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.
Year introduced: 2007
PubMed search builder options
Subheadings:
Tree Number(s): C16.320.850.475.440.500, C17.800.428.435.440.500, C17.800.827.475.440.500
MeSH Unique ID: D053546
Entry Terms:
- Unna-Thost Disease, Epidermolytic
- Epidermolytic Unna-Thost Disease
- Unna Thost Disease, Epidermolytic
- EPPK (Epidermolytic Palmoplantar Keratoderma)
- EPPKs (Epidermolytic Palmoplantar Keratoderma)
- Thost-Unna Disease, Epidermolytic
- Epidermolytic Thost-Unna Disease
- Thost Unna Disease, Epidermolytic
- Palmoplantar Keratoderma, Epidermolytic
- Keratoderma, Epidermolytic Palmoplantar
- Epidermolytic Palmoplantar Keratoderma
- Epidermolytic Palmoplantar Keratodermas
- Keratodermas, Epidermolytic Palmoplantar
- Palmoplantar Keratodermas, Epidermolytic
- Hyperkeratosis, Localized Epidermolytic
- Epidermolytic Hyperkeratoses, Localized
- Epidermolytic Hyperkeratosis, Localized
- Hyperkeratoses, Localized Epidermolytic
- Localized Epidermolytic Hyperkeratoses
- Localized Epidermolytic Hyperkeratosis
- Epidermolytic Palmoplantar Keratoderma Vorner Type
- Keratosis of Greither
- Greither Keratosis
Previous Indexing: