BabelNet

bn:01419294n

Noun Concept

No term available

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

مرض

مرض نادر

اضطراب جيني

انحلال البشرة الفقاعي الحثلي

عدم تنسج الجلد الخلقي

GENETIC ASSOCIATION

COL7A1