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Concept information

Preferred term

Keratoderma, Palmoplantar, Epidermolytic  

Type

  • mesh:Descriptor

Definition

  • 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.

Entry terms

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

In other languages

  • French

  • Hyperkératose palmoplantaire acanthokératolytique
  • Hyperkératose palmoplantaire épidermolytique
  • Kératodermie palmo-plantaire épidermolytique
  • Kératodermie palmo-plantaire épidermolytique de type Thost-Unna
  • Kératodermie palmoplantaire épidermolytique de type Thost-Unna

URI

http://data.loterre.fr/ark:/67375/JVR-K6Q8MZZW-5

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RDF/XML TURTLE JSON-LD Created 7/5/06, last modified 6/18/15