Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/4

From Wikipedia, the free encyclopedia

WikiProject Missing encyclopedic articles
v  d  e
Project page - The goal of this project is to ensure that Wikipedia has a corresponding article for every article in every other encyclopedia. Sign in!
Weekly focus : Hotlist of topics/I Only 286 remain!
Hotlist of topics - 79% done
1911 verification - 1.9%
General topics - 67.8% done
Other Wikipedias: de es fr
Biographies - 96.7% done
Science topics - 43% done
Catholic topics - 43.2% done
Easton's Bible Dictionary - 77.9% done
Gutenberg authors - 41.4% done
Literary Encyclopedia - 68% done
Find-A-Grave - 14.7% done
Miscellaneous
Many other lists of politicians, albums, films, TV shows and others.
Overall progress - 50.5%
Spread the word! {{Project missing articles}}


<< Previous · ^up^ · Next >>


  1. D ercole syndrome
  2. Daentl Towsend Siegel syndrome
  3. Dahlberg Borer Newcomer syndrome
  4. Daish Hardman Lamont syndrome
  5. Dandy Walker facial hemangioma
  6. Dandy Walker malformation postaxial polydactyly
  7. Dandy Walker syndrome recessive form
  8. Dandy-walker malformation with mental retardation, basal ganglia disease, and seizures
  9. Dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy
  10. Daneman Davy Mancer syndrome
  11. Davenport Donlan syndrome
  12. David syndrome
  13. Davis Lafer syndrome
  14. De Barsy syndrome
  15. De Hauwere Leroy Adriaenssens syndrome
  16. De Sanctis-Cacchione syndrome
  17. Deaf blind hypopigmentation
  18. Deafness conductive ptosis skeletal anomalies
  19. Deafness conductive stapedial ear malformation facial palsy
  20. Deafness congenital onychodystrophy recessive
  21. Deafness craniofacial syndrome
  22. Deafness enamel hypoplasia nail defects
  23. Deafness epiphyseal dysplasia short stature
  24. Deafness goiter stippled epiphyses
  25. Deafness hyperuricemia neurologic ataxia
  26. Deafness hypogonadism syndrome
  27. Deafness hypospadias metacarpal and metatarsal syndrome
  28. Deafness mesenteric diverticula of small bowel neuropathy
  29. Deafness mixed with perilymphatic Gusher, X-linked
  30. Deafness nephritis ano rectal malformation
  31. Deafness neurosensory pituitary dwarfism
  32. Deafness nonsyndromic, Connexin 26 linked
  33. Deafness oligodontia syndrome
  34. Deafness onychodystrophy dominant form
  35. Deafness peripheral neuropathy arterial disease
  36. Deafness progressive cataract autosomal dominant
  37. Deafness skeletal dysplasia lip granuloma
  38. Deafness symphalangism
  39. Deafness vitiligo achalasia
  40. Deafness white hair contractures papillomas
  41. Deafness X-linked, DFN3
  42. Deafness, autosomal dominant nonsyndromic sensorineural
  43. Deafness, isolated, due to mitochondrial transmission
  44. Deafness, neurosensory nonsyndromic recessive, DFN
  45. Deafness, X linked, DFN
  46. Deal Barratt Dillon syndrome
  47. Deciduous skin
  48. Decompensated phoria
  49. Defect in synthesis of adenosylcobalamin
  50. Defective apolipoprotein B-100
  51. Defective expression of HLA class 2
  52. Degenerative motor system disease
  53. Degenerative optic myopathy
  54. Degos 'en cocarde' erythrokeratoderma
  55. Dehydratase deficiency
  56. Dejerine-Sottas disease
  57. Delayed membranous cranial ossification
  58. Delayed speech facial asymmetry strabismus ear lobe creases
  59. Deletion 6q16 q21
  60. Delleman Oorthuys syndrome
  61. Delta-1-pyrroline-5-carboxylate dehydrogenase deficiency
  62. Delta-sarcoglycanopathy
  63. Dementia progressive lipomembranous polycysta
  64. Dementia, familial British
  65. Demodicidosis
  66. Dennis Cohen syndrome
  67. Dennis Fairhurst Moore syndrome
  68. Dent disease
  69. Dental aberrations steroid dehydrogenase deficienciency
  70. Dental tissue neoplasm
  71. Dentatorubral pallidoluysian atrophy
  72. Dentin dysplasia sclerotic bones
  73. Dentin dysplasia, coronal
  74. Dentin dysplasia, radicular
  75. Der kaloustian Jarudi Khoury syndrome
  76. Der Kaloustian Mcintosh Silver syndrome
  77. Dercum's disease
  78. Dermatocardioskeletal syndrome Boronne type
  79. Dermatoleukodystrophy
  80. Dermatoosteolysis Kirghizian type
  81. Dermatopathia pigmentosa reticularis
  82. Dermatophytids
  83. Dermochondrocorneal dystrophy of François
  84. Dermoodontodysplasia
  85. Desbuquois syndrome
  86. Desmin related myopathy
  87. Desmoid disease
  88. Desmoid tumor
  89. Developmental delay hypotonia extremities hypertrophy
  90. Developmental dysphasia familial
  91. Devic syndrome
  92. Devriendt Legius Fryns syndrome
  93. Devriendt Vandenberghe Fryns syndrome
  94. Dexamethasone sensitive hypertension
  95. Dextrocardia-bronchiectasis-sinusitis
  96. D-glycerate dehydrogenase deficiency
  97. D-glycericacidemia
  98. Diabetes hypogonadism deafness mental retardation
  99. Diabetes insipidus, diabetes mellitus, optic atrophy
  100. Diabetes insipidus, nephrogenic type 1
  101. Diabetes insipidus, nephrogenic type 2
  102. Diabetes insipidus, nephrogenic type 3
  103. Diabetes insipidus, nephrogenic, dominant type
  104. Diabetes insipidus, nephrogenic, recessive type
  105. Diabetes mellitus, transient neonatal
  106. Diabetes persistent mullerian ducts
  107. Diabetic embryopathy
  108. Diaphragmatic agenesia
  109. Diaphragmatic agenesis radial aplasia omphalocele
  110. Diaphragmatic defect limb deficiency skull defect
  111. Diaphragmatic hernia abnormal face limb
  112. Diaphragmatic hernia exomphalos corpus callosum agenesis
  113. Diaphragmatic hernia upper limb defects
  114. Diarrhea chronic with villous atrophy
  115. Diarrhea polyendocrinopathy infections X linked
  116. Diastematomyelia
  117. Dibasic aminoaciduria type 1
  118. Dicarboxylicaminoaciduria
  119. Die Smulders Droog Van Dijk syndrome
  120. Die Smulders Vles Fryns syndrome
  121. Diencephalic syndrome
  122. Dieterich's disease
  123. Diffuse idiopathic skeletal hyperostosis
  124. Diffuse leiomyomatosis with Alport syndrome
  125. Diffuse neonatal hemangiomatosis
  126. Diffuse palmoplantar keratoderma, Bothnian type
  127. Diffuse panbronchiolitis
  128. Digestive duplication
  129. Digitorenocerebral syndrome
  130. Dihydropteridine reductase deficiency
  131. Dihydropyrimidine dehydrogenase deficiency
  132. Dimitri Sturge Weber syndrome
  133. Dincsoy Salih Patel syndrome
  134. Dinno Shearer Weisskopf syndrome
  135. Diomedi Bernardi Placidi syndrome
  136. Dionisi Vici Sabetta Gambarara syndrome
  137. Diphallus rachischisis imperforate anus
  138. Diphosphoglycerate mutase deficiency of erythrocyte
  139. Disaccharide intolerance iii
  140. Dislocation of the hip dysmorphism
  141. Disorder in the hormonal synthesis with or without goiter
  142. Disorganization syndrome
  143. Dissecting cellulitis of the scalp
  144. Dissociative hysteria
  145. Distal arthrogryposis Moore Weaver type
  146. Distal myopathy Markesbery-Griggs type
  147. Distal myopathy with vocal cord weakness
  148. Distal myopathy, Nonaka type
  149. Distal myopathy
  150. Distal primary acidosis, familial
  151. Distichiasis heart congenital anomalies
  152. Distomatosis
  153. D-minus hemolytic uremic syndrome
  154. Dobrow syndrome
  155. Dominant cleft palate
  156. Dominant zonular cataract
  157. Donnai Barrow syndrome
  158. Door syndrome
  159. Dopamine beta-hydroxylase deficiency
  160. DOPA-responsive dystonia
  161. Double cortex
  162. Double discordia
  163. Double fingernail of fifth finger
  164. Double outlet left ventricle
  165. Double tachycardia induced by catecholamines
  166. Double uterus-hemivagina-renal agenesis
  167. Doyne honeycomb retinal dystrophy
  168. D-plus hemolytic uremic syndrome
  169. Drachtman Weinblatt Sitarz syndrome
  170. Duane anomaly mental retardation
  171. Duhring Brocq disease
  172. Duhring's disease
  173. Duker Weiss Siber syndrome
  174. Duodenal atresia tetralogy of Fallot
  175. Duodenal atresia
  176. Duplication of leg mirror foot
  177. Duplication of the thumb unilateral biphalangeal
  178. Duplication of urethra
  179. Dupont Sellier Chochillon syndrome
  180. Dupuytren subungual exostosis
  181. Dust-induced lung disease
  182. Dwarfism bluish sclerae
  183. Dwarfism deafness retinitis pigmentosa
  184. Dwarfism lethal type advanced bone age
  185. Dwarfism mental retardation eye abnormality
  186. Dwarfism short limb absent fibulas very short digits
  187. Dwarfism stiff joint ocular abnormalities
  188. Dwarfism syndesmodysplasic
  189. Dwarfism tall vertebrae
  190. Dwarfism thanatophoric
  191. Dwarfism thin bones multiple fractures
  192. Dyggve-Melchior-Clausen syndrome
  193. Dykes Markes Harper syndrome
  194. Dyschondrosteosis nephritis
  195. Dyschromatosis universalis
  196. Dysencephalia splachnocystica or Meckel Gruber
  197. Dysequilibrium syndrome
  198. Dyserythropoietic anemia, congenital type 1
  199. Dyserythropoietic anemia, congenital type 2
  200. Dyserythropoietic anemia, congenital type 3
  201. Dyserythropoietic anemia, congenital
  202. Dysferlinopathy
  203. Dysfibrinogenemia, familial
  204. Dysharmonic skeletal maturation muscular fiber disproportion
  205. Dyskeratosis congenita of Zinsser Cole Engman
  206. Dyskeratosis follicularis
  207. Dysmorphism abnormal vocalization mental retardation
  208. Dysmorphism cleft palate loose skin
  209. Dysmyelination
  210. Dysosteosclerosis
  211. Dysostosis acral with facial and genital abnormalities
  212. Dysostosis peripheral
  213. Dysostosis Stanescu type
  214. Dysostosis
  215. Dysphasic dementia, hereditary
  216. Dysphonia, chronic spasmodic
  217. Dysplasia epiphysealis hemimelica
  218. Dysplastic cortical hyperostosis
  219. Dysprothrombinemia
  220. Dysraphism cleft lip palate limb reduction defects
  221. Dyssegmental dysplasia glaucoma
  222. Dyssegmental dysplasia Silverman Handmaker type
  223. Dystonia musculorum deformans type 1
  224. Dystonia musculorum deformans type 2
  225. Dystonia musculorum deformans
  226. Dystonia progressive with diurnal variation
  227. Dystrophia myotonica
  228. Dystrophic epidermolysis bullosa
  229. Dystrophinopathy
  230. Ear, patella, short stature syndrome
  231. Earlobes thickened conductive deafness
  232. Eccentrochondrodysplasia
  233. Eccrine acrospiroma
  234. Ecp syndrome
  235. Ectodermal dysplasia absent dermatoglyphics
  236. Ectodermal dysplasia adrenal cyst
  237. Ectodermal dysplasia alopecia preaxial polydactyly
  238. Ectodermal dysplasia anhidrotic
  239. Ectodermal dysplasia arthrogryposis diabetes mellitus
  240. Ectodermal dysplasia Bartalos type
  241. Ectodermal dysplasia Berlin type
  242. Ectodermal dysplasia blindness
  243. Ectodermal dysplasia ectrodactyly macular dystrophy
  244. Ectodermal dysplasia hypohidrotic autosomal dominant
  245. Ectodermal dysplasia hypohidrotic hypothyroidism ciliary diskinesia
  246. Ectodermal dysplasia Margarita type
  247. Ectodermal dysplasia mental retardation CNS malformation
  248. Ectodermal dysplasia mental retardation syndactyly
  249. Ectodermal dysplasia neurosensory deafness
  250. Ectodermal dysplasia osteosclerosis
  251. Ectodermal dysplasia tricho odonto onychial type
  252. Ectodermal dysplasia, hydrotic
  253. Ectodermal dysplasia, hypohidrotic, autosomal recessive
  254. Ectodermal dysplasias
  255. Ectodermic dysplasia anhidrotic cleft lip
  256. Ectopia lentis isolated
  257. Ectopia pupillae
  258. Ectopic coarctation
  259. Ectopic ossification familial type
  260. Ectrodactyly cardiopathy dysmorphism
  261. Ectrodactyly cleft palate syndrome
  262. Ectrodactyly diaphragmatic hernia corpus callosum
  263. Ectrodactyly dominant form
  264. Ectrodactyly ectrodermal dysplasia
  265. Ectrodactyly polydactyly
  266. Ectrodactyly recessive form
  267. Ectrodactyly-ectodermal dysplasia-cleft lip/cleft palate
  268. Ectropion inferior cleft lip and or palate
  269. Edinburgh malformation syndrome
  270. Edwards Patton Dilly syndrome
  271. Eec syndrome without cleft lip palate
  272. Eec syndrome
  273. Eem syndrome
  274. Egg shaped pupils
  275. Eijkman's syndrome
  276. Eisenmenger syndrome
  277. Elattoproteus in context of NF
  278. Electron transfer flavoprotein, deficiency of
  279. Elejalde syndrome
  280. Elliott Ludman Teebi syndrome
  281. Ellis Yale Winter syndrome
  282. Emerinopathy
  283. Emery Nelson syndrome
  284. Emery-Dreifuss muscular dystrophy, dominant type
  285. Emery-Dreifuss muscular dystrophy, X-linked
  286. Emery-Dreifuss muscular dystrophy
  287. Emphysema, congenital lobar
  288. Emphysema-penoscrotal web-deafness-mental retardation
  289. Enamel hypoplasia cataract hydrocephaly
  290. Encephalo cranio cutaneous lipomatosis
  291. Encephalocele anterior
  292. Encephalocele frontal
  293. Encephalopathy intracerebral calcification retinal
  294. Encephalopathy progressive optic atrophy
  295. Encephalopathy subacute spongiform, Gerstmann-Stra
  296. Encephalopathy-basal ganglia-calcification
  297. Encephalophathy recurrent of childhood
  298. Encephalotrigeminal angiomatosis
  299. Enchondromatosis (benign)
  300. Enchondromatosis dwarfism deafness
  301. Endocardial fibroelastosis
  302. Endometrial stromal sarcoma
  303. Endomyocardial fibroelastosis
  304. Eng Strom syndrome
  305. Engelhard Yatziv syndrome
  306. Englemann disease
  307. Enolase deficiency type 1
  308. Enolase deficiency type 2
  309. Enolase deficiency type 3
  310. Enolase deficiency type 4
  311. Enolase deficiency
  312. Enteropathica
  313. Enterovirus antenatal infection
  314. Environment associated hypertension
  315. Eosinophilic cryptitis
  316. Eosinophilic cystitis
  317. Eosinophilic gastroenteritis
  318. Eosinophilic granuloma
  319. Eosinophilic lymphogranuloma
  320. Eosinophilic Pustular Folliculitis
  321. Eosinophilic synovitis
  322. Ependymoblastoma
  323. Epidemic encephalitis
  324. Epidemic encephalomyelitis
  325. Epidermal nevus vitamin D resistant rickets
  326. Epidermodysplasia verruciformis
  327. Epidermoid carcinoma
  328. Epidermolysa bullosa simplex and limb girdle muscular dystrophy
  329. Epidermolysis bullosa acquisita
  330. Epidermolysis bullosa dystrophica, Bart type
  331. Epidermolysis bullosa dystrophica, dominant type
  332. Epidermolysis bullosa herpetiformis, Dowling-Meara
  333. Epidermolysis bullosa intraepidermic
  334. Epidermolysis bullosa inversa dystrophica
  335. Epidermolysis bullosa simplex with anodontia, hair
  336. Epidermolysis bullosa simplex, Cockayne-Touraine type
  337. Epidermolysis bullosa simplex, Koebner type
  338. Epidermolysis bullosa simplex, Ogna type
  339. Epidermolysis bullosa, dermolytic
  340. Epidermolysis bullosa, generalized atrophic benign
  341. Epidermolysis bullosa, junctional, Herlitz-Pearson
  342. Epidermolysis bullosa, junctional, with pyloric atrophy
  343. Epidermolysis bullosa, junctional
  344. Epidermolysis bullosa, pretibial
  345. Epidermolytic palmoplantar keratoderma Vorner type
  346. Epilepsy benign neonatal dominant form
  347. Epilepsy benign neonatal recessive form
  348. Epilepsy mental deterioration Finnish type
  349. Epilepsy microcephaly skeletal dysplasia
  350. Epilepsy occipital calcifications
  351. Epilepsy progressive myoclonic type 2
  352. Epilepsy telangiectasia
  353. Epilepsy with myoclono-astatic crisis
  354. Epilepsy, benign occipital
  355. Epilepsy, myoclonic progressive familial
  356. Epilepsy, nocturnal, frontal lobe type
  357. Epilepsy, partial, familial
  358. Epimerase deficiency
  359. Epimetaphyseal dysplasia cataract
  360. Epimetaphyseal skeletal dysplasia
  361. Epiphyseal dysplasia dysmorphism camptodactyly
  362. Epiphyseal dysplasia hearing loss dysmorphism
  363. Epiphyseal dysplasia multiple
  364. Epiphysealis hemimelica dysplasia
  365. Epithelial-myoepithelial carcinoma
  366. Epitheliopathy (APMPPE)
  367. Epitheliopathy, acute posterior multifocal placoid
  368. Epstein syndrome
  369. Erb-Duchenne palsy
  370. Erdheim disease
  371. Eronen Somer Gustafsson syndrome
  372. Erosive pustular dermatosis of the scalp
  373. Erythroderma desquamativa of Leiner
  374. Erythroderma lethal congenital
  375. Erythrokeratodermia ataxia
  376. Erythrokeratodermia progressive symmetrica ichthyosis
  377. Erythrokeratodermia symmetrica progressiva
  378. Erythrokeratodermia variabilis ichthyosis
  379. Erythrokeratodermia variabilis, Mendes da Costa type
  380. Erythrokeratodermia with ataxia
  381. Erythrokeratolysis hiemalis ichthyosis
  382. Escher Hirt syndrome
  383. Esophageal atresia associated anomalies
  384. Esophageal atresia coloboma talipes
  385. Esophageal duodenal atresia abnormalities of hands
  386. Essential iris atrophy
  387. Essential mixed cryoglobulinemia
  388. Esthesioneuroblastoma
  389. Ethylmalonic aciduria
  390. Ethylmalonic adipic aciduria
  391. Euhidrotic ectodermal dysplasia
  392. Eunuchoidism familial
  393. Exercise induced anaphylaxis
  394. Exfoliative dermatitis
  395. Exner syndrome
  396. Exomphalos-macroglossia-gigantism syndrome
  397. Exostoses anetodermia brachydactyly type E
  398. Experimental allergic encephalomyelitis
  399. Extrasystoles short stature hyperpigmentation microcephaly
  400. Exudative retinopathy familial, autosomal dominant
  401. Exudative retinopathy familial, autosomal recessive
  402. Exudative retinopathy familial, X linked, recessive
  403. Exudative retinopathy, familial
  404. Eye defects arachnodactyly cardiopathy
  405. Eyebrows duplication syndactyly