Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/4

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