Category:Rare Diseases
From WikiMD's Wellness 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 352 total.
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- AADC deficiency
- Acrogeria
- Acute necrotizing encephalopathy
- Adenosine deaminase 2 deficiency
- 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
- Anomalous insertion of extensor tendons of fingers
- Anomalous pulmonary venous return
- Anophthalmia Waardenburg syndrome
- Antigen-peptide-transporter 2 deficiency
- Apert
- Aplasia cutis myopia
- Arthrogryposis multiplex with deafness, inguinal hernias, and early death
- Ataxia-oculomotor apraxia type 1
- 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
- Choanal atresia deafness cardiac defects dysmorphia
- Chondrodysplasia punctata, Sheffield type
- 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
- Corpus callosum agenesis polysyndactyly
- Corticobasal syndrome
- Costeff optic atrophy syndrome
- Coxoauricular syndrome
- Cramer–Niederdellmann syndrome
- Craniometaphyseal dysplasia dominant type
- Craniosynostosis mental retardation heart defects
- Crawfurd syndrome
- Crouzonodermoskeletal syndrome
- Curry–Hall syndrome
- Cystinoses
D
- Deaf blind hypopigmentation
- Deafness hypospadias metacarpal and metatarsal syndrome
- Dentin dysplasia
- Depersonalization/derealization disorder
- 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
- Dwarfism mental retardation eye abnormality
- Dwarfism short limb absent fibulas very short digits
- Dwarfism stiff joint ocular abnormalities
- Dysplastic cortical hyperostosis
E
- Ectodermal dysplasia hypohidrotic autosomal dominant
- Ectodermal dysplasia Margarita type
- Ectodermal dysplasia mental retardation syndactyly
- Ectodermal dysplasia, hypohidrotic, autosomal recessive
- Ectodermal dysplasia-skin fragility syndrome
- Ectopic ossification familial type
- Ectopic thymus
- Ectrodactyly-polydactyly syndrome
- Elisabeth Anderson Sierra
- Emery-Dreifuss syndrome
- Epidermolysis bullosa dystrophica, Bart type
- Epidermolysis bullosa, dermolytic
- Epidermolysis bullosa, junctional, Herlitz–Pearson
- Epiphyseal dysplasia dysmorphism camptodactyly
- Eprodisate disodium
- Erythrokeratoderma en cocardes (Degos syndrome)
- Erythrokeratodermia variabilis ichthyosis
- Escher Hirt syndrome
- Extrasystoles short stature hyperpigmentation microcephaly
- Exudative retinopathy, familial
F
- Feigenbaum Bergeron syndrome
- Fetal akinesia syndrome X linked
- Fibrosing colonopathy
- Fibular hypoplasia scapulo pelvic dysplasia absent
- Flail limb
- Floating limb syndrome
- Focal facial dermal dysplasia
- Follicular atrophoderma
- Folliculitis ulerythematosa reticulata
- Fraser-like syndrome
- Frias syndrome
- Frontonasal dysplasia phocomelic upper limbs
G
- Gastritis, familial giant hypertrophic
- Gaucher-like disease
- Generalized trichoepithelioma
- Giedion syndrome
- Gigantism partial, nevi, hemihypertrophy, macrocephaly
- Glycogen
- Glycogen debrancher deficiency
- GNE myopathy
- Goniodysgenesis mental retardation short stature
- Gorlin Syndrome
- Growth deficiency brachydactyly unusual facies
- Growth mental deficiency syndrome of Myhre
- Growth retardation alopecia pseudoanodontia optic
H
- Halal Setton Wang syndrome
- Hay–Wells syndrome recessive type
- Heart defect tongue hamartoma polysyndactyly
- Heide syndrome
- Hemangiopericytoma
- Hemicord syndrome
- Hemifacial atrophy agenesis of the caudate nucleus
- Hemihypertrophy intestinal web corneal opacity
- Heparane sulfamidase deficiency
- Hereditary Multiple Exostoses
- Hinson-Pepys disease
- Hirsutism congenital gingival hyperplasia
- Histidinuria renal tubular defect
- Histiocyte Society
- Holmes Collins syndrome
- Holmes–Collins syndrome
- Homologous wasting disease
- HSN2
- Hydrocephaly tall stature joint laxity
- Hydronephrosis with peculiar facial expression
- Hypernychthemeral syndrome
- Hypertrichosis congenital generalized X linked
- Hypertrophic hemangiectasia
- Hypertrophic osteoarthropathy, primary or idiopathic
- Hypoadrenocorticism hypoparathyroidism moniliasis
- Hypogonadotropic hypogonadism without anosmia, X linked
- Hypohidrotic ectodermal dysplasia with immune deficiency
- Hypoparathyroidism familial isolated
- Hypoparathyroidism short stature mental retardation
- Hypoplastic right heart microcephaly
- Hypovitaminosis D
