Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/4

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