EC23.1

ICD-11 MMS 2026-01

Syndromic genetically-determined hypermelanosis or lentiginosis

Index terms

  • Syndromic genetically-determined hypermelanosis or lentiginosis
  • Gastrocutaneous syndrome
  • Watson syndrome
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  • Café-au-lait macules with pulmonary stenosis

Foundation children elsewhere

  • LD27.00 – Incontinentia pigmenti
  • LD2D.0 – Peutz-Jeghers syndrome
  • LD2D.1 – Neurofibromatoses

Sibling codes

  • EC23.0 – Non-syndromic genetically-determined hypermelanosis or lentiginosis
  • EC23.2 – Albinism or other specified genetically-determined hypomelanotic disorders
  • EC23.Y – Other specified genetic disorders of skin pigmentation
  • EC23.Z – Genetic disorders of skin pigmentation, unspecified

Foundation entity

Syndromic genetically-determined hypermelanosis or lentiginosis – http://id.who.int/icd/entity/1465001518

Part of: EC23: Genetic disorders of skin pigmentation › 14: Diseases of the skin