957303_MONDO:0013073_MONDO:0010962_MONDO:0007758_MONDO:0968949,"palmoplantar keratoderma, nonepidermolytic, focal or diffuse",MONDO_grouped,disease,DISEASE_16583
16584,16584,16584,16584,16584,16584,16584,16584,MONDO:0005185,chronic childhood arthritis,MONDO,disease,DISEASE_16584
16585,16585,16585,16585,16585,16585,16585,16585,MONDO:0025369,Nairobi sheep disease,MONDO,disease,DISEASE_16585
16586,16586,16586,16586,16586,16586,16586,16586,MONDO:0000190,ventricular fibrillation,MONDO,disease,DISEASE_16586
16587,16587,16587,16587,16587,16587,16587,16587,MONDO:0017692,generalized galactose epimerase deficiency,MONDO,disease,DISEASE_16587
16588,16588,16588,16588,16588,16588,16588,16588,MONDO:0014238,severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome,MONDO,disease,DISEASE_16588
16589,16589,16589,16589,16589,16589,16589,16589,MONDO:0005114_MONDO:0005923_MONDO:0006913,pneumococcal infection,MONDO_grouped,disease,DISEASE_16589
16590,16590,16590,16590,16590,16590,16590,16590,MONDO:0015028,"48,XXYY syndrome",MONDO,disease,DISEASE_16590
16591,16591,16591,16591,16591,16591,16591,16591,MONDO:0011614,3-hydroxy-3-methylglutaryl-CoA synthase deficiency,MONDO,disease,DISEASE_16591
16592,16592,16592,16592,16592,16592,16592,16592,MONDO:0015742,periventricular leukomalacia,MONDO,disease,DISEASE_16592
16593,16593,16593,16593,16593,16593,16593,16593,MONDO:0019073,hypotrichosis-lymphedema-telangiectasia-renal defect syndrome,MONDO,disease,DISEASE_16593
16594,16594,16594,16594,16594,16594,16594,16594,MONDO:0017192,sporadic secreting paraganglioma,MONDO,disease,DISEASE_16594
16595,16595,16595,16595,16595,16595,16595,16595,MONDO:0020409,univentricular heart with single atrio-ventricular valve,MONDO,disease,DISEASE_16595
16596,16596,16596,16596,16596,16596,16596,16596,MONDO:0017572,tick-borne encephalitis,MONDO,disease,DISEASE_16596
16597,16597,16597,16597,16597,16597,16597,16597,MONDO:0017183,hyperinsulinism due to UCP2 deficiency,MONDO,disease,DISEASE_16597
16598,16598,16598,16598,16598,16598,16598,16598,MONDO:0009356,autosomal recessive humeroradial synostosis,MONDO,disease,DISEASE_16598
16599,16599,16599,16599,16599,16599,16599,16599,MONDO:0021804,silicotuberculosis,MONDO,disease,DISEASE_16599
16600,16600,16600,16600,16600,16600,16600,16600,MONDO:0001491,cough variant asthma,MONDO,disease,DISEASE_16600
16601,16601,16601,16601,16601,16601,16601,16601,MONDO:0006583,necrobiosis lipoidica,MONDO,disease,DISEASE_16601
16602,16602,16602,16602,16602,16602,16602,16602,MONDO:0001231,orbital periostitis,MONDO,disease,DISEASE_16602
16603,16603,16603,16603,16603,16603,16603,16603,MONDO:0020344,postsynaptic congenital myasthenic syndrome,MONDO,disease,DISEASE_16603
16604,16604,16604,16604,16604,16604,16604,16604,MONDO:0017289,fetal lung interstitial tumor,MONDO,disease,DISEASE_16604
16605,16605,16605,16605,16605,16605,16605,16605,MONDO:1011628,"paroxysm, non-human animal",MONDO,disease,DISEASE_16605
16606,16606,16606,16606,16606,16606,16606,16606,MONDO:0005430,early onset hypertension,MONDO,disease,DISEASE_16606
16607,16607,16607,16607,16607,16607,16607,16607,MONDO:0018739,neonatal alloimmune neutropenia,MONDO,disease,DISEASE_16607
16608,16608,16608,16608,16608,16608,16608,16608,MONDO:0016877,partial deletion of the long arm of chromosome 12,MONDO,disease,DISEASE_16608
16609,16609,16609,16609,16609,16609,16609,16609,MONDO:0008114_MONDO:0001158,obsessive-compulsive disorder,MONDO_grouped,disease,DISEASE_16609
16610,16610,16610,16610,16610,16610,16610,16610,MONDO:0014976,lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome,MONDO,disease,DISEASE_16610
16611,16611,16611,16611,16611,16611,16611,16611,MONDO:0001797,chancroid,MONDO,disease,DISEASE_16611
16612,16612,16612,16612,16612,16612,16612,16612,MONDO:0032904_MONDO:0020791,"corneal dystrophy, Meesmann",MONDO_grouped,disease,DISEASE_16612
16613,16613,16613,16613,16613,16613,16613,16613,MONDO:0011260,"pancreatic lymphoma, familial",MONDO,disease,DISEASE_16613
16614,16614,16614,16614,16614,16614,16614,16614,MONDO:0006815,jejunal cancer,MONDO,disease,DISEASE_16614
16615,16615,16615,16615,16615,16615,16615,16615,MONDO:0005125,borderline leprosy,MONDO,disease,DISEASE_16615
16616,16616,16616,16616,16616,16616,16616,16616,MONDO:0022782,cleft lower lip cleft lateral canthi chorioretinal,MONDO,disease,DISEASE_16616
16617,16617,16617,16617,16617,16617,16617,16617,MONDO:0958189_MONDO:0958174,basal cell nevus syndrome,MONDO_grouped,disease,DISEASE_16617
16618,16618,16618,16618,16618,16618,16618,16618,MONDO:0005650,Arenaviridae infectious disease,MONDO,disease,DISEASE_16618
16619,16619,16619,16619,16619,16619,16619,16619,MONDO:0015137,periodic fever syndrome,MONDO,disease,DISEASE_16619
16620,16620,16620,16620,16620,16620,16620,16620,MONDO:0001287,endometriosis in cutaneous scar,MONDO,disease,DISEASE_16620
16621,16621,16621,16621,16621,16621,16621,16621,MONDO:0036483_MONDO:0044328_MONDO:0014907_MONDO:0014688_MONDO:0800356,short-rib thoracic dysplasia 18 with polydactyly,MONDO_grouped,disease,DISEASE_16621
16622,16622,16622,16622,16622,16622,16622,16622,MONDO:0015539,progressive nodular histiocytosis,MONDO,disease,DISEASE_16622
16623,16623,16623,16623,16623,16623,16623,16623,MONDO:0004467,mature gastric teratoma,MONDO,disease,DISEASE_16623
16624,16624,16624,16624,16624,16624,16624,16624,MONDO:0017855,T-B- severe combined immunodeficiency,MONDO,disease,DISEASE_16624
16625,16625,16625,16625,16625,16625,16625,16625,MONDO:0008436,Sneddon syndrome,MONDO,disease,DISEASE_16625
16626,16626,16626,16626,16626,16626,16626,16626,MONDO:0019552,centrifugal lipodystrophy,MONDO,disease,DISEASE_16626
16627,16627,16627,16627,16627,16627,16627,16627,MONDO:0024239,congenital anomaly of cardiovascular system,MONDO,disease,DISEASE_16627
16628,16628,16628,16628,16628,16628,16628,16628,MONDO:0016199,qualitative or quantitative defects of protein SERCA1,MONDO,disease,DISEASE_16628
16629,16629,16629,16629,16629,16629,16629,16629,MONDO:0011797,infantile-onset ascending hereditary spastic paralysis,MONDO,disease,DISEASE_16629
16630,16630,16630,16630,16630,16630,16630,16630,MONDO:0023575,Krauss Herman Holmes syndrome,MONDO,disease,DISEASE_16630
16631,16631,16631,16631,16631,16631,16631,16631,MONDO:0017148,heritable pulmonary arterial hypertension,MONDO,disease,DISEASE_16631
16632,16632,16632,16632,16632,16632,16632,16632,MONDO:0007674,glucose-6-phosphate dehydrogenase-like,MONDO,disease,DISEASE_16632
16633,16633,16633,16633,16633,16633,16633,16633,MONDO:0009570,McDonough syndrome,MONDO,disease,DISEASE_16633
16634,16634,16634,16634,16634,16634,16634,16634,MONDO:1010227,"cauda equina syndrome, non-human animal",MONDO,disease,DISEASE_16634
16635,16635,16635,16635,16635,16635,16635,16635,MONDO:0043472,ectopic ACTH secretion syndrome,MONDO,disease,DISEASE_16635
16636,16636,16636,16636,16636,16636,16636,16636,MONDO:0002026_MONDO:0044070,candidiasis,MONDO_grouped,disease,DISEASE_16636
16637,16637,16637,16637,16637,16637,16637,16637,MONDO:0010618,familial isolated hypoparathyroidism due to agenesis of parathyroid gland,MONDO,disease,DISEASE_16637
16638,16638,16638,16638,16638,16638,16638,16638,MONDO:0008624,Upington disease,MONDO,disease,DISEASE_16638
16639,16639,16639,16639,16639,16639,16639,16639,MONDO:1010005,"autism spectrum disorder, non-human animal",MONDO,disease,DISEASE_16639
16640,16640,16640,16640,16640,16640,16640,16640,MONDO:0004103,tall cell variant thyroid gland papillary carcinoma,MONDO,disease,DISEASE_16640
16641,16641,16641,16641,16641,16641,16641,16641,MONDO:0004646,decubitus ulcer,MONDO,disease,DISEASE_16641
16642,16642,16642,16642,16642,16642,16642,16642,MONDO:0020823,infantile miliaria,MONDO,disease,DISEASE_16642
16643,16643,16643,16643,16643,16643,16643,16643,MONDO:0008465,Patterson-Stevenson-Fontaine syndrome,MONDO,disease,DISEASE_16643
16644,16644,16644,16644,16644,16644,16644,16644,MONDO:0007598,"factors VIII, IX and XI, combined deficiency of",MONDO,disease,DISEASE_16644
16645,16645,16645,16645,16645,16645,16645,16645,MONDO:0013487,recurrent Neisseria infections due to factor D deficiency,MONDO,disease,DISEASE_16645
16646,16646,16646,16646,16646,16646,16646,16646,MONDO:0025294_MONDO:0001621,tick-borne infectious disease,MONDO_grouped,disease,DISEASE_16646
16647,16647,16647,16647,16647,16647,16647,16647,MONDO:0006642,alcohol withdrawal delirium,MONDO,disease,DISEASE_16647
16648,16648,16648,16648,16648,16648,16648,16648,MONDO:0007328_MONDO:0971130,"choroidal osteoma, bilateral",MONDO_grouped,disease,DISEASE_16648
16649,16649,16649,16649,16649,16649,16649,16649,MONDO:0005463,aortic valve calcification,MONDO,disease,DISEASE_16649
16650,16650,16650,16650,16650,16650,16650,16650,MONDO:0019981_MONDO:0019982,unilateral multicystic dysplastic kidney,MONDO_grouped,disease,DISEASE_16650
16651,16651,16651,16651,16651,16651,16651,16651,MONDO:1012569,"hepatocellular fibrinogen storage disease, cattle",MONDO,disease,DISEASE_16651
16652,16652,16652,16652,16652,16652,16652,16652,MONDO:1012200,"esophageal motility disorder, dog",MONDO,disease,DISEASE_16652
16653,16653,16653,16653,16653,16653,16653,16653,MONDO:0009914,pseudodiastrophic dysplasia,MONDO,disease,DISEASE_16653
16654,16654,16654,16654,16654,16654,16654,16654,MONDO:0017558_MONDO:0017559_MONDO:0017562,"congenital elbow dislocation, unilateral",MONDO_grouped,disease,DISEASE_16654
16655,16655,16655,16655,16655,16655,16655,16655,MONDO:0044917,T-lymphoblastic lymphoma,MONDO,disease,DISEASE_16655
16656,16656,16656,16656,16656,16656,16656,16656,MONDO:0000951,thymus lymphoma,MONDO,disease,DISEASE_16656
16657,16657,16657,16657,16657,16657,16657,16657,MONDO:0006684,brain edema,MONDO,disease,DISEASE_16657
16658,16658,16658,16658,16658,16658,16658,16658,MONDO:0017415,multiple pterygium syndrome,MONDO,disease,DISEASE_16658
16659,16659,16659,16659,16659,16659,16659,16659,MONDO:0024557_MONDO:0014399_MONDO:0011457_MONDO:0018266,ataxia-telangiectasia-like disorder,MONDO_grouped,disease,DISEASE_16659
16660,16660,16660,16660,16660,16660,16660,16660,MONDO:0001166_MONDO:0006900,nephritis,MONDO_grouped,disease,DISEASE_16660
16661,16661,16661,16661,16661,16661,16661,16661,MONDO:0012284,"nephropathy, progressive, with deafness",MONDO,disease,DISEASE_16661
16662,16662,16662,16662,16662,16662,16662,16662,MONDO:0021073,paraneoplastic syndrome,MONDO,disease,DISEASE_16662
16663,16663,16663,16663,16663,16663,16663,16663,MONDO:0016277,malignant mixed epithelial and mesenchymal tumor of cervix uteri,MONDO,disease,DISEASE_16663
16664,16664,16664,16664,16664,16664,16664,16664,MONDO:0002123,calcinosis,MONDO,disease,DISEASE_16664
16665,16665,16665,16665,16665,16665,16665,16665,MONDO:1012054,"craniomandibular osteopathy, dog",MONDO,disease,DISEASE_16665
16666,16666,16666,16666,16666,16666,16666,16666,MONDO:1011679,"hereditary pancreatitis, non-human animal",MONDO,disease,DISEASE_16666
16667,16667,16667,16667,16667,16667,16667,16667,MONDO:0009352_MONDO:0004737,classic homocystinuria,MONDO_grouped,disease,DISEASE_16667
16668,16668,16668,16668,16668,16668,16668,16668,MONDO:0020647,"microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome",MONDO,disease,DISEASE_16668
16669,16669,16669,16669,16669,16669,16669,16669,MONDO:0015568,isolated congenital nasal pyriform aperture stenosis,MONDO,disease,DISEASE_16669
16670,16670,16670,16670,16670,16670,16670,16670,MONDO:0016378,maternal hyperthermia induced birth defects,MONDO,disease,DISEASE_16670
16671,16671,16671,16671,16671,16671,16671,16671,MONDO:0002107_MONDO:0004801,unilateral hyperactive labyrinth,MONDO_grouped,disease,DISEASE_16671
16672,16672,16672,16672,16672,16672,16672,16672,MONDO:0032758,"neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia",MONDO,disease,DISEASE_16672
16673,16673,16673,16673,16673,16673,16673,16673,MONDO:1011062,"primary hyperoxaluria, GRHPR-related, domestic cat",MONDO,disease,DISEASE_16673
16674,16674,16674,16674,16674,16674,16674,16674,MONDO:0004155,adult central nervous system embryonal carcinoma,MONDO,disease,DISEASE_16674
16675,16675,16675,16675,16675,16675,16675,16675,MONDO:0003735_MONDO:0003958,central nervous system immature teratoma,MONDO_grouped,disease,DISEASE_16675
16676,16676,16676,16676,16676,16676,16676,16676,MONDO:0009860,phenformin 4-hydroxylation,MONDO,disease,DISEASE_16676
16677,16677,16677,16677,16677,16677,16677,16677,MONDO:0019419,X-linked intellectual disability-macrocephaly-macroorchidism syndrome,MONDO,disease,DISEASE_16677
16678,16678,16678,16678,16678,16678,16678,16678,MONDO:0011575,cerebrooculonasal syndrome,MONDO,disease,DISEASE_16678
16679,16679,16679,16679,16679,16679,16679,16679,MONDO:0016473,familial rhabdoid tumor,MONDO,disease,DISEASE_16679
16680,16680,16680,16680,16680,16680,16680,16680,MONDO:0018939,muscle-eye-brain disease,MONDO,disease,DISEASE_16680
16681,16681,16681,16681,16681,16681,16681,16681,MONDO:0001087_MONDO:0001265,schizotypal personality disorder,MONDO_grouped,disease,DISEASE_16681
16682,16682,16682,16682,16682,16682,16682,16682,MONDO:0024467_MONDO:0003215,apocrine sweat gland disorder,MONDO_grouped,disease,DISEASE_16682
16683,16683,16683,16683,16683,16683,16683,16683,MONDO:0004911,cardiovascular syphilis,MONDO,disease,DISEASE_16683
16684,16684,16684,16684,16684,16684,16684,16684,MONDO:0018434_MONDO:0100377_MONDO:0100382_MONDO:0100384_MONDO:0100386_MONDO:0100400,acute myeloid leukemia with t(9;11)(p22;q23),MONDO_grouped,disease,DISEASE_16684
16685,16685,16685,16685,16685,16685,16685,16685,MONDO:1012587,"oculocutaneous albinism, TYR-related, American mink",MONDO,disease,DISEASE_16685
16686,16686,16686,16686,16686,16686,16686,16686,MONDO:0009623,Nijmegen breakage syndrome,MONDO,disease,DISEASE_16686
16687,16687,16687,16687,16687,16687,16687,16687,MONDO:0005892,otitis media with effusion,MONDO,disease,DISEASE_16687
16688,16688,16688,16688,16688,16688,16688,16688,MONDO:0021481,benign neoplasm of submandibular gland,MONDO,disease,DISEASE_16688
16689,16689,16689,16689,16689,16689,16689,16689,MONDO:1012870,"long QT syndrome, KCNE1-related, rabbit",MONDO,disease,DISEASE_16689
16690,16690,16690,16690,16690,16690,16690,16690,MONDO:0013272,chromosome 14q11-q22 deletion syndrome,MONDO,disease,DISEASE_16690
16691,16691,16691,16691,16691,16691,16691,16691,MONDO:0005929,postpartum depression,MONDO,disease,DISEASE_16691
16692,16692,16692,16692,16692,16692,16692,16692,MONDO:0859377,neurodevelopmental disorder with poor growth and behavioral abnormalities,MONDO,disease,DISEASE_16692
16693,16693,16693,16693,16693,16693,16693,16693,MONDO:0010271,X-linked myotubular myopathy-abnormal genitalia syndrome,MONDO,disease,DISEASE_16693
16694,16694,16694,16694,16694,16694,16694,16694,MONDO:0016160,X-linked intellectual disability-epilepsy syndrome,MONDO,disease,DISEASE_16694
16695,16695,16695,16695,16695,16695,16695,16695,MONDO:0957788_MONDO:0957308_MONDO:0859363,"spastic paraplegia 18a, autosomal dominant",MONDO_grouped,disease,DISEASE_16695
16696,16696,16696,16696,16696,16696,16696,16696,MONDO:0003137_MONDO:0003138,diffuse glomerulonephritis,MONDO_grouped,disease,DISEASE_16696
16697,16697,16697,16697,16697,16697,16697,16697,MONDO:0100580,"epilepsy, onset unknown",MONDO,disease,DISEASE_16697
16698,16698,16698,16698,16698,16698,16698,16698,MONDO:0011883,Curly hair - acral keratoderma - caries syndrome,MONDO,disease,DISEASE_16698
16699,16699,16699,16699,16699,16699,16699,16699,MONDO:0024475,squamous cell intraepithelial neoplasia,MONDO,disease,DISEASE_16699
16700,16700,16700,16700,16700,16700,16700,16700,MONDO:0002788,papillary craniopharyngioma,MONDO,disease,DISEASE_16700
16701,16701,16701,16701,16701,16701,16701,16701,MONDO:0008139,OSLAM syndrome,MONDO,disease,DISEASE_16701
16702,16702,16702,16702,16702,16702,16702,16702,MONDO:0019739,atypical hemolytic-uremic syndrome with anti-factor H antibodies,MONDO,disease,DISEASE_16702
16703,16703,16703,16703,16703,16703,16703,16703,MONDO:1011327,"inflammatory disease, non-human animal",MONDO,disease,DISEASE_16703
16704,16704,16704,16704,16704,16704,16704,16704,MONDO:0002907_MONDO:0002692_MONDO:0006809,intracranial thrombosis,MONDO_grouped,disease,DISEASE_16704
16705,16705,16705,16705,16705,16705,16705,16705,MONDO:0010840,pachygyria-intellectual disability-epilepsy syndrome,MONDO,disease,DISEASE_16705
16706,16706,16706,16706,16706,16706,16706,16706,MONDO:0011429,juvenile idiopathic arthritis,MONDO,disease,DISEASE_16706
16707,16707,16707,16707,16707,16707,16707,16707,MONDO:0018876,mantle cell lymphoma,MONDO,disease,DISEASE_16707
16708,16708,16708,16708,16708,16708,16708,16708,MONDO:0002779,central nervous system chondroma,MONDO,disease,DISEASE_16708
16709,16709,16709,16709,16709,16709,16709,16709,MONDO:0002120,neuroendocrine carcinoma,MONDO,disease,DISEASE_16709
16710,16710,16710,16710,16710,16710,16710,16710,MONDO:0007523,"Ehlers-Danlos syndrome, hypermobility type",MONDO,disease,DISEASE_16710
16711,16711,16711,16711,16711,16711,16711,16711,MONDO:1010440,"cardiomyopathy, hedgehogs",MONDO,disease,DISEASE_16711
16712,16712,16712,16712,16712,16712,16712,16712,MONDO:0019493,primary adult heart tumor,MONDO,disease,DISEASE_16712
16713,16713,16713,16713,16713,16713,16713,16713,MONDO:0006474,transitional cell carcinoma,MONDO,disease,DISEASE_16713
16714,16714,16714,16714,16714,16714,16714,16714,MONDO:0000525,cecum villous adenoma,MONDO,disease,DISEASE_16714
16715,16715,16715,16715,16715,16715,16715,16715,MONDO:0002937,nodular basal cell carcinoma,MONDO,disease,DISEASE_16715
16716,16716,16716,16716,16716,16716,16716,16716,MONDO:0006937,pulpitis,MONDO,disease,DISEASE_16716
16717,16717,16717,16717,16717,16717,16717,16717,MONDO:0850064,inherited hematologic cancer-predisposing syndrome,MONDO,disease,DISEASE_16717
16718,16718,16718,16718,16718,16718,16718,16718,MONDO:0007458,"digitotalar dysmorphism; ulnar drift, hereditary",MONDO,disease,DISEASE_16718
16719,16719,16719,16719,16719,16719,16719,16719,MONDO:0971129,stellate multiform amelanotic choroidopathy,MONDO,disease,DISEASE_16719
16720,16720,16720,16720,16720,16720,16720,16720,MONDO:0060760_MONDO:0015022,intellectual developmental disorder with dysmorphic facies and behavioral abnormalities,MONDO_grouped,disease,DISEASE_16720
16721,16721,16721,16721,16721,16721,16721,16721,MONDO:0008093,"nevus, epidermal",MONDO,disease,DISEASE_16721
16722,16722,16722,16722,16722,16722,16722,16722,MONDO:0018603,SFTPC- related interstitial lung disease,MONDO,disease,DISEASE_16722
16723,16723,16723,16723,16723,16723,16723,16723,MONDO:0012081,15q11q13 microduplication syndrome,MONDO,disease,DISEASE_16723
16724,16724,16724,16724,16724,16724,16724,16724,MONDO:0023415,congenital candidiasis,MONDO,disease,DISEASE_16724
16725,16725,16725,16725,16725,16725,16725,16725,MONDO:0000685,visual agnosia,MONDO,disease,DISEASE_16725
16726,16726,16726,16726,16726,16726,16726,16726,MONDO:0004647,in situ carcinoma,MONDO,disease,DISEASE_16726
16727,16727,16727,16727,16727,16727,16727,16727,MONDO:0018690,Holmes-Adie syndrome,MONDO,disease,DISEASE_16727
16728,16728,16728,16728,16728,16728,16728,16728,MONDO:1012334,"bone spavin, horse",MONDO,disease,DISEASE_16728
16729,16729,16729,16729,16729,16729,16729,16729,MONDO:0019179,monosomy 9q22.3,MONDO,disease,DISEASE_16729
16730,16730,16730,16730,16730,16730,16730,16730,MONDO:0020369,Chandler syndrome,MONDO,disease,DISEASE_16730
16731,16731,16731,16731,16731,16731,16731,16731,MONDO:0000015,classic complement early component deficiency,MONDO,disease,DISEASE_16731
16732,16732,16732,16732,16732,16732,16732,16732,MONDO:0012143,hereditary cryohydrocytosis with reduced stomatin,MONDO,disease,DISEASE_16732
16733,16733,16733,16733,16733,16733,16733,16733,MONDO:0001126,gastric ulcer,MONDO,disease,DISEASE_16733
16734,16734,16734,16734,16734,16734,16734,16734,MONDO:0000340,bulbospinal polio,MONDO,disease,DISEASE_16734
16735,16735,16735,16735,16735,16735,16735,16735,MONDO:0000451_MONDO:0000452,primary progressive multiple sclerosis,MONDO_grouped,disease,DISEASE_16735
16736,16736,16736,16736,16736,16736,16736,16736,MONDO:0001235,appendix cancer,MONDO,disease,DISEASE_16736
16737,16737,16737,16737,16737,16737,16737,16737,MONDO:0012394_MONDO:0054752_MONDO:0008519_MONDO:0013064_MONDO:0017923,multiple synostoses syndrome,MONDO_grouped,disease,DISEASE_16737
16738,16738,16738,16738,16738,16738,16738,16738,MONDO:0008669,"vulvovaginitis, allergic seminal",MONDO,disease,DISEASE_16738
16739,16739,16739,16739,16739,16739,16739,16739,MONDO:0957211,neurodegeneration and seizures due to copper transport defect,MONDO,disease,DISEASE_16739
16740,16740,16740,16740,16740,16740,16740,16740,MONDO:0100265,peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain,MONDO,disease,DISEASE_16740
16741,16741,16741,16741,16741,16741,16741,16741,MONDO:0015450,triatrial heart,MONDO,disease,DISEASE_16741
16742,16742,16742,16742,16742,16742,16742,16742,MONDO:0009460,indolylacroyl glycinuria with intellectual disability,MONDO,disease,DISEASE_16742
16743,16743,16743,16743,16743,16743,16743,16743,MONDO:0016621,juvenile Huntington disease,MONDO,disease,DISEASE_16743
16744,16744,16744,16744,16744,16744,16744,16744,MONDO:0032788_MONDO:0060551,cerebellar atrophy with seizures and variable developmental delay,MONDO_grouped,disease,DISEASE_16744
16745,16745,16745,16745,16745,16745,16745,16745,MONDO:0023221,Gaucher ichthyosis restrictive dermopathy,MONDO,disease,DISEASE_16745
16746,16746,16746,16746,16746,16746,16746,16746,MONDO:0971127,diffuse unilateral subacute neuroretinitis,MONDO,disease,DISEASE_16746
16747,16747,16747,16747,16747,16747,16747,16747,MONDO:0003300,appendix leiomyoma,MONDO,disease,DISEASE_16747
16748,16748,16748,16748,16748,16748,16748,16748,MONDO:0005864,muscle cancer,MONDO,disease,DISEASE_16748
16749,16749,16749,16749,16749,16749,16749,16749,MONDO:0010080_MONDO:0016394_MONDO:0015518,familial infantile bilateral striatal necrosis,MONDO_grouped,disease,DISEASE_16749
16750,16750,16750,16750,16750,16750,16750,16750,MONDO:0007879,larynx atresia,MONDO,disease,DISEASE_16750
16751,16751,16751,16751,16751,16751,16751,16751,MONDO:0004594,puerperal pulmonary embolism,MONDO,disease,DISEASE_16751
16752,16752,16752,16752,16752,16752,16752,16752,MONDO:0001949,acute thyroiditis,MONDO,disease,DISEASE_16752
16753,16753,16753,16753,16753,16753,16753,16753,MONDO:0006944,renal aminoaciduria,MONDO,disease,DISEASE_16753
16754,16754,16754,16754,16754,16754,16754,16754,MONDO:0014557_MONDO:0014084,ataxia - oculomotor apraxia type 4,MONDO_grouped,disease,DISEASE_16754
16755,16755,16755,16755,16755,16755,16755,16755,MONDO:1012163_MONDO:1012164,"micromelia, ducks",MONDO_grouped,disease,DISEASE_16755
16756,16756,16756,16756,16756,16756,16756,16756,MONDO:0022772_MONDO:0023067,classic Kaposi sarcoma,MONDO_grouped,disease,DISEASE_16756
16757,16757,16757,16757,16757,16757,16757,16757,MONDO:0003537,precursor T-lymphoblastic lymphoma/leukemia,MONDO,disease,DISEASE_16757
16758,16758,16758,16758,16758,16758,16758,16758,MONDO:0007817,"IgE responsiveness, atopic",MONDO,disease,DISEASE_16758
16759,16759,16759,16759,16759,16759,16759,16759,MONDO:0013638_MONDO:0013641_MONDO:0010822_MONDO:0014296_MONDO:0016649,Warburg micro syndrome,MONDO_grouped,disease,DISEASE_16759
16760,16760,16760,16760,16760,16760,16760,16760,MONDO:0003618,pyosalpinx,MONDO,disease,DISEASE_16760
16761,16761,16761,16761,16761,16761,16761,16761,MONDO:0010247,X-linked cerebral adrenoleukodystrophy,MONDO,disease,DISEASE_16761
16762,16762,16762,16762,16762,16762,16762,16762,MONDO:0020441_MONDO:0020448,right superior vena cava connecting to left-sided atrium,MONDO_grouped,disease,DISEASE_16762
16763,16763,16763,16763,16763,16763,16763,16763,MONDO:0030681,immunodeficiency 94 with autoinflammation and dysmorphic facies,MONDO,disease,DISEASE_16763
16764,16764,16764,16764,16764,16764,16764,16764,MONDO:0005419,methamphetamine dependence,MONDO,disease,DISEASE_16764
16765,16765,16765,16765,16765,16765,16765,16765,MONDO:0044726,psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome,MONDO,disease,DISEASE_16765
16766,16766,16766,16766,16766,16766,16766,16766,MONDO:0014044,dysmorphism-conductive hearing loss-heart defect syndrome,MONDO,disease,DISEASE_16766
16767,16767,16767,16767,16767,16767,16767,16767,MONDO:0017509_MONDO:0017510,"adactyly of foot, unilateral",MONDO_grouped,disease,DISEASE_16767
16768,16768,16768,16768,16768,16768,16768,16768,MONDO:0007979,metachondromatosis,MONDO,disease,DISEASE_16768
16769,16769,16769,16769,16769,16769,16769,16769,MONDO:0027652,5-fluorouracil toxicity,MONDO,disease,DISEASE_16769
16770,16770,16770,16770,16770,16770,16770,16770,MONDO:0008232,"phagocytosis, plasma-related defect 1N",MONDO,disease,DISEASE_16770
16771,16771,16771,16771,16771,16771,16771,16771,MONDO:0011651,"intellectual disability, short stature, facial anomalies, and joint dislocations",MONDO,disease,DISEASE_16771
16772,16772,16772,16772,16772,16772,16772,16772,MONDO:0004743_MONDO:1011535,hyperhomocysteinemia,MONDO_grouped,disease,DISEASE_16772
16773,16773,16773,16773,16773,16773,16773,16773,MONDO:0007422,keratoderma hereditarium mutilans,MONDO,disease,DISEASE_16773
16774,16774,16774,16774,16774,16774,16774,16774,MONDO:0014472,periodic fever-infantile enterocolitis-autoinflammatory syndrome,MONDO,disease,DISEASE_16774
16775,16775,16775,16775,16775,16775,16775,16775,MONDO:0003866_MONDO:0004360_MONDO:0004374,liver extraskeletal osteosarcoma,MONDO_grouped,disease,DISEASE_16775
16776,16776,16776,16776,16776,16776,16776,16776,MONDO:0018655,hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome,MONDO,disease,DISEASE_16776
16777,16777,16777,16777,16777,16777,16777,16777,MONDO:0023089,erythroplakia,MONDO,disease,DISEASE_16777
16778,16778,16778,16778,16778,16778,16778,16778,MONDO:0002796,melanotic medulloblastoma,MONDO,disease,DISEASE_16778
16779,16779,16779,16779,16779,16779,16779,16779,MONDO:0023148,fetal phenothiazine syndrome,MONDO,disease,DISEASE_16779
16780,16780,16780,16780,16780,16780,16780,16780,MONDO:0002800,thrombophlebitis,MONDO,disease,DISEASE_16780
16781,16781,16781,16781,16781,16781,16781,16781,MONDO:0859255_MONDO:0033546,"peripheral motor neuropathy, childhood-onset, biotin-responsive",MONDO_grouped,disease,DISEASE_16781
16782,16782,16782,16782,16782,16782,16782,16782,MONDO:1012429,"retinal dysplasia and internal hydrocephalus, cattle",MONDO,disease,DISEASE_16782
16783,16783,16783,16783,16783,16783,16783,16783,MONDO:1012612,"conjugated hyperbilirubinemia, golden lion tamarin",MONDO,disease,DISEASE_16783
16784,16784,16784,16784,16784,16784,16784,16784,MONDO:0016881,partial deletion of chromosome 19,MONDO,disease,DISEASE_16784
16785,16785,16785,16785,16785,16785,16785,16785,MONDO:0859171,Luo-Schoch-Yamamoto syndrome,MONDO,disease,DISEASE_16785
16786,16786,16786,16786,16786,16786,16786,16786,MONDO:1040032,EN1-related dorsoventral syndrome,MONDO,disease,DISEASE_16786
16787,16787,16787,16787,16787,16787,16787,16787,MONDO:0800463,KIF7-related ciliopathy,MONDO,disease,DISEASE_16787
16788,16788,16788,16788,16788,16788,16788,16788,MONDO:0013280_MONDO:0003359,myxoid liposarcoma,MONDO_grouped,disease,DISEASE_16788
16789,16789,16789,16789,16789,16789,16789,16789,MONDO:0013470_MONDO:0012346_MONDO:0011461_MONDO:0014517_MONDO:0011416_MONDO:0958324_MONDO:0032777_MONDO:0018214_MONDO:0012846_MONDO:0013448_MONDO:0800489,"generalized epilepsy with febrile seizures plus,",MONDO_grouped,disease,DISEASE_16789
16790,16790,16790,16790,16790,16790,16790,16790,MONDO:1011976,"Collie eye anomaly, non-human animal",MONDO,disease,DISEASE_16790
16791,16791,16791,16791,16791,16791,16791,16791,MONDO:0020841,neurodevelopmental disorder with cerebellar atrophy and with or without seizures,MONDO,disease,DISEASE_16791
16792,16792,16792,16792,16792,16792,16792,16792,MONDO:0011580,cerebellar ataxia and hypergonadotropic hypogonadism,MONDO,disease,DISEASE_16792
16793,16793,16793,16793,16793,16793,16793,16793,MONDO:0017586,onychocytic matricoma,MONDO,disease,DISEASE_16793
16794,16794,16794,16794,16794,16794,16794,16794,MONDO:0019164,6q terminal deletion syndrome,MONDO,disease,DISEASE_16794
16795,16795,16795,16795,16795,16795,16795,16795,MONDO:0017835,lymphocytic hypereosinophilic syndrome,MONDO,disease,DISEASE_16795
16796,16796,16796,16796,16796,16796,16796,16796,MONDO:0970958,transitional extramedullary conus spinal cord lipoma,MONDO,disease,DISEASE_16796
16797,16797,16797,16797,16797,16797,16797,16797,MONDO:0018067,triploidy,MONDO,disease,DISEASE_16797
16798,16798,16798,16798,16798,16798,16798,16798,MONDO:0005707,coccidiosis,MONDO,disease,DISEASE_16798
16799,16799,16799,16799,16799,16799,16799,16799,MONDO:0030019_MONDO:0054561_MONDO:0054560_MONDO:0011773,anauxetic dysplasia,MONDO_grouped,disease,DISEASE_16799
16800,16800,16800,16800,16800,16800,16800,16800,MONDO:0042727,sacrococcygeal teratoma,MONDO,disease,DISEASE_16800
16801,16801,16801,16801,16801,16801,16801,16801,MONDO:0011019,alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome,MONDO,disease,DISEASE_16801
16802,16802,16802,16802,16802,16802,16802,16802,MONDO:0005122,Pectobacterium carotovorum infection,MONDO,disease,DISEASE_16802
16803,16803,16803,16803,16803,16803,16803,16803,MONDO:0859311_MONDO:0030677_MONDO:0030689_MONDO:0033135,"Charcot-Marie-Tooth disease, demyelinating,",MONDO_grouped,disease,DISEASE_16803
16804,16804,16804,16804,16804,16804,16804,16804,MONDO:0014945,"myopathy, distal, with rimmed vacuoles",MONDO,disease,DISEASE_16804
16805,16805,16805,16805,16805,16805,16805,16805,MONDO:0019759,epispadias,MONDO,disease,DISEASE_16805
16806,16806,16806,16806,16806,16806,16806,16806,MONDO:1011603,"type 2 diabetes mellitus, crab-eating macaque",MONDO,disease,DISEASE_16806
16807,16807,16807,16807,16807,16807,16807,16807,MONDO:0005712,congenital nystagmus,MONDO,disease,DISEASE_16807
16808,16808,16808,16808,16808,16808,16808,16808,MONDO:0014425,obsolete hereditary persistence of alpha-fetoprotein,MONDO,disease,DISEASE_16808
16809,16809,16809,16809,16809,16809,16809,16809,MONDO:0016736,rosette-forming glioneuronal tumor of fourth ventricule,MONDO,disease,DISEASE_16809
16810,16810,16810,16810,16810,16810,16810,16810,MONDO:0009972,respiratory underresponsiveness to hypoxia and hypercapnia,MONDO,disease,DISEASE_16810
16811,16811,16811,16811,16811,16811,16811,16811,MONDO:0001941,blindness (disorder),MONDO,disease,DISEASE_16811
16812,16812,16812,16812,16812,16812,16812,16812,MONDO:1011844,"hypertrophic neuropathy, non-human animal",MONDO,disease,DISEASE_16812
16813,16813,16813,16813,16813,16813,16813,16813,MONDO:0003061,benign muscle neoplasm,MONDO,disease,DISEASE_16813
16814,16814,16814,16814,16814,16814,16814,16814,MONDO:0015929,thoracic malformation,MONDO,disease,DISEASE_16814
16815,16815,16815,16815,16815,16815,16815,16815,MONDO:0009887,desquamative interstitial pneumonia,MONDO,disease,DISEASE_16815
16816,16816,16816,16816,16816,16816,16816,16816,MONDO:0011705_MONDO:0006277,lymphangioleiomyomatosis,MONDO_grouped,disease,DISEASE_16816
16817,16817,16817,16817,16817,16817,16817,16817,MONDO:1010534,"gingival hypertrophy, red fox",MONDO,disease,DISEASE_16817
16818,16818,16818,16818,16818,16818,16818,16818,MONDO:0019978,Robinow syndrome,MONDO,disease,DISEASE_16818
16819,16819,16819,16819,16819,16819,16819,16819,MONDO:0007395,craniofacial-deafness-hand syndrome,MONDO,disease,DISEASE_16819
16820,16820,16820,16820,16820,16820,16820,16820,MONDO:0030026,retinal dystrophy with leukodystrophy,MONDO,disease,DISEASE_16820
16821,16821,16821,16821,16821,16821,16821,16821,MONDO:0008534,generalized essential telangiectasia,MONDO,disease,DISEASE_16821
16822,16822,16822,16822,16822,16822,16822,16822,MONDO:0005916,placenta accreta,MONDO,disease,DISEASE_16822
16823,16823,16823,16823,16823,16823,16823,16823,MONDO:0024322,disorder of glycosylation,MONDO,disease,DISEASE_16823
16824,16824,16824,16824,16824,16824,16824,16824,MONDO:1010461,"hypertrophic cardiomyopathy, Arabian camel",MONDO,disease,DISEASE_16824
16825,16825,16825,16825,16825,16825,16825,16825,MONDO:0017852,infantile spasms-broad thumbs syndrome,MONDO,disease,DISEASE_16825
16826,16826,16826,16826,16826,16826,16826,16826,MONDO:0011288,"spastic paraplegia, optic atrophy, microcephaly, and 10Y sex reversal",MONDO,disease,DISEASE_16826
16827,16827,16827,16827,16827,16827,16827,16827,MONDO:0016175,cutis laxa,MONDO,disease,DISEASE_16827
16828,16828,16828,16828,16828,16828,16828,16828,MONDO:0009933,congenital pulmonary lymphangiectasia,MONDO,disease,DISEASE_16828
16829,16829,16829,16829,16829,16829,16829,16829,MONDO:0011323,"arhinia, choanal atresia, and microphthalmia",MONDO,disease,DISEASE_16829
16830,16830,16830,16830,16830,16830,16830,16830,MONDO:0020450,azygos continuation of the inferior vena cava,MONDO,disease,DISEASE_16830
16831,16831,16831,16831,16831,16831,16831,16831,MONDO:0015606,Xp22.3 microdeletion syndrome,MONDO,disease,DISEASE_16831
16832,16832,16832,16832,16832,16832,16832,16832,MONDO:0008113,Schilbach-Rott syndrome,MONDO,disease,DISEASE_16832
16833,16833,16833,16833,16833,16833,16833,16833,MONDO:0011640,genitopatellar syndrome,MONDO,disease,DISEASE_16833
16834,16834,16834,16834,16834,16834,16834,16834,MONDO:0002828,Bartholin gland transitional cell carcinoma,MONDO,disease,DISEASE_16834
16835,16835,16835,16835,16835,16835,16835,16835,MONDO:0007315,cherubism,MONDO,disease,DISEASE_16835
16836,16836,16836,16836,16836,16836,16836,16836,MONDO:0010721,"reticuloendotheliosis, X-linked",MONDO,disease,DISEASE_16836
16837,16837,16837,16837,16837,16837,16837,16837,MONDO:0008761,obsolete alpha-2-deficient collagen disease,MONDO,disease,DISEASE_16837
16838,16838,16838,16838,16838,16838,16838,16838,MONDO:0004739,urea cycle disorder,MONDO,disease,DISEASE_16838
16839,16839,16839,16839,16839,16839,16839,16839,MONDO:0015317,laryngotracheal angioma,MONDO,disease,DISEASE_16839
16840,16840,16840,16840,16840,16840,16840,16840,MONDO:1012575,"X-linked disease, non-human animal",MONDO,disease,DISEASE_16840
16841,16841,16841,16841,16841,16841,16841,16841,MONDO:0000974,axillary lipoma,MONDO,disease,DISEASE_16841
16842,16842,16842,16842,16842,16842,16842,16842,MONDO:0015811,primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma,MONDO,disease,DISEASE_16842
16843,16843,16843,16843,16843,16843,16843,16843,MONDO:0007789,hypertrophia musculorum vera,MONDO,disease,DISEASE_16843
16844,16844,16844,16844,16844,16844,16844,16844,MONDO:0032782,immunodeficiency 63 with lymphoproliferation and autoimmunity,MONDO,disease,DISEASE_16844
16845,16845,16845,16845,16845,16845,16845,16845,MONDO:1040040,HGSNAT-related retinopathy,MONDO,disease,DISEASE_16845
16846,16846,16846,16846,16846,16846,16846,16846,MONDO:0030711,"Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive",MONDO,disease,DISEASE_16846
16847,16847,16847,16847,16847,16847,16847,16847,MONDO:1012767,"cancer, TP53-related, golden hamster",MONDO,disease,DISEASE_16847
16848,16848,16848,16848,16848,16848,16848,16848,MONDO:0002424,rectosigmoid carcinoma,MONDO,disease,DISEASE_16848
16849,16849,16849,16849,16849,16849,16849,16849,MONDO:0004190_MONDO:0004464,nephrogenic adenoma of urinary bladder,MONDO_grouped,disease,DISEASE_16849
16850,16850,16850,16850,16850,16850,16850,16850,MONDO:0859256,neurodevelopmental disorder with language delay and seizures,MONDO,disease,DISEASE_16850
16851,16851,16851,16851,16851,16851,16851,16851,MONDO:0003569,cranial nerve neuropathy,MONDO,disease,DISEASE_16851
16852,16852,16852,16852,16852,16852,16852,16852,MONDO:0024623_MONDO:0018751,otorhinolaryngologic disease,MONDO_grouped,disease,DISEASE_16852
16853,16853,16853,16853,16853,16853,16853,16853,MONDO:1012516,"goldenhar syndrome, domestic cat",MONDO,disease,DISEASE_16853
16854,16854,16854,16854,16854,16854,16854,16854,MONDO:0015556,nodular urticaria pigmentosa,MONDO,disease,DISEASE_16854
16855,16855,16855,16855,16855,16855,16855,16855,MONDO:0011829_MONDO:0013838_MONDO:0033615_MONDO:0014754,"coenzyme Q10 deficiency, primary",MONDO_grouped,disease,DISEASE_16855
16856,16856,16856,16856,16856,16856,16856,16856,MONDO:0006739,Ehrlich tumor carcinoma,MONDO,disease,DISEASE_16856
16857,16857,16857,16857,16857,16857,16857,16857,MONDO:0015833,pseudounicornuate uterus,MONDO,disease,DISEASE_16857
16858,16858,16858,16858,16858,16858,16858,16858,MONDO:0958175_MONDO:0958194_MONDO:0015397,craniofacial microsomia,MONDO_grouped,disease,DISEASE_16858
16859,16859,16859,16859,16859,16859,16859,16859,MONDO:0030517_MONDO:0030518_MONDO:0021013_MONDO:0014841_MONDO:0032806_MONDO:0010495,"trichothiodystrophy 8, nonphotosensitive",MONDO_grouped,disease,DISEASE_16859
16860,16860,16860,16860,16860,16860,16860,16860,MONDO:0001555,neonatal thyrotoxicosis,MONDO,disease,DISEASE_16860
16861,16861,16861,16861,16861,16861,16861,16861,MONDO:0021659,combined carcinoid and adenocarcinoma,MONDO,disease,DISEASE_16861
16862,16862,16862,16862,16862,16862,16862,16862,MONDO:0005445,visceral leishmaniasis,MONDO,disease,DISEASE_16862
16863,16863,16863,16863,16863,16863,16863,16863,MONDO:1010327,"strabismus, non-human animal",MONDO,disease,DISEASE_16863
16864,16864,16864,16864,16864,16864,16864,16864,MONDO:0032659,"mucocutaneous ulceration, chronic",MONDO,disease,DISEASE_16864
16865,16865,16865,16865,16865,16865,16865,16865,MONDO:0019694_MONDO:0800080,spondylodysplastic dysplasia,MONDO_grouped,disease,DISEASE_16865
16866,16866,16866,16866,16866,16866,16866,16866,MONDO:0021905,Apert-like polydactyly syndrome,MONDO,disease,DISEASE_16866
16867,16867,16867,16867,16867,16867,16867,16867,MONDO:0013548,acetyl-CoA acetyltransferase-2 deficiency,MONDO,disease,DISEASE_16867
16868,16868,16868,16868,16868,16868,16868,16868,MONDO:1010540,"pyloric stenosis, domestic cat",MONDO,disease,DISEASE_16868
16869,16869,16869,16869,16869,16869,16869,16869,MONDO:0016539,atypical hypotonia-cystinuria syndrome,MONDO,disease,DISEASE_16869
16870,16870,16870,16870,16870,16870,16870,16870,MONDO:0017013,trisomy 8p,MONDO,disease,DISEASE_16870
16871,16871,16871,16871,16871,16871,16871,16871,MONDO:0006807_MONDO:0004571_MONDO:0004570_MONDO:0957460,intestinal perforation,MONDO_grouped,disease,DISEASE_16871
16872,16872,16872,16872,16872,16872,16872,16872,MONDO:0032857,"diarrhea 11, malabsorptive, congenital",MONDO,disease,DISEASE_16872
16873,16873,16873,16873,16873,16873,16873,16873,MONDO:0100224_MONDO:0859320_MONDO:0100223,"mitochondrial complex I deficiency, nuclear",MONDO_grouped,disease,DISEASE_16873
16874,16874,16874,16874,16874,16874,16874,16874,MONDO:0958348,retained medullary cord,MONDO,disease,DISEASE_16874
16875,16875,16875,16875,16875,16875,16875,16875,MONDO:0005770,genital herpes,MONDO,disease,DISEASE_16875
16876,16876,16876,16876,16876,16876,16876,16876,MONDO:0019805,twin to twin transfusion syndrome,MONDO,disease,DISEASE_16876
16877,16877,16877,16877,16877,16877,16877,16877,MONDO:0100083,hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1,MONDO,disease,DISEASE_16877
16878,16878,16878,16878,16878,16878,16878,16878,MONDO:1010822,"split hand, domestic cat",MONDO,disease,DISEASE_16878
16879,16879,16879,16879,16879,16879,16879,16879,MONDO:0015810,primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma,MONDO,disease,DISEASE_16879
16880,16880,16880,16880,16880,16880,16880,16880,MONDO:0002002,postsurgical hypothyroidism,MONDO,disease,DISEASE_16880
16881,16881,16881,16881,16881,16881,16881,16881,MONDO:0004326,sphenoid sinus inverted papilloma,MONDO,disease,DISEASE_16881
16882,16882,16882,16882,16882,16882,16882,16882,MONDO:0045023,acquired adrenogenital syndrome,MONDO,disease,DISEASE_16882
16883,16883,16883,16883,16883,16883,16883,16883,MONDO:0006700,choroid cancer,MONDO,disease,DISEASE_16883
16884,16884,16884,16884,16884,16884,16884,16884,MONDO:0003622,pancreatic vasoactive intestinal peptide producing tumor,MONDO,disease,DISEASE_16884
16885,16885,16885,16885,16885,16885,16885,16885,MONDO:0003472,lice infestation,MONDO,disease,DISEASE_16885
16886,16886,16886,16886,16886,16886,16886,16886,MONDO:0001780,premature ejaculation,MONDO,disease,DISEASE_16886
16887,16887,16887,16887,16887,16887,16887,16887,MONDO:0004310,"adult embryonal tumor with multilayered rosettes, c19mc-altered",MONDO,disease,DISEASE_16887
16888,16888,16888,16888,16888,16888,16888,16888,MONDO:0005170,myeloid neoplasm,MONDO,disease,DISEASE_16888
16889,16889,16889,16889,16889,16889,16889,16889,MONDO:0005055,Kaposi's sarcoma,MONDO,disease,DISEASE_16889
16890,16890,16890,16890,16890,16890,16890,16890,MONDO:1011437,"neurofibromatosis, non-human animal",MONDO,disease,DISEASE_16890
16891,16891,16891,16891,16891,16891,16891,16891,MONDO:0008254,"platelet disorder, undefined",MONDO,disease,DISEASE_16891
16892,16892,16892,16892,16892,16892,16892,16892,MONDO:1011427_MONDO:1011764,"ichthyosis, non-human animal",MONDO_grouped,disease,DISEASE_16892
16893,16893,16893,16893,16893,16893,16893,16893,MONDO:0017771,Mayer-Rokitansky-Kuster-Hauser syndrome,MONDO,disease,DISEASE_16893
16894,16894,16894,16894,16894,16894,16894,16894,MONDO:0023002,double discordia,MONDO,disease,DISEASE_16894
16895,16895,16895,16895,16895,16895,16895,16895,MONDO:0004479,malignant childhood germ cell neoplasm,MONDO,disease,DISEASE_16895
16896,16896,16896,16896,16896,16896,16896,16896,MONDO:0001206,aqueous misdirection,MONDO,disease,DISEASE_16896
16897,16897,16897,16897,16897,16897,16897,16897,MONDO:0004562,breast apocrine carcinoma in situ,MONDO,disease,DISEASE_16897
16898,16898,16898,16898,16898,16898,16898,16898,MONDO:0007592,familial recurrent peripheral facial palsy,MONDO,disease,DISEASE_16898
16899,16899,16899,16899,16899,16899,16899,16899,MONDO:0004992,cancer,MONDO,disease,DISEASE_16899
16900,16900,16900,16900,16900,16900,16900,16900,MONDO:0007634,"intellectual disability, FRA12A type",MONDO,disease,DISEASE_16900
16901,16901,16901,16901,16901,16901,16901,16901,MONDO:0015520,late infantile CACH syndrome,MONDO,disease,DISEASE_16901
16902,16902,16902,16902,16902,16902,16902,16902,MONDO:0042494_MONDO:0002975,childhood malignant melanoma,MONDO_grouped,disease,DISEASE_16902
16903,16903,16903,16903,16903,16903,16903,16903,MONDO:0000428,Y-linked disease,MONDO,disease,DISEASE_16903
16904,16904,16904,16904,16904,16904,16904,16904,MONDO:0019463,non-amyloid monoclonal immunoglobulin deposition disease,MONDO,disease,DISEASE_16904
16905,16905,16905,16905,16905,16905,16905,16905,MONDO:0003406,sleep-wake disorder,MONDO,disease,DISEASE_16905
16906,16906,16906,16906,16906,16906,16906,16906,MONDO:0011116,lung agenesis-heart defect-thumb anomalies syndrome,MONDO,disease,DISEASE_16906
16907,16907,16907,16907,16907,16907,16907,16907,MONDO:0007382,Ramos-Arroyo syndrome,MONDO,disease,DISEASE_16907
16908,16908,16908,16908,16908,16908,16908,16908,MONDO:0018564,3p25.3 microdeletion syndrome,MONDO,disease,DISEASE_16908
16909,16909,16909,16909,16909,16909,16909,16909,MONDO:0004714,atrophic muscular disease,MONDO,disease,DISEASE_16909
16910,16910,16910,16910,16910,16910,16910,16910,MONDO:0009138,dysosteosclerosis,MONDO,disease,DISEASE_16910
16911,16911,16911,16911,16911,16911,16911,16911,MONDO:0035694,combined immunodeficiency due to RELA haploinsufficiency,MONDO,disease,DISEASE_16911
16912,16912,16912,16912,16912,16912,16912,16912,MONDO:0056796,obstructive nephropathy,MONDO,disease,DISEASE_16912
16913,16913,16913,16913,16913,16913,16913,16913,MONDO:1040008,CAMK2D-related neurodevelopmental disorder and dilated cardiomyopathy,MONDO,disease,DISEASE_16913
16914,16914,16914,16914,16914,16914,16914,16914,MONDO:0007253,"cancer, familial, with in vitro Radioresistance",MONDO,disease,DISEASE_16914
16915,16915,16915,16915,16915,16915,16915,16915,MONDO:1012060,"dermal allergy, horse",MONDO,disease,DISEASE_16915
16916,16916,16916,16916,16916,16916,16916,16916,MONDO:0017839,"classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form",MONDO,disease,DISEASE_16916
16917,16917,16917,16917,16917,16917,16917,16917,MONDO:0000755,ectopic pregnancy,MONDO,disease,DISEASE_16917
16918,16918,16918,16918,16918,16918,16918,16918,MONDO:0006816,arthropathy,MONDO,disease,DISEASE_16918
16919,16919,16919,16919,16919,16919,16919,16919,MONDO:0851095,KINSSHIP syndrome,MONDO,disease,DISEASE_16919
16920,16920,16920,16920,16920,16920,16920,16920,MONDO:0016798,ataxia neuropathy spectrum,MONDO,disease,DISEASE_16920
16921,16921,16921,16921,16921,16921,16921,16921,MONDO:0001334,hypertrichosis of eyelid,MONDO,disease,DISEASE_16921
16922,16922,16922,16922,16922,16922,16922,16922,MONDO:0010116,thoracomelic dysplasia,MONDO,disease,DISEASE_16922
16923,16923,16923,16923,16923,16923,16923,16923,MONDO:0000624,benign female reproductive system neoplasm,MONDO,disease,DISEASE_16923
16924,16924,16924,16924,16924,16924,16924,16924,MONDO:0008517,syndactyly-polydactyly-ear lobe syndrome,MONDO,disease,DISEASE_16924
16925,16925,16925,16925,16925,16925,16925,16925,MONDO:1012541,"idiopathic hypercalciuria, dog",MONDO,disease,DISEASE_16925
16926,16926,16926,16926,16926,16926,16926,16926,MONDO:0009054,"autosomal recessive cutis laxa type 2, classic type",MONDO,disease,DISEASE_16926
16927,16927,16927,16927,16927,16927,16927,16927,MONDO:0018906,follicular lymphoma,MONDO,disease,DISEASE_16927
16928,16928,16928,16928,16928,16928,16928,16928,MONDO:0004516,bulbomembranous urethral cancer,MONDO,disease,DISEASE_16928
16929,16929,16929,16929,16929,16929,16929,16929,MONDO:0008140,ossified ear cartilages,MONDO,disease,DISEASE_16929
16930,16930,16930,16930,16930,16930,16930,16930,MONDO:0035738,acquired factor VII deficiency,MONDO,disease,DISEASE_16930
16931,16931,16931,16931,16931,16931,16931,16931,MONDO:0009394,juvenile Paget disease,MONDO,disease,DISEASE_16931
16932,16932,16932,16932,16932,16932,16932,16932,MONDO:0003354,heart sarcoma,MONDO,disease,DISEASE_16932
16933,16933,16933,16933,16933,16933,16933,16933,MONDO:0016953,partial duplication of the long arm of chromosome 2,MONDO,disease,DISEASE_16933
16934,16934,16934,16934,16934,16934,16934,16934,MONDO:0024470,benign chondrogenic neoplasm,MONDO,disease,DISEASE_16934
16935,16935,16935,16935,16935,16935,16935,16935,MONDO:0060456,"cerebral sclerosis, diffuse, scholz type",MONDO,disease,DISEASE_16935
16936,16936,16936,16936,16936,16936,16936,16936,MONDO:0006879,optic papillitis,MONDO,disease,DISEASE_16936
16937,16937,16937,16937,16937,16937,16937,16937,MONDO:0044743,major salivary gland cancer,MONDO,disease,DISEASE_16937
16938,16938,16938,16938,16938,16938,16938,16938,MONDO:0859168,"myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy",MONDO,disease,DISEASE_16938
16939,16939,16939,16939,16939,16939,16939,16939,MONDO:0004425_MONDO:0001223,hyperthyroidism,MONDO_grouped,disease,DISEASE_16939
16940,16940,16940,16940,16940,16940,16940,16940,MONDO:0015232,radial deficiency-tibial hypoplasia syndrome,MONDO,disease,DISEASE_16940
16941,16941,16941,16941,16941,16941,16941,16941,MONDO:0001528_MONDO:0002187,vulva cancer,MONDO_grouped,disease,DISEASE_16941
16942,16942,16942,16942,16942,16942,16942,16942,MONDO:0971123,isolated retinal racemose hemangioma,MONDO,disease,DISEASE_16942
16943,16943,16943,16943,16943,16943,16943,16943,MONDO:0016604,dysraphism-cleft lip/palate-limb reduction defects syndrome,MONDO,disease,DISEASE_16943
16944,16944,16944,16944,16944,16944,16944,16944,MONDO:0027749,serpinopathy,MONDO,disease,DISEASE_16944
16945,16945,16945,16945,16945,16945,16945,16945,MONDO:0005487,schizoaffective disorder,MONDO,disease,DISEASE_16945
16946,16946,16946,16946,16946,16946,16946,16946,MONDO:0007711,Bencze syndrome,MONDO,disease,DISEASE_16946
16947,16947,16947,16947,16947,16947,16947,16947,MONDO:0054737_MONDO:0054738_MONDO:0054739_MONDO:0009046,Fraser syndrome,MONDO_grouped,disease,DISEASE_16947
16948,16948,16948,16948,16948,16948,16948,16948,MONDO:0011474_MONDO:0007240_MONDO:0007701_MONDO:0019490,progressive familial heart block,MONDO_grouped,disease,DISEASE_16948
16949,16949,16949,16949,16949,16949,16949,16949,MONDO:0005382,bone Paget disease,MONDO,disease,DISEASE_16949
16950,16950,16950,16950,16950,16950,16950,16950,MONDO:0011806,osteofibrous dysplasia,MONDO,disease,DISEASE_16950
16951,16951,16951,16951,16951,16951,16951,16951,MONDO:0700181,feline fibrosarcoma,MONDO,disease,DISEASE_16951
16952,16952,16952,16952,16952,16952,16952,16952,MONDO:0800464,SQSTM1-related multisystem proteinopathy,MONDO,disease,DISEASE_16952
16953,16953,16953,16953,16953,16953,16953,16953,MONDO:1010136,"vitiligo, non-human animal",MONDO,disease,DISEASE_16953
16954,16954,16954,16954,16954,16954,16954,16954,MONDO:0043678,chromosome inversion disorder,MONDO,disease,DISEASE_16954
16955,16955,16955,16955,16955,16955,16955,16955,MONDO:0010514,combined immunodeficiency due to moesin deficiency,MONDO,disease,DISEASE_16955
16956,16956,16956,16956,16956,16956,16956,16956,MONDO:0008134,"autosomal dominant optic atrophy, classic form",MONDO,disease,DISEASE_16956
16957,16957,16957,16957,16957,16957,16957,16957,MONDO:0004826,urethral calculus,MONDO,disease,DISEASE_16957
16958,16958,16958,16958,16958,16958,16958,16958,MONDO:0030326,mitochondrial dna depletion syndrome 16B (neuroophthalmic type),MONDO,disease,DISEASE_16958
16959,16959,16959,16959,16959,16959,16959,16959,MONDO:0100305,bile acid CoA:amino acid N-acyltransferase deficiency,MONDO,disease,DISEASE_16959
16960,16960,16960,16960,16960,16960,16960,16960,MONDO:0024893,toxocara canis infection (canine roundworms),MONDO,disease,DISEASE_16960
16961,16961,16961,16961,16961,16961,16961,16961,MONDO:0004572,cyclothymic disorder,MONDO,disease,DISEASE_16961
16962,16962,16962,16962,16962,16962,16962,16962,MONDO:0019849,isolated micropenis,MONDO,disease,DISEASE_16962
16963,16963,16963,16963,16963,16963,16963,16963,MONDO:0005932,pseudorabies,MONDO,disease,DISEASE_16963
16964,16964,16964,16964,16964,16964,16964,16964,MONDO:0001763_MONDO:0005756_MONDO:0004757,ethmoid sinus cancer,MONDO_grouped,disease,DISEASE_16964
16965,16965,16965,16965,16965,16965,16965,16965,MONDO:0018615,hemicrania continua,MONDO,disease,DISEASE_16965
16966,16966,16966,16966,16966,16966,16966,16966,MONDO:0016600,acute neonatal citrullinemia type I,MONDO,disease,DISEASE_16966
16967,16967,16967,16967,16967,16967,16967,16967,MONDO:0005647,anogenital human papillomavirus infection,MONDO,disease,DISEASE_16967
16968,16968,16968,16968,16968,16968,16968,16968,MONDO:0014034,severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome,MONDO,disease,DISEASE_16968
16969,16969,16969,16969,16969,16969,16969,16969,MONDO:0018893,Cobb syndrome,MONDO,disease,DISEASE_16969
16970,16970,16970,16970,16970,16970,16970,16970,MONDO:0005957,setariasis,MONDO,disease,DISEASE_16970
16971,16971,16971,16971,16971,16971,16971,16971,MONDO:0000294,mesocestoidiasis,MONDO,disease,DISEASE_16971
16972,16972,16972,16972,16972,16972,16972,16972,MONDO:0020652,immature teratoma of vulva,MONDO,disease,DISEASE_16972
16973,16973,16973,16973,16973,16973,16973,16973,MONDO:0022872,corpus callosum dysgenesis X-linked recessive,MONDO,disease,DISEASE_16973
16974,16974,16974,16974,16974,16974,16974,16974,MONDO:0044682,MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome,MONDO,disease,DISEASE_16974
16975,16975,16975,16975,16975,16975,16975,16975,MONDO:0009080,split hand-foot malformation 1 with sensorineural hearing loss,MONDO,disease,DISEASE_16975
16976,16976,16976,16976,16976,16976,16976,16976,MONDO:0018645,IgG4-related sclerosing cholangitis,MONDO,disease,DISEASE_16976
16977,16977,16977,16977,16977,16977,16977,16977,MONDO:0015129,chronic primary adrenal insufficiency,MONDO,disease,DISEASE_16977
16978,16978,16978,16978,16978,16978,16978,16978,MONDO:0016094,vaginal germ cell malignant tumor,MONDO,disease,DISEASE_16978
16979,16979,16979,16979,16979,16979,16979,16979,MONDO:0006712,corneal edema,MONDO,disease,DISEASE_16979
16980,16980,16980,16980,16980,16980,16980,16980,MONDO:0015570,isolated congenital auditory ossicle malformation,MONDO,disease,DISEASE_16980
16981,16981,16981,16981,16981,16981,16981,16981,MONDO:0000607,primary cutaneous T-cell non-Hodgkin lymphoma,MONDO,disease,DISEASE_16981
16982,16982,16982,16982,16982,16982,16982,16982,MONDO:0001627_MONDO:0004648,dementia,MONDO_grouped,disease,DISEASE_16982
16983,16983,16983,16983,16983,16983,16983,16983,MONDO:0013846,"peripartum cardiomyopathy, susceptibility to",MONDO,disease,DISEASE_16983
16984,16984,16984,16984,16984,16984,16984,16984,MONDO:0005277,migraine disorder,MONDO,disease,DISEASE_16984
16985,16985,16985,16985,16985,16985,16985,16985,MONDO:0013363,chromosome 2q31.1 duplication syndrome,MONDO,disease,DISEASE_16985
16986,16986,16986,16986,16986,16986,16986,16986,MONDO:0008080,"neurofibromatosis, type III, mixed central and peripheral",MONDO,disease,DISEASE_16986
16987,16987,16987,16987,16987,16987,16987,16987,MONDO:0030714,"osteogenesis imperfecta, IIA 22",MONDO,disease,DISEASE_16987
16988,16988,16988,16988,16988,16988,16988,16988,MONDO:1010044,"microvillus inclusion disease, non-human animal",MONDO,disease,DISEASE_16988
16989,16989,16989,16989,16989,16989,16989,16989,MONDO:0016868,partial deletion of chromosome 3,MONDO,disease,DISEASE_16989
16990,16990,16990,16990,16990,16990,16990,16990,MONDO:0010095,ataxia-tapetoretinal degeneration syndrome,MONDO,disease,DISEASE_16990
16991,16991,16991,16991,16991,16991,16991,16991,MONDO:0000588,autoimmune disorder of gastrointestinal tract,MONDO,disease,DISEASE_16991
16992,16992,16992,16992,16992,16992,16992,16992,MONDO:0016077,congenital aortopulmonary window,MONDO,disease,DISEASE_16992
16993,16993,16993,16993,16993,16993,16993,16993,MONDO:0007023,Yersinia infectious disease,MONDO,disease,DISEASE_16993
16994,16994,16994,16994,16994,16994,16994,16994,MONDO:0003128,classic pulmonary blastoma,MONDO,disease,DISEASE_16994
16995,16995,16995,16995,16995,16995,16995,16995,MONDO:0054591,Stankiewicz-Isidor syndrome,MONDO,disease,DISEASE_16995
16996,16996,16996,16996,16996,16996,16996,16996,MONDO:0800386,organophosphate poisoning,MONDO,disease,DISEASE_16996
16997,16997,16997,16997,16997,16997,16997,16997,MONDO:0015516,symbrachydactyly of hands and feet,MONDO,disease,DISEASE_16997
16998,16998,16998,16998,16998,16998,16998,16998,MONDO:0015306,Lemierre syndrome,MONDO,disease,DISEASE_16998
16999,16999,16999,16999,16999,16999,16999,16999,MONDO:0002869,heart valve disorder,MONDO,disease,DISEASE_16999
17000,17000,17000,17000,17000,17000,17000,17000,MONDO:0001261_MONDO:0020744,Mobitz type II atrioventricular block,MONDO_grouped,disease,DISEASE_17000
17001,17001,17001,17001,17001,17001,17001,17001,MONDO:0968955,hypocalcified amelogenesis imperfecta,MONDO,disease,DISEASE_17001
17002,17002,17002,17002,17002,17002,17002,17002,MONDO:0100004,mast cell activation syndrome,MONDO,disease,DISEASE_17002
17003,17003,17003,17003,17003,17003,17003,17003,MONDO:0030855_MONDO:0030854,combined osteogenesis imperfecta and Ehlers-Danlos syndrome,MONDO_grouped,disease,DISEASE_17003
17004,17004,17004,17004,17004,17004,17004,17004,MONDO:0010972,hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome,MONDO,disease,DISEASE_17004
17005,17005,17005,17005,17005,17005,17005,17005,MONDO:0018141,"pyruvate carboxylase deficiency, infantile form",MONDO,disease,DISEASE_17005
17006,17006,17006,17006,17006,17006,17006,17006,MONDO:0000671_MONDO:0000674,finger agnosia,MONDO_grouped,disease,DISEASE_17006
17007,17007,17007,17007,17007,17007,17007,17007,MONDO:0007427,deafness with anhidrotic ectodermal dysplasia,MONDO,disease,DISEASE_17007
17008,17008,17008,17008,17008,17008,17008,17008,MONDO:0008601_MONDO:0008602_MONDO:0000155,"triglyceride storage disease,",MONDO_grouped,disease,DISEASE_17008
17009,17009,17009,17009,17009,17009,17009,17009,MONDO:1010575_MONDO:1011600_MONDO:1011604,"diabetes mellitus, domestic cat",MONDO_grouped,disease,DISEASE_17009
17010,17010,17010,17010,17010,17010,17010,17010,MONDO:0008885,Elsahy-Waters syndrome,MONDO,disease,DISEASE_17010
17011,17011,17011,17011,17011,17011,17011,17011,MONDO:0700227,ELOVL4-related maculopathy,MONDO,disease,DISEASE_17011
17012,17012,17012,17012,17012,17012,17012,17012,MONDO:0006655,aortic valve prolapse,MONDO,disease,DISEASE_17012
17013,17013,17013,17013,17013,17013,17013,17013,MONDO:0700127,mosaic trisomy 21,MONDO,disease,DISEASE_17013
17014,17014,17014,17014,17014,17014,17014,17014,MONDO:0025139,white muscle disease,MONDO,disease,DISEASE_17014
17015,17015,17015,17015,17015,17015,17015,17015,MONDO:0700144,canine leukemia,MONDO,disease,DISEASE_17015
17016,17016,17016,17016,17016,17016,17016,17016,MONDO:0011953_MONDO:0016991,familial acute necrotizing encephalopathy,MONDO_grouped,disease,DISEASE_17016
17017,17017,17017,17017,17017,17017,17017,17017,MONDO:0015057,renin-angiotensin-aldosterone system-blocker-induced angioedema,MONDO,disease,DISEASE_17017
17018,17018,17018,17018,17018,17018,17018,17018,MONDO:0017239,familial progressive hyper- and hypopigmentation,MONDO,disease,DISEASE_17018
17019,17019,17019,17019,17019,17019,17019,17019,MONDO:0010051,spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome,MONDO,disease,DISEASE_17019
17020,17020,17020,17020,17020,17020,17020,17020,MONDO:0010605,hemopoietic proliferation,MONDO,disease,DISEASE_17020
17021,17021,17021,17021,17021,17021,17021,17021,MONDO:1010041,"Meckel diverticulum, non-human animal",MONDO,disease,DISEASE_17021
17022,17022,17022,17022,17022,17022,17022,17022,MONDO:1010812_MONDO:1010826,"polydactyly, domestic cat",MONDO_grouped,disease,DISEASE_17022
17023,17023,17023,17023,17023,17023,17023,17023,MONDO:0012819,diabetic ketoacidosis,MONDO,disease,DISEASE_17023
17024,17024,17024,17024,17024,17024,17024,17024,MONDO:0000293,coenurosis,MONDO,disease,DISEASE_17024
17025,17025,17025,17025,17025,17025,17025,17025,MONDO:0001580,lacrimal duct cancer,MONDO,disease,DISEASE_17025
17026,17026,17026,17026,17026,17026,17026,17026,MONDO:0001713,inherited aplastic anemia,MONDO,disease,DISEASE_17026
17027,17027,17027,17027,17027,17027,17027,17027,MONDO:0019896,Kleefstra syndrome due to 9q34 microdeletion,MONDO,disease,DISEASE_17027
17028,17028,17028,17028,17028,17028,17028,17028,MONDO:0700232,KIZ-related retinopathy,MONDO,disease,DISEASE_17028
17029,17029,17029,17029,17029,17029,17029,17029,MONDO:0007507,absence of fingerprints-congenital milia syndrome,MONDO,disease,DISEASE_17029
17030,17030,17030,17030,17030,17030,17030,17030,MONDO:0022236,colpocephaly,MONDO,disease,DISEASE_17030
17031,17031,17031,17031,17031,17031,17031,17031,MONDO:0019734,juvenile polymyositis,MONDO,disease,DISEASE_17031
17032,17032,17032,17032,17032,17032,17032,17032,MONDO:0011453,ulnar ray dysgenesis with postaxial polydactyly and renal cystic dysplasia,MONDO,disease,DISEASE_17032
17033,17033,17033,17033,17033,17033,17033,17033,MONDO:0005111_MONDO:0017342_MONDO:0000286,Epstein-Barr virus infection,MONDO_grouped,disease,DISEASE_17033
17034,17034,17034,17034,17034,17034,17034,17034,MONDO:0001922,pyoureter,MONDO,disease,DISEASE_17034
17035,17035,17035,17035,17035,17035,17035,17035,MONDO:1010171,"lysosomal storage disease, non-human animal",MONDO,disease,DISEASE_17035
17036,17036,17036,17036,17036,17036,17036,17036,MONDO:0001962,abnormality of glucagon secretion,MONDO,disease,DISEASE_17036
17037,17037,17037,17037,17037,17037,17037,17037,MONDO:0020429_MONDO:1010454,cor triatriatum dexter,MONDO_grouped,disease,DISEASE_17037
17038,17038,17038,17038,17038,17038,17038,17038,MONDO:0018484,semicircular canal dehiscence syndrome,MONDO,disease,DISEASE_17038
17039,17039,17039,17039,17039,17039,17039,17039,MONDO:1011918,"tetragametic chimerism, non-human animal",MONDO,disease,DISEASE_17039
17040,17040,17040,17040,17040,17040,17040,17040,MONDO:0000565,infective endocarditis,MONDO,disease,DISEASE_17040
17041,17041,17041,17041,17041,17041,17041,17041,MONDO:0957405,granulomatous autoinflammatory syndrome of childhood,MONDO,disease,DISEASE_17041
17042,17042,17042,17042,17042,17042,17042,17042,MONDO:0008845,atonic-astatic syndrome of Foerster,MONDO,disease,DISEASE_17042
17043,17043,17043,17043,17043,17043,17043,17043,MONDO:0032937,"myopathy, congenital proximal, with minicore lesions",MONDO,disease,DISEASE_17043
17044,17044,17044,17044,17044,17044,17044,17044,MONDO:0020458,hemolytic anemia due to erythrocyte adenosine deaminase overproduction,MONDO,disease,DISEASE_17044
17045,17045,17045,17045,17045,17045,17045,17045,MONDO:0016285,papillary carcinoma of the cervix uteri,MONDO,disease,DISEASE_17045
17046,17046,17046,17046,17046,17046,17046,17046,MONDO:0019904,ring chromosome 3,MONDO,disease,DISEASE_17046
17047,17047,17047,17047,17047,17047,17047,17047,MONDO:0007748_MONDO:0011802,"hypercalciuria, absorptive",MONDO_grouped,disease,DISEASE_17047
17048,17048,17048,17048,17048,17048,17048,17048,MONDO:0017778,lamellar ichthyosis,MONDO,disease,DISEASE_17048
17049,17049,17049,17049,17049,17049,17049,17049,MONDO:0009705,carnitine palmitoyl transferase 1A deficiency,MONDO,disease,DISEASE_17049
17050,17050,17050,17050,17050,17050,17050,17050,MONDO:1012399,"anal sac gland carcinoma, dog",MONDO,disease,DISEASE_17050
17051,17051,17051,17051,17051,17051,17051,17051,MONDO:0017056,DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion,MONDO,disease,DISEASE_17051
17052,17052,17052,17052,17052,17052,17052,17052,MONDO:0005965,spinal stenosis,MONDO,disease,DISEASE_17052
17053,17053,17053,17053,17053,17053,17053,17053,MONDO:0032655,visual impairment and progressive phthisis bulbi,MONDO,disease,DISEASE_17053
17054,17054,17054,17054,17054,17054,17054,17054,MONDO:0024339,lymph node neoplasm,MONDO,disease,DISEASE_17054
17055,17055,17055,17055,17055,17055,17055,17055,MONDO:0000727,scapuloperoneal myopathy,MONDO,disease,DISEASE_17055
17056,17056,17056,17056,17056,17056,17056,17056,MONDO:0006571,lichen nitidus,MONDO,disease,DISEASE_17056
17057,17057,17057,17057,17057,17057,17057,17057,MONDO:0004694,hepatopulmonary syndrome,MONDO,disease,DISEASE_17057
17058,17058,17058,17058,17058,17058,17058,17058,MONDO:0020685_MONDO:0020687_MONDO:0850340,infratentorial ependymal tumor,MONDO_grouped,disease,DISEASE_17058
17059,17059,17059,17059,17059,17059,17059,17059,MONDO:0015767,trisomy 4p,MONDO,disease,DISEASE_17059
17060,17060,17060,17060,17060,17060,17060,17060,MONDO:0001246,typhus,MONDO,disease,DISEASE_17060
17061,17061,17061,17061,17061,17061,17061,17061,MONDO:0015691,hypereosinophilic syndrome,MONDO,disease,DISEASE_17061
17062,17062,17062,17062,17062,17062,17062,17062,MONDO:0001196,psychologic dyspareunia,MONDO,disease,DISEASE_17062
17063,17063,17063,17063,17063,17063,17063,17063,MONDO:1040002_MONDO:1040004,PIK3CA-related overgrowth spectrum,MONDO_grouped,disease,DISEASE_17063
17064,17064,17064,17064,17064,17064,17064,17064,MONDO:0015663,diencephalic syndrome,MONDO,disease,DISEASE_17064
17065,17065,17065,17065,17065,17065,17065,17065,MONDO:0009597_MONDO:0009596_MONDO:0007982_MONDO:0009594,"metaphyseal chondrodysplasia, Spahr type",MONDO_grouped,disease,DISEASE_17065
17066,17066,17066,17066,17066,17066,17066,17066,MONDO:0005053,ischemic disease,MONDO,disease,DISEASE_17066
17067,17067,17067,17067,17067,17067,17067,17067,MONDO:0004414,tamoxifen-related endometrial lesion,MONDO,disease,DISEASE_17067
17068,17068,17068,17068,17068,17068,17068,17068,MONDO:0004507,atypical breast papilloma,MONDO,disease,DISEASE_17068
17069,17069,17069,17069,17069,17069,17069,17069,MONDO:0009942,pyknoachondrogenesis,MONDO,disease,DISEASE_17069
17070,17070,17070,17070,17070,17070,17070,17070,MONDO:0003574,external ear cancer,MONDO,disease,DISEASE_17070
17071,17071,17071,17071,17071,17071,17071,17071,MONDO:0000858,neuronal intestinal dysplasia,MONDO,disease,DISEASE_17071
17072,17072,17072,17072,17072,17072,17072,17072,MONDO:0007412,Beare-Stevenson cutis gyrata syndrome,MONDO,disease,DISEASE_17072
17073,17073,17073,17073,17073,17073,17073,17073,MONDO:0020316,acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22),MONDO,disease,DISEASE_17073
17074,17074,17074,17074,17074,17074,17074,17074,MONDO:0006864,necrotizing sialometaplasia,MONDO,disease,DISEASE_17074
17075,17075,17075,17075,17075,17075,17075,17075,MONDO:0017353,neonatal glycine encephalopathy,MONDO,disease,DISEASE_17075
17076,17076,17076,17076,17076,17076,17076,17076,MONDO:0003237,adenomyoma of uterine corpus,MONDO,disease,DISEASE_17076
17077,17077,17077,17077,17077,17077,17077,17077,MONDO:0000873,lymphoblastic lymphoma,MONDO,disease,DISEASE_17077
17078,17078,17078,17078,17078,17078,17078,17078,MONDO:0035548,autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiency,MONDO,disease,DISEASE_17078
17079,17079,17079,17079,17079,17079,17079,17079,MONDO:0010874,"enteropathy, familial, with villous edema and immunoglobulin G2 deficiency",MONDO,disease,DISEASE_17079
17080,17080,17080,17080,17080,17080,17080,17080,MONDO:0100460,"tobacco addiction, susceptibility to",MONDO,disease,DISEASE_17080
17081,17081,17081,17081,17081,17081,17081,17081,MONDO:0007913,"low density lipoprotein, variation in molecular weight of",MONDO,disease,DISEASE_17081
17082,17082,17082,17082,17082,17082,17082,17082,MONDO:0700028,chromosome Y disorder,MONDO,disease,DISEASE_17082
17083,17083,17083,17083,17083,17083,17083,17083,MONDO:0001614,intra-abdominal lymph node mast cell malignancy,MONDO,disease,DISEASE_17083
17084,17084,17084,17084,17084,17084,17084,17084,MONDO:0020765_MONDO:0020766,"neuropathy, congenital hypomyelinating",MONDO_grouped,disease,DISEASE_17084
17085,17085,17085,17085,17085,17085,17085,17085,MONDO:1050000,sycosis barbae,MONDO,disease,DISEASE_17085
17086,17086,17086,17086,17086,17086,17086,17086,MONDO:0017578,disorder of thiamine metabolism and transport,MONDO,disease,DISEASE_17086
17087,17087,17087,17087,17087,17087,17087,17087,MONDO:0012075,oligodontia-cancer predisposition syndrome,MONDO,disease,DISEASE_17087
17088,17088,17088,17088,17088,17088,17088,17088,MONDO:0018764,microcephalic primordial dwarfism due to RTTN deficiency,MONDO,disease,DISEASE_17088
17089,17089,17089,17089,17089,17089,17089,17089,MONDO:1011760,"symmetrical onychomadesis, non-human animal",MONDO,disease,DISEASE_17089
17090,17090,17090,17090,17090,17090,17090,17090,MONDO:0007005,ulcerative proctosigmoiditis,MONDO,disease,DISEASE_17090
17091,17091,17091,17091,17091,17091,17091,17091,MONDO:0020628_MONDO:0020629,"microcephaly, growth restriction, and increased sister chromatid exchange 2",MONDO_grouped,disease,DISEASE_17091
17092,17092,17092,17092,17092,17092,17092,17092,MONDO:1011653,"craniomandibular osteopathy, non-human animal",MONDO,disease,DISEASE_17092
17093,17093,17093,17093,17093,17093,17093,17093,MONDO:0002428,protozoa infectious disease,MONDO,disease,DISEASE_17093
17094,17094,17094,17094,17094,17094,17094,17094,MONDO:0007285_MONDO:0100436,cataract 1 multiple types,MONDO_grouped,disease,DISEASE_17094
17095,17095,17095,17095,17095,17095,17095,17095,MONDO:0001488_MONDO:0001717,anterior corneal pigmentation,MONDO_grouped,disease,DISEASE_17095
17096,17096,17096,17096,17096,17096,17096,17096,MONDO:0008054_MONDO:0001907_MONDO:0957456,juvenile dermatomyositis,MONDO_grouped,disease,DISEASE_17096
17097,17097,17097,17097,17097,17097,17097,17097,MONDO:0009024,cortical blindness-intellectual disability-polydactyly syndrome,MONDO,disease,DISEASE_17097
17098,17098,17098,17098,17098,17098,17098,17098,MONDO:0019919,maternal uniparental disomy of chromosome 22,MONDO,disease,DISEASE_17098
17099,17099,17099,17099,17099,17099,17099,17099,MONDO:0014061,Steel syndrome,MONDO,disease,DISEASE_17099
17100,17100,17100,17100,17100,17100,17100,17100,MONDO:0060704,neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures,MONDO,disease,DISEASE_17100
17101,17101,17101,17101,17101,17101,17101,17101,MONDO:0011973,"zinc deficiency, transient neonatal",MONDO,disease,DISEASE_17101
17102,17102,17102,17102,17102,17102,17102,17102,MONDO:0014911,"growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy",MONDO,disease,DISEASE_17102
17103,17103,17103,17103,17103,17103,17103,17103,MONDO:0016983,Bartter syndrome with hypocalcemia,MONDO,disease,DISEASE_17103
17104,17104,17104,17104,17104,17104,17104,17104,MONDO:0023201,Fryns Smeets Thiry syndrome,MONDO,disease,DISEASE_17104
17105,17105,17105,17105,17105,17105,17105,17105,MONDO:0015312,"choanal atresia, unilateral",MONDO,disease,DISEASE_17105
17106,17106,17106,17106,17106,17106,17106,17106,MONDO:1010258_MONDO:1011905,"glomerulonephritis, non-human animal",MONDO_grouped,disease,DISEASE_17106
17107,17107,17107,17107,17107,17107,17107,17107,MONDO:0015408,diffuse lymphatic malformation,MONDO,disease,DISEASE_17107
17108,17108,17108,17108,17108,17108,17108,17108,MONDO:0004838,orthostatic proteinuria,MONDO,disease,DISEASE_17108
17109,17109,17109,17109,17109,17109,17109,17109,MONDO:0012216,foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome,MONDO,disease,DISEASE_17109
17110,17110,17110,17110,17110,17110,17110,17110,MONDO:0016977,moderately-differentiated thymic neuroendocrine carcinoma,MONDO,disease,DISEASE_17110
17111,17111,17111,17111,17111,17111,17111,17111,MONDO:0009247,frontofacionasal dysplasia,MONDO,disease,DISEASE_17111
17112,17112,17112,17112,17112,17112,17112,17112,MONDO:0021508,benign neoplasm of epicardium,MONDO,disease,DISEASE_17112
17113,17113,17113,17113,17113,17113,17113,17113,MONDO:1012620,"congenital myasthenic syndrome, CHRNE-related, dog",MONDO,disease,DISEASE_17113
17114,17114,17114,17114,17114,17114,17114,17114,MONDO:1012014,"type-II collagen-immune complex arthritis, sheep",MONDO,disease,DISEASE_17114
17115,17115,17115,17115,17115,17115,17115,17115,MONDO:0008520,brachydactyly-elbow wrist dysplasia syndrome,MONDO,disease,DISEASE_17115
17116,17116,17116,17116,17116,17116,17116,17116,MONDO:0850282_MONDO:0956971,chronic asthma,MONDO_grouped,disease,DISEASE_17116
17117,17117,17117,17117,17117,17117,17117,17117,MONDO:0004634,vein disorder,MONDO,disease,DISEASE_17117
17118,17118,17118,17118,17118,17118,17118,17118,MONDO:0043373,sudden sensorineural hearing loss,MONDO,disease,DISEASE_17118
17119,17119,17119,17119,17119,17119,17119,17119,MONDO:0011368,papillary thyroid Microcarcinoma,MONDO,disease,DISEASE_17119
17120,17120,17120,17120,17120,17120,17120,17120,MONDO:0002305,thrombophilia,MONDO,disease,DISEASE_17120
17121,17121,17121,17121,17121,17121,17121,17121,MONDO:0002101,facial nerve neoplasm,MONDO,disease,DISEASE_17121
17122,17122,17122,17122,17122,17122,17122,17122,MONDO:0003223,meninges hemangiopericytoma,MONDO,disease,DISEASE_17122
17123,17123,17123,17123,17123,17123,17123,17123,MONDO:0850161,"B-lymphoblastic leukemia/lymphoma, BCR-ABL1–like",MONDO,disease,DISEASE_17123
17124,17124,17124,17124,17124,17124,17124,17124,MONDO:0005801,human T-lymphotropic virus 1 infectious disease,MONDO,disease,DISEASE_17124
17125,17125,17125,17125,17125,17125,17125,17125,MONDO:0013404,hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase,MONDO,disease,DISEASE_17125
17126,17126,17126,17126,17126,17126,17126,17126,MONDO:0017809,parkinsonism due to ATP13A2 deficiency,MONDO,disease,DISEASE_17126
17127,17127,17127,17127,17127,17127,17127,17127,MONDO:0008903,lung cancer,MONDO,disease,DISEASE_17127
17128,17128,17128,17128,17128,17128,17128,17128,MONDO:0002615_MONDO:0005236,xanthomatosis,MONDO_grouped,disease,DISEASE_17128
17129,17129,17129,17129,17129,17129,17129,17129,MONDO:0006968,shoulder impingement syndrome,MONDO,disease,DISEASE_17129
17130,17130,17130,17130,17130,17130,17130,17130,MONDO:0023650_MONDO:0975752,littoral cell angioma of the spleen,MONDO_grouped,disease,DISEASE_17130
17131,17131,17131,17131,17131,17131,17131,17131,MONDO:0018927,SUNCT syndrome,MONDO,disease,DISEASE_17131
17132,17132,17132,17132,17132,17132,17132,17132,MONDO:1012954,"amyotrophic lateral sclerosis, non-human animal",MONDO,disease,DISEASE_17132
17133,17133,17133,17133,17133,17133,17133,17133,MONDO:0007694,hairy nose tip,MONDO,disease,DISEASE_17133
17134,17134,17134,17134,17134,17134,17134,17134,MONDO:0016873,partial deletion of chromosome 8,MONDO,disease,DISEASE_17134
17135,17135,17135,17135,17135,17135,17135,17135,MONDO:0001593,rectal disorder,MONDO,disease,DISEASE_17135
17136,17136,17136,17136,17136,17136,17136,17136,MONDO:0041536,Far-East scarlet-like fever,MONDO,disease,DISEASE_17136
17137,17137,17137,17137,17137,17137,17137,17137,MONDO:0975761,"immunodeficiency 126, susceptibility to",MONDO,disease,DISEASE_17137
17138,17138,17138,17138,17138,17138,17138,17138,MONDO:0002892,skull base chordoma,MONDO,disease,DISEASE_17138
17139,17139,17139,17139,17139,17139,17139,17139,MONDO:1040024,myelin oligodendrocyte glycoprotein antibody-associated disease,MONDO,disease,DISEASE_17139
17140,17140,17140,17140,17140,17140,17140,17140,MONDO:0859351,obesity and hypopigmentation,MONDO,disease,DISEASE_17140
17141,17141,17141,17141,17141,17141,17141,17141,MONDO:0009190,"epiphyseal dysplasia of femoral head, myopia, and deafness",MONDO,disease,DISEASE_17141
17142,17142,17142,17142,17142,17142,17142,17142,MONDO:0006773,gonadal tissue neoplasm,MONDO,disease,DISEASE_17142
17143,17143,17143,17143,17143,17143,17143,17143,MONDO:1012380,"lymphoproliferative disease, dog",MONDO,disease,DISEASE_17143
17144,17144,17144,17144,17144,17144,17144,17144,MONDO:0000518,sacrum chordoma,MONDO,disease,DISEASE_17144
17145,17145,17145,17145,17145,17145,17145,17145,MONDO:0020404,shone complex,MONDO,disease,DISEASE_17145
17146,17146,17146,17146,17146,17146,17146,17146,MONDO:0018580,obsolete PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome,MONDO,disease,DISEASE_17146
17147,17147,17147,17147,17147,17147,17147,17147,MONDO:0859150,BDV syndrome,MONDO,disease,DISEASE_17147
17148,17148,17148,17148,17148,17148,17148,17148,MONDO:1011820_MONDO:1012408,"colorectal hamartomatous polyposis and ganglioneuromatosis, non-human animal",MONDO_grouped,disease,DISEASE_17148
17149,17149,17149,17149,17149,17149,17149,17149,MONDO:0009331,isolated hemihyperplasia,MONDO,disease,DISEASE_17149
17150,17150,17150,17150,17150,17150,17150,17150,MONDO:0008278,juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome,MONDO,disease,DISEASE_17150
17151,17151,17151,17151,17151,17151,17151,17151,MONDO:0012107,"neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia",MONDO,disease,DISEASE_17151
17152,17152,17152,17152,17152,17152,17152,17152,MONDO:1010670_MONDO:1010671,"methemoglobinemia, CYB5R3-related, dog",MONDO_grouped,disease,DISEASE_17152
17153,17153,17153,17153,17153,17153,17153,17153,MONDO:0008750,microcephaly-albinism-digital anomalies syndrome,MONDO,disease,DISEASE_17153
17154,17154,17154,17154,17154,17154,17154,17154,MONDO:0015315,neonatal brainstem dysfunction,MONDO,disease,DISEASE_17154
17155,17155,17155,17155,17155,17155,17155,17155,MONDO:0002060_MONDO:0004253_MONDO:0021099,intraductal papilloma,MONDO_grouped,disease,DISEASE_17155
17156,17156,17156,17156,17156,17156,17156,17156,MONDO:1011247_MONDO:1011246_MONDO:1012358,"retinal degeneration, cattle",MONDO_grouped,disease,DISEASE_17156
17157,17157,17157,17157,17157,17157,17157,17157,MONDO:0000686,alexia without agraphia,MONDO,disease,DISEASE_17157
17158,17158,17158,17158,17158,17158,17158,17158,MONDO:0008659,transcobalamin I deficiency,MONDO,disease,DISEASE_17158
17159,17159,17159,17159,17159,17159,17159,17159,MONDO:1010068,"situs inversus, non-human animal",MONDO,disease,DISEASE_17159
17160,17160,17160,17160,17160,17160,17160,17160,MONDO:0008167,dermoid cyst of ovary,MONDO,disease,DISEASE_17160
17161,17161,17161,17161,17161,17161,17161,17161,MONDO:0010772,Leber optic atrophy and dystonia,MONDO,disease,DISEASE_17161
17162,17162,17162,17162,17162,17162,17162,17162,MONDO:0020644,lung non-Hodgkin lymphoma,MONDO,disease,DISEASE_17162
17163,17163,17163,17163,17163,17163,17163,17163,MONDO:0011371,"hydroa vacciniforme, familial",MONDO,disease,DISEASE_17163
17164,17164,17164,17164,17164,17164,17164,17164,MONDO:0002493,prostatic acinar adenocarcinoma,MONDO,disease,DISEASE_17164
17165,17165,17165,17165,17165,17165,17165,17165,MONDO:0008858,Behr syndrome,MONDO,disease,DISEASE_17165
17166,17166,17166,17166,17166,17166,17166,17166,MONDO:0019390,Susac syndrome,MONDO,disease,DISEASE_17166
17167,17167,17167,17167,17167,17167,17167,17167,MONDO:0034217_MONDO:0034216,obsolete resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta,MONDO_grouped,disease,DISEASE_17167
17168,17168,17168,17168,17168,17168,17168,17168,MONDO:0018302,acquired kinky hair syndrome,MONDO,disease,DISEASE_17168
17169,17169,17169,17169,17169,17169,17169,17169,MONDO:0006059,nasal cavity squamous cell carcinoma,MONDO,disease,DISEASE_17169
17170,17170,17170,17170,17170,17170,17170,17170,MONDO:0800480,non-verbal learning disability,MONDO,disease,DISEASE_17170
17171,17171,17171,17171,17171,17171,17171,17171,MONDO:0011225,severe combined immunodeficiency due to DCLRE1C deficiency,MONDO,disease,DISEASE_17171
17172,17172,17172,17172,17172,17172,17172,17172,MONDO:0020117,alpha granule disease,MONDO,disease,DISEASE_17172
17173,17173,17173,17173,17173,17173,17173,17173,MONDO:0018137,temperature-sensitive oculocutaneous albinism type 1,MONDO,disease,DISEASE_17173
17174,17174,17174,17174,17174,17174,17174,17174,MONDO:0011446,"myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders",MONDO,disease,DISEASE_17174
17175,17175,17175,17175,17175,17175,17175,17175,MONDO:0001410,postmenopausal atrophic vaginitis,MONDO,disease,DISEASE_17175
17176,17176,17176,17176,17176,17176,17176,17176,MONDO:0009335_MONDO:0100590,"hemolytic uremic syndrome, atypical, susceptibility to",MONDO_grouped,disease,DISEASE_17176
17177,17177,17177,17177,17177,17177,17177,17177,MONDO:0037821,porphyrin metabolism disease,MONDO,disease,DISEASE_17177
17178,17178,17178,17178,17178,17178,17178,17178,MONDO:0022851,Dennis-Fairhurst-Moore syndrome,MONDO,disease,DISEASE_17178
17179,17179,17179,17179,17179,17179,17179,17179,MONDO:0019441,ATTRV122I amyloidosis,MONDO,disease,DISEASE_17179
17180,17180,17180,17180,17180,17180,17180,17180,MONDO:1011686,"contact activation defect, non-human animal",MONDO,disease,DISEASE_17180
17181,17181,17181,17181,17181,17181,17181,17181,MONDO:0000845,fibrous dysplasia,MONDO,disease,DISEASE_17181
17182,17182,17182,17182,17182,17182,17182,17182,MONDO:0008355_MONDO:0010411_MONDO:0012457_MONDO:0012785_MONDO:0012922,"pyloric stenosis, infantile hypertrophic",MONDO_grouped,disease,DISEASE_17182
17183,17183,17183,17183,17183,17183,17183,17183,MONDO:0006197,endometrial small cell carcinoma,MONDO,disease,DISEASE_17183
17184,17184,17184,17184,17184,17184,17184,17184,MONDO:0009652_MONDO:0100122,GNPTG-mucolipidosis,MONDO_grouped,disease,DISEASE_17184
17185,17185,17185,17185,17185,17185,17185,17185,MONDO:0007064,"severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency",MONDO,disease,DISEASE_17185
17186,17186,17186,17186,17186,17186,17186,17186,MONDO:0003383,fallopian tube clear cell adenocarcinoma,MONDO,disease,DISEASE_17186
17187,17187,17187,17187,17187,17187,17187,17187,MONDO:0014747,familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome,MONDO,disease,DISEASE_17187
17188,17188,17188,17188,17188,17188,17188,17188,MONDO:0009859,PHAVER syndrome,MONDO,disease,DISEASE_17188
17189,17189,17189,17189,17189,17189,17189,17189,MONDO:0008753,alkaptonuria,MONDO,disease,DISEASE_17189
17190,17190,17190,17190,17190,17190,17190,17190,MONDO:0010448,moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome,MONDO,disease,DISEASE_17190
17191,17191,17191,17191,17191,17191,17191,17191,MONDO:0016030,Evans syndrome,MONDO,disease,DISEASE_17191
17192,17192,17192,17192,17192,17192,17192,17192,MONDO:0018448,clear cell papillary renal cell carcinoma,MONDO,disease,DISEASE_17192
17193,17193,17193,17193,17193,17193,17193,17193,MONDO:0007782,"hyperthermia, cutaneous, with headaches and nausea",MONDO,disease,DISEASE_17193
17194,17194,17194,17194,17194,17194,17194,17194,MONDO:0041959,fibrosis of bile duct,MONDO,disease,DISEASE_17194
17195,17195,17195,17195,17195,17195,17195,17195,MONDO:0014067,short ulna-dysmorphism-hypotonia-intellectual disability syndrome,MONDO,disease,DISEASE_17195
17196,17196,17196,17196,17196,17196,17196,17196,MONDO:0008966,Aagenaes syndrome,MONDO,disease,DISEASE_17196
17197,17197,17197,17197,17197,17197,17197,17197,MONDO:0007562_MONDO:0012558,"multiple epiphyseal dysplasia, Beighton type",MONDO_grouped,disease,DISEASE_17197
17198,17198,17198,17198,17198,17198,17198,17198,MONDO:1011922,"retained placenta, non-human animal",MONDO,disease,DISEASE_17198
17199,17199,17199,17199,17199,17199,17199,17199,MONDO:0014246,"episodic pain syndrome, familial, 2",MONDO,disease,DISEASE_17199
17200,17200,17200,17200,17200,17200,17200,17200,MONDO:0100084,alpha-actinopathy,MONDO,disease,DISEASE_17200
17201,17201,17201,17201,17201,17201,17201,17201,MONDO:0021398_MONDO:0021390,polyp of rectum,MONDO_grouped,disease,DISEASE_17201
17202,17202,17202,17202,17202,17202,17202,17202,MONDO:0019497,nonsyndromic genetic hearing loss,MONDO,disease,DISEASE_17202
17203,17203,17203,17203,17203,17203,17203,17203,MONDO:0006760,fetal erythroblastosis,MONDO,disease,DISEASE_17203
17204,17204,17204,17204,17204,17204,17204,17204,MONDO:1011935,"growth and respiratory lethal syndrome, non-human animal",MONDO,disease,DISEASE_17204
17205,17205,17205,17205,17205,17205,17205,17205,MONDO:0020840_MONDO:0035529,pulmonary alveolar proteinosis with hypogammaglobulinemia,MONDO_grouped,disease,DISEASE_17205
17206,17206,17206,17206,17206,17206,17206,17206,MONDO:0012864,chromosome 2q32-q33 deletion syndrome,MONDO,disease,DISEASE_17206
17207,17207,17207,17207,17207,17207,17207,17207,MONDO:0007345,aorta coarctation,MONDO,disease,DISEASE_17207
17208,17208,17208,17208,17208,17208,17208,17208,MONDO:0005079_MONDO:0006258,polyp,MONDO_grouped,disease,DISEASE_17208
17209,17209,17209,17209,17209,17209,17209,17209,MONDO:1011308,"congenital nervous system disorder, non-human animal",MONDO,disease,DISEASE_17209
17210,17210,17210,17210,17210,17210,17210,17210,MONDO:0014880,Duane retraction syndrome 3 with or without deafness,MONDO,disease,DISEASE_17210
17211,17211,17211,17211,17211,17211,17211,17211,MONDO:0009007,Jalili syndrome,MONDO,disease,DISEASE_17211
17212,17212,17212,17212,17212,17212,17212,17212,MONDO:0018507,microcephaly-complex motor and sensory axonal neuropathy syndrome,MONDO,disease,DISEASE_17212
17213,17213,17213,17213,17213,17213,17213,17213,MONDO:0022894,craniosynostosis autosomal dominant,MONDO,disease,DISEASE_17213
17214,17214,17214,17214,17214,17214,17214,17214,MONDO:0015283,maternally-inherited cardiomyopathy and hearing loss,MONDO,disease,DISEASE_17214
17215,17215,17215,17215,17215,17215,17215,17215,MONDO:0004790_MONDO:0021104,fatty liver disease,MONDO_grouped,disease,DISEASE_17215
17216,17216,17216,17216,17216,17216,17216,17216,MONDO:0002507,gingival overgrowth,MONDO,disease,DISEASE_17216
17217,17217,17217,17217,17217,17217,17217,17217,MONDO:0025167,"reticuloendotheliosis, avian",MONDO,disease,DISEASE_17217
17218,17218,17218,17218,17218,17218,17218,17218,MONDO:1010058,"exocrine pancreatic insufficiency, non-human animal",MONDO,disease,DISEASE_17218
17219,17219,17219,17219,17219,17219,17219,17219,MONDO:0014669_MONDO:0013786_MONDO:0011395_MONDO:0014427_MONDO:0013002_MONDO:0014372_MONDO:0030440_MONDO:0011987_MONDO:0012464_MONDO:0957240_MONDO:0012983_MONDO:0011143_MONDO:0010905_MONDO:0011355_MONDO:0014068_MONDO:0010969_MONDO:0014153_MONDO:0011564_MONDO:0012483_MONDO:0007362_MONDO:0013348_MONDO:0015993_MONDO:0800326,cone-rod dystrophy,MONDO_grouped,disease,DISEASE_17219
17220,17220,17220,17220,17220,17220,17220,17220,MONDO:0019945_MONDO:0006599_MONDO:0850230,solar urticaria,MONDO_grouped,disease,DISEASE_17220
17221,17221,17221,17221,17221,17221,17221,17221,MONDO:0005997_MONDO:0002870,tricuspid valve stenosis,MONDO_grouped,disease,DISEASE_17221
17222,17222,17222,17222,17222,17222,17222,17222,MONDO:0000743,oral hairy leukoplakia,MONDO,disease,DISEASE_17222
17223,17223,17223,17223,17223,17223,17223,17223,MONDO:0010899_MONDO:0011297_MONDO:0012474_MONDO:0014002_MONDO:0011545_MONDO:0020300,autosomal dominant nocturnal frontal lobe epilepsy,MONDO_grouped,disease,DISEASE_17223
17224,17224,17224,17224,17224,17224,17224,17224,MONDO:0015340,drug rash with eosinophilia and systemic symptoms,MONDO,disease,DISEASE_17224
17225,17225,17225,17225,17225,17225,17225,17225,MONDO:0010881,mesomelia-synostoses syndrome,MONDO,disease,DISEASE_17225
17226,17226,17226,17226,17226,17226,17226,17226,MONDO:0022787,cleft palate heart disease polydactyly absent tibia,MONDO,disease,DISEASE_17226
17227,17227,17227,17227,17227,17227,17227,17227,MONDO:0006195,endometrial polyp,MONDO,disease,DISEASE_17227
17228,17228,17228,17228,17228,17228,17228,17228,MONDO:0000248,dengue shock syndrome,MONDO,disease,DISEASE_17228
17229,17229,17229,17229,17229,17229,17229,17229,MONDO:0030941_MONDO:0033015_MONDO:0033014_MONDO:0033013_MONDO:0033012_MONDO:0033010_MONDO:0032801,erythrokeratodermia variabilis et progressiva,MONDO_grouped,disease,DISEASE_17229
17230,17230,17230,17230,17230,17230,17230,17230,MONDO:0011790,Amish lethal microcephaly,MONDO,disease,DISEASE_17230
17231,17231,17231,17231,17231,17231,17231,17231,MONDO:0800487,variable-age onset idiopathic generalized epilepsy syndrome,MONDO,disease,DISEASE_17231
17232,17232,17232,17232,17232,17232,17232,17232,MONDO:0014576,lipoyl transferase 1 deficiency,MONDO,disease,DISEASE_17232
17233,17233,17233,17233,17233,17233,17233,17233,MONDO:0023561,Koone-Rizzo-Elias syndrome,MONDO,disease,DISEASE_17233
17234,17234,17234,17234,17234,17234,17234,17234,MONDO:0016430,Balo concentric sclerosis,MONDO,disease,DISEASE_17234
17235,17235,17235,17235,17235,17235,17235,17235,MONDO:1012517,"exercise induced metabolic myopathy, dog",MONDO,disease,DISEASE_17235
17236,17236,17236,17236,17236,17236,17236,17236,MONDO:0010680,X-linked Emery-Dreifuss muscular dystrophy,MONDO,disease,DISEASE_17236
17237,17237,17237,17237,17237,17237,17237,17237,MONDO:0002599,teratocarcinoma,MONDO,disease,DISEASE_17237
17238,17238,17238,17238,17238,17238,17238,17238,MONDO:0044335,benign soft tissue neoplasm,MONDO,disease,DISEASE_17238
17239,17239,17239,17239,17239,17239,17239,17239,MONDO:0005504_MONDO:0001479,diphtheria,MONDO_grouped,disease,DISEASE_17239
17240,17240,17240,17240,17240,17240,17240,17240,MONDO:0017815,acquired porencephaly,MONDO,disease,DISEASE_17240
17241,17241,17241,17241,17241,17241,17241,17241,MONDO:0021736,proctosigmoiditis,MONDO,disease,DISEASE_17241
17242,17242,17242,17242,17242,17242,17242,17242,MONDO:0002724,mast cell neoplasm,MONDO,disease,DISEASE_17242
17243,17243,17243,17243,17243,17243,17243,17243,MONDO:0015835,Bicervical bicornuate uterus and blind hemivagina,MONDO,disease,DISEASE_17243
17244,17244,17244,17244,17244,17244,17244,17244,MONDO:0010814,chondrodysplasia-pseudohermaphroditism syndrome,MONDO,disease,DISEASE_17244
17245,17245,17245,17245,17245,17245,17245,17245,MONDO:0018801,congenital bilateral absence of vas deferens,MONDO,disease,DISEASE_17245
17246,17246,17246,17246,17246,17246,17246,17246,MONDO:0100118_MONDO:0100191,hereditary skin disorder,MONDO_grouped,disease,DISEASE_17246
17247,17247,17247,17247,17247,17247,17247,17247,MONDO:0012711,"peripapillary atrophy, beta type",MONDO,disease,DISEASE_17247
17248,17248,17248,17248,17248,17248,17248,17248,MONDO:1012570,"cancer, dog",MONDO,disease,DISEASE_17248
17249,17249,17249,17249,17249,17249,17249,17249,MONDO:0008312,autosomal dominant prognathism,MONDO,disease,DISEASE_17249
17250,17250,17250,17250,17250,17250,17250,17250,MONDO:0018175,combined deficiency of factor V and factor VIII,MONDO,disease,DISEASE_17250
17251,17251,17251,17251,17251,17251,17251,17251,MONDO:0006082,anal squamous cell carcinoma,MONDO,disease,DISEASE_17251
17252,17252,17252,17252,17252,17252,17252,17252,MONDO:0014333,"polymicrogyria, bilateral perisylvian, autosomal recessive",MONDO,disease,DISEASE_17252
17253,17253,17253,17253,17253,17253,17253,17253,MONDO:0006708,Desulfovibrionaceae infectious disease,MONDO,disease,DISEASE_17253
17254,17254,17254,17254,17254,17254,17254,17254,MONDO:0030329_MONDO:0025708_MONDO:0030294_MONDO:0100354_MONDO:0030296_MONDO:0025986,megacystis-microcolon-intestinal hypoperistalsis syndrome,MONDO_grouped,disease,DISEASE_17254
17255,17255,17255,17255,17255,17255,17255,17255,MONDO:0004702,uterine cervix leukoplakia,MONDO,disease,DISEASE_17255
17256,17256,17256,17256,17256,17256,17256,17256,MONDO:0030953_MONDO:0100297_MONDO:0031439,"short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies",MONDO_grouped,disease,DISEASE_17256
17257,17257,17257,17257,17257,17257,17257,17257,MONDO:0020082,dendritic cell tumor,MONDO,disease,DISEASE_17257
17258,17258,17258,17258,17258,17258,17258,17258,MONDO:0004836,intravascular fasciitis,MONDO,disease,DISEASE_17258
17259,17259,17259,17259,17259,17259,17259,17259,MONDO:0013021,sterile multifocal osteomyelitis with periostitis and pustulosis,MONDO,disease,DISEASE_17259
17260,17260,17260,17260,17260,17260,17260,17260,MONDO:0016661,infantile onset panniculitis with uveitis and systemic granulomatosis,MONDO,disease,DISEASE_17260
17261,17261,17261,17261,17261,17261,17261,17261,MONDO:0014800,progressive scapulohumeroperoneal distal myopathy,MONDO,disease,DISEASE_17261
17262,17262,17262,17262,17262,17262,17262,17262,MONDO:0022639,Cantu Sanchez-Corona Garcia-Cruz syndrome,MONDO,disease,DISEASE_17262
17263,17263,17263,17263,17263,17263,17263,17263,MONDO:0019821,aneurysm or dilatation of ascending aorta,MONDO,disease,DISEASE_17263
17264,17264,17264,17264,17264,17264,17264,17264,MONDO:0015854,supernumerary breasts,MONDO,disease,DISEASE_17264
17265,17265,17265,17265,17265,17265,17265,17265,MONDO:0012809,"histiocytoma, Angiomatoid fibrous",MONDO,disease,DISEASE_17265
17266,17266,17266,17266,17266,17266,17266,17266,MONDO:1012985,"autoimmune disease, non-human animal",MONDO,disease,DISEASE_17266
17267,17267,17267,17267,17267,17267,17267,17267,MONDO:1012917,"Alzheimer disease, PSEN1-related, pig",MONDO,disease,DISEASE_17267
17268,17268,17268,17268,17268,17268,17268,17268,MONDO:0015095,Peters anomaly-cataract syndrome,MONDO,disease,DISEASE_17268
17269,17269,17269,17269,17269,17269,17269,17269,MONDO:1011233,"microphthalmia, golden hamster",MONDO,disease,DISEASE_17269
17270,17270,17270,17270,17270,17270,17270,17270,MONDO:0009372,encephalopathy due to hydroxykynureninuria,MONDO,disease,DISEASE_17270
17271,17271,17271,17271,17271,17271,17271,17271,MONDO:0017049,obsolete hypomyelination neuropathy-arthrogryposis syndrome,MONDO,disease,DISEASE_17271
17272,17272,17272,17272,17272,17272,17272,17272,MONDO:0018436,megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13),MONDO,disease,DISEASE_17272
17273,17273,17273,17273,17273,17273,17273,17273,MONDO:0032819_MONDO:0026732_MONDO:0026731_MONDO:0013757_MONDO:0009154_MONDO:0024264_MONDO:0000045_MONDO:0012360,"hypothyroidism, congenital, nongoitrous",MONDO_grouped,disease,DISEASE_17273
17274,17274,17274,17274,17274,17274,17274,17274,MONDO:0005310,atrial flutter,MONDO,disease,DISEASE_17274
17275,17275,17275,17275,17275,17275,17275,17275,MONDO:0800396,GPR179-related retinopathy,MONDO,disease,DISEASE_17275
17276,17276,17276,17276,17276,17276,17276,17276,MONDO:0009996,"rhizomelic syndrome, Urbach type",MONDO,disease,DISEASE_17276
17277,17277,17277,17277,17277,17277,17277,17277,MONDO:0015348,leukoencephalopathy with bilateral anterior temporal lobe cysts,MONDO,disease,DISEASE_17277
17278,17278,17278,17278,17278,17278,17278,17278,MONDO:0021326,malignant neoplasm of cervical esophagus,MONDO,disease,DISEASE_17278
17279,17279,17279,17279,17279,17279,17279,17279,MONDO:0009240,formiminoglutamic aciduria,MONDO,disease,DISEASE_17279
17280,17280,17280,17280,17280,17280,17280,17280,MONDO:0015290_MONDO:0001440,neurotrophic keratopathy,MONDO_grouped,disease,DISEASE_17280
17281,17281,17281,17281,17281,17281,17281,17281,MONDO:0021746,pyelocystitis,MONDO,disease,DISEASE_17281
17282,17282,17282,17282,17282,17282,17282,17282,MONDO:0009200,eyebrow duplication-syndactyly syndrome,MONDO,disease,DISEASE_17282
17283,17283,17283,17283,17283,17283,17283,17283,MONDO:0001642,hordeolum externum,MONDO,disease,DISEASE_17283
17284,17284,17284,17284,17284,17284,17284,17284,MONDO:0019087,cholangiocarcinoma,MONDO,disease,DISEASE_17284
17285,17285,17285,17285,17285,17285,17285,17285,MONDO:0004952,Hodgkins lymphoma,MONDO,disease,DISEASE_17285
17286,17286,17286,17286,17286,17286,17286,17286,MONDO:0018853,transgrediens et progrediens palmoplantar keratoderma,MONDO,disease,DISEASE_17286
17287,17287,17287,17287,17287,17287,17287,17287,MONDO:0006817,juxtacortical osteosarcoma,MONDO,disease,DISEASE_17287
17288,17288,17288,17288,17288,17288,17288,17288,MONDO:0700219,neoplastic meningitis,MONDO,disease,DISEASE_17288
17289,17289,17289,17289,17289,17289,17289,17289,MONDO:0013396,chromosome 1p32-p31 deletion syndrome,MONDO,disease,DISEASE_17289
17290,17290,17290,17290,17290,17290,17290,17290,MONDO:0001268,gingival recession,MONDO,disease,DISEASE_17290
17291,17291,17291,17291,17291,17291,17291,17291,MONDO:0007410,isolated cryptophthalmia,MONDO,disease,DISEASE_17291
17292,17292,17292,17292,17292,17292,17292,17292,MONDO:1012890_MONDO:1012925,"Rett syndrome, MECP2-related, crab-eating macaque",MONDO_grouped,disease,DISEASE_17292
17293,17293,17293,17293,17293,17293,17293,17293,MONDO:0010816,Qazi Markouizos syndrome,MONDO,disease,DISEASE_17293
17294,17294,17294,17294,17294,17294,17294,17294,MONDO:0001544,tibial nerve palsy,MONDO,disease,DISEASE_17294
17295,17295,17295,17295,17295,17295,17295,17295,MONDO:0007818,"hyper-IgE recurrent infection syndrome 1, autosomal dominant",MONDO,disease,DISEASE_17295
17296,17296,17296,17296,17296,17296,17296,17296,MONDO:0014515,macular dystrophy with central cone involvement,MONDO,disease,DISEASE_17296
17297,17297,17297,17297,17297,17297,17297,17297,MONDO:0858910,dropped head syndrome,MONDO,disease,DISEASE_17297
17298,17298,17298,17298,17298,17298,17298,17298,MONDO:0006734,benign duodenal neoplasm,MONDO,disease,DISEASE_17298
17299,17299,17299,17299,17299,17299,17299,17299,MONDO:1011596,"severe combined immunodeficiency disease, dog",MONDO,disease,DISEASE_17299
17300,17300,17300,17300,17300,17300,17300,17300,MONDO:0003241,central nervous system hemangioma,MONDO,disease,DISEASE_17300
17301,17301,17301,17301,17301,17301,17301,17301,MONDO:0011459_MONDO:0007152_MONDO:0011831_MONDO:0011460_MONDO:0012506_MONDO:0012180_MONDO:0011189_MONDO:0011188_MONDO:0012684_MONDO:0012434_MONDO:0000908_MONDO:0016587,arrhythmogenic right ventricular dysplasia,MONDO_grouped,disease,DISEASE_17301
17302,17302,17302,17302,17302,17302,17302,17302,MONDO:0009532,Miller-Dieker lissencephaly syndrome,MONDO,disease,DISEASE_17302
17303,17303,17303,17303,17303,17303,17303,17303,MONDO:0010553,"Charcot-Marie-Tooth peroneal muscular atrophy and Friedreich ataxia, combined",MONDO,disease,DISEASE_17303
17304,17304,17304,17304,17304,17304,17304,17304,MONDO:0030893,"leukoencephalopathy, progressive, infantile-onset, with or without deafness",MONDO,disease,DISEASE_17304
17305,17305,17305,17305,17305,17305,17305,17305,MONDO:0006681,Borrelia infectious disease,MONDO,disease,DISEASE_17305
17306,17306,17306,17306,17306,17306,17306,17306,MONDO:0018697,1p35.2 microdeletion syndrome,MONDO,disease,DISEASE_17306
17307,17307,17307,17307,17307,17307,17307,17307,MONDO:0004616,herpetic whitlow,MONDO,disease,DISEASE_17307
17308,17308,17308,17308,17308,17308,17308,17308,MONDO:1011071,"urolithiasis, American mink",MONDO,disease,DISEASE_17308
17309,17309,17309,17309,17309,17309,17309,17309,MONDO:0016515,Kallmann syndrome-heart disease syndrome,MONDO,disease,DISEASE_17309
17310,17310,17310,17310,17310,17310,17310,17310,MONDO:0060752,neurodevelopmental disorder with spasticity and poor growth,MONDO,disease,DISEASE_17310
17311,17311,17311,17311,17311,17311,17311,17311,MONDO:0007577,"esophageal ring, lower",MONDO,disease,DISEASE_17311
17312,17312,17312,17312,17312,17312,17312,17312,MONDO:0006727,diastolic heart failure,MONDO,disease,DISEASE_17312
17313,17313,17313,17313,17313,17313,17313,17313,MONDO:0015302,nodular cutaneous amyloidosis,MONDO,disease,DISEASE_17313
17314,17314,17314,17314,17314,17314,17314,17314,MONDO:0006947,renovascular hypertension,MONDO,disease,DISEASE_17314
17315,17315,17315,17315,17315,17315,17315,17315,MONDO:1011720,"subclinical hypocalcemia, non-human animal",MONDO,disease,DISEASE_17315
17316,17316,17316,17316,17316,17316,17316,17316,MONDO:1012540,"white skin color and iridophoroma, leopard gecko",MONDO,disease,DISEASE_17316
17317,17317,17317,17317,17317,17317,17317,17317,MONDO:0009732,"congenital nephrotic syndrome, Finnish type",MONDO,disease,DISEASE_17317
17318,17318,17318,17318,17318,17318,17318,17318,MONDO:0008244,piebaldism,MONDO,disease,DISEASE_17318
17319,17319,17319,17319,17319,17319,17319,17319,MONDO:0000723,stutter disorder,MONDO,disease,DISEASE_17319
17320,17320,17320,17320,17320,17320,17320,17320,MONDO:0043297,vibrio vulnificus infectious disease,MONDO,disease,DISEASE_17320
17321,17321,17321,17321,17321,17321,17321,17321,MONDO:0600005,venom allergy,MONDO,disease,DISEASE_17321
17322,17322,17322,17322,17322,17322,17322,17322,MONDO:0044784_MONDO:0006863,myxoma,MONDO_grouped,disease,DISEASE_17322
17323,17323,17323,17323,17323,17323,17323,17323,MONDO:0016100,rippling muscle disease with myasthenia gravis,MONDO,disease,DISEASE_17323
17324,17324,17324,17324,17324,17324,17324,17324,MONDO:0004762,Taylor syndrome,MONDO,disease,DISEASE_17324
17325,17325,17325,17325,17325,17325,17325,17325,MONDO:0000929,balloon cell malignant melanoma,MONDO,disease,DISEASE_17325
17326,17326,17326,17326,17326,17326,17326,17326,MONDO:0044718,alkaline ceramidase 3 deficiency,MONDO,disease,DISEASE_17326
17327,17327,17327,17327,17327,17327,17327,17327,MONDO:0009119,"diverticulosis, small-intestinal",MONDO,disease,DISEASE_17327
17328,17328,17328,17328,17328,17328,17328,17328,MONDO:0007205,diaphyseal medullary stenosis-bone malignancy syndrome,MONDO,disease,DISEASE_17328
17329,17329,17329,17329,17329,17329,17329,17329,MONDO:0007843_MONDO:0010465_MONDO:0016512,Kabuki syndrome,MONDO_grouped,disease,DISEASE_17329
17330,17330,17330,17330,17330,17330,17330,17330,MONDO:0016446,acquired cutis laxa,MONDO,disease,DISEASE_17330
17331,17331,17331,17331,17331,17331,17331,17331,MONDO:0019795,acalvaria,MONDO,disease,DISEASE_17331
17332,17332,17332,17332,17332,17332,17332,17332,MONDO:0019476,primary cutaneous peripheral T-cell lymphoma not otherwise specified,MONDO,disease,DISEASE_17332
17333,17333,17333,17333,17333,17333,17333,17333,MONDO:0041752,paucibacillary leprosy,MONDO,disease,DISEASE_17333
17334,17334,17334,17334,17334,17334,17334,17334,MONDO:0014059_MONDO:0014635_MONDO:0012408_MONDO:0012709_MONDO:0013376_MONDO:0013783_MONDO:0009630_MONDO:0000170_MONDO:0800324_MONDO:1011280,"microphthalmia, isolated, with coloboma",MONDO_grouped,disease,DISEASE_17334
17335,17335,17335,17335,17335,17335,17335,17335,MONDO:0004078,mucinous intrahepatic cholangiocarcinoma,MONDO,disease,DISEASE_17335
17336,17336,17336,17336,17336,17336,17336,17336,MONDO:0002103,factitious disorder,MONDO,disease,DISEASE_17336
17337,17337,17337,17337,17337,17337,17337,17337,MONDO:0000665,apraxia,MONDO,disease,DISEASE_17337
17338,17338,17338,17338,17338,17338,17338,17338,MONDO:0006154,colon mucosa-associated lymphoid tissue lymphoma,MONDO,disease,DISEASE_17338
17339,17339,17339,17339,17339,17339,17339,17339,MONDO:0004607,vallecula cancer,MONDO,disease,DISEASE_17339
17340,17340,17340,17340,17340,17340,17340,17340,MONDO:0008442,spastic paraplegia-neuropathy-poikiloderma syndrome,MONDO,disease,DISEASE_17340
17341,17341,17341,17341,17341,17341,17341,17341,MONDO:0015834,didelphys uterus,MONDO,disease,DISEASE_17341
17342,17342,17342,17342,17342,17342,17342,17342,MONDO:0011975,paternal uniparental disomy of chromosome 14,MONDO,disease,DISEASE_17342
17343,17343,17343,17343,17343,17343,17343,17343,MONDO:0008828,camptodactyly-arthropathy-coxa vara-pericarditis syndrome,MONDO,disease,DISEASE_17343
17344,17344,17344,17344,17344,17344,17344,17344,MONDO:0000082,pelvic organ prolapse,MONDO,disease,DISEASE_17344
17345,17345,17345,17345,17345,17345,17345,17345,MONDO:0001449,lymphocytic choriomeningitis,MONDO,disease,DISEASE_17345
17346,17346,17346,17346,17346,17346,17346,17346,MONDO:0015622,wound myiasis,MONDO,disease,DISEASE_17346
17347,17347,17347,17347,17347,17347,17347,17347,MONDO:0001858,Tietze syndrome,MONDO,disease,DISEASE_17347
17348,17348,17348,17348,17348,17348,17348,17348,MONDO:0011356,"exostosis, Dupuytren subungual",MONDO,disease,DISEASE_17348
17349,17349,17349,17349,17349,17349,17349,17349,MONDO:0008307,"presenile dementia, Kraepelin type",MONDO,disease,DISEASE_17349
17350,17350,17350,17350,17350,17350,17350,17350,MONDO:0006222,gastric choriocarcinoma,MONDO,disease,DISEASE_17350
17351,17351,17351,17351,17351,17351,17351,17351,MONDO:0009387,familial lipoprotein lipase deficiency,MONDO,disease,DISEASE_17351
17352,17352,17352,17352,17352,17352,17352,17352,MONDO:0008162,"otitis media, susceptibility to",MONDO,disease,DISEASE_17352
17353,17353,17353,17353,17353,17353,17353,17353,MONDO:0022941,deafness hypospadias metacarpal and metatarsal syndrome,MONDO,disease,DISEASE_17353
17354,17354,17354,17354,17354,17354,17354,17354,MONDO:0007824,"incisors, lower central, absence of",MONDO,disease,DISEASE_17354
17355,17355,17355,17355,17355,17355,17355,17355,MONDO:0012039_MONDO:0012058,"myocardial infarction, susceptibility to",MONDO_grouped,disease,DISEASE_17355
17356,17356,17356,17356,17356,17356,17356,17356,MONDO:0005522_MONDO:0003361_MONDO:0001852,small intestine carcinoma,MONDO_grouped,disease,DISEASE_17356
17357,17357,17357,17357,17357,17357,17357,17357,MONDO:0001005,kaolin pneumoconiosis,MONDO,disease,DISEASE_17357
17358,17358,17358,17358,17358,17358,17358,17358,MONDO:0001192,esophageal melanoma,MONDO,disease,DISEASE_17358
17359,17359,17359,17359,17359,17359,17359,17359,MONDO:0003143,angiokeratoma,MONDO,disease,DISEASE_17359
17360,17360,17360,17360,17360,17360,17360,17360,MONDO:0016643,frontonasal dysplasia,MONDO,disease,DISEASE_17360
17361,17361,17361,17361,17361,17361,17361,17361,MONDO:1011687,"cyclic neutropenia, non-human animal",MONDO,disease,DISEASE_17361
17362,17362,17362,17362,17362,17362,17362,17362,MONDO:0012446,seborrhea-like dermatitis with psoriasiform elements,MONDO,disease,DISEASE_17362
17363,17363,17363,17363,17363,17363,17363,17363,MONDO:0021300,adenoid cystic carcinoma of oropharynx,MONDO,disease,DISEASE_17363
17364,17364,17364,17364,17364,17364,17364,17364,MONDO:0018675,IgG4-related ophthalmic disorder,MONDO,disease,DISEASE_17364
17365,17365,17365,17365,17365,17365,17365,17365,MONDO:0010401,X-linked myopathy with postural muscle atrophy,MONDO,disease,DISEASE_17365
17366,17366,17366,17366,17366,17366,17366,17366,MONDO:1012686,"GM2 gangliosidosis, HEXA-related, American flamingo",MONDO,disease,DISEASE_17366
17367,17367,17367,17367,17367,17367,17367,17367,MONDO:0100051,idiopathic mast cell activation syndrome,MONDO,disease,DISEASE_17367
17368,17368,17368,17368,17368,17368,17368,17368,MONDO:1010035,"mandibulofacial dysostosis, non-human animal",MONDO,disease,DISEASE_17368
17369,17369,17369,17369,17369,17369,17369,17369,MONDO:0007122,anisocoria,MONDO,disease,DISEASE_17369
17370,17370,17370,17370,17370,17370,17370,17370,MONDO:0042604,Sandhaus-Ben-Ami syndrome,MONDO,disease,DISEASE_17370
17371,17371,17371,17371,17371,17371,17371,17371,MONDO:0044926,oropharyngeal carcinoma,MONDO,disease,DISEASE_17371
17372,17372,17372,17372,17372,17372,17372,17372,MONDO:1011225,"entropion, dog",MONDO,disease,DISEASE_17372
17373,17373,17373,17373,17373,17373,17373,17373,MONDO:0016467,isotretinoin syndrome,MONDO,disease,DISEASE_17373
17374,17374,17374,17374,17374,17374,17374,17374,MONDO:0002192,vulvar angiokeratoma,MONDO,disease,DISEASE_17374
17375,17375,17375,17375,17375,17375,17375,17375,MONDO:0006620,vulva fibroepithelial polyp,MONDO,disease,DISEASE_17375
17376,17376,17376,17376,17376,17376,17376,17376,MONDO:1010457,"hypertrophic cardiomyopathy, Rhesus monkey",MONDO,disease,DISEASE_17376
17377,17377,17377,17377,17377,17377,17377,17377,MONDO:0021483,benign neoplasm of frontal sinus,MONDO,disease,DISEASE_17377
17378,17378,17378,17378,17378,17378,17378,17378,MONDO:1011588,"porphyria, pig",MONDO,disease,DISEASE_17378
17379,17379,17379,17379,17379,17379,17379,17379,MONDO:0009664,mulibrey nanism,MONDO,disease,DISEASE_17379
17380,17380,17380,17380,17380,17380,17380,17380,MONDO:0010105,"teratoma, pineal",MONDO,disease,DISEASE_17380
17381,17381,17381,17381,17381,17381,17381,17381,MONDO:0024878,secondary carcinoma,MONDO,disease,DISEASE_17381
17382,17382,17382,17382,17382,17382,17382,17382,MONDO:0005298_MONDO:0017198,osteoporosis,MONDO_grouped,disease,DISEASE_17382
17383,17383,17383,17383,17383,17383,17383,17383,MONDO:0054601_MONDO:0054665,"pituitary adenoma 5, multiple types",MONDO_grouped,disease,DISEASE_17383
17384,17384,17384,17384,17384,17384,17384,17384,MONDO:0004956,metastatic prostate carcinoma,MONDO,disease,DISEASE_17384
17385,17385,17385,17385,17385,17385,17385,17385,MONDO:1010794,"Ehlers-Danlos syndrome, classic type, COL5A1-related, domestic cat",MONDO,disease,DISEASE_17385
17386,17386,17386,17386,17386,17386,17386,17386,MONDO:0003842,childhood cerebellar astrocytic neoplasm,MONDO,disease,DISEASE_17386
17387,17387,17387,17387,17387,17387,17387,17387,MONDO:0012020,chromosome 22q11.2 microduplication syndrome,MONDO,disease,DISEASE_17387
17388,17388,17388,17388,17388,17388,17388,17388,MONDO:0003872_MONDO:0003874,ovarian papillary cystadenoma,MONDO_grouped,disease,DISEASE_17388
17389,17389,17389,17389,17389,17389,17389,17389,MONDO:0008662,autosomal dominant vitreoretinochoroidopathy,MONDO,disease,DISEASE_17389
17390,17390,17390,17390,17390,17390,17390,17390,MONDO:0009619,microcephaly-micromelia syndrome,MONDO,disease,DISEASE_17390
17391,17391,17391,17391,17391,17391,17391,17391,MONDO:0017849,Siegler-Brewer-Carey syndrome,MONDO,disease,DISEASE_17391
17392,17392,17392,17392,17392,17392,17392,17392,MONDO:0007133,anonychia-onychodystrophy with brachydactyly type b and ectrodactyly,MONDO,disease,DISEASE_17392
17393,17393,17393,17393,17393,17393,17393,17393,MONDO:0008607,triphalangeal thumbs-brachyectrodactyly syndrome,MONDO,disease,DISEASE_17393
17394,17394,17394,17394,17394,17394,17394,17394,MONDO:0033558,"autoinflammation, immune dysregulation, and eosinophilia",MONDO,disease,DISEASE_17394
17395,17395,17395,17395,17395,17395,17395,17395,MONDO:0008296,familial porphyria cutanea tarda,MONDO,disease,DISEASE_17395
17396,17396,17396,17396,17396,17396,17396,17396,MONDO:0008527,tarsal coalition,MONDO,disease,DISEASE_17396
17397,17397,17397,17397,17397,17397,17397,17397,MONDO:0002236,ocular cancer,MONDO,disease,DISEASE_17397
17398,17398,17398,17398,17398,17398,17398,17398,MONDO:1011642,"spontaneous cardiomyopathy, non-human animal",MONDO,disease,DISEASE_17398
17399,17399,17399,17399,17399,17399,17399,17399,MONDO:0003322,epithelial predominant Wilms' tumor,MONDO,disease,DISEASE_17399
17400,17400,17400,17400,17400,17400,17400,17400,MONDO:0001577,respiratory syncytial virus infectious disease,MONDO,disease,DISEASE_17400
17401,17401,17401,17401,17401,17401,17401,17401,MONDO:0032601,"inflammatory bowel disease, immunodeficiency, and encephalopathy",MONDO,disease,DISEASE_17401
17402,17402,17402,17402,17402,17402,17402,17402,MONDO:0005306_MONDO:0020655_MONDO:1011150,ankylosing spondylitis,MONDO_grouped,disease,DISEASE_17402
17403,17403,17403,17403,17403,17403,17403,17403,MONDO:0033547,Li-Ghorbani-Weisz-Hubshman syndrome,MONDO,disease,DISEASE_17403
17404,17404,17404,17404,17404,17404,17404,17404,MONDO:0000510,synucleinopathy,MONDO,disease,DISEASE_17404
17405,17405,17405,17405,17405,17405,17405,17405,MONDO:0010049,spastic paraplegia-glaucoma-intellectual disability syndrome,MONDO,disease,DISEASE_17405
17406,17406,17406,17406,17406,17406,17406,17406,MONDO:0014039_MONDO:0008758_MONDO:0011283_MONDO:0012792_MONDO:0032815_MONDO:0014198_MONDO:0033545_MONDO:0032932_MONDO:0009504_MONDO:0013350_MONDO:0018158,mitochondrial DNA depletion syndrome,MONDO_grouped,disease,DISEASE_17406
17407,17407,17407,17407,17407,17407,17407,17407,MONDO:1012376,"acrochordonous plaque, dog",MONDO,disease,DISEASE_17407
17408,17408,17408,17408,17408,17408,17408,17408,MONDO:0014707,14q32 duplication syndrome,MONDO,disease,DISEASE_17408
17409,17409,17409,17409,17409,17409,17409,17409,MONDO:0005100,systemic sclerosis,MONDO,disease,DISEASE_17409
17410,17410,17410,17410,17410,17410,17410,17410,MONDO:0020748_MONDO:0020747_MONDO:0008863,sitosterolemia,MONDO_grouped,disease,DISEASE_17410
17411,17411,17411,17411,17411,17411,17411,17411,MONDO:0003109_MONDO:0003868_MONDO:0003921,foramen magnum meningioma,MONDO_grouped,disease,DISEASE_17411
17412,17412,17412,17412,17412,17412,17412,17412,MONDO:0017926,multiple paragangliomas associated with polycythemia,MONDO,disease,DISEASE_17412
17413,17413,17413,17413,17413,17413,17413,17413,MONDO:1011215,"coloboma, domestic cat",MONDO,disease,DISEASE_17413
17414,17414,17414,17414,17414,17414,17414,17414,MONDO:0013648,familial progressive hyperpigmentation,MONDO,disease,DISEASE_17414
17415,17415,17415,17415,17415,17415,17415,17415,MONDO:0019691,short rib dysplasia,MONDO,disease,DISEASE_17415
17416,17416,17416,17416,17416,17416,17416,17416,MONDO:0012739,microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome,MONDO,disease,DISEASE_17416
17417,17417,17417,17417,17417,17417,17417,17417,MONDO:0100553,OPTN-related open angle glaucoma,MONDO,disease,DISEASE_17417
17418,17418,17418,17418,17418,17418,17418,17418,MONDO:0001141,middle ear cholesterol granuloma,MONDO,disease,DISEASE_17418
17419,17419,17419,17419,17419,17419,17419,17419,MONDO:0003332_MONDO:0003333,malignant struma ovarii,MONDO_grouped,disease,DISEASE_17419
17420,17420,17420,17420,17420,17420,17420,17420,MONDO:0018896_MONDO:0019740_MONDO:0043768,thrombotic thrombocytopenic purpura,MONDO_grouped,disease,DISEASE_17420
17421,17421,17421,17421,17421,17421,17421,17421,MONDO:0011818_MONDO:0019009_MONDO:0017095_MONDO:0017101_MONDO:0017096_MONDO:0017097_MONDO:0017098_MONDO:0017102,isolated focal cortical dysplasia,MONDO_grouped,disease,DISEASE_17421
17422,17422,17422,17422,17422,17422,17422,17422,MONDO:0001368,phthisical cornea,MONDO,disease,DISEASE_17422
17423,17423,17423,17423,17423,17423,17423,17423,MONDO:0015458,intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome,MONDO,disease,DISEASE_17423
17424,17424,17424,17424,17424,17424,17424,17424,MONDO:0025100,"mastitis, bovine",MONDO,disease,DISEASE_17424
17425,17425,17425,17425,17425,17425,17425,17425,MONDO:0000701,ischemic colitis,MONDO,disease,DISEASE_17425
17426,17426,17426,17426,17426,17426,17426,17426,MONDO:0957337,isolated chorioretinal dystrophy,MONDO,disease,DISEASE_17426
17427,17427,17427,17427,17427,17427,17427,17427,MONDO:0006921,Actinomycetales infectious disease,MONDO,disease,DISEASE_17427
17428,17428,17428,17428,17428,17428,17428,17428,MONDO:0011012,African iron overload,MONDO,disease,DISEASE_17428
17429,17429,17429,17429,17429,17429,17429,17429,MONDO:0007164_MONDO:0012664_MONDO:0007165_MONDO:0013776_MONDO:0013354_MONDO:0012651_MONDO:0017845,spastic ataxia,MONDO_grouped,disease,DISEASE_17429
17430,17430,17430,17430,17430,17430,17430,17430,MONDO:0700124,chromosome 21 disorder,MONDO,disease,DISEASE_17430
17431,17431,17431,17431,17431,17431,17431,17431,MONDO:0037736,infratentorial neoplasm,MONDO,disease,DISEASE_17431
17432,17432,17432,17432,17432,17432,17432,17432,MONDO:0044915,salivary duct carcinoma,MONDO,disease,DISEASE_17432
17433,17433,17433,17433,17433,17433,17433,17433,MONDO:0020365,congenital hereditary endothelial dystrophy type I,MONDO,disease,DISEASE_17433
17434,17434,17434,17434,17434,17434,17434,17434,MONDO:0000252,inflammatory diarrhea,MONDO,disease,DISEASE_17434
17435,17435,17435,17435,17435,17435,17435,17435,MONDO:0014317,pancytopenia-developmental delay syndrome,MONDO,disease,DISEASE_17435
17436,17436,17436,17436,17436,17436,17436,17436,MONDO:0019983,multiloculated renal cyst,MONDO,disease,DISEASE_17436
17437,17437,17437,17437,17437,17437,17437,17437,MONDO:0030890,"pontocerebellar hypoplasia, IIA 17",MONDO,disease,DISEASE_17437
17438,17438,17438,17438,17438,17438,17438,17438,MONDO:0100365_MONDO:1012581,mucopolysaccharidosis or mucopolysaccharidosis-like disorder,MONDO_grouped,disease,DISEASE_17438
17439,17439,17439,17439,17439,17439,17439,17439,MONDO:0003707,distal biliary tract carcinoma,MONDO,disease,DISEASE_17439
17440,17440,17440,17440,17440,17440,17440,17440,MONDO:0009738_MONDO:0019346_MONDO:0017734,sialidosis,MONDO_grouped,disease,DISEASE_17440
17441,17441,17441,17441,17441,17441,17441,17441,MONDO:0013013,"question mark ears, isolated",MONDO,disease,DISEASE_17441
17442,17442,17442,17442,17442,17442,17442,17442,MONDO:0859251,Dentici-Novelli neurodevelopmental syndrome,MONDO,disease,DISEASE_17442
17443,17443,17443,17443,17443,17443,17443,17443,MONDO:0005746,enterobiasis,MONDO,disease,DISEASE_17443
17444,17444,17444,17444,17444,17444,17444,17444,MONDO:0003686,apocrine sweat gland neoplasm,MONDO,disease,DISEASE_17444
17445,17445,17445,17445,17445,17445,17445,17445,MONDO:0012994,dopa-responsive dystonia due to sepiapterin reductase deficiency,MONDO,disease,DISEASE_17445
17446,17446,17446,17446,17446,17446,17446,17446,MONDO:0005181,progressive external ophthalmoplegia,MONDO,disease,DISEASE_17446
17447,17447,17447,17447,17447,17447,17447,17447,MONDO:0006805,intermediate coronary syndrome,MONDO,disease,DISEASE_17447
17448,17448,17448,17448,17448,17448,17448,17448,MONDO:0859007,mosaic Legius syndrome,MONDO,disease,DISEASE_17448
17449,17449,17449,17449,17449,17449,17449,17449,MONDO:0009726,proteosome-associated autoinflammatory syndrome,MONDO,disease,DISEASE_17449
17450,17450,17450,17450,17450,17450,17450,17450,MONDO:0007194,familial bicuspid aortic valve,MONDO,disease,DISEASE_17450
17451,17451,17451,17451,17451,17451,17451,17451,MONDO:0015430,ring chromosome 1,MONDO,disease,DISEASE_17451
17452,17452,17452,17452,17452,17452,17452,17452,MONDO:0017063,total spina bifida aperta,MONDO,disease,DISEASE_17452
17453,17453,17453,17453,17453,17453,17453,17453,MONDO:1011750,"follicular dysplasia and interface dermatitis, non-human animal",MONDO,disease,DISEASE_17453
17454,17454,17454,17454,17454,17454,17454,17454,MONDO:0016555,transient congenital hypothyroidism due to maternal factor,MONDO,disease,DISEASE_17454
17455,17455,17455,17455,17455,17455,17455,17455,MONDO:0100063,Pericytoma with t(7;12),MONDO,disease,DISEASE_17455
17456,17456,17456,17456,17456,17456,17456,17456,MONDO:1011129_MONDO:1012814,"hypogonadotropic hypogonadism, KISS1-related, pig",MONDO_grouped,disease,DISEASE_17456
17457,17457,17457,17457,17457,17457,17457,17457,MONDO:0008627,ureter cancer,MONDO,disease,DISEASE_17457
17458,17458,17458,17458,17458,17458,17458,17458,MONDO:0010148,Mounier-Kuhn syndrome,MONDO,disease,DISEASE_17458
17459,17459,17459,17459,17459,17459,17459,17459,MONDO:0002597,notochordal tumor,MONDO,disease,DISEASE_17459
17460,17460,17460,17460,17460,17460,17460,17460,MONDO:0001803,myringitis bullosa hemorrhagica,MONDO,disease,DISEASE_17460
17461,17461,17461,17461,17461,17461,17461,17461,MONDO:0018487,autosomal recessive severe congenital neutropenia due to CXCR2 deficiency,MONDO,disease,DISEASE_17461
17462,17462,17462,17462,17462,17462,17462,17462,MONDO:0014645_MONDO:0005676,BENTA disease,MONDO_grouped,disease,DISEASE_17462
17463,17463,17463,17463,17463,17463,17463,17463,MONDO:0015864,mixed germ cell tumor,MONDO,disease,DISEASE_17463
17464,17464,17464,17464,17464,17464,17464,17464,MONDO:0019872,distal trisomy 3p,MONDO,disease,DISEASE_17464
17465,17465,17465,17465,17465,17465,17465,17465,MONDO:1010515,"triploidy, blue-and-yellow macaw",MONDO,disease,DISEASE_17465
17466,17466,17466,17466,17466,17466,17466,17466,MONDO:0032853,"myopathy, distal, 6, adult-onset, autosomal dominant",MONDO,disease,DISEASE_17466
17467,17467,17467,17467,17467,17467,17467,17467,MONDO:0022098,catamenial pneumothorax,MONDO,disease,DISEASE_17467
17468,17468,17468,17468,17468,17468,17468,17468,MONDO:0010960,protocadherin 3,MONDO,disease,DISEASE_17468
17469,17469,17469,17469,17469,17469,17469,17469,MONDO:1012383,"trapped neutrophil syndrome, dog",MONDO,disease,DISEASE_17469
17470,17470,17470,17470,17470,17470,17470,17470,MONDO:0002171,giant cell tumor,MONDO,disease,DISEASE_17470
17471,17471,17471,17471,17471,17471,17471,17471,MONDO:0023061,enamel hypoplasia cataract hydrocephaly,MONDO,disease,DISEASE_17471
17472,17472,17472,17472,17472,17472,17472,17472,MONDO:0003200,urethra adenocarcinoma,MONDO,disease,DISEASE_17472
17473,17473,17473,17473,17473,17473,17473,17473,MONDO:1010129_MONDO:1011737,"epidermolysis bullosa, non-human animal",MONDO_grouped,disease,DISEASE_17473
17474,17474,17474,17474,17474,17474,17474,17474,MONDO:0004831,proliferative fasciitis,MONDO,disease,DISEASE_17474
17475,17475,17475,17475,17475,17475,17475,17475,MONDO:0017568,Prata-Liberal-Goncalves syndrome,MONDO,disease,DISEASE_17475
17476,17476,17476,17476,17476,17476,17476,17476,MONDO:0015648,startle epilepsy,MONDO,disease,DISEASE_17476
17477,17477,17477,17477,17477,17477,17477,17477,MONDO:0001379,ureteric orifice cancer,MONDO,disease,DISEASE_17477
17478,17478,17478,17478,17478,17478,17478,17478,MONDO:0023283,ovarian granulosa cell tumor,MONDO,disease,DISEASE_17478
17479,17479,17479,17479,17479,17479,17479,17479,MONDO:0000105_MONDO:1011579,"anemia, nonspherocytic hemolytic",MONDO_grouped,disease,DISEASE_17479
17480,17480,17480,17480,17480,17480,17480,17480,MONDO:0000964,skin lipoma,MONDO,disease,DISEASE_17480
17481,17481,17481,17481,17481,17481,17481,17481,MONDO:0008971,chondrodysplasia calcificans Metaphysealis,MONDO,disease,DISEASE_17481
17482,17482,17482,17482,17482,17482,17482,17482,MONDO:0043133,microcephaly micropenis convulsions,MONDO,disease,DISEASE_17482
17483,17483,17483,17483,17483,17483,17483,17483,MONDO:0975847,autoimmune disease with susceptibility to mycobacterium tuberculosis,MONDO,disease,DISEASE_17483
17484,17484,17484,17484,17484,17484,17484,17484,MONDO:0006846_MONDO:0000959_MONDO:0001785_MONDO:0001133,malignant hypertension,MONDO_grouped,disease,DISEASE_17484
17485,17485,17485,17485,17485,17485,17485,17485,MONDO:0034846,primary desmosis coli,MONDO,disease,DISEASE_17485
17486,17486,17486,17486,17486,17486,17486,17486,MONDO:0010563,blue cone monochromacy,MONDO,disease,DISEASE_17486
17487,17487,17487,17487,17487,17487,17487,17487,MONDO:0018016,classic neuroendocrine tumor of appendix,MONDO,disease,DISEASE_17487
17488,17488,17488,17488,17488,17488,17488,17488,MONDO:0012007,"scimitar anomaly, multiple cardiac malformations, and craniofacial and central nervous system abnormalities",MONDO,disease,DISEASE_17488
17489,17489,17489,17489,17489,17489,17489,17489,MONDO:0006096,atypical endometrial hyperplasia,MONDO,disease,DISEASE_17489
17490,17490,17490,17490,17490,17490,17490,17490,MONDO:0005097,squamous cell lung carcinoma,MONDO,disease,DISEASE_17490
17491,17491,17491,17491,17491,17491,17491,17491,MONDO:0019865,mosaic trisomy 4,MONDO,disease,DISEASE_17491
17492,17492,17492,17492,17492,17492,17492,17492,MONDO:0009040,craniosynostosis-intellectual disability syndrome of 51N and Gettig,MONDO,disease,DISEASE_17492
17493,17493,17493,17493,17493,17493,17493,17493,MONDO:0100521,NOG-related symphalangism spectrum disorder,MONDO,disease,DISEASE_17493
17494,17494,17494,17494,17494,17494,17494,17494,MONDO:0010575,deafness-hypogonadism syndrome,MONDO,disease,DISEASE_17494
17495,17495,17495,17495,17495,17495,17495,17495,MONDO:0015419,midline cervical cleft,MONDO,disease,DISEASE_17495
17496,17496,17496,17496,17496,17496,17496,17496,MONDO:0018551,patent urachus,MONDO,disease,DISEASE_17496
17497,17497,17497,17497,17497,17497,17497,17497,MONDO:0010667,Prieto syndrome,MONDO,disease,DISEASE_17497
17498,17498,17498,17498,17498,17498,17498,17498,MONDO:1012851,"cataract, MIP-related, giant panda",MONDO,disease,DISEASE_17498
17499,17499,17499,17499,17499,17499,17499,17499,MONDO:0005549,renal cell adenocarcinoma,MONDO,disease,DISEASE_17499
17500,17500,17500,17500,17500,17500,17500,17500,MONDO:1010276,"hypogonadism, non-human animal",MONDO,disease,DISEASE_17500
17501,17501,17501,17501,17501,17501,17501,17501,MONDO:0001283,endosalpingiosis,MONDO,disease,DISEASE_17501
17502,17502,17502,17502,17502,17502,17502,17502,MONDO:0020068,postinfectious encephalitis,MONDO,disease,DISEASE_17502
17503,17503,17503,17503,17503,17503,17503,17503,MONDO:0012505_MONDO:0012509_MONDO:0013616_MONDO:0014359_MONDO:0015999_MONDO:0958262,"pigmented nodular adrenocortical disease, primary",MONDO_grouped,disease,DISEASE_17503
17504,17504,17504,17504,17504,17504,17504,17504,MONDO:0032865_MONDO:0957263_MONDO:0957294_MONDO:0014613_MONDO:0014612_MONDO:0957261_MONDO:0013879_MONDO:0013878_MONDO:0030690_MONDO:0000148,"pulmonary fibrosis and/or bone marrow failure, telomere-related",MONDO_grouped,disease,DISEASE_17504
17505,17505,17505,17505,17505,17505,17505,17505,MONDO:0016811,renal tubulopathy-encephalopathy-liver failure syndrome,MONDO,disease,DISEASE_17505
17506,17506,17506,17506,17506,17506,17506,17506,MONDO:0008922,Sengers syndrome,MONDO,disease,DISEASE_17506
17507,17507,17507,17507,17507,17507,17507,17507,MONDO:0000014,"colorblindness, partial",MONDO,disease,DISEASE_17507
17508,17508,17508,17508,17508,17508,17508,17508,MONDO:1012325_MONDO:1012326,"premature senesence, pig",MONDO_grouped,disease,DISEASE_17508
17509,17509,17509,17509,17509,17509,17509,17509,MONDO:0800496,epilepsy with auditory features,MONDO,disease,DISEASE_17509
17510,17510,17510,17510,17510,17510,17510,17510,MONDO:0015285,Carney complex,MONDO,disease,DISEASE_17510
17511,17511,17511,17511,17511,17511,17511,17511,MONDO:0003702,uterus intravascular leiomyomatosis,MONDO,disease,DISEASE_17511
17512,17512,17512,17512,17512,17512,17512,17512,MONDO:1012830,"craniomandibular osteopathy, SLC37A2-related, dog",MONDO,disease,DISEASE_17512
17513,17513,17513,17513,17513,17513,17513,17513,MONDO:0007551_MONDO:0007555_MONDO:0030489_MONDO:0007554_MONDO:0030527_MONDO:0007550_MONDO:0030525,"epidermolysis bullosa simplex 1C, localized",MONDO_grouped,disease,DISEASE_17513
17514,17514,17514,17514,17514,17514,17514,17514,MONDO:0956983,pleomorphic xanthoastrocytoma BRAF mutant,MONDO,disease,DISEASE_17514
17515,17515,17515,17515,17515,17515,17515,17515,MONDO:0006704,CNS demyelinating autoimmune disease,MONDO,disease,DISEASE_17515
17516,17516,17516,17516,17516,17516,17516,17516,MONDO:0009560,oculotrichoanal syndrome,MONDO,disease,DISEASE_17516
17517,17517,17517,17517,17517,17517,17517,17517,MONDO:0022623,CDK4 linked melanoma,MONDO,disease,DISEASE_17517
17518,17518,17518,17518,17518,17518,17518,17518,MONDO:1012567,"osseous choristoma of the ciliary body, domestic guinea pig",MONDO,disease,DISEASE_17518
17519,17519,17519,17519,17519,17519,17519,17519,MONDO:0013149,"hydrops fetalis, nonimmune, with gracile bones and dysmorphic features",MONDO,disease,DISEASE_17519
17520,17520,17520,17520,17520,17520,17520,17520,MONDO:0007046,hereditary papulotranslucent acrokeratoderma,MONDO,disease,DISEASE_17520
17521,17521,17521,17521,17521,17521,17521,17521,MONDO:1012375,"follicular dysplasia and interface dermatitis, dog",MONDO,disease,DISEASE_17521
17522,17522,17522,17522,17522,17522,17522,17522,MONDO:1011730,"complement component 4 deficiency, non-human animal",MONDO,disease,DISEASE_17522
17523,17523,17523,17523,17523,17523,17523,17523,MONDO:0002443,bruxism,MONDO,disease,DISEASE_17523
17524,17524,17524,17524,17524,17524,17524,17524,MONDO:0859240,intellectual developmental disorder with or without peripheral neuropathy,MONDO,disease,DISEASE_17524
17525,17525,17525,17525,17525,17525,17525,17525,MONDO:0010895,ABCD syndrome,MONDO,disease,DISEASE_17525
17526,17526,17526,17526,17526,17526,17526,17526,MONDO:0001030,"keratoconus, stable condition",MONDO,disease,DISEASE_17526
17527,17527,17527,17527,17527,17527,17527,17527,MONDO:0007041,Apert syndrome,MONDO,disease,DISEASE_17527
17528,17528,17528,17528,17528,17528,17528,17528,MONDO:1010352,"microphthalmia, isolated, with coloboma, non-human animal",MONDO,disease,DISEASE_17528
17529,17529,17529,17529,17529,17529,17529,17529,MONDO:0013445,complement component 9 deficiency,MONDO,disease,DISEASE_17529
17530,17530,17530,17530,17530,17530,17530,17530,MONDO:0006050,pleomorphic breast carcinoma,MONDO,disease,DISEASE_17530
17531,17531,17531,17531,17531,17531,17531,17531,MONDO:0006348,pancreatic small cell neuroendocrine carcinoma,MONDO,disease,DISEASE_17531
17532,17532,17532,17532,17532,17532,17532,17532,MONDO:0022890,craniosynostosis Fontaine type,MONDO,disease,DISEASE_17532
17533,17533,17533,17533,17533,17533,17533,17533,MONDO:0011468,"hereditary motor and sensory neuropathy, Okinawa type",MONDO,disease,DISEASE_17533
17534,17534,17534,17534,17534,17534,17534,17534,MONDO:0008900,camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia,MONDO,disease,DISEASE_17534
17535,17535,17535,17535,17535,17535,17535,17535,MONDO:0008528,"tear protein, anodal",MONDO,disease,DISEASE_17535
17536,17536,17536,17536,17536,17536,17536,17536,MONDO:0021333,carcinoma of lip,MONDO,disease,DISEASE_17536
17537,17537,17537,17537,17537,17537,17537,17537,MONDO:0100158,CHRNG-associated hypo-akinesia disorder of prenatal onset,MONDO,disease,DISEASE_17537
17538,17538,17538,17538,17538,17538,17538,17538,MONDO:0014958,Harel-Yoon syndrome,MONDO,disease,DISEASE_17538
17539,17539,17539,17539,17539,17539,17539,17539,MONDO:1011429,"hepatic lipidosis, non-human animal",MONDO,disease,DISEASE_17539
17540,17540,17540,17540,17540,17540,17540,17540,MONDO:0006932,pulmonary edema,MONDO,disease,DISEASE_17540
17541,17541,17541,17541,17541,17541,17541,17541,MONDO:0024772_MONDO:0026733_MONDO:0958322,"intellectual developmental disorder, X-linked, syndromic, Pilorge type",MONDO_grouped,disease,DISEASE_17541
17542,17542,17542,17542,17542,17542,17542,17542,MONDO:1010006,"Phelan-McDermid syndrome, non-human animal",MONDO,disease,DISEASE_17542
17543,17543,17543,17543,17543,17543,17543,17543,MONDO:0971047,PRC-2 complex-related overgrowth spectrum,MONDO,disease,DISEASE_17543
17544,17544,17544,17544,17544,17544,17544,17544,MONDO:0018459,isolated glycerol kinase deficiency,MONDO,disease,DISEASE_17544
17545,17545,17545,17545,17545,17545,17545,17545,MONDO:0012817,Ewing sarcoma,MONDO,disease,DISEASE_17545
17546,17546,17546,17546,17546,17546,17546,17546,MONDO:1012402,"caprine-like generalized hypoplasia syndrome, cattle",MONDO,disease,DISEASE_17546
17547,17547,17547,17547,17547,17547,17547,17547,MONDO:0015399,glossopalatine ankylosis,MONDO,disease,DISEASE_17547
17548,17548,17548,17548,17548,17548,17548,17548,MONDO:0016474,drug-induced lupus erythematosus,MONDO,disease,DISEASE_17548
17549,17549,17549,17549,17549,17549,17549,17549,MONDO:0000263,laryngotracheitis,MONDO,disease,DISEASE_17549
17550,17550,17550,17550,17550,17550,17550,17550,MONDO:0007120,aniridia-absent patella syndrome,MONDO,disease,DISEASE_17550
17551,17551,17551,17551,17551,17551,17551,17551,MONDO:0024275,amebic dysentery,MONDO,disease,DISEASE_17551
17552,17552,17552,17552,17552,17552,17552,17552,MONDO:0010174,Valinemia,MONDO,disease,DISEASE_17552
17553,17553,17553,17553,17553,17553,17553,17553,MONDO:0100130,adult acute respiratory distress syndrome,MONDO,disease,DISEASE_17553
17554,17554,17554,17554,17554,17554,17554,17554,MONDO:0011662,pathological gambling,MONDO,disease,DISEASE_17554
17555,17555,17555,17555,17555,17555,17555,17555,MONDO:0000337,exanthema subitum,MONDO,disease,DISEASE_17555
17556,17556,17556,17556,17556,17556,17556,17556,MONDO:0012351_MONDO:0017543_MONDO:0017544_MONDO:0017545,zygodactyly,MONDO_grouped,disease,DISEASE_17556
17557,17557,17557,17557,17557,17557,17557,17557,MONDO:0016836,16p13.11 microdeletion syndrome,MONDO,disease,DISEASE_17557
17558,17558,17558,17558,17558,17558,17558,17558,MONDO:0859246,"leukodystrophy, childhood-onset, remitting",MONDO,disease,DISEASE_17558
17559,17559,17559,17559,17559,17559,17559,17559,MONDO:0006915_MONDO:0022768,polyradiculoneuropathy,MONDO_grouped,disease,DISEASE_17559
17560,17560,17560,17560,17560,17560,17560,17560,MONDO:0005823,legionellosis,MONDO,disease,DISEASE_17560
17561,17561,17561,17561,17561,17561,17561,17561,MONDO:0014248,autism spectrum disorder - epilepsy - arthrogryposis syndrome,MONDO,disease,DISEASE_17561
17562,17562,17562,17562,17562,17562,17562,17562,MONDO:0024431,bilirubin metabolism disease,MONDO,disease,DISEASE_17562
17563,17563,17563,17563,17563,17563,17563,17563,MONDO:0008305,Currarino triad,MONDO,disease,DISEASE_17563
17564,17564,17564,17564,17564,17564,17564,17564,MONDO:0024665,indeterminate sex and/or pseudohermaphroditism,MONDO,disease,DISEASE_17564
17565,17565,17565,17565,17565,17565,17565,17565,MONDO:0016807,pure mitochondrial myopathy,MONDO,disease,DISEASE_17565
17566,17566,17566,17566,17566,17566,17566,17566,MONDO:0043303,hyperacusis,MONDO,disease,DISEASE_17566
17567,17567,17567,17567,17567,17567,17567,17567,MONDO:0010856,autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis,MONDO,disease,DISEASE_17567
17568,17568,17568,17568,17568,17568,17568,17568,MONDO:0004930_MONDO:0001996,steroid-induced glaucoma,MONDO_grouped,disease,DISEASE_17568
17569,17569,17569,17569,17569,17569,17569,17569,MONDO:0007151,"arms, malformation of",MONDO,disease,DISEASE_17569
17570,17570,17570,17570,17570,17570,17570,17570,MONDO:0001800,equatorial staphyloma,MONDO,disease,DISEASE_17570
17571,17571,17571,17571,17571,17571,17571,17571,MONDO:0100000,MED12-related intellectual disability syndrome,MONDO,disease,DISEASE_17571
17572,17572,17572,17572,17572,17572,17572,17572,MONDO:1012866,"hypercholesterolemia, PCSK9-related, rabbit",MONDO,disease,DISEASE_17572
17573,17573,17573,17573,17573,17573,17573,17573,MONDO:0014808_MONDO:0010036_MONDO:0008964_MONDO:0045032_MONDO:0015170,congenital secretory sodium diarrhea,MONDO_grouped,disease,DISEASE_17573
17574,17574,17574,17574,17574,17574,17574,17574,MONDO:1040036,IMPG1-related dominant retinopathy,MONDO,disease,DISEASE_17574
17575,17575,17575,17575,17575,17575,17575,17575,MONDO:0022140,Charles bonnet syndrome,MONDO,disease,DISEASE_17575
17576,17576,17576,17576,17576,17576,17576,17576,MONDO:0000222_MONDO:0001025,seminal vesicle acute gonorrhea,MONDO_grouped,disease,DISEASE_17576
17577,17577,17577,17577,17577,17577,17577,17577,MONDO:0019948,reducing body myopathy,MONDO,disease,DISEASE_17577
17578,17578,17578,17578,17578,17578,17578,17578,MONDO:0017801,atypical Meigs syndrome,MONDO,disease,DISEASE_17578
17579,17579,17579,17579,17579,17579,17579,17579,MONDO:0000066,mitochondrial complex deficiency,MONDO,disease,DISEASE_17579
17580,17580,17580,17580,17580,17580,17580,17580,MONDO:0007515_MONDO:0009153,ectopia pupillae,MONDO_grouped,disease,DISEASE_17580
17581,17581,17581,17581,17581,17581,17581,17581,MONDO:0018328,homozygous familial hypercholesterolemia,MONDO,disease,DISEASE_17581
17582,17582,17582,17582,17582,17582,17582,17582,MONDO:1010478,"arrhythmogenic right ventricular cardiomyopathy, dog",MONDO,disease,DISEASE_17582
17583,17583,17583,17583,17583,17583,17583,17583,MONDO:0032653,cardiac-urogenital syndrome,MONDO,disease,DISEASE_17583
17584,17584,17584,17584,17584,17584,17584,17584,MONDO:0015339,adrenomyeloneuropathy,MONDO,disease,DISEASE_17584
17585,17585,17585,17585,17585,17585,17585,17585,MONDO:0008481,"spondylosis, cervical",MONDO,disease,DISEASE_17585
17586,17586,17586,17586,17586,17586,17586,17586,MONDO:0015727,mosaic trisomy 15,MONDO,disease,DISEASE_17586
17587,17587,17587,17587,17587,17587,17587,17587,MONDO:0001526,labia minora cancer,MONDO,disease,DISEASE_17587
17588,17588,17588,17588,17588,17588,17588,17588,MONDO:0002659,uveal cancer,MONDO,disease,DISEASE_17588
17589,17589,17589,17589,17589,17589,17589,17589,MONDO:1011441,"mast cell tumor, non-human animal",MONDO,disease,DISEASE_17589
17590,17590,17590,17590,17590,17590,17590,17590,MONDO:0017164,hemolytic disease of the newborn with Kell alloimmunization,MONDO,disease,DISEASE_17590
17591,17591,17591,17591,17591,17591,17591,17591,MONDO:0011478,"growth and developintellectual disability, ocular ptosis, cardiac defect, and anal atresia",MONDO,disease,DISEASE_17591
17592,17592,17592,17592,17592,17592,17592,17592,MONDO:0032849,"neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies",MONDO,disease,DISEASE_17592
17593,17593,17593,17593,17593,17593,17593,17593,MONDO:0032877,neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures,MONDO,disease,DISEASE_17593
17594,17594,17594,17594,17594,17594,17594,17594,MONDO:1011637,"juvenile idiopathic epilepsy, non-human animal",MONDO,disease,DISEASE_17594
17595,17595,17595,17595,17595,17595,17595,17595,MONDO:0006563,inverted follicular keratosis,MONDO,disease,DISEASE_17595
17596,17596,17596,17596,17596,17596,17596,17596,MONDO:0004129,cloacogenic carcinoma,MONDO,disease,DISEASE_17596
17597,17597,17597,17597,17597,17597,17597,17597,MONDO:0008121,"onychogryposis, pedal, with keratosis plantaris and coarse hair",MONDO,disease,DISEASE_17597
17598,17598,17598,17598,17598,17598,17598,17598,MONDO:0000654,benign connective and soft tissue neoplasm,MONDO,disease,DISEASE_17598
17599,17599,17599,17599,17599,17599,17599,17599,MONDO:0021503,benign neoplasm of gallbladder,MONDO,disease,DISEASE_17599
17600,17600,17600,17600,17600,17600,17600,17600,MONDO:0035821,isolated female hypospadias,MONDO,disease,DISEASE_17600
17601,17601,17601,17601,17601,17601,17601,17601,MONDO:0005605,transitional cell papilloma,MONDO,disease,DISEASE_17601
17602,17602,17602,17602,17602,17602,17602,17602,MONDO:0010327,HSD10 mitochondrial disease,MONDO,disease,DISEASE_17602
17603,17603,17603,17603,17603,17603,17603,17603,MONDO:0021169_MONDO:0001939_MONDO:0003897_MONDO:0003945,epithelioid hemangioma,MONDO_grouped,disease,DISEASE_17603
17604,17604,17604,17604,17604,17604,17604,17604,MONDO:0009998,Richieri Costa-Pereira syndrome,MONDO,disease,DISEASE_17604
17605,17605,17605,17605,17605,17605,17605,17605,MONDO:0019839,panhypophysitis,MONDO,disease,DISEASE_17605
17606,17606,17606,17606,17606,17606,17606,17606,MONDO:0009233,Fibulo-ulnar hypoplasia-renal anomalies syndrome,MONDO,disease,DISEASE_17606
17607,17607,17607,17607,17607,17607,17607,17607,MONDO:0010083,succinic semialdehyde dehydrogenase deficiency,MONDO,disease,DISEASE_17607
17608,17608,17608,17608,17608,17608,17608,17608,MONDO:0017659,sporadic hyperekplexia,MONDO,disease,DISEASE_17608
17609,17609,17609,17609,17609,17609,17609,17609,MONDO:0002745,fallopian tube mucinous tumor,MONDO,disease,DISEASE_17609
17610,17610,17610,17610,17610,17610,17610,17610,MONDO:0014387,"leukoencephalopathy, progressive, with ovarian failure",MONDO,disease,DISEASE_17610
17611,17611,17611,17611,17611,17611,17611,17611,MONDO:0009286,"gluteal muscles, absence of",MONDO,disease,DISEASE_17611
17612,17612,17612,17612,17612,17612,17612,17612,MONDO:0018021,hypotrichosis-deafness syndrome,MONDO,disease,DISEASE_17612
17613,17613,17613,17613,17613,17613,17613,17613,MONDO:0018352,squamous cell carcinoma of penis,MONDO,disease,DISEASE_17613
17614,17614,17614,17614,17614,17614,17614,17614,MONDO:0700058,Morton neuroma,MONDO,disease,DISEASE_17614
17615,17615,17615,17615,17615,17615,17615,17615,MONDO:0015814,primary cutaneous follicle center lymphoma,MONDO,disease,DISEASE_17615
17616,17616,17616,17616,17616,17616,17616,17616,MONDO:0004343,pancreatic acinar cell cystadenocarcinoma,MONDO,disease,DISEASE_17616
17617,17617,17617,17617,17617,17617,17617,17617,MONDO:0015608,acute myeloid leukemia and myelodysplastic syndromes related to radiation,MONDO,disease,DISEASE_17617
17618,17618,17618,17618,17618,17618,17618,17618,MONDO:0017054,thiamine-responsive maple syrup urine disease,MONDO,disease,DISEASE_17618
17619,17619,17619,17619,17619,17619,17619,17619,MONDO:0024334,peripheral nerve lesion,MONDO,disease,DISEASE_17619
17620,17620,17620,17620,17620,17620,17620,17620,MONDO:0005094_MONDO:0002789,hemangiopericytoma,MONDO_grouped,disease,DISEASE_17620
17621,17621,17621,17621,17621,17621,17621,17621,MONDO:0015003_MONDO:0975837,"dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities",MONDO_grouped,disease,DISEASE_17621
17622,17622,17622,17622,17622,17622,17622,17622,MONDO:0014620_MONDO:0011844_MONDO:0008044,myoclonic dystonia,MONDO_grouped,disease,DISEASE_17622
17623,17623,17623,17623,17623,17623,17623,17623,MONDO:0014535_MONDO:0005804,hyperproinsulinemia,MONDO_grouped,disease,DISEASE_17623
17624,17624,17624,17624,17624,17624,17624,17624,MONDO:0002410,pyeloureteritis cystica,MONDO,disease,DISEASE_17624
17625,17625,17625,17625,17625,17625,17625,17625,MONDO:0006523,acrodermatitis,MONDO,disease,DISEASE_17625
17626,17626,17626,17626,17626,17626,17626,17626,MONDO:0007727,autosomal dominant familial periodic fever,MONDO,disease,DISEASE_17626
17627,17627,17627,17627,17627,17627,17627,17627,MONDO:0013663,platelet-activating factor acetylhydrolase deficiency,MONDO,disease,DISEASE_17627
17628,17628,17628,17628,17628,17628,17628,17628,MONDO:0020775_MONDO:0020777_MONDO:0060720,congenital disorder of glycosylation with defective fucosylation,MONDO_grouped,disease,DISEASE_17628
17629,17629,17629,17629,17629,17629,17629,17629,MONDO:0004260,peptic ulcer perforation,MONDO,disease,DISEASE_17629
17630,17630,17630,17630,17630,17630,17630,17630,MONDO:0003558,adenosquamous prostate carcinoma,MONDO,disease,DISEASE_17630
17631,17631,17631,17631,17631,17631,17631,17631,MONDO:0015800,osteosclerosis-developmental delay-craniosynostosis syndrome,MONDO,disease,DISEASE_17631
17632,17632,17632,17632,17632,17632,17632,17632,MONDO:0001906_MONDO:0002310,posterior dislocation of lens,MONDO_grouped,disease,DISEASE_17632
17633,17633,17633,17633,17633,17633,17633,17633,MONDO:0015643,photosensitive epilepsy,MONDO,disease,DISEASE_17633
17634,17634,17634,17634,17634,17634,17634,17634,MONDO:0000948,xerophthalmia,MONDO,disease,DISEASE_17634
17635,17635,17635,17635,17635,17635,17635,17635,MONDO:0700115,proliferative vitreoretinopathy,MONDO,disease,DISEASE_17635
17636,17636,17636,17636,17636,17636,17636,17636,MONDO:0014420,short stature due to primary acid-labile subunit deficiency,MONDO,disease,DISEASE_17636
17637,17637,17637,17637,17637,17637,17637,17637,MONDO:0003598,median nerve neuropathy,MONDO,disease,DISEASE_17637
17638,17638,17638,17638,17638,17638,17638,17638,MONDO:0003542,dental pulp calcification,MONDO,disease,DISEASE_17638
17639,17639,17639,17639,17639,17639,17639,17639,MONDO:1011705,"combined deficiency of factors VIII, IX, and X, non-human animal",MONDO,disease,DISEASE_17639
17640,17640,17640,17640,17640,17640,17640,17640,MONDO:0017941,chikungunya,MONDO,disease,DISEASE_17640
17641,17641,17641,17641,17641,17641,17641,17641,MONDO:0010904,"setting-Sun phenomenon, familial benign",MONDO,disease,DISEASE_17641
17642,17642,17642,17642,17642,17642,17642,17642,MONDO:0010086,obsolete sudden infant death syndrome,MONDO,disease,DISEASE_17642
17643,17643,17643,17643,17643,17643,17643,17643,MONDO:0003231,acute nonparalytic poliomyelitis,MONDO,disease,DISEASE_17643
17644,17644,17644,17644,17644,17644,17644,17644,MONDO:1011794,"spastic lameness, non-human animal",MONDO,disease,DISEASE_17644
17645,17645,17645,17645,17645,17645,17645,17645,MONDO:0850271,myeloid leukemia associated with down syndrome,MONDO,disease,DISEASE_17645
17646,17646,17646,17646,17646,17646,17646,17646,MONDO:1011643,"mitral valve disease, non-human animal",MONDO,disease,DISEASE_17646
17647,17647,17647,17647,17647,17647,17647,17647,MONDO:0008916,cardiomyopathy associated with myopathy and sudden death,MONDO,disease,DISEASE_17647
17648,17648,17648,17648,17648,17648,17648,17648,MONDO:1012424,"llama syndrome chondrodysplasia, sheep",MONDO,disease,DISEASE_17648
17649,17649,17649,17649,17649,17649,17649,17649,MONDO:0009225,"fever, familial lifelong persistent",MONDO,disease,DISEASE_17649
17650,17650,17650,17650,17650,17650,17650,17650,MONDO:0003184_MONDO:0001418,trachea carcinoma,MONDO_grouped,disease,DISEASE_17650
17651,17651,17651,17651,17651,17651,17651,17651,MONDO:0015850,transverse vaginal septum,MONDO,disease,DISEASE_17651
17652,17652,17652,17652,17652,17652,17652,17652,MONDO:0009127,"dwarfism, low-birth-weight type, with unresponsiveness to growth hormone",MONDO,disease,DISEASE_17652
17653,17653,17653,17653,17653,17653,17653,17653,MONDO:0002309_MONDO:0002308,papillary conjunctivitis,MONDO_grouped,disease,DISEASE_17653
17654,17654,17654,17654,17654,17654,17654,17654,MONDO:0019921,paternal uniparental disomy of chromosome 6,MONDO,disease,DISEASE_17654
17655,17655,17655,17655,17655,17655,17655,17655,MONDO:0009742,neuroectodermal melanolysosomal disease,MONDO,disease,DISEASE_17655
17656,17656,17656,17656,17656,17656,17656,17656,MONDO:0036915,benign ovarian mucinous tumor,MONDO,disease,DISEASE_17656
17657,17657,17657,17657,17657,17657,17657,17657,MONDO:1010859,"lysosomal storage disease, kangaroo",MONDO,disease,DISEASE_17657
17658,17658,17658,17658,17658,17658,17658,17658,MONDO:0021374,neoplasm of cerebral hemisphere,MONDO,disease,DISEASE_17658
17659,17659,17659,17659,17659,17659,17659,17659,MONDO:0000478,multifocal dystonia,MONDO,disease,DISEASE_17659
17660,17660,17660,17660,17660,17660,17660,17660,MONDO:0100451,CEP290-related ciliopathy,MONDO,disease,DISEASE_17660
17661,17661,17661,17661,17661,17661,17661,17661,MONDO:1010325,"congenital nystagmus, non-human animal",MONDO,disease,DISEASE_17661
17662,17662,17662,17662,17662,17662,17662,17662,MONDO:0018269,white platelet syndrome,MONDO,disease,DISEASE_17662
17663,17663,17663,17663,17663,17663,17663,17663,MONDO:0025419,"furunculosis, fish",MONDO,disease,DISEASE_17663
17664,17664,17664,17664,17664,17664,17664,17664,MONDO:0040671,class V glucose-6-phosphate dehydrogenase deficiency,MONDO,disease,DISEASE_17664
17665,17665,17665,17665,17665,17665,17665,17665,MONDO:0800045,"autoinflammatory syndrome, familial, Behcet-like 1",MONDO,disease,DISEASE_17665
17666,17666,17666,17666,17666,17666,17666,17666,MONDO:0022769,ciliary dyskinesia-bronchiectasis,MONDO,disease,DISEASE_17666
17667,17667,17667,17667,17667,17667,17667,17667,MONDO:0009146,ectodermal dysplasia-sensorineural deafness syndrome,MONDO,disease,DISEASE_17667
17668,17668,17668,17668,17668,17668,17668,17668,MONDO:1011439,"Wilms tumor, non-human animal",MONDO,disease,DISEASE_17668
17669,17669,17669,17669,17669,17669,17669,17669,MONDO:0009569,Hennekam-Beemer syndrome,MONDO,disease,DISEASE_17669
17670,17670,17670,17670,17670,17670,17670,17670,MONDO:1010959,"neurofibromatosis, NF1-related, pig",MONDO,disease,DISEASE_17670
17671,17671,17671,17671,17671,17671,17671,17671,MONDO:0017241,obsolete AP4-related intellectual disability and spastic paraplegia,MONDO,disease,DISEASE_17671
17672,17672,17672,17672,17672,17672,17672,17672,MONDO:0013562,"aspergillosis, susceptibility to",MONDO,disease,DISEASE_17672
17673,17673,17673,17673,17673,17673,17673,17673,MONDO:1011673,"spontaneous autoimmune thyroiditis, non-human animal",MONDO,disease,DISEASE_17673
17674,17674,17674,17674,17674,17674,17674,17674,MONDO:0010491,X-linked acrogigantism due to Xq26 microduplication,MONDO,disease,DISEASE_17674
17675,17675,17675,17675,17675,17675,17675,17675,MONDO:0043765,presbycusis,MONDO,disease,DISEASE_17675
17676,17676,17676,17676,17676,17676,17676,17676,MONDO:0001584,ocular motility disease,MONDO,disease,DISEASE_17676
17677,17677,17677,17677,17677,17677,17677,17677,MONDO:0004934,periostitis,MONDO,disease,DISEASE_17677
17678,17678,17678,17678,17678,17678,17678,17678,MONDO:0008785_MONDO:0030436_MONDO:0014804_MONDO:0020099_MONDO:0015194,sideroblastic anemia,MONDO_grouped,disease,DISEASE_17678
17679,17679,17679,17679,17679,17679,17679,17679,MONDO:0015554,typical urticaria pigmentosa,MONDO,disease,DISEASE_17679
17680,17680,17680,17680,17680,17680,17680,17680,MONDO:0011579,late-onset retinal degeneration,MONDO,disease,DISEASE_17680
17681,17681,17681,17681,17681,17681,17681,17681,MONDO:0800379,"17-alpha-hydroxylase/17,20-lyase deficiency, combined complete",MONDO,disease,DISEASE_17681
17682,17682,17682,17682,17682,17682,17682,17682,MONDO:0010437,severe X-linked mitochondrial encephalomyopathy,MONDO,disease,DISEASE_17682
17683,17683,17683,17683,17683,17683,17683,17683,MONDO:0022871,corpus callosum agenesis of blepharophimosis robin type,MONDO,disease,DISEASE_17683
17684,17684,17684,17684,17684,17684,17684,17684,MONDO:0957197,"diffuse glioma, H3 G34 mutant",MONDO,disease,DISEASE_17684
17685,17685,17685,17685,17685,17685,17685,17685,MONDO:0003508,choriocarcinoma of testis,MONDO,disease,DISEASE_17685
17686,17686,17686,17686,17686,17686,17686,17686,MONDO:0020049,autosomal anomaly,MONDO,disease,DISEASE_17686
17687,17687,17687,17687,17687,17687,17687,17687,MONDO:0859174,"Usmani-Riazuddin syndrome, autosomal dominant",MONDO,disease,DISEASE_17687
17688,17688,17688,17688,17688,17688,17688,17688,MONDO:0024888,mesonephric neoplasm,MONDO,disease,DISEASE_17688
17689,17689,17689,17689,17689,17689,17689,17689,MONDO:0001590,quadriplegia,MONDO,disease,DISEASE_17689
17690,17690,17690,17690,17690,17690,17690,17690,MONDO:1011310,"developmental defect during embryogenesis, non-human animal",MONDO,disease,DISEASE_17690
17691,17691,17691,17691,17691,17691,17691,17691,MONDO:0005920,Plasmodium falciparum malaria,MONDO,disease,DISEASE_17691
17692,17692,17692,17692,17692,17692,17692,17692,MONDO:0021162,carotenemia,MONDO,disease,DISEASE_17692
17693,17693,17693,17693,17693,17693,17693,17693,MONDO:0018373_MONDO:0018374_MONDO:0018379,avascular necrosis,MONDO_grouped,disease,DISEASE_17693
17694,17694,17694,17694,17694,17694,17694,17694,MONDO:0015849,longitudinal vaginal septum,MONDO,disease,DISEASE_17694
17695,17695,17695,17695,17695,17695,17695,17695,MONDO:0006665,chronic atrophic gastritis,MONDO,disease,DISEASE_17695
17696,17696,17696,17696,17696,17696,17696,17696,MONDO:0005630_MONDO:0006636,actinobacillosis,MONDO_grouped,disease,DISEASE_17696
17697,17697,17697,17697,17697,17697,17697,17697,MONDO:0008003_MONDO:0016810,autosomal dominant progressive external ophthalmoplegia,MONDO_grouped,disease,DISEASE_17697
17698,17698,17698,17698,17698,17698,17698,17698,MONDO:0002200,eccrine mixed tumor of skin,MONDO,disease,DISEASE_17698
17699,17699,17699,17699,17699,17699,17699,17699,MONDO:0020438,atrial septal aneurysm,MONDO,disease,DISEASE_17699
17700,17700,17700,17700,17700,17700,17700,17700,MONDO:0003447,clear cell hidradenoma,MONDO,disease,DISEASE_17700
17701,17701,17701,17701,17701,17701,17701,17701,MONDO:0007429,"optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy",MONDO,disease,DISEASE_17701
17702,17702,17702,17702,17702,17702,17702,17702,MONDO:0019738,atypical hemolytic-uremic syndrome with H factor anomaly,MONDO,disease,DISEASE_17702
17703,17703,17703,17703,17703,17703,17703,17703,MONDO:0007408,"cryptotia, familial",MONDO,disease,DISEASE_17703
17704,17704,17704,17704,17704,17704,17704,17704,MONDO:0020857_MONDO:0971176_MONDO:0054666_MONDO:0024463_MONDO:0030506_MONDO:0010349_MONDO:0032590_MONDO:0030736_MONDO:0054850_MONDO:0013689_MONDO:0001889,ovarian dysgenesis,MONDO_grouped,disease,DISEASE_17704
17705,17705,17705,17705,17705,17705,17705,17705,MONDO:0010650,Melnick-Needles syndrome,MONDO,disease,DISEASE_17705
17706,17706,17706,17706,17706,17706,17706,17706,MONDO:0013077,Santos syndrome,MONDO,disease,DISEASE_17706
17707,17707,17707,17707,17707,17707,17707,17707,MONDO:0006193,endometrial hyperplasia without atypia,MONDO,disease,DISEASE_17707
17708,17708,17708,17708,17708,17708,17708,17708,MONDO:0032935,rhizomelic limb shortening with dysmorphic features,MONDO,disease,DISEASE_17708
17709,17709,17709,17709,17709,17709,17709,17709,MONDO:0005477,ventricular tachycardia,MONDO,disease,DISEASE_17709
17710,17710,17710,17710,17710,17710,17710,17710,MONDO:0022444,amyloidosis bronchopulmonary,MONDO,disease,DISEASE_17710
17711,17711,17711,17711,17711,17711,17711,17711,MONDO:0006490,vaginal squamous cell carcinoma,MONDO,disease,DISEASE_17711
17712,17712,17712,17712,17712,17712,17712,17712,MONDO:1010641,"factor XII deficiency, killer whale",MONDO,disease,DISEASE_17712
17713,17713,17713,17713,17713,17713,17713,17713,MONDO:0002217,central nervous system sarcoma,MONDO,disease,DISEASE_17713
17714,17714,17714,17714,17714,17714,17714,17714,MONDO:1010799,"cutis laxa, sika deer",MONDO,disease,DISEASE_17714
17715,17715,17715,17715,17715,17715,17715,17715,MONDO:0003306,atypical neurofibroma,MONDO,disease,DISEASE_17715
17716,17716,17716,17716,17716,17716,17716,17716,MONDO:0010456,"renal cell carcinoma, Xp11-associated",MONDO,disease,DISEASE_17716
17717,17717,17717,17717,17717,17717,17717,17717,MONDO:0850284,extrinsic asthma,MONDO,disease,DISEASE_17717
17718,17718,17718,17718,17718,17718,17718,17718,MONDO:0003263,childhood cerebellar neoplasm,MONDO,disease,DISEASE_17718
17719,17719,17719,17719,17719,17719,17719,17719,MONDO:0019802,secondary short bowel syndrome,MONDO,disease,DISEASE_17719
17720,17720,17720,17720,17720,17720,17720,17720,MONDO:0004990,breast tumor luminal A or B,MONDO,disease,DISEASE_17720
17721,17721,17721,17721,17721,17721,17721,17721,MONDO:1010089,hypomyopathic dermatomyositis,MONDO,disease,DISEASE_17721
17722,17722,17722,17722,17722,17722,17722,17722,MONDO:0003049,ovarian large-cell neuroendocrine carcinoma,MONDO,disease,DISEASE_17722
17723,17723,17723,17723,17723,17723,17723,17723,MONDO:0025417,fowlpox,MONDO,disease,DISEASE_17723
17724,17724,17724,17724,17724,17724,17724,17724,MONDO:0006011_MONDO:0002251_MONDO:0001505,viral hepatitis,MONDO_grouped,disease,DISEASE_17724
17725,17725,17725,17725,17725,17725,17725,17725,MONDO:0021313,eyelid cancer,MONDO,disease,DISEASE_17725
17726,17726,17726,17726,17726,17726,17726,17726,MONDO:0018838,lissencephaly spectrum disorders,MONDO,disease,DISEASE_17726
17727,17727,17727,17727,17727,17727,17727,17727,MONDO:0005845_MONDO:0017079,meningoencephalitis,MONDO_grouped,disease,DISEASE_17727
17728,17728,17728,17728,17728,17728,17728,17728,MONDO:0019531,hemolytic anemia due to glutathione reductase deficiency,MONDO,disease,DISEASE_17728
17729,17729,17729,17729,17729,17729,17729,17729,MONDO:0019149,cholesteryl ester storage disease,MONDO,disease,DISEASE_17729
17730,17730,17730,17730,17730,17730,17730,17730,MONDO:0009638,mitochondrial myopathy with a defect in mitochondrial-protein transport,MONDO,disease,DISEASE_17730
17731,17731,17731,17731,17731,17731,17731,17731,MONDO:0024912,cat disease,MONDO,disease,DISEASE_17731
17732,17732,17732,17732,17732,17732,17732,17732,MONDO:0021235,external ear neoplasm,MONDO,disease,DISEASE_17732
17733,17733,17733,17733,17733,17733,17733,17733,MONDO:0003384,uterine ligament clear cell adenocarcinoma,MONDO,disease,DISEASE_17733
17734,17734,17734,17734,17734,17734,17734,17734,MONDO:0007425,"deafness, sensorineural, with peripheral neuropathy and arterial disease",MONDO,disease,DISEASE_17734
17735,17735,17735,17735,17735,17735,17735,17735,MONDO:0850418,diffuse large B-cell lymphoma activated B-cell type,MONDO,disease,DISEASE_17735
17736,17736,17736,17736,17736,17736,17736,17736,MONDO:0016103,isolated asymptomatic elevation of creatine phosphokinase,MONDO,disease,DISEASE_17736
17737,17737,17737,17737,17737,17737,17737,17737,MONDO:1040010,IRF6-related condition,MONDO,disease,DISEASE_17737
17738,17738,17738,17738,17738,17738,17738,17738,MONDO:0019127,polymyositis,MONDO,disease,DISEASE_17738
17739,17739,17739,17739,17739,17739,17739,17739,MONDO:0004134,benign dermal neurilemmoma,MONDO,disease,DISEASE_17739
17740,17740,17740,17740,17740,17740,17740,17740,MONDO:0035551,cathepsin a-related arteriopathy-strokes-leukoencephalopathy,MONDO,disease,DISEASE_17740
17741,17741,17741,17741,17741,17741,17741,17741,MONDO:0021727,aberrant subclavian artery,MONDO,disease,DISEASE_17741
17742,17742,17742,17742,17742,17742,17742,17742,MONDO:0000295,acanthocephaliasis,MONDO,disease,DISEASE_17742
17743,17743,17743,17743,17743,17743,17743,17743,MONDO:0021066,urinary system neoplasm,MONDO,disease,DISEASE_17743
17744,17744,17744,17744,17744,17744,17744,17744,MONDO:0015171,congenital enterocyte heparan sulfate deficiency,MONDO,disease,DISEASE_17744
17745,17745,17745,17745,17745,17745,17745,17745,MONDO:0859050,"Schistosoma mansoni infection, susceptibility/resistance to",MONDO,disease,DISEASE_17745
17746,17746,17746,17746,17746,17746,17746,17746,MONDO:0024240,eccrine carcinoma,MONDO,disease,DISEASE_17746
17747,17747,17747,17747,17747,17747,17747,17747,MONDO:0016241_MONDO:0013900_MONDO:0007087,alternating hemiplegia of childhood,MONDO_grouped,disease,DISEASE_17747
17748,17748,17748,17748,17748,17748,17748,17748,MONDO:0004377,pancreatic non-functioning delta cell tumor,MONDO,disease,DISEASE_17748
17749,17749,17749,17749,17749,17749,17749,17749,MONDO:1011309,"connective tissue disorder, non-human animal",MONDO,disease,DISEASE_17749
17750,17750,17750,17750,17750,17750,17750,17750,MONDO:0100535,hypodontia/oligodontia with orofacial cleft,MONDO,disease,DISEASE_17750
17751,17751,17751,17751,17751,17751,17751,17751,MONDO:0011401,Alzheimer disease without neurofibrillary tangles,MONDO,disease,DISEASE_17751
17752,17752,17752,17752,17752,17752,17752,17752,MONDO:0025096,malignant catarrh,MONDO,disease,DISEASE_17752
17753,17753,17753,17753,17753,17753,17753,17753,MONDO:0010758,Wieacker-Wolff syndrome,MONDO,disease,DISEASE_17753
17754,17754,17754,17754,17754,17754,17754,17754,MONDO:0971031,auto-brewery syndrome,MONDO,disease,DISEASE_17754
17755,17755,17755,17755,17755,17755,17755,17755,MONDO:0005984,tinea pedis,MONDO,disease,DISEASE_17755
17756,17756,17756,17756,17756,17756,17756,17756,MONDO:0009515,Norum disease,MONDO,disease,DISEASE_17756
17757,17757,17757,17757,17757,17757,17757,17757,MONDO:0009767,"oculocerebral hypopigmentation syndrome, Cross type",MONDO,disease,DISEASE_17757
17758,17758,17758,17758,17758,17758,17758,17758,MONDO:0012999,guanidinoacetate methyltransferase deficiency,MONDO,disease,DISEASE_17758
17759,17759,17759,17759,17759,17759,17759,17759,MONDO:0021211,brain neoplasm,MONDO,disease,DISEASE_17759
17760,17760,17760,17760,17760,17760,17760,17760,MONDO:0850451_MONDO:0850452,"mixed phenotype acute leukemia, B/myeloid",MONDO_grouped,disease,DISEASE_17760
17761,17761,17761,17761,17761,17761,17761,17761,MONDO:0010958,"cardiac arrhythmia, ankyrin-B-related",MONDO,disease,DISEASE_17761
17762,17762,17762,17762,17762,17762,17762,17762,MONDO:0000166,"encephalopathy, acute, infection-induced",MONDO,disease,DISEASE_17762
17763,17763,17763,17763,17763,17763,17763,17763,MONDO:0015249,mitral atresia disorder,MONDO,disease,DISEASE_17763
17764,17764,17764,17764,17764,17764,17764,17764,MONDO:0002350,familial nephrotic syndrome,MONDO,disease,DISEASE_17764
17765,17765,17765,17765,17765,17765,17765,17765,MONDO:0100414_MONDO:0100417_MONDO:0100421_MONDO:0100422_MONDO:0100423_MONDO:0100424,"acute myeloid leukemia, CEBPA gene mutation",MONDO_grouped,disease,DISEASE_17765
17766,17766,17766,17766,17766,17766,17766,17766,MONDO:0007313,cheilitis glandularis,MONDO,disease,DISEASE_17766
17767,17767,17767,17767,17767,17767,17767,17767,MONDO:0032736,"metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression",MONDO,disease,DISEASE_17767
17768,17768,17768,17768,17768,17768,17768,17768,MONDO:0032746_MONDO:0032747_MONDO:0009273_MONDO:0013671,"hydatidiform mole, recurrent",MONDO_grouped,disease,DISEASE_17768
17769,17769,17769,17769,17769,17769,17769,17769,MONDO:0019416,X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome,MONDO,disease,DISEASE_17769
17770,17770,17770,17770,17770,17770,17770,17770,MONDO:0003783,lymphopenia,MONDO,disease,DISEASE_17770
17771,17771,17771,17771,17771,17771,17771,17771,MONDO:0010031,Sjogren-Larsson syndrome,MONDO,disease,DISEASE_17771
17772,17772,17772,17772,17772,17772,17772,17772,MONDO:0006534,cholinergic urticaria,MONDO,disease,DISEASE_17772
17773,17773,17773,17773,17773,17773,17773,17773,MONDO:0013849_MONDO:0012106_MONDO:0054716_MONDO:0013923_MONDO:0054593_MONDO:0014908_MONDO:0014623_MONDO:0030339_MONDO:0012989_MONDO:0054761_MONDO:0011488_MONDO:0012029_MONDO:0032694_MONDO:0032583_MONDO:0009617_MONDO:0859342_MONDO:0031060_MONDO:0054805_MONDO:0054806_MONDO:0014473_MONDO:0014730_MONDO:0014173_MONDO:0014660_MONDO:0054804_MONDO:0011437_MONDO:0014484,"microcephaly 8, primary, autosomal recessive",MONDO_grouped,disease,DISEASE_17773
17774,17774,17774,17774,17774,17774,17774,17774,MONDO:0004315,cholangiolocellular carcinoma,MONDO,disease,DISEASE_17774
17775,17775,17775,17775,17775,17775,17775,17775,MONDO:0006618,vibratory urticaria,MONDO,disease,DISEASE_17775
17776,17776,17776,17776,17776,17776,17776,17776,MONDO:0017048,pseudomyxoma peritonei,MONDO,disease,DISEASE_17776
17777,17777,17777,17777,17777,17777,17777,17777,MONDO:0100058_MONDO:0009385,hypervalinemia and hyperleucine-isoleucinemia,MONDO_grouped,disease,DISEASE_17777
17778,17778,17778,17778,17778,17778,17778,17778,MONDO:0006877,oophoritis,MONDO,disease,DISEASE_17778
17779,17779,17779,17779,17779,17779,17779,17779,MONDO:0020315,obsolete unclassified myelodysplastic syndrome,MONDO,disease,DISEASE_17779
17780,17780,17780,17780,17780,17780,17780,17780,MONDO:0016176_MONDO:0016171,axonal polyneuropathy associated with IgG/IgM/IgA monoclonal gammopathy,MONDO_grouped,disease,DISEASE_17780
17781,17781,17781,17781,17781,17781,17781,17781,MONDO:0009957,Reese retinal dysplasia,MONDO,disease,DISEASE_17781
17782,17782,17782,17782,17782,17782,17782,17782,MONDO:0000548,ovarian clear cell cancer,MONDO,disease,DISEASE_17782
17783,17783,17783,17783,17783,17783,17783,17783,MONDO:0013662,Barrett esophagus,MONDO,disease,DISEASE_17783
17784,17784,17784,17784,17784,17784,17784,17784,MONDO:0958237,isolated hyperferritinemia,MONDO,disease,DISEASE_17784
17785,17785,17785,17785,17785,17785,17785,17785,MONDO:0010621,CHILD syndrome,MONDO,disease,DISEASE_17785
17786,17786,17786,17786,17786,17786,17786,17786,MONDO:0013362,THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome,MONDO,disease,DISEASE_17786
17787,17787,17787,17787,17787,17787,17787,17787,MONDO:0060764_MONDO:0060732,tetraamelia syndrome,MONDO_grouped,disease,DISEASE_17787
17788,17788,17788,17788,17788,17788,17788,17788,MONDO:0957451,non-terminal myelocystocele,MONDO,disease,DISEASE_17788
17789,17789,17789,17789,17789,17789,17789,17789,MONDO:0008894,cataract-hypertrichosis-intellectual disability syndrome,MONDO,disease,DISEASE_17789
17790,17790,17790,17790,17790,17790,17790,17790,MONDO:0006144,cervical Wilms tumor,MONDO,disease,DISEASE_17790
17791,17791,17791,17791,17791,17791,17791,17791,MONDO:0024539_MONDO:0013151_MONDO:0013137,"choroidal dystrophy, central areolar",MONDO_grouped,disease,DISEASE_17791
17792,17792,17792,17792,17792,17792,17792,17792,MONDO:0002146_MONDO:1011119,hypogonadism,MONDO_grouped,disease,DISEASE_17792
17793,17793,17793,17793,17793,17793,17793,17793,MONDO:0004299,infiltrating bladder lymphoepithelioma-like carcinoma,MONDO,disease,DISEASE_17793
17794,17794,17794,17794,17794,17794,17794,17794,MONDO:0001439,episcleritis periodica fugax,MONDO,disease,DISEASE_17794
17795,17795,17795,17795,17795,17795,17795,17795,MONDO:0019427,"X-linked neurodegenerative syndrome, Bertini type",MONDO,disease,DISEASE_17795
17796,17796,17796,17796,17796,17796,17796,17796,MONDO:0968976,neurodevelopmental disorder with progressive movement abnormalities,MONDO,disease,DISEASE_17796
17797,17797,17797,17797,17797,17797,17797,17797,MONDO:0019874,distal trisomy 7p,MONDO,disease,DISEASE_17797
17798,17798,17798,17798,17798,17798,17798,17798,MONDO:0700010,chromosome 3 disorder,MONDO,disease,DISEASE_17798
17799,17799,17799,17799,17799,17799,17799,17799,MONDO:0004822,bronchiectasis,MONDO,disease,DISEASE_17799
17800,17800,17800,17800,17800,17800,17800,17800,MONDO:0007621,Floating-Harbor syndrome,MONDO,disease,DISEASE_17800
17801,17801,17801,17801,17801,17801,17801,17801,MONDO:0006791,hyperemesis gravidarum,MONDO,disease,DISEASE_17801
17802,17802,17802,17802,17802,17802,17802,17802,MONDO:0958332,"neuromuscular disorder, congenital, with dysmorphic facies",MONDO,disease,DISEASE_17802
17803,17803,17803,17803,17803,17803,17803,17803,MONDO:0009765,ocular myopathy with curare sensitivity,MONDO,disease,DISEASE_17803
17804,17804,17804,17804,17804,17804,17804,17804,MONDO:0004102,columnar cell variant thyroid gland papillary carcinoma,MONDO,disease,DISEASE_17804
17805,17805,17805,17805,17805,17805,17805,17805,MONDO:0019154,androgen insensitivity syndrome,MONDO,disease,DISEASE_17805
17806,17806,17806,17806,17806,17806,17806,17806,MONDO:0009880,short stature-pituitary and cerebellar defects-small sella turcica syndrome,MONDO,disease,DISEASE_17806
17807,17807,17807,17807,17807,17807,17807,17807,MONDO:0007795,mullerian duct anomalies-limb anomalies syndrome,MONDO,disease,DISEASE_17807
17808,17808,17808,17808,17808,17808,17808,17808,MONDO:1011684,"alloimmune hemolytic anemia of the newborn, non-human animal",MONDO,disease,DISEASE_17808
17809,17809,17809,17809,17809,17809,17809,17809,MONDO:0009782,ophthalmoplegia totalis with ptosis and miosis,MONDO,disease,DISEASE_17809
17810,17810,17810,17810,17810,17810,17810,17810,MONDO:0013308_MONDO:0800465,CBL-related disorder,MONDO_grouped,disease,DISEASE_17810
17811,17811,17811,17811,17811,17811,17811,17811,MONDO:0002469,lacrimal gland carcinoma ex pleomorphic adenoma,MONDO,disease,DISEASE_17811
17812,17812,17812,17812,17812,17812,17812,17812,MONDO:1012857_MONDO:1012858,"pituitary dwarfism, LHX3-related, dog",MONDO_grouped,disease,DISEASE_17812
17813,17813,17813,17813,17813,17813,17813,17813,MONDO:1010628,"Chediak-Higashi syndrome, Arctic fox",MONDO,disease,DISEASE_17813
17814,17814,17814,17814,17814,17814,17814,17814,MONDO:0859219,Rauch-Steindl syndrome,MONDO,disease,DISEASE_17814
17815,17815,17815,17815,17815,17815,17815,17815,MONDO:0009483,Kapur-Toriello syndrome,MONDO,disease,DISEASE_17815
17816,17816,17816,17816,17816,17816,17816,17816,MONDO:0005348,keloid,MONDO,disease,DISEASE_17816
17817,17817,17817,17817,17817,17817,17817,17817,MONDO:0004905,intestinal disaccharidase deficiency,MONDO,disease,DISEASE_17817
17818,17818,17818,17818,17818,17818,17818,17818,MONDO:0016782,paternal 14q32.2 hypomethylation syndrome,MONDO,disease,DISEASE_17818
17819,17819,17819,17819,17819,17819,17819,17819,MONDO:0100183,"radioulnar synostosis, nonsyndromic, susceptibility to",MONDO,disease,DISEASE_17819
17820,17820,17820,17820,17820,17820,17820,17820,MONDO:0007955_MONDO:0000954_MONDO:0004551_MONDO:1010541,Meckel diverticulum,MONDO_grouped,disease,DISEASE_17820
17821,17821,17821,17821,17821,17821,17821,17821,MONDO:0014358,AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome,MONDO,disease,DISEASE_17821
17822,17822,17822,17822,17822,17822,17822,17822,MONDO:0001420,trigeminal nerve neoplasm,MONDO,disease,DISEASE_17822
17823,17823,17823,17823,17823,17823,17823,17823,MONDO:0011043,"myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay",MONDO,disease,DISEASE_17823
17824,17824,17824,17824,17824,17824,17824,17824,MONDO:0006170,conjunctival disorder,MONDO,disease,DISEASE_17824
17825,17825,17825,17825,17825,17825,17825,17825,MONDO:0003876,eyelid carcinoma,MONDO,disease,DISEASE_17825
17826,17826,17826,17826,17826,17826,17826,17826,MONDO:0011271,rigid spine muscular dystrophy 1,MONDO,disease,DISEASE_17826
17827,17827,17827,17827,17827,17827,17827,17827,MONDO:0016696,anaplastic oligodendroglioma,MONDO,disease,DISEASE_17827
17828,17828,17828,17828,17828,17828,17828,17828,MONDO:0001579,corneal staphyloma,MONDO,disease,DISEASE_17828
17829,17829,17829,17829,17829,17829,17829,17829,MONDO:0008993,cleft palate-stapes fixation-oligodontia syndrome,MONDO,disease,DISEASE_17829
17830,17830,17830,17830,17830,17830,17830,17830,MONDO:0009307,granulomatous disease with defect in neutrophil chemotaxis,MONDO,disease,DISEASE_17830
17831,17831,17831,17831,17831,17831,17831,17831,MONDO:0019702,neonatal osteosclerotic dysplasia,MONDO,disease,DISEASE_17831
17832,17832,17832,17832,17832,17832,17832,17832,MONDO:0018769,isosporiasis,MONDO,disease,DISEASE_17832
17833,17833,17833,17833,17833,17833,17833,17833,MONDO:0017700,"glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form",MONDO,disease,DISEASE_17833
17834,17834,17834,17834,17834,17834,17834,17834,MONDO:0800475,"NACC1-related neurodevelopmental disorder with epilepsy, cataracts and episodic irritability",MONDO,disease,DISEASE_17834
17835,17835,17835,17835,17835,17835,17835,17835,MONDO:0018131,neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion,MONDO,disease,DISEASE_17835
17836,17836,17836,17836,17836,17836,17836,17836,MONDO:0014529,cerebellar-facial-dental syndrome,MONDO,disease,DISEASE_17836
17837,17837,17837,17837,17837,17837,17837,17837,MONDO:0003708,extrahepatic bile duct small cell adenocarcinoma,MONDO,disease,DISEASE_17837
17838,17838,17838,17838,17838,17838,17838,17838,MONDO:0005850,milker's nodule,MONDO,disease,DISEASE_17838
17839,17839,17839,17839,17839,17839,17839,17839,MONDO:0014500,atrial conduction disease,MONDO,disease,DISEASE_17839
17840,17840,17840,17840,17840,17840,17840,17840,MONDO:0022465,anotia facial palsy cardiac defect,MONDO,disease,DISEASE_17840
17841,17841,17841,17841,17841,17841,17841,17841,MONDO:0023111,familial capillaro-venous leptomeningeal angiomatosis,MONDO,disease,DISEASE_17841
17842,17842,17842,17842,17842,17842,17842,17842,MONDO:1012101,"hemolytic uremic syndrome, cattle",MONDO,disease,DISEASE_17842
17843,17843,17843,17843,17843,17843,17843,17843,MONDO:0002256,cervix disorder,MONDO,disease,DISEASE_17843
17844,17844,17844,17844,17844,17844,17844,17844,MONDO:0018234,dysostosis,MONDO,disease,DISEASE_17844
17845,17845,17845,17845,17845,17845,17845,17845,MONDO:0957218,"neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities",MONDO,disease,DISEASE_17845
17846,17846,17846,17846,17846,17846,17846,17846,MONDO:0002872,trophoblastic neoplasm,MONDO,disease,DISEASE_17846
17847,17847,17847,17847,17847,17847,17847,17847,MONDO:0008905,predisposition to invasive fungal disease due to CARD9 deficiency,MONDO,disease,DISEASE_17847
17848,17848,17848,17848,17848,17848,17848,17848,MONDO:0007097,Finnish type amyloidosis,MONDO,disease,DISEASE_17848
17849,17849,17849,17849,17849,17849,17849,17849,MONDO:0010838,gonadal agenesis,MONDO,disease,DISEASE_17849
17850,17850,17850,17850,17850,17850,17850,17850,MONDO:0002169,rectum adenocarcinoma,MONDO,disease,DISEASE_17850
17851,17851,17851,17851,17851,17851,17851,17851,MONDO:0000534,trachea mucoepidermoid carcinoma,MONDO,disease,DISEASE_17851
17852,17852,17852,17852,17852,17852,17852,17852,MONDO:1012696,"multifocal symmetrical necrotizing encephalomyelopathy, Angus cattle",MONDO,disease,DISEASE_17852
17853,17853,17853,17853,17853,17853,17853,17853,MONDO:1011452,"intervertebral disc disease, non-human animal",MONDO,disease,DISEASE_17853
17854,17854,17854,17854,17854,17854,17854,17854,MONDO:0008333,"pseudoxanthoma elasticum, forme fruste",MONDO,disease,DISEASE_17854
17855,17855,17855,17855,17855,17855,17855,17855,MONDO:0021493,benign neoplasm of minor salivary gland,MONDO,disease,DISEASE_17855
17856,17856,17856,17856,17856,17856,17856,17856,MONDO:0005811,infectious myxomatosis,MONDO,disease,DISEASE_17856
17857,17857,17857,17857,17857,17857,17857,17857,MONDO:1011617,"Waardenburg syndrome, domestic cat",MONDO,disease,DISEASE_17857
17858,17858,17858,17858,17858,17858,17858,17858,MONDO:0004379,female breast carcinoma,MONDO,disease,DISEASE_17858
17859,17859,17859,17859,17859,17859,17859,17859,MONDO:0016051,cleft lip-retinopathy syndrome,MONDO,disease,DISEASE_17859
17860,17860,17860,17860,17860,17860,17860,17860,MONDO:0002193,Bartholin gland benign neoplasm,MONDO,disease,DISEASE_17860
17861,17861,17861,17861,17861,17861,17861,17861,MONDO:1012739,"xanthinuria, type II, dog",MONDO,disease,DISEASE_17861
17862,17862,17862,17862,17862,17862,17862,17862,MONDO:1012532,"calvarial hyperostotic syndrome, dog",MONDO,disease,DISEASE_17862
17863,17863,17863,17863,17863,17863,17863,17863,MONDO:0018321,atypical juvenile parkinsonism,MONDO,disease,DISEASE_17863
17864,17864,17864,17864,17864,17864,17864,17864,MONDO:0010870,tibial muscular dystrophy,MONDO,disease,DISEASE_17864
17865,17865,17865,17865,17865,17865,17865,17865,MONDO:0044033,posterior leukoencephalopathy syndrome,MONDO,disease,DISEASE_17865
17866,17866,17866,17866,17866,17866,17866,17866,MONDO:0002326_MONDO:0001423,alcohol-induced mental disorder,MONDO_grouped,disease,DISEASE_17866
17867,17867,17867,17867,17867,17867,17867,17867,MONDO:0015151,"muscular dystrophy, limb-girdle, autosomal dominant",MONDO,disease,DISEASE_17867
17868,17868,17868,17868,17868,17868,17868,17868,MONDO:0020721_MONDO:0010524,X-linked sideroblastic anemia 1,MONDO_grouped,disease,DISEASE_17868
17869,17869,17869,17869,17869,17869,17869,17869,MONDO:1011747,"recessive hypotrichosis, non-human animal",MONDO,disease,DISEASE_17869
17870,17870,17870,17870,17870,17870,17870,17870,MONDO:1010238_MONDO:1011897,"leukodystrophy, non-human animal",MONDO_grouped,disease,DISEASE_17870
17871,17871,17871,17871,17871,17871,17871,17871,MONDO:0019356,urogenital tract malformation,MONDO,disease,DISEASE_17871
17872,17872,17872,17872,17872,17872,17872,17872,MONDO:0014677_MONDO:0009875_MONDO:0009003_MONDO:0013465_MONDO:0018852_MONDO:0800196_MONDO:0800197,achromatopsia,MONDO_grouped,disease,DISEASE_17872
17873,17873,17873,17873,17873,17873,17873,17873,MONDO:0100144,Uner Tan Syndrome,MONDO,disease,DISEASE_17873
17874,17874,17874,17874,17874,17874,17874,17874,MONDO:0009798,Primrose syndrome,MONDO,disease,DISEASE_17874
17875,17875,17875,17875,17875,17875,17875,17875,MONDO:0024478_MONDO:0018308,mesenchymal hamartoma,MONDO_grouped,disease,DISEASE_17875
17876,17876,17876,17876,17876,17876,17876,17876,MONDO:0016364,Joubert syndrome with ocular defect,MONDO,disease,DISEASE_17876
17877,17877,17877,17877,17877,17877,17877,17877,MONDO:0008957,"cervical vertebrae, agenesis of",MONDO,disease,DISEASE_17877
17878,17878,17878,17878,17878,17878,17878,17878,MONDO:0100082_MONDO:0012691_MONDO:0013380,LEOPARD syndrome,MONDO_grouped,disease,DISEASE_17878
17879,17879,17879,17879,17879,17879,17879,17879,MONDO:0019296,subcutaneous tissue disorder,MONDO,disease,DISEASE_17879
17880,17880,17880,17880,17880,17880,17880,17880,MONDO:0006004,vasomotor rhinitis,MONDO,disease,DISEASE_17880
17881,17881,17881,17881,17881,17881,17881,17881,MONDO:0018024,hydroa vacciniforme,MONDO,disease,DISEASE_17881
17882,17882,17882,17882,17882,17882,17882,17882,MONDO:0016466,asbestosis,MONDO,disease,DISEASE_17882
17883,17883,17883,17883,17883,17883,17883,17883,MONDO:0100330,disease arising from reactivation of latent virus,MONDO,disease,DISEASE_17883
17884,17884,17884,17884,17884,17884,17884,17884,MONDO:0022859,cor biloculare,MONDO,disease,DISEASE_17884
17885,17885,17885,17885,17885,17885,17885,17885,MONDO:0008788,IRIDA syndrome,MONDO,disease,DISEASE_17885
17886,17886,17886,17886,17886,17886,17886,17886,MONDO:0018905,diffuse large B-cell lymphoma,MONDO,disease,DISEASE_17886
17887,17887,17887,17887,17887,17887,17887,17887,MONDO:0007853,palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome,MONDO,disease,DISEASE_17887
17888,17888,17888,17888,17888,17888,17888,17888,MONDO:0100124,NAA10-related syndrome,MONDO,disease,DISEASE_17888
17889,17889,17889,17889,17889,17889,17889,17889,MONDO:0011655,alveolar soft part sarcoma,MONDO,disease,DISEASE_17889
17890,17890,17890,17890,17890,17890,17890,17890,MONDO:0008318,Proteus syndrome,MONDO,disease,DISEASE_17890
17891,17891,17891,17891,17891,17891,17891,17891,MONDO:0009342,Hirschsprung disease-hearing loss-polydactyly syndrome,MONDO,disease,DISEASE_17891
17892,17892,17892,17892,17892,17892,17892,17892,MONDO:0021386,neoplasm of mediastinum,MONDO,disease,DISEASE_17892
17893,17893,17893,17893,17893,17893,17893,17893,MONDO:1012128,"immunoglobulin 7S deficiency, chicken",MONDO,disease,DISEASE_17893
17894,17894,17894,17894,17894,17894,17894,17894,MONDO:1011809,"multiple lipomatosis, non-human animal",MONDO,disease,DISEASE_17894
17895,17895,17895,17895,17895,17895,17895,17895,MONDO:0015634,isolated osteopoikilosis,MONDO,disease,DISEASE_17895
17896,17896,17896,17896,17896,17896,17896,17896,MONDO:0012137,Carney complex - trismus - pseudocamptodactyly syndrome,MONDO,disease,DISEASE_17896
17897,17897,17897,17897,17897,17897,17897,17897,MONDO:0044921,atypical lymphoproliferative disorder,MONDO,disease,DISEASE_17897
17898,17898,17898,17898,17898,17898,17898,17898,MONDO:0008430,skeletal dysplasia with delayed epiphyseal and carpal bone ossification,MONDO,disease,DISEASE_17898
17899,17899,17899,17899,17899,17899,17899,17899,MONDO:0022825,congenital cystic eye,MONDO,disease,DISEASE_17899
17900,17900,17900,17900,17900,17900,17900,17900,MONDO:0018898,primary cutaneous lymphoma,MONDO,disease,DISEASE_17900
17901,17901,17901,17901,17901,17901,17901,17901,MONDO:0020563,dedifferentiated liposarcoma,MONDO,disease,DISEASE_17901
17902,17902,17902,17902,17902,17902,17902,17902,MONDO:0002874,testicular pure germ cell tumor,MONDO,disease,DISEASE_17902
17903,17903,17903,17903,17903,17903,17903,17903,MONDO:0010685_MONDO:0010377,"myopia 1, X-linked",MONDO_grouped,disease,DISEASE_17903
17904,17904,17904,17904,17904,17904,17904,17904,MONDO:0060671_MONDO:0012655_MONDO:0013665_MONDO:0012134_MONDO:0020752_MONDO:0800271,"epilepsy, juvenile myoclonic, susceptibility to",MONDO_grouped,disease,DISEASE_17904
17905,17905,17905,17905,17905,17905,17905,17905,MONDO:1011479_MONDO:1011480,"Becker type muscular dystrophy, dog",MONDO_grouped,disease,DISEASE_17905
17906,17906,17906,17906,17906,17906,17906,17906,MONDO:0019197,folinic acid-responsive seizures,MONDO,disease,DISEASE_17906
17907,17907,17907,17907,17907,17907,17907,17907,MONDO:0015726,distal trisomy 14q,MONDO,disease,DISEASE_17907
17908,17908,17908,17908,17908,17908,17908,17908,MONDO:0006909,pituitary dwarfism,MONDO,disease,DISEASE_17908
17909,17909,17909,17909,17909,17909,17909,17909,MONDO:1012198,"ocular squamous cell carcinoma, goat",MONDO,disease,DISEASE_17909
17910,17910,17910,17910,17910,17910,17910,17910,MONDO:0005002,chronic obstructive pulmonary disease,MONDO,disease,DISEASE_17910
17911,17911,17911,17911,17911,17911,17911,17911,MONDO:0021453,benign neoplasm of retina,MONDO,disease,DISEASE_17911
17912,17912,17912,17912,17912,17912,17912,17912,MONDO:0002834,primary prostate urothelial carcinoma,MONDO,disease,DISEASE_17912
17913,17913,17913,17913,17913,17913,17913,17913,MONDO:0031001,vitreoretinopathy with phalangeal epiphyseal dysplasia,MONDO,disease,DISEASE_17913
17914,17914,17914,17914,17914,17914,17914,17914,MONDO:0018756,euthyroid Graves orbitopathy,MONDO,disease,DISEASE_17914
17915,17915,17915,17915,17915,17915,17915,17915,MONDO:0012714,early-onset myopathy with fatal cardiomyopathy,MONDO,disease,DISEASE_17915
17916,17916,17916,17916,17916,17916,17916,17916,MONDO:0002331_MONDO:0850149,nephrosis,MONDO_grouped,disease,DISEASE_17916
17917,17917,17917,17917,17917,17917,17917,17917,MONDO:0020359,congenital symblepharon,MONDO,disease,DISEASE_17917
17918,17918,17918,17918,17918,17918,17918,17918,MONDO:0004768_MONDO:0025431,keratoconjunctivitis,MONDO_grouped,disease,DISEASE_17918
17919,17919,17919,17919,17919,17919,17919,17919,MONDO:1011740,"primary seborrhea-oleosa, non-human animal",MONDO,disease,DISEASE_17919
17920,17920,17920,17920,17920,17920,17920,17920,MONDO:0009374,hydroxyprolinemia,MONDO,disease,DISEASE_17920
17921,17921,17921,17921,17921,17921,17921,17921,MONDO:1012387,"juvenile with age-dependent emphysema hypotrichosis, pig",MONDO,disease,DISEASE_17921
17922,17922,17922,17922,17922,17922,17922,17922,MONDO:0024479,epithelial tumor of colon,MONDO,disease,DISEASE_17922
17923,17923,17923,17923,17923,17923,17923,17923,MONDO:0001608,vagus nerve neoplasm,MONDO,disease,DISEASE_17923
17924,17924,17924,17924,17924,17924,17924,17924,MONDO:0005645,ancylostomiasis,MONDO,disease,DISEASE_17924
17925,17925,17925,17925,17925,17925,17925,17925,MONDO:0004410,sarcomatoid penile squamous cell carcinoma,MONDO,disease,DISEASE_17925
17926,17926,17926,17926,17926,17926,17926,17926,MONDO:0003356,epithelioid leiomyosarcoma,MONDO,disease,DISEASE_17926
17927,17927,17927,17927,17927,17927,17927,17927,MONDO:0013746_MONDO:0013748_MONDO:0013749_MONDO:0002070_MONDO:1010486_MONDO:1010487_MONDO:1010488_MONDO:1010489_MONDO:1010491_MONDO:1010492_MONDO:1010493_MONDO:1010494_MONDO:1010495,ventricular septal defect,MONDO_grouped,disease,DISEASE_17927
17928,17928,17928,17928,17928,17928,17928,17928,MONDO:1012404,"invasive transitional cell carcinoma, dog",MONDO,disease,DISEASE_17928
17929,17929,17929,17929,17929,17929,17929,17929,MONDO:0004876,myocardial stunning,MONDO,disease,DISEASE_17929
17930,17930,17930,17930,17930,17930,17930,17930,MONDO:0003173,brain stem astrocytic neoplasm,MONDO,disease,DISEASE_17930
17931,17931,17931,17931,17931,17931,17931,17931,MONDO:0016153,qualitative or quantitative defects of TRIM32,MONDO,disease,DISEASE_17931
17932,17932,17932,17932,17932,17932,17932,17932,MONDO:0008882,congenital bowing of long bones,MONDO,disease,DISEASE_17932
17933,17933,17933,17933,17933,17933,17933,17933,MONDO:0008690,"xeroderma pigmentosum, autosomal dominant, mild",MONDO,disease,DISEASE_17933
17934,17934,17934,17934,17934,17934,17934,17934,MONDO:0001135,voyeurism,MONDO,disease,DISEASE_17934
17935,17935,17935,17935,17935,17935,17935,17935,MONDO:0010857,semantic dementia,MONDO,disease,DISEASE_17935
17936,17936,17936,17936,17936,17936,17936,17936,MONDO:0017475_MONDO:0017474,macrodactyly of toes,MONDO_grouped,disease,DISEASE_17936
17937,17937,17937,17937,17937,17937,17937,17937,MONDO:0020496,familial porencephaly,MONDO,disease,DISEASE_17937
17938,17938,17938,17938,17938,17938,17938,17938,MONDO:0005628,male breast carcinoma,MONDO,disease,DISEASE_17938
17939,17939,17939,17939,17939,17939,17939,17939,MONDO:0008435,"Somatomedin, embryonic",MONDO,disease,DISEASE_17939
17940,17940,17940,17940,17940,17940,17940,17940,MONDO:0006590,palmoplantar keratosis,MONDO,disease,DISEASE_17940
17941,17941,17941,17941,17941,17941,17941,17941,MONDO:0018370,KLHL9-related early-onset distal myopathy,MONDO,disease,DISEASE_17941
17942,17942,17942,17942,17942,17942,17942,17942,MONDO:0001413,ulceroglandular tularemia,MONDO,disease,DISEASE_17942
17943,17943,17943,17943,17943,17943,17943,17943,MONDO:0016047_MONDO:0006884_MONDO:0017202_MONDO:0017203,endophthalmitis,MONDO_grouped,disease,DISEASE_17943
17944,17944,17944,17944,17944,17944,17944,17944,MONDO:0006486_MONDO:0004561,uveal melanoma,MONDO_grouped,disease,DISEASE_17944
17945,17945,17945,17945,17945,17945,17945,17945,MONDO:0005855,molluscum contagiosum,MONDO,disease,DISEASE_17945
17946,17946,17946,17946,17946,17946,17946,17946,MONDO:0002297,epidermal appendage tumor,MONDO,disease,DISEASE_17946
17947,17947,17947,17947,17947,17947,17947,17947,MONDO:0017722_MONDO:0017723_MONDO:0017721,"Sandhoff disease, juvenile form",MONDO_grouped,disease,DISEASE_17947
17948,17948,17948,17948,17948,17948,17948,17948,MONDO:0001318,functional gastric disease,MONDO,disease,DISEASE_17948
17949,17949,17949,17949,17949,17949,17949,17949,MONDO:0100308,atactic disorder,MONDO,disease,DISEASE_17949
17950,17950,17950,17950,17950,17950,17950,17950,MONDO:0044727,pancreatic carcinoma with mixed differentiation,MONDO,disease,DISEASE_17950
17951,17951,17951,17951,17951,17951,17951,17951,MONDO:0011166,lymphedema-atrial septal defects-facial changes syndrome,MONDO,disease,DISEASE_17951
17952,17952,17952,17952,17952,17952,17952,17952,MONDO:0022682,cennamo gangemi syndrome,MONDO,disease,DISEASE_17952
17953,17953,17953,17953,17953,17953,17953,17953,MONDO:0018908,non-Hodgkin lymphoma,MONDO,disease,DISEASE_17953
17954,17954,17954,17954,17954,17954,17954,17954,MONDO:0035500,congenital primary lymphedema of Gordon,MONDO,disease,DISEASE_17954
17955,17955,17955,17955,17955,17955,17955,17955,MONDO:0800375_MONDO:0800376,"developmental delay, epilepsy, and neonatal diabetes",MONDO_grouped,disease,DISEASE_17955
17956,17956,17956,17956,17956,17956,17956,17956,MONDO:0021948,cutaneous tuberculosis,MONDO,disease,DISEASE_17956
17957,17957,17957,17957,17957,17957,17957,17957,MONDO:0024988,sex cord-stromal benign neoplasm,MONDO,disease,DISEASE_17957
17958,17958,17958,17958,17958,17958,17958,17958,MONDO:0019570_MONDO:0019569_MONDO:0016006_MONDO:0008998,Cockayne syndrome,MONDO_grouped,disease,DISEASE_17958
17959,17959,17959,17959,17959,17959,17959,17959,MONDO:0010560,"cleft palate with or without ankyloglossia, X-linked",MONDO,disease,DISEASE_17959
17960,17960,17960,17960,17960,17960,17960,17960,MONDO:0043905_MONDO:0002572_MONDO:0001255_MONDO:0003479_MONDO:0043919,pneumonitis,MONDO_grouped,disease,DISEASE_17960
17961,17961,17961,17961,17961,17961,17961,17961,MONDO:0013283_MONDO:0013862_MONDO:0013286_MONDO:0013285_MONDO:0011864_MONDO:0958013_MONDO:0013284_MONDO:0014697_MONDO:0009413_MONDO:0054691_MONDO:0014260_MONDO:1010740,"immunodeficiency, common variable",MONDO_grouped,disease,DISEASE_17961
17962,17962,17962,17962,17962,17962,17962,17962,MONDO:0010125,upper limb defect-eye and ear abnormalities syndrome,MONDO,disease,DISEASE_17962
17963,17963,17963,17963,17963,17963,17963,17963,MONDO:0023154,fibromatosis multiple non ossifying,MONDO,disease,DISEASE_17963
17964,17964,17964,17964,17964,17964,17964,17964,MONDO:0957813,"spastic paraplegia 91, autosomal dominant, with or without cerebellar ataxia",MONDO,disease,DISEASE_17964
17965,17965,17965,17965,17965,17965,17965,17965,MONDO:0021350,neoplasm of thorax,MONDO,disease,DISEASE_17965
17966,17966,17966,17966,17966,17966,17966,17966,MONDO:1010714,"multiple acyl-CoA dehydrogenase deficiency, domestic cat",MONDO,disease,DISEASE_17966
17967,17967,17967,17967,17967,17967,17967,17967,MONDO:0100509,IFT140-related recessive ciliopathy,MONDO,disease,DISEASE_17967
17968,17968,17968,17968,17968,17968,17968,17968,MONDO:0010082,subaortic stenosis-short stature syndrome,MONDO,disease,DISEASE_17968
17969,17969,17969,17969,17969,17969,17969,17969,MONDO:1012233,"quaking, golden hamster",MONDO,disease,DISEASE_17969
17970,17970,17970,17970,17970,17970,17970,17970,MONDO:0024886_MONDO:0005182,serous adenofibroma,MONDO_grouped,disease,DISEASE_17970
17971,17971,17971,17971,17971,17971,17971,17971,MONDO:1011867,"neuronal abiotrophy, non-human animal",MONDO,disease,DISEASE_17971
17972,17972,17972,17972,17972,17972,17972,17972,MONDO:0013898,karyomegalic interstitial nephritis,MONDO,disease,DISEASE_17972
17973,17973,17973,17973,17973,17973,17973,17973,MONDO:0021465,benign neoplasm of appendix,MONDO,disease,DISEASE_17973
17974,17974,17974,17974,17974,17974,17974,17974,MONDO:0001050,malignant otitis externa,MONDO,disease,DISEASE_17974
17975,17975,17975,17975,17975,17975,17975,17975,MONDO:0009219,"fascial dystrophy, congenital",MONDO,disease,DISEASE_17975
17976,17976,17976,17976,17976,17976,17976,17976,MONDO:0009548,renal hypomagnesemia 5 with ocular involvement,MONDO,disease,DISEASE_17976
17977,17977,17977,17977,17977,17977,17977,17977,MONDO:0031010,odontochondrodysplasia 2 with hearing loss and diabetes,MONDO,disease,DISEASE_17977
17978,17978,17978,17978,17978,17978,17978,17978,MONDO:0022453,angiomyomatous hamartoma,MONDO,disease,DISEASE_17978
17979,17979,17979,17979,17979,17979,17979,17979,MONDO:0007230,Brachymorphism-onychodysplasia-dysphalangism syndrome,MONDO,disease,DISEASE_17979
17980,17980,17980,17980,17980,17980,17980,17980,MONDO:0013232,"brachydactylous dwarfism, Mseleni type",MONDO,disease,DISEASE_17980
17981,17981,17981,17981,17981,17981,17981,17981,MONDO:0002261,keratopathy,MONDO,disease,DISEASE_17981
17982,17982,17982,17982,17982,17982,17982,17982,MONDO:0001108,broad ligament malignant neoplasm,MONDO,disease,DISEASE_17982
17983,17983,17983,17983,17983,17983,17983,17983,MONDO:0005102_MONDO:0020661,undifferentiated (embryonal) sarcoma,MONDO_grouped,disease,DISEASE_17983
17984,17984,17984,17984,17984,17984,17984,17984,MONDO:0001851_MONDO:0002124,primary lacrimal atrophy,MONDO_grouped,disease,DISEASE_17984
17985,17985,17985,17985,17985,17985,17985,17985,MONDO:0700026,chromosome 22 disorder,MONDO,disease,DISEASE_17985
17986,17986,17986,17986,17986,17986,17986,17986,MONDO:1010104,"trimethylaminuria (fishy taint), non-human animal",MONDO,disease,DISEASE_17986
17987,17987,17987,17987,17987,17987,17987,17987,MONDO:0020445,agenesis of the superior vena cava,MONDO,disease,DISEASE_17987
17988,17988,17988,17988,17988,17988,17988,17988,MONDO:0011041,"ectodermal dysplasia with natal teeth, Turnpenny type",MONDO,disease,DISEASE_17988
17989,17989,17989,17989,17989,17989,17989,17989,MONDO:0007839,Aase-Smith syndrome,MONDO,disease,DISEASE_17989
17990,17990,17990,17990,17990,17990,17990,17990,MONDO:0005520,rickets,MONDO,disease,DISEASE_17990
17991,17991,17991,17991,17991,17991,17991,17991,MONDO:0017439,tetra-amelia,MONDO,disease,DISEASE_17991
17992,17992,17992,17992,17992,17992,17992,17992,MONDO:1012161,"cutaneous malignant melanoma in Sinclair swine, pig",MONDO,disease,DISEASE_17992
17993,17993,17993,17993,17993,17993,17993,17993,MONDO:1011539_MONDO:1011540,"hypokalaemic periodic paralysis, domestic cat",MONDO_grouped,disease,DISEASE_17993
17994,17994,17994,17994,17994,17994,17994,17994,MONDO:1012121_MONDO:1012122,"primary hypothyroidism, dog",MONDO_grouped,disease,DISEASE_17994
17995,17995,17995,17995,17995,17995,17995,17995,MONDO:0009088,"deafness, neural, with atypical atopic dermatitis",MONDO,disease,DISEASE_17995
17996,17996,17996,17996,17996,17996,17996,17996,MONDO:0005871,Nematoda infectious disease,MONDO,disease,DISEASE_17996
17997,17997,17997,17997,17997,17997,17997,17997,MONDO:0008779,arthrogryposis,MONDO,disease,DISEASE_17997
17998,17998,17998,17998,17998,17998,17998,17998,MONDO:0008242,"photomyoclonus, diabetes mellitus, deafness, nephropathy, and cerebral dysfunction",MONDO,disease,DISEASE_17998
17999,17999,17999,17999,17999,17999,17999,17999,MONDO:0014478_MONDO:0032641_MONDO:0008002_MONDO:0013790,mirror movements,MONDO_grouped,disease,DISEASE_17999
18000,18000,18000,18000,18000,18000,18000,18000,MONDO:0000840,dysbaric osteonecrosis,MONDO,disease,DISEASE_18000
18001,18001,18001,18001,18001,18001,18001,18001,MONDO:0010677,"muscular dystrophy, Mabry type",MONDO,disease,DISEASE_18001
18002,18002,18002,18002,18002,18002,18002,18002,MONDO:0018695,avian influenza,MONDO,disease,DISEASE_18002
18003,18003,18003,18003,18003,18003,18003,18003,MONDO:0000331,Rickettsia helvetica spotted fever,MONDO,disease,DISEASE_18003
18004,18004,18004,18004,18004,18004,18004,18004,MONDO:0017642,intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome,MONDO,disease,DISEASE_18004
18005,18005,18005,18005,18005,18005,18005,18005,MONDO:0033555,immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia,MONDO,disease,DISEASE_18005
18006,18006,18006,18006,18006,18006,18006,18006,MONDO:0019010,congenital isolated hyperinsulinism,MONDO,disease,DISEASE_18006
18007,18007,18007,18007,18007,18007,18007,18007,MONDO:0011454,patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome,MONDO,disease,DISEASE_18007
18008,18008,18008,18008,18008,18008,18008,18008,MONDO:0003002,dysgerminoma,MONDO,disease,DISEASE_18008
18009,18009,18009,18009,18009,18009,18009,18009,MONDO:0800357,"hyperpigmentation, progressive cribriform and zosteriform",MONDO,disease,DISEASE_18009
18010,18010,18010,18010,18010,18010,18010,18010,MONDO:0009685,Miyoshi myopathy,MONDO,disease,DISEASE_18010
18011,18011,18011,18011,18011,18011,18011,18011,MONDO:0001398,ureter benign neoplasm,MONDO,disease,DISEASE_18011
18012,18012,18012,18012,18012,18012,18012,18012,MONDO:0015536,papular xanthoma,MONDO,disease,DISEASE_18012
18013,18013,18013,18013,18013,18013,18013,18013,MONDO:0019395,Hinman syndrome,MONDO,disease,DISEASE_18013
18014,18014,18014,18014,18014,18014,18014,18014,MONDO:0004843,pathologic nystagmus,MONDO,disease,DISEASE_18014
18015,18015,18015,18015,18015,18015,18015,18015,MONDO:1011160_MONDO:1011161,"osteoarthritis, dog",MONDO_grouped,disease,DISEASE_18015
18016,18016,18016,18016,18016,18016,18016,18016,MONDO:0003159,vascular hemostatic disease,MONDO,disease,DISEASE_18016
18017,18017,18017,18017,18017,18017,18017,18017,MONDO:0015838,cordiform uterus,MONDO,disease,DISEASE_18017
18018,18018,18018,18018,18018,18018,18018,18018,MONDO:0020772,"epilepsy, juvenile absence, susceptibility to, 1",MONDO,disease,DISEASE_18018
18019,18019,18019,18019,18019,18019,18019,18019,MONDO:0700338,"autoinflammation, panniculitis, and dermatosis syndrome, autosomal dominant",MONDO,disease,DISEASE_18019
18020,18020,18020,18020,18020,18020,18020,18020,MONDO:0016776,frontal fibrosing alopecia,MONDO,disease,DISEASE_18020
18021,18021,18021,18021,18021,18021,18021,18021,MONDO:0022884,craniofacial dysostosis arthrogryposis progeroid appearance,MONDO,disease,DISEASE_18021
18022,18022,18022,18022,18022,18022,18022,18022,MONDO:0009432,"hypopituitarism, congenital, with central diabetes insipidus",MONDO,disease,DISEASE_18022
18023,18023,18023,18023,18023,18023,18023,18023,MONDO:0013087_MONDO:0008887_MONDO:0013112,bronchiectasis with or without elevated sweat chloride,MONDO_grouped,disease,DISEASE_18023
18024,18024,18024,18024,18024,18024,18024,18024,MONDO:0012148,"obsolete drug metabolism, poor, CYP2D6-related",MONDO,disease,DISEASE_18024
18025,18025,18025,18025,18025,18025,18025,18025,MONDO:0030815_MONDO:0008892_MONDO:0031040_MONDO:0030800_MONDO:0030360_MONDO:0030810_MONDO:0014381_MONDO:0014884_MONDO:0030505_MONDO:0011214_MONDO:0011156_MONDO:0017290_MONDO:0975807,"cholestasis, progressive familial intrahepatic",MONDO_grouped,disease,DISEASE_18025
18026,18026,18026,18026,18026,18026,18026,18026,MONDO:0001725,balanitis xerotica obliterans,MONDO,disease,DISEASE_18026
18027,18027,18027,18027,18027,18027,18027,18027,MONDO:0001309_MONDO:0002434,oculomotor nerve paralysis,MONDO_grouped,disease,DISEASE_18027
18028,18028,18028,18028,18028,18028,18028,18028,MONDO:0700116,microcephaly with lissencephaly and/or hydranencephaly,MONDO,disease,DISEASE_18028
18029,18029,18029,18029,18029,18029,18029,18029,MONDO:0018533,undifferentiated carcinoma of liver and intrahepatic biliary tract,MONDO,disease,DISEASE_18029
18030,18030,18030,18030,18030,18030,18030,18030,MONDO:0100497,titinopathy with congenital contractures,MONDO,disease,DISEASE_18030
18031,18031,18031,18031,18031,18031,18031,18031,MONDO:0018472,familial isolated trichomegaly,MONDO,disease,DISEASE_18031
18032,18032,18032,18032,18032,18032,18032,18032,MONDO:0001843,uterus interstitial leiomyoma,MONDO,disease,DISEASE_18032
18033,18033,18033,18033,18033,18033,18033,18033,MONDO:0013773_MONDO:0017410,porencephaly 2,MONDO_grouped,disease,DISEASE_18033
18034,18034,18034,18034,18034,18034,18034,18034,MONDO:0017442_MONDO:0017444_MONDO:0017496_MONDO:0017497,congenital absence of thigh and lower leg with foot present,MONDO_grouped,disease,DISEASE_18034
18035,18035,18035,18035,18035,18035,18035,18035,MONDO:0008773,"amino aciduria with mental deficiency, dwarfism, muscular dystrophy, osteoporosis, and acidosis",MONDO,disease,DISEASE_18035
18036,18036,18036,18036,18036,18036,18036,18036,MONDO:0003864,chronic lymphocytic leukemia/small lymphocytic lymphoma,MONDO,disease,DISEASE_18036
18037,18037,18037,18037,18037,18037,18037,18037,MONDO:0020121,muscular dystrophy,MONDO,disease,DISEASE_18037
18038,18038,18038,18038,18038,18038,18038,18038,MONDO:0010629,"impacted teeth, multiple",MONDO,disease,DISEASE_18038
18039,18039,18039,18039,18039,18039,18039,18039,MONDO:0100215_MONDO:0100220_MONDO:0100214,Rajab interstitial lung disease with brain calcifications,MONDO_grouped,disease,DISEASE_18039
18040,18040,18040,18040,18040,18040,18040,18040,MONDO:0009337_MONDO:0014454_MONDO:0032564,Hennekam lymphangiectasia-lymphedema syndrome,MONDO_grouped,disease,DISEASE_18040
18041,18041,18041,18041,18041,18041,18041,18041,MONDO:0100128,coinfection,MONDO,disease,DISEASE_18041
18042,18042,18042,18042,18042,18042,18042,18042,MONDO:0018754,cyanide poisoning,MONDO,disease,DISEASE_18042
18043,18043,18043,18043,18043,18043,18043,18043,MONDO:0004854,ophthalmia neonatorum,MONDO,disease,DISEASE_18043
18044,18044,18044,18044,18044,18044,18044,18044,MONDO:0005492,urticaria,MONDO,disease,DISEASE_18044
18045,18045,18045,18045,18045,18045,18045,18045,MONDO:0100539,hemiplegic migraine-developmental and epileptic encephalopathy spectrum,MONDO,disease,DISEASE_18045
18046,18046,18046,18046,18046,18046,18046,18046,MONDO:0002667,gallbladder signet ring cell adenocarcinoma,MONDO,disease,DISEASE_18046
18047,18047,18047,18047,18047,18047,18047,18047,MONDO:0004126_MONDO:0015074_MONDO:0002108_MONDO:0006996,thyroiditis,MONDO_grouped,disease,DISEASE_18047
18048,18048,18048,18048,18048,18048,18048,18048,MONDO:0021469,benign neoplasm of anus,MONDO,disease,DISEASE_18048
18049,18049,18049,18049,18049,18049,18049,18049,MONDO:0016236,kaposiform hemangioendothelioma,MONDO,disease,DISEASE_18049
18050,18050,18050,18050,18050,18050,18050,18050,MONDO:0019640,posterior urethral valve,MONDO,disease,DISEASE_18050
18051,18051,18051,18051,18051,18051,18051,18051,MONDO:0700339,DNM1-encephalopathy and neurodevelopmental disorder,MONDO,disease,DISEASE_18051
18052,18052,18052,18052,18052,18052,18052,18052,MONDO:0007485_MONDO:0009136_MONDO:0014076_MONDO:0013521_MONDO:0013520_MONDO:0014600_MONDO:0014690_MONDO:0013522_MONDO:0013519_MONDO:0859319_MONDO:0027353_MONDO:0800366_MONDO:0800370,"dyskeratosis congenita, autosomal dominant",MONDO_grouped,disease,DISEASE_18052
18053,18053,18053,18053,18053,18053,18053,18053,MONDO:1012077,"faded shaker, chicken",MONDO,disease,DISEASE_18053
18054,18054,18054,18054,18054,18054,18054,18054,MONDO:0021377,hypertrophic lichen planus,MONDO,disease,DISEASE_18054
18055,18055,18055,18055,18055,18055,18055,18055,MONDO:0021723,vaginismus,MONDO,disease,DISEASE_18055
18056,18056,18056,18056,18056,18056,18056,18056,MONDO:0018682,congenital insensitivity to pain with severe intellectual disability,MONDO,disease,DISEASE_18056
18057,18057,18057,18057,18057,18057,18057,18057,MONDO:0015704,familial scaphocephaly syndrome,MONDO,disease,DISEASE_18057
18058,18058,18058,18058,18058,18058,18058,18058,MONDO:0002162,fallopian tube adenosarcoma,MONDO,disease,DISEASE_18058
18059,18059,18059,18059,18059,18059,18059,18059,MONDO:0012200_MONDO:0007378_MONDO:0012199_MONDO:0013027_MONDO:0054832_MONDO:0020364,posterior polymorphous corneal dystrophy,MONDO_grouped,disease,DISEASE_18059
18060,18060,18060,18060,18060,18060,18060,18060,MONDO:0008403,scalp defects-postaxial polydactyly syndrome,MONDO,disease,DISEASE_18060
18061,18061,18061,18061,18061,18061,18061,18061,MONDO:0012347,"hamartoma, Precalcaneal congenital fibrolipomatous",MONDO,disease,DISEASE_18061
18062,18062,18062,18062,18062,18062,18062,18062,MONDO:0021539,hamartoma of skin appendage,MONDO,disease,DISEASE_18062
18063,18063,18063,18063,18063,18063,18063,18063,MONDO:0044642,c11orf73-related autosomal recessive hypomyelinating leukodystrophy,MONDO,disease,DISEASE_18063
18064,18064,18064,18064,18064,18064,18064,18064,MONDO:0024981,rodent disease,MONDO,disease,DISEASE_18064
18065,18065,18065,18065,18065,18065,18065,18065,MONDO:0021966,baker Vinters syndrome,MONDO,disease,DISEASE_18065
18066,18066,18066,18066,18066,18066,18066,18066,MONDO:0021670,post-infectious syndrome,MONDO,disease,DISEASE_18066
18067,18067,18067,18067,18067,18067,18067,18067,MONDO:0010727,"Russell-silver syndrome, X-linked",MONDO,disease,DISEASE_18067
18068,18068,18068,18068,18068,18068,18068,18068,MONDO:0010670,X-linked intellectual disability-spastic quadriparesis syndrome,MONDO,disease,DISEASE_18068
18069,18069,18069,18069,18069,18069,18069,18069,MONDO:0858959,polymorphous low grade neuroepithelial tumor of the young,MONDO,disease,DISEASE_18069
18070,18070,18070,18070,18070,18070,18070,18070,MONDO:0010668,skeletal dysplasia-intellectual disability syndrome,MONDO,disease,DISEASE_18070
18071,18071,18071,18071,18071,18071,18071,18071,MONDO:0007162,asymmetric short stature syndrome,MONDO,disease,DISEASE_18071
18072,18072,18072,18072,18072,18072,18072,18072,MONDO:0008272_MONDO:0008286_MONDO:0021003_MONDO:0017529_MONDO:0017530,polysyndactyly,MONDO_grouped,disease,DISEASE_18072
18073,18073,18073,18073,18073,18073,18073,18073,MONDO:0004754,rectal prolapse,MONDO,disease,DISEASE_18073
18074,18074,18074,18074,18074,18074,18074,18074,MONDO:0000210,thiopurine metabolic disease,MONDO,disease,DISEASE_18074
18075,18075,18075,18075,18075,18075,18075,18075,MONDO:0013125,CLAPO syndrome,MONDO,disease,DISEASE_18075
18076,18076,18076,18076,18076,18076,18076,18076,MONDO:0004305,parathyroid oncocytic adenoma,MONDO,disease,DISEASE_18076
18077,18077,18077,18077,18077,18077,18077,18077,MONDO:0021480,benign neoplasm of soft palate,MONDO,disease,DISEASE_18077
18078,18078,18078,18078,18078,18078,18078,18078,MONDO:1012761_MONDO:1012835,"muscular dystrophy, COL6A1-related, dog",MONDO_grouped,disease,DISEASE_18078
18079,18079,18079,18079,18079,18079,18079,18079,MONDO:0030909_MONDO:0010407_MONDO:0010512,"intellectual disability, X-linked, syndromic, Houge type",MONDO_grouped,disease,DISEASE_18079
18080,18080,18080,18080,18080,18080,18080,18080,MONDO:0005648,aortic valve insufficiency,MONDO,disease,DISEASE_18080
18081,18081,18081,18081,18081,18081,18081,18081,MONDO:0700104,"respiratory system disorder, non-human animal",MONDO,disease,DISEASE_18081
18082,18082,18082,18082,18082,18082,18082,18082,MONDO:1011325,"immunodeficiency-related disorder, non-human animal",MONDO,disease,DISEASE_18082
18083,18083,18083,18083,18083,18083,18083,18083,MONDO:0010267,"episodic muscle weakness, X-linked",MONDO,disease,DISEASE_18083
18084,18084,18084,18084,18084,18084,18084,18084,MONDO:0010622_MONDO:0017264,recessive X-linked ichthyosis,MONDO_grouped,disease,DISEASE_18084
18085,18085,18085,18085,18085,18085,18085,18085,MONDO:0010653,Renpenning syndrome,MONDO,disease,DISEASE_18085
18086,18086,18086,18086,18086,18086,18086,18086,MONDO:0019151,oligocone trichromacy,MONDO,disease,DISEASE_18086
18087,18087,18087,18087,18087,18087,18087,18087,MONDO:0003656,hemoglobinuria,MONDO,disease,DISEASE_18087
18088,18088,18088,18088,18088,18088,18088,18088,MONDO:0005269,carotid artery disorder,MONDO,disease,DISEASE_18088
18089,18089,18089,18089,18089,18089,18089,18089,MONDO:0016542,IL10-related early-onset inflammatory bowel disease,MONDO,disease,DISEASE_18089
18090,18090,18090,18090,18090,18090,18090,18090,MONDO:1010158_MONDO:1010160,"polydactyly, non-human animal",MONDO_grouped,disease,DISEASE_18090
18091,18091,18091,18091,18091,18091,18091,18091,MONDO:0000430,mature T-cell and NK-cell non-Hodgkin lymphoma,MONDO,disease,DISEASE_18091
18092,18092,18092,18092,18092,18092,18092,18092,MONDO:0850349,"astroblastoma, MN1-altered",MONDO,disease,DISEASE_18092
18093,18093,18093,18093,18093,18093,18093,18093,MONDO:0004574,pyridoxine deficiency anemia,MONDO,disease,DISEASE_18093
18094,18094,18094,18094,18094,18094,18094,18094,MONDO:0851103,Bartholin's gland disease,MONDO,disease,DISEASE_18094
18095,18095,18095,18095,18095,18095,18095,18095,MONDO:1012268,"androgen insensitivity syndrome, cattle",MONDO,disease,DISEASE_18095
18096,18096,18096,18096,18096,18096,18096,18096,MONDO:0008291,porokeratosis plantaris palmaris et disseminata,MONDO,disease,DISEASE_18096
18097,18097,18097,18097,18097,18097,18097,18097,MONDO:0005649,appendicitis,MONDO,disease,DISEASE_18097
18098,18098,18098,18098,18098,18098,18098,18098,MONDO:0001016_MONDO:0850128,epididymis cancer,MONDO_grouped,disease,DISEASE_18098
18099,18099,18099,18099,18099,18099,18099,18099,MONDO:0017761,disorder of mineral absorption and transport,MONDO,disease,DISEASE_18099
18100,18100,18100,18100,18100,18100,18100,18100,MONDO:0800159_MONDO:0100477_MONDO:0017352,disorder of polyamine metabolism,MONDO_grouped,disease,DISEASE_18100
18101,18101,18101,18101,18101,18101,18101,18101,MONDO:0006804,inflammatory breast carcinoma,MONDO,disease,DISEASE_18101
18102,18102,18102,18102,18102,18102,18102,18102,MONDO:0010008,sarcosinemia,MONDO,disease,DISEASE_18102
18103,18103,18103,18103,18103,18103,18103,18103,MONDO:0019136,Zygomycosis,MONDO,disease,DISEASE_18103
18104,18104,18104,18104,18104,18104,18104,18104,MONDO:0010979_MONDO:0035678_MONDO:0035679,Timothy syndrome,MONDO_grouped,disease,DISEASE_18104
18105,18105,18105,18105,18105,18105,18105,18105,MONDO:0012308,Joubert syndrome with renal defect,MONDO,disease,DISEASE_18105
18106,18106,18106,18106,18106,18106,18106,18106,MONDO:0009377,hyperammonemia due to N-acetylglutamate synthase deficiency,MONDO,disease,DISEASE_18106
18107,18107,18107,18107,18107,18107,18107,18107,MONDO:0044304,hyperphenylalaninemia due to DNAJC12 deficiency,MONDO,disease,DISEASE_18107
18108,18108,18108,18108,18108,18108,18108,18108,MONDO:0003660,adult lymphoma,MONDO,disease,DISEASE_18108
18109,18109,18109,18109,18109,18109,18109,18109,MONDO:1010199,"muscular dystrophy, Duchenne type, non-human animal",MONDO,disease,DISEASE_18109
18110,18110,18110,18110,18110,18110,18110,18110,MONDO:0007156,"arthritis, sacroiliac",MONDO,disease,DISEASE_18110
18111,18111,18111,18111,18111,18111,18111,18111,MONDO:0001356,iron deficiency anemia,MONDO,disease,DISEASE_18111
18112,18112,18112,18112,18112,18112,18112,18112,MONDO:0023224,inherited reflex epilepsy,MONDO,disease,DISEASE_18112
18113,18113,18113,18113,18113,18113,18113,18113,MONDO:1011811_MONDO:1011827,"congenital melanoma, non-human animal",MONDO_grouped,disease,DISEASE_18113
18114,18114,18114,18114,18114,18114,18114,18114,MONDO:0019924,paternal uniparental disomy of chromosome 20,MONDO,disease,DISEASE_18114
18115,18115,18115,18115,18115,18115,18115,18115,MONDO:0021653_MONDO:0021654,cutaneous focal mucinosis,MONDO_grouped,disease,DISEASE_18115
18116,18116,18116,18116,18116,18116,18116,18116,MONDO:0006060,nasopharyngeal squamous cell carcinoma,MONDO,disease,DISEASE_18116
18117,18117,18117,18117,18117,18117,18117,18117,MONDO:0010991,"laterality defects, autosomal dominant",MONDO,disease,DISEASE_18117
18118,18118,18118,18118,18118,18118,18118,18118,MONDO:0001711,hepatic encephalopathy,MONDO,disease,DISEASE_18118
18119,18119,18119,18119,18119,18119,18119,18119,MONDO:0008839,ataxia-microcephaly-cataract syndrome,MONDO,disease,DISEASE_18119
18120,18120,18120,18120,18120,18120,18120,18120,MONDO:0016979,MRCS syndrome,MONDO,disease,DISEASE_18120
18121,18121,18121,18121,18121,18121,18121,18121,MONDO:0024508_MONDO:0013230,"epilepsy, hot water",MONDO_grouped,disease,DISEASE_18121
18122,18122,18122,18122,18122,18122,18122,18122,MONDO:0010290_MONDO:0011635,"goiter, multinodular",MONDO_grouped,disease,DISEASE_18122
18123,18123,18123,18123,18123,18123,18123,18123,MONDO:0006931,pulmonary coin lesion,MONDO,disease,DISEASE_18123
18124,18124,18124,18124,18124,18124,18124,18124,MONDO:0019330,pili gemini,MONDO,disease,DISEASE_18124
18125,18125,18125,18125,18125,18125,18125,18125,MONDO:0001820,focal labyrinthitis,MONDO,disease,DISEASE_18125
18126,18126,18126,18126,18126,18126,18126,18126,MONDO:0002233,enamel caries,MONDO,disease,DISEASE_18126
18127,18127,18127,18127,18127,18127,18127,18127,MONDO:1010137,"bullous pemphigoid, non-human animal",MONDO,disease,DISEASE_18127
18128,18128,18128,18128,18128,18128,18128,18128,MONDO:0009164,"encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts",MONDO,disease,DISEASE_18128
18129,18129,18129,18129,18129,18129,18129,18129,MONDO:0006808,intracranial arterial disease,MONDO,disease,DISEASE_18129
18130,18130,18130,18130,18130,18130,18130,18130,MONDO:1012191,"neurological syndrome, dog",MONDO,disease,DISEASE_18130
18131,18131,18131,18131,18131,18131,18131,18131,MONDO:0035402_MONDO:0035401_MONDO:0017089,isolated exencephaly,MONDO_grouped,disease,DISEASE_18131
18132,18132,18132,18132,18132,18132,18132,18132,MONDO:0008016,trismus-pseudocamptodactyly syndrome,MONDO,disease,DISEASE_18132
18133,18133,18133,18133,18133,18133,18133,18133,MONDO:0007391,coxa vara,MONDO,disease,DISEASE_18133
18134,18134,18134,18134,18134,18134,18134,18134,MONDO:0014332,hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency,MONDO,disease,DISEASE_18134
18135,18135,18135,18135,18135,18135,18135,18135,MONDO:0019060,bone neoplasm,MONDO,disease,DISEASE_18135
18136,18136,18136,18136,18136,18136,18136,18136,MONDO:0021532,fibroma of prostate,MONDO,disease,DISEASE_18136
18137,18137,18137,18137,18137,18137,18137,18137,MONDO:0016482,silver-Russell syndrome due to maternal uniparental disomy of chromosome 11,MONDO,disease,DISEASE_18137
18138,18138,18138,18138,18138,18138,18138,18138,MONDO:0012393,congenital brain dysgenesis due to glutamine synthetase deficiency,MONDO,disease,DISEASE_18138
18139,18139,18139,18139,18139,18139,18139,18139,MONDO:0015675,distomatosis,MONDO,disease,DISEASE_18139
18140,18140,18140,18140,18140,18140,18140,18140,MONDO:1012531,"digital dermatitis, cattle",MONDO,disease,DISEASE_18140
18141,18141,18141,18141,18141,18141,18141,18141,MONDO:1011990,"retinal dysplasia and persistent primary vitreous, non-human animal",MONDO,disease,DISEASE_18141
18142,18142,18142,18142,18142,18142,18142,18142,MONDO:0017145,beta-thalassemia and related diseases,MONDO,disease,DISEASE_18142
18143,18143,18143,18143,18143,18143,18143,18143,MONDO:0017514,"split foot, bilateral",MONDO,disease,DISEASE_18143
18144,18144,18144,18144,18144,18144,18144,18144,MONDO:0018845,focal myositis,MONDO,disease,DISEASE_18144
18145,18145,18145,18145,18145,18145,18145,18145,MONDO:0004855,tenosynovitis,MONDO,disease,DISEASE_18145
18146,18146,18146,18146,18146,18146,18146,18146,MONDO:0956979,nocturnal asthma,MONDO,disease,DISEASE_18146
18147,18147,18147,18147,18147,18147,18147,18147,MONDO:0041154,disorder of neck of urinary bladder,MONDO,disease,DISEASE_18147
18148,18148,18148,18148,18148,18148,18148,18148,MONDO:0009180_MONDO:0009182_MONDO:0019307_MONDO:0016673,"junctional epidermolysis bullosa, non-Herlitz type",MONDO_grouped,disease,DISEASE_18148
18149,18149,18149,18149,18149,18149,18149,18149,MONDO:1011414,"vestibular disease, non-human animal",MONDO,disease,DISEASE_18149
18150,18150,18150,18150,18150,18150,18150,18150,MONDO:0010630,imprinting gene related to retinoblastoma,MONDO,disease,DISEASE_18150
18151,18151,18151,18151,18151,18151,18151,18151,MONDO:1011137,"primary ciliary dyskinesia CCDC39-related, dog",MONDO,disease,DISEASE_18151
18152,18152,18152,18152,18152,18152,18152,18152,MONDO:0056804,benign neoplasm of peripheral nervous system,MONDO,disease,DISEASE_18152
18153,18153,18153,18153,18153,18153,18153,18153,MONDO:0006420,small intestinal mucosa-associated lymphoid tissue lymphoma,MONDO,disease,DISEASE_18153
18154,18154,18154,18154,18154,18154,18154,18154,MONDO:0007002,trochlear nerve disorder,MONDO,disease,DISEASE_18154
18155,18155,18155,18155,18155,18155,18155,18155,MONDO:1010456,"hypertrophic cardiomyopathy, woolly monkeys",MONDO,disease,DISEASE_18155
18156,18156,18156,18156,18156,18156,18156,18156,MONDO:1010239,"peripheral neuropathy, non-human animal",MONDO,disease,DISEASE_18156
18157,18157,18157,18157,18157,18157,18157,18157,MONDO:0013433_MONDO:0018646_MONDO:0018647,primary sclerosing cholangitis,MONDO_grouped,disease,DISEASE_18157
18158,18158,18158,18158,18158,18158,18158,18158,MONDO:0022338,ALK+ histiocytosis,MONDO,disease,DISEASE_18158
18159,18159,18159,18159,18159,18159,18159,18159,MONDO:0011284,astigmatism,MONDO,disease,DISEASE_18159
18160,18160,18160,18160,18160,18160,18160,18160,MONDO:0020581,benign PEComa,MONDO,disease,DISEASE_18160
18161,18161,18161,18161,18161,18161,18161,18161,MONDO:0100009,"structural congenital heart disease, multiple types - GATA4",MONDO,disease,DISEASE_18161
18162,18162,18162,18162,18162,18162,18162,18162,MONDO:0015974,severe combined immunodeficiency,MONDO,disease,DISEASE_18162
18163,18163,18163,18163,18163,18163,18163,18163,MONDO:1012875,"Parkinson disease, PINK1-related, crab-eating macaque",MONDO,disease,DISEASE_18163
18164,18164,18164,18164,18164,18164,18164,18164,MONDO:0017010,partial duplication of the long arm of chromosome X,MONDO,disease,DISEASE_18164
18165,18165,18165,18165,18165,18165,18165,18165,MONDO:0011210,"mitochondrial intermembrane space protein Tim12, yeast, homolog of",MONDO,disease,DISEASE_18165
18166,18166,18166,18166,18166,18166,18166,18166,MONDO:0009781,Onychotrichodysplasia and neutropenia,MONDO,disease,DISEASE_18166
18167,18167,18167,18167,18167,18167,18167,18167,MONDO:0021225,uvea neoplasm,MONDO,disease,DISEASE_18167
18168,18168,18168,18168,18168,18168,18168,18168,MONDO:0014128,TCF12-related craniosynostosis,MONDO,disease,DISEASE_18168
18169,18169,18169,18169,18169,18169,18169,18169,MONDO:1012064,"Ancon dwarfism, sheep",MONDO,disease,DISEASE_18169
18170,18170,18170,18170,18170,18170,18170,18170,MONDO:0044321,structural heart defects and renal anomalies syndrome,MONDO,disease,DISEASE_18170
18171,18171,18171,18171,18171,18171,18171,18171,MONDO:1012342,"renal cysts, pig",MONDO,disease,DISEASE_18171
18172,18172,18172,18172,18172,18172,18172,18172,MONDO:0001218,acute laryngopharyngitis,MONDO,disease,DISEASE_18172
18173,18173,18173,18173,18173,18173,18173,18173,MONDO:0015824,oculomaxillofacial dysostosis,MONDO,disease,DISEASE_18173
18174,18174,18174,18174,18174,18174,18174,18174,MONDO:0024662_MONDO:0006395,colorectal tubulovillous adenoma,MONDO_grouped,disease,DISEASE_18174
18175,18175,18175,18175,18175,18175,18175,18175,MONDO:0016217,mal de Debarquement,MONDO,disease,DISEASE_18175
18176,18176,18176,18176,18176,18176,18176,18176,MONDO:0018976,schisis association,MONDO,disease,DISEASE_18176
18177,18177,18177,18177,18177,18177,18177,18177,MONDO:0019935,isochromosome Y,MONDO,disease,DISEASE_18177
18178,18178,18178,18178,18178,18178,18178,18178,MONDO:0020324,intravascular large B-cell lymphoma,MONDO,disease,DISEASE_18178
18179,18179,18179,18179,18179,18179,18179,18179,MONDO:0004621,upper lip cancer,MONDO,disease,DISEASE_18179
18180,18180,18180,18180,18180,18180,18180,18180,MONDO:0016004,aminopterin/methotrexate embryofetopathy,MONDO,disease,DISEASE_18180
18181,18181,18181,18181,18181,18181,18181,18181,MONDO:0100189,obsolete apolipoprotein A-I deficiency,MONDO,disease,DISEASE_18181
18182,18182,18182,18182,18182,18182,18182,18182,MONDO:0006869,nodular goiter,MONDO,disease,DISEASE_18182
18183,18183,18183,18183,18183,18183,18183,18183,MONDO:0019366,free sialic acid storage disease,MONDO,disease,DISEASE_18183
18184,18184,18184,18184,18184,18184,18184,18184,MONDO:0024280,polyarticular arthritis,MONDO,disease,DISEASE_18184
18185,18185,18185,18185,18185,18185,18185,18185,MONDO:0015431,ring chromosome 10,MONDO,disease,DISEASE_18185
18186,18186,18186,18186,18186,18186,18186,18186,MONDO:0010074,"brachyolmia type 1, toledo type",MONDO,disease,DISEASE_18186
18187,18187,18187,18187,18187,18187,18187,18187,MONDO:0002099,Histoplasma capsulatum infectious disease,MONDO,disease,DISEASE_18187
18188,18188,18188,18188,18188,18188,18188,18188,MONDO:0001044,esophageal atresia,MONDO,disease,DISEASE_18188
18189,18189,18189,18189,18189,18189,18189,18189,MONDO:0013007,combined immunodeficiency due to ORAI1 deficiency,MONDO,disease,DISEASE_18189
18190,18190,18190,18190,18190,18190,18190,18190,MONDO:0013332,"brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability",MONDO,disease,DISEASE_18190
18191,18191,18191,18191,18191,18191,18191,18191,MONDO:0019392,syringocystadenoma papilliferum,MONDO,disease,DISEASE_18191
18192,18192,18192,18192,18192,18192,18192,18192,MONDO:0100254,CACNA1A-related complex neurodevelopmental disorder,MONDO,disease,DISEASE_18192
18193,18193,18193,18193,18193,18193,18193,18193,MONDO:0019628,Rieger anomaly,MONDO,disease,DISEASE_18193
18194,18194,18194,18194,18194,18194,18194,18194,MONDO:0013944,autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation,MONDO,disease,DISEASE_18194
18195,18195,18195,18195,18195,18195,18195,18195,MONDO:0001694,diffuse interstitial keratitis,MONDO,disease,DISEASE_18195
18196,18196,18196,18196,18196,18196,18196,18196,MONDO:0017326,infective dermatitis associated with HTLV-1,MONDO,disease,DISEASE_18196
18197,18197,18197,18197,18197,18197,18197,18197,MONDO:0018989,recurrent acute pancreatitis,MONDO,disease,DISEASE_18197
18198,18198,18198,18198,18198,18198,18198,18198,MONDO:0007688,Myhre syndrome,MONDO,disease,DISEASE_18198
18199,18199,18199,18199,18199,18199,18199,18199,MONDO:0002252,granulomatous hepatitis,MONDO,disease,DISEASE_18199
18200,18200,18200,18200,18200,18200,18200,18200,MONDO:0003721,kidney osteogenic sarcoma,MONDO,disease,DISEASE_18200
18201,18201,18201,18201,18201,18201,18201,18201,MONDO:0015325,cataract-deafness-hypogonadism syndrome,MONDO,disease,DISEASE_18201
18202,18202,18202,18202,18202,18202,18202,18202,MONDO:0024284,demodicidosis of sebaceous gland,MONDO,disease,DISEASE_18202
18203,18203,18203,18203,18203,18203,18203,18203,MONDO:0022883,craniofacial and skeletal defects,MONDO,disease,DISEASE_18203
18204,18204,18204,18204,18204,18204,18204,18204,MONDO:0000480,anismus,MONDO,disease,DISEASE_18204
18205,18205,18205,18205,18205,18205,18205,18205,MONDO:0859762,SLC12A2-related autosomal dominant infantile-developmental delay-intellectual disability-sensorineural deafness syndrome,MONDO,disease,DISEASE_18205
18206,18206,18206,18206,18206,18206,18206,18206,MONDO:0005773,Gerstmann syndrome,MONDO,disease,DISEASE_18206
18207,18207,18207,18207,18207,18207,18207,18207,MONDO:0019263_MONDO:0001676,autosomal erythropoietic protoporphyria,MONDO_grouped,disease,DISEASE_18207
18208,18208,18208,18208,18208,18208,18208,18208,MONDO:0007401,craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome,MONDO,disease,DISEASE_18208
18209,18209,18209,18209,18209,18209,18209,18209,MONDO:0015729,mosaic trisomy 16,MONDO,disease,DISEASE_18209
18210,18210,18210,18210,18210,18210,18210,18210,MONDO:0002137,noninfectious dermatoses of eyelid,MONDO,disease,DISEASE_18210
18211,18211,18211,18211,18211,18211,18211,18211,MONDO:0018548,acute poisoning by drugs with membrane-stabilizing effect,MONDO,disease,DISEASE_18211
18212,18212,18212,18212,18212,18212,18212,18212,MONDO:0000831,thrombotic disease,MONDO,disease,DISEASE_18212
18213,18213,18213,18213,18213,18213,18213,18213,MONDO:0010179,isolated right ventricular hypoplasia,MONDO,disease,DISEASE_18213
18214,18214,18214,18214,18214,18214,18214,18214,MONDO:0025690_MONDO:0031481_MONDO:0100328,"microcephaly, epilepsy, and diabetes syndrome",MONDO_grouped,disease,DISEASE_18214
18215,18215,18215,18215,18215,18215,18215,18215,MONDO:0021655,secondary catabolic mucinosis of skin,MONDO,disease,DISEASE_18215
18216,18216,18216,18216,18216,18216,18216,18216,MONDO:1010042,"protein-losing enteropathy, non-human animal",MONDO,disease,DISEASE_18216
18217,18217,18217,18217,18217,18217,18217,18217,MONDO:0007531,electroencephalographic peculiarity: fronto-precentral beta wave groups,MONDO,disease,DISEASE_18217
18218,18218,18218,18218,18218,18218,18218,18218,MONDO:1010573,"diabetes mellitus, koala",MONDO,disease,DISEASE_18218
18219,18219,18219,18219,18219,18219,18219,18219,MONDO:0007371,cornea guttata with anterior polar cataracts,MONDO,disease,DISEASE_18219
18220,18220,18220,18220,18220,18220,18220,18220,MONDO:0017297,chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids,MONDO,disease,DISEASE_18220
18221,18221,18221,18221,18221,18221,18221,18221,MONDO:0016195,qualitative or quantitative defects of beta-myosin heavy chain (MYH7),MONDO,disease,DISEASE_18221
18222,18222,18222,18222,18222,18222,18222,18222,MONDO:0009545,"macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance",MONDO,disease,DISEASE_18222
18223,18223,18223,18223,18223,18223,18223,18223,MONDO:0017088,isolated amyelia,MONDO,disease,DISEASE_18223
18224,18224,18224,18224,18224,18224,18224,18224,MONDO:0032799,mitochondrial DNA depletion syndrome 16 (hepatic type),MONDO,disease,DISEASE_18224
18225,18225,18225,18225,18225,18225,18225,18225,MONDO:0850030,complete hemimelia,MONDO,disease,DISEASE_18225
18226,18226,18226,18226,18226,18226,18226,18226,MONDO:0002763,urethral verrucous carcinoma,MONDO,disease,DISEASE_18226
18227,18227,18227,18227,18227,18227,18227,18227,MONDO:1010115,"c8 deficiency, non-human animal",MONDO,disease,DISEASE_18227
18228,18228,18228,18228,18228,18228,18228,18228,MONDO:0016140,sarcoglycanopathy,MONDO,disease,DISEASE_18228
18229,18229,18229,18229,18229,18229,18229,18229,MONDO:0043310,amaurosis fugax,MONDO,disease,DISEASE_18229
18230,18230,18230,18230,18230,18230,18230,18230,MONDO:0023167,focal alopecia congenital megalencephaly,MONDO,disease,DISEASE_18230
18231,18231,18231,18231,18231,18231,18231,18231,MONDO:1012453,"selective ADP deficiency, dog",MONDO,disease,DISEASE_18231
18232,18232,18232,18232,18232,18232,18232,18232,MONDO:0017007,partial deletion of the long arm of chromosome X,MONDO,disease,DISEASE_18232
18233,18233,18233,18233,18233,18233,18233,18233,MONDO:0008994,"cleidocranial dysplasia, recessive form",MONDO,disease,DISEASE_18233
18234,18234,18234,18234,18234,18234,18234,18234,MONDO:0019910,maternal uniparental disomy of chromosome 2,MONDO,disease,DISEASE_18234
18235,18235,18235,18235,18235,18235,18235,18235,MONDO:0022841,congenital hypotrichosis milia,MONDO,disease,DISEASE_18235
18236,18236,18236,18236,18236,18236,18236,18236,MONDO:0850112,breast implant-associated anaplastic large cell lymphoma,MONDO,disease,DISEASE_18236
18237,18237,18237,18237,18237,18237,18237,18237,MONDO:0010142_MONDO:0043103,hypothyroidism due to TSH receptor mutations,MONDO_grouped,disease,DISEASE_18237
18238,18238,18238,18238,18238,18238,18238,18238,MONDO:1011322,"iatrogenic disease, non-human animal",MONDO,disease,DISEASE_18238
18239,18239,18239,18239,18239,18239,18239,18239,MONDO:0032852,"myopathy, congenital, with structured cores and z-line abnormalities",MONDO,disease,DISEASE_18239
18240,18240,18240,18240,18240,18240,18240,18240,MONDO:0019344,antisynthetase syndrome,MONDO,disease,DISEASE_18240
18241,18241,18241,18241,18241,18241,18241,18241,MONDO:0005464,rhegmatogenous retinal detachment,MONDO,disease,DISEASE_18241
18242,18242,18242,18242,18242,18242,18242,18242,MONDO:0016266,squamous cell carcinoma of the corpus uteri,MONDO,disease,DISEASE_18242
18243,18243,18243,18243,18243,18243,18243,18243,MONDO:0035586,Cramp-fasciculation syndrome,MONDO,disease,DISEASE_18243
18244,18244,18244,18244,18244,18244,18244,18244,MONDO:0042605,Y chromosome infertility due to DAZ1 deletion,MONDO,disease,DISEASE_18244
18245,18245,18245,18245,18245,18245,18245,18245,MONDO:0020108_MONDO:0019535_MONDO:0018358_MONDO:0021559_MONDO:1012098_MONDO:1012099,autoimmune hemolytic anemia,MONDO_grouped,disease,DISEASE_18245
18246,18246,18246,18246,18246,18246,18246,18246,MONDO:1010535,"megacolon, domestic cat",MONDO,disease,DISEASE_18246
18247,18247,18247,18247,18247,18247,18247,18247,MONDO:0013044,atypical hemolytic-uremic syndrome with thrombomodulin anomaly,MONDO,disease,DISEASE_18247
18248,18248,18248,18248,18248,18248,18248,18248,MONDO:0957999_MONDO:0030785,"intellectual developmental disorder, autosomal recessive 80, with variant lissencephaly",MONDO_grouped,disease,DISEASE_18248
18249,18249,18249,18249,18249,18249,18249,18249,MONDO:0021165,Paget disease,MONDO,disease,DISEASE_18249
18250,18250,18250,18250,18250,18250,18250,18250,MONDO:0021468,benign neoplasm of adrenal medulla,MONDO,disease,DISEASE_18250
18251,18251,18251,18251,18251,18251,18251,18251,MONDO:0015540,hemophagocytic syndrome,MONDO,disease,DISEASE_18251
18252,18252,18252,18252,18252,18252,18252,18252,MONDO:0007357,colonic varices without portal hypertension,MONDO,disease,DISEASE_18252
18253,18253,18253,18253,18253,18253,18253,18253,MONDO:0015769,distal trisomy 6p,MONDO,disease,DISEASE_18253
18254,18254,18254,18254,18254,18254,18254,18254,MONDO:0016954,partial duplication of the long arm of chromosome 3,MONDO,disease,DISEASE_18254
18255,18255,18255,18255,18255,18255,18255,18255,MONDO:0010101,Teebi-Shaltout syndrome,MONDO,disease,DISEASE_18255
18256,18256,18256,18256,18256,18256,18256,18256,MONDO:0016652,2q31.1 microdeletion syndrome,MONDO,disease,DISEASE_18256
18257,18257,18257,18257,18257,18257,18257,18257,MONDO:0009197,transient erythroblastopenia of childhood,MONDO,disease,DISEASE_18257
18258,18258,18258,18258,18258,18258,18258,18258,MONDO:0002914,childhood brain stem neoplasm,MONDO,disease,DISEASE_18258
18259,18259,18259,18259,18259,18259,18259,18259,MONDO:1030010,precerebral artery stenosis,MONDO,disease,DISEASE_18259
18260,18260,18260,18260,18260,18260,18260,18260,MONDO:0013814,"podoconiosis, susceptibility to",MONDO,disease,DISEASE_18260
18261,18261,18261,18261,18261,18261,18261,18261,MONDO:0021249,lip neoplasm,MONDO,disease,DISEASE_18261
18262,18262,18262,18262,18262,18262,18262,18262,MONDO:0003940,Kummell disease,MONDO,disease,DISEASE_18262
18263,18263,18263,18263,18263,18263,18263,18263,MONDO:0006998,tonsil cancer,MONDO,disease,DISEASE_18263
18264,18264,18264,18264,18264,18264,18264,18264,MONDO:0006446,testicular embryonal carcinoma,MONDO,disease,DISEASE_18264
18265,18265,18265,18265,18265,18265,18265,18265,MONDO:0017683,methylcobalamin deficiency type cblDv1,MONDO,disease,DISEASE_18265
18266,18266,18266,18266,18266,18266,18266,18266,MONDO:0009644_MONDO:0014212_MONDO:0009643_MONDO:0020480,sulfite oxidase deficiency due to molybdenum cofactor deficiency,MONDO_grouped,disease,DISEASE_18266
18267,18267,18267,18267,18267,18267,18267,18267,MONDO:0015722,congenital vitamin K-dependent coagulation factors deficiency,MONDO,disease,DISEASE_18267
18268,18268,18268,18268,18268,18268,18268,18268,MONDO:1012053,"congenital copper deficiency, goat",MONDO,disease,DISEASE_18268
18269,18269,18269,18269,18269,18269,18269,18269,MONDO:1010320_MONDO:1010350_MONDO:1011980,"corneal dystrophy, non-human animal",MONDO_grouped,disease,DISEASE_18269
18270,18270,18270,18270,18270,18270,18270,18270,MONDO:0010060,mitochondrial DNA depletion syndrome 7 (hepatocerebral type),MONDO,disease,DISEASE_18270
18271,18271,18271,18271,18271,18271,18271,18271,MONDO:0002035_MONDO:0002032_MONDO:0003352_MONDO:0000527,colon lymphoma,MONDO_grouped,disease,DISEASE_18271
18272,18272,18272,18272,18272,18272,18272,18272,MONDO:0009477,Stromme syndrome,MONDO,disease,DISEASE_18272
18273,18273,18273,18273,18273,18273,18273,18273,MONDO:0016572,central bilateral macrogyria,MONDO,disease,DISEASE_18273
18274,18274,18274,18274,18274,18274,18274,18274,MONDO:0018315,X-linked osteoporosis with fractures,MONDO,disease,DISEASE_18274
18275,18275,18275,18275,18275,18275,18275,18275,MONDO:0003880,ceruminous carcinoma,MONDO,disease,DISEASE_18275
18276,18276,18276,18276,18276,18276,18276,18276,MONDO:0025556,isocyanate induced asthma,MONDO,disease,DISEASE_18276
18277,18277,18277,18277,18277,18277,18277,18277,MONDO:0002407_MONDO:0003896,capillary hemangioma,MONDO_grouped,disease,DISEASE_18277
18278,18278,18278,18278,18278,18278,18278,18278,MONDO:1011138,"choanal atresia, alpaca",MONDO,disease,DISEASE_18278
18279,18279,18279,18279,18279,18279,18279,18279,MONDO:0017812,segmental progressive overgrowth syndrome with fibroadipose hyperplasia,MONDO,disease,DISEASE_18279
18280,18280,18280,18280,18280,18280,18280,18280,MONDO:0020597,angiokeratoma of scrotum,MONDO,disease,DISEASE_18280
18281,18281,18281,18281,18281,18281,18281,18281,MONDO:0005783,hemopericardium,MONDO,disease,DISEASE_18281
18282,18282,18282,18282,18282,18282,18282,18282,MONDO:0859223,"congenital disorder of glycosylation, type Iw, autosomal dominant",MONDO,disease,DISEASE_18282
18283,18283,18283,18283,18283,18283,18283,18283,MONDO:0024652,embryonic cyst of fallopian tube,MONDO,disease,DISEASE_18283
18284,18284,18284,18284,18284,18284,18284,18284,MONDO:1010305,"craniosynostosis, non-human animal",MONDO,disease,DISEASE_18284
18285,18285,18285,18285,18285,18285,18285,18285,MONDO:1011677,"congenital hypoplasia of mammary gland, non-human animal",MONDO,disease,DISEASE_18285
18286,18286,18286,18286,18286,18286,18286,18286,MONDO:1011708,"dyserythropoietic anemia and myopathy syndrome, non-human animal",MONDO,disease,DISEASE_18286
18287,18287,18287,18287,18287,18287,18287,18287,MONDO:0024777,"immunodeficiency 98 with autoinflammation, X-linked",MONDO,disease,DISEASE_18287
18288,18288,18288,18288,18288,18288,18288,18288,MONDO:0011537,macrocephaly-autism syndrome,MONDO,disease,DISEASE_18288
18289,18289,18289,18289,18289,18289,18289,18289,MONDO:0017611,pituitary tumor,MONDO,disease,DISEASE_18289
18290,18290,18290,18290,18290,18290,18290,18290,MONDO:1012050,"chronic interstitial nephropathy, ducks",MONDO,disease,DISEASE_18290
18291,18291,18291,18291,18291,18291,18291,18291,MONDO:0022873,corpus callosum dysgenesis cleft spasm,MONDO,disease,DISEASE_18291
18292,18292,18292,18292,18292,18292,18292,18292,MONDO:0009896,"polymyoclonus, infantile",MONDO,disease,DISEASE_18292
18293,18293,18293,18293,18293,18293,18293,18293,MONDO:0100304,disorder of bile acid aminotransferase,MONDO,disease,DISEASE_18293
18294,18294,18294,18294,18294,18294,18294,18294,MONDO:0004477,adrenal gland ganglioneuroblastoma,MONDO,disease,DISEASE_18294
18295,18295,18295,18295,18295,18295,18295,18295,MONDO:0007958,familial medullary thyroid carcinoma,MONDO,disease,DISEASE_18295
18296,18296,18296,18296,18296,18296,18296,18296,MONDO:0000597,Munchausen by proxy,MONDO,disease,DISEASE_18296
18297,18297,18297,18297,18297,18297,18297,18297,MONDO:0004307,sarcomatosis of the meninges,MONDO,disease,DISEASE_18297
18298,18298,18298,18298,18298,18298,18298,18298,MONDO:0022912,cutis verticis gyrata mental deficiency,MONDO,disease,DISEASE_18298
18299,18299,18299,18299,18299,18299,18299,18299,MONDO:1011657,"goldenhar syndrome, non-human animal",MONDO,disease,DISEASE_18299
18300,18300,18300,18300,18300,18300,18300,18300,MONDO:0020654,renal pelvis/ureter urothelial carcinoma,MONDO,disease,DISEASE_18300
18301,18301,18301,18301,18301,18301,18301,18301,MONDO:0009186,"epilepsy, photogenic, with spastic diplegia and intellectual disability",MONDO,disease,DISEASE_18301
18302,18302,18302,18302,18302,18302,18302,18302,MONDO:1010642,"factor XII deficiency, common bottlenose dolphin",MONDO,disease,DISEASE_18302
18303,18303,18303,18303,18303,18303,18303,18303,MONDO:0020743,mixed phenotype acute leukemia,MONDO,disease,DISEASE_18303
18304,18304,18304,18304,18304,18304,18304,18304,MONDO:0010627,X-linked lymphoproliferative syndrome,MONDO,disease,DISEASE_18304
18305,18305,18305,18305,18305,18305,18305,18305,MONDO:0700033,complete trisomy 13,MONDO,disease,DISEASE_18305
18306,18306,18306,18306,18306,18306,18306,18306,MONDO:0017946,"ABeta amyloidosis, Iowa type",MONDO,disease,DISEASE_18306
18307,18307,18307,18307,18307,18307,18307,18307,MONDO:0016681,gliosarcoma,MONDO,disease,DISEASE_18307
18308,18308,18308,18308,18308,18308,18308,18308,MONDO:0017219,microform holoprosencephaly,MONDO,disease,DISEASE_18308
18309,18309,18309,18309,18309,18309,18309,18309,MONDO:0007104,amyotrophic lateral sclerosis-parkinsonism-dementia complex,MONDO,disease,DISEASE_18309
18310,18310,18310,18310,18310,18310,18310,18310,MONDO:0031384,"autoinflammatory syndrome, familial, Behcet-like",MONDO,disease,DISEASE_18310
18311,18311,18311,18311,18311,18311,18311,18311,MONDO:0007930,"Bernard-Soulier syndrome, type A2, autosomal dominant",MONDO,disease,DISEASE_18311
18312,18312,18312,18312,18312,18312,18312,18312,MONDO:0019088,post-transplant lymphoproliferative disease,MONDO,disease,DISEASE_18312
18313,18313,18313,18313,18313,18313,18313,18313,MONDO:0034041,congenital axonal neuropathy with encephalopathy,MONDO,disease,DISEASE_18313
18314,18314,18314,18314,18314,18314,18314,18314,MONDO:0007276,cat-eye syndrome,MONDO,disease,DISEASE_18314
18315,18315,18315,18315,18315,18315,18315,18315,MONDO:1012413,"neonatal pancytopenia, cattle",MONDO,disease,DISEASE_18315
18316,18316,18316,18316,18316,18316,18316,18316,MONDO:1011409,"portosystemic shunt, non-human animal",MONDO,disease,DISEASE_18316