EE41.1

ICD-11 MMS 2026-01

Anetoderma

Description

A condition presenting as focal areas of thinned, flaccid skin and resulting from focal defects in dermal elastin. The involved skin is often elevated above the surrounding normal skin but can be depressed. The condition may be primary and without identifiable cause or may be a sequela of a large number of different conditions which may damage elastin in the dermis.

Index terms

  • Anetoderma
  • Macular atrophy
  • Primary anetoderma
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  • Familial anetoderma
  • Anetoderma of Jadassohn-Pellizzari
  • Anetoderma of Schweninger-Buzzi
  • Secondary anetoderma

Sibling codes

  • EE41.0 – Cutis laxa
  • EE41.Y – Other specified dermatoses characterised by abnormal dermal elastin
  • EE41.Z – Abnormalities of dermal elastin, unspecified

Foundation entity

Anetoderma – http://id.who.int/icd/entity/1490033315

Part of: EE41: Abnormalities of dermal elastin › 14: Diseases of the skin