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Aplasia cutis congenita

rare

Aplasia cutis congenita (ACC) is a rare skin disorder characterized by localized absence of skin that is usually located on the scalp but can occur anywhere on the body including the face, trunk and extremities. ACC may occasionally be associated with other anomalies.

Identifiers
MONDO:0007145 OMIM:107600Orphanet:1114
Causal genes
BMS1
Part of
Hereditary skin disorderMixed dermis disorder
Also known as
ACC · aplasia cutis congenita (disease) · aplasia cutis congenita nonsyndromic · aplasia cutis congenita recessive · aplasia cutis congenita, nonsyndromic

Subtypes

All diseases Rare only
Disease Subtypes
Aplasia cutis autosomal recessive
Aplasia cutis congenita dominant
Aplasia cutis-myopia syndrome

Rare disease

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