Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/6

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  1. Hair defect with photosensitivity and mental retardation
  2. Hairy ears, y-linked
  3. Hairy ears
  4. Hairy nose tip
  5. Halal Setton Wang syndrome
  6. Hall Riggs mental retardation syndrome
  7. Hamanishi Ueba Tsuji syndrome
  8. Hamano Tsukamoto syndrome
  9. Hand and foot deformity flat facies
  10. Hard skin syndrome Parana type
  11. Harrod Doman Keele syndrome
  12. Hartsfield Bixler Demyer syndrome
  13. Haspeslagh Fryns Muelenaere syndrome
  14. Hay Wells syndrome recessive type
  15. Heart block progressive, familial
  16. Heart defect round face congenital retarded development
  17. Heart defect tongue hamartoma polysyndactyly
  18. Heart defects limb shortening
  19. Heart hand syndrome Spanish type
  20. Hecht Scott syndrome
  21. Heckenlively syndrome
  22. Heide syndrome
  23. Helmerhorst Heaton Crossen syndrome
  24. HEM dysplasia
  25. Hemangiomatosis, familial pulmonary capillary
  26. Hemeralopia, congenital essential
  27. Hemeralopia, familial
  28. Hemi 3 syndrome
  29. Hemifacial atrophy agenesis of the caudate nucleus
  30. Hemifacial atrophy progressive
  31. Hemifacial hyperplasia strabismus
  32. Hemihypertrophy in context of NF
  33. Hemihypertrophy intestinal web corneal opacity
  34. Hemolytic anemia lethal genital anomalies
  35. Hemorrhagic thrombocythemia
  36. Hennekam Beemer syndrome
  37. Hennekam Koss de Geest syndrome
  38. Hennekam Van der Horst syndrome
  39. Heparane sulfamidase deficiency
  40. Hepatic cystic hamartoma
  41. Hepatic ductular hypoplasia
  42. Hepatic fibrosis renal cysts mental retardation
  43. Hereditary alpha tryptasemia syndrome
  44. Hereditary carnitine deficiency syndrome
  45. Hereditary macrothrombocytopenia
  46. Hereditary myopathy with intranuclear filamentous
  47. Hereditary nodular heterotopia
  48. Hereditary paroxysmal cerebral ataxia
  49. Hereditary resistance to anti-vitamin K
  50. Hereditary sensory neuropathy type I
  51. Hereditary sensory neuropathy type II
  52. Hereditary spherocytic hemolytic anemia
  53. Hereditary type 1 neuropathy
  54. Hereditary type 2 neuropathy
  55. Hernandez Aguire Negrete syndrome
  56. Herpetic embryopathy
  57. Herrmann Opitz arthrogryposis syndrome
  58. Herrmann Opitz craniosynostosis
  59. Hersh Podruch Weisskopk syndrome
  60. Heterotaxia autosomal dominant type
  61. Heterotaxy with polysplenia or asplenia
  62. Heterotaxy, visceral, X-linked
  63. Hexosaminidases A and B deficiency
  64. Hidradenitis suppurativa familial
  65. Hidrotic ectodermal dysplasia type Christianson Fouris
  66. High-molecular-weight kininogen deficiency, congenital
  67. Hillig syndrome
  68. Hing Torack Dowston syndrome
  69. Hinson-Pepys disease
  70. Hip dysplasia Beukes type
  71. Hip subluxation -> Should this redirect to sublixation or dislocation of hip?
  72. Hipo syndrome
  73. Hirschsprung disease ganglioneuroblastoma
  74. Hirschsprung disease polydactyly heart disease
  75. Hirschsprung disease type 2
  76. Hirschsprung disease type 3
  77. Hirschsprung disease type d brachydactyly
  78. Hirschsprung microcephaly cleft palate
  79. Hirschsprung nail hypoplasia dysmorphism
  80. Hirsutism congenital gingival hyperplasia
  81. Hirsutism skeletal dysplasia mental retardation
  82. Histidinuria renal tubular defect
  83. Hittner Hirsch Kreh syndrome
  84. HMG CoA synthetase deficiency
  85. Hoepffner Dreyer Reimers syndrome
  86. Hollow visceral myopathy
  87. Holmes Benacerraf syndrome
  88. Holmes Borden syndrome
  89. Holmes Collins syndrome
  90. Holoacardius amorphus
  91. Holoprosencephaly caudal dysgenesis
  92. Holoprosencephaly deletion 2p
  93. Holoprosencephaly ectrodactyly cleft lip palate
  94. Holoprosencephaly radial heart renal anomalies
  95. Holzgreve Wagner Rehder syndrome
  96. Homocarnosinase deficiency
  97. Homocarnosinosis
  98. Homocystinuria due to defect in methylation (cbl g)
  99. Homocystinuria due to defect in methylation cbl e
  100. Homocystinuria due to defect in methylation, MTHFR deficiency
  101. Homologous wasting disease
  102. Homozygous hypobetalipoproteinemia
  103. Hoon Hall syndrome
  104. Hordnes Engebretsen Knudtson syndrome
  105. Hornova Dlurosova syndrome
  106. Houlston Ironton Temple syndrome
  107. Howard Young syndrome
  108. Hoyeraal syndrome
  109. Humero spinal dysostosis congenital heart disease
  110. Humeroradial synostosis
  111. Humeroradioulnar synostosis
  112. Humerus trochlea aplasia of
  113. Hungry Tumor Syndrome
  114. Hunter Carpenter Mc donald syndrome
  115. Hunter Jurenka Thompson syndrome
  116. Hunter Macpherson syndrome
  117. Hunter Mcalpine syndrome
  118. Hunter Mcdonald syndrome
  119. Hunter Rudd Hoffmann syndrome
  120. Huriez scleroatrophic syndrome
  121. Hurst Hallam Hockey syndrome
  122. Hutteroth Spranger syndrome
  123. Hyalinosis systemic short stature
  124. Hyaloideoretinal degeneration of wagner
  125. Hyde Forster Mccarthy Berry syndrome
  126. Hydrocephalus autosomal recessive
  127. Hydrocephalus costovertebral dysplasia Sprengel anomaly
  128. Hydrocephalus craniosynostosis bifid nose
  129. Hydrocephalus endocardial fibroelastosis cataract
  130. Hydrocephalus growth retardation skeletal anomalies
  131. Hydrocephalus obesity hypogonadism
  132. Hydrocephalus skeletal anomalies
  133. Hydrocephaly corpus callosum agenesis diaphragmatic hernia
  134. Hydrocephaly low insertion umbilicus
  135. Hydrocephaly tall stature joint laxity
  136. Hydronephrosis peculiar facial expression
  137. Hydrops ectrodactyly syndactyly
  138. Hydrops fetalis anemia immune disorder absent thumb
  139. Hyperbilirubinemia transient familial neonatal
  140. Hyperbilirubinemia type 1
  141. Hyperbilirubinemia type 2
  142. Hypercalcemia, familial benign type 1
  143. Hypercalcemia, familial benign type 2
  144. Hypercalcemia, familial benign type 3
  145. Hypercalcemia, familial benign
  146. Hypercalcinuria idiopathic
  147. Hypercalcinuria macular coloboma
  148. Hypercholesterolemia due to arg3500 mutation of Apo B-100
  149. Hypercholesterolemia due to LDL receptor deficiency
  150. Hyperferritinemia, hereditary, with congenital cataracts
  151. Hyperglycinemia, isolated nonketotic type 1
  152. Hyperglycinemia, isolated nonketotic type 2
  153. Hyperglycinemia, isolated nonketotic
  154. Hypergonadotropic ovarian failure, familial or sporadic
  155. Hyperimidodipeptiduria
  156. Hyperimmunoglobulin E - reccurrent infection syndrome
  157. Hyperimmunoglobulinemia D with periodic fever
  158. Hyperinsulinism due to focal adenomatous hyperplasia
  159. Hyperinsulinism due to glucokinase deficiency
  160. Hyperinsulinism due to glutamodehydrogenase deficiency
  161. Hyperkeratosis palmoplantar localized acanthokeratolytic
  162. Hyperkeratosis palmoplantar localized epidermolytic
  163. Hyperkeratosis palmoplantar with palmar crease hyperkeratosis
  164. Hyperornithinemia
  165. Hyperostosid corticalis deformans juvenilis
  166. Hyperoxaluria type 2
  167. Hyperparathyroidism, familial, primary
  168. Hyperparathyroidism, neonatal severe primary
  169. Hyperphalangism dysmorphy bronchomalacia
  170. Hyperphenilalaninemia due to pterin-4-alpha-carbin
  171. Hyperphenylalalinemia due to dihydropteridine reductase deficiency
  172. Hyperphenylalaninemia due to 6-pyruvoyltetrahydrop
  173. Hyperphenylalaninemia due to dehydratase deficiency
  174. Hyperphenylalaninemia due to GTP cyclohydrolase deficiency
  175. Hyperphenylalaninemic embryopathy
  176. Hyperprolinemia type II
  177. Hypertelorism and tetralogy of Fallot
  178. Hypertelorism hypospadias syndrome
  179. Hypertensive hyperkalemia, familial
  180. Hypertensive hypokalemia familial
  181. Hyperthermia induced defects
  182. Hyperthyroidism due to mutations in TSH receptor
  183. Hypertrichosis atrophic skin ectropion macrostomia
  184. Hypertrichosis brachydactyly obesity and mental retardation
  185. Hypertrichosis congenital generalized X linked
  186. Hypertrichosis retinopathy dysmorphism
  187. Hypertrichosis, anterior cervical
  188. Hypertrichotic osteochondrodysplasia
  189. Hypertrophic branchial myopathy
  190. Hypertrophic hemangiectasia
  191. Hypertrophic myocardiopathy
  192. Hypertrophic osteoarthropathy, primary or idiopathic
  193. Hypertropic neuropathy of Dejerine-Sottas
  194. Hypoadrenocorticism hypoparathyroidism moniliasis
  195. Hypo-alphalipoproteinemia primary
  196. Hypobetalipoproteinaemia ataxia hearing loss
  197. Hypocalcemia, autosomal dominant
  198. Hypocalcinuric hypercalcemia, familial type 1
  199. Hypocalcinuric hypercalcemia, familial type 2
  200. Hypocalcinuric hypercalcemia, familial type 3
  201. Hypocalcinuric hypercalcemia, familial
  202. Hypodontia dysplasia of nails
  203. Hypofibrinogenemia, familial
  204. Hypoglycemia with deficiency of glycogen synthetase in the liver
  205. Hypogonadism cardiomyopathy
  206. Hypogonadism hypogonadotropic due to mutations in GR hormone
  207. Hypogonadism male mental retardation skeletal anomaly
  208. Hypogonadism mitral valve prolapse mental retardation
  209. Hypogonadism primary partial alopecia
  210. Hypogonadism retinitis pigmentosa
  211. Hypogonadotropic hypogonadism syndactyly
  212. Hypogonadotropic hypogonadism without anosmia, X linked
  213. Hypogonadotropic hypogonadism-anosmia, X linked
  214. Hypogonadotropic hypogonadism-anosmia
  215. Hypokalemic alkalosis with hypercalcinuria
  216. Hypoketonemic hypoglycemia
  217. Hypomagnesemia primary
  218. Hypomandibular faciocranial dysostosis
  219. Hypomelia mullerian duct anomalies
  220. Hypoparathyroidism familial isolated
  221. Hypoparathyroidism nerve deafness nephrosis
  222. Hypoparathyroidism short stature mental retardation
  223. Hypoparathyroidism short stature
  224. Hypoparathyroidism X linked
  225. Hypophosphatasia, infantile
  226. Hypopigmentation oculocerebral syndrome Cross type
  227. Hypopituitarism micropenis cleft lip palate
  228. Hypopituitarism postaxial polydactyly
  229. Hypoplasia hepatic ductular
  230. Hypoplasia of the tibia with polydactyly
  231. Hypoplastic right heart microcephaly
  232. Hypoplastic thumbs hydranencephaly
  233. Hypoproconvertinemia
  234. Hyporeninemic hypoaldosteronism - double check?
  235. Hyposmia nasal hypoplasia hypogonadism
  236. Hypospadias mental retardation Goldblatt type
  237. Hypotelorism cleft palate hypospadias
  238. Hypothalamic hamartomas
  239. Hypothyroidism due to iodide transport defect
  240. Hypothyroidism postaxial polydactyly mental retardation
  241. Hypotonic sclerotic muscular dystrophy
  242. Hypotrichosis mental retardation Lopes type
  243. Hypoxanthine guanine phosphoribosyltransferase deficiency
  244. Ichthyosiform erythroderma corneal involvement deafness
  245. Ichthyosis alopecia eclabion ectropion mental retardation
  246. Ichthyosis and male hypogonadism
  247. Ichthyosis cheek eyebrow syndrome
  248. Ichthyosis congenita biliary atresia
  249. Ichthyosis hepatosplenomegaly cerebellar degeneration
  250. Ichthyosis hystrix, Curth Macklin type
  251. Ichthyosis male hypogonadism
  252. Ichthyosis mental retardation Devriendt type
  253. Ichthyosis mental retardation dwarfism renal impairment
  254. Ichthyosis microphthalmos
  255. Ichthyosis tapered fingers midline groove up
  256. Ichthyosis, erythrokeratolysis hemalis
  257. Ichthyosis, keratosis follicularis spinulosa Decalvans
  258. Ichthyosis, lamellar recessive
  259. Idaho syndrome
  260. Idiopathic adult neutropenia
  261. Idiopathic alveolar hypoventilation syndrome
  262. Idiopathic congenital nystagmus, dominant, X- linked
  263. Idiopathic diffuse interstitial fibrosis
  264. Idiopathic dilatation of the pulmonary artery
  265. Idiopathic double athetosis
  266. [[Idiopathic edema]]
  267. Idiopathic facial palsy
  268. Idiopathic hypereosinophilic syndrome
  269. Idiopathic infection caused by BCG or atypical mycobacteria
  270. IGDA syndrome
  271. Ilyina Amoashy Grygory syndrome
  272. Imaizumi Kuroki syndrome
  273. Immotile cilia syndrome, due to defective radial spokes
  274. Immotile cilia syndrome, due to excessively long cilia
  275. Immotile cilia syndrome, Kartagener type
  276. Immune deficiency, familial variable
  277. Immunodeficiency with short limb dwarfism
  278. Immunodeficiency, microcephaly with normal intelligence
  279. Imperforate oropharynx costo vetebral anomalies
  280. Inactive colon
  281. Incontinentia pigmenti type 1
  282. Incontinentia pigmenti type 2
  283. Infant epilepsy with migrant focal crisis
  284. Infantile axonal neuropathy
  285. Infantile convulsions and paroxysmal choreoathetosis, familial
  286. Infantile dysphagia
  287. Infantile multisystem inflammatory disease
  288. Infantile onset spinocerebellar ataxia
  289. Infantile recurrent chronic multifocal osteomyolitis
  290. Infantile spasms broad thumbs
  291. Infantile striato thalamic degeneration
  292. Infundibulopelvic stenosis multicystic kidney
  293. Insensitivity to pain with anhidrosis
  294. Instability mitotic non disjunction syndrome
  295. Insulin-resistance type B
  296. Insulin-resistant acanthosis nigricans, type A
  297. Intercellular cholesterol esterification disease
  298. Interferon gamma, receptor 1, deficiency
  299. Internal carotid agenesis
  300. Intestinal atresia multiple
  301. Intestinal lipodystrophy
  302. Intestinal lymphangiectasia
  303. Intestinal malrotation facial anomalies familial type
  304. Intracranial aneurysms multiple congenital anomaly
  305. Intracranial arterioveinous malformation
  306. Intractable singultus
  307. Intrathoracic kidney vertebral fusion
  308. Intrauterine growth retardation mandibular malar hypoplasia
  309. Intrinsic factor, congenital deficiency of
  310. Iris dysplasia hypertelorism deafness
  311. Irons Bhan syndrome
  312. Isaacs Mertens syndrome
  313. Ischiadic hypoplasia renal dysfunction immunodeficiency
  314. Ischiopatellar dysplasia
  315. Isthmian coarctation
  316. Ivic Syndrome
  317. Jaffer Beighton syndrome
  318. Jancar syndrome
  319. Jansen type metaphyseal chondrodysplasia
  320. Jensen syndrome
  321. Jequier Kozlowski skeletal dysplasia
  322. Jeune syndrome situs inversus
  323. Johnson Hall Krous syndrome
  324. Johnston Aarons Schelley syndrome
  325. Jones Hersh Yusk syndrome
  326. Jones syndrome
  327. Jorgenson Lenz syndrome
  328. Joseph disease
  329. Joubert syndrome bilateral chorioretinal coloboma
  330. Juberg Hayward syndrome
  331. Judge Misch Wright syndrome
  332. Jung Wolff Back Stahl syndrome
  333. Juvenile cataract cerebellar atrophy myopathy mental retardation
  334. Juvenile gastrointestinal polyposis
  335. Juvenile macular degeneration hypotrichosis
  336. Juvenile muscular atrophy of the distal upper limb
  337. Juvenile temporal arteritis