diff --git "a/synonyms/terms.jsonl" "b/synonyms/terms.jsonl"
--- "a/synonyms/terms.jsonl"
+++ "b/synonyms/terms.jsonl"
@@ -1,103 +1,2026 @@
-{"_id": "0", "text": "Hereditary Motor and Sensory Neuropathy"}
-{"_id": "1", "text": "Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy"}
-{"_id": "2", "text": "Alzheimer's Disease 3"}
-{"_id": "3", "text": "Early-onset autosomal dominant Alzheimer disease"}
-{"_id": "4", "text": "Alzheimer Disease"}
-{"_id": "5", "text": "Neuroblastoma of Adrenal"}
-{"_id": "6", "text": "Neuroblastoma"}
-{"_id": "7", "text": "Noninsulin Dependent Diabetes"}
-{"_id": "8", "text": "ADENOCARCINOMA, ENDOMETRIAL, MALIGNANT"}
-{"_id": "9", "text": "Human Papillomavirus-Related Endocervical Adenocarcinoma"}
-{"_id": "10", "text": "Sandhoff Disease"}
-{"_id": "11", "text": "Sandhoff disease"}
-{"_id": "12", "text": "Fucosidosis"}
-{"_id": "13", "text": "Fucosidosis"}
-{"_id": "14", "text": "Acute Intermittent Porphyria"}
-{"_id": "15", "text": "Acute intermittent porphyria"}
-{"_id": "16", "text": "Maple Syrup Urine Disease"}
-{"_id": "17", "text": "Maple syrup urine disease"}
-{"_id": "18", "text": "Ataxia Telangiectasia Syndrome"}
-{"_id": "19", "text": "Ataxia-telangiectasia"}
-{"_id": "20", "text": "Gaucher Disease"}
-{"_id": "21", "text": "Gaucher disease"}
-{"_id": "22", "text": "Lesch-Nyhan Syndrome"}
-{"_id": "23", "text": "Lesch-Nyhan syndrome"}
-{"_id": "24", "text": "Huntington's Chorea"}
-{"_id": "25", "text": "Huntington disease"}
-{"_id": "26", "text": "Retinitis Pigmentosa"}
-{"_id": "27", "text": "Retinitis pigmentosa"}
-{"_id": "28", "text": "Steinert Syndrome"}
-{"_id": "29", "text": "Steinert myotonic dystrophy"}
-{"_id": "30", "text": "cystic fibrosis"}
-{"_id": "31", "text": "Cystic fibrosis"}
-{"_id": "32", "text": "Hereditary Spherocytosis"}
-{"_id": "33", "text": "Hereditary spherocytosis"}
-{"_id": "34", "text": "Hepatocyte Nuclear Factor 4-Alpha Associated Monogenic Diabetes"}
-{"_id": "35", "text": "MODY"}
-{"_id": "36", "text": "D-Bifunctional Protein Deficiency"}
-{"_id": "37", "text": "Bifunctional enzyme deficiency"}
-{"_id": "38", "text": "Langer Syndrome"}
-{"_id": "39", "text": "Langer mesomelic dysplasia"}
-{"_id": "40", "text": "18P Syndrome"}
-{"_id": "41", "text": "Monosomy 18p syndrome"}
-{"_id": "42", "text": "Embryonal rhabdomyosarcoma"}
-{"_id": "43", "text": "Embryonal rhabdomyosarcoma"}
-{"_id": "44", "text": "Blast Phase Chronic Myelocytic Leukemia"}
-{"_id": "45", "text": "Chronic myeloid leukemia"}
-{"_id": "46", "text": "idiopathic pulmonary fibrosis"}
-{"_id": "47", "text": "Idiopathic pulmonary fibrosis"}
-{"_id": "48", "text": "Melanoma, NOS"}
-{"_id": "49", "text": "Lung Small Cell Carcinoma"}
-{"_id": "50", "text": "Small cell lung cancer"}
-{"_id": "51", "text": "Parkinson's Disease"}
-{"_id": "52", "text": "ISCHEMIC STROKE"}
-{"_id": "53", "text": "Subarachnoid hemorrhage"}
-{"_id": "54", "text": "Lewy Body Disease"}
-{"_id": "55", "text": "ALS"}
-{"_id": "56", "text": "Amyotrophic lateral sclerosis"}
-{"_id": "57", "text": "Primary Lateral Sclerosis"}
-{"_id": "58", "text": "Primary lateral sclerosis"}
-{"_id": "59", "text": "Frontotemporal Dementia"}
-{"_id": "60", "text": "Behavioral variant of frontotemporal dementia"}
-{"_id": "61", "text": "MELANOMA, AMELANOTIC, MALIGNANT"}
-{"_id": "62", "text": "Ovarian Cystadenocarcinoma"}
-{"_id": "63", "text": "Neural Crest Tumor, Malignant"}
-{"_id": "64", "text": "Thyroid Gland Squamous Cell Carcinoma"}
-{"_id": "65", "text": "Rare thyroid carcinoma"}
-{"_id": "66", "text": "49,XXXXY Syndrome"}
-{"_id": "67", "text": "49,XXXXY syndrome"}
-{"_id": "68", "text": "Leigh Disease"}
-{"_id": "69", "text": "Leigh syndrome"}
-{"_id": "70", "text": "skin of arm"}
-{"_id": "71", "text": "vertebrate blood"}
-{"_id": "72", "text": "entire skin"}
-{"_id": "73", "text": "glandula adrenalis"}
-{"_id": "74", "text": "tunica mucosa uteri"}
-{"_id": "75", "text": "canalis cervicis uteri"}
-{"_id": "76", "text": "amniotic fluid"}
-{"_id": "77", "text": "leg skin"}
-{"_id": "78", "text": "lung primordium"}
-{"_id": "79", "text": "epithelium corne\u00e6 anterior layer"}
-{"_id": "80", "text": "splenic primordium"}
-{"_id": "81", "text": "foreskin of penis"}
-{"_id": "82", "text": "trunk zone of skin"}
-{"_id": "83", "text": "kidney"}
-{"_id": "84", "text": "outer pigmented layer of retina"}
-{"_id": "85", "text": "pleural effusion"}
-{"_id": "86", "text": "pulmo"}
-{"_id": "87", "text": "spleen"}
-{"_id": "88", "text": "medulla ossea"}
-{"_id": "89", "text": "gluteal part of pelvic girdle"}
-{"_id": "90", "text": "hypoderm"}
-{"_id": "91", "text": "ascitic fluid"}
-{"_id": "92", "text": "thyroid"}
-{"_id": "93", "text": "skin fibroblast"}
-{"_id": "94", "text": "fibroblast"}
-{"_id": "95", "text": "B-lymphocyte"}
-{"_id": "96", "text": "fibroblast of lung"}
-{"_id": "97", "text": "epitheliocyte"}
-{"_id": "98", "text": "retinal pigment epithelial cell"}
-{"_id": "99", "text": "Epstein-Barr virus EBV"}
-{"_id": "100", "text": "Human papillomavirus type 18"}
-{"_id": "101", "text": "Ad12-SV40 hybrid virus"}
-{"_id": "102", "text": "Simian virus 40"}
+{"_id": "0", "text": "Spongioblastoma multiforme"}
+{"_id": "1", "text": "Glioblastoma"}
+{"_id": "2", "text": "Human Papillomavirus-Associated Cervical Adenocarcinoma"}
+{"_id": "3", "text": "Carcinoma of the Prostate"}
+{"_id": "4", "text": "Chondrosarcoma"}
+{"_id": "5", "text": "Chondrosarcoma"}
+{"_id": "6", "text": "Adenocarcinoma of Lung"}
+{"_id": "7", "text": "Invasive Ductal Carcinoma, Not Otherwise Specified"}
+{"_id": "8", "text": "melanoma"}
+{"_id": "9", "text": "Cutaneous Melanoma"}
+{"_id": "10", "text": "Endometriosis"}
+{"_id": "11", "text": "Childhood T Acute Lymphoblastic Leukemia"}
+{"_id": "12", "text": "Precursor T-cell acute lymphoblastic leukemia"}
+{"_id": "13", "text": "Astrocytoma"}
+{"_id": "14", "text": "Astrocytoma"}
+{"_id": "15", "text": "osteogenic sarcoma"}
+{"_id": "16", "text": "Osteosarcoma"}
+{"_id": "17", "text": "Hereditary Adenomatous Polyposis Coli"}
+{"_id": "18", "text": "Familial adenomatous polyposis"}
+{"_id": "19", "text": "LIG4 Syndrome"}
+{"_id": "20", "text": "LIG4 syndrome"}
+{"_id": "21", "text": "HPV-Associated Cervical Squamous Cell Carcinoma"}
+{"_id": "22", "text": "Squamous cell carcinoma of the cervix uteri"}
+{"_id": "23", "text": "Serous Adenocarcinoma of the Ovary"}
+{"_id": "24", "text": "Carcinoma, Embryonal, Malignant"}
+{"_id": "25", "text": "Embryonal carcinoma"}
+{"_id": "26", "text": "Mixed Germ Cell Tumor of Ovary"}
+{"_id": "27", "text": "Mixed germ cell tumor"}
+{"_id": "28", "text": "Gastric Adenocarcinoma, NOS"}
+{"_id": "29", "text": "Carcinoma of the Bladder"}
+{"_id": "30", "text": "Myxoliposarcoma"}
+{"_id": "31", "text": "Myxoid/round cell liposarcoma"}
+{"_id": "32", "text": "Amyotrophic Lateral Sclerosis 1"}
+{"_id": "33", "text": "Amyotrophic lateral sclerosis"}
+{"_id": "34", "text": "EBV Related Burkitt's Lymphoma"}
+{"_id": "35", "text": "Burkitt lymphoma"}
+{"_id": "36", "text": "Cernunnos / XLF deficiency"}
+{"_id": "37", "text": "Cernunnos-XLF deficiency"}
+{"_id": "38", "text": "FIBROSARCOMA, MALIGNANT"}
+{"_id": "39", "text": "Fibrosarcoma"}
+{"_id": "40", "text": "AIDS-Associated Burkitt's Lymphoma"}
+{"_id": "41", "text": "HIV-associated cancer"}
+{"_id": "42", "text": "B Cell Pediatric ALL"}
+{"_id": "43", "text": "Precursor B-cell acute lymphoblastic leukemia"}
+{"_id": "44", "text": "High Grade Ovarian Serous Adenocarcinoma"}
+{"_id": "45", "text": "DNA Ligase I Deficiency"}
+{"_id": "46", "text": "hypogammaglobulinemia"}
+{"_id": "47", "text": "Clear Cell Adenocarcinoma of Kidney"}
+{"_id": "48", "text": "Clear cell renal carcinoma"}
+{"_id": "49", "text": "hepatitis C"}
+{"_id": "50", "text": "Lung Lymphangioleiomyomatosis"}
+{"_id": "51", "text": "Lymphangioleiomyomatosis"}
+{"_id": "52", "text": "Ureteral Transitional Cell Carcinoma"}
+{"_id": "53", "text": "Upper tract urothelial carcinoma"}
+{"_id": "54", "text": "B-Acute Lymphoblastic Leukemia with TCF3::PBX1 Fusion"}
+{"_id": "55", "text": "B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3)"}
+{"_id": "56", "text": "CARCINOMA, RENAL CELL, MALIGNANT"}
+{"_id": "57", "text": "Renal cell carcinoma"}
+{"_id": "58", "text": "Anaplastic Carcinoma of the Thyroid"}
+{"_id": "59", "text": "Anaplastic thyroid carcinoma"}
+{"_id": "60", "text": "Lung Large Cell Carcinoma"}
+{"_id": "61", "text": "Small Cell Neuroendocrine Carcinoma of Lung"}
+{"_id": "62", "text": "Small cell lung cancer"}
+{"_id": "63", "text": "Cystic Fibrosis"}
+{"_id": "64", "text": "Cystic fibrosis"}
+{"_id": "65", "text": "MPNST, NOS"}
+{"_id": "66", "text": "neurofibromatosis type 1"}
+{"_id": "67", "text": "Malignant peripheral nerve sheath tumor"}
+{"_id": "68", "text": "Neurofibromatosis type 1"}
+{"_id": "69", "text": "MELANOMA, UVEAL, MALIGNANT"}
+{"_id": "70", "text": "Uveal melanoma"}
+{"_id": "71", "text": "embryonal rhabdomyosarcoma"}
+{"_id": "72", "text": "Embryonal rhabdomyosarcoma"}
+{"_id": "73", "text": "Squamous Cell Carcinoma of Submandibular Gland"}
+{"_id": "74", "text": "OBSOLETE: Squamous cell carcinoma of salivary glands"}
+{"_id": "75", "text": "MELANOMA, AMELANOTIC, MALIGNANT"}
+{"_id": "76", "text": "Squamous Cell Carcinoma of the Skin"}
+{"_id": "77", "text": "Ewing's Sarcoma"}
+{"_id": "78", "text": "Skeletal Ewing sarcoma"}
+{"_id": "79", "text": "Down Syndrome"}
+{"_id": "80", "text": "Down syndrome"}
+{"_id": "81", "text": "M5b Pediatric Acute Differentiated Monocytic Leukemia"}
+{"_id": "82", "text": "Acute monoblastic/monocytic leukemia"}
+{"_id": "83", "text": "Werner's Syndrome"}
+{"_id": "84", "text": "Werner syndrome"}
+{"_id": "85", "text": "Ovarian Carcinoma"}
+{"_id": "86", "text": "Endometrioid Adenocarcinoma of Ovary"}
+{"_id": "87", "text": "Endometrioid carcinoma of ovary"}
+{"_id": "88", "text": "Non-follicular (diffuse) lymphoma, unspecified, unspecified site"}
+{"_id": "89", "text": "Diffuse large B-cell lymphoma"}
+{"_id": "90", "text": "B-Cell Adult Acute Lymphoblastic Leukemia"}
+{"_id": "91", "text": "Adenosquamous Lung Carcinoma"}
+{"_id": "92", "text": "Kaposi Disease"}
+{"_id": "93", "text": "Xeroderma pigmentosum"}
+{"_id": "94", "text": "non-small cell lung cancer"}
+{"_id": "95", "text": "Pleural Epithelioid Mesothelioma"}
+{"_id": "96", "text": "Pleural mesothelioma"}
+{"_id": "97", "text": "Papillary Renal Cell Cancer"}
+{"_id": "98", "text": "Papillary renal cell carcinoma"}
+{"_id": "99", "text": "Uterine Malignant Mixed Mesodermal (Mullerian) Tumor"}
+{"_id": "100", "text": "Carcinosarcoma of the corpus uteri"}
+{"_id": "101", "text": "Ehlers-Danlos Syndrome, Type II"}
+{"_id": "102", "text": "Classical Ehlers-Danlos syndrome"}
+{"_id": "103", "text": "Hutchinson-Gilford Disease"}
+{"_id": "104", "text": "Hutchinson-Gilford progeria syndrome"}
+{"_id": "105", "text": "Perheentupa Syndrome"}
+{"_id": "106", "text": "Mulibrey nanism"}
+{"_id": "107", "text": "Louis-Bar Syndrome"}
+{"_id": "108", "text": "Ataxia-telangiectasia"}
+{"_id": "109", "text": "Rothmund-Thomson Syndrome"}
+{"_id": "110", "text": "Rothmund-Thomson syndrome"}
+{"_id": "111", "text": "DKC"}
+{"_id": "112", "text": "Dyskeratosis congenita"}
+{"_id": "113", "text": "Atypical Werner syndrome"}
+{"_id": "114", "text": "Familial Alzheimer Disease, Type 3"}
+{"_id": "115", "text": "Early-onset autosomal dominant Alzheimer disease"}
+{"_id": "116", "text": "Alzheimer's disease, unspecified"}
+{"_id": "117", "text": "Steinert Myotonic Dystrophy Syndrome"}
+{"_id": "118", "text": "Steinert myotonic dystrophy"}
+{"_id": "119", "text": "Cockayne Syndrome Type A"}
+{"_id": "120", "text": "Cockayne syndrome"}
+{"_id": "121", "text": "Triploid Syndrome"}
+{"_id": "122", "text": "Triploidy syndrome"}
+{"_id": "123", "text": "Bloom-Torre-Machacek syndrome"}
+{"_id": "124", "text": "Bloom syndrome"}
+{"_id": "125", "text": "Type II Diabetes Mellitus"}
+{"_id": "126", "text": "Hereditary Sensorimotor Neuropathy"}
+{"_id": "127", "text": "Charcot-Marie-Tooth disease/Hereditary motor and sensory neuropathy"}
+{"_id": "128", "text": "Xeroderma Pigmentosum Group A"}
+{"_id": "129", "text": "MADA"}
+{"_id": "130", "text": "Mandibuloacral dysplasia with type A lipodystrophy"}
+{"_id": "131", "text": "Trisomy 18"}
+{"_id": "132", "text": "Trisomy 18 syndrome"}
+{"_id": "133", "text": "Turner syndrome"}
+{"_id": "134", "text": "Turner syndrome"}
+{"_id": "135", "text": "Parkinson Disease"}
+{"_id": "136", "text": "Neonatal Progeroid Syndrome"}
+{"_id": "137", "text": "Wiedemann-Rautenstrauch syndrome"}
+{"_id": "138", "text": "Familial Alzheimer's Disease, Type 4"}
+{"_id": "139", "text": "Type 1 Diabetes Mellitus"}
+{"_id": "140", "text": "Gerstmann-Straussler-Scheinker Disease"}
+{"_id": "141", "text": "Gerstmann-Straussler-Scheinker syndrome"}
+{"_id": "142", "text": "Trisomy-13"}
+{"_id": "143", "text": "Trisomy 13 syndrome"}
+{"_id": "144", "text": "Pick Disease"}
+{"_id": "145", "text": "Frontotemporal dementia"}
+{"_id": "146", "text": "Gynecomastia"}
+{"_id": "147", "text": "Transient ischemic attack"}
+{"_id": "148", "text": "B-Cell Acute Lymphoblastic Leukemia with t(v;11q23.3); MLL Rearranged"}
+{"_id": "149", "text": "B-lymphoblastic leukemia/lymphoma with t(v;11q23.3)"}
+{"_id": "150", "text": "Osteogenesis imperfecta"}
+{"_id": "151", "text": "Osteogenesis imperfecta"}
+{"_id": "152", "text": "Methylmalonic Aciduria Due to Methylmalonyl-CoA Mutase Deficiency"}
+{"_id": "153", "text": "Vitamin B12-unresponsive methylmalonic acidemia"}
+{"_id": "154", "text": "Pediatric Acute Myeloblastic Leukemia"}
+{"_id": "155", "text": "Acute myeloid leukemia"}
+{"_id": "156", "text": "Adult AML"}
+{"_id": "157", "text": "Plasma Cell Myeloma/Multiple Myeloma"}
+{"_id": "158", "text": "Multiple myeloma"}
+{"_id": "159", "text": "Marfan syndrome"}
+{"_id": "160", "text": "Marfan syndrome"}
+{"_id": "161", "text": "Acanthosis Nigricans"}
+{"_id": "162", "text": "Endometrial Adenocarcinoma"}
+{"_id": "163", "text": "Colonic Adenocarcinoma"}
+{"_id": "164", "text": "Biphasic Sarcoma of the Synovium"}
+{"_id": "165", "text": "Synovial sarcoma"}
+{"_id": "166", "text": "Ductal Adenocarcinoma of Pancreas"}
+{"_id": "167", "text": "Pyruvate Dehydrogenase Deficiency"}
+{"_id": "168", "text": "Pyruvate dehydrogenase deficiency"}
+{"_id": "169", "text": "Adult Precursor T-Lymphoblastic Leukemia"}
+{"_id": "170", "text": "Colon Cancer"}
+{"_id": "171", "text": "Pervasive Developmental Disorders"}
+{"_id": "172", "text": "Pervasive Developmental Disorder"}
+{"_id": "173", "text": "Mammary adenocarcinoma"}
+{"_id": "174", "text": "Hereditary Orotic Aciduria"}
+{"_id": "175", "text": "Hereditary orotic aciduria"}
+{"_id": "176", "text": "Duodenal Adenocarcinoma"}
+{"_id": "177", "text": "Poorly Differentiated Thyroid Gland Carcinoma"}
+{"_id": "178", "text": "Rare thyroid carcinoma"}
+{"_id": "179", "text": "Squamous Cell Lung Carcinoma"}
+{"_id": "180", "text": "Squamous Cell Carcinoma of the Head and Neck"}
+{"_id": "181", "text": "SCC of the Floor of Mouth"}
+{"_id": "182", "text": "Squamous cell carcinoma of the oral cavity"}
+{"_id": "183", "text": "primary effusion lymphoma"}
+{"_id": "184", "text": "Primary effusion lymphoma"}
+{"_id": "185", "text": "AIDS Associated Immunoblastic Lymphoma"}
+{"_id": "186", "text": "Waldenstrom Macroglobulinemia"}
+{"_id": "187", "text": "Waldenstr\u00f6m macroglobulinemia"}
+{"_id": "188", "text": "Fanconi Anemia, Complementation Group C"}
+{"_id": "189", "text": "Fanconi anemia"}
+{"_id": "190", "text": "Acute Myelogenous Leukemia"}
+{"_id": "191", "text": "Barrett Adenocarcinoma"}
+{"_id": "192", "text": "Adenocarcinoma of the esophagus"}
+{"_id": "193", "text": "Meningothelial Meningioma"}
+{"_id": "194", "text": "Meningioma"}
+{"_id": "195", "text": "Gestational Choriocarcinoma"}
+{"_id": "196", "text": "Gestational choriocarcinoma"}
+{"_id": "197", "text": "Transitional Cell Carcinoma of Renal Pelvis"}
+{"_id": "198", "text": "Adenocarcinoma of the Ovary"}
+{"_id": "199", "text": "Adenocarcinoma of ovary"}
+{"_id": "200", "text": "Alveolar Ridge Squamous Cell Carcinoma"}
+{"_id": "201", "text": "Ehlers-Danlos Syndrome"}
+{"_id": "202", "text": "Ehlers-Danlos syndrome"}
+{"_id": "203", "text": "SCC of Buccal Mucosa"}
+{"_id": "204", "text": "SCC of Tongue"}
+{"_id": "205", "text": "Squamous cell carcinoma of the oral tongue"}
+{"_id": "206", "text": "Ovarian Small Cell Carcinoma, Hypercalcemic Type"}
+{"_id": "207", "text": "Small cell carcinoma of the ovary"}
+{"_id": "208", "text": "Small Non-Cleaved Cell Lymphoma, Burkitt's Type"}
+{"_id": "209", "text": "Ehlers-Danlos Syndrome, Type I"}
+{"_id": "210", "text": "Pancreatic Serotonin-Producing Neuroendocrine Tumor"}
+{"_id": "211", "text": "Serotonin-producing neuroendocrine tumor of pancreas"}
+{"_id": "212", "text": "Leukemic reticuloendotheliosis"}
+{"_id": "213", "text": "Classic hairy cell leukemia"}
+{"_id": "214", "text": "Prostatic Hyperplasia"}
+{"_id": "215", "text": "Bare Lymphocyte Syndrome Type 1"}
+{"_id": "216", "text": "Immunodeficiency by defective expression of MHC class I"}
+{"_id": "217", "text": "Chronic Myelogenous Leukemia"}
+{"_id": "218", "text": "Chronic myeloid leukemia"}
+{"_id": "219", "text": "HPV-Independent Cervical Squamous Cell Carcinoma"}
+{"_id": "220", "text": "Large Intestine Adenocarcinoma"}
+{"_id": "221", "text": "Cri-du-Chat Syndrome"}
+{"_id": "222", "text": "Monosomy 5p syndrome"}
+{"_id": "223", "text": "Secondary Chondrosarcoma"}
+{"_id": "224", "text": "Enchondromatosis"}
+{"_id": "225", "text": "Nasopharyngeal Throat Cancer"}
+{"_id": "226", "text": "Nasopharyngeal carcinoma"}
+{"_id": "227", "text": "Porokeratosis"}
+{"_id": "228", "text": "Porokeratosis"}
+{"_id": "229", "text": "Gingival SCC"}
+{"_id": "230", "text": "Ovarian Serous Surface Papillary Adenocarcinoma"}
+{"_id": "231", "text": "Cancer of Breast"}
+{"_id": "232", "text": "Tongue Adenosquamous Carcinoma"}
+{"_id": "233", "text": "Squamous Cell Carcinoma of Vulva"}
+{"_id": "234", "text": "Vulvar squamous cell carcinoma"}
+{"_id": "235", "text": "Dedifferentiated Chondrosarcoma"}
+{"_id": "236", "text": "Rectal Adenocarcinoma"}
+{"_id": "237", "text": "Intrahepatic bile duct carcinoma"}
+{"_id": "238", "text": "Cholangiocarcinoma"}
+{"_id": "239", "text": "Polycystic Kidney Disease"}
+{"_id": "240", "text": "Poikiloderma"}
+{"_id": "241", "text": "Thyroid Gland Squamous Cell Carcinoma"}
+{"_id": "242", "text": "Well-differentiated Follicular Carcinoma"}
+{"_id": "243", "text": "Differentiated thyroid carcinoma"}
+{"_id": "244", "text": "Papillary Carcinoma of Thyroid"}
+{"_id": "245", "text": "Bronchus Cancer"}
+{"_id": "246", "text": "Large Intestine Cancer"}
+{"_id": "247", "text": "Neuroblastoma (Schwannian Stroma-poor)"}
+{"_id": "248", "text": "Neuroblastoma"}
+{"_id": "249", "text": "Galactosemia"}
+{"_id": "250", "text": "Galactosemia"}
+{"_id": "251", "text": "Neuroblastoma of the Adrenal Gland"}
+{"_id": "252", "text": "Childhood Acute M7 Leukemia"}
+{"_id": "253", "text": "Acute megakaryoblastic leukemia"}
+{"_id": "254", "text": "B-Cell Non-Hodgkin Lymphoma"}
+{"_id": "255", "text": "B-cell non-Hodgkin lymphoma"}
+{"_id": "256", "text": "Argininosuccinate Synthetase Deficiency"}
+{"_id": "257", "text": "Citrullinemia type I"}
+{"_id": "258", "text": "Squamous Cell Carcinoma of the Mouth"}
+{"_id": "259", "text": "Lactic Acidosis"}
+{"_id": "260", "text": "Fatal infantile lactic acidosis with methylmalonic aciduria"}
+{"_id": "261", "text": "Invasive Breast Lobular Carcinoma"}
+{"_id": "262", "text": "Monophasic Sarcoma of Synovium"}
+{"_id": "263", "text": "AML Occurring in Children with Down Syndrome"}
+{"_id": "264", "text": "Acute megakaryoblastic leukemia in children with Down syndrome"}
+{"_id": "265", "text": "Hereditary Colorectal Endometrial Cancer Syndrome"}
+{"_id": "266", "text": "Lynch syndrome"}
+{"_id": "267", "text": "Adenosquamous carcinoma"}
+{"_id": "268", "text": "Squamous cell carcinoma of pancreas"}
+{"_id": "269", "text": "Esophageal Squamous Cell Carcinoma, Not Otherwise Specified"}
+{"_id": "270", "text": "Squamous cell carcinoma of the esophagus"}
+{"_id": "271", "text": "Ehlers-Danlos Syndrome, Type IV"}
+{"_id": "272", "text": "Vascular Ehlers-Danlos syndrome"}
+{"_id": "273", "text": "Lung cancer, NOS"}
+{"_id": "274", "text": "Mucinous Carcinoma of the Ovary"}
+{"_id": "275", "text": "Mucinous adenocarcinoma of ovary"}
+{"_id": "276", "text": "Lou Gehrig Disease"}
+{"_id": "277", "text": "Cockayne Syndrome Type B"}
+{"_id": "278", "text": "Cockayne syndrome"}
+{"_id": "279", "text": "Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1"}
+{"_id": "280", "text": "Severe Infantile Spinal Muscular Atrophy"}
+{"_id": "281", "text": "Proximal spinal muscular atrophy type 1"}
+{"_id": "282", "text": "HD"}
+{"_id": "283", "text": "Huntington disease"}
+{"_id": "284", "text": "Childhood T-Lymphoblastic Lymphoma"}
+{"_id": "285", "text": "T-cell non-Hodgkin lymphoma"}
+{"_id": "286", "text": "gliosarcoma"}
+{"_id": "287", "text": "Gliosarcoma"}
+{"_id": "288", "text": "Medulloblastoma, Non-WNT/Non-SHH, Group 3"}
+{"_id": "289", "text": "Medulloblastoma"}
+{"_id": "290", "text": "MEDULLOBLASTOMA, MALIGNANT"}
+{"_id": "291", "text": "Stiff Skin Syndrome"}
+{"_id": "292", "text": "Stiff skin syndrome"}
+{"_id": "293", "text": "Ehlers-Danlos Syndrome, Type V"}
+{"_id": "294", "text": "X-linked Ehlers-Danlos syndrome"}
+{"_id": "295", "text": "Erythroleukemia"}
+{"_id": "296", "text": "Acute erythroid leukemia"}
+{"_id": "297", "text": "Adenocarcinoma of Pancreas"}
+{"_id": "298", "text": "Medulloblastoma, SHH-activated and TP53-mutant"}
+{"_id": "299", "text": "Diffuse Large B-Cell Lymphoma Germinal Center B-Cell Type"}
+{"_id": "300", "text": "Grade 3 Astrocytic Neoplasm"}
+{"_id": "301", "text": "Anaplastic astrocytoma"}
+{"_id": "302", "text": "ALCL, ALK+"}
+{"_id": "303", "text": "ALK-positive anaplastic large cell lymphoma"}
+{"_id": "304", "text": "XXY Syndrome"}
+{"_id": "305", "text": "Hepatosplenic gamma-delta cell lymphoma"}
+{"_id": "306", "text": "Hepatosplenic T-cell lymphoma"}
+{"_id": "307", "text": "Pharyngeal squam. cell carcinoma"}
+{"_id": "308", "text": "Gardner's Syndrome"}
+{"_id": "309", "text": "Gardner syndrome"}
+{"_id": "310", "text": "SMARCA4-Deficient Thoracic Sarcomatoid Tumor"}
+{"_id": "311", "text": "OED"}
+{"_id": "312", "text": "Cancer of Cervix"}
+{"_id": "313", "text": "Pediatric Hepatoblastoma"}
+{"_id": "314", "text": "Hepatoblastoma"}
+{"_id": "315", "text": "LYMPHANGIECTASIS"}
+{"_id": "316", "text": "RAD"}
+{"_id": "317", "text": "Dyschromatosis symmetrica hereditaria"}
+{"_id": "318", "text": "Infectious Mononucleosis"}
+{"_id": "319", "text": "Small Cell Carcinoma of Stomach"}
+{"_id": "320", "text": "Ehlers-Danlos Syndrome, Type III"}
+{"_id": "321", "text": "Hypermobile Ehlers-Danlos syndrome"}
+{"_id": "322", "text": "Ehlers-Danlos Syndrome, Type VII"}
+{"_id": "323", "text": "Arthrochalasia Ehlers-Danlos syndrome"}
+{"_id": "324", "text": "Acute Erythroid Leukemia"}
+{"_id": "325", "text": "CARCINOMA, ENDOMETRIAL, MALIGNANT"}
+{"_id": "326", "text": "Breast Ductal Carcinoma"}
+{"_id": "327", "text": "Ovarian Serous Cystadenocarcinoma"}
+{"_id": "328", "text": "Cholangiocellular Carcinoma"}
+{"_id": "329", "text": "Acute Monocytic Leukemia"}
+{"_id": "330", "text": "Childhood Chronic Myelogenous Leukemia, BCR::ABL1 Positive"}
+{"_id": "331", "text": "Chronic eosinophilic leukemia/hypereosinophilic syndrome"}
+{"_id": "332", "text": "Chronic eosinophilic leukemia"}
+{"_id": "333", "text": "Lung Mucoepidermoid Cancer"}
+{"_id": "334", "text": "Ovarian Clear Cell Adenocarcinoma"}
+{"_id": "335", "text": "Clear cell adenocarcinoma of the ovary"}
+{"_id": "336", "text": "Endometrial stromal sarcoma"}
+{"_id": "337", "text": "Endometrial stromal sarcoma"}
+{"_id": "338", "text": "Fanconi Anemia, Complementation Group F"}
+{"_id": "339", "text": "Fanconi Anemia, Complementation Group N"}
+{"_id": "340", "text": "Fanconi Anemia, Complementation Group G"}
+{"_id": "341", "text": "Myelodysplastic Syndrome/Neoplasm"}
+{"_id": "342", "text": "meningioma"}
+{"_id": "343", "text": "Hypopharyngeal Throat Squamous Cell Cancer"}
+{"_id": "344", "text": "Squamous cell carcinoma of the hypopharynx"}
+{"_id": "345", "text": "AOA1"}
+{"_id": "346", "text": "Ataxia-oculomotor apraxia type 1"}
+{"_id": "347", "text": "Anaplastic large cell lymphoma, ALK negative"}
+{"_id": "348", "text": "ALK-negative anaplastic large cell lymphoma"}
+{"_id": "349", "text": "Adult Primary Hepatocellular Carcinoma"}
+{"_id": "350", "text": "Adult hepatocellular carcinoma"}
+{"_id": "351", "text": "Mucopolysaccharidosis IV"}
+{"_id": "352", "text": "Mucopolysaccharidosis type 4"}
+{"_id": "353", "text": "Pseudoxanthoma Elasticum"}
+{"_id": "354", "text": "Follicle Center Lymphoma"}
+{"_id": "355", "text": "Follicular lymphoma"}
+{"_id": "356", "text": "PNET"}
+{"_id": "357", "text": "Rhabdoid Tumor of the Kidney (RTK)"}
+{"_id": "358", "text": "Rhabdoid tumor"}
+{"_id": "359", "text": "Renal Neoplasm"}
+{"_id": "360", "text": "Cancer of the Gallbladder"}
+{"_id": "361", "text": "Carcinoma of gallbladder and extrahepatic biliary tract"}
+{"_id": "362", "text": "L3 Adult Acute Lymphoblastic Leukemia"}
+{"_id": "363", "text": "Vulvar Melanoma"}
+{"_id": "364", "text": "FIBROSARCOMA, PLEOMORPHIC, MALIGNANT"}
+{"_id": "365", "text": "Undifferentiated pleomorphic sarcoma"}
+{"_id": "366", "text": "Gastrointestinal Stromal Neoplasm"}
+{"_id": "367", "text": "Gastrointestinal stromal tumor"}
+{"_id": "368", "text": "Familial Glomangioma"}
+{"_id": "369", "text": "Glomuvenous malformation"}
+{"_id": "370", "text": "Acute lymphoblastic leukemia"}
+{"_id": "371", "text": "Acute lymphoblastic leukemia"}
+{"_id": "372", "text": "phenylketonuria"}
+{"_id": "373", "text": "Phenylketonuria"}
+{"_id": "374", "text": "Nephropathic Cystinosis"}
+{"_id": "375", "text": "Infantile nephropathic cystinosis"}
+{"_id": "376", "text": "Mitochondrial Myopathy"}
+{"_id": "377", "text": "Mitochondrial myopathy"}
+{"_id": "378", "text": "Hepatolenticular Degeneration"}
+{"_id": "379", "text": "Wilson disease"}
+{"_id": "380", "text": "Hurler Syndrome"}
+{"_id": "381", "text": "Hurler syndrome"}
+{"_id": "382", "text": "Mucopolysaccharidosis Type II"}
+{"_id": "383", "text": "Mucopolysaccharidosis type 2"}
+{"_id": "384", "text": "Cornelia De Lange Syndrome"}
+{"_id": "385", "text": "Cornelia de Lange syndrome"}
+{"_id": "386", "text": "46,XY Sex Reversal 1"}
+{"_id": "387", "text": "46,XY complete gonadal dysgenesis"}
+{"_id": "388", "text": "Propionic Acidemia"}
+{"_id": "389", "text": "Propionic acidemia"}
+{"_id": "390", "text": "Canavan Disease"}
+{"_id": "391", "text": "Canavan disease"}
+{"_id": "392", "text": "Lesch-Nyhan Syndrome"}
+{"_id": "393", "text": "Lesch-Nyhan syndrome"}
+{"_id": "394", "text": "Wolf-Hirschhorn Syndrome"}
+{"_id": "395", "text": "Wolf-Hirschhorn syndrome"}
+{"_id": "396", "text": "Tay Sachs Disease"}
+{"_id": "397", "text": "Tay-Sachs disease"}
+{"_id": "398", "text": "Metachromatic Leukodystrophy"}
+{"_id": "399", "text": "Metachromatic leukodystrophy"}
+{"_id": "400", "text": "Trisomy 22"}
+{"_id": "401", "text": "Total autosomal trisomy syndrome"}
+{"_id": "402", "text": "SGBS1"}
+{"_id": "403", "text": "Simpson-Golabi-Behmel syndrome"}
+{"_id": "404", "text": "Alpha-Galactosidase A Deficiency"}
+{"_id": "405", "text": "Fabry disease"}
+{"_id": "406", "text": "Supernumerary Circular Chromosome"}
+{"_id": "407", "text": "Type C1 Niemann-Pick Disease"}
+{"_id": "408", "text": "Niemann-Pick disease type C"}
+{"_id": "409", "text": "Glycogen Storage Disease Type III"}
+{"_id": "410", "text": "Glycogen storage disease due to glycogen debranching enzyme deficiency"}
+{"_id": "411", "text": "Niemann-Pick Disease, Type A"}
+{"_id": "412", "text": "Infantile neurovisceral acid sphingomyelinase deficiency"}
+{"_id": "413", "text": "Mucolipidosis Type IIIA"}
+{"_id": "414", "text": "Mucolipidosis type III alpha/beta"}
+{"_id": "415", "text": "Mucopolysaccharidosis Type VII"}
+{"_id": "416", "text": "Mucopolysaccharidosis type 7"}
+{"_id": "417", "text": "MPS III B"}
+{"_id": "418", "text": "Sanfilippo syndrome type B"}
+{"_id": "419", "text": "49,XXXXY Syndrome"}
+{"_id": "420", "text": "49,XXXXY syndrome"}
+{"_id": "421", "text": "Niemann-Pick Disease"}
+{"_id": "422", "text": "Sandhoff Disease"}
+{"_id": "423", "text": "Sandhoff disease"}
+{"_id": "424", "text": "Methylmalonic Aciduria, cblA Type"}
+{"_id": "425", "text": "Vitamin B12-responsive methylmalonic acidemia type cblA"}
+{"_id": "426", "text": "Menkes Kinky Hair Syndrome"}
+{"_id": "427", "text": "Menkes disease"}
+{"_id": "428", "text": "Zellweger Syndrome"}
+{"_id": "429", "text": "Zellweger syndrome"}
+{"_id": "430", "text": "Chondrodystrophy"}
+{"_id": "431", "text": "Glycogen Storage Disease Type II"}
+{"_id": "432", "text": "Glycogen storage disease due to acid maltase deficiency"}
+{"_id": "433", "text": "Fructose-1,6-Bisphosphatase Deficiency"}
+{"_id": "434", "text": "Fructose-1,6-bisphosphatase deficiency"}
+{"_id": "435", "text": "Type IIa Hyperlipidemia"}
+{"_id": "436", "text": "Homozygous familial hypercholesterolemia"}
+{"_id": "437", "text": "Ring Chromosome 13 Syndrome"}
+{"_id": "438", "text": "Ring chromosome 13 syndrome"}
+{"_id": "439", "text": "Tyrosinemia Type I"}
+{"_id": "440", "text": "Tyrosinemia type 1"}
+{"_id": "441", "text": "Fucosidosis"}
+{"_id": "442", "text": "Fucosidosis"}
+{"_id": "443", "text": "Maple Syrup Urine Disease"}
+{"_id": "444", "text": "Maple syrup urine disease"}
+{"_id": "445", "text": "Mucopolysaccharidosis Type IIIA"}
+{"_id": "446", "text": "Sanfilippo syndrome type A"}
+{"_id": "447", "text": "G6PD Deficiency"}
+{"_id": "448", "text": "Class I glucose-6-phosphate dehydrogenase deficiency"}
+{"_id": "449", "text": "GALK Deficiency"}
+{"_id": "450", "text": "Galactokinase deficiency"}
+{"_id": "451", "text": "Isodicentric Chromosome"}
+{"_id": "452", "text": "Homocystinuria"}
+{"_id": "453", "text": "Homocystinuria due to cystathionine beta-synthase deficiency"}
+{"_id": "454", "text": "Beckwith-Wiedemann"}
+{"_id": "455", "text": "Beckwith-Wiedemann syndrome"}
+{"_id": "456", "text": "Bruton's X-Linked Agammaglobulinemia"}
+{"_id": "457", "text": "X-linked agammaglobulinemia"}
+{"_id": "458", "text": "Fanconi's Anemia"}
+{"_id": "459", "text": "Fanconi Anemia, Complementation Group A"}
+{"_id": "460", "text": "Gaucher Disease"}
+{"_id": "461", "text": "Gaucher disease"}
+{"_id": "462", "text": "Trisomy 8"}
+{"_id": "463", "text": "Gout"}
+{"_id": "464", "text": "Pyruvate Carboxylase Deficiency Disease"}
+{"_id": "465", "text": "Pyruvate carboxylase deficiency"}
+{"_id": "466", "text": "Adenosine Deaminase Severe Combined Immunodeficiency"}
+{"_id": "467", "text": "Severe combined immunodeficiency due to adenosine deaminase deficiency"}
+{"_id": "468", "text": "Cutis Laxa"}
+{"_id": "469", "text": "Cutis laxa"}
+{"_id": "470", "text": "Incontinentia Pigmenti"}
+{"_id": "471", "text": "Incontinentia pigmenti"}
+{"_id": "472", "text": "Mental Retardation"}
+{"_id": "473", "text": "MPS I H-S"}
+{"_id": "474", "text": "Hurler-Scheie syndrome"}
+{"_id": "475", "text": "Fibrodysplasia Ossificans Progressiva"}
+{"_id": "476", "text": "Fibrodysplasia ossificans progressiva"}
+{"_id": "477", "text": "Adenine Phosphoribosyltransferase Deficiency"}
+{"_id": "478", "text": "Adenine phosphoribosyltransferase deficiency"}
+{"_id": "479", "text": "Mucopolysaccharidosis VI"}
+{"_id": "480", "text": "Mucopolysaccharidosis type 6"}
+{"_id": "481", "text": "Argininosuccinate Lyase Deficiency"}
+{"_id": "482", "text": "Argininosuccinic aciduria"}
+{"_id": "483", "text": "Aspartylglycosaminuria"}
+{"_id": "484", "text": "Aspartylglucosaminuria"}
+{"_id": "485", "text": "Glycogen Storage Disease Type IV"}
+{"_id": "486", "text": "Glycogen storage disease due to glycogen branching enzyme deficiency"}
+{"_id": "487", "text": "Glycogen Storage Disease Type Ia"}
+{"_id": "488", "text": "Glycogen storage disease due to glucose-6-phosphatase deficiency type Ia"}
+{"_id": "489", "text": "Glycogen Storage Disease Type IX"}
+{"_id": "490", "text": "Glycogen storage disease due to phosphorylase kinase deficiency"}
+{"_id": "491", "text": "Glycogen Storage Disease Type V"}
+{"_id": "492", "text": "Glycogen storage disease due to muscle glycogen phosphorylase deficiency"}
+{"_id": "493", "text": "Glycogen Storage Disease Type VI"}
+{"_id": "494", "text": "Glycogen storage disease due to liver glycogen phosphorylase deficiency"}
+{"_id": "495", "text": "MPS IV A"}
+{"_id": "496", "text": "Mucopolysaccharidosis type 4A"}
+{"_id": "497", "text": "Familial Dysautonomia"}
+{"_id": "498", "text": "Familial dysautonomia"}
+{"_id": "499", "text": "Asthma"}
+{"_id": "500", "text": "Alpha-Mannosidosis"}
+{"_id": "501", "text": "Alpha-mannosidosis"}
+{"_id": "502", "text": "Hypercholesterolemia, Familial, 4"}
+{"_id": "503", "text": "Thanatophoric Dysplasia"}
+{"_id": "504", "text": "Thanatophoric dysplasia"}
+{"_id": "505", "text": "Peripheral sensory neuropathy"}
+{"_id": "506", "text": "Rare peripheral neuropathy"}
+{"_id": "507", "text": "Rhizomelic Dwarfism"}
+{"_id": "508", "text": "Rhizomelic chondrodysplasia punctata"}
+{"_id": "509", "text": "Phosphoglycerate Kinase 1 Deficiency"}
+{"_id": "510", "text": "Glycogen storage disease due to phosphoglycerate kinase 1 deficiency"}
+{"_id": "511", "text": "Glycine Encephalopathy"}
+{"_id": "512", "text": "Glycine encephalopathy"}
+{"_id": "513", "text": "Sea-Blue Histiocyte Syndrome"}
+{"_id": "514", "text": "Sea-blue histiocytosis"}
+{"_id": "515", "text": "Wolman Disease"}
+{"_id": "516", "text": "Wolman disease"}
+{"_id": "517", "text": "Methylmalonic Aciduria, cblB Type"}
+{"_id": "518", "text": "Vitamin B12-responsive methylmalonic acidemia type cblB"}
+{"_id": "519", "text": "Isolated Persistent Hypermethioninemia"}
+{"_id": "520", "text": "Methionine adenosyltransferase I/III deficiency"}
+{"_id": "521", "text": "Sporadic Retinoblastoma"}
+{"_id": "522", "text": "Retinoblastoma"}
+{"_id": "523", "text": "GM1 Gangliosidosis"}
+{"_id": "524", "text": "GM1 gangliosidosis"}
+{"_id": "525", "text": "Methylmalonic Acidemia"}
+{"_id": "526", "text": "Methylmalonic acidemia without homocystinuria"}
+{"_id": "527", "text": "Acute Intermittent Porphyria"}
+{"_id": "528", "text": "Acute intermittent porphyria"}
+{"_id": "529", "text": "Isovaleric Acidemia"}
+{"_id": "530", "text": "Isovaleric acidemia"}
+{"_id": "531", "text": "Scleromyxedema"}
+{"_id": "532", "text": "Scleromyxedema"}
+{"_id": "533", "text": "Hyperargininemia"}
+{"_id": "534", "text": "Argininemia"}
+{"_id": "535", "text": "Porphyria Cutanea Tarda"}
+{"_id": "536", "text": "Porphyria cutanea tarda"}
+{"_id": "537", "text": "Hereditary Coproporphyria"}
+{"_id": "538", "text": "Hereditary coproporphyria"}
+{"_id": "539", "text": "Erythropoietic Porphyria"}
+{"_id": "540", "text": "Congenital erythropoietic porphyria"}
+{"_id": "541", "text": "Maturity-Onset Diabetes of the Young, Type 1"}
+{"_id": "542", "text": "MODY"}
+{"_id": "543", "text": "Retinoblastoma"}
+{"_id": "544", "text": "Retinal Macular Dystrophy-1"}
+{"_id": "545", "text": "North Carolina macular dystrophy"}
+{"_id": "546", "text": "Xeroderma Pigmentosum, Complementation Group E"}
+{"_id": "547", "text": "Nonsyndromic X-Linked Cognitive Disability"}
+{"_id": "548", "text": "X-linked non-syndromic intellectual disability"}
+{"_id": "549", "text": "Maturity-Onset Diabetes of the Young"}
+{"_id": "550", "text": "XYY Syndrome"}
+{"_id": "551", "text": "47,XYY syndrome"}
+{"_id": "552", "text": "MPS I S"}
+{"_id": "553", "text": "Scheie syndrome"}
+{"_id": "554", "text": "Dermoid Cyst of the Ovary"}
+{"_id": "555", "text": "Hereditary Persistence of Fetal Hemoglobin"}
+{"_id": "556", "text": "Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome"}
+{"_id": "557", "text": "Testicular Feminization Syndrome"}
+{"_id": "558", "text": "Androgen insensitivity syndrome"}
+{"_id": "559", "text": "Abetalipoproteinemia"}
+{"_id": "560", "text": "Abetalipoproteinemia"}
+{"_id": "561", "text": "Cystathioninuria"}
+{"_id": "562", "text": "Cystathioninuria"}
+{"_id": "563", "text": "Hyperlipoproteinemia, Type IIb"}
+{"_id": "564", "text": "Familial chylomicronemia syndrome"}
+{"_id": "565", "text": "Schizophrenia"}
+{"_id": "566", "text": "Anorexia nervosa"}
+{"_id": "567", "text": "Leigh's Disease"}
+{"_id": "568", "text": "Leigh syndrome"}
+{"_id": "569", "text": "Delayed developmental milestones"}
+{"_id": "570", "text": "Basal Cell Nevus Syndrome"}
+{"_id": "571", "text": "Gorlin syndrome"}
+{"_id": "572", "text": "Hypophosphatasia"}
+{"_id": "573", "text": "Hypophosphatasia"}
+{"_id": "574", "text": "Mucolipidosis Type II"}
+{"_id": "575", "text": "Mucolipidosis type II"}
+{"_id": "576", "text": "Aldrich syndrome"}
+{"_id": "577", "text": "Wiskott-Aldrich syndrome"}
+{"_id": "578", "text": "Sitosterolemia"}
+{"_id": "579", "text": "Sitosterolemia"}
+{"_id": "580", "text": "MPS IV B"}
+{"_id": "581", "text": "Mucopolysaccharidosis type 4B"}
+{"_id": "582", "text": "Wolfram Syndrome"}
+{"_id": "583", "text": "Wolfram syndrome"}
+{"_id": "584", "text": "Inosine Triphosphatase Deficiency"}
+{"_id": "585", "text": "ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement"}
+{"_id": "586", "text": "Tuberous Sclerosis 1"}
+{"_id": "587", "text": "Tuberous sclerosis complex"}
+{"_id": "588", "text": "Cartilage Hair Hypoplasia"}
+{"_id": "589", "text": "Cartilage-hair hypoplasia"}
+{"_id": "590", "text": "GM2-Gangliosidosis, AB Variant"}
+{"_id": "591", "text": "GM2 gangliosidosis, AB variant"}
+{"_id": "592", "text": "Oculocerebrorenal Syndrome"}
+{"_id": "593", "text": "Oculocerebrorenal syndrome of Lowe"}
+{"_id": "594", "text": "Duchenne Muscular Dystrophy"}
+{"_id": "595", "text": "Duchenne muscular dystrophy"}
+{"_id": "596", "text": "gonadal dysgenesis"}
+{"_id": "597", "text": "Mucolipidosis I"}
+{"_id": "598", "text": "Sialidosis type 2"}
+{"_id": "599", "text": "XP-C"}
+{"_id": "600", "text": "CMD"}
+{"_id": "601", "text": "Campomelic dysplasia"}
+{"_id": "602", "text": "CPT II Deficiency"}
+{"_id": "603", "text": "Carnitine palmitoyltransferase II deficiency"}
+{"_id": "604", "text": "Krabbe Disease"}
+{"_id": "605", "text": "Krabbe disease"}
+{"_id": "606", "text": "Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1"}
+{"_id": "607", "text": "Kyphoscoliotic Ehlers-Danlos syndrome"}
+{"_id": "608", "text": "Neurofibroma (WHO Grade I)"}
+{"_id": "609", "text": "Neurofibroma"}
+{"_id": "610", "text": "XX Male"}
+{"_id": "611", "text": "46,XX testicular difference of sex development"}
+{"_id": "612", "text": "AVED"}
+{"_id": "613", "text": "Ataxia with vitamin E deficiency"}
+{"_id": "614", "text": "Amyloidosis, Familial"}
+{"_id": "615", "text": "Hereditary ATTR amyloidosis"}
+{"_id": "616", "text": "Mucolipidosis IV"}
+{"_id": "617", "text": "Mucolipidosis type IV"}
+{"_id": "618", "text": "Chediak-Higashi Syndrome"}
+{"_id": "619", "text": "Ch\u00e9diak-Higashi syndrome"}
+{"_id": "620", "text": "Autosomal Dominant Torsion Dystonia 1"}
+{"_id": "621", "text": "Early-onset generalized limb-onset dystonia"}
+{"_id": "622", "text": "Alkaptonuria"}
+{"_id": "623", "text": "Alkaptonuria"}
+{"_id": "624", "text": "Thalassemia Major"}
+{"_id": "625", "text": "Beta-thalassemia major"}
+{"_id": "626", "text": "Congenital Adrenal Hyperplasia 1"}
+{"_id": "627", "text": "Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency"}
+{"_id": "628", "text": "Autosomal Recessive Torsion Dystonia 2"}
+{"_id": "629", "text": "Primary dystonia, DYT2 type"}
+{"_id": "630", "text": "WNCHRS"}
+{"_id": "631", "text": "Multicentric osteolysis-nodulosis-arthropathy spectrum"}
+{"_id": "632", "text": "Becker's Muscular Dystrophy"}
+{"_id": "633", "text": "Becker muscular dystrophy"}
+{"_id": "634", "text": "Variegate Porphyria"}
+{"_id": "635", "text": "Variegate porphyria"}
+{"_id": "636", "text": "Farber Lipogranulomatosis"}
+{"_id": "637", "text": "Farber disease"}
+{"_id": "638", "text": "Trisomy 9"}
+{"_id": "639", "text": "Sickle-cell Disorders"}
+{"_id": "640", "text": "Sickle cell anemia"}
+{"_id": "641", "text": "Coffin-Lowry Syndrome"}
+{"_id": "642", "text": "Coffin-Lowry syndrome"}
+{"_id": "643", "text": "DMC"}
+{"_id": "644", "text": "Dyggve-Melchior-Clausen disease"}
+{"_id": "645", "text": "Goldberg Syndrome"}
+{"_id": "646", "text": "Galactosialidosis"}
+{"_id": "647", "text": "Schilder Disease"}
+{"_id": "648", "text": "X-linked cerebral adrenoleukodystrophy"}
+{"_id": "649", "text": "Methylmalonic Aciduria and Homocystinuria, cblC Type"}
+{"_id": "650", "text": "Methylmalonic acidemia with homocystinuria, type cblC"}
+{"_id": "651", "text": "Alpha 1-Antitrypsin Disease"}
+{"_id": "652", "text": "Alpha-1-antitrypsin deficiency"}
+{"_id": "653", "text": "Hemoglobin Lepore Syndrome"}
+{"_id": "654", "text": "Hemoglobin Lepore-beta-thalassemia syndrome"}
+{"_id": "655", "text": "Carnosinemia"}
+{"_id": "656", "text": "Carnosinase deficiency"}
+{"_id": "657", "text": "Turcot Syndrome"}
+{"_id": "658", "text": "Turcot syndrome with polyposis"}
+{"_id": "659", "text": "Tourette Syndrome"}
+{"_id": "660", "text": "Hard Skin Syndrome Parana Type"}
+{"_id": "661", "text": "Parana hard skin syndrome"}
+{"_id": "662", "text": "Sialidosis type 1"}
+{"_id": "663", "text": "Carbonic Anhydrase I Deficiency"}
+{"_id": "664", "text": "depression"}
+{"_id": "665", "text": "Nasal Polyp"}
+{"_id": "666", "text": "Acrodermatitis Enteropathica"}
+{"_id": "667", "text": "Acrodermatitis enteropathica"}
+{"_id": "668", "text": "Dubowitz Syndrome"}
+{"_id": "669", "text": "Dubowitz syndrome"}
+{"_id": "670", "text": "Epidermolysis Bullosa Dystrophica"}
+{"_id": "671", "text": "Dystrophic epidermolysis bullosa"}
+{"_id": "672", "text": "Eosinophilic Fasciitis"}
+{"_id": "673", "text": "Eosinophilic fasciitis"}
+{"_id": "674", "text": "Leri-Weill Dyschondrosteosis"}
+{"_id": "675", "text": "L\u00e9ri-Weill dyschondrosteosis"}
+{"_id": "676", "text": "5-Alpha-Reductase Deficiency"}
+{"_id": "677", "text": "46,XY difference of sex development due to 5-alpha-reductase 2 deficiency"}
+{"_id": "678", "text": "FACES"}
+{"_id": "679", "text": "22q11.2 deletion syndrome"}
+{"_id": "680", "text": "Hereditary Sensory and Autonomic Neuropathy Type IV"}
+{"_id": "681", "text": "Hereditary sensory and autonomic neuropathy type 4"}
+{"_id": "682", "text": "Epidermodysplasia Verruciformis"}
+{"_id": "683", "text": "Inherited epidermodysplasia verruciformis"}
+{"_id": "684", "text": "Ring Chromosome 14 Syndrome"}
+{"_id": "685", "text": "Ring chromosome 14 syndrome"}
+{"_id": "686", "text": "Telangiectasia, Hereditary Hemorrahagic, of Rendu, Osler"}
+{"_id": "687", "text": "Hereditary hemorrhagic telangiectasia"}
+{"_id": "688", "text": "Ichthyosis, X-linked"}
+{"_id": "689", "text": "X-linked ichthyosis syndrome"}
+{"_id": "690", "text": "Alpha Thalassemia"}
+{"_id": "691", "text": "Alpha-thalassemia"}
+{"_id": "692", "text": "Smith-Lemli-Opitz Syndrome"}
+{"_id": "693", "text": "Smith-Lemli-Opitz syndrome"}
+{"_id": "694", "text": "Congenital Sucrase-Isomaltase Deficiency"}
+{"_id": "695", "text": "Congenital sucrase-isomaltase deficiency"}
+{"_id": "696", "text": "MMDD"}
+{"_id": "697", "text": "Adenosine monophosphate deaminase deficiency"}
+{"_id": "698", "text": "Wagr Syndrome"}
+{"_id": "699", "text": "WAGR syndrome"}
+{"_id": "700", "text": "TETRALOGY OF FALLOT"}
+{"_id": "701", "text": "Tetralogy of Fallot"}
+{"_id": "702", "text": "Pseudoachondroplasia"}
+{"_id": "703", "text": "Pseudoachondroplasia"}
+{"_id": "704", "text": "Tarui Disease"}
+{"_id": "705", "text": "Glycogen storage disease due to muscle phosphofructokinase deficiency"}
+{"_id": "706", "text": "Anetoderma"}
+{"_id": "707", "text": "Primary anetoderma"}
+{"_id": "708", "text": "Glutaric Aciduria, Type 2"}
+{"_id": "709", "text": "Multiple acyl-CoA dehydrogenase deficiency"}
+{"_id": "710", "text": "Fragile X Syndrome"}
+{"_id": "711", "text": "Fragile X syndrome"}
+{"_id": "712", "text": "Meckel-Gruber Syndrome"}
+{"_id": "713", "text": "Meckel syndrome"}
+{"_id": "714", "text": "Idiopathic Torsion Dystonia"}
+{"_id": "715", "text": "Rare dystonia"}
+{"_id": "716", "text": "Idiopathic Basal Ganglia Calcification 1"}
+{"_id": "717", "text": "Bilateral striopallidodentate calcinosis"}
+{"_id": "718", "text": "Multiple Sulfatase Deficiency Disease"}
+{"_id": "719", "text": "Multiple sulfatase deficiency"}
+{"_id": "720", "text": "Ichthyosis"}
+{"_id": "721", "text": "Inherited ichthyosis"}
+{"_id": "722", "text": "Mucolipidosis III Gamma"}
+{"_id": "723", "text": "Mucolipidosis type III gamma"}
+{"_id": "724", "text": "Niemann-Pick Disease, Type B"}
+{"_id": "725", "text": "Chronic visceral acid sphingomyelinase deficiency"}
+{"_id": "726", "text": "Carbamoyl Phosphate Synthetase Deficiency"}
+{"_id": "727", "text": "Carbamoyl-phosphate synthetase 1 deficiency"}
+{"_id": "728", "text": "Embryonal Nephroma"}
+{"_id": "729", "text": "Nephroblastoma"}
+{"_id": "730", "text": "Asphyxiating Thoracic Dystrophy"}
+{"_id": "731", "text": "Jeune syndrome"}
+{"_id": "732", "text": "Neonatal Multiple Carboxylase Deficiency"}
+{"_id": "733", "text": "Holocarboxylase synthetase deficiency"}
+{"_id": "734", "text": "17 beta HSD3 Deficiency"}
+{"_id": "735", "text": "46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency"}
+{"_id": "736", "text": "Spinocerebellar Ataxia Type 7"}
+{"_id": "737", "text": "Spinocerebellar ataxia type 7"}
+{"_id": "738", "text": "Trisomy 2"}
+{"_id": "739", "text": "Trisomy 21"}
+{"_id": "740", "text": "Pipecolic Acidemia"}
+{"_id": "741", "text": "Pipecolic acidemia"}
+{"_id": "742", "text": "Friedreich's Ataxia"}
+{"_id": "743", "text": "Friedreich ataxia"}
+{"_id": "744", "text": "Glycogen Storage Disease Type I non-a"}
+{"_id": "745", "text": "Glycogen storage disease due to glucose-6-phosphatase deficiency type Ib"}
+{"_id": "746", "text": "Central Core Myopathy"}
+{"_id": "747", "text": "Central core disease"}
+{"_id": "748", "text": "Deletion 18p Syndrome"}
+{"_id": "749", "text": "Monosomy 18p syndrome"}
+{"_id": "750", "text": "SMA2"}
+{"_id": "751", "text": "Proximal spinal muscular atrophy type 2"}
+{"_id": "752", "text": "Retinitis Pigmentosa"}
+{"_id": "753", "text": "Retinitis pigmentosa"}
+{"_id": "754", "text": "Leber Congenital Amaurosis"}
+{"_id": "755", "text": "Leber congenital amaurosis"}
+{"_id": "756", "text": "Usher Syndrome Type 1"}
+{"_id": "757", "text": "Usher syndrome type 1"}
+{"_id": "758", "text": "Hereditary Optic Atrophy"}
+{"_id": "759", "text": "Hereditary optic neuropathy"}
+{"_id": "760", "text": "Glutathione Synthetase Deficiency"}
+{"_id": "761", "text": "Glutathione synthetase deficiency"}
+{"_id": "762", "text": "Klippel-Feil Syndrome"}
+{"_id": "763", "text": "Isolated Klippel-Feil syndrome"}
+{"_id": "764", "text": "Refsum Disease"}
+{"_id": "765", "text": "Refsum disease"}
+{"_id": "766", "text": "Roberts-SC Phocomelia Syndrome"}
+{"_id": "767", "text": "Roberts syndrome"}
+{"_id": "768", "text": "Limb-Girdle Muscular Dystrophy Type 2A"}
+{"_id": "769", "text": "Calpain-3-related limb-girdle muscular dystrophy R1"}
+{"_id": "770", "text": "Tuberous Sclerosis 2"}
+{"_id": "771", "text": "Familial Essential Hyperlipemia"}
+{"_id": "772", "text": "Renal Carnitine Transport Defect"}
+{"_id": "773", "text": "Systemic primary carnitine deficiency"}
+{"_id": "774", "text": "LEOPARD Syndrome"}
+{"_id": "775", "text": "Noonan syndrome with multiple lentigines"}
+{"_id": "776", "text": "Osteogenesis Imperfecta Type II"}
+{"_id": "777", "text": "Osteogenesis imperfecta type 2"}
+{"_id": "778", "text": "Kniest Dysplasia"}
+{"_id": "779", "text": "Kniest dysplasia"}
+{"_id": "780", "text": "Pterygium"}
+{"_id": "781", "text": "Familial pterygium of the conjunctiva"}
+{"_id": "782", "text": "Prader-Willi-Labhart Syndrome"}
+{"_id": "783", "text": "Prader-Willi syndrome"}
+{"_id": "784", "text": "Spinocerebellar Ataxia"}
+{"_id": "785", "text": "Hereditary ataxia"}
+{"_id": "786", "text": "Kearns-Sayre Syndrome"}
+{"_id": "787", "text": "Kearns-Sayre syndrome"}
+{"_id": "788", "text": "Tyrosinemia Type II"}
+{"_id": "789", "text": "Tyrosinemia type 2"}
+{"_id": "790", "text": "Pseudohypoparathyroidism, Type IA"}
+{"_id": "791", "text": "Albright hereditary osteodystrophy"}
+{"_id": "792", "text": "Trisomy 16"}
+{"_id": "793", "text": "Schwartz-Jampel Syndrome"}
+{"_id": "794", "text": "Schwartz-Jampel syndrome"}
+{"_id": "795", "text": "Acyl-CoA Dehydrogenase, Medium-Chain Deficiency"}
+{"_id": "796", "text": "Medium chain acyl-CoA dehydrogenase deficiency"}
+{"_id": "797", "text": "Sideroblastic Anemia"}
+{"_id": "798", "text": "Sideroblastic anemia"}
+{"_id": "799", "text": "CMTX1"}
+{"_id": "800", "text": "X-linked Charcot-Marie-Tooth disease type 1"}
+{"_id": "801", "text": "Glucocorticoid Resistance"}
+{"_id": "802", "text": "Generalized glucocorticoid resistance syndrome"}
+{"_id": "803", "text": "Bannayan Syndrome"}
+{"_id": "804", "text": "Bannayan-Riley-Ruvalcaba syndrome"}
+{"_id": "805", "text": "Manic Depressive Disorder"}
+{"_id": "806", "text": "Glutaric Acidemia Type 1"}
+{"_id": "807", "text": "Glutaryl-CoA dehydrogenase deficiency"}
+{"_id": "808", "text": "Hartnup Disease"}
+{"_id": "809", "text": "Hartnup disease"}
+{"_id": "810", "text": "Erythropoietic Protoporphyria"}
+{"_id": "811", "text": "Autosomal erythropoietic protoporphyria"}
+{"_id": "812", "text": "XXXXX Syndrome"}
+{"_id": "813", "text": "Pentasomy X syndrome"}
+{"_id": "814", "text": "Sanfilippo D"}
+{"_id": "815", "text": "Sanfilippo syndrome type D"}
+{"_id": "816", "text": "Charcot-Marie-Tooth Disease Type 1A"}
+{"_id": "817", "text": "Charcot-Marie-Tooth disease type 1A"}
+{"_id": "818", "text": "MPS III C"}
+{"_id": "819", "text": "Sanfilippo syndrome type C"}
+{"_id": "820", "text": "Osteogenesis Imperfecta Type I"}
+{"_id": "821", "text": "Osteogenesis imperfecta type 1"}
+{"_id": "822", "text": "Anxiety Disorder"}
+{"_id": "823", "text": "Leprechaunism"}
+{"_id": "824", "text": "Leprechaunism"}
+{"_id": "825", "text": "Kartagener Syndrome"}
+{"_id": "826", "text": "Primary Ciliary Dyskinesia 1"}
+{"_id": "827", "text": "Primary ciliary dyskinesia, Kartagener type"}
+{"_id": "828", "text": "Fragile Site"}
+{"_id": "829", "text": "Sialic Acid Storage Disease"}
+{"_id": "830", "text": "Free sialic acid storage disease"}
+{"_id": "831", "text": "Alagille Syndrome"}
+{"_id": "832", "text": "Alagille syndrome"}
+{"_id": "833", "text": "Manic Bipolar Affective Disorder"}
+{"_id": "834", "text": "Laurence-Moon-Bardet-Biedl Syndrome"}
+{"_id": "835", "text": "Bardet-Biedl syndrome"}
+{"_id": "836", "text": "Major Depression"}
+{"_id": "837", "text": "Miller-Dieker Syndrome"}
+{"_id": "838", "text": "Miller-Dieker syndrome"}
+{"_id": "839", "text": "Osteopetrosis with Renal Tubular Acidosis"}
+{"_id": "840", "text": "Osteopetrosis with renal tubular acidosis"}
+{"_id": "841", "text": "VLCAD"}
+{"_id": "842", "text": "Very long chain acyl-CoA dehydrogenase deficiency"}
+{"_id": "843", "text": "Machado-Joseph Disease"}
+{"_id": "844", "text": "Spinocerebellar ataxia type 3"}
+{"_id": "845", "text": "Schinzel-Giedion Syndrome"}
+{"_id": "846", "text": "Schinzel-Giedion syndrome"}
+{"_id": "847", "text": "Ring Chromosome 21 Syndrome"}
+{"_id": "848", "text": "Ring chromosome 21 syndrome"}
+{"_id": "849", "text": "PBD8A"}
+{"_id": "850", "text": "Peroxisome biogenesis disorder"}
+{"_id": "851", "text": "Analbuminemia"}
+{"_id": "852", "text": "Congenital analbuminemia"}
+{"_id": "853", "text": "Infantile Neuroaxonal Dystrophy"}
+{"_id": "854", "text": "Infantile neuroaxonal dystrophy"}
+{"_id": "855", "text": "Gyrate Atrophy"}
+{"_id": "856", "text": "Gyrate atrophy of choroid and retina"}
+{"_id": "857", "text": "Trichothiodystrophy 4, Nonphotosensitive"}
+{"_id": "858", "text": "Trichothiodystrophy"}
+{"_id": "859", "text": "Ring Chromosome 22 Syndrome"}
+{"_id": "860", "text": "Ring chromosome 22 syndrome"}
+{"_id": "861", "text": "Ectopia Lentis"}
+{"_id": "862", "text": "Isolated ectopia lentis"}
+{"_id": "863", "text": "MTM"}
+{"_id": "864", "text": "X-linked centronuclear myopathy"}
+{"_id": "865", "text": "Aniridia"}
+{"_id": "866", "text": "Isolated aniridia"}
+{"_id": "867", "text": "Ornithine Carbamoyltransferase Deficiency Disease"}
+{"_id": "868", "text": "Ornithine transcarbamylase deficiency"}
+{"_id": "869", "text": "CMM2"}
+{"_id": "870", "text": "Familial melanoma"}
+{"_id": "871", "text": "SCA1"}
+{"_id": "872", "text": "Spinocerebellar ataxia type 1"}
+{"_id": "873", "text": "Progressive Choroidal Atrophy"}
+{"_id": "874", "text": "Choroideremia"}
+{"_id": "875", "text": "Combined Lipase Deficiency"}
+{"_id": "876", "text": "Familial lipase maturation factor 1 deficiency"}
+{"_id": "877", "text": "Harlequin Ichthyosis"}
+{"_id": "878", "text": "Harlequin ichthyosis"}
+{"_id": "879", "text": "Acute Disseminated Langerhans Cell Histiocytosis"}
+{"_id": "880", "text": "Langerhans cell histiocytosis"}
+{"_id": "881", "text": "Nijmegen Breakage Syndrome"}
+{"_id": "882", "text": "Nijmegen breakage syndrome"}
+{"_id": "883", "text": "Achromatopsia 2"}
+{"_id": "884", "text": "Achromatopsia"}
+{"_id": "885", "text": "fHLH"}
+{"_id": "886", "text": "Familial hemophagocytic lymphohistiocytosis"}
+{"_id": "887", "text": "Pelizaeus-Merzbacher Disease"}
+{"_id": "888", "text": "Pelizaeus-Merzbacher disease"}
+{"_id": "889", "text": "Hypomanic Mood"}
+{"_id": "890", "text": "Holoprosencephaly Sequence"}
+{"_id": "891", "text": "Holoprosencephaly"}
+{"_id": "892", "text": "Hyperlysinemia"}
+{"_id": "893", "text": "Hyperlysinemia"}
+{"_id": "894", "text": "Peroxisome Biogenesis Disorder 7A"}
+{"_id": "895", "text": "Trisomy 20"}
+{"_id": "896", "text": "Wilms tumor (WT)"}
+{"_id": "897", "text": "Hydatid Mole"}
+{"_id": "898", "text": "Wernicke Encephalopathy"}
+{"_id": "899", "text": "Chronic Granulomatous Disease"}
+{"_id": "900", "text": "Chronic granulomatous disease"}
+{"_id": "901", "text": "Psychosis"}
+{"_id": "902", "text": "Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency"}
+{"_id": "903", "text": "Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency"}
+{"_id": "904", "text": "Hypochondrogenesis"}
+{"_id": "905", "text": "Achondrogenesis type 2"}
+{"_id": "906", "text": "Rett's syndrome"}
+{"_id": "907", "text": "Rett syndrome"}
+{"_id": "908", "text": "Triosephosphate-Isomerase Deficiency"}
+{"_id": "909", "text": "Triose phosphate-isomerase deficiency"}
+{"_id": "910", "text": "Hereditary Spherocytosis"}
+{"_id": "911", "text": "Hereditary spherocytosis"}
+{"_id": "912", "text": "Perlman Syndrome"}
+{"_id": "913", "text": "Perlman syndrome"}
+{"_id": "914", "text": "3-OH 3-Methyl Glutaric Aciduria"}
+{"_id": "915", "text": "3-hydroxy-3-methylglutaric aciduria"}
+{"_id": "916", "text": "Biotinidase Deficiency"}
+{"_id": "917", "text": "Biotinidase deficiency"}
+{"_id": "918", "text": "cirrhosis"}
+{"_id": "919", "text": "Hereditary Factor X Deficiency"}
+{"_id": "920", "text": "Congenital factor X deficiency"}
+{"_id": "921", "text": "Factor IX Deficiency"}
+{"_id": "922", "text": "Hemophilia B"}
+{"_id": "923", "text": "Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1"}
+{"_id": "924", "text": "ICF syndrome"}
+{"_id": "925", "text": "Autosomal Dominant Polycystic Kidney Disease"}
+{"_id": "926", "text": "Autosomal dominant polycystic kidney disease"}
+{"_id": "927", "text": "Cystinosis"}
+{"_id": "928", "text": "Ocular cystinosis"}
+{"_id": "929", "text": "Multiple Endocrine Neoplasia Type 2"}
+{"_id": "930", "text": "Multiple endocrine neoplasia type 2"}
+{"_id": "931", "text": "Infantile Refsum Disease"}
+{"_id": "932", "text": "Infantile Refsum disease"}
+{"_id": "933", "text": "PBD7B"}
+{"_id": "934", "text": "Adrenal Hypoplasia Congenita"}
+{"_id": "935", "text": "Adrenal hypoplasia congenita"}
+{"_id": "936", "text": "Neuronal Ceroid Lipofuscinosis Type 3"}
+{"_id": "937", "text": "OBSOLETE: Congenital neuronal ceroid lipofuscinosis"}
+{"_id": "938", "text": "Multiple sclerosis"}
+{"_id": "939", "text": "Achondroplasia"}
+{"_id": "940", "text": "Achondroplasia"}
+{"_id": "941", "text": "SCAD"}
+{"_id": "942", "text": "Short chain acyl-CoA dehydrogenase deficiency"}
+{"_id": "943", "text": "Lafora Disease"}
+{"_id": "944", "text": "Lafora disease"}
+{"_id": "945", "text": "Usher Syndrome Type 2"}
+{"_id": "946", "text": "Usher syndrome type 2"}
+{"_id": "947", "text": "Crigler-Najjar Syndrome"}
+{"_id": "948", "text": "Crigler-Najjar syndrome"}
+{"_id": "949", "text": "von Hippel-Lindau syndrome"}
+{"_id": "950", "text": "Von Hippel-Lindau disease"}
+{"_id": "951", "text": "Carboxypeptidase N Deficiency"}
+{"_id": "952", "text": "Acoustic Neurofibromatosis"}
+{"_id": "953", "text": "Full NF2-related schwannomatosis"}
+{"_id": "954", "text": "Late Infantile Neuronal Ceroid Lipofuscinosis"}
+{"_id": "955", "text": "Xeroderma Pigmentosum, Complementation Group D"}
+{"_id": "956", "text": "Neonatal Hemochromatosis"}
+{"_id": "957", "text": "Neonatal hemochromatosis"}
+{"_id": "958", "text": "Hereditary Factor II Deficiency"}
+{"_id": "959", "text": "Congenital factor II deficiency"}
+{"_id": "960", "text": "Junctional Epidermolysis Bullosa"}
+{"_id": "961", "text": "Junctional epidermolysis bullosa"}
+{"_id": "962", "text": "Hereditary Factor VII Deficiency"}
+{"_id": "963", "text": "Congenital factor VII deficiency"}
+{"_id": "964", "text": "Hereditary Multiple Exostoses"}
+{"_id": "965", "text": "Multiple osteochondromas"}
+{"_id": "966", "text": "Seckel Syndrome"}
+{"_id": "967", "text": "Seckel syndrome"}
+{"_id": "968", "text": "Langer-Giedion Syndrome"}
+{"_id": "969", "text": "Trichorhinophalangeal syndrome type 2"}
+{"_id": "970", "text": "Syndromic aniridia"}
+{"_id": "971", "text": "Epidermolysis Bullosa Simplex"}
+{"_id": "972", "text": "Autosomal dominant generalized epidermolysis bullosa simplex, severe form"}
+{"_id": "973", "text": "Cowden's Disease"}
+{"_id": "974", "text": "Cowden syndrome"}
+{"_id": "975", "text": "MDDGA1"}
+{"_id": "976", "text": "Walker-Warburg syndrome"}
+{"_id": "977", "text": "Orofacial Cleft 1"}
+{"_id": "978", "text": "Cleft lip/palate"}
+{"_id": "979", "text": "Hyperglycerolemia"}
+{"_id": "980", "text": "Isolated glycerol kinase deficiency"}
+{"_id": "981", "text": "Polycystic Kidney Disease, Infantile Type"}
+{"_id": "982", "text": "Autosomal recessive polycystic kidney disease"}
+{"_id": "983", "text": "Carnitine-Acylcarnitine Translocase Deficiency"}
+{"_id": "984", "text": "Carnitine-acylcarnitine translocase deficiency"}
+{"_id": "985", "text": "Fraser Syndrome"}
+{"_id": "986", "text": "Fraser syndrome"}
+{"_id": "987", "text": "MDDGA4"}
+{"_id": "988", "text": "Congenital muscular dystrophy, Fukuyama type"}
+{"_id": "989", "text": "Truncus Arteriosus"}
+{"_id": "990", "text": "Common arterial trunk"}
+{"_id": "991", "text": "Great Vessels Transposition"}
+{"_id": "992", "text": "Transposition of the great arteries"}
+{"_id": "993", "text": "Reye Syndrome"}
+{"_id": "994", "text": "Reye syndrome"}
+{"_id": "995", "text": "Generalized Arterial Calcification of Infancy 1"}
+{"_id": "996", "text": "Generalized arterial calcification of infancy"}
+{"_id": "997", "text": "Platelet Glycoprotein Ib Deficiency"}
+{"_id": "998", "text": "Bernard-Soulier syndrome"}
+{"_id": "999", "text": "Kallmann Syndrome"}
+{"_id": "1000", "text": "Kallmann syndrome"}
+{"_id": "1001", "text": "Greig Cephalosyndactyly Syndrome"}
+{"_id": "1002", "text": "Greig cephalopolysyndactyly syndrome"}
+{"_id": "1003", "text": "D-Glyceric Aciduria"}
+{"_id": "1004", "text": "D-glyceric aciduria"}
+{"_id": "1005", "text": "Sjogren-Larsson Syndrome"}
+{"_id": "1006", "text": "Sj\u00f6gren-Larsson syndrome"}
+{"_id": "1007", "text": "Thyroid Follicular Adenoma"}
+{"_id": "1008", "text": "Leber Hereditary Optic Atrophy"}
+{"_id": "1009", "text": "Leber hereditary optic neuropathy"}
+{"_id": "1010", "text": "Fryns Syndrome"}
+{"_id": "1011", "text": "Fryns syndrome"}
+{"_id": "1012", "text": "De Sanctis-Cacchione Syndrome"}
+{"_id": "1013", "text": "De Sanctis-Cacchione syndrome"}
+{"_id": "1014", "text": "Familial Hypotransferrinemia"}
+{"_id": "1015", "text": "Congenital atransferrinemia"}
+{"_id": "1016", "text": "Leiomyoma of Uterine Corpus"}
+{"_id": "1017", "text": "Marshall Syndrome"}
+{"_id": "1018", "text": "Marshall syndrome"}
+{"_id": "1019", "text": "Kennedy Disease"}
+{"_id": "1020", "text": "Kennedy disease"}
+{"_id": "1021", "text": "Renal Agenesis"}
+{"_id": "1022", "text": "Renal agenesis"}
+{"_id": "1023", "text": "Chondroectodermal Dysplasia"}
+{"_id": "1024", "text": "Ellis Van Creveld syndrome"}
+{"_id": "1025", "text": "OCA1A"}
+{"_id": "1026", "text": "Oculocutaneous albinism type 1A"}
+{"_id": "1027", "text": "albinism"}
+{"_id": "1028", "text": "Oculocutaneous albinism"}
+{"_id": "1029", "text": "Pena-Shokeir syndrome, Type 1"}
+{"_id": "1030", "text": "Fetal akinesia deformation sequence"}
+{"_id": "1031", "text": "Angelman Syndrome"}
+{"_id": "1032", "text": "Angelman syndrome"}
+{"_id": "1033", "text": "WVS"}
+{"_id": "1034", "text": "Weaver syndrome"}
+{"_id": "1035", "text": "Multiple Endocrine Adenomatosis Type IIB"}
+{"_id": "1036", "text": "Multiple endocrine neoplasia type 2B"}
+{"_id": "1037", "text": "Wermer Syndrome"}
+{"_id": "1038", "text": "Multiple endocrine neoplasia type 1"}
+{"_id": "1039", "text": "Hypomelanosis of Ito"}
+{"_id": "1040", "text": "Nevus of Ito"}
+{"_id": "1041", "text": "Spondyloepimetaphyseal Dysplasia, Sponastrime Type"}
+{"_id": "1042", "text": "SPONASTRIME dysplasia"}
+{"_id": "1043", "text": "myasthenia gravis"}
+{"_id": "1044", "text": "Myasthenia gravis"}
+{"_id": "1045", "text": "Spondyloperipheral Dysplasia"}
+{"_id": "1046", "text": "Spondyloperipheral dysplasia-short ulna syndrome"}
+{"_id": "1047", "text": "MERRF Syndrome"}
+{"_id": "1048", "text": "MERRF"}
+{"_id": "1049", "text": "Chromosome 18q Deletion Syndrome"}
+{"_id": "1050", "text": "Monosomy 18q syndrome"}
+{"_id": "1051", "text": "Potocki-Shaffer Syndrome"}
+{"_id": "1052", "text": "Potocki-Shaffer syndrome"}
+{"_id": "1053", "text": "Mevalonic Aciduria"}
+{"_id": "1054", "text": "Mevalonic aciduria"}
+{"_id": "1055", "text": "Achalasia-Addisonianism-Alacrima Syndrome"}
+{"_id": "1056", "text": "Triple A syndrome"}
+{"_id": "1057", "text": "Proteus Syndrome"}
+{"_id": "1058", "text": "Proteus syndrome"}
+{"_id": "1059", "text": "Pyruvate dehydrogenase E1-alpha deficiency"}
+{"_id": "1060", "text": "ALAD Deficiency"}
+{"_id": "1061", "text": "Porphyria due to ALA dehydratase deficiency"}
+{"_id": "1062", "text": "Norrie Syndrome"}
+{"_id": "1063", "text": "Norrie disease"}
+{"_id": "1064", "text": "Acrocephalosyndactyly Type I"}
+{"_id": "1065", "text": "Apert syndrome"}
+{"_id": "1066", "text": "Pettigrew Syndrome"}
+{"_id": "1067", "text": "X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome"}
+{"_id": "1068", "text": "Hypoplastic left heart syndrome"}
+{"_id": "1069", "text": "Hypoplastic left heart syndrome"}
+{"_id": "1070", "text": "CMS5"}
+{"_id": "1071", "text": "Synaptic congenital myasthenic syndromes"}
+{"_id": "1072", "text": "Dandy-Walker Syndrome"}
+{"_id": "1073", "text": "Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome"}
+{"_id": "1074", "text": "CAVD"}
+{"_id": "1075", "text": "Congenital bilateral absence of vas deferens"}
+{"_id": "1076", "text": "46,XY Sex Reversal 4"}
+{"_id": "1077", "text": "HPS1"}
+{"_id": "1078", "text": "Hermansky-Pudlak syndrome due to BLOC-3 deficiency"}
+{"_id": "1079", "text": "Juvenile Myoclonic Epilepsy"}
+{"_id": "1080", "text": "Juvenile myoclonic epilepsy"}
+{"_id": "1081", "text": "Schimke Immuno-Osseous Dysplasia"}
+{"_id": "1082", "text": "Schimke immuno-osseous dysplasia"}
+{"_id": "1083", "text": "Rubinstein-Taybi Syndrome"}
+{"_id": "1084", "text": "Rubinstein-Taybi syndrome"}
+{"_id": "1085", "text": "Progressive Familial Intrahepatic Cholestasis"}
+{"_id": "1086", "text": "Progressive familial intrahepatic cholestasis"}
+{"_id": "1087", "text": "Lipoid Proteinosis of Urbach and Wiethe"}
+{"_id": "1088", "text": "Lipoid proteinosis"}
+{"_id": "1089", "text": "Multifunctional Enzyme Deficiency"}
+{"_id": "1090", "text": "Bifunctional enzyme deficiency"}
+{"_id": "1091", "text": "Neonatal Adrenoleukodystrophy"}
+{"_id": "1092", "text": "Neonatal adrenoleukodystrophy"}
+{"_id": "1093", "text": "Pancreatic Lipase Deficiency"}
+{"_id": "1094", "text": "Pancreatic triacylglycerol lipase deficiency"}
+{"_id": "1095", "text": "Trichothiodystrophy"}
+{"_id": "1096", "text": "Holt-Oram Syndrome"}
+{"_id": "1097", "text": "Holt-Oram syndrome"}
+{"_id": "1098", "text": "Adrenal Gland Hyperplasia II"}
+{"_id": "1099", "text": "Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency"}
+{"_id": "1100", "text": "Charcot-Marie-Tooth Disease Type 1B"}
+{"_id": "1101", "text": "Charcot-Marie-Tooth disease type 1B"}
+{"_id": "1102", "text": "MTHFR"}
+{"_id": "1103", "text": "Homocystinuria due to methylene tetrahydrofolate reductase deficiency"}
+{"_id": "1104", "text": "Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency"}
+{"_id": "1105", "text": "SPG1"}
+{"_id": "1106", "text": "MASA syndrome"}
+{"_id": "1107", "text": "Shprintzen-Goldberg Craniosynostosis Syndrome"}
+{"_id": "1108", "text": "Shprintzen-Goldberg syndrome"}
+{"_id": "1109", "text": "Williams-Beuren Syndrome (WBS)"}
+{"_id": "1110", "text": "Williams syndrome"}
+{"_id": "1111", "text": "Chromosome 17p11.2 Deletion Syndrome"}
+{"_id": "1112", "text": "Smith-Magenis syndrome"}
+{"_id": "1113", "text": "Denys-Drash syndrome"}
+{"_id": "1114", "text": "Denys-Drash syndrome"}
+{"_id": "1115", "text": "Maturity-Onset Diabetes of the Young, Type 2"}
+{"_id": "1116", "text": "Familial Female Breast Carcinoma"}
+{"_id": "1117", "text": "Hereditary breast cancer"}
+{"_id": "1118", "text": "Glomus Tumor"}
+{"_id": "1119", "text": "Glomus tumor"}
+{"_id": "1120", "text": "Generalized Epilepsy"}
+{"_id": "1121", "text": "BRCA1 Syndrome"}
+{"_id": "1122", "text": "Hereditary breast and/or ovarian cancer syndrome"}
+{"_id": "1123", "text": "DRPLA"}
+{"_id": "1124", "text": "Dentatorubral pallidoluysian atrophy"}
+{"_id": "1125", "text": "Cleft Palate"}
+{"_id": "1126", "text": "Cleft palate"}
+{"_id": "1127", "text": "Nemaline Myopathy 2"}
+{"_id": "1128", "text": "Typical nemaline myopathy"}
+{"_id": "1129", "text": "Spinal Myelocele"}
+{"_id": "1130", "text": "Neural tube closure defect"}
+{"_id": "1131", "text": "Mosaic Variegated Aneuploidy Syndrome 1"}
+{"_id": "1132", "text": "Mosaic variegated aneuploidy syndrome"}
+{"_id": "1133", "text": "Site Specific Early Onset Breast Cancer Syndrome"}
+{"_id": "1134", "text": "Morbid Obesity"}
+{"_id": "1135", "text": "Leiomyomatous Tumor"}
+{"_id": "1136", "text": "HFE-Associated Hereditary Hemochromatosis"}
+{"_id": "1137", "text": "Symptomatic form of HFE-related hemochromatosis"}
+{"_id": "1138", "text": "NIID"}
+{"_id": "1139", "text": "Neuronal intranuclear inclusion disease"}
+{"_id": "1140", "text": "Short-Rib Thoracic Dysplasia 6 with or without Polydactyly"}
+{"_id": "1141", "text": "Short rib-polydactyly syndrome, Majewski type"}
+{"_id": "1142", "text": "Cleft Lip/Palate-Ectodermal Dysplasia Syndrome"}
+{"_id": "1143", "text": "Cleft lip/palate-ectodermal dysplasia syndrome"}
+{"_id": "1144", "text": "Owren Disease"}
+{"_id": "1145", "text": "Congenital factor V deficiency"}
+{"_id": "1146", "text": "Partial Epilepsy"}
+{"_id": "1147", "text": "FMF"}
+{"_id": "1148", "text": "Familial Mediterranean fever"}
+{"_id": "1149", "text": "Parkinson Disease 4, Autosomal Dominant"}
+{"_id": "1150", "text": "Hereditary late-onset Parkinson disease"}
+{"_id": "1151", "text": "Anhidrotic Ectodermal Dysplasia 1"}
+{"_id": "1152", "text": "Hypohidrotic ectodermal dysplasia"}
+{"_id": "1153", "text": "Atrial Fibrillation"}
+{"_id": "1154", "text": "Familial atrial fibrillation"}
+{"_id": "1155", "text": "Childhood Absence Epilepsy"}
+{"_id": "1156", "text": "Childhood absence epilepsy"}
+{"_id": "1157", "text": "Progressive supranuclear ophthalmoplegia"}
+{"_id": "1158", "text": "Progressive supranuclear palsy"}
+{"_id": "1159", "text": "Deep Vein Thrombosis (DVT)"}
+{"_id": "1160", "text": "Santavuori Disease"}
+{"_id": "1161", "text": "Facioscapulohumeral Muscular Dystrophy 1"}
+{"_id": "1162", "text": "Facioscapulohumeral dystrophy"}
+{"_id": "1163", "text": "Sanjad-Sakati Syndrome"}
+{"_id": "1164", "text": "Sanjad-Sakati syndrome"}
+{"_id": "1165", "text": "BPS"}
+{"_id": "1166", "text": "Bartsocas-Papas syndrome"}
+{"_id": "1167", "text": "Common Atrioventricular Canal"}
+{"_id": "1168", "text": "Atrioventricular septal defect"}
+{"_id": "1169", "text": "Cystinuria"}
+{"_id": "1170", "text": "Cystinuria"}
+{"_id": "1171", "text": "Peroxisome Biogenesis Disorder 1A"}
+{"_id": "1172", "text": "Eagle-Barrett Syndrome"}
+{"_id": "1173", "text": "Prune belly syndrome"}
+{"_id": "1174", "text": "Congenital Nephrotic Syndrome"}
+{"_id": "1175", "text": "Genetic nephrotic syndrome"}
+{"_id": "1176", "text": "Fanconi Anemia, Complementation Group D2"}
+{"_id": "1177", "text": "Aspermia"}
+{"_id": "1178", "text": "Chromosome Y microdeletion syndrome"}
+{"_id": "1179", "text": "Osteogenesis Imperfecta Type IV"}
+{"_id": "1180", "text": "Osteogenesis imperfecta type 4"}
+{"_id": "1181", "text": "Alexander Disease"}
+{"_id": "1182", "text": "Alexander disease"}
+{"_id": "1183", "text": "EDMD1"}
+{"_id": "1184", "text": "X-linked Emery-Dreifuss muscular dystrophy"}
+{"_id": "1185", "text": "Isobutyryl-CoA Dehydrogenase Deficiency"}
+{"_id": "1186", "text": "Isobutyryl-CoA dehydrogenase deficiency"}
+{"_id": "1187", "text": "2-Methylbutyryl-CoA Dehydrogenase Deficiency"}
+{"_id": "1188", "text": "2-methylbutyryl-CoA dehydrogenase deficiency"}
+{"_id": "1189", "text": "Mitochondrial Trifunctional Protein Deficiency"}
+{"_id": "1190", "text": "Mitochondrial trifunctional protein deficiency"}
+{"_id": "1191", "text": "Mucopolysaccharidosis Type IX"}
+{"_id": "1192", "text": "Hyaluronidase deficiency"}
+{"_id": "1193", "text": "Autosomal Recessive Congenital Ichthyosis 2"}
+{"_id": "1194", "text": "Congenital ichthyosiform erythroderma"}
+{"_id": "1195", "text": "47,XXX"}
+{"_id": "1196", "text": "Trisomy X syndrome"}
+{"_id": "1197", "text": "Pantothenate Kinase-Associated Neurodegeneration"}
+{"_id": "1198", "text": "Atypical pantothenate kinase-associated neurodegeneration"}
+{"_id": "1199", "text": "ADHD"}
+{"_id": "1200", "text": "HPS6"}
+{"_id": "1201", "text": "Hermansky-Pudlak syndrome due to BLOC-2 deficiency"}
+{"_id": "1202", "text": "HPS2"}
+{"_id": "1203", "text": "Hermansky-Pudlak syndrome due to AP-3 deficiency"}
+{"_id": "1204", "text": "Frontonasal Dysplasia 1"}
+{"_id": "1205", "text": "Frontorhiny"}
+{"_id": "1206", "text": "Cleidocranial Dysostosis"}
+{"_id": "1207", "text": "Cleidocranial dysplasia"}
+{"_id": "1208", "text": "Niemann-Pick Disease, Type C2"}
+{"_id": "1209", "text": "Congenital Cerebellar Hypoplasia"}
+{"_id": "1210", "text": "Coenzyme Q10 deficiency"}
+{"_id": "1211", "text": "Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate"}
+{"_id": "1212", "text": "Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome"}
+{"_id": "1213", "text": "Brown-Vialetto-Van Laere Syndrome 1"}
+{"_id": "1214", "text": "RFVT3-related riboflavin transporter deficiency"}
+{"_id": "1215", "text": "Peroxisomal Acyl-CoA Oxidase Deficiency"}
+{"_id": "1216", "text": "Peroxisomal acyl-CoA oxidase deficiency"}
+{"_id": "1217", "text": "Varadi-Papp Syndrome"}
+{"_id": "1218", "text": "Orofaciodigital syndrome type 6"}
+{"_id": "1219", "text": "Holoprosencephaly-Polydactyly Syndrome"}
+{"_id": "1220", "text": "Holoprosencephaly-postaxial polydactyly syndrome"}
+{"_id": "1221", "text": "Familial Multilocular Cystic Disease of the Jaws"}
+{"_id": "1222", "text": "Cherubism"}
+{"_id": "1223", "text": "Pearson Syndrome"}
+{"_id": "1224", "text": "Pearson syndrome"}
+{"_id": "1225", "text": "Oromandibular-Limb Hypogenesis Spectrum"}
+{"_id": "1226", "text": "Moebius syndrome"}
+{"_id": "1227", "text": "Hypochondroplasia"}
+{"_id": "1228", "text": "Hypochondroplasia"}
+{"_id": "1229", "text": "Hyperphosphatemic Familial Tumoral Calcinosis"}
+{"_id": "1230", "text": "Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome"}
+{"_id": "1231", "text": "Hashimoto disease"}
+{"_id": "1232", "text": "Vitiligo"}
+{"_id": "1233", "text": "Charcot-Marie-Tooth Disease Type 2D"}
+{"_id": "1234", "text": "Autosomal dominant Charcot-Marie-Tooth disease type 2D"}
+{"_id": "1235", "text": "Sotos Syndrome"}
+{"_id": "1236", "text": "Sotos syndrome"}
+{"_id": "1237", "text": "Leukoencephalopathy with Vanishing White Matter"}
+{"_id": "1238", "text": "Cree leukoencephalopathy"}
+{"_id": "1239", "text": "LGS"}
+{"_id": "1240", "text": "Lennox-Gastaut syndrome"}
+{"_id": "1241", "text": "CDGIg"}
+{"_id": "1242", "text": "ALG12-CDG"}
+{"_id": "1243", "text": "Deafness, Autosomal Recessive 49"}
+{"_id": "1244", "text": "Rare autosomal recessive non-syndromic sensorineural deafness type DFNB"}
+{"_id": "1245", "text": "Deafness, Autosomal Recessive 28"}
+{"_id": "1246", "text": "Langer Type Mesomelic Dysplasia"}
+{"_id": "1247", "text": "Langer mesomelic dysplasia"}
+{"_id": "1248", "text": "FXTAS"}
+{"_id": "1249", "text": "Fragile X-associated tremor/ataxia syndrome"}
+{"_id": "1250", "text": "X-linked Hypophosphatemic Rickets"}
+{"_id": "1251", "text": "X-linked hypophosphatemia"}
+{"_id": "1252", "text": "Molybdenum Cofactor Deficiency"}
+{"_id": "1253", "text": "Sulfite oxidase deficiency due to molybdenum cofactor deficiency"}
+{"_id": "1254", "text": "Nephrotic Syndrome - NPHS1 Associated"}
+{"_id": "1255", "text": "Congenital nephrotic syndrome, Finnish type"}
+{"_id": "1256", "text": "Peters-Plus Syndrome"}
+{"_id": "1257", "text": "Peters plus syndrome"}
+{"_id": "1258", "text": "SEMDJL2"}
+{"_id": "1259", "text": "Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type"}
+{"_id": "1260", "text": "Jackson-Weiss Syndrome"}
+{"_id": "1261", "text": "Jackson-Weiss syndrome"}
+{"_id": "1262", "text": "IBMPFD1"}
+{"_id": "1263", "text": "Adult-onset distal myopathy due to VCP mutation"}
+{"_id": "1264", "text": "Congenital Disorder of Glycosylation Type Ij"}
+{"_id": "1265", "text": "DPAGT1-CDG"}
+{"_id": "1266", "text": "CDGIa"}
+{"_id": "1267", "text": "PMM2-CDG"}
+{"_id": "1268", "text": "Congenital Disorder of Glycosylation Type Ie"}
+{"_id": "1269", "text": "DPM1-CDG"}
+{"_id": "1270", "text": "CDGId"}
+{"_id": "1271", "text": "ALG3-CDG"}
+{"_id": "1272", "text": "CDGIc"}
+{"_id": "1273", "text": "ALG6-CDG"}
+{"_id": "1274", "text": "CDGIf"}
+{"_id": "1275", "text": "MPDU1-CDG"}
+{"_id": "1276", "text": "Mayer-Rokitansky-Kuster-Hauser Syndrome"}
+{"_id": "1277", "text": "Mayer-Rokitansky-K\u00fcster-Hauser syndrome"}
+{"_id": "1278", "text": "Otopalatodigital Syndrome Type 1"}
+{"_id": "1279", "text": "Otopalatodigital syndrome type 1"}
+{"_id": "1280", "text": "Mosaic Variegated Aneuploidy Syndrome 2"}
+{"_id": "1281", "text": "Cerebrooculofacioskeletal Syndrome"}
+{"_id": "1282", "text": "COFS syndrome"}
+{"_id": "1283", "text": "Gastric Signet Ring Cell Adenocarcinoma"}
+{"_id": "1284", "text": "Mantle cell lymphoma, unspecified site"}
+{"_id": "1285", "text": "Mantle cell lymphoma"}
+{"_id": "1286", "text": "Cancer of Stomach"}
+{"_id": "1287", "text": "Gastric Tubular Adenocarcinoma"}
+{"_id": "1288", "text": "Extraskeletal Chondrosarcoma"}
+{"_id": "1289", "text": "Extraskeletal myxoid chondrosarcoma"}
+{"_id": "1290", "text": "Pleural Biphasic Mesothelioma"}
+{"_id": "1291", "text": "Sezary disease"}
+{"_id": "1292", "text": "S\u00e9zary syndrome"}
+{"_id": "1293", "text": "B Acute Lymphoblastic Leukemia with TCF3-HLF Fusion"}
+{"_id": "1294", "text": "B-lymphoblastic leukemia/lymphoma with t(17;19)"}
+{"_id": "1295", "text": "Epidermolysis Bullosa"}
+{"_id": "1296", "text": "Inherited epidermolysis bullosa"}
+{"_id": "1297", "text": "ABC DLBCL"}
+{"_id": "1298", "text": "Renal Cystadenocarcinoma"}
+{"_id": "1299", "text": "Multilocular cystic renal neoplasm of low malignant potential"}
+{"_id": "1300", "text": "Giant Cell Carcinoma of the Lung"}
+{"_id": "1301", "text": "Endocervical Carcinoma"}
+{"_id": "1302", "text": "Adenocarcinoma of the cervix uteri"}
+{"_id": "1303", "text": "Adrenocortical Carcinoma"}
+{"_id": "1304", "text": "Adrenocortical carcinoma"}
+{"_id": "1305", "text": "Breast Squamous Cell Carcinoma, Acantholytic Variant"}
+{"_id": "1306", "text": "Metastatic Breast Lobular Carcinoma"}
+{"_id": "1307", "text": "NUT Midline Carcinoma"}
+{"_id": "1308", "text": "NUT midline carcinoma"}
+{"_id": "1309", "text": "Hemimegalencephaly"}
+{"_id": "1310", "text": "Hemimegalencephaly"}
+{"_id": "1311", "text": "Adult Precursor T-Lymphoblastic Lymphoma"}
+{"_id": "1312", "text": "Hodgkin Lymphoma"}
+{"_id": "1313", "text": "Hodgkin lymphoma"}
+{"_id": "1314", "text": "Acoustic Neurilemmoma"}
+{"_id": "1315", "text": "Vestibular schwannoma"}
+{"_id": "1316", "text": "Childhood Carcinoma of Liver Cell"}
+{"_id": "1317", "text": "Pediatric hepatocellular carcinoma"}
+{"_id": "1318", "text": "Primary Carcinoma of the Liver Cells"}
+{"_id": "1319", "text": "Hepatocellular carcinoma"}
+{"_id": "1320", "text": "Mature Teratoma of Stomach"}
+{"_id": "1321", "text": "Extragonadal teratoma"}
+{"_id": "1322", "text": "Primary Cutaneous T-Cell Non-Hodgkin's Lymphoma"}
+{"_id": "1323", "text": "Primary cutaneous T-cell lymphoma"}
+{"_id": "1324", "text": "Malignant Lymphomas of the CNS"}
+{"_id": "1325", "text": "Primary central nervous system lymphoma"}
+{"_id": "1326", "text": "Laryngeal Squamous Cell Carcinoma"}
+{"_id": "1327", "text": "Squamous cell carcinoma of the larynx"}
+{"_id": "1328", "text": "Mast cell leukaemia"}
+{"_id": "1329", "text": "Mast cell leukemia"}
+{"_id": "1330", "text": "Vaginal Melanoma"}
+{"_id": "1331", "text": "Cervical Adenosquamous Carcinoma, Glassy Cell Variant"}
+{"_id": "1332", "text": "Glassy cell carcinoma of the cervix uteri"}
+{"_id": "1333", "text": "Cervical Melanoma"}
+{"_id": "1334", "text": "Spindle cell sarcoma"}
+{"_id": "1335", "text": "neoplasia"}
+{"_id": "1336", "text": "Lymphoma (Hodgkin's and Non-Hodgkin's)"}
+{"_id": "1337", "text": "Histiocytic Sarcoma"}
+{"_id": "1338", "text": "Histiocytic sarcoma"}
+{"_id": "1339", "text": "Chronic Lymphadenitis"}
+{"_id": "1340", "text": "Dermatofibrosarcoma protuberans, NOS"}
+{"_id": "1341", "text": "Dermatofibrosarcoma protuberans"}
+{"_id": "1342", "text": "Teratoma of the Ovary"}
+{"_id": "1343", "text": "Synovial sarcoma"}
+{"_id": "1344", "text": "hyperplasia"}
+{"_id": "1345", "text": "Chronic Unifocal Langerhans Cell Histiocytosis"}
+{"_id": "1346", "text": "Skin Inflammation/ Irritation"}
+{"_id": "1347", "text": "Small cell B-cell lymphoma, unspecified site"}
+{"_id": "1348", "text": "Leiomyosarcoma (excluding uterine leiomyosarcoma)"}
+{"_id": "1349", "text": "Leiomyosarcoma"}
+{"_id": "1350", "text": "WHO Grade 2 Oligodendroglial Neoplasm"}
+{"_id": "1351", "text": "Oligodendroglioma"}
+{"_id": "1352", "text": "Giant Cell Sarcoma of the Bone"}
+{"_id": "1353", "text": "Giant cell tumor of bone"}
+{"_id": "1354", "text": "Granulomatous Lesion"}
+{"_id": "1355", "text": "Urethra Transitional Cell Carcinoma"}
+{"_id": "1356", "text": "Bladder Urothelial Cancer"}
+{"_id": "1357", "text": "Non-papillary transitional cell carcinoma of the bladder"}
+{"_id": "1358", "text": "Fibrous Dysplasia"}
+{"_id": "1359", "text": "Fibrous dysplasia of bone"}
+{"_id": "1360", "text": "Histiocytoma"}
+{"_id": "1361", "text": "Skin Keratoacanthoma"}
+{"_id": "1362", "text": "Osteoid Osteoma"}
+{"_id": "1363", "text": "Paget Cell Neoplasm"}
+{"_id": "1364", "text": "rhabdomyosarcoma"}
+{"_id": "1365", "text": "Rhabdomyosarcoma"}
+{"_id": "1366", "text": "Epithelioid Cell Sarcoma"}
+{"_id": "1367", "text": "Epithelioid sarcoma"}
+{"_id": "1368", "text": "Fanconi Anemia, Complementation Group B"}
+{"_id": "1369", "text": "Fanconi Anemia, Complementation Group D1"}
+{"_id": "1370", "text": "Krukenberg Neoplasm"}
+{"_id": "1371", "text": "Epidermoid Carcinoma of Maxillary Sinus"}
+{"_id": "1372", "text": "Squamous cell carcinoma of the nasal cavity and paranasal sinuses"}
+{"_id": "1373", "text": "Relapsed Cancer of the Bladder"}
+{"_id": "1374", "text": "senile keratosis"}
+{"_id": "1375", "text": "Pre-Sacral Teratoma"}
+{"_id": "1376", "text": "Sacrococcygeal teratoma"}
+{"_id": "1377", "text": "Mycosis fungoides, unspecified site"}
+{"_id": "1378", "text": "Classic mycosis fungoides"}
+{"_id": "1379", "text": "Immunodeficiency with Hyper-IgM"}
+{"_id": "1380", "text": "X-linked hyper-IgM syndrome"}
+{"_id": "1381", "text": "Common variable immune deficiency (CVID)"}
+{"_id": "1382", "text": "Common variable immunodeficiency"}
+{"_id": "1383", "text": "IGAD1"}
+{"_id": "1384", "text": "Recurrent infections associated with rare immunoglobulin isotypes deficiency"}
+{"_id": "1385", "text": "Selective Antibody Deficiency with Normal Immunoglobulins"}
+{"_id": "1386", "text": "Specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells"}
+{"_id": "1387", "text": "Immunodeficiency 5"}
+{"_id": "1388", "text": "X-linked lymphoproliferative disease due to SAP deficiency"}
+{"_id": "1389", "text": "X-Linked Severe Combined Immunodeficiency"}
+{"_id": "1390", "text": "T-B+ severe combined immunodeficiency due to gamma chain deficiency"}
+{"_id": "1391", "text": "Intracranial Meningioma"}
+{"_id": "1392", "text": "Ovarian Squamous Cell Carcinoma"}
+{"_id": "1393", "text": "Adenosquamous Cell Carcinoma of the Uterine Cervix"}
+{"_id": "1394", "text": "Cervical Squamous Cell Carcinoma, Not Otherwise Specified"}
+{"_id": "1395", "text": "Primary Bone Chondrosarcoma"}
+{"_id": "1396", "text": "B-ALL"}
+{"_id": "1397", "text": "B-Cell Prolymphocytic Leukemia"}
+{"_id": "1398", "text": "B-cell prolymphocytic leukemia"}
+{"_id": "1399", "text": "Blastic Phase Chronic Myelogenous Leukemia"}
+{"_id": "1400", "text": "Mediastinal (thymic) large B-cell lymphoma, unspecified site"}
+{"_id": "1401", "text": "Primary mediastinal large B-cell lymphoma"}
+{"_id": "1402", "text": "Childhood Acute Myeloblastic Leukemia with Maturation (M2)"}
+{"_id": "1403", "text": "Acute myeloblastic leukemia with maturation"}
+{"_id": "1404", "text": "Adult Acute Myeloid Leukemia Minimally Differentiated"}
+{"_id": "1405", "text": "Acute myeloid leukemia with minimal differentiation"}
+{"_id": "1406", "text": "Acute Myelomonocytic Leukemia"}
+{"_id": "1407", "text": "Acute myelomonocytic leukemia"}
+{"_id": "1408", "text": "Granulosa Cell Neoplasm of the Ovary"}
+{"_id": "1409", "text": "Malignant granulosa cell tumor of the ovary"}
+{"_id": "1410", "text": "Precursor Natural Killer Cell Lymphoblastic Leukemia/Lymphoma"}
+{"_id": "1411", "text": "T Cell Prolymphocytic Leukemia"}
+{"_id": "1412", "text": "T-cell prolymphocytic leukemia"}
+{"_id": "1413", "text": "Perihilar Cholangiocarcinoma"}
+{"_id": "1414", "text": "Liver Fluke-Related Cholangiocarcinoma"}
+{"_id": "1415", "text": "Klatskin tumor"}
+{"_id": "1416", "text": "B Lymphoblastic Leukemia/Lymphoma with ETV6::RUNX1 Fusion"}
+{"_id": "1417", "text": "B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1)"}
+{"_id": "1418", "text": "Liver and Intrahepatic Biliary Tract Carcinoma"}
+{"_id": "1419", "text": "Combined hepatocellular carcinoma and cholangiocarcinoma"}
+{"_id": "1420", "text": "Pheochromocytoma"}
+{"_id": "1421", "text": "Sporadic pheochromocytoma/secreting paraganglioma"}
+{"_id": "1422", "text": "NCIT_C207229"}
+{"_id": "1423", "text": "Inflammatory carcinoma"}
+{"_id": "1424", "text": "AIDS-Related Kaposi's Sarcoma"}
+{"_id": "1425", "text": "Kaposi sarcoma"}
+{"_id": "1426", "text": "Peripheral Neuroectodermal Tumor of Bone"}
+{"_id": "1427", "text": "Peripheral primitive neuroectodermal tumor"}
+{"_id": "1428", "text": "anemia"}
+{"_id": "1429", "text": "HIGM2"}
+{"_id": "1430", "text": "Hyper-IgM syndrome type 2"}
+{"_id": "1431", "text": "Darier Disease"}
+{"_id": "1432", "text": "Darier disease"}
+{"_id": "1433", "text": "idiopathic pulmonary fibrosis"}
+{"_id": "1434", "text": "Idiopathic pulmonary fibrosis"}
+{"_id": "1435", "text": "Epithelioid Angiosarcoma"}
+{"_id": "1436", "text": "Epithelioid hemangioendothelioma"}
+{"_id": "1437", "text": "Adenocarcinoma of the Cecum"}
+{"_id": "1438", "text": "M0 Acute Myelogenous Leukemia with Minimal Differentiation"}
+{"_id": "1439", "text": "Malignant Mesothelioma of the Pleura"}
+{"_id": "1440", "text": "Nodular Malignant Melanoma of the Skin"}
+{"_id": "1441", "text": "Adult Acute Megakaryoblastic Leukemia"}
+{"_id": "1442", "text": "Mucinous Cystadenocarcinoma of Ovary"}
+{"_id": "1443", "text": "Squamous Cell Carcinoma of Retromolar Trigone"}
+{"_id": "1444", "text": "Oropharyngeal Squamous Cell Carcinoma"}
+{"_id": "1445", "text": "Squamous cell carcinoma of the oropharynx"}
+{"_id": "1446", "text": "B Cell Chronic Lymphocytic Leukemia"}
+{"_id": "1447", "text": "B-cell chronic lymphocytic leukemia"}
+{"_id": "1448", "text": "Sarcoma of Corpus Uteri"}
+{"_id": "1449", "text": "Sarcoma of the corpus uteri"}
+{"_id": "1450", "text": "Endometrial Adenosquamous Carcinoma"}
+{"_id": "1451", "text": "Gastric (Stomach) Adenosquamous Cancer"}
+{"_id": "1452", "text": "Acute Myeloid Leukemia with t(6;11)(q27;q23.3); KMT2A::MLLT4"}
+{"_id": "1453", "text": "Ovarian Serous Cystadenofibroma"}
+{"_id": "1454", "text": "Benign Ovarian Serous Cystadenoma"}
+{"_id": "1455", "text": "Pleural Sarcomatoid Mesothelioma"}
+{"_id": "1456", "text": "Oral Leukoplakia"}
+{"_id": "1457", "text": "Thyroid Gland Neuroendocrine Carcinoma"}
+{"_id": "1458", "text": "Medullary thyroid carcinoma"}
+{"_id": "1459", "text": "Acute Myeloid Leukemia (AML) with Maturation"}
+{"_id": "1460", "text": "Acute Myeloid Leukemia with inv(3)(q21.3;q26.2) or t(3;3)(q21.3;q26.2); GATA2, MECOM(EVI1)"}
+{"_id": "1461", "text": "Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)"}
+{"_id": "1462", "text": "Acute biphenotypic leukemia"}
+{"_id": "1463", "text": "Mixed phenotype acute leukemia"}
+{"_id": "1464", "text": "Askin tumor"}
+{"_id": "1465", "text": "Pediatric Acute Lymphocytic Leukemia"}
+{"_id": "1466", "text": "Adult B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1"}
+{"_id": "1467", "text": "B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)"}
+{"_id": "1468", "text": "Acute Promyelocytic Leukemia with t(15;17)(q24.1;q21.2); PML-RARA"}
+{"_id": "1469", "text": "Acute promyelocytic leukemia"}
+{"_id": "1470", "text": "Testicular Embryonal Carcinoma"}
+{"_id": "1471", "text": "Non-central nervous system-localized embryonal carcinoma"}
+{"_id": "1472", "text": "Bilateral Retinoblastoma"}
+{"_id": "1473", "text": "Unilateral Retinoblastoma"}
+{"_id": "1474", "text": "Bronchiolo-Alveolar Lung Carcinoma"}
+{"_id": "1475", "text": "Cervix Uteri Small Cell Carcinoma"}
+{"_id": "1476", "text": "High-grade neuroendocrine carcinoma of the cervix uteri"}
+{"_id": "1477", "text": "Papillary Lung Adenocarcinoma"}
+{"_id": "1478", "text": "Lung Sarcomatoid Carcinoma"}
+{"_id": "1479", "text": "Prostate Small Cell Carcinoma"}
+{"_id": "1480", "text": "Lung NET"}
+{"_id": "1481", "text": "Extraosseous Ewing's Sarcoma"}
+{"_id": "1482", "text": "Extraskeletal Ewing sarcoma"}
+{"_id": "1483", "text": "Testicular Yolk Sac Tumor"}
+{"_id": "1484", "text": "Yolk sac tumor"}
+{"_id": "1485", "text": "Multiple System Atrophy"}
+{"_id": "1486", "text": "Multiple system atrophy"}
+{"_id": "1487", "text": "Lewy Body Disease"}
+{"_id": "1488", "text": "PARK8"}
+{"_id": "1489", "text": "Acute ischemic stroke"}
+{"_id": "1490", "text": "Dissection of carotid artery"}
+{"_id": "1491", "text": "Epilepsy"}
+{"_id": "1492", "text": "Parkinson Disease 2, Autosomal Recessive Juvenile"}
+{"_id": "1493", "text": "Young-onset Parkinson disease"}
+{"_id": "1494", "text": "Cortical Basal Ganglionic Degeneration"}
+{"_id": "1495", "text": "Striatonigral Degeneration"}
+{"_id": "1496", "text": "Arteriovenous Angioma"}
+{"_id": "1497", "text": "Subarachnoid Hemorrhage"}
+{"_id": "1498", "text": "Intracerebral hemorrhage"}
+{"_id": "1499", "text": "Intracranial Aneurysm"}
+{"_id": "1500", "text": "Pathologic AV Fistula"}
+{"_id": "1501", "text": "Progressive Muscular Atrophy"}
+{"_id": "1502", "text": "Progressive muscular atrophy"}
+{"_id": "1503", "text": "Primary lateral sclerosis"}
+{"_id": "1504", "text": "Primary lateral sclerosis"}
+{"_id": "1505", "text": "Amyotrophic Lateral Sclerosis 14, With or Without Frontotemporal Dementia"}
+{"_id": "1506", "text": "Amyotrophic Lateral Sclerosis 6, With or Without Frontotemporal Dementia"}
+{"_id": "1507", "text": "Frontotemporal Dementia"}
+{"_id": "1508", "text": "Behavioral variant of frontotemporal dementia"}
+{"_id": "1509", "text": "Man-in-barrel Syndrome"}
+{"_id": "1510", "text": "Pseudobulbar Palsy"}
+{"_id": "1511", "text": "Progressive bulbar palsy"}
+{"_id": "1512", "text": "Bulbospinal muscular atrophy of adult"}
+{"_id": "1513", "text": "Myxofibrosarcoma"}
+{"_id": "1514", "text": "Myxofibrosarcoma"}
+{"_id": "1515", "text": "Yolk Sac Tumor of Ovary"}
+{"_id": "1516", "text": "Alveolar rhabdomyosarcoma"}
+{"_id": "1517", "text": "Alveolar rhabdomyosarcoma"}
+{"_id": "1518", "text": "Adenocarcinoma of Esophagus"}
+{"_id": "1519", "text": "Anaplastic Gastric Carcinoma"}
+{"_id": "1520", "text": "Undifferentiated carcinoma of stomach"}
+{"_id": "1521", "text": "HTLV-I Associated Adult T-Cell Leukemia/Lymphoma"}
+{"_id": "1522", "text": "Adult T-cell leukemia/lymphoma"}
+{"_id": "1523", "text": "Medulloblastoma, SHH-Activated, TP53-Wildtype"}
+{"_id": "1524", "text": "Cystadenocarcinoma of the Ovary"}
+{"_id": "1525", "text": "Pyriform Fossa Squamous Cell Carcinoma"}
+{"_id": "1526", "text": "Head and Neck Basaloid Carcinoma"}
+{"_id": "1527", "text": "Pancreatic Somatostatinoma"}
+{"_id": "1528", "text": "Somatostatinoma"}
+{"_id": "1529", "text": "Grade 1 Astrocytic Tumor"}
+{"_id": "1530", "text": "Pilocytic astrocytoma"}
+{"_id": "1531", "text": "Leiomyosarcoma of the Ovary"}
+{"_id": "1532", "text": "Thyroid Sarcoma"}
+{"_id": "1533", "text": "Squamous Cell Carcinoma of the Upper Gingiva"}
+{"_id": "1534", "text": "Adenoid Cystic Carcinoma of Salivary Gland"}
+{"_id": "1535", "text": "Squamous Cell Carcinoma of the Bladder"}
+{"_id": "1536", "text": "Gastric Choriocarcinoma"}
+{"_id": "1537", "text": "Soft Tissue Fibrosarcoma"}
+{"_id": "1538", "text": "Soft tissue sarcoma"}
+{"_id": "1539", "text": "Epithelial Hepatic and Intrahepatic Bile Duct Neoplasm"}
+{"_id": "1540", "text": "Vulvar Leiomyosarcoma"}
+{"_id": "1541", "text": "Amelanotic Melanoma of Skin"}
+{"_id": "1542", "text": "Leiomyosarcoma of the uterus"}
+{"_id": "1543", "text": "Leiomyosarcoma of the corpus uteri"}
+{"_id": "1544", "text": "DIPG"}
+{"_id": "1545", "text": "Diffuse intrinsic pontine glioma"}
+{"_id": "1546", "text": "Pleomorphic Breast Carcinoma"}
+{"_id": "1547", "text": "Philadelphia-Positive ALL"}
+{"_id": "1548", "text": "Renal Angiomyolipoma"}
+{"_id": "1549", "text": "LIPOSARCOMA, MALIGNANT"}
+{"_id": "1550", "text": "Liposarcoma"}
+{"_id": "1551", "text": "Carcinoma of the Vulva"}
+{"_id": "1552", "text": "Vulvar carcinoma"}
+{"_id": "1553", "text": "Acute T Cell Leukemia"}
+{"_id": "1554", "text": "Testicular seminoma"}
+{"_id": "1555", "text": "Testicular seminomatous germ cell tumor"}
+{"_id": "1556", "text": "Squamous Cell Carcinoma, Keratinizing"}
+{"_id": "1557", "text": "Non-Hodgkin lymphoma, NOS"}
+{"_id": "1558", "text": "Basal Cell Skin Carcinoma"}
+{"_id": "1559", "text": "Invasive Adenocarcinoma of the Ampullary Region"}
+{"_id": "1560", "text": "Carcinoma of the ampulla of Vater"}
+{"_id": "1561", "text": "Undifferentiated Gallbladder Cancer"}
+{"_id": "1562", "text": "Ampulla of Vater Adenosquamous Carcinoma"}
+{"_id": "1563", "text": "Clear Cell Carcinoma of Endometrium"}
+{"_id": "1564", "text": "Familial Thyroid Gland Medullary Carcinoma"}
+{"_id": "1565", "text": "Familial medullary thyroid carcinoma"}
+{"_id": "1566", "text": "Malignant Extrarenal Rhabdoid Neoplasm"}
+{"_id": "1567", "text": "Trichothiodystrophy 1, Photosensitive"}
+{"_id": "1568", "text": "Trichothiodystrophy 3, Photosensitive"}
+{"_id": "1569", "text": "LBL"}
+{"_id": "1570", "text": "Non-Hodgkin lymphoma"}
+{"_id": "1571", "text": "Sacral Chordoma"}
+{"_id": "1572", "text": "Chordoma"}
+{"_id": "1573", "text": "essential thrombocythemia"}
+{"_id": "1574", "text": "Essential thrombocythemia"}
+{"_id": "1575", "text": "Tonsil Squamous Cell Carcinoma"}
+{"_id": "1576", "text": "Kidney Pelvis Carcinoma"}
+{"_id": "1577", "text": "hereditary leiomyomatosis and renal cell cancer syndrome"}
+{"_id": "1578", "text": "Hereditary leiomyomatosis and renal cell cancer"}
+{"_id": "1579", "text": "Splenic Marginal Zone B-Cell Lymphoma"}
+{"_id": "1580", "text": "Splenic marginal zone lymphoma"}
+{"_id": "1581", "text": "WHO Follicular Lymphoma Histologic Grade 1"}
+{"_id": "1582", "text": "XPV"}
+{"_id": "1583", "text": "Xeroderma pigmentosum variant"}
+{"_id": "1584", "text": "XP-CS"}
+{"_id": "1585", "text": "Xeroderma pigmentosum-Cockayne syndrome complex"}
+{"_id": "1586", "text": "Xeroderma Pigmentosum Group G"}
+{"_id": "1587", "text": "Xeroderma Pigmentosum, Complementation Group F"}
+{"_id": "1588", "text": "Xeroderma Pigmentosum Group B"}
+{"_id": "1589", "text": "Benign Schwannoma"}
+{"_id": "1590", "text": "brain"}
+{"_id": "1591", "text": "canalis cervicis uteri"}
+{"_id": "1592", "text": "calcium tissue"}
+{"_id": "1593", "text": "external epithelium of cornea"}
+{"_id": "1594", "text": "vertebrate blood"}
+{"_id": "1595", "text": "distal femoral epiphysis"}
+{"_id": "1596", "text": "pulmo"}
+{"_id": "1597", "text": "mammary part of chest"}
+{"_id": "1598", "text": "lung primordium"}
+{"_id": "1599", "text": "entire skin"}
+{"_id": "1600", "text": "epithelial tissue of endometrium"}
+{"_id": "1601", "text": "thigh bone"}
+{"_id": "1602", "text": "prostate"}
+{"_id": "1603", "text": "bronchi epithelial tissue"}
+{"_id": "1604", "text": "vertebrate dermis"}
+{"_id": "1605", "text": "skin of arm"}
+{"_id": "1606", "text": "breast epithelium"}
+{"_id": "1607", "text": "pancreatic primordium"}
+{"_id": "1608", "text": "tracheobronchial epithelium"}
+{"_id": "1609", "text": "omentum"}
+{"_id": "1610", "text": "gonada of female organism reproductive system"}
+{"_id": "1611", "text": "gonad of male genitalia"}
+{"_id": "1612", "text": "ascitic fluid"}
+{"_id": "1613", "text": "stomach"}
+{"_id": "1614", "text": "mammary gland milk"}
+{"_id": "1615", "text": "retroperitoneal node"}
+{"_id": "1616", "text": "prostate gland epithelial tissue"}
+{"_id": "1617", "text": "kidney"}
+{"_id": "1618", "text": "acetabular region"}
+{"_id": "1619", "text": "lymph node"}
+{"_id": "1620", "text": "foreskin of penis"}
+{"_id": "1621", "text": "vertebrate epidermis"}
+{"_id": "1622", "text": "allantoic placenta"}
+{"_id": "1623", "text": "lobus temporalis"}
+{"_id": "1624", "text": "vesica urinaria"}
+{"_id": "1625", "text": "pleural effusion"}
+{"_id": "1626", "text": "ureter"}
+{"_id": "1627", "text": "medulla ossea"}
+{"_id": "1628", "text": "lobus frontalis"}
+{"_id": "1629", "text": "thyroid"}
+{"_id": "1630", "text": "lymph node of neck"}
+{"_id": "1631", "text": "soft palate"}
+{"_id": "1632", "text": "hypoderm"}
+{"_id": "1633", "text": "spleen"}
+{"_id": "1634", "text": "optic cup"}
+{"_id": "1635", "text": "tunica vasculosa of eyeball"}
+{"_id": "1636", "text": "muscle organ"}
+{"_id": "1637", "text": "mandibular gland"}
+{"_id": "1638", "text": "leg zone of skin"}
+{"_id": "1639", "text": "right frontal lobe"}
+{"_id": "1640", "text": "late embryo"}
+{"_id": "1641", "text": "lower chamber of heart"}
+{"_id": "1642", "text": "wall of pleural sac"}
+{"_id": "1643", "text": "tunica mucosa uteri"}
+{"_id": "1644", "text": "zone of skin of abdomen"}
+{"_id": "1645", "text": "skin of sacral region"}
+{"_id": "1646", "text": "hip region zone of skin"}
+{"_id": "1647", "text": "skin of buttock"}
+{"_id": "1648", "text": "zone of skin of anterolateral part of thorax"}
+{"_id": "1649", "text": "funiculus umbilicalis"}
+{"_id": "1650", "text": "amniotic fluid"}
+{"_id": "1651", "text": "hind limb stylopod skin"}
+{"_id": "1652", "text": "skin of posterior part of leg"}
+{"_id": "1653", "text": "zone of skin of shoulder"}
+{"_id": "1654", "text": "gums"}
+{"_id": "1655", "text": "gonada"}
+{"_id": "1656", "text": "skin of digitus pedis"}
+{"_id": "1657", "text": "zone of skin of neck"}
+{"_id": "1658", "text": "iliac artery endothelium"}
+{"_id": "1659", "text": "umbilical vein"}
+{"_id": "1660", "text": "zone of skin of adult scalp"}
+{"_id": "1661", "text": "skin of breast"}
+{"_id": "1662", "text": "interlobular stroma of mammary gland"}
+{"_id": "1663", "text": "fat"}
+{"_id": "1664", "text": "regio glutealis"}
+{"_id": "1665", "text": "pelvis skin"}
+{"_id": "1666", "text": "stylopod of hindlimb"}
+{"_id": "1667", "text": "subcutaneous abdominal fat"}
+{"_id": "1668", "text": "left supraclavicular lymph node"}
+{"_id": "1669", "text": "left occipital lobe"}
+{"_id": "1670", "text": "large bowel"}
+{"_id": "1671", "text": "retinal pigment epithelium"}
+{"_id": "1672", "text": "duodenum"}
+{"_id": "1673", "text": "epithelium of eye lens"}
+{"_id": "1674", "text": "regio parietalis"}
+{"_id": "1675", "text": "trophoblast layer"}
+{"_id": "1676", "text": "colon ascendens"}
+{"_id": "1677", "text": "supraclavicular node"}
+{"_id": "1678", "text": "cerebral falx"}
+{"_id": "1679", "text": "brain rudiment"}
+{"_id": "1680", "text": "kidney pelvis"}
+{"_id": "1681", "text": "blastocyst"}
+{"_id": "1682", "text": "margo alveolaris"}
+{"_id": "1683", "text": "buccal mucosa"}
+{"_id": "1684", "text": "tongue"}
+{"_id": "1685", "text": "pelvis region"}
+{"_id": "1686", "text": "inguen"}
+{"_id": "1687", "text": "mandibular arch skeleton"}
+{"_id": "1688", "text": "pancreas"}
+{"_id": "1689", "text": "costal cartilage"}
+{"_id": "1690", "text": "humeri"}
+{"_id": "1691", "text": "proximal end of tibia"}
+{"_id": "1692", "text": "umbilical cord blood"}
+{"_id": "1693", "text": "wall of abdomen proper"}
+{"_id": "1694", "text": "small intestine"}
+{"_id": "1695", "text": "puboperineal region"}
+{"_id": "1696", "text": "patella"}
+{"_id": "1697", "text": "muscle of thigh"}
+{"_id": "1698", "text": "subserosa of uterine tube"}
+{"_id": "1699", "text": "liver"}
+{"_id": "1700", "text": "inguinal lymph node"}
+{"_id": "1701", "text": "forearm skin"}
+{"_id": "1702", "text": "face skin"}
+{"_id": "1703", "text": "windpipe"}
+{"_id": "1704", "text": "skull"}
+{"_id": "1705", "text": "cavum extradurale"}
+{"_id": "1706", "text": "retroperitoneum"}
+{"_id": "1707", "text": "glandula suprarenalis"}
+{"_id": "1708", "text": "eye socket"}
+{"_id": "1709", "text": "chest cavity"}
+{"_id": "1710", "text": "regio oralis"}
+{"_id": "1711", "text": "peritoneal fluid"}
+{"_id": "1712", "text": "coronary arterial tree"}
+{"_id": "1713", "text": "colon descendens"}
+{"_id": "1714", "text": "sigmoid colon"}
+{"_id": "1715", "text": "celiac node"}
+{"_id": "1716", "text": "external soft tissue zone"}
+{"_id": "1717", "text": "oesophagus"}
+{"_id": "1718", "text": "pelvic wall"}
+{"_id": "1719", "text": "axillary node"}
+{"_id": "1720", "text": "urinary bladder fundus"}
+{"_id": "1721", "text": "stratum granulosum of ovarian follicle"}
+{"_id": "1722", "text": "vertebra thoracica"}
+{"_id": "1723", "text": "zone of skin of inguinal region"}
+{"_id": "1724", "text": "lens crystallina"}
+{"_id": "1725", "text": "pericardial fluid"}
+{"_id": "1726", "text": "epencephalon-1"}
+{"_id": "1727", "text": "posterior cranial fossa"}
+{"_id": "1728", "text": "skin of heel"}
+{"_id": "1729", "text": "Brain, right parasagittal parietal region."}
+{"_id": "1730", "text": "right parietal lobe"}
+{"_id": "1731", "text": "maxilla"}
+{"_id": "1732", "text": "terminal portion of intestine"}
+{"_id": "1733", "text": "exocervical epithelium"}
+{"_id": "1734", "text": "bile duct"}
+{"_id": "1735", "text": "uterine glands set"}
+{"_id": "1736", "text": "endocervical glandular epithelium"}
+{"_id": "1737", "text": "mediastinal node"}
+{"_id": "1738", "text": "thymic primordium"}
+{"_id": "1739", "text": "laryngopharynx"}
+{"_id": "1740", "text": "gall bladder"}
+{"_id": "1741", "text": "stomach epithelium"}
+{"_id": "1742", "text": "Brain, left fronto-parietal lobe."}
+{"_id": "1743", "text": "tunica muscularis (myometrium)"}
+{"_id": "1744", "text": "pericardium"}
+{"_id": "1745", "text": "cartilage tissue"}
+{"_id": "1746", "text": "tunica conjunctiva"}
+{"_id": "1747", "text": "cornea of camera-type eye"}
+{"_id": "1748", "text": "uterus"}
+{"_id": "1749", "text": "uterine tube (sensu Mammalia)"}
+{"_id": "1750", "text": "skin of external genitalia"}
+{"_id": "1751", "text": "epididymis"}
+{"_id": "1752", "text": "nasal conduit space"}
+{"_id": "1753", "text": "abdominopelvic region"}
+{"_id": "1754", "text": "amnios"}
+{"_id": "1755", "text": "spleen mesenchyme"}
+{"_id": "1756", "text": "skin of iliac crest region"}
+{"_id": "1757", "text": "skin of umbilical area"}
+{"_id": "1758", "text": "future eye"}
+{"_id": "1759", "text": "chorionic villus"}
+{"_id": "1760", "text": "auricular region of head zone of skin"}
+{"_id": "1761", "text": "Achilles tendon"}
+{"_id": "1762", "text": "future diaphragm"}
+{"_id": "1763", "text": "skeletal muscle tissue of diaphragm"}
+{"_id": "1764", "text": "skin of armpit"}
+{"_id": "1765", "text": "chambered heart"}
+{"_id": "1766", "text": "tunica albuginea"}
+{"_id": "1767", "text": "skeletal muscle tissue"}
+{"_id": "1768", "text": "tonsil"}
+{"_id": "1769", "text": "stomach pyloric antrum"}
+{"_id": "1770", "text": "kidney epithelial tissue"}
+{"_id": "1771", "text": "pars abdominalis aortae"}
+{"_id": "1772", "text": "skin, dorsal region"}
+{"_id": "1773", "text": "presumptive telencephalon"}
+{"_id": "1774", "text": "optic nerve (II) foramen"}
+{"_id": "1775", "text": "floor of oval cavity"}
+{"_id": "1776", "text": "conjunctival epithelium"}
+{"_id": "1777", "text": "blood microvessel"}
+{"_id": "1778", "text": "cortex of cerebral hemisphere"}
+{"_id": "1779", "text": "vestibular root of eighth cranial nerve"}
+{"_id": "1780", "text": "oral roof"}
+{"_id": "1781", "text": "left parietal lobe"}
+{"_id": "1782", "text": "femoral artery"}
+{"_id": "1783", "text": "bone of limb"}
+{"_id": "1784", "text": "peritoneum"}
+{"_id": "1785", "text": "iliac artery smooth muscle tissue"}
+{"_id": "1786", "text": "cellular trophoblast"}
+{"_id": "1787", "text": "thoracic aorta smooth muscle tissue"}
+{"_id": "1788", "text": "iliac vein endothelium"}
+{"_id": "1789", "text": "iliac vein smooth muscle tissue"}
+{"_id": "1790", "text": "proximal kidney tubule"}
+{"_id": "1791", "text": "neck"}
+{"_id": "1792", "text": "vagina"}
+{"_id": "1793", "text": "Rivinus' gland"}
+{"_id": "1794", "text": "ovary germinal epithelium"}
+{"_id": "1795", "text": "pulmonary artery endothelial tube"}
+{"_id": "1796", "text": "parotid epithelium"}
+{"_id": "1797", "text": "respiratory portion of lung"}
+{"_id": "1798", "text": "pulmonary venous tree organ part"}
+{"_id": "1799", "text": "bowel"}
+{"_id": "1800", "text": "thymus organ"}
+{"_id": "1801", "text": "mesenteric node"}
+{"_id": "1802", "text": "terminal segment of free upper limb digit skin"}
+{"_id": "1803", "text": "bronchi"}
+{"_id": "1804", "text": "textus connectivus"}
+{"_id": "1805", "text": "zone of skin of torso"}
+{"_id": "1806", "text": "future tongue"}
+{"_id": "1807", "text": "left temporal lobe"}
+{"_id": "1808", "text": "os sacrum [vertebrae sacrales I - V]"}
+{"_id": "1809", "text": "muscle of thigh or crus"}
+{"_id": "1810", "text": "urethra"}
+{"_id": "1811", "text": "shankbone"}
+{"_id": "1812", "text": "proximal humeral epiphysis"}
+{"_id": "1813", "text": "vertebral column"}
+{"_id": "1814", "text": "pharynx"}
+{"_id": "1815", "text": "parotid"}
+{"_id": "1816", "text": "bone marrow stroma"}
+{"_id": "1817", "text": "sciatic nerve"}
+{"_id": "1818", "text": "hand skin"}
+{"_id": "1819", "text": "sinus maxilliaris"}
+{"_id": "1820", "text": "coccyx [coccygeal vertebrae I-IV]"}
+{"_id": "1821", "text": "saphenous vein smooth muscle tissue"}
+{"_id": "1822", "text": "trunk of aortic tree"}
+{"_id": "1823", "text": "cortex renalis"}
+{"_id": "1824", "text": "lactiferous gland"}
+{"_id": "1825", "text": "larynx"}
+{"_id": "1826", "text": "pretracheal node"}
+{"_id": "1827", "text": "suprarenal medulla"}
+{"_id": "1828", "text": "Brain, right fronto-parietal lobe."}
+{"_id": "1829", "text": "Right pararenal lymph node."}
+{"_id": "1830", "text": "ileum"}
+{"_id": "1831", "text": "cluster of meninges"}
+{"_id": "1832", "text": "pectoralis major muscle structure"}
+{"_id": "1833", "text": "Brain, fronto-temporal lobe."}
+{"_id": "1834", "text": "right temporal lobe"}
+{"_id": "1835", "text": "Brain, temporo-occipital lobe."}
+{"_id": "1836", "text": "Brain, right frontal parieto-occipital cortex."}
+{"_id": "1837", "text": "Brain, right fronto-temporal lobe."}
+{"_id": "1838", "text": "Brain, right parieto-occipital lobe."}
+{"_id": "1839", "text": "Brain, left fronto-temporal lobe."}
+{"_id": "1840", "text": "temporoparietal junction"}
+{"_id": "1841", "text": "right caudal lobe of lung"}
+{"_id": "1842", "text": "cecum"}
+{"_id": "1843", "text": "valva ileocaecalis (valva ilealis)"}
+{"_id": "1844", "text": "retromolar triangle"}
+{"_id": "1845", "text": "iliac lymph node"}
+{"_id": "1846", "text": "cortex (glandula suprarenalis)"}
+{"_id": "1847", "text": "synovium"}
+{"_id": "1848", "text": "bone of pelvis"}
+{"_id": "1849", "text": "retina of camera-type eye"}
+{"_id": "1850", "text": "CSF"}
+{"_id": "1851", "text": "Brain, left occipital-parietal region."}
+{"_id": "1852", "text": "right occipital lobe"}
+{"_id": "1853", "text": "Brain, occipito-medial region."}
+{"_id": "1854", "text": "Brain, right occipital-parietal region."}
+{"_id": "1855", "text": "Brain, left temporo-medial region."}
+{"_id": "1856", "text": "Brain, left temporo-occipital lobe."}
+{"_id": "1857", "text": "left frontal lobe"}
+{"_id": "1858", "text": "mucosa of large bowel"}
+{"_id": "1859", "text": "knee region"}
+{"_id": "1860", "text": "nasal part of pharynx"}
+{"_id": "1861", "text": "lower leg muscle"}
+{"_id": "1862", "text": "perigastric node"}
+{"_id": "1863", "text": "Casserio's muscle"}
+{"_id": "1864", "text": "ampulla of uterine tube"}
+{"_id": "1865", "text": "innominate bone"}
+{"_id": "1866", "text": "buccal cavity"}
+{"_id": "1867", "text": "pancreatic insula"}
+{"_id": "1868", "text": "pelvic muscle"}
+{"_id": "1869", "text": "pyloric node"}
+{"_id": "1870", "text": "muscle organ of perineum"}
+{"_id": "1871", "text": "urachus"}
+{"_id": "1872", "text": "future retinal pigmented epithelium"}
+{"_id": "1873", "text": "presumptive rhombencephalon"}
+{"_id": "1874", "text": "anterior part of tongue"}
+{"_id": "1875", "text": "left upper lobe of lung"}
+{"_id": "1876", "text": "esophagus distal third"}
+{"_id": "1877", "text": "lymph node of thorax"}
+{"_id": "1878", "text": "eye region"}
+{"_id": "1879", "text": "fascia of Zuckerkandl"}
+{"_id": "1880", "text": "obturator node"}
+{"_id": "1881", "text": "eye"}
+{"_id": "1882", "text": "scapulae"}
+{"_id": "1883", "text": "pons Varolii"}
+{"_id": "1884", "text": "chest wall"}
+{"_id": "1885", "text": "renal glomeruli"}
+{"_id": "1886", "text": "sebaceous gland of skin"}
+{"_id": "1887", "text": "mandibulla"}
+{"_id": "1888", "text": "aortic smooth muscle"}
+{"_id": "1889", "text": "thyroid primordium"}
+{"_id": "1890", "text": "os ilii"}
+{"_id": "1891", "text": "fascia cluster"}
+{"_id": "1892", "text": "extrahepatic bile duct"}
+{"_id": "1893", "text": "ampulla biliaropancreatica"}
+{"_id": "1894", "text": "ileocaecal lymph node"}
+{"_id": "1895", "text": "back"}
+{"_id": "1896", "text": "tonsillar sinus"}
+{"_id": "1897", "text": "supraglottis"}
+{"_id": "1898", "text": "urinary bladder transitional epithelium"}
+{"_id": "1899", "text": "glottis"}
+{"_id": "1900", "text": "vertebrae"}
+{"_id": "1901", "text": "vagina mucosa of organ"}
+{"_id": "1902", "text": "fibula"}
+{"_id": "1903", "text": "eye globe"}
+{"_id": "1904", "text": "prostate stroma"}
+{"_id": "1905", "text": "Brain, right temporo-occipital lobe."}
+{"_id": "1906", "text": "arm"}
+{"_id": "1907", "text": "Human papilloma virus type 18"}
+{"_id": "1908", "text": "Rhesus macaque polyomavirus"}
+{"_id": "1909", "text": "Epstein Barr virus"}
+{"_id": "1910", "text": "benzo[pqr]tetraphene"}
+{"_id": "1911", "text": "ethyl methanesulfonate"}
+{"_id": "1912", "text": "Adenovirus 5"}
+{"_id": "1913", "text": "Human papillomavirus - 68"}
+{"_id": "1914", "text": "N-(2-chloroethyl)-N'-(6-chloro-2-methoxyacridin-9-yl)propane-1,3-diamine dihydrochloride"}
+{"_id": "1915", "text": "Human papillomavirus type 38"}
+{"_id": "1916", "text": "human papillomavirus type 16 HPV16"}
+{"_id": "1917", "text": "asbestos"}
+{"_id": "1918", "text": "Ad12-SV40 hybrid virus"}
+{"_id": "1919", "text": "Human herpesvirus 8 type P"}
+{"_id": "1920", "text": "N-Methyl-N'-nitro-N-nitrosoguanidine"}
+{"_id": "1921", "text": "Human T-cell lymphotropic virus type I"}
+{"_id": "1922", "text": "hepatitis B virus (HBV)"}
+{"_id": "1923", "text": "Ad5-SV40 hybrid virus"}
+{"_id": "1924", "text": "v-Myc"}
+{"_id": "1925", "text": "Ad-SV40 hybrid virus"}
+{"_id": "1926", "text": "Astatine-211 Alpha Radiation"}
+{"_id": "1927", "text": "GAMMA RAY"}
+{"_id": "1928", "text": "Human papillomavirus - 56"}
+{"_id": "1929", "text": "Kirsten murine sarcoma virus"}
+{"_id": "1930", "text": "Human papillomavirus type 30"}
+{"_id": "1931", "text": "nickel(II) cation"}
+{"_id": "1932", "text": "Cesium-137 Gamma Radiation"}
+{"_id": "1933", "text": "Cobalt-60 Gamma Radiation"}
+{"_id": "1934", "text": "3-Methylcholanthrene"}
+{"_id": "1935", "text": "Human T-cell lymphotropic virus type II"}
+{"_id": "1936", "text": "Human papillomavirus - 45"}
+{"_id": "1937", "text": "4-nitroquinoline 1-oxide"}
+{"_id": "1938", "text": "herpes simplex virus type-1 HSV-1"}
+{"_id": "1939", "text": "Herpes simplex virus type 2 (HSV-2)"}
+{"_id": "1940", "text": "N-Methyl-N-nitrosourea"}
+{"_id": "1941", "text": "epithelial cell of cornea"}
+{"_id": "1942", "text": "fibroblast of lung"}
+{"_id": "1943", "text": "skin fibroblast"}
+{"_id": "1944", "text": "epitheliocyte"}
+{"_id": "1945", "text": "T-cell"}
+{"_id": "1946", "text": "bronchial epithelial cell"}
+{"_id": "1947", "text": "B-cell"}
+{"_id": "1948", "text": "epithelial cell of tracheobronchial tree"}
+{"_id": "1949", "text": "luminal cell of lactiferous duct"}
+{"_id": "1950", "text": "prostate epithelial cell"}
+{"_id": "1951", "text": "malpighian cell"}
+{"_id": "1952", "text": "breast epithelial cell"}
+{"_id": "1953", "text": "fibroblast"}
+{"_id": "1954", "text": "retinal stem cell"}
+{"_id": "1955", "text": "kidney epithelial cell"}
+{"_id": "1956", "text": "embryonic cardiomyocyte"}
+{"_id": "1957", "text": "foreskin fibroblast"}
+{"_id": "1958", "text": "endothelial cell of umbilical vein"}
+{"_id": "1959", "text": "stromal cell"}
+{"_id": "1960", "text": "retinal pigment epithelial cell"}
+{"_id": "1961", "text": "lens epithelial cell"}
+{"_id": "1962", "text": "ESC"}
+{"_id": "1963", "text": "cartilage cell"}
+{"_id": "1964", "text": "epithelial cell of uterus"}
+{"_id": "1965", "text": "Treg"}
+{"_id": "1966", "text": "tracheocyte"}
+{"_id": "1967", "text": "smooth muscle cell of the coronary artery"}
+{"_id": "1968", "text": "colon epithelial cell"}
+{"_id": "1969", "text": "stromal cell of endometrium"}
+{"_id": "1970", "text": "hepatocyte"}
+{"_id": "1971", "text": "intestinal epithelial cell"}
+{"_id": "1972", "text": "melanocyte of foreskin"}
+{"_id": "1973", "text": "epithelial cell of stomach"}
+{"_id": "1974", "text": "ICC"}
+{"_id": "1975", "text": "cardiac fibroblast"}
+{"_id": "1976", "text": "splenic fibroblast"}
+{"_id": "1977", "text": "fibroblast of the conjunctiva"}
+{"_id": "1978", "text": "fibroblast of gingiva"}
+{"_id": "1979", "text": "ovarian fibroblast"}
+{"_id": "1980", "text": "muscle fibroblast"}
+{"_id": "1981", "text": "skeleton muscle fibroblast"}
+{"_id": "1982", "text": "myoblast"}
+{"_id": "1983", "text": "aortic endothelial cell"}
+{"_id": "1984", "text": "endotheliocyte"}
+{"_id": "1985", "text": "nerve cell"}
+{"_id": "1986", "text": "neurolemmocyte"}
+{"_id": "1987", "text": "mesenchyme cell"}
+{"_id": "1988", "text": "epithelial cell of esophagus"}
+{"_id": "1989", "text": "arterial endothelial cell"}
+{"_id": "1990", "text": "osteoblast"}
+{"_id": "1991", "text": "vascular smooth muscle cell"}
+{"_id": "1992", "text": "endothelial cell of vein"}
+{"_id": "1993", "text": "kidney proximal tubule epithelial cell"}
+{"_id": "1994", "text": "histaminocyte"}
+{"_id": "1995", "text": "ovarian surface epithelial cell"}
+{"_id": "1996", "text": "pancreatic ductal cell"}
+{"_id": "1997", "text": "marrow fibroblast"}
+{"_id": "1998", "text": "hepatic stellate cell"}
+{"_id": "1999", "text": "myometrium smooth muscle cell"}
+{"_id": "2000", "text": "smooth muscle cell of the umbilical vein"}
+{"_id": "2001", "text": "myeloblast"}
+{"_id": "2002", "text": "phaeochromocyte"}
+{"_id": "2003", "text": "BaP"}
+{"_id": "2004", "text": "mononuclear leukocyte"}
+{"_id": "2005", "text": "MFB"}
+{"_id": "2006", "text": "mesotheliocyte"}
+{"_id": "2007", "text": "fibroblast-like synoviocyte"}
+{"_id": "2008", "text": "Muller cell"}
+{"_id": "2009", "text": "monocyte"}
+{"_id": "2010", "text": "Clara cell"}
+{"_id": "2011", "text": "melanocyte"}
+{"_id": "2012", "text": "NK cell"}
+{"_id": "2013", "text": "thyroid gland follicular cell"}
+{"_id": "2014", "text": "gingival epithelial cell"}
+{"_id": "2015", "text": "pancreatic delta cell"}
+{"_id": "2016", "text": "skin melanocyte"}
+{"_id": "2017", "text": "bone marrow stromal cell"}
+{"_id": "2018", "text": "glomerular endothelial cell"}
+{"_id": "2019", "text": "astrocyte"}
+{"_id": "2020", "text": "sebocyte"}
+{"_id": "2021", "text": "clear cell of thyroid gland"}
+{"_id": "2022", "text": "mesenchymal stem cell of the bone marrow"}
+{"_id": "2023", "text": "mesenchymal stem cell of umbilical cord"}
+{"_id": "2024", "text": "urothelial cell"}
+{"_id": "2025", "text": "prostate stromal cell"}