{
  "0": "11 beta hydroxylase deficiency",
  "1": "15q13.3 microdeletion",
  "2": "15q24 microdeletion",
  "3": "16p11.2 deletion syndrome",
  "4": "17 alpha hydroxylase/17,20 lyase deficiency",
  "5": "17 beta hydroxysteroid dehydrogenase 3 deficiency",
  "6": "17q23.1q23.2 microdeletion syndrome",
  "7": "18q deletion syndrome",
  "8": "1p36 deletion syndrome",
  "9": "1q21.1 microdeletion",
  "10": "2 hydroxyglutaric aciduria",
  "11": "2 methylbutyryl coa dehydrogenase deficiency",
  "12": "21 hydroxylase deficiency",
  "13": "22q11.2 deletion syndrome",
  "14": "22q11.2 duplication",
  "15": "22q13.3 deletion syndrome",
  "16": "2q37 deletion syndrome",
  "17": "3 beta hydroxysteroid dehydrogenase deficiency",
  "18": "3 hydroxy 3 methylglutaryl coa lyase deficiency",
  "19": "3 hydroxyacyl coa dehydrogenase deficiency",
  "20": "3 hydroxyisobutyric aciduria",
  "21": "3 m syndrome",
  "22": "3 methylcrotonyl coa carboxylase deficiency",
  "23": "3 methylglutaconyl coa hydratase deficiency",
  "24": "3mc syndrome",
  "25": "46,xx testicular disorder of sex development",
  "26": "47 xxx syndrome",
  "27": "47,xyy syndrome",
  "28": "48,xxyy syndrome",
  "29": "5 alpha reductase deficiency",
  "30": "5q minus syndrome",
  "31": "6q24 related transient neonatal diabetes mellitus",
  "32": "7q11.23 duplication syndrome",
  "33": "8p11 myeloproliferative syndrome",
  "34": "9q22.3 microdeletion",
  "35": "aarskog scott syndrome",
  "36": "abdominal adhesions",
  "37": "abdominal wall defect",
  "38": "abetalipoproteinemia",
  "39": "absence of the septum pellucidum",
  "40": "acanthamoeba granulomatous amebic encephalitis (gae); keratitis",
  "41": "acatalasemia",
  "42": "accessory navicular bone",
  "43": "aceruloplasminemia",
  "44": "achalasia",
  "45": "achondrogenesis",
  "46": "achondroplasia",
  "47": "achromatopsia",
  "48": "acid lipase disease",
  "49": "acinetobacter in healthcare settings",
  "50": "acquired cystic kidney disease",
  "51": "acral peeling skin syndrome",
  "52": "acromegaly",
  "53": "acromicric dysplasia",
  "54": "actin accumulation myopathy",
  "55": "activated pi3k delta syndrome",
  "56": "acute disseminated encephalomyelitis",
  "57": "acute febrile neutrophilic dermatosis",
  "58": "acute intermittent porphyria",
  "59": "acute promyelocytic leukemia",
  "60": "adams oliver syndrome",
  "61": "adcy5 related dyskinesia",
  "62": "adenine phosphoribosyltransferase deficiency",
  "63": "adenosine deaminase deficiency",
  "64": "adenosine monophosphate deaminase deficiency",
  "65": "adenylosuccinate lyase deficiency",
  "66": "adermatoglyphia",
  "67": "adiposis dolorosa",
  "68": "adolescent idiopathic scoliosis",
  "69": "adrenal insufficiency and addison's disease",
  "70": "adrenoleukodystrophy",
  "71": "adult acute lymphoblastic leukemia",
  "72": "adult acute myeloid leukemia",
  "73": "adult central nervous system tumors",
  "74": "adult hodgkin lymphoma",
  "75": "adult non hodgkin lymphoma",
  "76": "adult onset leukoencephalopathy with axonal spheroids and pigmented glia",
  "77": "adult onset vitelliform macular dystrophy",
  "78": "adult polyglucosan body disease",
  "79": "adult primary liver cancer",
  "80": "adult soft tissue sarcoma",
  "81": "afibrinogenemia",
  "82": "african iron overload",
  "83": "age related macular degeneration",
  "84": "agenesis of the corpus callosum",
  "85": "agenesis of the dorsal pancreas",
  "86": "agnosia",
  "87": "aicardi goutieres syndrome",
  "88": "aicardi goutieres syndrome disorder",
  "89": "aicardi syndrome",
  "90": "aids related lymphoma",
  "91": "alagille syndrome",
  "92": "albright's hereditary osteodystrophy",
  "93": "alcohol use and older adults",
  "94": "alexander disease",
  "95": "alg1 congenital disorder of glycosylation",
  "96": "alg12 congenital disorder of glycosylation",
  "97": "alg6 congenital disorder of glycosylation",
  "98": "alkaptonuria",
  "99": "alkhurma hemorrhagic fever (ahf)",
  "100": "allan herndon dudley syndrome",
  "101": "allergic asthma",
  "102": "alopecia universalis",
  "103": "alpers huttenlocher syndrome",
  "104": "alpers' disease",
  "105": "alpha 1 antitrypsin deficiency",
  "106": "alpha mannosidosis",
  "107": "alpha methylacyl coa racemase deficiency",
  "108": "alpha thalassemia",
  "109": "alpha thalassemia x linked intellectual disability syndrome",
  "110": "alport syndrome",
  "111": "alstrm syndrome",
  "112": "alternating hemiplegia",
  "113": "alternating hemiplegia of childhood",
  "114": "alveolar capillary dysplasia with misalignment of pulmonary veins",
  "115": "alzheimer disease",
  "116": "alzheimer's caregiving",
  "117": "alzheimer's disease",
  "118": "am i at risk for type 2 diabetes? taking steps to lower your risk of getting diabetes",
  "119": "amelogenesis imperfecta",
  "120": "aminoacylase 1 deficiency",
  "121": "amish lethal microcephaly",
  "122": "amniotic band syndrome",
  "123": "amyloidosis and kidney disease",
  "124": "amyotrophic lateral sclerosis",
  "125": "anal cancer",
  "126": "andermann syndrome",
  "127": "andersen tawil syndrome",
  "128": "androgen insensitivity syndrome",
  "129": "androgenetic alopecia",
  "130": "anemia",
  "131": "anemia in chronic kidney disease",
  "132": "anemia of inflammation and chronic disease",
  "133": "anencephaly",
  "134": "aneurysm",
  "135": "angelman syndrome",
  "136": "angina",
  "137": "anhidrotic ectodermal dysplasia with immune deficiency",
  "138": "aniridia",
  "139": "ankyloblepharon ectodermal defects cleft lip/palate syndrome",
  "140": "ankylosing spondylitis",
  "141": "antiphospholipid antibody syndrome",
  "142": "antiphospholipid syndrome",
  "143": "antisynthetase syndrome",
  "144": "anxiety disorders",
  "145": "apert syndrome",
  "146": "aphasia",
  "147": "aplasia cutis congenita",
  "148": "aplastic anemia",
  "149": "apraxia",
  "150": "aquagenic pruritus",
  "151": "arachnoid cysts",
  "152": "arachnoiditis",
  "153": "ards",
  "154": "arginase deficiency",
  "155": "arginine:glycine amidinotransferase deficiency",
  "156": "argininosuccinic aciduria",
  "157": "aromatase deficiency",
  "158": "aromatase excess syndrome",
  "159": "aromatic l amino acid decarboxylase deficiency",
  "160": "arrhythmia",
  "161": "arrhythmogenic right ventricular cardiomyopathy",
  "162": "arterial tortuosity syndrome",
  "163": "arteriovenous malformation",
  "164": "arts syndrome",
  "165": "asbestos related lung diseases",
  "166": "aspartylglucosaminuria",
  "167": "asperger syndrome",
  "168": "asphyxiating thoracic dystrophy",
  "169": "asthma",
  "170": "ataxia",
  "171": "ataxia neuropathy spectrum",
  "172": "ataxia telangiectasia",
  "173": "ataxia with oculomotor apraxia",
  "174": "ataxia with vitamin e deficiency",
  "175": "atelosteogenesis type 1",
  "176": "atelosteogenesis type 2",
  "177": "atelosteogenesis type 3",
  "178": "atherosclerosis",
  "179": "atopic dermatitis",
  "180": "atrial fibrillation",
  "181": "atrial fibrillation and stroke",
  "182": "attention deficit hyperactivity disorder",
  "183": "atypical chronic myelogenous leukemia",
  "184": "atypical hemolytic uremic syndrome",
  "185": "auriculo condylar syndrome",
  "186": "autism",
  "187": "autoimmune addison disease",
  "188": "autoimmune atrophic gastritis",
  "189": "autoimmune autonomic ganglionopathy",
  "190": "autoimmune hemolytic anemia",
  "191": "autoimmune hepatitis",
  "192": "autoimmune lymphoproliferative syndrome",
  "193": "autoimmune polyglandular syndrome, type 1",
  "194": "autosomal dominant congenital stationary night blindness",
  "195": "autosomal dominant hyper ige syndrome",
  "196": "autosomal dominant hypocalcemia",
  "197": "autosomal dominant nocturnal frontal lobe epilepsy",
  "198": "autosomal dominant partial epilepsy with auditory features",
  "199": "autosomal dominant vitreoretinochoroidopathy",
  "200": "autosomal recessive axonal neuropathy with neuromyotonia",
  "201": "autosomal recessive cerebellar ataxia type 1",
  "202": "autosomal recessive congenital methemoglobinemia",
  "203": "autosomal recessive congenital stationary night blindness",
  "204": "autosomal recessive hyper ige syndrome",
  "205": "autosomal recessive hypotrichosis",
  "206": "autosomal recessive polycystic kidney disease",
  "207": "autosomal recessive primary microcephaly",
  "208": "autosomal recessive spastic ataxia of charlevoix saguenay",
  "209": "axenfeld rieger syndrome",
  "210": "axenfeld rieger syndrome type 1",
  "211": "back pain",
  "212": "balance problems",
  "213": "baller gerold syndrome",
  "214": "bannayan riley ruvalcaba syndrome",
  "215": "baraitser winter syndrome",
  "216": "bardet biedl syndrome",
  "217": "barrett esophagus",
  "218": "bart pumphrey syndrome",
  "219": "barth syndrome",
  "220": "bartter syndrome",
  "221": "basilar migraine",
  "222": "batten disease",
  "223": "beare stevenson cutis gyrata syndrome",
  "224": "beckwith wiedemann syndrome",
  "225": "behcet's disease",
  "226": "behet disease",
  "227": "behr syndrome",
  "228": "bell's palsy",
  "229": "benign chronic pemphigus",
  "230": "benign essential blepharospasm",
  "231": "benign familial neonatal seizures",
  "232": "benign recurrent intrahepatic cholestasis",
  "233": "benign rolandic epilepsy (bre)",
  "234": "benign schwannoma",
  "235": "best vitelliform macular dystrophy",
  "236": "beta ketothiolase deficiency",
  "237": "beta mannosidosis",
  "238": "beta thalassemia",
  "239": "beta ureidopropionase deficiency",
  "240": "bethlem myopathy",
  "241": "bietti crystalline dystrophy",
  "242": "bilateral perisylvian polymicrogyria",
  "243": "bile duct cancer (cholangiocarcinoma)",
  "244": "biliary atresia",
  "245": "binswanger's disease",
  "246": "biotin thiamine responsive basal ganglia disease",
  "247": "biotinidase deficiency",
  "248": "birt hogg dub syndrome",
  "249": "bjrnstad syndrome",
  "250": "bladder cancer",
  "251": "blau syndrome",
  "252": "blepharophimosis, ptosis, and epicanthus inversus syndrome",
  "253": "blepharophimosis, ptosis, and epicanthus inversus syndrome type 1",
  "254": "bloom syndrome",
  "255": "blue rubber bleb nevus syndrome",
  "256": "book syndrome",
  "257": "boomerang dysplasia",
  "258": "botulism",
  "259": "bowen conradi syndrome",
  "260": "brachial plexus injuries",
  "261": "bradyopsia",
  "262": "brain and spinal tumors",
  "263": "branchio oculo facial syndrome",
  "264": "branchiooculofacial syndrome",
  "265": "branchiootorenal syndrome",
  "266": "branchiootorenal/branchiootic syndrome",
  "267": "breast cancer",
  "268": "brittle diabetes",
  "269": "brody myopathy",
  "270": "broken heart syndrome",
  "271": "bronchiectasis",
  "272": "bronchiolitis obliterans organizing pneumonia",
  "273": "bronchitis",
  "274": "bronchopulmonary dysplasia",
  "275": "brooke spiegler syndrome",
  "276": "brown sequard syndrome",
  "277": "brugada syndrome",
  "278": "buerger disease",
  "279": "buschke ollendorff syndrome",
  "280": "c3 glomerulopathy",
  "281": "cadasil",
  "282": "caffey disease",
  "283": "campomelic dysplasia",
  "284": "camurati engelmann disease",
  "285": "canavan disease",
  "286": "cant syndrome",
  "287": "cap myopathy",
  "288": "capillary malformation arteriovenous malformation syndrome",
  "289": "carbamoyl phosphate synthetase i deficiency",
  "290": "cardiofaciocutaneous syndrome",
  "291": "cardiogenic shock",
  "292": "cardiomyopathy",
  "293": "carney complex",
  "294": "carnitine acylcarnitine translocase deficiency",
  "295": "carnitine palmitoyltransferase i deficiency",
  "296": "carnitine palmitoyltransferase ii deficiency",
  "297": "carotid artery disease",
  "298": "carpal tunnel syndrome",
  "299": "carpenter syndrome",
  "300": "cartilage hair hypoplasia",
  "301": "cask related intellectual disability",
  "302": "catamenial pneumothorax",
  "303": "cataract",
  "304": "catecholaminergic polymorphic ventricular tachycardia",
  "305": "catsper1 related nonsyndromic male infertility",
  "306": "caudal regression syndrome",
  "307": "causes of diabetes",
  "308": "cav3 related distal myopathy",
  "309": "cavernous malformation",
  "310": "celiac artery compression syndrome",
  "311": "celiac disease",
  "312": "central cord syndrome",
  "313": "central core disease",
  "314": "central pain syndrome",
  "315": "central pontine myelinolysis",
  "316": "centronuclear myopathy",
  "317": "cephalic disorders",
  "318": "cerebellar degeneration",
  "319": "cerebellar hypoplasia",
  "320": "cerebral aneurysms",
  "321": "cerebral arteriosclerosis",
  "322": "cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy",
  "323": "cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy",
  "324": "cerebral cavernous malformation",
  "325": "cerebral hypoxia",
  "326": "cerebral palsy",
  "327": "cerebro oculo facio skeletal syndrome (cofs)",
  "328": "cerebrotendinous xanthomatosis",
  "329": "chanarin dorfman syndrome",
  "330": "chandler's syndrome",
  "331": "chapare hemorrhagic fever (chhf)",
  "332": "char syndrome",
  "333": "charcot marie tooth disease",
  "334": "charcot marie tooth disease type 2f",
  "335": "charge syndrome",
  "336": "chediak higashi syndrome",
  "337": "cherubism",
  "338": "chiari malformation",
  "339": "chiari malformation type 1",
  "340": "chilaiditi syndrome",
  "341": "childhood acute lymphoblastic leukemia",
  "342": "childhood acute myeloid leukemia and other myeloid malignancies",
  "343": "childhood astrocytomas",
  "344": "childhood brain and spinal cord tumors",
  "345": "childhood brain stem glioma",
  "346": "childhood central nervous system atypical teratoid/rhabdoid tumor",
  "347": "childhood central nervous system embryonal tumors",
  "348": "childhood central nervous system germ cell tumors",
  "349": "childhood craniopharyngioma",
  "350": "childhood ependymoma",
  "351": "childhood extracranial germ cell tumors",
  "352": "childhood hodgkin lymphoma",
  "353": "childhood interstitial lung disease",
  "354": "childhood liver cancer",
  "355": "childhood myocerebrohepatopathy spectrum",
  "356": "childhood nephrotic syndrome",
  "357": "childhood non hodgkin lymphoma",
  "358": "childhood rhabdomyosarcoma",
  "359": "childhood soft tissue sarcoma",
  "360": "childhood vascular tumors",
  "361": "chmp2b related frontotemporal dementia",
  "362": "cholesteatoma",
  "363": "cholesteryl ester storage disease",
  "364": "chondrocalcinosis 2",
  "365": "chops syndrome",
  "366": "chordoma",
  "367": "chorea",
  "368": "chorea acanthocytosis",
  "369": "choroideremia",
  "370": "christianson syndrome",
  "371": "chromosome 3p syndrome",
  "372": "chromosome 4q deletion",
  "373": "chronic atrial and intestinal dysrhythmia",
  "374": "chronic diarrhea in children",
  "375": "chronic fatigue syndrome",
  "376": "chronic fatigue syndrome (cfs)",
  "377": "chronic granulomatous disease",
  "378": "chronic hiccups",
  "379": "chronic inflammatory demyelinating polyneuropathy",
  "380": "chronic inflammatory demyelinating polyneuropathy (cidp)",
  "381": "chronic lymphocytic leukemia",
  "382": "chronic myelogenous leukemia",
  "383": "chronic myelomonocytic leukemia",
  "384": "chronic myeloproliferative neoplasms",
  "385": "chronic pain",
  "386": "chronic progressive external ophthalmoplegia",
  "387": "chst3 related skeletal dysplasia",
  "388": "chylomicron retention disease",
  "389": "cirrhosis",
  "390": "citrullinemia",
  "391": "citrullinemia type i",
  "392": "cleidocranial dysplasia",
  "393": "clouston syndrome",
  "394": "coats disease",
  "395": "coats plus syndrome",
  "396": "coccygodynia",
  "397": "cockayne syndrome",
  "398": "coffin lowry syndrome",
  "399": "coffin siris syndrome",
  "400": "cog5 congenital disorder of glycosylation",
  "401": "cohen syndrome",
  "402": "col4a1 related brain small vessel disease",
  "403": "cold agglutinin disease",
  "404": "cold induced sweating syndrome",
  "405": "cold urticaria",
  "406": "cole disease",
  "407": "collagen vi related myopathy",
  "408": "coloboma",
  "409": "colon cancer",
  "410": "color vision deficiency",
  "411": "colorectal cancer",
  "412": "colpocephaly",
  "413": "coma",
  "414": "combined malonic and methylmalonic aciduria",
  "415": "combined pituitary hormone deficiency",
  "416": "common variable immune deficiency",
  "417": "common variable immunodeficiency",
  "418": "complement component 2 deficiency",
  "419": "complement factor i deficiency",
  "420": "complete lcat deficiency",
  "421": "complex regional pain syndrome",
  "422": "cone rod dystrophy",
  "423": "congenital adrenal hyperplasia",
  "424": "congenital adrenal hyperplasia due to 11 beta hydroxylase deficiency",
  "425": "congenital afibrinogenemia",
  "426": "congenital anosmia",
  "427": "congenital bilateral absence of the vas deferens",
  "428": "congenital cataracts, facial dysmorphism, and neuropathy",
  "429": "congenital central hypoventilation syndrome",
  "430": "congenital contractural arachnodactyly",
  "431": "congenital deafness with labyrinthine aplasia, microtia, and microdontia",
  "432": "congenital diaphragmatic hernia",
  "433": "congenital dyserythropoietic anemia",
  "434": "congenital fiber type disproportion",
  "435": "congenital fibrosis of the extraocular muscles",
  "436": "congenital generalized lipodystrophy",
  "437": "congenital heart defects",
  "438": "congenital hemidysplasia with ichthyosiform erythroderma and limb defects",
  "439": "congenital hepatic fibrosis",
  "440": "congenital hyperinsulinism",
  "441": "congenital hypothyroidism",
  "442": "congenital insensitivity to pain",
  "443": "congenital insensitivity to pain with anhidrosis",
  "444": "congenital laryngeal palsy",
  "445": "congenital leptin deficiency",
  "446": "congenital mirror movement disorder",
  "447": "congenital myasthenia",
  "448": "congenital myasthenic syndrome",
  "449": "congenital myopathy",
  "450": "congenital neuronal ceroid lipofuscinosis",
  "451": "congenital plasminogen deficiency",
  "452": "congenital radio ulnar synostosis",
  "453": "congenital stromal corneal dystrophy",
  "454": "congenital sucrase isomaltase deficiency",
  "455": "copd",
  "456": "core binding factor acute myeloid leukemia",
  "457": "cornelia de lange syndrome",
  "458": "coronary heart disease",
  "459": "coronary microvascular disease",
  "460": "corticobasal degeneration",
  "461": "corticosteroid binding globulin deficiency",
  "462": "costeff syndrome",
  "463": "costello syndrome",
  "464": "cough",
  "465": "cowden syndrome",
  "466": "cramp fasciculation syndrome",
  "467": "cranioectodermal dysplasia",
  "468": "craniofacial deafness hand syndrome",
  "469": "craniofacial microsomia",
  "470": "craniometaphyseal dysplasia",
  "471": "craniometaphyseal dysplasia, autosomal dominant",
  "472": "craniometaphyseal dysplasia, autosomal recessive type",
  "473": "craniopharyngioma",
  "474": "craniosynostosis",
  "475": "creating a family health history",
  "476": "crest syndrome",
  "477": "creutzfeldt jakob disease",
  "478": "cri du chat syndrome",
  "479": "crigler najjar syndrome",
  "480": "crimean congo hemorrhagic fever (cchf)",
  "481": "critical congenital heart disease",
  "482": "crohn disease",
  "483": "crohn's disease",
  "484": "crouzon syndrome",
  "485": "crouzonodermoskeletal syndrome",
  "486": "cryptogenic cirrhosis",
  "487": "cryptogenic organizing pneumonia",
  "488": "currarino triad",
  "489": "cushing disease",
  "490": "cushing's syndrome",
  "491": "cutaneous mastocytosis",
  "492": "cutis laxa",
  "493": "cyclic neutropenia",
  "494": "cyclic vomiting syndrome",
  "495": "cystic fibrosis",
  "496": "cystinosis",
  "497": "cystinuria",
  "498": "cystocele",
  "499": "cytochrome c oxidase deficiency",
  "500": "cytochrome p450 oxidoreductase deficiency",
  "501": "cytogenetically normal acute myeloid leukemia",
  "502": "czech dysplasia",
  "503": "d bifunctional protein deficiency",
  "504": "dandy walker malformation",
  "505": "dandy walker syndrome",
  "506": "danon disease",
  "507": "darier disease",
  "508": "deafness and myopia syndrome",
  "509": "deafness dystonia optic neuronopathy syndrome",
  "510": "deep brain stimulation for parkinson's disease",
  "511": "deep vein thrombosis",
  "512": "dementia",
  "513": "dementia with lewy bodies",
  "514": "dentatorubral pallidoluysian atrophy",
  "515": "dentinogenesis imperfecta",
  "516": "denys drash syndrome",
  "517": "deoxyguanosine kinase deficiency",
  "518": "depression",
  "519": "dermatitis herpetiformis: skin manifestation of celiac disease (for health care professionals)",
  "520": "dermatofibrosarcoma protuberans",
  "521": "dermatomyositis",
  "522": "desmoid tumor",
  "523": "desmoplastic infantile ganglioglioma",
  "524": "desmosterolosis",
  "525": "developmental dyspraxia",
  "526": "dextrocardia with situs inversus",
  "527": "diabetes",
  "528": "diabetes, heart disease, and stroke",
  "529": "diabetic heart disease",
  "530": "diabetic kidney disease",
  "531": "diabetic mastopathy",
  "532": "diabetic neuropathies: the nerve damage of diabetes",
  "533": "diabetic neuropathy",
  "534": "diabetic retinopathy",
  "535": "diagnosis of diabetes and prediabetes",
  "536": "diamond blackfan anemia",
  "537": "diarrhea",
  "538": "diastrophic dysplasia",
  "539": "dicer1 syndrome",
  "540": "diffuse gastric cancer",
  "541": "diffuse idiopathic skeletal hyperostosis",
  "542": "dihydrolipoamide dehydrogenase deficiency",
  "543": "dihydropyrimidinase deficiency",
  "544": "dihydropyrimidine dehydrogenase deficiency",
  "545": "dilated cardiomyopathy with ataxia syndrome",
  "546": "disseminated intravascular coagulation",
  "547": "disseminated peritoneal leiomyomatosis",
  "548": "distal arthrogryposis type 1",
  "549": "distal hereditary motor neuropathy, type ii",
  "550": "distal hereditary motor neuropathy, type v",
  "551": "distal myopathy 2",
  "552": "diverticular disease",
  "553": "dmd associated dilated cardiomyopathy",
  "554": "dolk congenital disorder of glycosylation",
  "555": "dominant dystrophic epidermolysis bullosa",
  "556": "donnai barrow syndrome",
  "557": "donohue syndrome",
  "558": "doors syndrome",
  "559": "dopa responsive dystonia",
  "560": "dopamine beta hydroxylase deficiency",
  "561": "dopamine transporter deficiency syndrome",
  "562": "dowling degos disease",
  "563": "down syndrome",
  "564": "doyne honeycomb retinal dystrophy",
  "565": "dravet syndrome",
  "566": "dry eye",
  "567": "dry mouth",
  "568": "duane radial ray syndrome",
  "569": "dubin johnson syndrome",
  "570": "duchenne and becker muscular dystrophy",
  "571": "duchenne muscular dystrophy",
  "572": "dumping syndrome",
  "573": "dyggve melchior clausen syndrome",
  "574": "dysautonomia",
  "575": "dyserythropoietic anemia and thrombocytopenia",
  "576": "dysgraphia",
  "577": "dyskeratosis congenita",
  "578": "dyslexia",
  "579": "dyssynergia cerebellaris myoclonica",
  "580": "dystonia 6",
  "581": "dystonias",
  "582": "dystrophic epidermolysis bullosa",
  "583": "early onset glaucoma",
  "584": "early onset primary dystonia",
  "585": "ectopic kidney",
  "586": "eec syndrome",
  "587": "ehlers danlos syndrome",
  "588": "ehlers danlos syndrome, dermatosparaxis type",
  "589": "ehlers danlos syndrome, kyphoscoliosis type",
  "590": "ehlers danlos syndrome, progeroid type",
  "591": "ehlers danlos syndrome, vascular type",
  "592": "eisenmenger syndrome",
  "593": "electrocardiogram",
  "594": "ellis van creveld syndrome",
  "595": "emanuel syndrome",
  "596": "emery dreifuss muscular dystrophy",
  "597": "empty sella syndrome",
  "598": "encephalitis lethargica",
  "599": "encephaloceles",
  "600": "encephalopathy",
  "601": "endocarditis",
  "602": "endometrial cancer",
  "603": "enlarged parietal foramina",
  "604": "eosinophil peroxidase deficiency",
  "605": "eosinophilic enteropathy",
  "606": "epidermal nevus",
  "607": "epidermolysis bullosa acquisita",
  "608": "epidermolysis bullosa simplex",
  "609": "epidermolysis bullosa with pyloric atresia",
  "610": "epidermolytic hyperkeratosis",
  "611": "epilepsy",
  "612": "episodic ataxia",
  "613": "erb duchenne and dejerine klumpke palsies",
  "614": "erdheim chester disease",
  "615": "erythrokeratodermia variabilis et progressiva",
  "616": "erythromelalgia",
  "617": "erythropoietic protoporphyria",
  "618": "esophageal atresia/tracheoesophageal fistula",
  "619": "essential pentosuria",
  "620": "essential thrombocythemia",
  "621": "essential tremor",
  "622": "esthesioneuroblastoma",
  "623": "ethylmalonic encephalopathy",
  "624": "ewing sarcoma",
  "625": "extragonadal germ cell tumors",
  "626": "fabry disease",
  "627": "facioscapulohumeral muscular dystrophy",
  "628": "factor v deficiency",
  "629": "factor v leiden thrombophilia",
  "630": "factor x deficiency",
  "631": "factor xiii deficiency",
  "632": "fahr's syndrome",
  "633": "familial acute myeloid leukemia with mutated cebpa",
  "634": "familial adenomatous polyposis",
  "635": "familial atrial fibrillation",
  "636": "familial cold autoinflammatory syndrome",
  "637": "familial cylindromatosis",
  "638": "familial dilated cardiomyopathy",
  "639": "familial dysautonomia",
  "640": "familial encephalopathy with neuroserpin inclusion bodies",
  "641": "familial erythrocytosis",
  "642": "familial exudative vitreoretinopathy",
  "643": "familial glucocorticoid deficiency",
  "644": "familial hdl deficiency",
  "645": "familial hemiplegic migraine",
  "646": "familial hemophagocytic lymphohistiocytosis",
  "647": "familial hyperaldosteronism",
  "648": "familial hypercholesterolemia",
  "649": "familial hypertrophic cardiomyopathy",
  "650": "familial hypobetalipoproteinemia",
  "651": "familial idiopathic basal ganglia calcification",
  "652": "familial isolated hyperparathyroidism",
  "653": "familial isolated pituitary adenoma",
  "654": "familial lipoprotein lipase deficiency",
  "655": "familial male limited precocious puberty",
  "656": "familial mediterranean fever",
  "657": "familial osteochondritis dissecans",
  "658": "familial paroxysmal kinesigenic dyskinesia",
  "659": "familial paroxysmal nonkinesigenic dyskinesia",
  "660": "familial periodic paralyses",
  "661": "familial pityriasis rubra pilaris",
  "662": "familial porencephaly",
  "663": "familial restrictive cardiomyopathy",
  "664": "familial thoracic aortic aneurysm and dissection",
  "665": "fanconi anemia",
  "666": "farber lipogranulomatosis",
  "667": "farber's disease",
  "668": "fatal familial insomnia",
  "669": "fatty acid hydroxylase associated neurodegeneration",
  "670": "febrile seizures",
  "671": "febrile ulceronecrotic mucha habermann disease",
  "672": "fecal incontinence",
  "673": "feingold syndrome",
  "674": "felty's syndrome",
  "675": "fg syndrome",
  "676": "fibrochondrogenesis",
  "677": "fibrodysplasia ossificans progressiva",
  "678": "fibrolamellar carcinoma",
  "679": "fibromuscular dysplasia",
  "680": "fibronectin glomerulopathy",
  "681": "fibrous dysplasia",
  "682": "financial help for diabetes care",
  "683": "fine lubinsky syndrome",
  "684": "fish eye disease",
  "685": "floating harbor syndrome",
  "686": "florid cemento osseous dysplasia",
  "687": "focal dermal hypoplasia",
  "688": "foodborne illnesses",
  "689": "foot drop",
  "690": "fowler's syndrome",
  "691": "foxg1 syndrome",
  "692": "fragile x associated primary ovarian insufficiency",
  "693": "fragile x associated tremor/ataxia syndrome",
  "694": "fragile x syndrome",
  "695": "fragile xe syndrome",
  "696": "fraser syndrome",
  "697": "frasier syndrome",
  "698": "freeman sheldon syndrome",
  "699": "freiberg's disease",
  "700": "friedreich ataxia",
  "701": "friedreich's ataxia",
  "702": "froelich syndrome",
  "703": "frontal fibrosing alopecia",
  "704": "frontometaphyseal dysplasia",
  "705": "frontonasal dysplasia",
  "706": "frontotemporal dementia",
  "707": "frontotemporal dementia with parkinsonism 17",
  "708": "fryns syndrome",
  "709": "fuchs endothelial dystrophy",
  "710": "fucosidosis",
  "711": "fukuyama congenital muscular dystrophy",
  "712": "fumarase deficiency",
  "713": "galactosemia",
  "714": "galactosialidosis",
  "715": "gallbladder cancer",
  "716": "galloway mowat syndrome",
  "717": "gallstones",
  "718": "gamma heavy chain disease",
  "719": "gardner diamond syndrome",
  "720": "gardner syndrome",
  "721": "gas in the digestive tract",
  "722": "gastritis",
  "723": "gastrointestinal carcinoid tumors",
  "724": "gastrointestinal stromal tumor",
  "725": "gastrointestinal stromal tumors",
  "726": "gastroparesis",
  "727": "gaucher disease",
  "728": "geleophysic dysplasia",
  "729": "generalized arterial calcification of infancy",
  "730": "generalized gangliosidoses",
  "731": "geniospasm",
  "732": "genitopatellar syndrome",
  "733": "geographic tongue",
  "734": "gerstmann straussler scheinker disease",
  "735": "gerstmann's syndrome",
  "736": "gestational trophoblastic disease",
  "737": "ghosal hematodiaphyseal dysplasia",
  "738": "giant axonal neuropathy",
  "739": "giant congenital melanocytic nevus",
  "740": "gilbert syndrome",
  "741": "gillespie syndrome",
  "742": "gitelman syndrome",
  "743": "glanzmann thrombasthenia",
  "744": "glass chapman hockley syndrome",
  "745": "glaucoma",
  "746": "glioblastoma",
  "747": "globozoospermia",
  "748": "glomerular diseases",
  "749": "glossopharyngeal neuralgia",
  "750": "glucose 6 phosphate dehydrogenase deficiency",
  "751": "glucose galactose malabsorption",
  "752": "glucose phosphate isomerase deficiency",
  "753": "glucose transporter type 1 deficiency syndrome",
  "754": "glut1 deficiency syndrome",
  "755": "glutamate formiminotransferase deficiency",
  "756": "glutaric acidemia type i",
  "757": "glutaric acidemia type ii",
  "758": "glutathione synthetase deficiency",
  "759": "glycine encephalopathy",
  "760": "glycogen storage disease type 0",
  "761": "glycogen storage disease type 13",
  "762": "glycogen storage disease type 4",
  "763": "glycogen storage disease type i",
  "764": "glycogen storage disease type iii",
  "765": "glycogen storage disease type iv",
  "766": "glycogen storage disease type ix",
  "767": "glycogen storage disease type v",
  "768": "glycogen storage disease type vi",
  "769": "glycogen storage disease type vii",
  "770": "gm1 gangliosidosis",
  "771": "gm2 gangliosidosis, ab variant",
  "772": "gm3 synthase deficiency",
  "773": "gnathodiaphyseal dysplasia",
  "774": "goodpasture syndrome",
  "775": "gorlin syndrome",
  "776": "gout",
  "777": "gracile syndrome",
  "778": "granuloma annulare",
  "779": "granulomatosis with polyangiitis",
  "780": "graves disease",
  "781": "graves' disease",
  "782": "gray platelet syndrome",
  "783": "greenberg dysplasia",
  "784": "greig cephalopolysyndactyly syndrome",
  "785": "griscelli syndrome",
  "786": "grn related frontotemporal dementia",
  "787": "growth failure in children with chronic kidney disease",
  "788": "guanidinoacetate methyltransferase deficiency",
  "789": "guillain barr syndrome",
  "790": "gum (periodontal) disease",
  "791": "gyrate atrophy of the choroid and retina",
  "792": "hailey hailey disease",
  "793": "hairy cell leukemia",
  "794": "hajdu cheney syndrome",
  "795": "hallermann streiff syndrome",
  "796": "hand foot genital syndrome",
  "797": "hanhart syndrome",
  "798": "hantavirus",
  "799": "harlequin ichthyosis",
  "800": "hashimoto thyroiditis",
  "801": "hashimoto's disease",
  "802": "hashimoto's encephalitis",
  "803": "hashimoto's syndrome",
  "804": "head and neck squamous cell carcinoma",
  "805": "headache",
  "806": "hearing loss",
  "807": "heart attack",
  "808": "heart block",
  "809": "heart disease in women",
  "810": "heart failure",
  "811": "heart murmur",
  "812": "heart palpitations",
  "813": "heart valve disease",
  "814": "hemangiopericytoma",
  "815": "hematuria (blood in the urine)",
  "816": "hemicrania continua",
  "817": "hemifacial microsomia",
  "818": "hemifacial spasm",
  "819": "hemochromatosis",
  "820": "hemoglobin e disease",
  "821": "hemolytic anemia",
  "822": "hemolytic uremic syndrome in children",
  "823": "hemophagocytic lymphohistiocytosis",
  "824": "hemophilia",
  "825": "hemorrhoids",
  "826": "hendra virus disease (hev)",
  "827": "hennekam syndrome",
  "828": "henoch schnlein purpura",
  "829": "henoch schonlein purpura",
  "830": "hepatic lipase deficiency",
  "831": "hepatic veno occlusive disease with immunodeficiency",
  "832": "hepatitis b: what asian and pacific islander americans need to know",
  "833": "hereditary angioedema",
  "834": "hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome",
  "835": "hereditary antithrombin deficiency",
  "836": "hereditary cerebral amyloid angiopathy",
  "837": "hereditary cerebral hemorrhage with amyloidosis",
  "838": "hereditary diffuse gastric cancer",
  "839": "hereditary diffuse leukoencephalopathy with spheroids",
  "840": "hereditary endotheliopathy, retinopathy, nephropathy, and stroke",
  "841": "hereditary folate malabsorption",
  "842": "hereditary fructose intolerance",
  "843": "hereditary hemochromatosis",
  "844": "hereditary hemorrhagic telangiectasia",
  "845": "hereditary hyperekplexia",
  "846": "hereditary hypophosphatemic rickets",
  "847": "hereditary leiomyomatosis and renal cell cancer",
  "848": "hereditary lymphedema type ii",
  "849": "hereditary multiple osteochondromas",
  "850": "hereditary myopathy with early respiratory failure",
  "851": "hereditary neuralgic amyotrophy",
  "852": "hereditary neuropathies",
  "853": "hereditary neuropathy with liability to pressure palsies",
  "854": "hereditary pancreatitis",
  "855": "hereditary paraganglioma pheochromocytoma",
  "856": "hereditary sensory and autonomic neuropathy type ie",
  "857": "hereditary sensory and autonomic neuropathy type ii",
  "858": "hereditary sensory and autonomic neuropathy type v",
  "859": "hereditary sensory neuropathy type 1",
  "860": "hereditary sensory neuropathy type ia",
  "861": "hereditary sensory neuropathy type ie",
  "862": "hereditary spastic paraplegia",
  "863": "hereditary spherocytosis",
  "864": "hereditary xanthinuria",
  "865": "hermansky pudlak syndrome",
  "866": "herpes zoster oticus",
  "867": "heterotaxy syndrome",
  "868": "hidradenitis suppurativa",
  "869": "high blood cholesterol",
  "870": "high blood pressure",
  "871": "high blood pressure and kidney disease",
  "872": "hirschsprung disease",
  "873": "hirschsprung's disease",
  "874": "histidinemia",
  "875": "histiocytosis lymphadenopathy plus syndrome",
  "876": "holes in the heart",
  "877": "holocarboxylase synthetase deficiency",
  "878": "holoprosencephaly",
  "879": "holt oram syndrome",
  "880": "homocystinuria",
  "881": "horizontal gaze palsy with progressive scoliosis",
  "882": "horner syndrome",
  "883": "human t cell leukemia virus type 1",
  "884": "human t cell leukemia virus type 2",
  "885": "huntington disease",
  "886": "huntington disease like syndrome",
  "887": "huntington's disease",
  "888": "hutchinson gilford progeria syndrome",
  "889": "hydranencephaly",
  "890": "hydrocephalus",
  "891": "hydrocephalus due to congenital stenosis of aqueduct of sylvius",
  "892": "hydromyelia",
  "893": "hydrops, ectopic calcification, moth eaten skeletal dysplasia",
  "894": "hyper igd syndrome",
  "895": "hypercholesterolemia",
  "896": "hyperferritinemia cataract syndrome",
  "897": "hyperkalemic periodic paralysis",
  "898": "hyperlysinemia",
  "899": "hypermanganesemia with dystonia, polycythemia, and cirrhosis",
  "900": "hypermethioninemia",
  "901": "hyperparathyroidism jaw tumor syndrome",
  "902": "hyperphosphatemic familial tumoral calcinosis",
  "903": "hyperprolinemia",
  "904": "hypersensitivity pneumonitis",
  "905": "hypersomnia",
  "906": "hyperthyroidism",
  "907": "hypertonia",
  "908": "hypochondrogenesis",
  "909": "hypochondroplasia",
  "910": "hypochromic microcytic anemia with iron overload",
  "911": "hypoglycemia",
  "912": "hypohidrotic ectodermal dysplasia",
  "913": "hypokalemic periodic paralysis",
  "914": "hypomagnesemia with secondary hypocalcemia",
  "915": "hypomyelination and congenital cataract",
  "916": "hypomyelination with atrophy of basal ganglia and cerebellum",
  "917": "hypopharyngeal cancer",
  "918": "hypophosphatasia",
  "919": "hypophosphatemic rickets",
  "920": "hypotension",
  "921": "hypothalamic dysfunction",
  "922": "hypothyroidism",
  "923": "hypotonia",
  "924": "hystrix like ichthyosis with deafness",
  "925": "i can lower my risk for type 2 diabetes: a guide for american indians",
  "926": "ibids syndrome",
  "927": "ichthyosis with confetti",
  "928": "idiopathic inflammatory myopathy",
  "929": "idiopathic juxtafoveal retinal telangiectasia",
  "930": "idiopathic pulmonary fibrosis",
  "931": "iga nephropathy",
  "932": "imerslund grsbeck syndrome",
  "933": "immune dysregulation, polyendocrinopathy, enteropathy, x linked syndrome",
  "934": "immune thrombocytopenia",
  "935": "immunodeficiency with hyper igm type 1",
  "936": "inclusion body myopathy 2",
  "937": "inclusion body myopathy with early onset paget disease and frontotemporal dementia",
  "938": "inclusion body myositis",
  "939": "incontinentia pigmenti",
  "940": "indigestion",
  "941": "infantile neuroaxonal dystrophy",
  "942": "infantile neuronal ceroid lipofuscinosis",
  "943": "infantile onset ascending hereditary spastic paralysis",
  "944": "infantile onset spinocerebellar ataxia",
  "945": "infantile refsum disease",
  "946": "infantile spasms",
  "947": "infantile systemic hyalinosis",
  "948": "inflammatory myopathies",
  "949": "inguinal hernia",
  "950": "inherited thyroxine binding globulin deficiency",
  "951": "iniencephaly",
  "952": "insomnia",
  "953": "insulin resistance and prediabetes",
  "954": "intestinal pseudo obstruction",
  "955": "intrahepatic cholestasis of pregnancy",
  "956": "intranuclear rod myopathy",
  "957": "intraocular (uveal) melanoma",
  "958": "intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies",
  "959": "irak 4 deficiency",
  "960": "iridocorneal endothelial syndrome",
  "961": "iron deficiency anemia",
  "962": "iron refractory iron deficiency anemia",
  "963": "irritable bowel syndrome in children",
  "964": "isaacs' syndrome",
  "965": "isobutyryl coa dehydrogenase deficiency",
  "966": "isodicentric chromosome 15 syndrome",
  "967": "isolated duane retraction syndrome",
  "968": "isolated ectopia lentis",
  "969": "isolated growth hormone deficiency",
  "970": "isolated lissencephaly sequence",
  "971": "isolated pierre robin sequence",
  "972": "isovaleric acidemia",
  "973": "jackson weiss syndrome",
  "974": "jacobsen syndrome",
  "975": "jejunal atresia",
  "976": "jervell and lange nielsen syndrome",
  "977": "jones syndrome",
  "978": "joubert syndrome",
  "979": "junctional epidermolysis bullosa",
  "980": "juvenile amyotrophic lateral sclerosis",
  "981": "juvenile batten disease",
  "982": "juvenile huntington disease",
  "983": "juvenile hyaline fibromatosis",
  "984": "juvenile idiopathic arthritis",
  "985": "juvenile myelomonocytic leukemia",
  "986": "juvenile myoclonic epilepsy",
  "987": "juvenile paget disease",
  "988": "juvenile polyposis syndrome",
  "989": "juvenile primary lateral sclerosis",
  "990": "juvenile primary osteoporosis",
  "991": "juvenile retinoschisis",
  "992": "kabuki syndrome",
  "993": "kallmann syndrome",
  "994": "kaposi sarcoma",
  "995": "kawasaki disease",
  "996": "kawasaki syndrome",
  "997": "kbg syndrome",
  "998": "kearns sayre syndrome",
  "999": "kennedy's disease",
  "1000": "keratitis ichthyosis deafness syndrome",
  "1001": "keratoderma with woolly hair",
  "1002": "kidney disease",
  "1003": "kidney disease of diabetes",
  "1004": "kidney dysplasia",
  "1005": "kidney failure: choosing a treatment that's right for you",
  "1006": "kidney failure: eat right to feel right on hemodialysis",
  "1007": "kidney stones in adults",
  "1008": "kidney stones in children",
  "1009": "kienbock's disease",
  "1010": "klebsiella infection",
  "1011": "kleefstra syndrome",
  "1012": "kleine levin syndrome",
  "1013": "klinefelter syndrome",
  "1014": "klippel feil syndrome",
  "1015": "klippel trenaunay syndrome",
  "1016": "klippel trenaunay syndrome (kts)",
  "1017": "klver bucy syndrome",
  "1018": "knee replacement",
  "1019": "kniest dysplasia",
  "1020": "knobloch syndrome",
  "1021": "konigsmark knox hussels syndrome",
  "1022": "koolen de vries syndrome",
  "1023": "krabbe disease",
  "1024": "kufs disease",
  "1025": "kuru",
  "1026": "kuskokwim syndrome",
  "1027": "kyasanur forest disease (kfd)",
  "1028": "kyrle disease",
  "1029": "l1 syndrome",
  "1030": "la crosse encephalitis",
  "1031": "lacrimo auriculo dento digital syndrome",
  "1032": "lactate dehydrogenase deficiency",
  "1033": "lactose intolerance",
  "1034": "lafora disease",
  "1035": "lafora progressive myoclonus epilepsy",
  "1036": "laing distal myopathy",
  "1037": "lama2 related muscular dystrophy",
  "1038": "lambert eaton myasthenic syndrome",
  "1039": "lamellar ichthyosis",
  "1040": "landau kleffner syndrome",
  "1041": "langer giedion syndrome",
  "1042": "langer mesomelic dysplasia",
  "1043": "langerhans cell histiocytosis",
  "1044": "laron syndrome",
  "1045": "larsen syndrome",
  "1046": "laryngeal cancer",
  "1047": "laryngeal cleft",
  "1048": "laryngo onycho cutaneous syndrome",
  "1049": "late infantile neuronal ceroid lipofuscinosis",
  "1050": "lattice corneal dystrophy type i",
  "1051": "lattice corneal dystrophy type ii",
  "1052": "learning disabilities",
  "1053": "leber congenital amaurosis",
  "1054": "leber hereditary optic neuropathy",
  "1055": "legg calv perthes disease",
  "1056": "legius syndrome",
  "1057": "leigh syndrome",
  "1058": "leigh's disease",
  "1059": "lemierre syndrome",
  "1060": "lennox gastaut syndrome",
  "1061": "lenz microphthalmia syndrome",
  "1062": "leptin receptor deficiency",
  "1063": "lesch nyhan syndrome",
  "1064": "leukemia",
  "1065": "leukocyte adhesion deficiency type 1",
  "1066": "leukodystrophy",
  "1067": "leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation",
  "1068": "leukoencephalopathy with vanishing white matter",
  "1069": "leukonychia totalis",
  "1070": "leydig cell hypoplasia",
  "1071": "li fraumeni syndrome",
  "1072": "lichen planus pigmentosus",
  "1073": "lichen sclerosus",
  "1074": "liddle syndrome",
  "1075": "limb girdle muscular dystrophy",
  "1076": "limbic encephalitis",
  "1077": "lip and oral cavity cancer",
  "1078": "lipedema",
  "1079": "lipodermatosclerosis",
  "1080": "lipoid proteinosis",
  "1081": "lissencephaly",
  "1082": "lissencephaly with cerebellar hypoplasia",
  "1083": "liver (hepatocellular) cancer",
  "1084": "localized scleroderma",
  "1085": "locked in syndrome",
  "1086": "loeys dietz syndrome",
  "1087": "loin pain hematuria syndrome",
  "1088": "long chain 3 hydroxyacyl coa dehydrogenase deficiency",
  "1089": "long qt syndrome",
  "1090": "low vision",
  "1091": "lowe syndrome",
  "1092": "lujan syndrome",
  "1093": "lujo hemorrhagic fever (luhf)",
  "1094": "lung cancer",
  "1095": "lupus",
  "1096": "lupus nephritis",
  "1097": "lymphangioleiomyomatosis",
  "1098": "lymphedema distichiasis syndrome",
  "1099": "lymphocytic choriomeningitis (lcm)",
  "1100": "lymphomatoid papulosis",
  "1101": "lynch syndrome",
  "1102": "lysinuric protein intolerance",
  "1103": "mabry syndrome",
  "1104": "machado joseph disease",
  "1105": "madelung disease",
  "1106": "maffucci syndrome",
  "1107": "mainzer saldino syndrome",
  "1108": "majeed syndrome",
  "1109": "mal de meleda",
  "1110": "male breast cancer",
  "1111": "malignant hyperthermia",
  "1112": "malignant migrating partial seizures of infancy",
  "1113": "malonyl coa decarboxylase deficiency",
  "1114": "mandibuloacral dysplasia",
  "1115": "mandibulofacial dysostosis with microcephaly",
  "1116": "manitoba oculotrichoanal syndrome",
  "1117": "mannose binding lectin deficiency",
  "1118": "mantle cell lymphoma",
  "1119": "maple syrup urine disease",
  "1120": "marburg hemorrhagic fever (marburg hf)",
  "1121": "marden walker syndrome",
  "1122": "marfan syndrome",
  "1123": "marine toxins",
  "1124": "marinesco sjgren syndrome",
  "1125": "mastocytic enterocolitis",
  "1126": "maternally inherited diabetes and deafness",
  "1127": "mayer rokitansky kster hauser syndrome",
  "1128": "mccune albright syndrome",
  "1129": "mckusick kaufman syndrome",
  "1130": "mcleod neuroacanthocytosis syndrome",
  "1131": "meckel syndrome",
  "1132": "mecp2 duplication syndrome",
  "1133": "mecp2 related severe neonatal encephalopathy",
  "1134": "medicare and continuing care",
  "1135": "medium chain acyl coa dehydrogenase deficiency",
  "1136": "medium chain acyl coenzyme a dehydrogenase deficiency",
  "1137": "medullary cystic kidney disease",
  "1138": "medullary cystic kidney disease type 1",
  "1139": "medullary sponge kidney",
  "1140": "meesmann corneal dystrophy",
  "1141": "megalencephalic leukoencephalopathy with subcortical cysts",
  "1142": "megalencephaly",
  "1143": "megalencephaly capillary malformation syndrome",
  "1144": "megdel syndrome",
  "1145": "meier gorlin syndrome",
  "1146": "meige disease",
  "1147": "melanoma",
  "1148": "melkersson rosenthal syndrome",
  "1149": "melnick needles syndrome",
  "1150": "menetrier disease",
  "1151": "meningitis and encephalitis",
  "1152": "menkes disease",
  "1153": "menkes syndrome",
  "1154": "meralgia paresthetica",
  "1155": "merkel cell carcinoma",
  "1156": "metabolic syndrome",
  "1157": "metachromatic leukodystrophy",
  "1158": "metastatic squamous neck cancer with occult primary",
  "1159": "metatropic dysplasia",
  "1160": "methemoglobinemia, beta globin type",
  "1161": "methylmalonic acidemia",
  "1162": "methylmalonic acidemia with homocystinuria",
  "1163": "mevalonate kinase deficiency",
  "1164": "microcephalic osteodysplastic primordial dwarfism type 1",
  "1165": "microcephalic osteodysplastic primordial dwarfism type ii",
  "1166": "microcephaly",
  "1167": "microcephaly capillary malformation syndrome",
  "1168": "microhydranencephaly",
  "1169": "microphthalmia",
  "1170": "microphthalmia with linear skin defects syndrome",
  "1171": "microscopic colitis: collagenous colitis and lymphocytic colitis",
  "1172": "microscopic polyangiitis",
  "1173": "microvillus inclusion disease",
  "1174": "migraine",
  "1175": "miller dieker syndrome",
  "1176": "miller fisher syndrome",
  "1177": "miller syndrome",
  "1178": "milroy disease",
  "1179": "mineral and bone disorder in chronic kidney disease",
  "1180": "mitochondrial complex ii deficiency",
  "1181": "mitochondrial complex iii deficiency",
  "1182": "mitochondrial encephalomyopathy lactic acidosis and stroke like episodes",
  "1183": "mitochondrial encephalomyopathy, lactic acidosis, and stroke like episodes",
  "1184": "mitochondrial genetic disorders",
  "1185": "mitochondrial membrane protein associated neurodegeneration",
  "1186": "mitochondrial myopathy",
  "1187": "mitochondrial neurogastrointestinal encephalopathy disease",
  "1188": "mitochondrial neurogastrointestinal encephalopathy syndrome",
  "1189": "mitochondrial trifunctional protein deficiency",
  "1190": "mitral valve prolapse",
  "1191": "mixed connective tissue disease",
  "1192": "miyoshi myopathy",
  "1193": "mnire's disease",
  "1194": "mntriers disease",
  "1195": "moebius syndrome",
  "1196": "molybdenum cofactor deficiency",
  "1197": "mondini dysplasia",
  "1198": "monilethrix",
  "1199": "monogenic forms of diabetes: neonatal diabetes mellitus and maturity onset diabetes of the young",
  "1200": "monomelic amyotrophy",
  "1201": "mosaic trisomy 14",
  "1202": "mosaic trisomy 9",
  "1203": "motor neuron diseases",
  "1204": "mowat wilson syndrome",
  "1205": "moyamoya disease",
  "1206": "mpv17 related hepatocerebral mitochondrial dna depletion syndrome",
  "1207": "mthfr gene mutation",
  "1208": "muckle wells syndrome",
  "1209": "mucolipidoses",
  "1210": "mucolipidosis ii alpha/beta",
  "1211": "mucolipidosis iii alpha/beta",
  "1212": "mucolipidosis iii gamma",
  "1213": "mucolipidosis type iv",
  "1214": "mucopolysaccharidoses",
  "1215": "mucopolysaccharidosis type i",
  "1216": "mucopolysaccharidosis type ii",
  "1217": "mucopolysaccharidosis type iii",
  "1218": "mucopolysaccharidosis type iv",
  "1219": "mucopolysaccharidosis type vi",
  "1220": "mucopolysaccharidosis type vii",
  "1221": "muenke syndrome",
  "1222": "muir torre syndrome",
  "1223": "multi infarct dementia",
  "1224": "multicentric castleman disease",
  "1225": "multicentric osteolysis, nodulosis, and arthropathy",
  "1226": "multifocal choroiditis",
  "1227": "multifocal motor neuropathy",
  "1228": "multiminicore disease",
  "1229": "multiple cutaneous and mucosal venous malformations",
  "1230": "multiple endocrine neoplasia",
  "1231": "multiple endocrine neoplasia type 1",
  "1232": "multiple epiphyseal dysplasia",
  "1233": "multiple familial trichoepithelioma",
  "1234": "multiple lentigines syndrome",
  "1235": "multiple mitochondrial dysfunctions syndrome",
  "1236": "multiple myeloma",
  "1237": "multiple pterygium syndrome",
  "1238": "multiple pterygium syndrome escobar type",
  "1239": "multiple sclerosis",
  "1240": "multiple sulfatase deficiency",
  "1241": "multiple system atrophy",
  "1242": "multiple system atrophy with orthostatic hypotension",
  "1243": "muscular dystrophy",
  "1244": "myasthenia gravis",
  "1245": "mycosis fungoides",
  "1246": "mycosis fungoides and the szary syndrome",
  "1247": "myd88 deficiency",
  "1248": "myelodysplastic syndromes",
  "1249": "myelodysplastic/ myeloproliferative neoplasms",
  "1250": "myh7 related scapuloperoneal myopathy",
  "1251": "myh9 related disorder",
  "1252": "myhre syndrome",
  "1253": "myoclonic epilepsy myopathy sensory ataxia",
  "1254": "myoclonic epilepsy with ragged red fibers",
  "1255": "myoclonus",
  "1256": "myoclonus dystonia",
  "1257": "myofibrillar myopathy",
  "1258": "myopathy",
  "1259": "myopathy with deficiency of iron sulfur cluster assembly enzyme",
  "1260": "myosin storage myopathy",
  "1261": "myostatin related muscle hypertrophy",
  "1262": "myotonia",
  "1263": "myotonia congenita",
  "1264": "myotonic dystrophy",
  "1265": "myotonic dystrophy type 1",
  "1266": "n acetylglutamate synthase deficiency",
  "1267": "naegeli franceschetti jadassohn syndrome/dermatopathia pigmentosa reticularis",
  "1268": "naegeli syndrome",
  "1269": "nager syndrome",
  "1270": "nail patella syndrome",
  "1271": "nakajo nishimura syndrome",
  "1272": "nan",
  "1273": "nance horan syndrome",
  "1274": "narcolepsy",
  "1275": "nasopharyngeal cancer",
  "1276": "national hormone and pituitary program (nhpp): information for people treated with pituitary human growth hormone (comprehensive report)",
  "1277": "necrotizing fasciitis",
  "1278": "nemaline myopathy",
  "1279": "neonatal onset multisystem inflammatory disease",
  "1280": "neonatal progeroid syndrome",
  "1281": "nephrocalcinosis",
  "1282": "nephrogenic diabetes insipidus",
  "1283": "nephronophthisis",
  "1284": "nephrotic syndrome in adults",
  "1285": "nerve disease and bladder control",
  "1286": "netherton syndrome",
  "1287": "neuroacanthocytosis",
  "1288": "neuroaxonal dystrophy",
  "1289": "neuroblastoma",
  "1290": "neurodegeneration with brain iron accumulation",
  "1291": "neuroferritinopathy",
  "1292": "neurofibromatosis",
  "1293": "neurofibromatosis type 1",
  "1294": "neurofibromatosis type 2",
  "1295": "neurohypophyseal diabetes insipidus",
  "1296": "neuroleptic malignant syndrome",
  "1297": "neurological complications of aids",
  "1298": "neurological consequences of cytomegalovirus infection",
  "1299": "neurological sequelae of lupus",
  "1300": "neuromyelitis optica",
  "1301": "neuronal migration disorders",
  "1302": "neuropathy, ataxia, and retinitis pigmentosa",
  "1303": "neurosarcoidosis",
  "1304": "neurosyphilis",
  "1305": "neurotoxicity",
  "1306": "neutral lipid storage disease with myopathy",
  "1307": "nevoid basal cell carcinoma syndrome",
  "1308": "nicolaides baraitser syndrome",
  "1309": "niemann pick disease",
  "1310": "nijmegen breakage syndrome",
  "1311": "nocardiosis",
  "1312": "non classic congenital adrenal hyperplasia due to 21 hydroxylase deficiency",
  "1313": "non small cell lung cancer",
  "1314": "nonalcoholic steatohepatitis",
  "1315": "nonbullous congenital ichthyosiform erythroderma",
  "1316": "nonspherocytic hemolytic anemia due to hexokinase deficiency",
  "1317": "nonsyndromic aplasia cutis congenita",
  "1318": "nonsyndromic hearing loss",
  "1319": "nonsyndromic holoprosencephaly",
  "1320": "nonsyndromic paraganglioma",
  "1321": "noonan syndrome",
  "1322": "normal pressure hydrocephalus",
  "1323": "norrie disease",
  "1324": "north american indian childhood cirrhosis",
  "1325": "northern epilepsy",
  "1326": "norum disease",
  "1327": "nutrition for advanced chronic kidney disease in adults",
  "1328": "nutrition for early chronic kidney disease in adults",
  "1329": "obesity hypoventilation syndrome",
  "1330": "occipital neuralgia",
  "1331": "ochoa syndrome",
  "1332": "ocular albinism",
  "1333": "oculocutaneous albinism",
  "1334": "oculodentodigital dysplasia",
  "1335": "oculofaciocardiodental syndrome",
  "1336": "oculopharyngeal muscular dystrophy",
  "1337": "ohdo syndrome, maat kievit brunner type",
  "1338": "ohdo syndrome, say barber biesecker young simpson variant",
  "1339": "ohtahara syndrome",
  "1340": "olivopontocerebellar atrophy",
  "1341": "ollier disease",
  "1342": "omenn syndrome",
  "1343": "omsk hemorrhagic fever (ohf)",
  "1344": "ophthalmo acromelic syndrome",
  "1345": "opitz g/bbb syndrome",
  "1346": "opsoclonus myoclonus",
  "1347": "optic atrophy type 1",
  "1348": "oral cavity and oropharyngeal cancer",
  "1349": "oral facial digital syndrome",
  "1350": "ornithine transcarbamylase deficiency",
  "1351": "ornithine translocase deficiency",
  "1352": "orofaciodigital syndrome 2",
  "1353": "oropharyngeal cancer",
  "1354": "orthostatic hypotension",
  "1355": "osteoarthritis",
  "1356": "osteochondritis dissecans",
  "1357": "osteogenesis imperfecta",
  "1358": "osteogenesis imperfecta type vi",
  "1359": "osteoglophonic dysplasia",
  "1360": "osteopetrosis",
  "1361": "osteoporosis",
  "1362": "osteoporosis pseudoglioma syndrome",
  "1363": "osteosarcoma and malignant fibrous histiocytoma of bone",
  "1364": "otopalatodigital syndrome type 1",
  "1365": "otopalatodigital syndrome type 2",
  "1366": "otospondylomegaepiphyseal dysplasia",
  "1367": "ovarian cancer",
  "1368": "ovarian epithelial, fallopian tube, and primary peritoneal cancer",
  "1369": "ovarian germ cell tumors",
  "1370": "ovarian low malignant potential tumors",
  "1371": "ovarian, fallopian tube, and primary peritoneal cancer",
  "1372": "overview of kidney disease in children",
  "1373": "overweight and obesity",
  "1374": "oxygen therapy",
  "1375": "pachygyria",
  "1376": "pachyonychia congenita",
  "1377": "paget disease of bone",
  "1378": "paget's disease of bone",
  "1379": "pallister hall syndrome",
  "1380": "pallister killian mosaic syndrome",
  "1381": "palmoplantar keratoderma with deafness",
  "1382": "pancreatic cancer",
  "1383": "pancreatic neuroendocrine tumors (islet cell tumors)",
  "1384": "pantothenate kinase associated neurodegeneration",
  "1385": "paramyotonia congenita",
  "1386": "paranasal sinus and nasal cavity cancer",
  "1387": "paraneoplastic syndromes",
  "1388": "parasites african trypanosomiasis (also known as sleeping sickness)",
  "1389": "parasites american trypanosomiasis (also known as chagas disease)",
  "1390": "parasites angiostrongyliasis (also known as angiostrongylus infection)",
  "1391": "parasites ascariasis",
  "1392": "parasites babesiosis",
  "1393": "parasites baylisascaris infection",
  "1394": "parasites cyclosporiasis (cyclospora infection)",
  "1395": "parasites cysticercosis",
  "1396": "parasites echinococcosis",
  "1397": "parasites enterobiasis (also known as pinworm infection)",
  "1398": "parasites fascioliasis (fasciola infection)",
  "1399": "parasites hookworm",
  "1400": "parasites leishmaniasis",
  "1401": "parasites lice body lice",
  "1402": "parasites lice head lice",
  "1403": "parasites lice pubic \"crab\" lice",
  "1404": "parasites loiasis",
  "1405": "parasites lymphatic filariasis",
  "1406": "parasites paragonimiasis (also known as paragonimus infection)",
  "1407": "parasites scabies",
  "1408": "parasites schistosomiasis",
  "1409": "parasites taeniasis",
  "1410": "parasites toxocariasis (also known as roundworm infection)",
  "1411": "parasites toxoplasmosis (toxoplasma infection)",
  "1412": "parasites trichinellosis (also known as trichinosis)",
  "1413": "parasites trichuriasis (also known as whipworm infection)",
  "1414": "parasites zoonotic hookworm",
  "1415": "parathyroid cancer",
  "1416": "paresthesia",
  "1417": "parkes weber syndrome",
  "1418": "parkinson disease",
  "1419": "parkinson's disease",
  "1420": "paroxysmal choreoathetosis",
  "1421": "paroxysmal extreme pain disorder",
  "1422": "paroxysmal hemicrania",
  "1423": "paroxysmal nocturnal hemoglobinuria",
  "1424": "parry romberg",
  "1425": "pars planitis",
  "1426": "parsonage turner syndrome",
  "1427": "partington syndrome",
  "1428": "patent ductus arteriosus",
  "1429": "pdgfra associated chronic eosinophilic leukemia",
  "1430": "pdgfrb associated chronic eosinophilic leukemia",
  "1431": "pearson marrow pancreas syndrome",
  "1432": "pelizaeus merzbacher disease",
  "1433": "pendred syndrome",
  "1434": "penile cancer",
  "1435": "pericarditis",
  "1436": "perineal injury in males",
  "1437": "periodic fever, aphthous stomatitis, pharyngitis and adenitis",
  "1438": "peripheral arterial disease (p.a.d.)",
  "1439": "peripheral artery disease",
  "1440": "peripheral neuropathy",
  "1441": "periventricular heterotopia",
  "1442": "periventricular leukomalacia",
  "1443": "permanent neonatal diabetes mellitus",
  "1444": "pernicious anemia",
  "1445": "peroxisomal acyl coa oxidase deficiency",
  "1446": "perrault syndrome",
  "1447": "perry syndrome",
  "1448": "persistent mllerian duct syndrome",
  "1449": "pervasive developmental disorders",
  "1450": "peters plus syndrome",
  "1451": "peutz jeghers syndrome",
  "1452": "peyronie's disease",
  "1453": "pfeiffer syndrome",
  "1454": "phacomatosis pigmentovascularis",
  "1455": "phenylketonuria",
  "1456": "phosphoglycerate dehydrogenase deficiency",
  "1457": "phosphoglycerate kinase deficiency",
  "1458": "phosphoglycerate mutase deficiency",
  "1459": "phosphoribosylpyrophosphate synthetase superactivity",
  "1460": "piebaldism",
  "1461": "pierson syndrome",
  "1462": "pigmented purpuric eruption",
  "1463": "pigmented villonodular synovitis",
  "1464": "pilocytic astrocytoma",
  "1465": "pilomatricoma",
  "1466": "pilomatrixoma",
  "1467": "pinched nerve",
  "1468": "pineal cyst",
  "1469": "piriformis syndrome",
  "1470": "pitt hopkins syndrome",
  "1471": "pituitary tumors",
  "1472": "pityriasis lichenoides chronica",
  "1473": "pityriasis lichenoides et varioliformis acuta",
  "1474": "pityriasis rubra pilaris",
  "1475": "plasma cell neoplasms (including multiple myeloma)",
  "1476": "platelet storage pool deficiency",
  "1477": "platyspondylic lethal skeletal dysplasia, torrance type",
  "1478": "pleurisy and other pleural disorders",
  "1479": "pmm2 congenital disorder of glycosylation",
  "1480": "pneumonia",
  "1481": "pol iii related leukodystrophy",
  "1482": "poland syndrome",
  "1483": "polycystic kidney disease",
  "1484": "polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy",
  "1485": "polycythemia vera",
  "1486": "polymicrogyria",
  "1487": "polymyositis",
  "1488": "pompe disease",
  "1489": "pontocerebellar hypoplasia",
  "1490": "pontocerebellar hypoplasia type 1",
  "1491": "popliteal pterygium syndrome",
  "1492": "porencephaly",
  "1493": "porphyria",
  "1494": "post polio syndrome",
  "1495": "postural orthostatic tachycardia syndrome",
  "1496": "postural tachycardia syndrome",
  "1497": "potassium aggravated myotonia",
  "1498": "potocki shaffer syndrome",
  "1499": "ppm x syndrome",
  "1500": "prader willi syndrome",
  "1501": "preeclampsia",
  "1502": "pregnancy and thyroid disease",
  "1503": "prekallikrein deficiency",
  "1504": "prescription and illicit drug abuse",
  "1505": "prevent diabetes problems: keep your diabetes under control",
  "1506": "prevent diabetes problems: keep your heart and blood vessels healthy",
  "1507": "prevent diabetes problems: keep your kidneys healthy",
  "1508": "prevent diabetes problems: keep your nervous system healthy",
  "1509": "prickle1 related progressive myoclonus epilepsy with ataxia",
  "1510": "primary biliary cirrhosis",
  "1511": "primary carnitine deficiency",
  "1512": "primary ciliary dyskinesia",
  "1513": "primary cns lymphoma",
  "1514": "primary familial brain calcification",
  "1515": "primary gastrointestinal melanoma",
  "1516": "primary hyperoxaluria",
  "1517": "primary hyperoxaluria type 2",
  "1518": "primary hyperparathyroidism",
  "1519": "primary lateral sclerosis",
  "1520": "primary macronodular adrenal hyperplasia",
  "1521": "primary myelofibrosis",
  "1522": "primary sclerosing cholangitis",
  "1523": "primary spontaneous pneumothorax",
  "1524": "prinzmetal's variant angina",
  "1525": "prion disease",
  "1526": "problems with smell",
  "1527": "problems with taste",
  "1528": "proctitis",
  "1529": "progeria",
  "1530": "progressive deafness with stapes fixation",
  "1531": "progressive external ophthalmoplegia",
  "1532": "progressive familial heart block",
  "1533": "progressive familial intrahepatic cholestasis",
  "1534": "progressive multifocal leukoencephalopathy",
  "1535": "progressive osseous heteroplasia",
  "1536": "progressive pseudorheumatoid dysplasia",
  "1537": "progressive supranuclear palsy",
  "1538": "prolactinoma",
  "1539": "prolidase deficiency",
  "1540": "proopiomelanocortin deficiency",
  "1541": "propionic acidemia",
  "1542": "prosopagnosia",
  "1543": "prostate cancer",
  "1544": "prostate enlargement: benign prostatic hyperplasia",
  "1545": "protein c deficiency",
  "1546": "protein s deficiency",
  "1547": "proteinuria",
  "1548": "proteus syndrome",
  "1549": "prothrombin deficiency",
  "1550": "prothrombin thrombophilia",
  "1551": "proud syndrome",
  "1552": "prune belly syndrome",
  "1553": "pseudoachondroplasia",
  "1554": "pseudocholinesterase deficiency",
  "1555": "pseudohypoaldosteronism type 1",
  "1556": "pseudohypoaldosteronism type 2",
  "1557": "pseudotumor cerebri",
  "1558": "pseudoxanthoma elasticum",
  "1559": "psoriasis",
  "1560": "psoriatic arthritis",
  "1561": "pulmonary alveolar microlithiasis",
  "1562": "pulmonary arterial hypertension",
  "1563": "pulmonary embolism",
  "1564": "pulmonary hypertension",
  "1565": "pulmonary veno occlusive disease",
  "1566": "punctate palmoplantar keratoderma type i",
  "1567": "purine nucleoside phosphorylase deficiency",
  "1568": "pyelonephritis: kidney infection",
  "1569": "pyridoxal 5' phosphate dependent epilepsy",
  "1570": "pyridoxine dependent epilepsy",
  "1571": "pyruvate carboxylase deficiency",
  "1572": "pyruvate dehydrogenase deficiency",
  "1573": "pyruvate kinase deficiency",
  "1574": "q fever",
  "1575": "quitting smoking for older adults",
  "1576": "rabies",
  "1577": "rabson mendenhall syndrome",
  "1578": "rapadilino syndrome",
  "1579": "rapid onset dystonia parkinsonism",
  "1580": "rasmussen's encephalitis",
  "1581": "recombinant 8 syndrome",
  "1582": "rectal cancer",
  "1583": "recurrent hydatidiform mole",
  "1584": "refsum disease",
  "1585": "relapsing polychondritis",
  "1586": "ren related kidney disease",
  "1587": "renal artery stenosis",
  "1588": "renal cell cancer",
  "1589": "renal coloboma syndrome",
  "1590": "renal hypouricemia",
  "1591": "renal nutcracker syndrome",
  "1592": "renal oncocytoma",
  "1593": "renal tubular acidosis",
  "1594": "renal tubular acidosis with deafness",
  "1595": "renal tubular dysgenesis",
  "1596": "renpenning syndrome",
  "1597": "repetitive motion disorders",
  "1598": "respiratory distress syndrome",
  "1599": "respiratory failure",
  "1600": "restless legs syndrome",
  "1601": "reticulohistiocytoma",
  "1602": "retinal arterial macroaneurysm with supravalvular pulmonic stenosis",
  "1603": "retinitis pigmentosa",
  "1604": "retinoblastoma",
  "1605": "retroperitoneal fibrosis",
  "1606": "rett syndrome",
  "1607": "reye's syndrome",
  "1608": "rh incompatibility",
  "1609": "rheumatic fever",
  "1610": "rheumatoid arthritis",
  "1611": "rhizomelic chondrodysplasia punctata",
  "1612": "rickets",
  "1613": "ring chromosome 14 syndrome",
  "1614": "ring chromosome 20 syndrome",
  "1615": "rippling muscle disease",
  "1616": "roberts syndrome",
  "1617": "robinow syndrome",
  "1618": "romano ward syndrome",
  "1619": "rothmund thomson syndrome",
  "1620": "rotor syndrome",
  "1621": "rubinstein taybi syndrome",
  "1622": "russell silver syndrome",
  "1623": "saddan",
  "1624": "saethre chotzen syndrome",
  "1625": "salih myopathy",
  "1626": "salivary gland cancer",
  "1627": "sandhoff disease",
  "1628": "sarcoidosis",
  "1629": "schilder's disease",
  "1630": "schimke immuno osseous dysplasia",
  "1631": "schimke immunoosseous dysplasia",
  "1632": "schindler disease",
  "1633": "schindler disease type 1",
  "1634": "schinzel giedion syndrome",
  "1635": "schizencephaly",
  "1636": "schnitzler syndrome",
  "1637": "schwannomatosis",
  "1638": "schwartz jampel syndrome",
  "1639": "schwartz jampel syndrome type 1",
  "1640": "scleroderma",
  "1641": "scot deficiency",
  "1642": "senior lken syndrome",
  "1643": "sensorineural deafness and male infertility",
  "1644": "sepiapterin reductase deficiency",
  "1645": "septo optic dysplasia",
  "1646": "serpiginous choroiditis",
  "1647": "severe congenital neutropenia",
  "1648": "shaken baby syndrome",
  "1649": "sheldon hall syndrome",
  "1650": "shingles",
  "1651": "short bowel syndrome",
  "1652": "short chain acyl coa dehydrogenase deficiency",
  "1653": "short qt syndrome",
  "1654": "short stature, hyperextensibility, hernia, ocular depression, rieger anomaly, and teething delay",
  "1655": "short syndrome",
  "1656": "shprintzen goldberg syndrome",
  "1657": "shwachman diamond syndrome",
  "1658": "sialadenitis",
  "1659": "sialic acid storage disease",
  "1660": "sialidosis",
  "1661": "sialuria",
  "1662": "sick sinus syndrome",
  "1663": "sickle cell disease",
  "1664": "sideroblastic anemia",
  "1665": "sideroblastic anemia pyridoxine refractory autosomal recessive",
  "1666": "silver syndrome",
  "1667": "simple kidney cysts",
  "1668": "simpson golabi behmel syndrome",
  "1669": "singleton merten syndrome",
  "1670": "sitosterolemia",
  "1671": "situs inversus",
  "1672": "sjgren larsson syndrome",
  "1673": "sjgren syndrome",
  "1674": "sjgren's syndrome",
  "1675": "sjogren syndrome",
  "1676": "skin cancer",
  "1677": "slc4a1 associated distal renal tubular acidosis",
  "1678": "sleep apnea",
  "1679": "small cell lung cancer",
  "1680": "small fiber neuropathy",
  "1681": "small intestine cancer",
  "1682": "smith lemli opitz syndrome",
  "1683": "smith magenis syndrome",
  "1684": "smoking and the digestive system",
  "1685": "snyder robinson syndrome",
  "1686": "solitary kidney",
  "1687": "sost related sclerosing bone dysplasia",
  "1688": "sotos syndrome",
  "1689": "sox2 anophthalmia syndrome",
  "1690": "spastic diplegia cerebral palsy",
  "1691": "spastic paraplegia type 11",
  "1692": "spastic paraplegia type 15",
  "1693": "spastic paraplegia type 2",
  "1694": "spastic paraplegia type 31",
  "1695": "spastic paraplegia type 3a",
  "1696": "spastic paraplegia type 4",
  "1697": "spastic paraplegia type 7",
  "1698": "spastic paraplegia type 8",
  "1699": "spasticity",
  "1700": "spina bifida",
  "1701": "spinal and bulbar muscular atrophy",
  "1702": "spinal cord infarction",
  "1703": "spinal cord injury",
  "1704": "spinal muscular atrophy",
  "1705": "spinal muscular atrophy with progressive myoclonic epilepsy",
  "1706": "spinal muscular atrophy with respiratory distress type 1",
  "1707": "spinocerebellar ataxia 2",
  "1708": "spinocerebellar ataxia type 1",
  "1709": "spinocerebellar ataxia type 2",
  "1710": "spinocerebellar ataxia type 3",
  "1711": "spinocerebellar ataxia type 36",
  "1712": "spinocerebellar ataxia type 6",
  "1713": "spondylocarpotarsal synostosis syndrome",
  "1714": "spondylocostal dysostosis",
  "1715": "spondyloenchondrodysplasia with immune dysregulation",
  "1716": "spondyloepimetaphyseal dysplasia, strudwick type",
  "1717": "spondyloepiphyseal dysplasia congenita",
  "1718": "spondyloperipheral dysplasia",
  "1719": "spondylothoracic dysostosis",
  "1720": "sporadic hemiplegic migraine",
  "1721": "stargardt disease",
  "1722": "stargardt macular degeneration",
  "1723": "steatocystoma multiplex",
  "1724": "stenotrophomonas maltophilia infection",
  "1725": "stevens johnson syndrome",
  "1726": "stevens johnson syndrome/toxic epidermal necrolysis",
  "1727": "stickler syndrome",
  "1728": "stiff person syndrome",
  "1729": "sting associated vasculopathy with onset in infancy",
  "1730": "stormorken syndrome",
  "1731": "striatonigral degeneration",
  "1732": "stroke",
  "1733": "sturge weber syndrome",
  "1734": "stve wiedemann syndrome",
  "1735": "subacute sclerosing panencephalitis",
  "1736": "succinate coa ligase deficiency",
  "1737": "succinic semialdehyde dehydrogenase deficiency",
  "1738": "succinyl coa:3 ketoacid coa transferase deficiency",
  "1739": "sudden cardiac arrest",
  "1740": "sudden infant death with dysgenesis of the testes syndrome",
  "1741": "sunct headache",
  "1742": "supravalvular aortic stenosis",
  "1743": "surfactant dysfunction",
  "1744": "surviving cancer",
  "1745": "swallowing disorders",
  "1746": "swyer james syndrome",
  "1747": "swyer syndrome",
  "1748": "sydenham chorea",
  "1749": "syncope",
  "1750": "syndrome of inappropriate antidiuretic hormone",
  "1751": "syngap1 related intellectual disability",
  "1752": "syringomyelia",
  "1753": "systemic lupus erythematosus",
  "1754": "systemic scleroderma",
  "1755": "t cell immunodeficiency, congenital alopecia, and nail dystrophy",
  "1756": "tabes dorsalis",
  "1757": "tangier disease",
  "1758": "tardive dyskinesia",
  "1759": "tarlov cysts",
  "1760": "tarp syndrome",
  "1761": "tarsal carpal coalition syndrome",
  "1762": "tarsal tunnel syndrome",
  "1763": "task specific focal dystonia",
  "1764": "tay sachs disease",
  "1765": "testicular cancer",
  "1766": "tethered spinal cord syndrome",
  "1767": "tetra amelia syndrome",
  "1768": "tetrahydrobiopterin deficiency",
  "1769": "tetralogy of fallot",
  "1770": "tetrasomy 18p",
  "1771": "thalassemia",
  "1772": "thalassemias",
  "1773": "thanatophoric dysplasia",
  "1774": "thiamine responsive megaloblastic anemia syndrome",
  "1775": "thiopurine s methyltransferase deficiency",
  "1776": "thoracic outlet syndrome",
  "1777": "thrombocythemia and thrombocytosis",
  "1778": "thrombocytopenia",
  "1779": "thrombocytopenia absent radius syndrome",
  "1780": "thrombotic thrombocytopenic purpura",
  "1781": "thymoma and thymic carcinoma",
  "1782": "thyrotoxic myopathy",
  "1783": "tibial muscular dystrophy",
  "1784": "tietz syndrome",
  "1785": "tietze syndrome",
  "1786": "timothy syndrome",
  "1787": "tk2 related mitochondrial dna depletion syndrome, myopathic form",
  "1788": "todd's paralysis",
  "1789": "tourette syndrome",
  "1790": "townes brocks syndrome",
  "1791": "tracheobronchomalacia",
  "1792": "tracheobronchopathia osteoplastica",
  "1793": "transient ischemic attack",
  "1794": "transitional cell cancer of the renal pelvis and ureter",
  "1795": "transmissible spongiform encephalopathies",
  "1796": "transthyretin amyloidosis",
  "1797": "transverse myelitis",
  "1798": "traumatic brain injury",
  "1799": "treacher collins syndrome",
  "1800": "treatment methods for kidney failure: peritoneal dialysis",
  "1801": "tremor",
  "1802": "trichohepatoenteric syndrome",
  "1803": "trichothiodystrophy",
  "1804": "trigeminal neuralgia",
  "1805": "trimethylaminuria",
  "1806": "triosephosphate isomerase deficiency",
  "1807": "triple a syndrome",
  "1808": "triple x syndrome",
  "1809": "trisomy 13",
  "1810": "trisomy 18",
  "1811": "tropical spastic paraparesis",
  "1812": "troyer syndrome",
  "1813": "tuberculosis (tb)",
  "1814": "tuberous sclerosis",
  "1815": "tuberous sclerosis complex",
  "1816": "tubular aggregate myopathy",
  "1817": "tularemia",
  "1818": "tumor necrosis factor receptor associated periodic syndrome",
  "1819": "turner syndrome",
  "1820": "tylosis with esophageal cancer",
  "1821": "type 1 diabetes",
  "1822": "type 1 plasminogen deficiency",
  "1823": "type a insulin resistance syndrome",
  "1824": "tyrosine hydroxylase deficiency",
  "1825": "tyrosinemia",
  "1826": "ulcerative colitis",
  "1827": "uncombable hair syndrome",
  "1828": "unverricht lundborg disease",
  "1829": "urachal cyst",
  "1830": "urethral cancer",
  "1831": "urinary incontinence",
  "1832": "urinary incontinence in children",
  "1833": "urinary incontinence in men",
  "1834": "urinary retention",
  "1835": "urinary tract infection in adults",
  "1836": "urinary tract infections",
  "1837": "urinary tract infections in children",
  "1838": "urine blockage in newborns",
  "1839": "uromodulin associated kidney disease",
  "1840": "usher syndrome",
  "1841": "uterine sarcoma",
  "1842": "uv sensitive syndrome",
  "1843": "vacterl association",
  "1844": "van der woude syndrome",
  "1845": "varicose veins",
  "1846": "vasculitis",
  "1847": "vasculitis syndromes of the central and peripheral nervous systems",
  "1848": "very long chain acyl coa dehydrogenase deficiency",
  "1849": "vesicoureteral reflux",
  "1850": "viral gastroenteritis",
  "1851": "viral hepatitis: a through e and beyond",
  "1852": "vitamin d dependent rickets",
  "1853": "vitelliform macular dystrophy",
  "1854": "vitiligo",
  "1855": "vlcad deficiency",
  "1856": "vldlr associated cerebellar hypoplasia",
  "1857": "vohwinkel syndrome",
  "1858": "von hippel lindau disease",
  "1859": "von hippel lindau disease (vhl)",
  "1860": "von hippel lindau syndrome",
  "1861": "von willebrand disease",
  "1862": "vulvar cancer",
  "1863": "waardenburg syndrome",
  "1864": "wagner syndrome",
  "1865": "wagr syndrome",
  "1866": "waldenstrm macroglobulinemia",
  "1867": "walker warburg syndrome",
  "1868": "wallenberg's syndrome",
  "1869": "warfarin resistance",
  "1870": "warfarin sensitivity",
  "1871": "warsaw breakage syndrome",
  "1872": "warthin tumor",
  "1873": "waterhousefriderichsen syndrome",
  "1874": "weaver syndrome",
  "1875": "weill marchesani syndrome",
  "1876": "weissenbacher zweymller syndrome",
  "1877": "werner syndrome",
  "1878": "wernicke korsakoff syndrome",
  "1879": "weyers acrofacial dysostosis",
  "1880": "what i need to know about bladder control for women",
  "1881": "what i need to know about cirrhosis",
  "1882": "what i need to know about crohn's disease",
  "1883": "what i need to know about diarrhea",
  "1884": "what i need to know about diverticular disease",
  "1885": "what i need to know about erectile dysfunction",
  "1886": "what i need to know about gas",
  "1887": "what i need to know about gestational diabetes",
  "1888": "what i need to know about hepatitis a",
  "1889": "what i need to know about hepatitis b",
  "1890": "what i need to know about hepatitis c",
  "1891": "what i need to know about hirschsprung disease",
  "1892": "what i need to know about interstitial cystitis/painful bladder syndrome",
  "1893": "what i need to know about kidney failure and how its treated",
  "1894": "what i need to know about kidney stones",
  "1895": "what i need to know about lactose intolerance",
  "1896": "what i need to know about living with kidney failure",
  "1897": "what i need to know about my child's urinary tract infection",
  "1898": "whiplash",
  "1899": "whipple disease",
  "1900": "whipple's disease",
  "1901": "white sponge nevus",
  "1902": "wildervanck syndrome",
  "1903": "williams syndrome",
  "1904": "wilms tumor and other childhood kidney tumors",
  "1905": "wilson disease",
  "1906": "winchester syndrome",
  "1907": "wiskott aldrich syndrome",
  "1908": "wolf hirschhorn syndrome",
  "1909": "wolff parkinson white syndrome",
  "1910": "wolfram syndrome",
  "1911": "wolman disease",
  "1912": "x linked adrenal hypoplasia congenita",
  "1913": "x linked adrenoleukodystrophy",
  "1914": "x linked agammaglobulinemia",
  "1915": "x linked chondrodysplasia punctata 1",
  "1916": "x linked chondrodysplasia punctata 2",
  "1917": "x linked congenital stationary night blindness",
  "1918": "x linked creatine deficiency",
  "1919": "x linked dominant scapuloperoneal myopathy",
  "1920": "x linked dystonia parkinsonism",
  "1921": "x linked hyper igm syndrome",
  "1922": "x linked hypophosphatemia",
  "1923": "x linked immunodeficiency with magnesium defect, epstein barr virus infection, and neoplasia",
  "1924": "x linked infantile nystagmus",
  "1925": "x linked infantile spasm syndrome",
  "1926": "x linked intellectual disability, siderius type",
  "1927": "x linked juvenile retinoschisis",
  "1928": "x linked lissencephaly with abnormal genitalia",
  "1929": "x linked lymphoproliferative disease",
  "1930": "x linked myotubular myopathy",
  "1931": "x linked severe combined immunodeficiency",
  "1932": "x linked sideroblastic anemia",
  "1933": "x linked sideroblastic anemia and ataxia",
  "1934": "x linked spondyloepiphyseal dysplasia tarda",
  "1935": "x linked thrombocytopenia",
  "1936": "xeroderma pigmentosum",
  "1937": "y chromosome infertility",
  "1938": "yellow nail syndrome",
  "1939": "yersinia",
  "1940": "zap70 related severe combined immunodeficiency",
  "1941": "zellweger spectrum disorder",
  "1942": "zellweger syndrome",
  "1943": "zollinger ellison syndrome"
}