EC23.0

ICD-11 MMS 2026-01

Non-syndromic genetically-determined hypermelanosis or lentiginosis

Index terms

  • Non-syndromic genetically-determined hypermelanosis or lentiginosis
  • Familial progressive hyperpigmentation
  • Familial generalised lentiginosis
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  • Inherited patterned lentiginosis
  • Centrofacial lentiginosis
  • Familial multiple café-au-lait macules
  • Café-au-lait spots syndrome
  • NF6 - [Neurofibromatosis type 6]
  • Neurofibromatosis type 6
  • Dowling-Degos disease
  • Reticulate pigmented anomaly of the flexures
  • Galli-Galli disease
  • Hypermelanotic pigmentary mosaicism
  • Linear or whorled naevoid hypermelanosis
  • Segmental lentiginosis
  • Partial unilateral lentiginosis

Sibling codes

  • EC23.1 – 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

Non-syndromic genetically-determined hypermelanosis or lentiginosis – http://id.who.int/icd/entity/1654612170

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