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
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)
留言 (0)