LC60 Aplasia cutis congenita

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Congenital absence of skin. The commonest form presents as a defect limited to the scalp. It is also a component of a number of genetic syndromes.

Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.

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