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bn:01419294n
Noun Concept
JA
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
Relations
Sources
IS A
病気
希少疾患
遺伝子疾患
EN
Epidermolysis bullosa dystrophica
EN
aplasia cutis congenita
GENETIC ASSOCIATION
EN
COL7A1

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