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