Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja 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 Klasyfikacja Malformation syndrome Kod ORPHA 1114 Kod OMIM 107600 Kod ICD10 Q84.8 Kod ICD11 LC60 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl