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Concept information

Preferred term

Keratoderma, Palmoplantar, Epidermolytic  

Type

  • Topical Descriptor

Entry terms

  • Epidermolytic Hyperkeratoses, Localized
  • Epidermolytic Hyperkeratosis, Localized
  • Epidermolytic Palmoplantar Keratoderma
  • Epidermolytic Palmoplantar Keratodermas
  • Epidermolytic Thost-Unna Disease
  • Epidermolytic Unna-Thost Disease
  • EPPK (Epidermolytic Palmoplantar Keratoderma)
  • EPPKs (Epidermolytic Palmoplantar Keratoderma)
  • Hyperkeratoses, Localized Epidermolytic
  • Hyperkeratosis, Localized Epidermolytic
  • Keratoderma, Epidermolytic Palmoplantar
  • Keratodermas, Epidermolytic Palmoplantar
  • Localized Epidermolytic Hyperkeratoses
  • Localized Epidermolytic Hyperkeratosis
  • Palmoplantar Keratoderma, Epidermolytic
  • Palmoplantar Keratodermas, Epidermolytic
  • Thost Unna Disease, Epidermolytic
  • Thost-Unna Disease, Epidermolytic
  • Unna Thost Disease, Epidermolytic
  • Unna-Thost Disease, Epidermolytic

Scope note

  • An autosomal dominant hereditary skin disease characterized by epidermolytic hyperkeratosis that is strictly confined to the palms and soles. It has been associated with mutations in the gene that codes for KERATIN-9.

History note

  • 2007

URI

http://www.yso.fi/onto/mesh/D053546

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