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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.
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Specific anatomy - multiple selections are allowed
synonyms
- Aplasia cutis congenita
- Syndromic aplasia cutis congenita
- Aplasia cutis congenita due to adverse intrauterine events
- Aplasia cutis congenita secondary to adverse intrauterine events
- Aplasia cutis congenita of limbs
- Recessive aplasia cutis congenita of limbs
- Aplasia cutis congenita of scalp
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