Category:Rare Diseases
From WikiMD.com Medical Encyclopedia
This is a category page. It lists all of the pages in category "Rare Diseases" as well as all subcategories of category "Rare Diseases" if any exist.
Pages in category "Rare Diseases"
The following 200 pages are in this category, out of 267 total.
(previous page) (next page)A
- AADC deficiency
- Acute necrotizing encephalopathy
- Akesson syndrome
- Albinism, yellow mutant type
- Alipogene tiparvovec
- Amylo-1,6-glucosidase deficiency
- Amyoplasia
- Andre syndrome
- Angiolipoleiomyoma
- Aniridia renal agenesis psychomotor retardation
- Annular constricting bands
- Anophthalmia Waardenburg syndrome
- Apert
- Aplasia cutis myopia
- Atmit
B
C
- Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
- Carcinoma, merkel cell
- Carnitine uptake defect
- Caudal regression syndrome
- CCA syndrome
- Cerebrofaciothoracic dysplasia
- Chemke–Oliver–Mallek syndrome
- Cleft lip palate mental retardation corneal opacity
- Cleft lip palate oligodontia syndactyly pili torti
- Cleft lip palate-tetraphocomelia
- Cole–Carpenter syndrome
- Combarros Calleja Leno syndrome
- Congenital epulis
- Congenital hypoplastic anemia
- Coproporphyria
- Cormier–Rustin–Munnich syndrome
- Corticobasal syndrome
- Costeff optic atrophy syndrome
- Coxoauricular syndrome
- Cramer–Niederdellmann syndrome
- Craniosynostosis mental retardation heart defects
- Crawfurd syndrome
- Crouzonodermoskeletal syndrome
- Curry–Hall syndrome
- Cystinoses
D
- Deaf blind hypopigmentation
- Deafness hypospadias metacarpal and metatarsal syndrome
- Desmons syndrome
- Diaphragmatic agenesis radial aplasia omphalocele
- Diaphragmatic defect limb deficiency skull defect
- Dienoyl-CoA reductase deficiency
- Diffuse alopecia
- Diffuse neonatal hemangiomatosis
- Diprosopus
- Distal arthrogryposis Moore–Weaver type
- Distal myopathy Markesbery–Griggs type
- Dominant cleft palate
- Doose syndrome
- Dupuytren subungual exostosis
- Dwarfism bluish sclerae
E
- Ectodermal dysplasia hypohidrotic autosomal dominant
- Ectodermal dysplasia Margarita type
- Ectodermal dysplasia mental retardation syndactyly
- Ectodermal dysplasia-skin fragility syndrome
- Ectopic ossification familial type
- Ectopic thymus
- Ectrodactyly-polydactyly syndrome
- Emery-Dreifuss syndrome
- Epidermolysis bullosa, junctional, Herlitz–Pearson
- Epiphyseal dysplasia dysmorphism camptodactyly
- Eprodisate disodium
- Erythrokeratoderma en cocardes (Degos syndrome)
- Escher Hirt syndrome
- Extrasystoles short stature hyperpigmentation microcephaly
- Exudative retinopathy, familial
F
G
H
- Halal Setton Wang syndrome
- Hay–Wells syndrome recessive type
- Heide syndrome
- Hemangiopericytoma
- Hemicord syndrome
- Hemifacial atrophy agenesis of the caudate nucleus
- Heparane sulfamidase deficiency
- Hereditary Multiple Exostoses
- Hinson-Pepys disease
- Hirsutism congenital gingival hyperplasia
- Holmes Collins syndrome
- Holmes–Collins syndrome
- Homologous wasting disease
- HSN2
- Hypernychthemeral syndrome
- Hypertrichosis congenital generalized X linked
- Hypertrophic hemangiectasia
- Hypertrophic osteoarthropathy, primary or idiopathic
- Hypohidrotic ectodermal dysplasia with immune deficiency
- Hypoparathyroidism familial isolated
- Hypoparathyroidism short stature mental retardation
- Hypoplastic right heart microcephaly
- Hypovitaminosis D
I
K
L
M
- Major affective disorder
- Mandibulofacial dysostosis-microcephaly syndrome
- Marfanoid craniosynostosis syndrome
- Markel–Vikkula–Mulliken syndrome
- Maroteaux–Fonfria syndrome
- Massa Casaer Ceulemans syndrome
- McDowall syndrome
- Medeira Dennis Donnai syndrome
- Megalocornea mental retardation syndrome
- Meige's syndrome
- Menetrier's disease
- Menke-Hennekam syndrome
- Mental retardation arachnodactyly hypotonia telangiectasia
- Mental retardation cataracts calcified pinnae myopathy
- Mental retardation microcephaly unusual facies
- Mental retardation nasal hypoplasia obesity genital hypoplasia
- Mental retardation short stature absent phalanges
- Mental retardation short stature deafness genital
- Mental retardation short stature hand contractures genital anomalies
- Mental retardation short stature wedge shaped epiphyses
- Mental retardation-polydactyly-uncombable hair
- Mesenteric panniculitis
- Microspherophakia with hernia
- Mirror polydactyly-vertebral segmentation-limb defects syndrome
- Mmih syndrome
- MMIH syndrome
- Monosomy 18p
- Monosomy 1p36 syndrome
- Morgagni Stewart Morel syndrome
- Morgani–Turner–Albright syndrome
- Morgellon's
- Multiple pterygium syndrome lethal type
- Muscular dystrophy limb girdle type 2A, Erb type
- Muscular dystrophy limb-girdle autosomal dominant
- Muscular dystrophy limb-girdle with delta-sarcoglyan deficiency
- Myopathy tubular aggregates
O
- Ocular flutter
- Oculodental syndrome Rutherfurd syndrome
- OEIS complex
- Oliver McFarlane syndrome
- Olivopontocerebellar atrophy type 1
- Ophthalmomandibulomelic dysplasia
- Ophthalmoplegia mental retardation lingua scrotalis
- Ossifying fibroma
- Osteoectasia familial
- Osteopathia condensans disseminata with osteopoikilosis
- Otoonychoperoneal syndrome
