EC20.31

ICD-11 MMS 2026-01

Focal palmoplantar keratodermas

Description

Palmoplantar keratoderma in which there is focal epidermal thickening with areas of normal intervening palmar and plantar skin.

Index terms

  • Focal palmoplantar keratodermas
  • Non-syndromic nummular or linear palmoplantar keratodermas
  • Striate palmoplantar keratoderma
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  • Brunauer-Fuhs-Siemens keratoderma
  • Keratoderma palmoplantaris striata
  • Nummular palmoplantar keratoderma
  • Hereditary painful callosities
  • Keratosis palmoplantaris nummularis
  • Syndromic nummular or linear palmoplantar keratodermas
  • Palmoplantar keratoderma – oral leukokeratosis – oesophageal carcinoma
  • Howel-Evans syndrome
  • Tylosis with oesophageal cancer
  • Papillomatoverrucous palmoplantar keratoderma – dysplastic dentition
  • Jakac-Wolf keratoderma
  • Hypotrichosis – acro-osteolysis – onychogryphosis – palmoplantar keratoderma – periodontitis syndrome
  • HOPP - [Hypotrichosis – acro-osteolysis – onychogryphosis – palmoplantar keratoderma – periodontitis] syndrome

Foundation children elsewhere

Sibling codes

  • EC20.30 – Diffuse palmoplantar keratodermas
  • EC20.32 – Papular palmoplantar keratodermas
  • EC20.3Z – Hereditary palmoplantar keratoderma of unspecified type

Foundation entity

Focal palmoplantar keratodermas – http://id.who.int/icd/entity/1676945961

Part of: EC20.3: Hereditary palmoplantar keratodermas › EC20: Genetic disorders of keratinisation › 14: Diseases of the skin