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Epidermolysis Bullosa Dystrophica
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Epidermolysis Bullosa Dystrophica 8 coordinate concepts∟ ∟ ∟ ∟ ∟ Epidermolysis Bullosa Dystrophica 8 coordinate concepts∟ ∟ ∟ ∟ Epidermolysis Bullosa Dystrophica 8 coordinate concepts∟ ∟ ∟ ∟ ∟ Epidermolysis Bullosa Dystrophica 8 coordinate concepts∟ ∟ ∟ ∟ ∟ Epidermolysis Bullosa Dystrophica 8 coordinate concepts∟ ∟ ∟ ∟ ∟ Epidermolysis Bullosa Dystrophica 8 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ ∟ Epidermolysis Bullosa Dystrophica ∟ ∟ ∟ ∟ ∟ Epidermolysis Bullosa Dystrophica ∟ ∟ ∟ ∟ Epidermolysis Bullosa Dystrophica ∟ ∟ ∟ ∟ ∟ Epidermolysis Bullosa Dystrophica ∟ ∟ ∟ ∟ ∟ Epidermolysis Bullosa Dystrophica ∟ ∟ ∟ ∟ ∟ Epidermolysis Bullosa Dystrophica |
History note: | Epidermolysis Bullosa (1966-1990)X |
historyNote*: | 91
X |
publicMeSHNote*: | 91
X |
Scope note: | Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in COLLAGEN TYPE VII, a major component fibrils of BASEMENT MEMBRANE and EPIDERMIS.
X |
activeMeSHYear*: | 2007X |
dateCreated*: | 1990-02-12X |
dateEstablished*: | 1991-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | AGSX |
Type: | |
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Labels and equivalent concepts: | Dystrofinen rakkulainen epidermolyysi (fi) XDystrofinen epidermolysis bullosa (fi, replaced) Epidermolysis Bullosa, Dystrophic (en, replaced) Epidermolysis Bullosa Dystrophica, Recessive (en, replaced) Epidermolysis Bullosa Dystrophica, Hallopeau-Siemens Type (en, replaced) Epidermolysis Bullosa Dystrophica, Cockayne-Touraine Type (en, replaced) Epidermolysis Bullosa Dystrophica, Dominant (en, replaced) Dystrophic Epidermolysis Bullosa (en, replaced) Epidermolysis bullosa dystrophica (la-FI, replaced) |
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