| { |
| "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" |
| } |
