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bn:01419294n
Noun Concept
NL
No term available
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
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EN
Epidermolysis bullosa dystrophica
Aplasia cutis congenita
GENETIC ASSOCIATION
COL7A1

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