Create id2label.json
Browse files- id2label.json +1946 -0
id2label.json
ADDED
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@@ -0,0 +1,1946 @@
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|
|
|
|
|
|
|
|
|
|
|
|
|
|
| 1 |
+
{
|
| 2 |
+
"0": "11 beta hydroxylase deficiency",
|
| 3 |
+
"1": "15q13.3 microdeletion",
|
| 4 |
+
"2": "15q24 microdeletion",
|
| 5 |
+
"3": "16p11.2 deletion syndrome",
|
| 6 |
+
"4": "17 alpha hydroxylase/17,20 lyase deficiency",
|
| 7 |
+
"5": "17 beta hydroxysteroid dehydrogenase 3 deficiency",
|
| 8 |
+
"6": "17q23.1q23.2 microdeletion syndrome",
|
| 9 |
+
"7": "18q deletion syndrome",
|
| 10 |
+
"8": "1p36 deletion syndrome",
|
| 11 |
+
"9": "1q21.1 microdeletion",
|
| 12 |
+
"10": "2 hydroxyglutaric aciduria",
|
| 13 |
+
"11": "2 methylbutyryl coa dehydrogenase deficiency",
|
| 14 |
+
"12": "21 hydroxylase deficiency",
|
| 15 |
+
"13": "22q11.2 deletion syndrome",
|
| 16 |
+
"14": "22q11.2 duplication",
|
| 17 |
+
"15": "22q13.3 deletion syndrome",
|
| 18 |
+
"16": "2q37 deletion syndrome",
|
| 19 |
+
"17": "3 beta hydroxysteroid dehydrogenase deficiency",
|
| 20 |
+
"18": "3 hydroxy 3 methylglutaryl coa lyase deficiency",
|
| 21 |
+
"19": "3 hydroxyacyl coa dehydrogenase deficiency",
|
| 22 |
+
"20": "3 hydroxyisobutyric aciduria",
|
| 23 |
+
"21": "3 m syndrome",
|
| 24 |
+
"22": "3 methylcrotonyl coa carboxylase deficiency",
|
| 25 |
+
"23": "3 methylglutaconyl coa hydratase deficiency",
|
| 26 |
+
"24": "3mc syndrome",
|
| 27 |
+
"25": "46,xx testicular disorder of sex development",
|
| 28 |
+
"26": "47 xxx syndrome",
|
| 29 |
+
"27": "47,xyy syndrome",
|
| 30 |
+
"28": "48,xxyy syndrome",
|
| 31 |
+
"29": "5 alpha reductase deficiency",
|
| 32 |
+
"30": "5q minus syndrome",
|
| 33 |
+
"31": "6q24 related transient neonatal diabetes mellitus",
|
| 34 |
+
"32": "7q11.23 duplication syndrome",
|
| 35 |
+
"33": "8p11 myeloproliferative syndrome",
|
| 36 |
+
"34": "9q22.3 microdeletion",
|
| 37 |
+
"35": "aarskog scott syndrome",
|
| 38 |
+
"36": "abdominal adhesions",
|
| 39 |
+
"37": "abdominal wall defect",
|
| 40 |
+
"38": "abetalipoproteinemia",
|
| 41 |
+
"39": "absence of the septum pellucidum",
|
| 42 |
+
"40": "acanthamoeba granulomatous amebic encephalitis (gae); keratitis",
|
| 43 |
+
"41": "acatalasemia",
|
| 44 |
+
"42": "accessory navicular bone",
|
| 45 |
+
"43": "aceruloplasminemia",
|
| 46 |
+
"44": "achalasia",
|
| 47 |
+
"45": "achondrogenesis",
|
| 48 |
+
"46": "achondroplasia",
|
| 49 |
+
"47": "achromatopsia",
|
| 50 |
+
"48": "acid lipase disease",
|
| 51 |
+
"49": "acinetobacter in healthcare settings",
|
| 52 |
+
"50": "acquired cystic kidney disease",
|
| 53 |
+
"51": "acral peeling skin syndrome",
|
| 54 |
+
"52": "acromegaly",
|
| 55 |
+
"53": "acromicric dysplasia",
|
| 56 |
+
"54": "actin accumulation myopathy",
|
| 57 |
+
"55": "activated pi3k delta syndrome",
|
| 58 |
+
"56": "acute disseminated encephalomyelitis",
|
| 59 |
+
"57": "acute febrile neutrophilic dermatosis",
|
| 60 |
+
"58": "acute intermittent porphyria",
|
| 61 |
+
"59": "acute promyelocytic leukemia",
|
| 62 |
+
"60": "adams oliver syndrome",
|
| 63 |
+
"61": "adcy5 related dyskinesia",
|
| 64 |
+
"62": "adenine phosphoribosyltransferase deficiency",
|
| 65 |
+
"63": "adenosine deaminase deficiency",
|
| 66 |
+
"64": "adenosine monophosphate deaminase deficiency",
|
| 67 |
+
"65": "adenylosuccinate lyase deficiency",
|
| 68 |
+
"66": "adermatoglyphia",
|
| 69 |
+
"67": "adiposis dolorosa",
|
| 70 |
+
"68": "adolescent idiopathic scoliosis",
|
| 71 |
+
"69": "adrenal insufficiency and addison's disease",
|
| 72 |
+
"70": "adrenoleukodystrophy",
|
| 73 |
+
"71": "adult acute lymphoblastic leukemia",
|
| 74 |
+
"72": "adult acute myeloid leukemia",
|
| 75 |
+
"73": "adult central nervous system tumors",
|
| 76 |
+
"74": "adult hodgkin lymphoma",
|
| 77 |
+
"75": "adult non hodgkin lymphoma",
|
| 78 |
+
"76": "adult onset leukoencephalopathy with axonal spheroids and pigmented glia",
|
| 79 |
+
"77": "adult onset vitelliform macular dystrophy",
|
| 80 |
+
"78": "adult polyglucosan body disease",
|
| 81 |
+
"79": "adult primary liver cancer",
|
| 82 |
+
"80": "adult soft tissue sarcoma",
|
| 83 |
+
"81": "afibrinogenemia",
|
| 84 |
+
"82": "african iron overload",
|
| 85 |
+
"83": "age related macular degeneration",
|
| 86 |
+
"84": "agenesis of the corpus callosum",
|
| 87 |
+
"85": "agenesis of the dorsal pancreas",
|
| 88 |
+
"86": "agnosia",
|
| 89 |
+
"87": "aicardi goutieres syndrome",
|
| 90 |
+
"88": "aicardi goutieres syndrome disorder",
|
| 91 |
+
"89": "aicardi syndrome",
|
| 92 |
+
"90": "aids related lymphoma",
|
| 93 |
+
"91": "alagille syndrome",
|
| 94 |
+
"92": "albright's hereditary osteodystrophy",
|
| 95 |
+
"93": "alcohol use and older adults",
|
| 96 |
+
"94": "alexander disease",
|
| 97 |
+
"95": "alg1 congenital disorder of glycosylation",
|
| 98 |
+
"96": "alg12 congenital disorder of glycosylation",
|
| 99 |
+
"97": "alg6 congenital disorder of glycosylation",
|
| 100 |
+
"98": "alkaptonuria",
|
| 101 |
+
"99": "alkhurma hemorrhagic fever (ahf)",
|
| 102 |
+
"100": "allan herndon dudley syndrome",
|
| 103 |
+
"101": "allergic asthma",
|
| 104 |
+
"102": "alopecia universalis",
|
| 105 |
+
"103": "alpers huttenlocher syndrome",
|
| 106 |
+
"104": "alpers' disease",
|
| 107 |
+
"105": "alpha 1 antitrypsin deficiency",
|
| 108 |
+
"106": "alpha mannosidosis",
|
| 109 |
+
"107": "alpha methylacyl coa racemase deficiency",
|
| 110 |
+
"108": "alpha thalassemia",
|
| 111 |
+
"109": "alpha thalassemia x linked intellectual disability syndrome",
|
| 112 |
+
"110": "alport syndrome",
|
| 113 |
+
"111": "alstrm syndrome",
|
| 114 |
+
"112": "alternating hemiplegia",
|
| 115 |
+
"113": "alternating hemiplegia of childhood",
|
| 116 |
+
"114": "alveolar capillary dysplasia with misalignment of pulmonary veins",
|
| 117 |
+
"115": "alzheimer disease",
|
| 118 |
+
"116": "alzheimer's caregiving",
|
| 119 |
+
"117": "alzheimer's disease",
|
| 120 |
+
"118": "am i at risk for type 2 diabetes? taking steps to lower your risk of getting diabetes",
|
| 121 |
+
"119": "amelogenesis imperfecta",
|
| 122 |
+
"120": "aminoacylase 1 deficiency",
|
| 123 |
+
"121": "amish lethal microcephaly",
|
| 124 |
+
"122": "amniotic band syndrome",
|
| 125 |
+
"123": "amyloidosis and kidney disease",
|
| 126 |
+
"124": "amyotrophic lateral sclerosis",
|
| 127 |
+
"125": "anal cancer",
|
| 128 |
+
"126": "andermann syndrome",
|
| 129 |
+
"127": "andersen tawil syndrome",
|
| 130 |
+
"128": "androgen insensitivity syndrome",
|
| 131 |
+
"129": "androgenetic alopecia",
|
| 132 |
+
"130": "anemia",
|
| 133 |
+
"131": "anemia in chronic kidney disease",
|
| 134 |
+
"132": "anemia of inflammation and chronic disease",
|
| 135 |
+
"133": "anencephaly",
|
| 136 |
+
"134": "aneurysm",
|
| 137 |
+
"135": "angelman syndrome",
|
| 138 |
+
"136": "angina",
|
| 139 |
+
"137": "anhidrotic ectodermal dysplasia with immune deficiency",
|
| 140 |
+
"138": "aniridia",
|
| 141 |
+
"139": "ankyloblepharon ectodermal defects cleft lip/palate syndrome",
|
| 142 |
+
"140": "ankylosing spondylitis",
|
| 143 |
+
"141": "antiphospholipid antibody syndrome",
|
| 144 |
+
"142": "antiphospholipid syndrome",
|
| 145 |
+
"143": "antisynthetase syndrome",
|
| 146 |
+
"144": "anxiety disorders",
|
| 147 |
+
"145": "apert syndrome",
|
| 148 |
+
"146": "aphasia",
|
| 149 |
+
"147": "aplasia cutis congenita",
|
| 150 |
+
"148": "aplastic anemia",
|
| 151 |
+
"149": "apraxia",
|
| 152 |
+
"150": "aquagenic pruritus",
|
| 153 |
+
"151": "arachnoid cysts",
|
| 154 |
+
"152": "arachnoiditis",
|
| 155 |
+
"153": "ards",
|
| 156 |
+
"154": "arginase deficiency",
|
| 157 |
+
"155": "arginine:glycine amidinotransferase deficiency",
|
| 158 |
+
"156": "argininosuccinic aciduria",
|
| 159 |
+
"157": "aromatase deficiency",
|
| 160 |
+
"158": "aromatase excess syndrome",
|
| 161 |
+
"159": "aromatic l amino acid decarboxylase deficiency",
|
| 162 |
+
"160": "arrhythmia",
|
| 163 |
+
"161": "arrhythmogenic right ventricular cardiomyopathy",
|
| 164 |
+
"162": "arterial tortuosity syndrome",
|
| 165 |
+
"163": "arteriovenous malformation",
|
| 166 |
+
"164": "arts syndrome",
|
| 167 |
+
"165": "asbestos related lung diseases",
|
| 168 |
+
"166": "aspartylglucosaminuria",
|
| 169 |
+
"167": "asperger syndrome",
|
| 170 |
+
"168": "asphyxiating thoracic dystrophy",
|
| 171 |
+
"169": "asthma",
|
| 172 |
+
"170": "ataxia",
|
| 173 |
+
"171": "ataxia neuropathy spectrum",
|
| 174 |
+
"172": "ataxia telangiectasia",
|
| 175 |
+
"173": "ataxia with oculomotor apraxia",
|
| 176 |
+
"174": "ataxia with vitamin e deficiency",
|
| 177 |
+
"175": "atelosteogenesis type 1",
|
| 178 |
+
"176": "atelosteogenesis type 2",
|
| 179 |
+
"177": "atelosteogenesis type 3",
|
| 180 |
+
"178": "atherosclerosis",
|
| 181 |
+
"179": "atopic dermatitis",
|
| 182 |
+
"180": "atrial fibrillation",
|
| 183 |
+
"181": "atrial fibrillation and stroke",
|
| 184 |
+
"182": "attention deficit hyperactivity disorder",
|
| 185 |
+
"183": "atypical chronic myelogenous leukemia",
|
| 186 |
+
"184": "atypical hemolytic uremic syndrome",
|
| 187 |
+
"185": "auriculo condylar syndrome",
|
| 188 |
+
"186": "autism",
|
| 189 |
+
"187": "autoimmune addison disease",
|
| 190 |
+
"188": "autoimmune atrophic gastritis",
|
| 191 |
+
"189": "autoimmune autonomic ganglionopathy",
|
| 192 |
+
"190": "autoimmune hemolytic anemia",
|
| 193 |
+
"191": "autoimmune hepatitis",
|
| 194 |
+
"192": "autoimmune lymphoproliferative syndrome",
|
| 195 |
+
"193": "autoimmune polyglandular syndrome, type 1",
|
| 196 |
+
"194": "autosomal dominant congenital stationary night blindness",
|
| 197 |
+
"195": "autosomal dominant hyper ige syndrome",
|
| 198 |
+
"196": "autosomal dominant hypocalcemia",
|
| 199 |
+
"197": "autosomal dominant nocturnal frontal lobe epilepsy",
|
| 200 |
+
"198": "autosomal dominant partial epilepsy with auditory features",
|
| 201 |
+
"199": "autosomal dominant vitreoretinochoroidopathy",
|
| 202 |
+
"200": "autosomal recessive axonal neuropathy with neuromyotonia",
|
| 203 |
+
"201": "autosomal recessive cerebellar ataxia type 1",
|
| 204 |
+
"202": "autosomal recessive congenital methemoglobinemia",
|
| 205 |
+
"203": "autosomal recessive congenital stationary night blindness",
|
| 206 |
+
"204": "autosomal recessive hyper ige syndrome",
|
| 207 |
+
"205": "autosomal recessive hypotrichosis",
|
| 208 |
+
"206": "autosomal recessive polycystic kidney disease",
|
| 209 |
+
"207": "autosomal recessive primary microcephaly",
|
| 210 |
+
"208": "autosomal recessive spastic ataxia of charlevoix saguenay",
|
| 211 |
+
"209": "axenfeld rieger syndrome",
|
| 212 |
+
"210": "axenfeld rieger syndrome type 1",
|
| 213 |
+
"211": "back pain",
|
| 214 |
+
"212": "balance problems",
|
| 215 |
+
"213": "baller gerold syndrome",
|
| 216 |
+
"214": "bannayan riley ruvalcaba syndrome",
|
| 217 |
+
"215": "baraitser winter syndrome",
|
| 218 |
+
"216": "bardet biedl syndrome",
|
| 219 |
+
"217": "barrett esophagus",
|
| 220 |
+
"218": "bart pumphrey syndrome",
|
| 221 |
+
"219": "barth syndrome",
|
| 222 |
+
"220": "bartter syndrome",
|
| 223 |
+
"221": "basilar migraine",
|
| 224 |
+
"222": "batten disease",
|
| 225 |
+
"223": "beare stevenson cutis gyrata syndrome",
|
| 226 |
+
"224": "beckwith wiedemann syndrome",
|
| 227 |
+
"225": "behcet's disease",
|
| 228 |
+
"226": "behet disease",
|
| 229 |
+
"227": "behr syndrome",
|
| 230 |
+
"228": "bell's palsy",
|
| 231 |
+
"229": "benign chronic pemphigus",
|
| 232 |
+
"230": "benign essential blepharospasm",
|
| 233 |
+
"231": "benign familial neonatal seizures",
|
| 234 |
+
"232": "benign recurrent intrahepatic cholestasis",
|
| 235 |
+
"233": "benign rolandic epilepsy (bre)",
|
| 236 |
+
"234": "benign schwannoma",
|
| 237 |
+
"235": "best vitelliform macular dystrophy",
|
| 238 |
+
"236": "beta ketothiolase deficiency",
|
| 239 |
+
"237": "beta mannosidosis",
|
| 240 |
+
"238": "beta thalassemia",
|
| 241 |
+
"239": "beta ureidopropionase deficiency",
|
| 242 |
+
"240": "bethlem myopathy",
|
| 243 |
+
"241": "bietti crystalline dystrophy",
|
| 244 |
+
"242": "bilateral perisylvian polymicrogyria",
|
| 245 |
+
"243": "bile duct cancer (cholangiocarcinoma)",
|
| 246 |
+
"244": "biliary atresia",
|
| 247 |
+
"245": "binswanger's disease",
|
| 248 |
+
"246": "biotin thiamine responsive basal ganglia disease",
|
| 249 |
+
"247": "biotinidase deficiency",
|
| 250 |
+
"248": "birt hogg dub syndrome",
|
| 251 |
+
"249": "bjrnstad syndrome",
|
| 252 |
+
"250": "bladder cancer",
|
| 253 |
+
"251": "blau syndrome",
|
| 254 |
+
"252": "blepharophimosis, ptosis, and epicanthus inversus syndrome",
|
| 255 |
+
"253": "blepharophimosis, ptosis, and epicanthus inversus syndrome type 1",
|
| 256 |
+
"254": "bloom syndrome",
|
| 257 |
+
"255": "blue rubber bleb nevus syndrome",
|
| 258 |
+
"256": "book syndrome",
|
| 259 |
+
"257": "boomerang dysplasia",
|
| 260 |
+
"258": "botulism",
|
| 261 |
+
"259": "bowen conradi syndrome",
|
| 262 |
+
"260": "brachial plexus injuries",
|
| 263 |
+
"261": "bradyopsia",
|
| 264 |
+
"262": "brain and spinal tumors",
|
| 265 |
+
"263": "branchio oculo facial syndrome",
|
| 266 |
+
"264": "branchiooculofacial syndrome",
|
| 267 |
+
"265": "branchiootorenal syndrome",
|
| 268 |
+
"266": "branchiootorenal/branchiootic syndrome",
|
| 269 |
+
"267": "breast cancer",
|
| 270 |
+
"268": "brittle diabetes",
|
| 271 |
+
"269": "brody myopathy",
|
| 272 |
+
"270": "broken heart syndrome",
|
| 273 |
+
"271": "bronchiectasis",
|
| 274 |
+
"272": "bronchiolitis obliterans organizing pneumonia",
|
| 275 |
+
"273": "bronchitis",
|
| 276 |
+
"274": "bronchopulmonary dysplasia",
|
| 277 |
+
"275": "brooke spiegler syndrome",
|
| 278 |
+
"276": "brown sequard syndrome",
|
| 279 |
+
"277": "brugada syndrome",
|
| 280 |
+
"278": "buerger disease",
|
| 281 |
+
"279": "buschke ollendorff syndrome",
|
| 282 |
+
"280": "c3 glomerulopathy",
|
| 283 |
+
"281": "cadasil",
|
| 284 |
+
"282": "caffey disease",
|
| 285 |
+
"283": "campomelic dysplasia",
|
| 286 |
+
"284": "camurati engelmann disease",
|
| 287 |
+
"285": "canavan disease",
|
| 288 |
+
"286": "cant syndrome",
|
| 289 |
+
"287": "cap myopathy",
|
| 290 |
+
"288": "capillary malformation arteriovenous malformation syndrome",
|
| 291 |
+
"289": "carbamoyl phosphate synthetase i deficiency",
|
| 292 |
+
"290": "cardiofaciocutaneous syndrome",
|
| 293 |
+
"291": "cardiogenic shock",
|
| 294 |
+
"292": "cardiomyopathy",
|
| 295 |
+
"293": "carney complex",
|
| 296 |
+
"294": "carnitine acylcarnitine translocase deficiency",
|
| 297 |
+
"295": "carnitine palmitoyltransferase i deficiency",
|
| 298 |
+
"296": "carnitine palmitoyltransferase ii deficiency",
|
| 299 |
+
"297": "carotid artery disease",
|
| 300 |
+
"298": "carpal tunnel syndrome",
|
| 301 |
+
"299": "carpenter syndrome",
|
| 302 |
+
"300": "cartilage hair hypoplasia",
|
| 303 |
+
"301": "cask related intellectual disability",
|
| 304 |
+
"302": "catamenial pneumothorax",
|
| 305 |
+
"303": "cataract",
|
| 306 |
+
"304": "catecholaminergic polymorphic ventricular tachycardia",
|
| 307 |
+
"305": "catsper1 related nonsyndromic male infertility",
|
| 308 |
+
"306": "caudal regression syndrome",
|
| 309 |
+
"307": "causes of diabetes",
|
| 310 |
+
"308": "cav3 related distal myopathy",
|
| 311 |
+
"309": "cavernous malformation",
|
| 312 |
+
"310": "celiac artery compression syndrome",
|
| 313 |
+
"311": "celiac disease",
|
| 314 |
+
"312": "central cord syndrome",
|
| 315 |
+
"313": "central core disease",
|
| 316 |
+
"314": "central pain syndrome",
|
| 317 |
+
"315": "central pontine myelinolysis",
|
| 318 |
+
"316": "centronuclear myopathy",
|
| 319 |
+
"317": "cephalic disorders",
|
| 320 |
+
"318": "cerebellar degeneration",
|
| 321 |
+
"319": "cerebellar hypoplasia",
|
| 322 |
+
"320": "cerebral aneurysms",
|
| 323 |
+
"321": "cerebral arteriosclerosis",
|
| 324 |
+
"322": "cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy",
|
| 325 |
+
"323": "cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy",
|
| 326 |
+
"324": "cerebral cavernous malformation",
|
| 327 |
+
"325": "cerebral hypoxia",
|
| 328 |
+
"326": "cerebral palsy",
|
| 329 |
+
"327": "cerebro oculo facio skeletal syndrome (cofs)",
|
| 330 |
+
"328": "cerebrotendinous xanthomatosis",
|
| 331 |
+
"329": "chanarin dorfman syndrome",
|
| 332 |
+
"330": "chandler's syndrome",
|
| 333 |
+
"331": "chapare hemorrhagic fever (chhf)",
|
| 334 |
+
"332": "char syndrome",
|
| 335 |
+
"333": "charcot marie tooth disease",
|
| 336 |
+
"334": "charcot marie tooth disease type 2f",
|
| 337 |
+
"335": "charge syndrome",
|
| 338 |
+
"336": "chediak higashi syndrome",
|
| 339 |
+
"337": "cherubism",
|
| 340 |
+
"338": "chiari malformation",
|
| 341 |
+
"339": "chiari malformation type 1",
|
| 342 |
+
"340": "chilaiditi syndrome",
|
| 343 |
+
"341": "childhood acute lymphoblastic leukemia",
|
| 344 |
+
"342": "childhood acute myeloid leukemia and other myeloid malignancies",
|
| 345 |
+
"343": "childhood astrocytomas",
|
| 346 |
+
"344": "childhood brain and spinal cord tumors",
|
| 347 |
+
"345": "childhood brain stem glioma",
|
| 348 |
+
"346": "childhood central nervous system atypical teratoid/rhabdoid tumor",
|
| 349 |
+
"347": "childhood central nervous system embryonal tumors",
|
| 350 |
+
"348": "childhood central nervous system germ cell tumors",
|
| 351 |
+
"349": "childhood craniopharyngioma",
|
| 352 |
+
"350": "childhood ependymoma",
|
| 353 |
+
"351": "childhood extracranial germ cell tumors",
|
| 354 |
+
"352": "childhood hodgkin lymphoma",
|
| 355 |
+
"353": "childhood interstitial lung disease",
|
| 356 |
+
"354": "childhood liver cancer",
|
| 357 |
+
"355": "childhood myocerebrohepatopathy spectrum",
|
| 358 |
+
"356": "childhood nephrotic syndrome",
|
| 359 |
+
"357": "childhood non hodgkin lymphoma",
|
| 360 |
+
"358": "childhood rhabdomyosarcoma",
|
| 361 |
+
"359": "childhood soft tissue sarcoma",
|
| 362 |
+
"360": "childhood vascular tumors",
|
| 363 |
+
"361": "chmp2b related frontotemporal dementia",
|
| 364 |
+
"362": "cholesteatoma",
|
| 365 |
+
"363": "cholesteryl ester storage disease",
|
| 366 |
+
"364": "chondrocalcinosis 2",
|
| 367 |
+
"365": "chops syndrome",
|
| 368 |
+
"366": "chordoma",
|
| 369 |
+
"367": "chorea",
|
| 370 |
+
"368": "chorea acanthocytosis",
|
| 371 |
+
"369": "choroideremia",
|
| 372 |
+
"370": "christianson syndrome",
|
| 373 |
+
"371": "chromosome 3p syndrome",
|
| 374 |
+
"372": "chromosome 4q deletion",
|
| 375 |
+
"373": "chronic atrial and intestinal dysrhythmia",
|
| 376 |
+
"374": "chronic diarrhea in children",
|
| 377 |
+
"375": "chronic fatigue syndrome",
|
| 378 |
+
"376": "chronic fatigue syndrome (cfs)",
|
| 379 |
+
"377": "chronic granulomatous disease",
|
| 380 |
+
"378": "chronic hiccups",
|
| 381 |
+
"379": "chronic inflammatory demyelinating polyneuropathy",
|
| 382 |
+
"380": "chronic inflammatory demyelinating polyneuropathy (cidp)",
|
| 383 |
+
"381": "chronic lymphocytic leukemia",
|
| 384 |
+
"382": "chronic myelogenous leukemia",
|
| 385 |
+
"383": "chronic myelomonocytic leukemia",
|
| 386 |
+
"384": "chronic myeloproliferative neoplasms",
|
| 387 |
+
"385": "chronic pain",
|
| 388 |
+
"386": "chronic progressive external ophthalmoplegia",
|
| 389 |
+
"387": "chst3 related skeletal dysplasia",
|
| 390 |
+
"388": "chylomicron retention disease",
|
| 391 |
+
"389": "cirrhosis",
|
| 392 |
+
"390": "citrullinemia",
|
| 393 |
+
"391": "citrullinemia type i",
|
| 394 |
+
"392": "cleidocranial dysplasia",
|
| 395 |
+
"393": "clouston syndrome",
|
| 396 |
+
"394": "coats disease",
|
| 397 |
+
"395": "coats plus syndrome",
|
| 398 |
+
"396": "coccygodynia",
|
| 399 |
+
"397": "cockayne syndrome",
|
| 400 |
+
"398": "coffin lowry syndrome",
|
| 401 |
+
"399": "coffin siris syndrome",
|
| 402 |
+
"400": "cog5 congenital disorder of glycosylation",
|
| 403 |
+
"401": "cohen syndrome",
|
| 404 |
+
"402": "col4a1 related brain small vessel disease",
|
| 405 |
+
"403": "cold agglutinin disease",
|
| 406 |
+
"404": "cold induced sweating syndrome",
|
| 407 |
+
"405": "cold urticaria",
|
| 408 |
+
"406": "cole disease",
|
| 409 |
+
"407": "collagen vi related myopathy",
|
| 410 |
+
"408": "coloboma",
|
| 411 |
+
"409": "colon cancer",
|
| 412 |
+
"410": "color vision deficiency",
|
| 413 |
+
"411": "colorectal cancer",
|
| 414 |
+
"412": "colpocephaly",
|
| 415 |
+
"413": "coma",
|
| 416 |
+
"414": "combined malonic and methylmalonic aciduria",
|
| 417 |
+
"415": "combined pituitary hormone deficiency",
|
| 418 |
+
"416": "common variable immune deficiency",
|
| 419 |
+
"417": "common variable immunodeficiency",
|
| 420 |
+
"418": "complement component 2 deficiency",
|
| 421 |
+
"419": "complement factor i deficiency",
|
| 422 |
+
"420": "complete lcat deficiency",
|
| 423 |
+
"421": "complex regional pain syndrome",
|
| 424 |
+
"422": "cone rod dystrophy",
|
| 425 |
+
"423": "congenital adrenal hyperplasia",
|
| 426 |
+
"424": "congenital adrenal hyperplasia due to 11 beta hydroxylase deficiency",
|
| 427 |
+
"425": "congenital afibrinogenemia",
|
| 428 |
+
"426": "congenital anosmia",
|
| 429 |
+
"427": "congenital bilateral absence of the vas deferens",
|
| 430 |
+
"428": "congenital cataracts, facial dysmorphism, and neuropathy",
|
| 431 |
+
"429": "congenital central hypoventilation syndrome",
|
| 432 |
+
"430": "congenital contractural arachnodactyly",
|
| 433 |
+
"431": "congenital deafness with labyrinthine aplasia, microtia, and microdontia",
|
| 434 |
+
"432": "congenital diaphragmatic hernia",
|
| 435 |
+
"433": "congenital dyserythropoietic anemia",
|
| 436 |
+
"434": "congenital fiber type disproportion",
|
| 437 |
+
"435": "congenital fibrosis of the extraocular muscles",
|
| 438 |
+
"436": "congenital generalized lipodystrophy",
|
| 439 |
+
"437": "congenital heart defects",
|
| 440 |
+
"438": "congenital hemidysplasia with ichthyosiform erythroderma and limb defects",
|
| 441 |
+
"439": "congenital hepatic fibrosis",
|
| 442 |
+
"440": "congenital hyperinsulinism",
|
| 443 |
+
"441": "congenital hypothyroidism",
|
| 444 |
+
"442": "congenital insensitivity to pain",
|
| 445 |
+
"443": "congenital insensitivity to pain with anhidrosis",
|
| 446 |
+
"444": "congenital laryngeal palsy",
|
| 447 |
+
"445": "congenital leptin deficiency",
|
| 448 |
+
"446": "congenital mirror movement disorder",
|
| 449 |
+
"447": "congenital myasthenia",
|
| 450 |
+
"448": "congenital myasthenic syndrome",
|
| 451 |
+
"449": "congenital myopathy",
|
| 452 |
+
"450": "congenital neuronal ceroid lipofuscinosis",
|
| 453 |
+
"451": "congenital plasminogen deficiency",
|
| 454 |
+
"452": "congenital radio ulnar synostosis",
|
| 455 |
+
"453": "congenital stromal corneal dystrophy",
|
| 456 |
+
"454": "congenital sucrase isomaltase deficiency",
|
| 457 |
+
"455": "copd",
|
| 458 |
+
"456": "core binding factor acute myeloid leukemia",
|
| 459 |
+
"457": "cornelia de lange syndrome",
|
| 460 |
+
"458": "coronary heart disease",
|
| 461 |
+
"459": "coronary microvascular disease",
|
| 462 |
+
"460": "corticobasal degeneration",
|
| 463 |
+
"461": "corticosteroid binding globulin deficiency",
|
| 464 |
+
"462": "costeff syndrome",
|
| 465 |
+
"463": "costello syndrome",
|
| 466 |
+
"464": "cough",
|
| 467 |
+
"465": "cowden syndrome",
|
| 468 |
+
"466": "cramp fasciculation syndrome",
|
| 469 |
+
"467": "cranioectodermal dysplasia",
|
| 470 |
+
"468": "craniofacial deafness hand syndrome",
|
| 471 |
+
"469": "craniofacial microsomia",
|
| 472 |
+
"470": "craniometaphyseal dysplasia",
|
| 473 |
+
"471": "craniometaphyseal dysplasia, autosomal dominant",
|
| 474 |
+
"472": "craniometaphyseal dysplasia, autosomal recessive type",
|
| 475 |
+
"473": "craniopharyngioma",
|
| 476 |
+
"474": "craniosynostosis",
|
| 477 |
+
"475": "creating a family health history",
|
| 478 |
+
"476": "crest syndrome",
|
| 479 |
+
"477": "creutzfeldt jakob disease",
|
| 480 |
+
"478": "cri du chat syndrome",
|
| 481 |
+
"479": "crigler najjar syndrome",
|
| 482 |
+
"480": "crimean congo hemorrhagic fever (cchf)",
|
| 483 |
+
"481": "critical congenital heart disease",
|
| 484 |
+
"482": "crohn disease",
|
| 485 |
+
"483": "crohn's disease",
|
| 486 |
+
"484": "crouzon syndrome",
|
| 487 |
+
"485": "crouzonodermoskeletal syndrome",
|
| 488 |
+
"486": "cryptogenic cirrhosis",
|
| 489 |
+
"487": "cryptogenic organizing pneumonia",
|
| 490 |
+
"488": "currarino triad",
|
| 491 |
+
"489": "cushing disease",
|
| 492 |
+
"490": "cushing's syndrome",
|
| 493 |
+
"491": "cutaneous mastocytosis",
|
| 494 |
+
"492": "cutis laxa",
|
| 495 |
+
"493": "cyclic neutropenia",
|
| 496 |
+
"494": "cyclic vomiting syndrome",
|
| 497 |
+
"495": "cystic fibrosis",
|
| 498 |
+
"496": "cystinosis",
|
| 499 |
+
"497": "cystinuria",
|
| 500 |
+
"498": "cystocele",
|
| 501 |
+
"499": "cytochrome c oxidase deficiency",
|
| 502 |
+
"500": "cytochrome p450 oxidoreductase deficiency",
|
| 503 |
+
"501": "cytogenetically normal acute myeloid leukemia",
|
| 504 |
+
"502": "czech dysplasia",
|
| 505 |
+
"503": "d bifunctional protein deficiency",
|
| 506 |
+
"504": "dandy walker malformation",
|
| 507 |
+
"505": "dandy walker syndrome",
|
| 508 |
+
"506": "danon disease",
|
| 509 |
+
"507": "darier disease",
|
| 510 |
+
"508": "deafness and myopia syndrome",
|
| 511 |
+
"509": "deafness dystonia optic neuronopathy syndrome",
|
| 512 |
+
"510": "deep brain stimulation for parkinson's disease",
|
| 513 |
+
"511": "deep vein thrombosis",
|
| 514 |
+
"512": "dementia",
|
| 515 |
+
"513": "dementia with lewy bodies",
|
| 516 |
+
"514": "dentatorubral pallidoluysian atrophy",
|
| 517 |
+
"515": "dentinogenesis imperfecta",
|
| 518 |
+
"516": "denys drash syndrome",
|
| 519 |
+
"517": "deoxyguanosine kinase deficiency",
|
| 520 |
+
"518": "depression",
|
| 521 |
+
"519": "dermatitis herpetiformis: skin manifestation of celiac disease (for health care professionals)",
|
| 522 |
+
"520": "dermatofibrosarcoma protuberans",
|
| 523 |
+
"521": "dermatomyositis",
|
| 524 |
+
"522": "desmoid tumor",
|
| 525 |
+
"523": "desmoplastic infantile ganglioglioma",
|
| 526 |
+
"524": "desmosterolosis",
|
| 527 |
+
"525": "developmental dyspraxia",
|
| 528 |
+
"526": "dextrocardia with situs inversus",
|
| 529 |
+
"527": "diabetes",
|
| 530 |
+
"528": "diabetes, heart disease, and stroke",
|
| 531 |
+
"529": "diabetic heart disease",
|
| 532 |
+
"530": "diabetic kidney disease",
|
| 533 |
+
"531": "diabetic mastopathy",
|
| 534 |
+
"532": "diabetic neuropathies: the nerve damage of diabetes",
|
| 535 |
+
"533": "diabetic neuropathy",
|
| 536 |
+
"534": "diabetic retinopathy",
|
| 537 |
+
"535": "diagnosis of diabetes and prediabetes",
|
| 538 |
+
"536": "diamond blackfan anemia",
|
| 539 |
+
"537": "diarrhea",
|
| 540 |
+
"538": "diastrophic dysplasia",
|
| 541 |
+
"539": "dicer1 syndrome",
|
| 542 |
+
"540": "diffuse gastric cancer",
|
| 543 |
+
"541": "diffuse idiopathic skeletal hyperostosis",
|
| 544 |
+
"542": "dihydrolipoamide dehydrogenase deficiency",
|
| 545 |
+
"543": "dihydropyrimidinase deficiency",
|
| 546 |
+
"544": "dihydropyrimidine dehydrogenase deficiency",
|
| 547 |
+
"545": "dilated cardiomyopathy with ataxia syndrome",
|
| 548 |
+
"546": "disseminated intravascular coagulation",
|
| 549 |
+
"547": "disseminated peritoneal leiomyomatosis",
|
| 550 |
+
"548": "distal arthrogryposis type 1",
|
| 551 |
+
"549": "distal hereditary motor neuropathy, type ii",
|
| 552 |
+
"550": "distal hereditary motor neuropathy, type v",
|
| 553 |
+
"551": "distal myopathy 2",
|
| 554 |
+
"552": "diverticular disease",
|
| 555 |
+
"553": "dmd associated dilated cardiomyopathy",
|
| 556 |
+
"554": "dolk congenital disorder of glycosylation",
|
| 557 |
+
"555": "dominant dystrophic epidermolysis bullosa",
|
| 558 |
+
"556": "donnai barrow syndrome",
|
| 559 |
+
"557": "donohue syndrome",
|
| 560 |
+
"558": "doors syndrome",
|
| 561 |
+
"559": "dopa responsive dystonia",
|
| 562 |
+
"560": "dopamine beta hydroxylase deficiency",
|
| 563 |
+
"561": "dopamine transporter deficiency syndrome",
|
| 564 |
+
"562": "dowling degos disease",
|
| 565 |
+
"563": "down syndrome",
|
| 566 |
+
"564": "doyne honeycomb retinal dystrophy",
|
| 567 |
+
"565": "dravet syndrome",
|
| 568 |
+
"566": "dry eye",
|
| 569 |
+
"567": "dry mouth",
|
| 570 |
+
"568": "duane radial ray syndrome",
|
| 571 |
+
"569": "dubin johnson syndrome",
|
| 572 |
+
"570": "duchenne and becker muscular dystrophy",
|
| 573 |
+
"571": "duchenne muscular dystrophy",
|
| 574 |
+
"572": "dumping syndrome",
|
| 575 |
+
"573": "dyggve melchior clausen syndrome",
|
| 576 |
+
"574": "dysautonomia",
|
| 577 |
+
"575": "dyserythropoietic anemia and thrombocytopenia",
|
| 578 |
+
"576": "dysgraphia",
|
| 579 |
+
"577": "dyskeratosis congenita",
|
| 580 |
+
"578": "dyslexia",
|
| 581 |
+
"579": "dyssynergia cerebellaris myoclonica",
|
| 582 |
+
"580": "dystonia 6",
|
| 583 |
+
"581": "dystonias",
|
| 584 |
+
"582": "dystrophic epidermolysis bullosa",
|
| 585 |
+
"583": "early onset glaucoma",
|
| 586 |
+
"584": "early onset primary dystonia",
|
| 587 |
+
"585": "ectopic kidney",
|
| 588 |
+
"586": "eec syndrome",
|
| 589 |
+
"587": "ehlers danlos syndrome",
|
| 590 |
+
"588": "ehlers danlos syndrome, dermatosparaxis type",
|
| 591 |
+
"589": "ehlers danlos syndrome, kyphoscoliosis type",
|
| 592 |
+
"590": "ehlers danlos syndrome, progeroid type",
|
| 593 |
+
"591": "ehlers danlos syndrome, vascular type",
|
| 594 |
+
"592": "eisenmenger syndrome",
|
| 595 |
+
"593": "electrocardiogram",
|
| 596 |
+
"594": "ellis van creveld syndrome",
|
| 597 |
+
"595": "emanuel syndrome",
|
| 598 |
+
"596": "emery dreifuss muscular dystrophy",
|
| 599 |
+
"597": "empty sella syndrome",
|
| 600 |
+
"598": "encephalitis lethargica",
|
| 601 |
+
"599": "encephaloceles",
|
| 602 |
+
"600": "encephalopathy",
|
| 603 |
+
"601": "endocarditis",
|
| 604 |
+
"602": "endometrial cancer",
|
| 605 |
+
"603": "enlarged parietal foramina",
|
| 606 |
+
"604": "eosinophil peroxidase deficiency",
|
| 607 |
+
"605": "eosinophilic enteropathy",
|
| 608 |
+
"606": "epidermal nevus",
|
| 609 |
+
"607": "epidermolysis bullosa acquisita",
|
| 610 |
+
"608": "epidermolysis bullosa simplex",
|
| 611 |
+
"609": "epidermolysis bullosa with pyloric atresia",
|
| 612 |
+
"610": "epidermolytic hyperkeratosis",
|
| 613 |
+
"611": "epilepsy",
|
| 614 |
+
"612": "episodic ataxia",
|
| 615 |
+
"613": "erb duchenne and dejerine klumpke palsies",
|
| 616 |
+
"614": "erdheim chester disease",
|
| 617 |
+
"615": "erythrokeratodermia variabilis et progressiva",
|
| 618 |
+
"616": "erythromelalgia",
|
| 619 |
+
"617": "erythropoietic protoporphyria",
|
| 620 |
+
"618": "esophageal atresia/tracheoesophageal fistula",
|
| 621 |
+
"619": "essential pentosuria",
|
| 622 |
+
"620": "essential thrombocythemia",
|
| 623 |
+
"621": "essential tremor",
|
| 624 |
+
"622": "esthesioneuroblastoma",
|
| 625 |
+
"623": "ethylmalonic encephalopathy",
|
| 626 |
+
"624": "ewing sarcoma",
|
| 627 |
+
"625": "extragonadal germ cell tumors",
|
| 628 |
+
"626": "fabry disease",
|
| 629 |
+
"627": "facioscapulohumeral muscular dystrophy",
|
| 630 |
+
"628": "factor v deficiency",
|
| 631 |
+
"629": "factor v leiden thrombophilia",
|
| 632 |
+
"630": "factor x deficiency",
|
| 633 |
+
"631": "factor xiii deficiency",
|
| 634 |
+
"632": "fahr's syndrome",
|
| 635 |
+
"633": "familial acute myeloid leukemia with mutated cebpa",
|
| 636 |
+
"634": "familial adenomatous polyposis",
|
| 637 |
+
"635": "familial atrial fibrillation",
|
| 638 |
+
"636": "familial cold autoinflammatory syndrome",
|
| 639 |
+
"637": "familial cylindromatosis",
|
| 640 |
+
"638": "familial dilated cardiomyopathy",
|
| 641 |
+
"639": "familial dysautonomia",
|
| 642 |
+
"640": "familial encephalopathy with neuroserpin inclusion bodies",
|
| 643 |
+
"641": "familial erythrocytosis",
|
| 644 |
+
"642": "familial exudative vitreoretinopathy",
|
| 645 |
+
"643": "familial glucocorticoid deficiency",
|
| 646 |
+
"644": "familial hdl deficiency",
|
| 647 |
+
"645": "familial hemiplegic migraine",
|
| 648 |
+
"646": "familial hemophagocytic lymphohistiocytosis",
|
| 649 |
+
"647": "familial hyperaldosteronism",
|
| 650 |
+
"648": "familial hypercholesterolemia",
|
| 651 |
+
"649": "familial hypertrophic cardiomyopathy",
|
| 652 |
+
"650": "familial hypobetalipoproteinemia",
|
| 653 |
+
"651": "familial idiopathic basal ganglia calcification",
|
| 654 |
+
"652": "familial isolated hyperparathyroidism",
|
| 655 |
+
"653": "familial isolated pituitary adenoma",
|
| 656 |
+
"654": "familial lipoprotein lipase deficiency",
|
| 657 |
+
"655": "familial male limited precocious puberty",
|
| 658 |
+
"656": "familial mediterranean fever",
|
| 659 |
+
"657": "familial osteochondritis dissecans",
|
| 660 |
+
"658": "familial paroxysmal kinesigenic dyskinesia",
|
| 661 |
+
"659": "familial paroxysmal nonkinesigenic dyskinesia",
|
| 662 |
+
"660": "familial periodic paralyses",
|
| 663 |
+
"661": "familial pityriasis rubra pilaris",
|
| 664 |
+
"662": "familial porencephaly",
|
| 665 |
+
"663": "familial restrictive cardiomyopathy",
|
| 666 |
+
"664": "familial thoracic aortic aneurysm and dissection",
|
| 667 |
+
"665": "fanconi anemia",
|
| 668 |
+
"666": "farber lipogranulomatosis",
|
| 669 |
+
"667": "farber's disease",
|
| 670 |
+
"668": "fatal familial insomnia",
|
| 671 |
+
"669": "fatty acid hydroxylase associated neurodegeneration",
|
| 672 |
+
"670": "febrile seizures",
|
| 673 |
+
"671": "febrile ulceronecrotic mucha habermann disease",
|
| 674 |
+
"672": "fecal incontinence",
|
| 675 |
+
"673": "feingold syndrome",
|
| 676 |
+
"674": "felty's syndrome",
|
| 677 |
+
"675": "fg syndrome",
|
| 678 |
+
"676": "fibrochondrogenesis",
|
| 679 |
+
"677": "fibrodysplasia ossificans progressiva",
|
| 680 |
+
"678": "fibrolamellar carcinoma",
|
| 681 |
+
"679": "fibromuscular dysplasia",
|
| 682 |
+
"680": "fibronectin glomerulopathy",
|
| 683 |
+
"681": "fibrous dysplasia",
|
| 684 |
+
"682": "financial help for diabetes care",
|
| 685 |
+
"683": "fine lubinsky syndrome",
|
| 686 |
+
"684": "fish eye disease",
|
| 687 |
+
"685": "floating harbor syndrome",
|
| 688 |
+
"686": "florid cemento osseous dysplasia",
|
| 689 |
+
"687": "focal dermal hypoplasia",
|
| 690 |
+
"688": "foodborne illnesses",
|
| 691 |
+
"689": "foot drop",
|
| 692 |
+
"690": "fowler's syndrome",
|
| 693 |
+
"691": "foxg1 syndrome",
|
| 694 |
+
"692": "fragile x associated primary ovarian insufficiency",
|
| 695 |
+
"693": "fragile x associated tremor/ataxia syndrome",
|
| 696 |
+
"694": "fragile x syndrome",
|
| 697 |
+
"695": "fragile xe syndrome",
|
| 698 |
+
"696": "fraser syndrome",
|
| 699 |
+
"697": "frasier syndrome",
|
| 700 |
+
"698": "freeman sheldon syndrome",
|
| 701 |
+
"699": "freiberg's disease",
|
| 702 |
+
"700": "friedreich ataxia",
|
| 703 |
+
"701": "friedreich's ataxia",
|
| 704 |
+
"702": "froelich syndrome",
|
| 705 |
+
"703": "frontal fibrosing alopecia",
|
| 706 |
+
"704": "frontometaphyseal dysplasia",
|
| 707 |
+
"705": "frontonasal dysplasia",
|
| 708 |
+
"706": "frontotemporal dementia",
|
| 709 |
+
"707": "frontotemporal dementia with parkinsonism 17",
|
| 710 |
+
"708": "fryns syndrome",
|
| 711 |
+
"709": "fuchs endothelial dystrophy",
|
| 712 |
+
"710": "fucosidosis",
|
| 713 |
+
"711": "fukuyama congenital muscular dystrophy",
|
| 714 |
+
"712": "fumarase deficiency",
|
| 715 |
+
"713": "galactosemia",
|
| 716 |
+
"714": "galactosialidosis",
|
| 717 |
+
"715": "gallbladder cancer",
|
| 718 |
+
"716": "galloway mowat syndrome",
|
| 719 |
+
"717": "gallstones",
|
| 720 |
+
"718": "gamma heavy chain disease",
|
| 721 |
+
"719": "gardner diamond syndrome",
|
| 722 |
+
"720": "gardner syndrome",
|
| 723 |
+
"721": "gas in the digestive tract",
|
| 724 |
+
"722": "gastritis",
|
| 725 |
+
"723": "gastrointestinal carcinoid tumors",
|
| 726 |
+
"724": "gastrointestinal stromal tumor",
|
| 727 |
+
"725": "gastrointestinal stromal tumors",
|
| 728 |
+
"726": "gastroparesis",
|
| 729 |
+
"727": "gaucher disease",
|
| 730 |
+
"728": "geleophysic dysplasia",
|
| 731 |
+
"729": "generalized arterial calcification of infancy",
|
| 732 |
+
"730": "generalized gangliosidoses",
|
| 733 |
+
"731": "geniospasm",
|
| 734 |
+
"732": "genitopatellar syndrome",
|
| 735 |
+
"733": "geographic tongue",
|
| 736 |
+
"734": "gerstmann straussler scheinker disease",
|
| 737 |
+
"735": "gerstmann's syndrome",
|
| 738 |
+
"736": "gestational trophoblastic disease",
|
| 739 |
+
"737": "ghosal hematodiaphyseal dysplasia",
|
| 740 |
+
"738": "giant axonal neuropathy",
|
| 741 |
+
"739": "giant congenital melanocytic nevus",
|
| 742 |
+
"740": "gilbert syndrome",
|
| 743 |
+
"741": "gillespie syndrome",
|
| 744 |
+
"742": "gitelman syndrome",
|
| 745 |
+
"743": "glanzmann thrombasthenia",
|
| 746 |
+
"744": "glass chapman hockley syndrome",
|
| 747 |
+
"745": "glaucoma",
|
| 748 |
+
"746": "glioblastoma",
|
| 749 |
+
"747": "globozoospermia",
|
| 750 |
+
"748": "glomerular diseases",
|
| 751 |
+
"749": "glossopharyngeal neuralgia",
|
| 752 |
+
"750": "glucose 6 phosphate dehydrogenase deficiency",
|
| 753 |
+
"751": "glucose galactose malabsorption",
|
| 754 |
+
"752": "glucose phosphate isomerase deficiency",
|
| 755 |
+
"753": "glucose transporter type 1 deficiency syndrome",
|
| 756 |
+
"754": "glut1 deficiency syndrome",
|
| 757 |
+
"755": "glutamate formiminotransferase deficiency",
|
| 758 |
+
"756": "glutaric acidemia type i",
|
| 759 |
+
"757": "glutaric acidemia type ii",
|
| 760 |
+
"758": "glutathione synthetase deficiency",
|
| 761 |
+
"759": "glycine encephalopathy",
|
| 762 |
+
"760": "glycogen storage disease type 0",
|
| 763 |
+
"761": "glycogen storage disease type 13",
|
| 764 |
+
"762": "glycogen storage disease type 4",
|
| 765 |
+
"763": "glycogen storage disease type i",
|
| 766 |
+
"764": "glycogen storage disease type iii",
|
| 767 |
+
"765": "glycogen storage disease type iv",
|
| 768 |
+
"766": "glycogen storage disease type ix",
|
| 769 |
+
"767": "glycogen storage disease type v",
|
| 770 |
+
"768": "glycogen storage disease type vi",
|
| 771 |
+
"769": "glycogen storage disease type vii",
|
| 772 |
+
"770": "gm1 gangliosidosis",
|
| 773 |
+
"771": "gm2 gangliosidosis, ab variant",
|
| 774 |
+
"772": "gm3 synthase deficiency",
|
| 775 |
+
"773": "gnathodiaphyseal dysplasia",
|
| 776 |
+
"774": "goodpasture syndrome",
|
| 777 |
+
"775": "gorlin syndrome",
|
| 778 |
+
"776": "gout",
|
| 779 |
+
"777": "gracile syndrome",
|
| 780 |
+
"778": "granuloma annulare",
|
| 781 |
+
"779": "granulomatosis with polyangiitis",
|
| 782 |
+
"780": "graves disease",
|
| 783 |
+
"781": "graves' disease",
|
| 784 |
+
"782": "gray platelet syndrome",
|
| 785 |
+
"783": "greenberg dysplasia",
|
| 786 |
+
"784": "greig cephalopolysyndactyly syndrome",
|
| 787 |
+
"785": "griscelli syndrome",
|
| 788 |
+
"786": "grn related frontotemporal dementia",
|
| 789 |
+
"787": "growth failure in children with chronic kidney disease",
|
| 790 |
+
"788": "guanidinoacetate methyltransferase deficiency",
|
| 791 |
+
"789": "guillain barr syndrome",
|
| 792 |
+
"790": "gum (periodontal) disease",
|
| 793 |
+
"791": "gyrate atrophy of the choroid and retina",
|
| 794 |
+
"792": "hailey hailey disease",
|
| 795 |
+
"793": "hairy cell leukemia",
|
| 796 |
+
"794": "hajdu cheney syndrome",
|
| 797 |
+
"795": "hallermann streiff syndrome",
|
| 798 |
+
"796": "hand foot genital syndrome",
|
| 799 |
+
"797": "hanhart syndrome",
|
| 800 |
+
"798": "hantavirus",
|
| 801 |
+
"799": "harlequin ichthyosis",
|
| 802 |
+
"800": "hashimoto thyroiditis",
|
| 803 |
+
"801": "hashimoto's disease",
|
| 804 |
+
"802": "hashimoto's encephalitis",
|
| 805 |
+
"803": "hashimoto's syndrome",
|
| 806 |
+
"804": "head and neck squamous cell carcinoma",
|
| 807 |
+
"805": "headache",
|
| 808 |
+
"806": "hearing loss",
|
| 809 |
+
"807": "heart attack",
|
| 810 |
+
"808": "heart block",
|
| 811 |
+
"809": "heart disease in women",
|
| 812 |
+
"810": "heart failure",
|
| 813 |
+
"811": "heart murmur",
|
| 814 |
+
"812": "heart palpitations",
|
| 815 |
+
"813": "heart valve disease",
|
| 816 |
+
"814": "hemangiopericytoma",
|
| 817 |
+
"815": "hematuria (blood in the urine)",
|
| 818 |
+
"816": "hemicrania continua",
|
| 819 |
+
"817": "hemifacial microsomia",
|
| 820 |
+
"818": "hemifacial spasm",
|
| 821 |
+
"819": "hemochromatosis",
|
| 822 |
+
"820": "hemoglobin e disease",
|
| 823 |
+
"821": "hemolytic anemia",
|
| 824 |
+
"822": "hemolytic uremic syndrome in children",
|
| 825 |
+
"823": "hemophagocytic lymphohistiocytosis",
|
| 826 |
+
"824": "hemophilia",
|
| 827 |
+
"825": "hemorrhoids",
|
| 828 |
+
"826": "hendra virus disease (hev)",
|
| 829 |
+
"827": "hennekam syndrome",
|
| 830 |
+
"828": "henoch schnlein purpura",
|
| 831 |
+
"829": "henoch schonlein purpura",
|
| 832 |
+
"830": "hepatic lipase deficiency",
|
| 833 |
+
"831": "hepatic veno occlusive disease with immunodeficiency",
|
| 834 |
+
"832": "hepatitis b: what asian and pacific islander americans need to know",
|
| 835 |
+
"833": "hereditary angioedema",
|
| 836 |
+
"834": "hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome",
|
| 837 |
+
"835": "hereditary antithrombin deficiency",
|
| 838 |
+
"836": "hereditary cerebral amyloid angiopathy",
|
| 839 |
+
"837": "hereditary cerebral hemorrhage with amyloidosis",
|
| 840 |
+
"838": "hereditary diffuse gastric cancer",
|
| 841 |
+
"839": "hereditary diffuse leukoencephalopathy with spheroids",
|
| 842 |
+
"840": "hereditary endotheliopathy, retinopathy, nephropathy, and stroke",
|
| 843 |
+
"841": "hereditary folate malabsorption",
|
| 844 |
+
"842": "hereditary fructose intolerance",
|
| 845 |
+
"843": "hereditary hemochromatosis",
|
| 846 |
+
"844": "hereditary hemorrhagic telangiectasia",
|
| 847 |
+
"845": "hereditary hyperekplexia",
|
| 848 |
+
"846": "hereditary hypophosphatemic rickets",
|
| 849 |
+
"847": "hereditary leiomyomatosis and renal cell cancer",
|
| 850 |
+
"848": "hereditary lymphedema type ii",
|
| 851 |
+
"849": "hereditary multiple osteochondromas",
|
| 852 |
+
"850": "hereditary myopathy with early respiratory failure",
|
| 853 |
+
"851": "hereditary neuralgic amyotrophy",
|
| 854 |
+
"852": "hereditary neuropathies",
|
| 855 |
+
"853": "hereditary neuropathy with liability to pressure palsies",
|
| 856 |
+
"854": "hereditary pancreatitis",
|
| 857 |
+
"855": "hereditary paraganglioma pheochromocytoma",
|
| 858 |
+
"856": "hereditary sensory and autonomic neuropathy type ie",
|
| 859 |
+
"857": "hereditary sensory and autonomic neuropathy type ii",
|
| 860 |
+
"858": "hereditary sensory and autonomic neuropathy type v",
|
| 861 |
+
"859": "hereditary sensory neuropathy type 1",
|
| 862 |
+
"860": "hereditary sensory neuropathy type ia",
|
| 863 |
+
"861": "hereditary sensory neuropathy type ie",
|
| 864 |
+
"862": "hereditary spastic paraplegia",
|
| 865 |
+
"863": "hereditary spherocytosis",
|
| 866 |
+
"864": "hereditary xanthinuria",
|
| 867 |
+
"865": "hermansky pudlak syndrome",
|
| 868 |
+
"866": "herpes zoster oticus",
|
| 869 |
+
"867": "heterotaxy syndrome",
|
| 870 |
+
"868": "hidradenitis suppurativa",
|
| 871 |
+
"869": "high blood cholesterol",
|
| 872 |
+
"870": "high blood pressure",
|
| 873 |
+
"871": "high blood pressure and kidney disease",
|
| 874 |
+
"872": "hirschsprung disease",
|
| 875 |
+
"873": "hirschsprung's disease",
|
| 876 |
+
"874": "histidinemia",
|
| 877 |
+
"875": "histiocytosis lymphadenopathy plus syndrome",
|
| 878 |
+
"876": "holes in the heart",
|
| 879 |
+
"877": "holocarboxylase synthetase deficiency",
|
| 880 |
+
"878": "holoprosencephaly",
|
| 881 |
+
"879": "holt oram syndrome",
|
| 882 |
+
"880": "homocystinuria",
|
| 883 |
+
"881": "horizontal gaze palsy with progressive scoliosis",
|
| 884 |
+
"882": "horner syndrome",
|
| 885 |
+
"883": "human t cell leukemia virus type 1",
|
| 886 |
+
"884": "human t cell leukemia virus type 2",
|
| 887 |
+
"885": "huntington disease",
|
| 888 |
+
"886": "huntington disease like syndrome",
|
| 889 |
+
"887": "huntington's disease",
|
| 890 |
+
"888": "hutchinson gilford progeria syndrome",
|
| 891 |
+
"889": "hydranencephaly",
|
| 892 |
+
"890": "hydrocephalus",
|
| 893 |
+
"891": "hydrocephalus due to congenital stenosis of aqueduct of sylvius",
|
| 894 |
+
"892": "hydromyelia",
|
| 895 |
+
"893": "hydrops, ectopic calcification, moth eaten skeletal dysplasia",
|
| 896 |
+
"894": "hyper igd syndrome",
|
| 897 |
+
"895": "hypercholesterolemia",
|
| 898 |
+
"896": "hyperferritinemia cataract syndrome",
|
| 899 |
+
"897": "hyperkalemic periodic paralysis",
|
| 900 |
+
"898": "hyperlysinemia",
|
| 901 |
+
"899": "hypermanganesemia with dystonia, polycythemia, and cirrhosis",
|
| 902 |
+
"900": "hypermethioninemia",
|
| 903 |
+
"901": "hyperparathyroidism jaw tumor syndrome",
|
| 904 |
+
"902": "hyperphosphatemic familial tumoral calcinosis",
|
| 905 |
+
"903": "hyperprolinemia",
|
| 906 |
+
"904": "hypersensitivity pneumonitis",
|
| 907 |
+
"905": "hypersomnia",
|
| 908 |
+
"906": "hyperthyroidism",
|
| 909 |
+
"907": "hypertonia",
|
| 910 |
+
"908": "hypochondrogenesis",
|
| 911 |
+
"909": "hypochondroplasia",
|
| 912 |
+
"910": "hypochromic microcytic anemia with iron overload",
|
| 913 |
+
"911": "hypoglycemia",
|
| 914 |
+
"912": "hypohidrotic ectodermal dysplasia",
|
| 915 |
+
"913": "hypokalemic periodic paralysis",
|
| 916 |
+
"914": "hypomagnesemia with secondary hypocalcemia",
|
| 917 |
+
"915": "hypomyelination and congenital cataract",
|
| 918 |
+
"916": "hypomyelination with atrophy of basal ganglia and cerebellum",
|
| 919 |
+
"917": "hypopharyngeal cancer",
|
| 920 |
+
"918": "hypophosphatasia",
|
| 921 |
+
"919": "hypophosphatemic rickets",
|
| 922 |
+
"920": "hypotension",
|
| 923 |
+
"921": "hypothalamic dysfunction",
|
| 924 |
+
"922": "hypothyroidism",
|
| 925 |
+
"923": "hypotonia",
|
| 926 |
+
"924": "hystrix like ichthyosis with deafness",
|
| 927 |
+
"925": "i can lower my risk for type 2 diabetes: a guide for american indians",
|
| 928 |
+
"926": "ibids syndrome",
|
| 929 |
+
"927": "ichthyosis with confetti",
|
| 930 |
+
"928": "idiopathic inflammatory myopathy",
|
| 931 |
+
"929": "idiopathic juxtafoveal retinal telangiectasia",
|
| 932 |
+
"930": "idiopathic pulmonary fibrosis",
|
| 933 |
+
"931": "iga nephropathy",
|
| 934 |
+
"932": "imerslund grsbeck syndrome",
|
| 935 |
+
"933": "immune dysregulation, polyendocrinopathy, enteropathy, x linked syndrome",
|
| 936 |
+
"934": "immune thrombocytopenia",
|
| 937 |
+
"935": "immunodeficiency with hyper igm type 1",
|
| 938 |
+
"936": "inclusion body myopathy 2",
|
| 939 |
+
"937": "inclusion body myopathy with early onset paget disease and frontotemporal dementia",
|
| 940 |
+
"938": "inclusion body myositis",
|
| 941 |
+
"939": "incontinentia pigmenti",
|
| 942 |
+
"940": "indigestion",
|
| 943 |
+
"941": "infantile neuroaxonal dystrophy",
|
| 944 |
+
"942": "infantile neuronal ceroid lipofuscinosis",
|
| 945 |
+
"943": "infantile onset ascending hereditary spastic paralysis",
|
| 946 |
+
"944": "infantile onset spinocerebellar ataxia",
|
| 947 |
+
"945": "infantile refsum disease",
|
| 948 |
+
"946": "infantile spasms",
|
| 949 |
+
"947": "infantile systemic hyalinosis",
|
| 950 |
+
"948": "inflammatory myopathies",
|
| 951 |
+
"949": "inguinal hernia",
|
| 952 |
+
"950": "inherited thyroxine binding globulin deficiency",
|
| 953 |
+
"951": "iniencephaly",
|
| 954 |
+
"952": "insomnia",
|
| 955 |
+
"953": "insulin resistance and prediabetes",
|
| 956 |
+
"954": "intestinal pseudo obstruction",
|
| 957 |
+
"955": "intrahepatic cholestasis of pregnancy",
|
| 958 |
+
"956": "intranuclear rod myopathy",
|
| 959 |
+
"957": "intraocular (uveal) melanoma",
|
| 960 |
+
"958": "intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies",
|
| 961 |
+
"959": "irak 4 deficiency",
|
| 962 |
+
"960": "iridocorneal endothelial syndrome",
|
| 963 |
+
"961": "iron deficiency anemia",
|
| 964 |
+
"962": "iron refractory iron deficiency anemia",
|
| 965 |
+
"963": "irritable bowel syndrome in children",
|
| 966 |
+
"964": "isaacs' syndrome",
|
| 967 |
+
"965": "isobutyryl coa dehydrogenase deficiency",
|
| 968 |
+
"966": "isodicentric chromosome 15 syndrome",
|
| 969 |
+
"967": "isolated duane retraction syndrome",
|
| 970 |
+
"968": "isolated ectopia lentis",
|
| 971 |
+
"969": "isolated growth hormone deficiency",
|
| 972 |
+
"970": "isolated lissencephaly sequence",
|
| 973 |
+
"971": "isolated pierre robin sequence",
|
| 974 |
+
"972": "isovaleric acidemia",
|
| 975 |
+
"973": "jackson weiss syndrome",
|
| 976 |
+
"974": "jacobsen syndrome",
|
| 977 |
+
"975": "jejunal atresia",
|
| 978 |
+
"976": "jervell and lange nielsen syndrome",
|
| 979 |
+
"977": "jones syndrome",
|
| 980 |
+
"978": "joubert syndrome",
|
| 981 |
+
"979": "junctional epidermolysis bullosa",
|
| 982 |
+
"980": "juvenile amyotrophic lateral sclerosis",
|
| 983 |
+
"981": "juvenile batten disease",
|
| 984 |
+
"982": "juvenile huntington disease",
|
| 985 |
+
"983": "juvenile hyaline fibromatosis",
|
| 986 |
+
"984": "juvenile idiopathic arthritis",
|
| 987 |
+
"985": "juvenile myelomonocytic leukemia",
|
| 988 |
+
"986": "juvenile myoclonic epilepsy",
|
| 989 |
+
"987": "juvenile paget disease",
|
| 990 |
+
"988": "juvenile polyposis syndrome",
|
| 991 |
+
"989": "juvenile primary lateral sclerosis",
|
| 992 |
+
"990": "juvenile primary osteoporosis",
|
| 993 |
+
"991": "juvenile retinoschisis",
|
| 994 |
+
"992": "kabuki syndrome",
|
| 995 |
+
"993": "kallmann syndrome",
|
| 996 |
+
"994": "kaposi sarcoma",
|
| 997 |
+
"995": "kawasaki disease",
|
| 998 |
+
"996": "kawasaki syndrome",
|
| 999 |
+
"997": "kbg syndrome",
|
| 1000 |
+
"998": "kearns sayre syndrome",
|
| 1001 |
+
"999": "kennedy's disease",
|
| 1002 |
+
"1000": "keratitis ichthyosis deafness syndrome",
|
| 1003 |
+
"1001": "keratoderma with woolly hair",
|
| 1004 |
+
"1002": "kidney disease",
|
| 1005 |
+
"1003": "kidney disease of diabetes",
|
| 1006 |
+
"1004": "kidney dysplasia",
|
| 1007 |
+
"1005": "kidney failure: choosing a treatment that's right for you",
|
| 1008 |
+
"1006": "kidney failure: eat right to feel right on hemodialysis",
|
| 1009 |
+
"1007": "kidney stones in adults",
|
| 1010 |
+
"1008": "kidney stones in children",
|
| 1011 |
+
"1009": "kienbock's disease",
|
| 1012 |
+
"1010": "klebsiella infection",
|
| 1013 |
+
"1011": "kleefstra syndrome",
|
| 1014 |
+
"1012": "kleine levin syndrome",
|
| 1015 |
+
"1013": "klinefelter syndrome",
|
| 1016 |
+
"1014": "klippel feil syndrome",
|
| 1017 |
+
"1015": "klippel trenaunay syndrome",
|
| 1018 |
+
"1016": "klippel trenaunay syndrome (kts)",
|
| 1019 |
+
"1017": "klver bucy syndrome",
|
| 1020 |
+
"1018": "knee replacement",
|
| 1021 |
+
"1019": "kniest dysplasia",
|
| 1022 |
+
"1020": "knobloch syndrome",
|
| 1023 |
+
"1021": "konigsmark knox hussels syndrome",
|
| 1024 |
+
"1022": "koolen de vries syndrome",
|
| 1025 |
+
"1023": "krabbe disease",
|
| 1026 |
+
"1024": "kufs disease",
|
| 1027 |
+
"1025": "kuru",
|
| 1028 |
+
"1026": "kuskokwim syndrome",
|
| 1029 |
+
"1027": "kyasanur forest disease (kfd)",
|
| 1030 |
+
"1028": "kyrle disease",
|
| 1031 |
+
"1029": "l1 syndrome",
|
| 1032 |
+
"1030": "la crosse encephalitis",
|
| 1033 |
+
"1031": "lacrimo auriculo dento digital syndrome",
|
| 1034 |
+
"1032": "lactate dehydrogenase deficiency",
|
| 1035 |
+
"1033": "lactose intolerance",
|
| 1036 |
+
"1034": "lafora disease",
|
| 1037 |
+
"1035": "lafora progressive myoclonus epilepsy",
|
| 1038 |
+
"1036": "laing distal myopathy",
|
| 1039 |
+
"1037": "lama2 related muscular dystrophy",
|
| 1040 |
+
"1038": "lambert eaton myasthenic syndrome",
|
| 1041 |
+
"1039": "lamellar ichthyosis",
|
| 1042 |
+
"1040": "landau kleffner syndrome",
|
| 1043 |
+
"1041": "langer giedion syndrome",
|
| 1044 |
+
"1042": "langer mesomelic dysplasia",
|
| 1045 |
+
"1043": "langerhans cell histiocytosis",
|
| 1046 |
+
"1044": "laron syndrome",
|
| 1047 |
+
"1045": "larsen syndrome",
|
| 1048 |
+
"1046": "laryngeal cancer",
|
| 1049 |
+
"1047": "laryngeal cleft",
|
| 1050 |
+
"1048": "laryngo onycho cutaneous syndrome",
|
| 1051 |
+
"1049": "late infantile neuronal ceroid lipofuscinosis",
|
| 1052 |
+
"1050": "lattice corneal dystrophy type i",
|
| 1053 |
+
"1051": "lattice corneal dystrophy type ii",
|
| 1054 |
+
"1052": "learning disabilities",
|
| 1055 |
+
"1053": "leber congenital amaurosis",
|
| 1056 |
+
"1054": "leber hereditary optic neuropathy",
|
| 1057 |
+
"1055": "legg calv perthes disease",
|
| 1058 |
+
"1056": "legius syndrome",
|
| 1059 |
+
"1057": "leigh syndrome",
|
| 1060 |
+
"1058": "leigh's disease",
|
| 1061 |
+
"1059": "lemierre syndrome",
|
| 1062 |
+
"1060": "lennox gastaut syndrome",
|
| 1063 |
+
"1061": "lenz microphthalmia syndrome",
|
| 1064 |
+
"1062": "leptin receptor deficiency",
|
| 1065 |
+
"1063": "lesch nyhan syndrome",
|
| 1066 |
+
"1064": "leukemia",
|
| 1067 |
+
"1065": "leukocyte adhesion deficiency type 1",
|
| 1068 |
+
"1066": "leukodystrophy",
|
| 1069 |
+
"1067": "leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation",
|
| 1070 |
+
"1068": "leukoencephalopathy with vanishing white matter",
|
| 1071 |
+
"1069": "leukonychia totalis",
|
| 1072 |
+
"1070": "leydig cell hypoplasia",
|
| 1073 |
+
"1071": "li fraumeni syndrome",
|
| 1074 |
+
"1072": "lichen planus pigmentosus",
|
| 1075 |
+
"1073": "lichen sclerosus",
|
| 1076 |
+
"1074": "liddle syndrome",
|
| 1077 |
+
"1075": "limb girdle muscular dystrophy",
|
| 1078 |
+
"1076": "limbic encephalitis",
|
| 1079 |
+
"1077": "lip and oral cavity cancer",
|
| 1080 |
+
"1078": "lipedema",
|
| 1081 |
+
"1079": "lipodermatosclerosis",
|
| 1082 |
+
"1080": "lipoid proteinosis",
|
| 1083 |
+
"1081": "lissencephaly",
|
| 1084 |
+
"1082": "lissencephaly with cerebellar hypoplasia",
|
| 1085 |
+
"1083": "liver (hepatocellular) cancer",
|
| 1086 |
+
"1084": "localized scleroderma",
|
| 1087 |
+
"1085": "locked in syndrome",
|
| 1088 |
+
"1086": "loeys dietz syndrome",
|
| 1089 |
+
"1087": "loin pain hematuria syndrome",
|
| 1090 |
+
"1088": "long chain 3 hydroxyacyl coa dehydrogenase deficiency",
|
| 1091 |
+
"1089": "long qt syndrome",
|
| 1092 |
+
"1090": "low vision",
|
| 1093 |
+
"1091": "lowe syndrome",
|
| 1094 |
+
"1092": "lujan syndrome",
|
| 1095 |
+
"1093": "lujo hemorrhagic fever (luhf)",
|
| 1096 |
+
"1094": "lung cancer",
|
| 1097 |
+
"1095": "lupus",
|
| 1098 |
+
"1096": "lupus nephritis",
|
| 1099 |
+
"1097": "lymphangioleiomyomatosis",
|
| 1100 |
+
"1098": "lymphedema distichiasis syndrome",
|
| 1101 |
+
"1099": "lymphocytic choriomeningitis (lcm)",
|
| 1102 |
+
"1100": "lymphomatoid papulosis",
|
| 1103 |
+
"1101": "lynch syndrome",
|
| 1104 |
+
"1102": "lysinuric protein intolerance",
|
| 1105 |
+
"1103": "mabry syndrome",
|
| 1106 |
+
"1104": "machado joseph disease",
|
| 1107 |
+
"1105": "madelung disease",
|
| 1108 |
+
"1106": "maffucci syndrome",
|
| 1109 |
+
"1107": "mainzer saldino syndrome",
|
| 1110 |
+
"1108": "majeed syndrome",
|
| 1111 |
+
"1109": "mal de meleda",
|
| 1112 |
+
"1110": "male breast cancer",
|
| 1113 |
+
"1111": "malignant hyperthermia",
|
| 1114 |
+
"1112": "malignant migrating partial seizures of infancy",
|
| 1115 |
+
"1113": "malonyl coa decarboxylase deficiency",
|
| 1116 |
+
"1114": "mandibuloacral dysplasia",
|
| 1117 |
+
"1115": "mandibulofacial dysostosis with microcephaly",
|
| 1118 |
+
"1116": "manitoba oculotrichoanal syndrome",
|
| 1119 |
+
"1117": "mannose binding lectin deficiency",
|
| 1120 |
+
"1118": "mantle cell lymphoma",
|
| 1121 |
+
"1119": "maple syrup urine disease",
|
| 1122 |
+
"1120": "marburg hemorrhagic fever (marburg hf)",
|
| 1123 |
+
"1121": "marden walker syndrome",
|
| 1124 |
+
"1122": "marfan syndrome",
|
| 1125 |
+
"1123": "marine toxins",
|
| 1126 |
+
"1124": "marinesco sjgren syndrome",
|
| 1127 |
+
"1125": "mastocytic enterocolitis",
|
| 1128 |
+
"1126": "maternally inherited diabetes and deafness",
|
| 1129 |
+
"1127": "mayer rokitansky kster hauser syndrome",
|
| 1130 |
+
"1128": "mccune albright syndrome",
|
| 1131 |
+
"1129": "mckusick kaufman syndrome",
|
| 1132 |
+
"1130": "mcleod neuroacanthocytosis syndrome",
|
| 1133 |
+
"1131": "meckel syndrome",
|
| 1134 |
+
"1132": "mecp2 duplication syndrome",
|
| 1135 |
+
"1133": "mecp2 related severe neonatal encephalopathy",
|
| 1136 |
+
"1134": "medicare and continuing care",
|
| 1137 |
+
"1135": "medium chain acyl coa dehydrogenase deficiency",
|
| 1138 |
+
"1136": "medium chain acyl coenzyme a dehydrogenase deficiency",
|
| 1139 |
+
"1137": "medullary cystic kidney disease",
|
| 1140 |
+
"1138": "medullary cystic kidney disease type 1",
|
| 1141 |
+
"1139": "medullary sponge kidney",
|
| 1142 |
+
"1140": "meesmann corneal dystrophy",
|
| 1143 |
+
"1141": "megalencephalic leukoencephalopathy with subcortical cysts",
|
| 1144 |
+
"1142": "megalencephaly",
|
| 1145 |
+
"1143": "megalencephaly capillary malformation syndrome",
|
| 1146 |
+
"1144": "megdel syndrome",
|
| 1147 |
+
"1145": "meier gorlin syndrome",
|
| 1148 |
+
"1146": "meige disease",
|
| 1149 |
+
"1147": "melanoma",
|
| 1150 |
+
"1148": "melkersson rosenthal syndrome",
|
| 1151 |
+
"1149": "melnick needles syndrome",
|
| 1152 |
+
"1150": "menetrier disease",
|
| 1153 |
+
"1151": "meningitis and encephalitis",
|
| 1154 |
+
"1152": "menkes disease",
|
| 1155 |
+
"1153": "menkes syndrome",
|
| 1156 |
+
"1154": "meralgia paresthetica",
|
| 1157 |
+
"1155": "merkel cell carcinoma",
|
| 1158 |
+
"1156": "metabolic syndrome",
|
| 1159 |
+
"1157": "metachromatic leukodystrophy",
|
| 1160 |
+
"1158": "metastatic squamous neck cancer with occult primary",
|
| 1161 |
+
"1159": "metatropic dysplasia",
|
| 1162 |
+
"1160": "methemoglobinemia, beta globin type",
|
| 1163 |
+
"1161": "methylmalonic acidemia",
|
| 1164 |
+
"1162": "methylmalonic acidemia with homocystinuria",
|
| 1165 |
+
"1163": "mevalonate kinase deficiency",
|
| 1166 |
+
"1164": "microcephalic osteodysplastic primordial dwarfism type 1",
|
| 1167 |
+
"1165": "microcephalic osteodysplastic primordial dwarfism type ii",
|
| 1168 |
+
"1166": "microcephaly",
|
| 1169 |
+
"1167": "microcephaly capillary malformation syndrome",
|
| 1170 |
+
"1168": "microhydranencephaly",
|
| 1171 |
+
"1169": "microphthalmia",
|
| 1172 |
+
"1170": "microphthalmia with linear skin defects syndrome",
|
| 1173 |
+
"1171": "microscopic colitis: collagenous colitis and lymphocytic colitis",
|
| 1174 |
+
"1172": "microscopic polyangiitis",
|
| 1175 |
+
"1173": "microvillus inclusion disease",
|
| 1176 |
+
"1174": "migraine",
|
| 1177 |
+
"1175": "miller dieker syndrome",
|
| 1178 |
+
"1176": "miller fisher syndrome",
|
| 1179 |
+
"1177": "miller syndrome",
|
| 1180 |
+
"1178": "milroy disease",
|
| 1181 |
+
"1179": "mineral and bone disorder in chronic kidney disease",
|
| 1182 |
+
"1180": "mitochondrial complex ii deficiency",
|
| 1183 |
+
"1181": "mitochondrial complex iii deficiency",
|
| 1184 |
+
"1182": "mitochondrial encephalomyopathy lactic acidosis and stroke like episodes",
|
| 1185 |
+
"1183": "mitochondrial encephalomyopathy, lactic acidosis, and stroke like episodes",
|
| 1186 |
+
"1184": "mitochondrial genetic disorders",
|
| 1187 |
+
"1185": "mitochondrial membrane protein associated neurodegeneration",
|
| 1188 |
+
"1186": "mitochondrial myopathy",
|
| 1189 |
+
"1187": "mitochondrial neurogastrointestinal encephalopathy disease",
|
| 1190 |
+
"1188": "mitochondrial neurogastrointestinal encephalopathy syndrome",
|
| 1191 |
+
"1189": "mitochondrial trifunctional protein deficiency",
|
| 1192 |
+
"1190": "mitral valve prolapse",
|
| 1193 |
+
"1191": "mixed connective tissue disease",
|
| 1194 |
+
"1192": "miyoshi myopathy",
|
| 1195 |
+
"1193": "mnire's disease",
|
| 1196 |
+
"1194": "mntriers disease",
|
| 1197 |
+
"1195": "moebius syndrome",
|
| 1198 |
+
"1196": "molybdenum cofactor deficiency",
|
| 1199 |
+
"1197": "mondini dysplasia",
|
| 1200 |
+
"1198": "monilethrix",
|
| 1201 |
+
"1199": "monogenic forms of diabetes: neonatal diabetes mellitus and maturity onset diabetes of the young",
|
| 1202 |
+
"1200": "monomelic amyotrophy",
|
| 1203 |
+
"1201": "mosaic trisomy 14",
|
| 1204 |
+
"1202": "mosaic trisomy 9",
|
| 1205 |
+
"1203": "motor neuron diseases",
|
| 1206 |
+
"1204": "mowat wilson syndrome",
|
| 1207 |
+
"1205": "moyamoya disease",
|
| 1208 |
+
"1206": "mpv17 related hepatocerebral mitochondrial dna depletion syndrome",
|
| 1209 |
+
"1207": "mthfr gene mutation",
|
| 1210 |
+
"1208": "muckle wells syndrome",
|
| 1211 |
+
"1209": "mucolipidoses",
|
| 1212 |
+
"1210": "mucolipidosis ii alpha/beta",
|
| 1213 |
+
"1211": "mucolipidosis iii alpha/beta",
|
| 1214 |
+
"1212": "mucolipidosis iii gamma",
|
| 1215 |
+
"1213": "mucolipidosis type iv",
|
| 1216 |
+
"1214": "mucopolysaccharidoses",
|
| 1217 |
+
"1215": "mucopolysaccharidosis type i",
|
| 1218 |
+
"1216": "mucopolysaccharidosis type ii",
|
| 1219 |
+
"1217": "mucopolysaccharidosis type iii",
|
| 1220 |
+
"1218": "mucopolysaccharidosis type iv",
|
| 1221 |
+
"1219": "mucopolysaccharidosis type vi",
|
| 1222 |
+
"1220": "mucopolysaccharidosis type vii",
|
| 1223 |
+
"1221": "muenke syndrome",
|
| 1224 |
+
"1222": "muir torre syndrome",
|
| 1225 |
+
"1223": "multi infarct dementia",
|
| 1226 |
+
"1224": "multicentric castleman disease",
|
| 1227 |
+
"1225": "multicentric osteolysis, nodulosis, and arthropathy",
|
| 1228 |
+
"1226": "multifocal choroiditis",
|
| 1229 |
+
"1227": "multifocal motor neuropathy",
|
| 1230 |
+
"1228": "multiminicore disease",
|
| 1231 |
+
"1229": "multiple cutaneous and mucosal venous malformations",
|
| 1232 |
+
"1230": "multiple endocrine neoplasia",
|
| 1233 |
+
"1231": "multiple endocrine neoplasia type 1",
|
| 1234 |
+
"1232": "multiple epiphyseal dysplasia",
|
| 1235 |
+
"1233": "multiple familial trichoepithelioma",
|
| 1236 |
+
"1234": "multiple lentigines syndrome",
|
| 1237 |
+
"1235": "multiple mitochondrial dysfunctions syndrome",
|
| 1238 |
+
"1236": "multiple myeloma",
|
| 1239 |
+
"1237": "multiple pterygium syndrome",
|
| 1240 |
+
"1238": "multiple pterygium syndrome escobar type",
|
| 1241 |
+
"1239": "multiple sclerosis",
|
| 1242 |
+
"1240": "multiple sulfatase deficiency",
|
| 1243 |
+
"1241": "multiple system atrophy",
|
| 1244 |
+
"1242": "multiple system atrophy with orthostatic hypotension",
|
| 1245 |
+
"1243": "muscular dystrophy",
|
| 1246 |
+
"1244": "myasthenia gravis",
|
| 1247 |
+
"1245": "mycosis fungoides",
|
| 1248 |
+
"1246": "mycosis fungoides and the szary syndrome",
|
| 1249 |
+
"1247": "myd88 deficiency",
|
| 1250 |
+
"1248": "myelodysplastic syndromes",
|
| 1251 |
+
"1249": "myelodysplastic/ myeloproliferative neoplasms",
|
| 1252 |
+
"1250": "myh7 related scapuloperoneal myopathy",
|
| 1253 |
+
"1251": "myh9 related disorder",
|
| 1254 |
+
"1252": "myhre syndrome",
|
| 1255 |
+
"1253": "myoclonic epilepsy myopathy sensory ataxia",
|
| 1256 |
+
"1254": "myoclonic epilepsy with ragged red fibers",
|
| 1257 |
+
"1255": "myoclonus",
|
| 1258 |
+
"1256": "myoclonus dystonia",
|
| 1259 |
+
"1257": "myofibrillar myopathy",
|
| 1260 |
+
"1258": "myopathy",
|
| 1261 |
+
"1259": "myopathy with deficiency of iron sulfur cluster assembly enzyme",
|
| 1262 |
+
"1260": "myosin storage myopathy",
|
| 1263 |
+
"1261": "myostatin related muscle hypertrophy",
|
| 1264 |
+
"1262": "myotonia",
|
| 1265 |
+
"1263": "myotonia congenita",
|
| 1266 |
+
"1264": "myotonic dystrophy",
|
| 1267 |
+
"1265": "myotonic dystrophy type 1",
|
| 1268 |
+
"1266": "n acetylglutamate synthase deficiency",
|
| 1269 |
+
"1267": "naegeli franceschetti jadassohn syndrome/dermatopathia pigmentosa reticularis",
|
| 1270 |
+
"1268": "naegeli syndrome",
|
| 1271 |
+
"1269": "nager syndrome",
|
| 1272 |
+
"1270": "nail patella syndrome",
|
| 1273 |
+
"1271": "nakajo nishimura syndrome",
|
| 1274 |
+
"1272": "nan",
|
| 1275 |
+
"1273": "nance horan syndrome",
|
| 1276 |
+
"1274": "narcolepsy",
|
| 1277 |
+
"1275": "nasopharyngeal cancer",
|
| 1278 |
+
"1276": "national hormone and pituitary program (nhpp): information for people treated with pituitary human growth hormone (comprehensive report)",
|
| 1279 |
+
"1277": "necrotizing fasciitis",
|
| 1280 |
+
"1278": "nemaline myopathy",
|
| 1281 |
+
"1279": "neonatal onset multisystem inflammatory disease",
|
| 1282 |
+
"1280": "neonatal progeroid syndrome",
|
| 1283 |
+
"1281": "nephrocalcinosis",
|
| 1284 |
+
"1282": "nephrogenic diabetes insipidus",
|
| 1285 |
+
"1283": "nephronophthisis",
|
| 1286 |
+
"1284": "nephrotic syndrome in adults",
|
| 1287 |
+
"1285": "nerve disease and bladder control",
|
| 1288 |
+
"1286": "netherton syndrome",
|
| 1289 |
+
"1287": "neuroacanthocytosis",
|
| 1290 |
+
"1288": "neuroaxonal dystrophy",
|
| 1291 |
+
"1289": "neuroblastoma",
|
| 1292 |
+
"1290": "neurodegeneration with brain iron accumulation",
|
| 1293 |
+
"1291": "neuroferritinopathy",
|
| 1294 |
+
"1292": "neurofibromatosis",
|
| 1295 |
+
"1293": "neurofibromatosis type 1",
|
| 1296 |
+
"1294": "neurofibromatosis type 2",
|
| 1297 |
+
"1295": "neurohypophyseal diabetes insipidus",
|
| 1298 |
+
"1296": "neuroleptic malignant syndrome",
|
| 1299 |
+
"1297": "neurological complications of aids",
|
| 1300 |
+
"1298": "neurological consequences of cytomegalovirus infection",
|
| 1301 |
+
"1299": "neurological sequelae of lupus",
|
| 1302 |
+
"1300": "neuromyelitis optica",
|
| 1303 |
+
"1301": "neuronal migration disorders",
|
| 1304 |
+
"1302": "neuropathy, ataxia, and retinitis pigmentosa",
|
| 1305 |
+
"1303": "neurosarcoidosis",
|
| 1306 |
+
"1304": "neurosyphilis",
|
| 1307 |
+
"1305": "neurotoxicity",
|
| 1308 |
+
"1306": "neutral lipid storage disease with myopathy",
|
| 1309 |
+
"1307": "nevoid basal cell carcinoma syndrome",
|
| 1310 |
+
"1308": "nicolaides baraitser syndrome",
|
| 1311 |
+
"1309": "niemann pick disease",
|
| 1312 |
+
"1310": "nijmegen breakage syndrome",
|
| 1313 |
+
"1311": "nocardiosis",
|
| 1314 |
+
"1312": "non classic congenital adrenal hyperplasia due to 21 hydroxylase deficiency",
|
| 1315 |
+
"1313": "non small cell lung cancer",
|
| 1316 |
+
"1314": "nonalcoholic steatohepatitis",
|
| 1317 |
+
"1315": "nonbullous congenital ichthyosiform erythroderma",
|
| 1318 |
+
"1316": "nonspherocytic hemolytic anemia due to hexokinase deficiency",
|
| 1319 |
+
"1317": "nonsyndromic aplasia cutis congenita",
|
| 1320 |
+
"1318": "nonsyndromic hearing loss",
|
| 1321 |
+
"1319": "nonsyndromic holoprosencephaly",
|
| 1322 |
+
"1320": "nonsyndromic paraganglioma",
|
| 1323 |
+
"1321": "noonan syndrome",
|
| 1324 |
+
"1322": "normal pressure hydrocephalus",
|
| 1325 |
+
"1323": "norrie disease",
|
| 1326 |
+
"1324": "north american indian childhood cirrhosis",
|
| 1327 |
+
"1325": "northern epilepsy",
|
| 1328 |
+
"1326": "norum disease",
|
| 1329 |
+
"1327": "nutrition for advanced chronic kidney disease in adults",
|
| 1330 |
+
"1328": "nutrition for early chronic kidney disease in adults",
|
| 1331 |
+
"1329": "obesity hypoventilation syndrome",
|
| 1332 |
+
"1330": "occipital neuralgia",
|
| 1333 |
+
"1331": "ochoa syndrome",
|
| 1334 |
+
"1332": "ocular albinism",
|
| 1335 |
+
"1333": "oculocutaneous albinism",
|
| 1336 |
+
"1334": "oculodentodigital dysplasia",
|
| 1337 |
+
"1335": "oculofaciocardiodental syndrome",
|
| 1338 |
+
"1336": "oculopharyngeal muscular dystrophy",
|
| 1339 |
+
"1337": "ohdo syndrome, maat kievit brunner type",
|
| 1340 |
+
"1338": "ohdo syndrome, say barber biesecker young simpson variant",
|
| 1341 |
+
"1339": "ohtahara syndrome",
|
| 1342 |
+
"1340": "olivopontocerebellar atrophy",
|
| 1343 |
+
"1341": "ollier disease",
|
| 1344 |
+
"1342": "omenn syndrome",
|
| 1345 |
+
"1343": "omsk hemorrhagic fever (ohf)",
|
| 1346 |
+
"1344": "ophthalmo acromelic syndrome",
|
| 1347 |
+
"1345": "opitz g/bbb syndrome",
|
| 1348 |
+
"1346": "opsoclonus myoclonus",
|
| 1349 |
+
"1347": "optic atrophy type 1",
|
| 1350 |
+
"1348": "oral cavity and oropharyngeal cancer",
|
| 1351 |
+
"1349": "oral facial digital syndrome",
|
| 1352 |
+
"1350": "ornithine transcarbamylase deficiency",
|
| 1353 |
+
"1351": "ornithine translocase deficiency",
|
| 1354 |
+
"1352": "orofaciodigital syndrome 2",
|
| 1355 |
+
"1353": "oropharyngeal cancer",
|
| 1356 |
+
"1354": "orthostatic hypotension",
|
| 1357 |
+
"1355": "osteoarthritis",
|
| 1358 |
+
"1356": "osteochondritis dissecans",
|
| 1359 |
+
"1357": "osteogenesis imperfecta",
|
| 1360 |
+
"1358": "osteogenesis imperfecta type vi",
|
| 1361 |
+
"1359": "osteoglophonic dysplasia",
|
| 1362 |
+
"1360": "osteopetrosis",
|
| 1363 |
+
"1361": "osteoporosis",
|
| 1364 |
+
"1362": "osteoporosis pseudoglioma syndrome",
|
| 1365 |
+
"1363": "osteosarcoma and malignant fibrous histiocytoma of bone",
|
| 1366 |
+
"1364": "otopalatodigital syndrome type 1",
|
| 1367 |
+
"1365": "otopalatodigital syndrome type 2",
|
| 1368 |
+
"1366": "otospondylomegaepiphyseal dysplasia",
|
| 1369 |
+
"1367": "ovarian cancer",
|
| 1370 |
+
"1368": "ovarian epithelial, fallopian tube, and primary peritoneal cancer",
|
| 1371 |
+
"1369": "ovarian germ cell tumors",
|
| 1372 |
+
"1370": "ovarian low malignant potential tumors",
|
| 1373 |
+
"1371": "ovarian, fallopian tube, and primary peritoneal cancer",
|
| 1374 |
+
"1372": "overview of kidney disease in children",
|
| 1375 |
+
"1373": "overweight and obesity",
|
| 1376 |
+
"1374": "oxygen therapy",
|
| 1377 |
+
"1375": "pachygyria",
|
| 1378 |
+
"1376": "pachyonychia congenita",
|
| 1379 |
+
"1377": "paget disease of bone",
|
| 1380 |
+
"1378": "paget's disease of bone",
|
| 1381 |
+
"1379": "pallister hall syndrome",
|
| 1382 |
+
"1380": "pallister killian mosaic syndrome",
|
| 1383 |
+
"1381": "palmoplantar keratoderma with deafness",
|
| 1384 |
+
"1382": "pancreatic cancer",
|
| 1385 |
+
"1383": "pancreatic neuroendocrine tumors (islet cell tumors)",
|
| 1386 |
+
"1384": "pantothenate kinase associated neurodegeneration",
|
| 1387 |
+
"1385": "paramyotonia congenita",
|
| 1388 |
+
"1386": "paranasal sinus and nasal cavity cancer",
|
| 1389 |
+
"1387": "paraneoplastic syndromes",
|
| 1390 |
+
"1388": "parasites african trypanosomiasis (also known as sleeping sickness)",
|
| 1391 |
+
"1389": "parasites american trypanosomiasis (also known as chagas disease)",
|
| 1392 |
+
"1390": "parasites angiostrongyliasis (also known as angiostrongylus infection)",
|
| 1393 |
+
"1391": "parasites ascariasis",
|
| 1394 |
+
"1392": "parasites babesiosis",
|
| 1395 |
+
"1393": "parasites baylisascaris infection",
|
| 1396 |
+
"1394": "parasites cyclosporiasis (cyclospora infection)",
|
| 1397 |
+
"1395": "parasites cysticercosis",
|
| 1398 |
+
"1396": "parasites echinococcosis",
|
| 1399 |
+
"1397": "parasites enterobiasis (also known as pinworm infection)",
|
| 1400 |
+
"1398": "parasites fascioliasis (fasciola infection)",
|
| 1401 |
+
"1399": "parasites hookworm",
|
| 1402 |
+
"1400": "parasites leishmaniasis",
|
| 1403 |
+
"1401": "parasites lice body lice",
|
| 1404 |
+
"1402": "parasites lice head lice",
|
| 1405 |
+
"1403": "parasites lice pubic \"crab\" lice",
|
| 1406 |
+
"1404": "parasites loiasis",
|
| 1407 |
+
"1405": "parasites lymphatic filariasis",
|
| 1408 |
+
"1406": "parasites paragonimiasis (also known as paragonimus infection)",
|
| 1409 |
+
"1407": "parasites scabies",
|
| 1410 |
+
"1408": "parasites schistosomiasis",
|
| 1411 |
+
"1409": "parasites taeniasis",
|
| 1412 |
+
"1410": "parasites toxocariasis (also known as roundworm infection)",
|
| 1413 |
+
"1411": "parasites toxoplasmosis (toxoplasma infection)",
|
| 1414 |
+
"1412": "parasites trichinellosis (also known as trichinosis)",
|
| 1415 |
+
"1413": "parasites trichuriasis (also known as whipworm infection)",
|
| 1416 |
+
"1414": "parasites zoonotic hookworm",
|
| 1417 |
+
"1415": "parathyroid cancer",
|
| 1418 |
+
"1416": "paresthesia",
|
| 1419 |
+
"1417": "parkes weber syndrome",
|
| 1420 |
+
"1418": "parkinson disease",
|
| 1421 |
+
"1419": "parkinson's disease",
|
| 1422 |
+
"1420": "paroxysmal choreoathetosis",
|
| 1423 |
+
"1421": "paroxysmal extreme pain disorder",
|
| 1424 |
+
"1422": "paroxysmal hemicrania",
|
| 1425 |
+
"1423": "paroxysmal nocturnal hemoglobinuria",
|
| 1426 |
+
"1424": "parry romberg",
|
| 1427 |
+
"1425": "pars planitis",
|
| 1428 |
+
"1426": "parsonage turner syndrome",
|
| 1429 |
+
"1427": "partington syndrome",
|
| 1430 |
+
"1428": "patent ductus arteriosus",
|
| 1431 |
+
"1429": "pdgfra associated chronic eosinophilic leukemia",
|
| 1432 |
+
"1430": "pdgfrb associated chronic eosinophilic leukemia",
|
| 1433 |
+
"1431": "pearson marrow pancreas syndrome",
|
| 1434 |
+
"1432": "pelizaeus merzbacher disease",
|
| 1435 |
+
"1433": "pendred syndrome",
|
| 1436 |
+
"1434": "penile cancer",
|
| 1437 |
+
"1435": "pericarditis",
|
| 1438 |
+
"1436": "perineal injury in males",
|
| 1439 |
+
"1437": "periodic fever, aphthous stomatitis, pharyngitis and adenitis",
|
| 1440 |
+
"1438": "peripheral arterial disease (p.a.d.)",
|
| 1441 |
+
"1439": "peripheral artery disease",
|
| 1442 |
+
"1440": "peripheral neuropathy",
|
| 1443 |
+
"1441": "periventricular heterotopia",
|
| 1444 |
+
"1442": "periventricular leukomalacia",
|
| 1445 |
+
"1443": "permanent neonatal diabetes mellitus",
|
| 1446 |
+
"1444": "pernicious anemia",
|
| 1447 |
+
"1445": "peroxisomal acyl coa oxidase deficiency",
|
| 1448 |
+
"1446": "perrault syndrome",
|
| 1449 |
+
"1447": "perry syndrome",
|
| 1450 |
+
"1448": "persistent mllerian duct syndrome",
|
| 1451 |
+
"1449": "pervasive developmental disorders",
|
| 1452 |
+
"1450": "peters plus syndrome",
|
| 1453 |
+
"1451": "peutz jeghers syndrome",
|
| 1454 |
+
"1452": "peyronie's disease",
|
| 1455 |
+
"1453": "pfeiffer syndrome",
|
| 1456 |
+
"1454": "phacomatosis pigmentovascularis",
|
| 1457 |
+
"1455": "phenylketonuria",
|
| 1458 |
+
"1456": "phosphoglycerate dehydrogenase deficiency",
|
| 1459 |
+
"1457": "phosphoglycerate kinase deficiency",
|
| 1460 |
+
"1458": "phosphoglycerate mutase deficiency",
|
| 1461 |
+
"1459": "phosphoribosylpyrophosphate synthetase superactivity",
|
| 1462 |
+
"1460": "piebaldism",
|
| 1463 |
+
"1461": "pierson syndrome",
|
| 1464 |
+
"1462": "pigmented purpuric eruption",
|
| 1465 |
+
"1463": "pigmented villonodular synovitis",
|
| 1466 |
+
"1464": "pilocytic astrocytoma",
|
| 1467 |
+
"1465": "pilomatricoma",
|
| 1468 |
+
"1466": "pilomatrixoma",
|
| 1469 |
+
"1467": "pinched nerve",
|
| 1470 |
+
"1468": "pineal cyst",
|
| 1471 |
+
"1469": "piriformis syndrome",
|
| 1472 |
+
"1470": "pitt hopkins syndrome",
|
| 1473 |
+
"1471": "pituitary tumors",
|
| 1474 |
+
"1472": "pityriasis lichenoides chronica",
|
| 1475 |
+
"1473": "pityriasis lichenoides et varioliformis acuta",
|
| 1476 |
+
"1474": "pityriasis rubra pilaris",
|
| 1477 |
+
"1475": "plasma cell neoplasms (including multiple myeloma)",
|
| 1478 |
+
"1476": "platelet storage pool deficiency",
|
| 1479 |
+
"1477": "platyspondylic lethal skeletal dysplasia, torrance type",
|
| 1480 |
+
"1478": "pleurisy and other pleural disorders",
|
| 1481 |
+
"1479": "pmm2 congenital disorder of glycosylation",
|
| 1482 |
+
"1480": "pneumonia",
|
| 1483 |
+
"1481": "pol iii related leukodystrophy",
|
| 1484 |
+
"1482": "poland syndrome",
|
| 1485 |
+
"1483": "polycystic kidney disease",
|
| 1486 |
+
"1484": "polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy",
|
| 1487 |
+
"1485": "polycythemia vera",
|
| 1488 |
+
"1486": "polymicrogyria",
|
| 1489 |
+
"1487": "polymyositis",
|
| 1490 |
+
"1488": "pompe disease",
|
| 1491 |
+
"1489": "pontocerebellar hypoplasia",
|
| 1492 |
+
"1490": "pontocerebellar hypoplasia type 1",
|
| 1493 |
+
"1491": "popliteal pterygium syndrome",
|
| 1494 |
+
"1492": "porencephaly",
|
| 1495 |
+
"1493": "porphyria",
|
| 1496 |
+
"1494": "post polio syndrome",
|
| 1497 |
+
"1495": "postural orthostatic tachycardia syndrome",
|
| 1498 |
+
"1496": "postural tachycardia syndrome",
|
| 1499 |
+
"1497": "potassium aggravated myotonia",
|
| 1500 |
+
"1498": "potocki shaffer syndrome",
|
| 1501 |
+
"1499": "ppm x syndrome",
|
| 1502 |
+
"1500": "prader willi syndrome",
|
| 1503 |
+
"1501": "preeclampsia",
|
| 1504 |
+
"1502": "pregnancy and thyroid disease",
|
| 1505 |
+
"1503": "prekallikrein deficiency",
|
| 1506 |
+
"1504": "prescription and illicit drug abuse",
|
| 1507 |
+
"1505": "prevent diabetes problems: keep your diabetes under control",
|
| 1508 |
+
"1506": "prevent diabetes problems: keep your heart and blood vessels healthy",
|
| 1509 |
+
"1507": "prevent diabetes problems: keep your kidneys healthy",
|
| 1510 |
+
"1508": "prevent diabetes problems: keep your nervous system healthy",
|
| 1511 |
+
"1509": "prickle1 related progressive myoclonus epilepsy with ataxia",
|
| 1512 |
+
"1510": "primary biliary cirrhosis",
|
| 1513 |
+
"1511": "primary carnitine deficiency",
|
| 1514 |
+
"1512": "primary ciliary dyskinesia",
|
| 1515 |
+
"1513": "primary cns lymphoma",
|
| 1516 |
+
"1514": "primary familial brain calcification",
|
| 1517 |
+
"1515": "primary gastrointestinal melanoma",
|
| 1518 |
+
"1516": "primary hyperoxaluria",
|
| 1519 |
+
"1517": "primary hyperoxaluria type 2",
|
| 1520 |
+
"1518": "primary hyperparathyroidism",
|
| 1521 |
+
"1519": "primary lateral sclerosis",
|
| 1522 |
+
"1520": "primary macronodular adrenal hyperplasia",
|
| 1523 |
+
"1521": "primary myelofibrosis",
|
| 1524 |
+
"1522": "primary sclerosing cholangitis",
|
| 1525 |
+
"1523": "primary spontaneous pneumothorax",
|
| 1526 |
+
"1524": "prinzmetal's variant angina",
|
| 1527 |
+
"1525": "prion disease",
|
| 1528 |
+
"1526": "problems with smell",
|
| 1529 |
+
"1527": "problems with taste",
|
| 1530 |
+
"1528": "proctitis",
|
| 1531 |
+
"1529": "progeria",
|
| 1532 |
+
"1530": "progressive deafness with stapes fixation",
|
| 1533 |
+
"1531": "progressive external ophthalmoplegia",
|
| 1534 |
+
"1532": "progressive familial heart block",
|
| 1535 |
+
"1533": "progressive familial intrahepatic cholestasis",
|
| 1536 |
+
"1534": "progressive multifocal leukoencephalopathy",
|
| 1537 |
+
"1535": "progressive osseous heteroplasia",
|
| 1538 |
+
"1536": "progressive pseudorheumatoid dysplasia",
|
| 1539 |
+
"1537": "progressive supranuclear palsy",
|
| 1540 |
+
"1538": "prolactinoma",
|
| 1541 |
+
"1539": "prolidase deficiency",
|
| 1542 |
+
"1540": "proopiomelanocortin deficiency",
|
| 1543 |
+
"1541": "propionic acidemia",
|
| 1544 |
+
"1542": "prosopagnosia",
|
| 1545 |
+
"1543": "prostate cancer",
|
| 1546 |
+
"1544": "prostate enlargement: benign prostatic hyperplasia",
|
| 1547 |
+
"1545": "protein c deficiency",
|
| 1548 |
+
"1546": "protein s deficiency",
|
| 1549 |
+
"1547": "proteinuria",
|
| 1550 |
+
"1548": "proteus syndrome",
|
| 1551 |
+
"1549": "prothrombin deficiency",
|
| 1552 |
+
"1550": "prothrombin thrombophilia",
|
| 1553 |
+
"1551": "proud syndrome",
|
| 1554 |
+
"1552": "prune belly syndrome",
|
| 1555 |
+
"1553": "pseudoachondroplasia",
|
| 1556 |
+
"1554": "pseudocholinesterase deficiency",
|
| 1557 |
+
"1555": "pseudohypoaldosteronism type 1",
|
| 1558 |
+
"1556": "pseudohypoaldosteronism type 2",
|
| 1559 |
+
"1557": "pseudotumor cerebri",
|
| 1560 |
+
"1558": "pseudoxanthoma elasticum",
|
| 1561 |
+
"1559": "psoriasis",
|
| 1562 |
+
"1560": "psoriatic arthritis",
|
| 1563 |
+
"1561": "pulmonary alveolar microlithiasis",
|
| 1564 |
+
"1562": "pulmonary arterial hypertension",
|
| 1565 |
+
"1563": "pulmonary embolism",
|
| 1566 |
+
"1564": "pulmonary hypertension",
|
| 1567 |
+
"1565": "pulmonary veno occlusive disease",
|
| 1568 |
+
"1566": "punctate palmoplantar keratoderma type i",
|
| 1569 |
+
"1567": "purine nucleoside phosphorylase deficiency",
|
| 1570 |
+
"1568": "pyelonephritis: kidney infection",
|
| 1571 |
+
"1569": "pyridoxal 5' phosphate dependent epilepsy",
|
| 1572 |
+
"1570": "pyridoxine dependent epilepsy",
|
| 1573 |
+
"1571": "pyruvate carboxylase deficiency",
|
| 1574 |
+
"1572": "pyruvate dehydrogenase deficiency",
|
| 1575 |
+
"1573": "pyruvate kinase deficiency",
|
| 1576 |
+
"1574": "q fever",
|
| 1577 |
+
"1575": "quitting smoking for older adults",
|
| 1578 |
+
"1576": "rabies",
|
| 1579 |
+
"1577": "rabson mendenhall syndrome",
|
| 1580 |
+
"1578": "rapadilino syndrome",
|
| 1581 |
+
"1579": "rapid onset dystonia parkinsonism",
|
| 1582 |
+
"1580": "rasmussen's encephalitis",
|
| 1583 |
+
"1581": "recombinant 8 syndrome",
|
| 1584 |
+
"1582": "rectal cancer",
|
| 1585 |
+
"1583": "recurrent hydatidiform mole",
|
| 1586 |
+
"1584": "refsum disease",
|
| 1587 |
+
"1585": "relapsing polychondritis",
|
| 1588 |
+
"1586": "ren related kidney disease",
|
| 1589 |
+
"1587": "renal artery stenosis",
|
| 1590 |
+
"1588": "renal cell cancer",
|
| 1591 |
+
"1589": "renal coloboma syndrome",
|
| 1592 |
+
"1590": "renal hypouricemia",
|
| 1593 |
+
"1591": "renal nutcracker syndrome",
|
| 1594 |
+
"1592": "renal oncocytoma",
|
| 1595 |
+
"1593": "renal tubular acidosis",
|
| 1596 |
+
"1594": "renal tubular acidosis with deafness",
|
| 1597 |
+
"1595": "renal tubular dysgenesis",
|
| 1598 |
+
"1596": "renpenning syndrome",
|
| 1599 |
+
"1597": "repetitive motion disorders",
|
| 1600 |
+
"1598": "respiratory distress syndrome",
|
| 1601 |
+
"1599": "respiratory failure",
|
| 1602 |
+
"1600": "restless legs syndrome",
|
| 1603 |
+
"1601": "reticulohistiocytoma",
|
| 1604 |
+
"1602": "retinal arterial macroaneurysm with supravalvular pulmonic stenosis",
|
| 1605 |
+
"1603": "retinitis pigmentosa",
|
| 1606 |
+
"1604": "retinoblastoma",
|
| 1607 |
+
"1605": "retroperitoneal fibrosis",
|
| 1608 |
+
"1606": "rett syndrome",
|
| 1609 |
+
"1607": "reye's syndrome",
|
| 1610 |
+
"1608": "rh incompatibility",
|
| 1611 |
+
"1609": "rheumatic fever",
|
| 1612 |
+
"1610": "rheumatoid arthritis",
|
| 1613 |
+
"1611": "rhizomelic chondrodysplasia punctata",
|
| 1614 |
+
"1612": "rickets",
|
| 1615 |
+
"1613": "ring chromosome 14 syndrome",
|
| 1616 |
+
"1614": "ring chromosome 20 syndrome",
|
| 1617 |
+
"1615": "rippling muscle disease",
|
| 1618 |
+
"1616": "roberts syndrome",
|
| 1619 |
+
"1617": "robinow syndrome",
|
| 1620 |
+
"1618": "romano ward syndrome",
|
| 1621 |
+
"1619": "rothmund thomson syndrome",
|
| 1622 |
+
"1620": "rotor syndrome",
|
| 1623 |
+
"1621": "rubinstein taybi syndrome",
|
| 1624 |
+
"1622": "russell silver syndrome",
|
| 1625 |
+
"1623": "saddan",
|
| 1626 |
+
"1624": "saethre chotzen syndrome",
|
| 1627 |
+
"1625": "salih myopathy",
|
| 1628 |
+
"1626": "salivary gland cancer",
|
| 1629 |
+
"1627": "sandhoff disease",
|
| 1630 |
+
"1628": "sarcoidosis",
|
| 1631 |
+
"1629": "schilder's disease",
|
| 1632 |
+
"1630": "schimke immuno osseous dysplasia",
|
| 1633 |
+
"1631": "schimke immunoosseous dysplasia",
|
| 1634 |
+
"1632": "schindler disease",
|
| 1635 |
+
"1633": "schindler disease type 1",
|
| 1636 |
+
"1634": "schinzel giedion syndrome",
|
| 1637 |
+
"1635": "schizencephaly",
|
| 1638 |
+
"1636": "schnitzler syndrome",
|
| 1639 |
+
"1637": "schwannomatosis",
|
| 1640 |
+
"1638": "schwartz jampel syndrome",
|
| 1641 |
+
"1639": "schwartz jampel syndrome type 1",
|
| 1642 |
+
"1640": "scleroderma",
|
| 1643 |
+
"1641": "scot deficiency",
|
| 1644 |
+
"1642": "senior lken syndrome",
|
| 1645 |
+
"1643": "sensorineural deafness and male infertility",
|
| 1646 |
+
"1644": "sepiapterin reductase deficiency",
|
| 1647 |
+
"1645": "septo optic dysplasia",
|
| 1648 |
+
"1646": "serpiginous choroiditis",
|
| 1649 |
+
"1647": "severe congenital neutropenia",
|
| 1650 |
+
"1648": "shaken baby syndrome",
|
| 1651 |
+
"1649": "sheldon hall syndrome",
|
| 1652 |
+
"1650": "shingles",
|
| 1653 |
+
"1651": "short bowel syndrome",
|
| 1654 |
+
"1652": "short chain acyl coa dehydrogenase deficiency",
|
| 1655 |
+
"1653": "short qt syndrome",
|
| 1656 |
+
"1654": "short stature, hyperextensibility, hernia, ocular depression, rieger anomaly, and teething delay",
|
| 1657 |
+
"1655": "short syndrome",
|
| 1658 |
+
"1656": "shprintzen goldberg syndrome",
|
| 1659 |
+
"1657": "shwachman diamond syndrome",
|
| 1660 |
+
"1658": "sialadenitis",
|
| 1661 |
+
"1659": "sialic acid storage disease",
|
| 1662 |
+
"1660": "sialidosis",
|
| 1663 |
+
"1661": "sialuria",
|
| 1664 |
+
"1662": "sick sinus syndrome",
|
| 1665 |
+
"1663": "sickle cell disease",
|
| 1666 |
+
"1664": "sideroblastic anemia",
|
| 1667 |
+
"1665": "sideroblastic anemia pyridoxine refractory autosomal recessive",
|
| 1668 |
+
"1666": "silver syndrome",
|
| 1669 |
+
"1667": "simple kidney cysts",
|
| 1670 |
+
"1668": "simpson golabi behmel syndrome",
|
| 1671 |
+
"1669": "singleton merten syndrome",
|
| 1672 |
+
"1670": "sitosterolemia",
|
| 1673 |
+
"1671": "situs inversus",
|
| 1674 |
+
"1672": "sjgren larsson syndrome",
|
| 1675 |
+
"1673": "sjgren syndrome",
|
| 1676 |
+
"1674": "sjgren's syndrome",
|
| 1677 |
+
"1675": "sjogren syndrome",
|
| 1678 |
+
"1676": "skin cancer",
|
| 1679 |
+
"1677": "slc4a1 associated distal renal tubular acidosis",
|
| 1680 |
+
"1678": "sleep apnea",
|
| 1681 |
+
"1679": "small cell lung cancer",
|
| 1682 |
+
"1680": "small fiber neuropathy",
|
| 1683 |
+
"1681": "small intestine cancer",
|
| 1684 |
+
"1682": "smith lemli opitz syndrome",
|
| 1685 |
+
"1683": "smith magenis syndrome",
|
| 1686 |
+
"1684": "smoking and the digestive system",
|
| 1687 |
+
"1685": "snyder robinson syndrome",
|
| 1688 |
+
"1686": "solitary kidney",
|
| 1689 |
+
"1687": "sost related sclerosing bone dysplasia",
|
| 1690 |
+
"1688": "sotos syndrome",
|
| 1691 |
+
"1689": "sox2 anophthalmia syndrome",
|
| 1692 |
+
"1690": "spastic diplegia cerebral palsy",
|
| 1693 |
+
"1691": "spastic paraplegia type 11",
|
| 1694 |
+
"1692": "spastic paraplegia type 15",
|
| 1695 |
+
"1693": "spastic paraplegia type 2",
|
| 1696 |
+
"1694": "spastic paraplegia type 31",
|
| 1697 |
+
"1695": "spastic paraplegia type 3a",
|
| 1698 |
+
"1696": "spastic paraplegia type 4",
|
| 1699 |
+
"1697": "spastic paraplegia type 7",
|
| 1700 |
+
"1698": "spastic paraplegia type 8",
|
| 1701 |
+
"1699": "spasticity",
|
| 1702 |
+
"1700": "spina bifida",
|
| 1703 |
+
"1701": "spinal and bulbar muscular atrophy",
|
| 1704 |
+
"1702": "spinal cord infarction",
|
| 1705 |
+
"1703": "spinal cord injury",
|
| 1706 |
+
"1704": "spinal muscular atrophy",
|
| 1707 |
+
"1705": "spinal muscular atrophy with progressive myoclonic epilepsy",
|
| 1708 |
+
"1706": "spinal muscular atrophy with respiratory distress type 1",
|
| 1709 |
+
"1707": "spinocerebellar ataxia 2",
|
| 1710 |
+
"1708": "spinocerebellar ataxia type 1",
|
| 1711 |
+
"1709": "spinocerebellar ataxia type 2",
|
| 1712 |
+
"1710": "spinocerebellar ataxia type 3",
|
| 1713 |
+
"1711": "spinocerebellar ataxia type 36",
|
| 1714 |
+
"1712": "spinocerebellar ataxia type 6",
|
| 1715 |
+
"1713": "spondylocarpotarsal synostosis syndrome",
|
| 1716 |
+
"1714": "spondylocostal dysostosis",
|
| 1717 |
+
"1715": "spondyloenchondrodysplasia with immune dysregulation",
|
| 1718 |
+
"1716": "spondyloepimetaphyseal dysplasia, strudwick type",
|
| 1719 |
+
"1717": "spondyloepiphyseal dysplasia congenita",
|
| 1720 |
+
"1718": "spondyloperipheral dysplasia",
|
| 1721 |
+
"1719": "spondylothoracic dysostosis",
|
| 1722 |
+
"1720": "sporadic hemiplegic migraine",
|
| 1723 |
+
"1721": "stargardt disease",
|
| 1724 |
+
"1722": "stargardt macular degeneration",
|
| 1725 |
+
"1723": "steatocystoma multiplex",
|
| 1726 |
+
"1724": "stenotrophomonas maltophilia infection",
|
| 1727 |
+
"1725": "stevens johnson syndrome",
|
| 1728 |
+
"1726": "stevens johnson syndrome/toxic epidermal necrolysis",
|
| 1729 |
+
"1727": "stickler syndrome",
|
| 1730 |
+
"1728": "stiff person syndrome",
|
| 1731 |
+
"1729": "sting associated vasculopathy with onset in infancy",
|
| 1732 |
+
"1730": "stormorken syndrome",
|
| 1733 |
+
"1731": "striatonigral degeneration",
|
| 1734 |
+
"1732": "stroke",
|
| 1735 |
+
"1733": "sturge weber syndrome",
|
| 1736 |
+
"1734": "stve wiedemann syndrome",
|
| 1737 |
+
"1735": "subacute sclerosing panencephalitis",
|
| 1738 |
+
"1736": "succinate coa ligase deficiency",
|
| 1739 |
+
"1737": "succinic semialdehyde dehydrogenase deficiency",
|
| 1740 |
+
"1738": "succinyl coa:3 ketoacid coa transferase deficiency",
|
| 1741 |
+
"1739": "sudden cardiac arrest",
|
| 1742 |
+
"1740": "sudden infant death with dysgenesis of the testes syndrome",
|
| 1743 |
+
"1741": "sunct headache",
|
| 1744 |
+
"1742": "supravalvular aortic stenosis",
|
| 1745 |
+
"1743": "surfactant dysfunction",
|
| 1746 |
+
"1744": "surviving cancer",
|
| 1747 |
+
"1745": "swallowing disorders",
|
| 1748 |
+
"1746": "swyer james syndrome",
|
| 1749 |
+
"1747": "swyer syndrome",
|
| 1750 |
+
"1748": "sydenham chorea",
|
| 1751 |
+
"1749": "syncope",
|
| 1752 |
+
"1750": "syndrome of inappropriate antidiuretic hormone",
|
| 1753 |
+
"1751": "syngap1 related intellectual disability",
|
| 1754 |
+
"1752": "syringomyelia",
|
| 1755 |
+
"1753": "systemic lupus erythematosus",
|
| 1756 |
+
"1754": "systemic scleroderma",
|
| 1757 |
+
"1755": "t cell immunodeficiency, congenital alopecia, and nail dystrophy",
|
| 1758 |
+
"1756": "tabes dorsalis",
|
| 1759 |
+
"1757": "tangier disease",
|
| 1760 |
+
"1758": "tardive dyskinesia",
|
| 1761 |
+
"1759": "tarlov cysts",
|
| 1762 |
+
"1760": "tarp syndrome",
|
| 1763 |
+
"1761": "tarsal carpal coalition syndrome",
|
| 1764 |
+
"1762": "tarsal tunnel syndrome",
|
| 1765 |
+
"1763": "task specific focal dystonia",
|
| 1766 |
+
"1764": "tay sachs disease",
|
| 1767 |
+
"1765": "testicular cancer",
|
| 1768 |
+
"1766": "tethered spinal cord syndrome",
|
| 1769 |
+
"1767": "tetra amelia syndrome",
|
| 1770 |
+
"1768": "tetrahydrobiopterin deficiency",
|
| 1771 |
+
"1769": "tetralogy of fallot",
|
| 1772 |
+
"1770": "tetrasomy 18p",
|
| 1773 |
+
"1771": "thalassemia",
|
| 1774 |
+
"1772": "thalassemias",
|
| 1775 |
+
"1773": "thanatophoric dysplasia",
|
| 1776 |
+
"1774": "thiamine responsive megaloblastic anemia syndrome",
|
| 1777 |
+
"1775": "thiopurine s methyltransferase deficiency",
|
| 1778 |
+
"1776": "thoracic outlet syndrome",
|
| 1779 |
+
"1777": "thrombocythemia and thrombocytosis",
|
| 1780 |
+
"1778": "thrombocytopenia",
|
| 1781 |
+
"1779": "thrombocytopenia absent radius syndrome",
|
| 1782 |
+
"1780": "thrombotic thrombocytopenic purpura",
|
| 1783 |
+
"1781": "thymoma and thymic carcinoma",
|
| 1784 |
+
"1782": "thyrotoxic myopathy",
|
| 1785 |
+
"1783": "tibial muscular dystrophy",
|
| 1786 |
+
"1784": "tietz syndrome",
|
| 1787 |
+
"1785": "tietze syndrome",
|
| 1788 |
+
"1786": "timothy syndrome",
|
| 1789 |
+
"1787": "tk2 related mitochondrial dna depletion syndrome, myopathic form",
|
| 1790 |
+
"1788": "todd's paralysis",
|
| 1791 |
+
"1789": "tourette syndrome",
|
| 1792 |
+
"1790": "townes brocks syndrome",
|
| 1793 |
+
"1791": "tracheobronchomalacia",
|
| 1794 |
+
"1792": "tracheobronchopathia osteoplastica",
|
| 1795 |
+
"1793": "transient ischemic attack",
|
| 1796 |
+
"1794": "transitional cell cancer of the renal pelvis and ureter",
|
| 1797 |
+
"1795": "transmissible spongiform encephalopathies",
|
| 1798 |
+
"1796": "transthyretin amyloidosis",
|
| 1799 |
+
"1797": "transverse myelitis",
|
| 1800 |
+
"1798": "traumatic brain injury",
|
| 1801 |
+
"1799": "treacher collins syndrome",
|
| 1802 |
+
"1800": "treatment methods for kidney failure: peritoneal dialysis",
|
| 1803 |
+
"1801": "tremor",
|
| 1804 |
+
"1802": "trichohepatoenteric syndrome",
|
| 1805 |
+
"1803": "trichothiodystrophy",
|
| 1806 |
+
"1804": "trigeminal neuralgia",
|
| 1807 |
+
"1805": "trimethylaminuria",
|
| 1808 |
+
"1806": "triosephosphate isomerase deficiency",
|
| 1809 |
+
"1807": "triple a syndrome",
|
| 1810 |
+
"1808": "triple x syndrome",
|
| 1811 |
+
"1809": "trisomy 13",
|
| 1812 |
+
"1810": "trisomy 18",
|
| 1813 |
+
"1811": "tropical spastic paraparesis",
|
| 1814 |
+
"1812": "troyer syndrome",
|
| 1815 |
+
"1813": "tuberculosis (tb)",
|
| 1816 |
+
"1814": "tuberous sclerosis",
|
| 1817 |
+
"1815": "tuberous sclerosis complex",
|
| 1818 |
+
"1816": "tubular aggregate myopathy",
|
| 1819 |
+
"1817": "tularemia",
|
| 1820 |
+
"1818": "tumor necrosis factor receptor associated periodic syndrome",
|
| 1821 |
+
"1819": "turner syndrome",
|
| 1822 |
+
"1820": "tylosis with esophageal cancer",
|
| 1823 |
+
"1821": "type 1 diabetes",
|
| 1824 |
+
"1822": "type 1 plasminogen deficiency",
|
| 1825 |
+
"1823": "type a insulin resistance syndrome",
|
| 1826 |
+
"1824": "tyrosine hydroxylase deficiency",
|
| 1827 |
+
"1825": "tyrosinemia",
|
| 1828 |
+
"1826": "ulcerative colitis",
|
| 1829 |
+
"1827": "uncombable hair syndrome",
|
| 1830 |
+
"1828": "unverricht lundborg disease",
|
| 1831 |
+
"1829": "urachal cyst",
|
| 1832 |
+
"1830": "urethral cancer",
|
| 1833 |
+
"1831": "urinary incontinence",
|
| 1834 |
+
"1832": "urinary incontinence in children",
|
| 1835 |
+
"1833": "urinary incontinence in men",
|
| 1836 |
+
"1834": "urinary retention",
|
| 1837 |
+
"1835": "urinary tract infection in adults",
|
| 1838 |
+
"1836": "urinary tract infections",
|
| 1839 |
+
"1837": "urinary tract infections in children",
|
| 1840 |
+
"1838": "urine blockage in newborns",
|
| 1841 |
+
"1839": "uromodulin associated kidney disease",
|
| 1842 |
+
"1840": "usher syndrome",
|
| 1843 |
+
"1841": "uterine sarcoma",
|
| 1844 |
+
"1842": "uv sensitive syndrome",
|
| 1845 |
+
"1843": "vacterl association",
|
| 1846 |
+
"1844": "van der woude syndrome",
|
| 1847 |
+
"1845": "varicose veins",
|
| 1848 |
+
"1846": "vasculitis",
|
| 1849 |
+
"1847": "vasculitis syndromes of the central and peripheral nervous systems",
|
| 1850 |
+
"1848": "very long chain acyl coa dehydrogenase deficiency",
|
| 1851 |
+
"1849": "vesicoureteral reflux",
|
| 1852 |
+
"1850": "viral gastroenteritis",
|
| 1853 |
+
"1851": "viral hepatitis: a through e and beyond",
|
| 1854 |
+
"1852": "vitamin d dependent rickets",
|
| 1855 |
+
"1853": "vitelliform macular dystrophy",
|
| 1856 |
+
"1854": "vitiligo",
|
| 1857 |
+
"1855": "vlcad deficiency",
|
| 1858 |
+
"1856": "vldlr associated cerebellar hypoplasia",
|
| 1859 |
+
"1857": "vohwinkel syndrome",
|
| 1860 |
+
"1858": "von hippel lindau disease",
|
| 1861 |
+
"1859": "von hippel lindau disease (vhl)",
|
| 1862 |
+
"1860": "von hippel lindau syndrome",
|
| 1863 |
+
"1861": "von willebrand disease",
|
| 1864 |
+
"1862": "vulvar cancer",
|
| 1865 |
+
"1863": "waardenburg syndrome",
|
| 1866 |
+
"1864": "wagner syndrome",
|
| 1867 |
+
"1865": "wagr syndrome",
|
| 1868 |
+
"1866": "waldenstrm macroglobulinemia",
|
| 1869 |
+
"1867": "walker warburg syndrome",
|
| 1870 |
+
"1868": "wallenberg's syndrome",
|
| 1871 |
+
"1869": "warfarin resistance",
|
| 1872 |
+
"1870": "warfarin sensitivity",
|
| 1873 |
+
"1871": "warsaw breakage syndrome",
|
| 1874 |
+
"1872": "warthin tumor",
|
| 1875 |
+
"1873": "waterhousefriderichsen syndrome",
|
| 1876 |
+
"1874": "weaver syndrome",
|
| 1877 |
+
"1875": "weill marchesani syndrome",
|
| 1878 |
+
"1876": "weissenbacher zweymller syndrome",
|
| 1879 |
+
"1877": "werner syndrome",
|
| 1880 |
+
"1878": "wernicke korsakoff syndrome",
|
| 1881 |
+
"1879": "weyers acrofacial dysostosis",
|
| 1882 |
+
"1880": "what i need to know about bladder control for women",
|
| 1883 |
+
"1881": "what i need to know about cirrhosis",
|
| 1884 |
+
"1882": "what i need to know about crohn's disease",
|
| 1885 |
+
"1883": "what i need to know about diarrhea",
|
| 1886 |
+
"1884": "what i need to know about diverticular disease",
|
| 1887 |
+
"1885": "what i need to know about erectile dysfunction",
|
| 1888 |
+
"1886": "what i need to know about gas",
|
| 1889 |
+
"1887": "what i need to know about gestational diabetes",
|
| 1890 |
+
"1888": "what i need to know about hepatitis a",
|
| 1891 |
+
"1889": "what i need to know about hepatitis b",
|
| 1892 |
+
"1890": "what i need to know about hepatitis c",
|
| 1893 |
+
"1891": "what i need to know about hirschsprung disease",
|
| 1894 |
+
"1892": "what i need to know about interstitial cystitis/painful bladder syndrome",
|
| 1895 |
+
"1893": "what i need to know about kidney failure and how its treated",
|
| 1896 |
+
"1894": "what i need to know about kidney stones",
|
| 1897 |
+
"1895": "what i need to know about lactose intolerance",
|
| 1898 |
+
"1896": "what i need to know about living with kidney failure",
|
| 1899 |
+
"1897": "what i need to know about my child's urinary tract infection",
|
| 1900 |
+
"1898": "whiplash",
|
| 1901 |
+
"1899": "whipple disease",
|
| 1902 |
+
"1900": "whipple's disease",
|
| 1903 |
+
"1901": "white sponge nevus",
|
| 1904 |
+
"1902": "wildervanck syndrome",
|
| 1905 |
+
"1903": "williams syndrome",
|
| 1906 |
+
"1904": "wilms tumor and other childhood kidney tumors",
|
| 1907 |
+
"1905": "wilson disease",
|
| 1908 |
+
"1906": "winchester syndrome",
|
| 1909 |
+
"1907": "wiskott aldrich syndrome",
|
| 1910 |
+
"1908": "wolf hirschhorn syndrome",
|
| 1911 |
+
"1909": "wolff parkinson white syndrome",
|
| 1912 |
+
"1910": "wolfram syndrome",
|
| 1913 |
+
"1911": "wolman disease",
|
| 1914 |
+
"1912": "x linked adrenal hypoplasia congenita",
|
| 1915 |
+
"1913": "x linked adrenoleukodystrophy",
|
| 1916 |
+
"1914": "x linked agammaglobulinemia",
|
| 1917 |
+
"1915": "x linked chondrodysplasia punctata 1",
|
| 1918 |
+
"1916": "x linked chondrodysplasia punctata 2",
|
| 1919 |
+
"1917": "x linked congenital stationary night blindness",
|
| 1920 |
+
"1918": "x linked creatine deficiency",
|
| 1921 |
+
"1919": "x linked dominant scapuloperoneal myopathy",
|
| 1922 |
+
"1920": "x linked dystonia parkinsonism",
|
| 1923 |
+
"1921": "x linked hyper igm syndrome",
|
| 1924 |
+
"1922": "x linked hypophosphatemia",
|
| 1925 |
+
"1923": "x linked immunodeficiency with magnesium defect, epstein barr virus infection, and neoplasia",
|
| 1926 |
+
"1924": "x linked infantile nystagmus",
|
| 1927 |
+
"1925": "x linked infantile spasm syndrome",
|
| 1928 |
+
"1926": "x linked intellectual disability, siderius type",
|
| 1929 |
+
"1927": "x linked juvenile retinoschisis",
|
| 1930 |
+
"1928": "x linked lissencephaly with abnormal genitalia",
|
| 1931 |
+
"1929": "x linked lymphoproliferative disease",
|
| 1932 |
+
"1930": "x linked myotubular myopathy",
|
| 1933 |
+
"1931": "x linked severe combined immunodeficiency",
|
| 1934 |
+
"1932": "x linked sideroblastic anemia",
|
| 1935 |
+
"1933": "x linked sideroblastic anemia and ataxia",
|
| 1936 |
+
"1934": "x linked spondyloepiphyseal dysplasia tarda",
|
| 1937 |
+
"1935": "x linked thrombocytopenia",
|
| 1938 |
+
"1936": "xeroderma pigmentosum",
|
| 1939 |
+
"1937": "y chromosome infertility",
|
| 1940 |
+
"1938": "yellow nail syndrome",
|
| 1941 |
+
"1939": "yersinia",
|
| 1942 |
+
"1940": "zap70 related severe combined immunodeficiency",
|
| 1943 |
+
"1941": "zellweger spectrum disorder",
|
| 1944 |
+
"1942": "zellweger syndrome",
|
| 1945 |
+
"1943": "zollinger ellison syndrome"
|
| 1946 |
+
}
|