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bn:01419294n
Noun Concept
Categories: Syndromes affecting the skin, Collagen disease, Genodermatoses
EN
Bart syndrome  Epidermolysis Bullosa Dystrophica, Bart Type  EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN AND DEFORMITY OF NAILS
EN
Bart syndrome, also known as aplasia cutis congenita type VI, is a rare genetic disorder characterized by the association of congenital localized absence of skin, mucocutaneous blistering and absent and dystrophic nails. Wikipedia
Definitions
Relations
Sources
EN
Bart syndrome, also known as aplasia cutis congenita type VI, is a rare genetic disorder characterized by the association of congenital localized absence of skin, mucocutaneous blistering and absent and dystrophic nails. Wikipedia
A genetic disorder characterized by congenital localized absence of skin, epidermolysis bullosa, lesions of the mouth mucosa, and dystrophic nails. Wiktionary
IS A
disease
rare disease
genetic disease
Epidermolysis bullosa dystrophica
aplasia cutis congenita
GENETIC ASSOCIATION
COL7A1
Wikipedia
EN
Bart syndrome
Wikidata
EN
Bart syndrome
Wiktionary
EN
Bart syndrome
Wikidata Alias
EN
Epidermolysis Bullosa Dystrophica, Bart Type, EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN AND DEFORMITY OF NAILS

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