| { | |
| "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" | |
| } |