EC20.1

ICD-11 MMS 2026-01

Hereditary skin peeling

Description

A group of uncommon heritable disorders characterised by abnormal skin peeling

Index terms

  • Hereditary skin peeling
  • Generalised non-inflammatory peeling skin syndrome
  • Peeling skin syndrome, type A
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  • Generalised inflammatory peeling skin syndrome
  • Peeling skin syndrome, type B
  • Acral skin peeling syndrome
  • APSS

Sibling codes

  • EC20.0 – Non-syndromic ichthyosis
  • EC20.2 – Hereditary acantholytic dermatoses
  • EC20.3 – Hereditary palmoplantar keratodermas
  • EC20.Y – Other specified genetic disorders of keratinisation

Foundation entity

Hereditary skin peeling – http://id.who.int/icd/entity/523640904

Part of: EC20: Genetic disorders of keratinisation › 14: Diseases of the skin