LC7ZICD-11 MMS 2026-01
Structural developmental anomalies of the skin, unspecified
Exclusions from above levels
5C58.12– Congenital erythropoietic porphyria5C64.20– Acrodermatitis enteropathicaEG63– pilonidal cyst or sinus
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- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Sibling codes
Foundation entity
Structural developmental anomalies of the skin – http://id.who.int/icd/entity/653663824
Allowed postcoordination axes
Part of: 20: Developmental anomalies