EC10

ICD-11 MMS 2026-01

Genetic syndromes with poikiloderma

Description

Hereditary syndromes in which poikiloderma (cutaneous pigmentation, atrophy and telangiectasia) is a conspicuous feature.

Index terms

  • Genetic syndromes with poikiloderma
  • Poikiloderma with neutropaenia
  • Poikiloderma with neutropaenia, Clericuzio type
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  • Hereditary sclerosing poikiloderma
  • Hereditary sclerosing poikiloderma (MIM 173700)
  • Hereditary sclerosing poikiloderma, Weary type
  • Hereditary sclerosing poikiloderma with cardiac anomalies
  • Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
  • Congenital or hereditary poikiloderma of uncertain or unspecified type

Sibling codes

  • EC1Y – Other specified genetic syndromes affecting the skin

Foundation entity

Genetic syndromes with poikiloderma – http://id.who.int/icd/entity/1343350087

Part of: 14: Diseases of the skin