MeSH 搜索器

Keratoderma, Palmoplantar, Epidermolytic

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.
推出的年份: 2007
副标题
树号: C16.320.850.475.440.500, C17.800.428.435.440.500, C17.800.827.475.440.500
MeSH 单一 ID: D053546
进入的组:
  • EPPK (Epidermolytic Palmoplantar Keratoderma)
  • EPPKs (Epidermolytic Palmoplantar Keratoderma)
  • Hyperkeratosis, Localized Epidermolytic
  • Epidermolytic Hyperkeratoses, Localized
  • Epidermolytic Hyperkeratosis, Localized
  • Hyperkeratoses, Localized Epidermolytic
  • Localized Epidermolytic Hyperkeratoses
  • Localized Epidermolytic Hyperkeratosis
  • Palmoplantar Keratoderma, Epidermolytic
  • Keratoderma, Epidermolytic Palmoplantar
  • Epidermolytic Palmoplantar Keratoderma
  • Epidermolytic Palmoplantar Keratodermas
  • Keratodermas, Epidermolytic Palmoplantar
  • Palmoplantar Keratodermas, Epidermolytic
  • Unna-Thost Disease, Epidermolytic
  • Epidermolytic Unna-Thost Disease
  • Unna Thost Disease, Epidermolytic
  • Thost-Unna Disease, Epidermolytic
  • Epidermolytic Thost-Unna Disease
  • Thost Unna Disease, Epidermolytic
  • Keratosis of Greither
  • Greither Keratosis
  • Epidermolytic Palmoplantar Keratoderma Vorner Type
早前的内容:
  • Keratoderma, Palmoplantar, Diffuse (1989-2006)

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