| { |
| "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, |
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| "dystonia 6": 580, |
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| "epidermolysis bullosa acquisita": 607, |
| "epidermolysis bullosa simplex": 608, |
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| "erythropoietic protoporphyria": 617, |
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| "essential thrombocythemia": 620, |
| "essential tremor": 621, |
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| "ethylmalonic encephalopathy": 623, |
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| "extragonadal germ cell tumors": 625, |
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| "factor v leiden thrombophilia": 629, |
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| "familial cold autoinflammatory syndrome": 636, |
| "familial cylindromatosis": 637, |
| "familial dilated cardiomyopathy": 638, |
| "familial dysautonomia": 639, |
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| "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, |
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| "familial pityriasis rubra pilaris": 661, |
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| "familial restrictive cardiomyopathy": 663, |
| "familial thoracic aortic aneurysm and dissection": 664, |
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| "fibrodysplasia ossificans progressiva": 677, |
| "fibrolamellar carcinoma": 678, |
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| "fragile x associated primary ovarian insufficiency": 692, |
| "fragile x associated tremor/ataxia syndrome": 693, |
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| "fragile xe syndrome": 695, |
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| "frontotemporal dementia": 706, |
| "frontotemporal dementia with parkinsonism 17": 707, |
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| "fuchs endothelial dystrophy": 709, |
| "fucosidosis": 710, |
| "fukuyama congenital muscular dystrophy": 711, |
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| "giant axonal neuropathy": 738, |
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| "glutaric acidemia type ii": 757, |
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| "glycogen storage disease type 0": 760, |
| "glycogen storage disease type 13": 761, |
| "glycogen storage disease type 4": 762, |
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| "glycogen storage disease type iii": 764, |
| "glycogen storage disease type iv": 765, |
| "glycogen storage disease type ix": 766, |
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| "glycogen storage disease type vi": 768, |
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| "gm2 gangliosidosis, ab variant": 771, |
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| "gracile syndrome": 777, |
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| "granulomatosis with polyangiitis": 779, |
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| "grn related frontotemporal dementia": 786, |
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| "gyrate atrophy of the choroid and retina": 791, |
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| "hairy cell leukemia": 793, |
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| "hand foot genital syndrome": 796, |
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| "harlequin ichthyosis": 799, |
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| "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, |
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| "hereditary cerebral amyloid angiopathy": 836, |
| "hereditary cerebral hemorrhage with amyloidosis": 837, |
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| "hereditary fructose intolerance": 842, |
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| "hereditary hemorrhagic telangiectasia": 844, |
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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, |
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| "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, |
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| "hereditary sensory neuropathy type ia": 860, |
| "hereditary sensory neuropathy type ie": 861, |
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| "hereditary xanthinuria": 864, |
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| "human t cell leukemia virus type 2": 884, |
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| "infantile neuronal ceroid lipofuscinosis": 942, |
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| "intraocular (uveal) melanoma": 957, |
| "intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies": 958, |
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| "iridocorneal endothelial syndrome": 960, |
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| "iron refractory iron deficiency anemia": 962, |
| "irritable bowel syndrome in children": 963, |
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| "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, |
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| "jervell and lange nielsen syndrome": 976, |
| "jones syndrome": 977, |
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| "junctional epidermolysis bullosa": 979, |
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| "juvenile huntington disease": 982, |
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| "juvenile polyposis syndrome": 988, |
| "juvenile primary lateral sclerosis": 989, |
| "juvenile primary osteoporosis": 990, |
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| "kallmann syndrome": 993, |
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| "kawasaki syndrome": 996, |
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| "kearns sayre syndrome": 998, |
| "kennedy's disease": 999, |
| "keratitis ichthyosis deafness syndrome": 1000, |
| "keratoderma with woolly hair": 1001, |
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| "kidney disease of diabetes": 1003, |
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| "kidney failure: choosing a treatment that's right for you": 1005, |
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| "kidney stones in adults": 1007, |
| "kidney stones in children": 1008, |
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| "klinefelter syndrome": 1013, |
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| "klippel trenaunay syndrome": 1015, |
| "klippel trenaunay syndrome (kts)": 1016, |
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| "kyrle disease": 1028, |
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| "lacrimo auriculo dento digital syndrome": 1031, |
| "lactate dehydrogenase deficiency": 1032, |
| "lactose intolerance": 1033, |
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| "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, |
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| "laryngo onycho cutaneous syndrome": 1048, |
| "late infantile neuronal ceroid lipofuscinosis": 1049, |
| "lattice corneal dystrophy type i": 1050, |
| "lattice corneal dystrophy type ii": 1051, |
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| "leber hereditary optic neuropathy": 1054, |
| "legg calv perthes disease": 1055, |
| "legius syndrome": 1056, |
| "leigh syndrome": 1057, |
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| "lemierre syndrome": 1059, |
| "lennox gastaut syndrome": 1060, |
| "lenz microphthalmia syndrome": 1061, |
| "leptin receptor deficiency": 1062, |
| "lesch nyhan syndrome": 1063, |
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| "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, |
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| "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, |
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| "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, |
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| "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, |
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| "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, |
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| "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, |
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| "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 |
| } |
