Aplasia cutis congenita

Orpha code: 1114OMIM code: 107600

Definition

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. Aplasia cutis congenita (ACC) may occasionally be associated with other anomalies.

Disease data
Classification

Malformation syndrome

ORPHA code
1114
OMIM code
107600
ICD10 code
Q84.8
ICD11 code
LC60

No additional description.

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