Upload label2id.json

label2id.json

@@ -0,0 +1,1946 @@
+{
+  "11 beta hydroxylase deficiency": 0,
+  "15q13.3 microdeletion": 1,
+  "15q24 microdeletion": 2,
+  "16p11.2 deletion syndrome": 3,
+  "17 alpha hydroxylase/17,20 lyase deficiency": 4,
+  "17 beta hydroxysteroid dehydrogenase 3 deficiency": 5,
+  "17q23.1q23.2 microdeletion syndrome": 6,
+  "18q deletion syndrome": 7,
+  "1p36 deletion syndrome": 8,
+  "1q21.1 microdeletion": 9,
+  "2 hydroxyglutaric aciduria": 10,
+  "2 methylbutyryl coa dehydrogenase deficiency": 11,
+  "21 hydroxylase deficiency": 12,
+  "22q11.2 deletion syndrome": 13,
+  "22q11.2 duplication": 14,
+  "22q13.3 deletion syndrome": 15,
+  "2q37 deletion syndrome": 16,
+  "3 beta hydroxysteroid dehydrogenase deficiency": 17,
+  "3 hydroxy 3 methylglutaryl coa lyase deficiency": 18,
+  "3 hydroxyacyl coa dehydrogenase deficiency": 19,
+  "3 hydroxyisobutyric aciduria": 20,
+  "3 m syndrome": 21,
+  "3 methylcrotonyl coa carboxylase deficiency": 22,
+  "3 methylglutaconyl coa hydratase deficiency": 23,
+  "3mc syndrome": 24,
+  "46,xx testicular disorder of sex development": 25,
+  "47 xxx syndrome": 26,
+  "47,xyy syndrome": 27,
+  "48,xxyy syndrome": 28,
+  "5 alpha reductase deficiency": 29,
+  "5q minus syndrome": 30,
+  "6q24 related transient neonatal diabetes mellitus": 31,
+  "7q11.23 duplication syndrome": 32,
+  "8p11 myeloproliferative syndrome": 33,
+  "9q22.3 microdeletion": 34,
+  "aarskog scott syndrome": 35,
+  "abdominal adhesions": 36,
+  "abdominal wall defect": 37,
+  "abetalipoproteinemia": 38,
+  "absence of the septum pellucidum": 39,
+  "acanthamoeba granulomatous amebic encephalitis (gae); keratitis": 40,
+  "acatalasemia": 41,
+  "accessory navicular bone": 42,
+  "aceruloplasminemia": 43,
+  "achalasia": 44,
+  "achondrogenesis": 45,
+  "achondroplasia": 46,
+  "achromatopsia": 47,
+  "acid lipase disease": 48,
+  "acinetobacter in healthcare settings": 49,
+  "acquired cystic kidney disease": 50,
+  "acral peeling skin syndrome": 51,
+  "acromegaly": 52,
+  "acromicric dysplasia": 53,
+  "actin accumulation myopathy": 54,
+  "activated pi3k delta syndrome": 55,
+  "acute disseminated encephalomyelitis": 56,
+  "acute febrile neutrophilic dermatosis": 57,
+  "acute intermittent porphyria": 58,
+  "acute promyelocytic leukemia": 59,
+  "adams oliver syndrome": 60,
+  "adcy5 related dyskinesia": 61,
+  "adenine phosphoribosyltransferase deficiency": 62,
+  "adenosine deaminase deficiency": 63,
+  "adenosine monophosphate deaminase deficiency": 64,
+  "adenylosuccinate lyase deficiency": 65,
+  "adermatoglyphia": 66,
+  "adiposis dolorosa": 67,
+  "adolescent idiopathic scoliosis": 68,
+  "adrenal insufficiency and addison's disease": 69,
+  "adrenoleukodystrophy": 70,
+  "adult acute lymphoblastic leukemia": 71,
+  "adult acute myeloid leukemia": 72,
+  "adult central nervous system tumors": 73,
+  "adult hodgkin lymphoma": 74,
+  "adult non hodgkin lymphoma": 75,
+  "adult onset leukoencephalopathy with axonal spheroids and pigmented glia": 76,
+  "adult onset vitelliform macular dystrophy": 77,
+  "adult polyglucosan body disease": 78,
+  "adult primary liver cancer": 79,
+  "adult soft tissue sarcoma": 80,
+  "afibrinogenemia": 81,
+  "african iron overload": 82,
+  "age related macular degeneration": 83,
+  "agenesis of the corpus callosum": 84,
+  "agenesis of the dorsal pancreas": 85,
+  "agnosia": 86,
+  "aicardi goutieres syndrome": 87,
+  "aicardi goutieres syndrome disorder": 88,
+  "aicardi syndrome": 89,
+  "aids related lymphoma": 90,
+  "alagille syndrome": 91,
+  "albright's hereditary osteodystrophy": 92,
+  "alcohol use and older adults": 93,
+  "alexander disease": 94,
+  "alg1 congenital disorder of glycosylation": 95,
+  "alg12 congenital disorder of glycosylation": 96,
+  "alg6 congenital disorder of glycosylation": 97,
+  "alkaptonuria": 98,
+  "alkhurma hemorrhagic fever (ahf)": 99,
+  "allan herndon dudley syndrome": 100,
+  "allergic asthma": 101,
+  "alopecia universalis": 102,
+  "alpers huttenlocher syndrome": 103,
+  "alpers' disease": 104,
+  "alpha 1 antitrypsin deficiency": 105,
+  "alpha mannosidosis": 106,
+  "alpha methylacyl coa racemase deficiency": 107,
+  "alpha thalassemia": 108,
+  "alpha thalassemia x linked intellectual disability syndrome": 109,
+  "alport syndrome": 110,
+  "alstrm syndrome": 111,
+  "alternating hemiplegia": 112,
+  "alternating hemiplegia of childhood": 113,
+  "alveolar capillary dysplasia with misalignment of pulmonary veins": 114,
+  "alzheimer disease": 115,
+  "alzheimer's caregiving": 116,
+  "alzheimer's disease": 117,
+  "am i at risk for type 2 diabetes? taking steps to lower your risk of getting diabetes": 118,
+  "amelogenesis imperfecta": 119,
+  "aminoacylase 1 deficiency": 120,
+  "amish lethal microcephaly": 121,
+  "amniotic band syndrome": 122,
+  "amyloidosis and kidney disease": 123,
+  "amyotrophic lateral sclerosis": 124,
+  "anal cancer": 125,
+  "andermann syndrome": 126,
+  "andersen tawil syndrome": 127,
+  "androgen insensitivity syndrome": 128,
+  "androgenetic alopecia": 129,
+  "anemia": 130,
+  "anemia in chronic kidney disease": 131,
+  "anemia of inflammation and chronic disease": 132,
+  "anencephaly": 133,
+  "aneurysm": 134,
+  "angelman syndrome": 135,
+  "angina": 136,
+  "anhidrotic ectodermal dysplasia with immune deficiency": 137,
+  "aniridia": 138,
+  "ankyloblepharon ectodermal defects cleft lip/palate syndrome": 139,
+  "ankylosing spondylitis": 140,
+  "antiphospholipid antibody syndrome": 141,
+  "antiphospholipid syndrome": 142,
+  "antisynthetase syndrome": 143,
+  "anxiety disorders": 144,
+  "apert syndrome": 145,
+  "aphasia": 146,
+  "aplasia cutis congenita": 147,
+  "aplastic anemia": 148,
+  "apraxia": 149,
+  "aquagenic pruritus": 150,
+  "arachnoid cysts": 151,
+  "arachnoiditis": 152,
+  "ards": 153,
+  "arginase deficiency": 154,
+  "arginine:glycine amidinotransferase deficiency": 155,
+  "argininosuccinic aciduria": 156,
+  "aromatase deficiency": 157,
+  "aromatase excess syndrome": 158,
+  "aromatic l amino acid decarboxylase deficiency": 159,
+  "arrhythmia": 160,
+  "arrhythmogenic right ventricular cardiomyopathy": 161,
+  "arterial tortuosity syndrome": 162,
+  "arteriovenous malformation": 163,
+  "arts syndrome": 164,
+  "asbestos related lung diseases": 165,
+  "aspartylglucosaminuria": 166,
+  "asperger syndrome": 167,
+  "asphyxiating thoracic dystrophy": 168,
+  "asthma": 169,
+  "ataxia": 170,
+  "ataxia neuropathy spectrum": 171,
+  "ataxia telangiectasia": 172,
+  "ataxia with oculomotor apraxia": 173,
+  "ataxia with vitamin e deficiency": 174,
+  "atelosteogenesis type 1": 175,
+  "atelosteogenesis type 2": 176,
+  "atelosteogenesis type 3": 177,
+  "atherosclerosis": 178,
+  "atopic dermatitis": 179,
+  "atrial fibrillation": 180,
+  "atrial fibrillation and stroke": 181,
+  "attention deficit hyperactivity disorder": 182,
+  "atypical chronic myelogenous leukemia": 183,
+  "atypical hemolytic uremic syndrome": 184,
+  "auriculo condylar syndrome": 185,
+  "autism": 186,
+  "autoimmune addison disease": 187,
+  "autoimmune atrophic gastritis": 188,
+  "autoimmune autonomic ganglionopathy": 189,
+  "autoimmune hemolytic anemia": 190,
+  "autoimmune hepatitis": 191,
+  "autoimmune lymphoproliferative syndrome": 192,
+  "autoimmune polyglandular syndrome, type 1": 193,
+  "autosomal dominant congenital stationary night blindness": 194,
+  "autosomal dominant hyper ige syndrome": 195,
+  "autosomal dominant hypocalcemia": 196,
+  "autosomal dominant nocturnal frontal lobe epilepsy": 197,
+  "autosomal dominant partial epilepsy with auditory features": 198,
+  "autosomal dominant vitreoretinochoroidopathy": 199,
+  "autosomal recessive axonal neuropathy with neuromyotonia": 200,
+  "autosomal recessive cerebellar ataxia type 1": 201,
+  "autosomal recessive congenital methemoglobinemia": 202,
+  "autosomal recessive congenital stationary night blindness": 203,
+  "autosomal recessive hyper ige syndrome": 204,
+  "autosomal recessive hypotrichosis": 205,
+  "autosomal recessive polycystic kidney disease": 206,
+  "autosomal recessive primary microcephaly": 207,
+  "autosomal recessive spastic ataxia of charlevoix saguenay": 208,
+  "axenfeld rieger syndrome": 209,
+  "axenfeld rieger syndrome type 1": 210,
+  "back pain": 211,
+  "balance problems": 212,
+  "baller gerold syndrome": 213,
+  "bannayan riley ruvalcaba syndrome": 214,
+  "baraitser winter syndrome": 215,
+  "bardet biedl syndrome": 216,
+  "barrett esophagus": 217,
+  "bart pumphrey syndrome": 218,
+  "barth syndrome": 219,
+  "bartter syndrome": 220,
+  "basilar migraine": 221,
+  "batten disease": 222,
+  "beare stevenson cutis gyrata syndrome": 223,
+  "beckwith wiedemann syndrome": 224,
+  "behcet's disease": 225,
+  "behet disease": 226,
+  "behr syndrome": 227,
+  "bell's palsy": 228,
+  "benign chronic pemphigus": 229,
+  "benign essential blepharospasm": 230,
+  "benign familial neonatal seizures": 231,
+  "benign recurrent intrahepatic cholestasis": 232,
+  "benign rolandic epilepsy (bre)": 233,
+  "benign schwannoma": 234,
+  "best vitelliform macular dystrophy": 235,
+  "beta ketothiolase deficiency": 236,
+  "beta mannosidosis": 237,
+  "beta thalassemia": 238,
+  "beta ureidopropionase deficiency": 239,
+  "bethlem myopathy": 240,
+  "bietti crystalline dystrophy": 241,
+  "bilateral perisylvian polymicrogyria": 242,
+  "bile duct cancer (cholangiocarcinoma)": 243,
+  "biliary atresia": 244,
+  "binswanger's disease": 245,
+  "biotin thiamine responsive basal ganglia disease": 246,
+  "biotinidase deficiency": 247,
+  "birt hogg dub syndrome": 248,
+  "bjrnstad syndrome": 249,
+  "bladder cancer": 250,
+  "blau syndrome": 251,
+  "blepharophimosis, ptosis, and epicanthus inversus syndrome": 252,
+  "blepharophimosis, ptosis, and epicanthus inversus syndrome type 1": 253,
+  "bloom syndrome": 254,
+  "blue rubber bleb nevus syndrome": 255,
+  "book syndrome": 256,
+  "boomerang dysplasia": 257,
+  "botulism": 258,
+  "bowen conradi syndrome": 259,
+  "brachial plexus injuries": 260,
+  "bradyopsia": 261,
+  "brain and spinal tumors": 262,
+  "branchio oculo facial syndrome": 263,
+  "branchiooculofacial syndrome": 264,
+  "branchiootorenal syndrome": 265,
+  "branchiootorenal/branchiootic syndrome": 266,
+  "breast cancer": 267,
+  "brittle diabetes": 268,
+  "brody myopathy": 269,
+  "broken heart syndrome": 270,
+  "bronchiectasis": 271,
+  "bronchiolitis obliterans organizing pneumonia": 272,
+  "bronchitis": 273,
+  "bronchopulmonary dysplasia": 274,
+  "brooke spiegler syndrome": 275,
+  "brown sequard syndrome": 276,
+  "brugada syndrome": 277,
+  "buerger disease": 278,
+  "buschke ollendorff syndrome": 279,
+  "c3 glomerulopathy": 280,
+  "cadasil": 281,
+  "caffey disease": 282,
+  "campomelic dysplasia": 283,
+  "camurati engelmann disease": 284,
+  "canavan disease": 285,
+  "cant syndrome": 286,
+  "cap myopathy": 287,
+  "capillary malformation arteriovenous malformation syndrome": 288,
+  "carbamoyl phosphate synthetase i deficiency": 289,
+  "cardiofaciocutaneous syndrome": 290,
+  "cardiogenic shock": 291,
+  "cardiomyopathy": 292,
+  "carney complex": 293,
+  "carnitine acylcarnitine translocase deficiency": 294,
+  "carnitine palmitoyltransferase i deficiency": 295,
+  "carnitine palmitoyltransferase ii deficiency": 296,
+  "carotid artery disease": 297,
+  "carpal tunnel syndrome": 298,
+  "carpenter syndrome": 299,
+  "cartilage hair hypoplasia": 300,
+  "cask related intellectual disability": 301,
+  "catamenial pneumothorax": 302,
+  "cataract": 303,
+  "catecholaminergic polymorphic ventricular tachycardia": 304,
+  "catsper1 related nonsyndromic male infertility": 305,
+  "caudal regression syndrome": 306,
+  "causes of diabetes": 307,
+  "cav3 related distal myopathy": 308,
+  "cavernous malformation": 309,
+  "celiac artery compression syndrome": 310,
+  "celiac disease": 311,
+  "central cord syndrome": 312,
+  "central core disease": 313,
+  "central pain syndrome": 314,
+  "central pontine myelinolysis": 315,
+  "centronuclear myopathy": 316,
+  "cephalic disorders": 317,
+  "cerebellar degeneration": 318,
+  "cerebellar hypoplasia": 319,
+  "cerebral aneurysms": 320,
+  "cerebral arteriosclerosis": 321,
+  "cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy": 322,
+  "cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy": 323,
+  "cerebral cavernous malformation": 324,
+  "cerebral hypoxia": 325,
+  "cerebral palsy": 326,
+  "cerebro oculo facio skeletal syndrome (cofs)": 327,
+  "cerebrotendinous xanthomatosis": 328,
+  "chanarin dorfman syndrome": 329,
+  "chandler's syndrome": 330,
+  "chapare hemorrhagic fever (chhf)": 331,
+  "char syndrome": 332,
+  "charcot marie tooth disease": 333,
+  "charcot marie tooth disease type 2f": 334,
+  "charge syndrome": 335,
+  "chediak higashi syndrome": 336,
+  "cherubism": 337,
+  "chiari malformation": 338,
+  "chiari malformation type 1": 339,
+  "chilaiditi syndrome": 340,
+  "childhood acute lymphoblastic leukemia": 341,
+  "childhood acute myeloid leukemia and other myeloid malignancies": 342,
+  "childhood astrocytomas": 343,
+  "childhood brain and spinal cord tumors": 344,
+  "childhood brain stem glioma": 345,
+  "childhood central nervous system atypical teratoid/rhabdoid tumor": 346,
+  "childhood central nervous system embryonal tumors": 347,
+  "childhood central nervous system germ cell tumors": 348,
+  "childhood craniopharyngioma": 349,
+  "childhood ependymoma": 350,
+  "childhood extracranial germ cell tumors": 351,
+  "childhood hodgkin lymphoma": 352,
+  "childhood interstitial lung disease": 353,
+  "childhood liver cancer": 354,
+  "childhood myocerebrohepatopathy spectrum": 355,
+  "childhood nephrotic syndrome": 356,
+  "childhood non hodgkin lymphoma": 357,
+  "childhood rhabdomyosarcoma": 358,
+  "childhood soft tissue sarcoma": 359,
+  "childhood vascular tumors": 360,
+  "chmp2b related frontotemporal dementia": 361,
+  "cholesteatoma": 362,
+  "cholesteryl ester storage disease": 363,
+  "chondrocalcinosis 2": 364,
+  "chops syndrome": 365,
+  "chordoma": 366,
+  "chorea": 367,
+  "chorea acanthocytosis": 368,
+  "choroideremia": 369,
+  "christianson syndrome": 370,
+  "chromosome 3p syndrome": 371,
+  "chromosome 4q deletion": 372,
+  "chronic atrial and intestinal dysrhythmia": 373,
+  "chronic diarrhea in children": 374,
+  "chronic fatigue syndrome": 375,
+  "chronic fatigue syndrome (cfs)": 376,
+  "chronic granulomatous disease": 377,
+  "chronic hiccups": 378,
+  "chronic inflammatory demyelinating polyneuropathy": 379,
+  "chronic inflammatory demyelinating polyneuropathy (cidp)": 380,
+  "chronic lymphocytic leukemia": 381,
+  "chronic myelogenous leukemia": 382,
+  "chronic myelomonocytic leukemia": 383,
+  "chronic myeloproliferative neoplasms": 384,
+  "chronic pain": 385,
+  "chronic progressive external ophthalmoplegia": 386,
+  "chst3 related skeletal dysplasia": 387,
+  "chylomicron retention disease": 388,
+  "cirrhosis": 389,
+  "citrullinemia": 390,
+  "citrullinemia type i": 391,
+  "cleidocranial dysplasia": 392,
+  "clouston syndrome": 393,
+  "coats disease": 394,
+  "coats plus syndrome": 395,
+  "coccygodynia": 396,
+  "cockayne syndrome": 397,
+  "coffin lowry syndrome": 398,
+  "coffin siris syndrome": 399,
+  "cog5 congenital disorder of glycosylation": 400,
+  "cohen syndrome": 401,
+  "col4a1 related brain small vessel disease": 402,
+  "cold agglutinin disease": 403,
+  "cold induced sweating syndrome": 404,
+  "cold urticaria": 405,
+  "cole disease": 406,
+  "collagen vi related myopathy": 407,
+  "coloboma": 408,
+  "colon cancer": 409,
+  "color vision deficiency": 410,
+  "colorectal cancer": 411,
+  "colpocephaly": 412,
+  "coma": 413,
+  "combined malonic and methylmalonic aciduria": 414,
+  "combined pituitary hormone deficiency": 415,
+  "common variable immune deficiency": 416,
+  "common variable immunodeficiency": 417,
+  "complement component 2 deficiency": 418,
+  "complement factor i deficiency": 419,
+  "complete lcat deficiency": 420,
+  "complex regional pain syndrome": 421,
+  "cone rod dystrophy": 422,
+  "congenital adrenal hyperplasia": 423,
+  "congenital adrenal hyperplasia due to 11 beta hydroxylase deficiency": 424,
+  "congenital afibrinogenemia": 425,
+  "congenital anosmia": 426,
+  "congenital bilateral absence of the vas deferens": 427,
+  "congenital cataracts, facial dysmorphism, and neuropathy": 428,
+  "congenital central hypoventilation syndrome": 429,
+  "congenital contractural arachnodactyly": 430,
+  "congenital deafness with labyrinthine aplasia, microtia, and microdontia": 431,
+  "congenital diaphragmatic hernia": 432,
+  "congenital dyserythropoietic anemia": 433,
+  "congenital fiber type disproportion": 434,
+  "congenital fibrosis of the extraocular muscles": 435,
+  "congenital generalized lipodystrophy": 436,
+  "congenital heart defects": 437,
+  "congenital hemidysplasia with ichthyosiform erythroderma and limb defects": 438,
+  "congenital hepatic fibrosis": 439,
+  "congenital hyperinsulinism": 440,
+  "congenital hypothyroidism": 441,
+  "congenital insensitivity to pain": 442,
+  "congenital insensitivity to pain with anhidrosis": 443,
+  "congenital laryngeal palsy": 444,
+  "congenital leptin deficiency": 445,
+  "congenital mirror movement disorder": 446,
+  "congenital myasthenia": 447,
+  "congenital myasthenic syndrome": 448,
+  "congenital myopathy": 449,
+  "congenital neuronal ceroid lipofuscinosis": 450,
+  "congenital plasminogen deficiency": 451,
+  "congenital radio ulnar synostosis": 452,
+  "congenital stromal corneal dystrophy": 453,
+  "congenital sucrase isomaltase deficiency": 454,
+  "copd": 455,
+  "core binding factor acute myeloid leukemia": 456,
+  "cornelia de lange syndrome": 457,
+  "coronary heart disease": 458,
+  "coronary microvascular disease": 459,
+  "corticobasal degeneration": 460,
+  "corticosteroid binding globulin deficiency": 461,
+  "costeff syndrome": 462,
+  "costello syndrome": 463,
+  "cough": 464,
+  "cowden syndrome": 465,
+  "cramp fasciculation syndrome": 466,
+  "cranioectodermal dysplasia": 467,
+  "craniofacial deafness hand syndrome": 468,
+  "craniofacial microsomia": 469,
+  "craniometaphyseal dysplasia": 470,
+  "craniometaphyseal dysplasia, autosomal dominant": 471,
+  "craniometaphyseal dysplasia, autosomal recessive type": 472,
+  "craniopharyngioma": 473,
+  "craniosynostosis": 474,
+  "creating a family health history": 475,
+  "crest syndrome": 476,
+  "creutzfeldt jakob disease": 477,
+  "cri du chat syndrome": 478,
+  "crigler najjar syndrome": 479,
+  "crimean congo hemorrhagic fever (cchf)": 480,
+  "critical congenital heart disease": 481,
+  "crohn disease": 482,
+  "crohn's disease": 483,
+  "crouzon syndrome": 484,
+  "crouzonodermoskeletal syndrome": 485,
+  "cryptogenic cirrhosis": 486,
+  "cryptogenic organizing pneumonia": 487,
+  "currarino triad": 488,
+  "cushing disease": 489,
+  "cushing's syndrome": 490,
+  "cutaneous mastocytosis": 491,
+  "cutis laxa": 492,
+  "cyclic neutropenia": 493,
+  "cyclic vomiting syndrome": 494,
+  "cystic fibrosis": 495,
+  "cystinosis": 496,
+  "cystinuria": 497,
+  "cystocele": 498,
+  "cytochrome c oxidase deficiency": 499,
+  "cytochrome p450 oxidoreductase deficiency": 500,
+  "cytogenetically normal acute myeloid leukemia": 501,
+  "czech dysplasia": 502,
+  "d bifunctional protein deficiency": 503,
+  "dandy walker malformation": 504,
+  "dandy walker syndrome": 505,
+  "danon disease": 506,
+  "darier disease": 507,
+  "deafness and myopia syndrome": 508,
+  "deafness dystonia optic neuronopathy syndrome": 509,
+  "deep brain stimulation for parkinson's disease": 510,
+  "deep vein thrombosis": 511,
+  "dementia": 512,
+  "dementia with lewy bodies": 513,
+  "dentatorubral pallidoluysian atrophy": 514,
+  "dentinogenesis imperfecta": 515,
+  "denys drash syndrome": 516,
+  "deoxyguanosine kinase deficiency": 517,
+  "depression": 518,
+  "dermatitis herpetiformis: skin manifestation of celiac disease (for health care professionals)": 519,
+  "dermatofibrosarcoma protuberans": 520,
+  "dermatomyositis": 521,
+  "desmoid tumor": 522,
+  "desmoplastic infantile ganglioglioma": 523,
+  "desmosterolosis": 524,
+  "developmental dyspraxia": 525,
+  "dextrocardia with situs inversus": 526,
+  "diabetes": 527,
+  "diabetes, heart disease, and stroke": 528,
+  "diabetic heart disease": 529,
+  "diabetic kidney disease": 530,
+  "diabetic mastopathy": 531,
+  "diabetic neuropathies: the nerve damage of diabetes": 532,
+  "diabetic neuropathy": 533,
+  "diabetic retinopathy": 534,
+  "diagnosis of diabetes and prediabetes": 535,
+  "diamond blackfan anemia": 536,
+  "diarrhea": 537,
+  "diastrophic dysplasia": 538,
+  "dicer1 syndrome": 539,
+  "diffuse gastric cancer": 540,
+  "diffuse idiopathic skeletal hyperostosis": 541,
+  "dihydrolipoamide dehydrogenase deficiency": 542,
+  "dihydropyrimidinase deficiency": 543,
+  "dihydropyrimidine dehydrogenase deficiency": 544,
+  "dilated cardiomyopathy with ataxia syndrome": 545,
+  "disseminated intravascular coagulation": 546,
+  "disseminated peritoneal leiomyomatosis": 547,
+  "distal arthrogryposis type 1": 548,
+  "distal hereditary motor neuropathy, type ii": 549,
+  "distal hereditary motor neuropathy, type v": 550,
+  "distal myopathy 2": 551,
+  "diverticular disease": 552,
+  "dmd associated dilated cardiomyopathy": 553,
+  "dolk congenital disorder of glycosylation": 554,
+  "dominant dystrophic epidermolysis bullosa": 555,
+  "donnai barrow syndrome": 556,
+  "donohue syndrome": 557,
+  "doors syndrome": 558,
+  "dopa responsive dystonia": 559,
+  "dopamine beta hydroxylase deficiency": 560,
+  "dopamine transporter deficiency syndrome": 561,
+  "dowling degos disease": 562,
+  "down syndrome": 563,
+  "doyne honeycomb retinal dystrophy": 564,
+  "dravet syndrome": 565,
+  "dry eye": 566,
+  "dry mouth": 567,
+  "duane radial ray syndrome": 568,
+  "dubin johnson syndrome": 569,
+  "duchenne and becker muscular dystrophy": 570,
+  "duchenne muscular dystrophy": 571,
+  "dumping syndrome": 572,
+  "dyggve melchior clausen syndrome": 573,
+  "dysautonomia": 574,
+  "dyserythropoietic anemia and thrombocytopenia": 575,
+  "dysgraphia": 576,
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+  "steatocystoma multiplex": 1723,
+  "stenotrophomonas maltophilia infection": 1724,
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+  "syndrome of inappropriate antidiuretic hormone": 1750,
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+  "thalassemia": 1771,
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+  "thanatophoric dysplasia": 1773,
+  "thiamine responsive megaloblastic anemia syndrome": 1774,
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+  "thrombocythemia and thrombocytosis": 1777,
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+  "thrombocytopenia absent radius syndrome": 1779,
+  "thrombotic thrombocytopenic purpura": 1780,
+  "thymoma and thymic carcinoma": 1781,
+  "thyrotoxic myopathy": 1782,
+  "tibial muscular dystrophy": 1783,
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+  "townes brocks syndrome": 1790,
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+  "tracheobronchopathia osteoplastica": 1792,
+  "transient ischemic attack": 1793,
+  "transitional cell cancer of the renal pelvis and ureter": 1794,
+  "transmissible spongiform encephalopathies": 1795,
+  "transthyretin amyloidosis": 1796,
+  "transverse myelitis": 1797,
+  "traumatic brain injury": 1798,
+  "treacher collins syndrome": 1799,
+  "treatment methods for kidney failure: peritoneal dialysis": 1800,
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+  "trigeminal neuralgia": 1804,
+  "trimethylaminuria": 1805,
+  "triosephosphate isomerase deficiency": 1806,
+  "triple a syndrome": 1807,
+  "triple x syndrome": 1808,
+  "trisomy 13": 1809,
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+  "tropical spastic paraparesis": 1811,
+  "troyer syndrome": 1812,
+  "tuberculosis (tb)": 1813,
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+  "tuberous sclerosis complex": 1815,
+  "tubular aggregate myopathy": 1816,
+  "tularemia": 1817,
+  "tumor necrosis factor receptor associated periodic syndrome": 1818,
+  "turner syndrome": 1819,
+  "tylosis with esophageal cancer": 1820,
+  "type 1 diabetes": 1821,
+  "type 1 plasminogen deficiency": 1822,
+  "type a insulin resistance syndrome": 1823,
+  "tyrosine hydroxylase deficiency": 1824,
+  "tyrosinemia": 1825,
+  "ulcerative colitis": 1826,
+  "uncombable hair syndrome": 1827,
+  "unverricht lundborg disease": 1828,
+  "urachal cyst": 1829,
+  "urethral cancer": 1830,
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+  "urinary incontinence in children": 1832,
+  "urinary incontinence in men": 1833,
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+  "urinary tract infection in adults": 1835,
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+  "urinary tract infections in children": 1837,
+  "urine blockage in newborns": 1838,
+  "uromodulin associated kidney disease": 1839,
+  "usher syndrome": 1840,
+  "uterine sarcoma": 1841,
+  "uv sensitive syndrome": 1842,
+  "vacterl association": 1843,
+  "van der woude syndrome": 1844,
+  "varicose veins": 1845,
+  "vasculitis": 1846,
+  "vasculitis syndromes of the central and peripheral nervous systems": 1847,
+  "very long chain acyl coa dehydrogenase deficiency": 1848,
+  "vesicoureteral reflux": 1849,
+  "viral gastroenteritis": 1850,
+  "viral hepatitis: a through e and beyond": 1851,
+  "vitamin d dependent rickets": 1852,
+  "vitelliform macular dystrophy": 1853,
+  "vitiligo": 1854,
+  "vlcad deficiency": 1855,
+  "vldlr associated cerebellar hypoplasia": 1856,
+  "vohwinkel syndrome": 1857,
+  "von hippel lindau disease": 1858,
+  "von hippel lindau disease (vhl)": 1859,
+  "von hippel lindau syndrome": 1860,
+  "von willebrand disease": 1861,
+  "vulvar cancer": 1862,
+  "waardenburg syndrome": 1863,
+  "wagner syndrome": 1864,
+  "wagr syndrome": 1865,
+  "waldenstrm macroglobulinemia": 1866,
+  "walker warburg syndrome": 1867,
+  "wallenberg's syndrome": 1868,
+  "warfarin resistance": 1869,
+  "warfarin sensitivity": 1870,
+  "warsaw breakage syndrome": 1871,
+  "warthin tumor": 1872,
+  "waterhousefriderichsen syndrome": 1873,
+  "weaver syndrome": 1874,
+  "weill marchesani syndrome": 1875,
+  "weissenbacher zweymller syndrome": 1876,
+  "werner syndrome": 1877,
+  "wernicke korsakoff syndrome": 1878,
+  "weyers acrofacial dysostosis": 1879,
+  "what i need to know about bladder control for women": 1880,
+  "what i need to know about cirrhosis": 1881,
+  "what i need to know about crohn's disease": 1882,
+  "what i need to know about diarrhea": 1883,
+  "what i need to know about diverticular disease": 1884,
+  "what i need to know about erectile dysfunction": 1885,
+  "what i need to know about gas": 1886,
+  "what i need to know about gestational diabetes": 1887,
+  "what i need to know about hepatitis a": 1888,
+  "what i need to know about hepatitis b": 1889,
+  "what i need to know about hepatitis c": 1890,
+  "what i need to know about hirschsprung disease": 1891,
+  "what i need to know about interstitial cystitis/painful bladder syndrome": 1892,
+  "what i need to know about kidney failure and how its treated": 1893,
+  "what i need to know about kidney stones": 1894,
+  "what i need to know about lactose intolerance": 1895,
+  "what i need to know about living with kidney failure": 1896,
+  "what i need to know about my child's urinary tract infection": 1897,
+  "whiplash": 1898,
+  "whipple disease": 1899,
+  "whipple's disease": 1900,
+  "white sponge nevus": 1901,
+  "wildervanck syndrome": 1902,
+  "williams syndrome": 1903,
+  "wilms tumor and other childhood kidney tumors": 1904,
+  "wilson disease": 1905,
+  "winchester syndrome": 1906,
+  "wiskott aldrich syndrome": 1907,
+  "wolf hirschhorn syndrome": 1908,
+  "wolff parkinson white syndrome": 1909,
+  "wolfram syndrome": 1910,
+  "wolman disease": 1911,
+  "x linked adrenal hypoplasia congenita": 1912,
+  "x linked adrenoleukodystrophy": 1913,
+  "x linked agammaglobulinemia": 1914,
+  "x linked chondrodysplasia punctata 1": 1915,
+  "x linked chondrodysplasia punctata 2": 1916,
+  "x linked congenital stationary night blindness": 1917,
+  "x linked creatine deficiency": 1918,
+  "x linked dominant scapuloperoneal myopathy": 1919,
+  "x linked dystonia parkinsonism": 1920,
+  "x linked hyper igm syndrome": 1921,
+  "x linked hypophosphatemia": 1922,
+  "x linked immunodeficiency with magnesium defect, epstein barr virus infection, and neoplasia": 1923,
+  "x linked infantile nystagmus": 1924,
+  "x linked infantile spasm syndrome": 1925,
+  "x linked intellectual disability, siderius type": 1926,
+  "x linked juvenile retinoschisis": 1927,
+  "x linked lissencephaly with abnormal genitalia": 1928,
+  "x linked lymphoproliferative disease": 1929,
+  "x linked myotubular myopathy": 1930,
+  "x linked severe combined immunodeficiency": 1931,
+  "x linked sideroblastic anemia": 1932,
+  "x linked sideroblastic anemia and ataxia": 1933,
+  "x linked spondyloepiphyseal dysplasia tarda": 1934,
+  "x linked thrombocytopenia": 1935,
+  "xeroderma pigmentosum": 1936,
+  "y chromosome infertility": 1937,
+  "yellow nail syndrome": 1938,
+  "yersinia": 1939,
+  "zap70 related severe combined immunodeficiency": 1940,
+  "zellweger spectrum disorder": 1941,
+  "zellweger syndrome": 1942,
+  "zollinger ellison syndrome": 1943
+}