Keratoderma, Palmoplantar, Epidermolytic
"Keratoderma, Palmoplantar, Epidermolytic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D053546
|
| MeSH Number(s) |
C16.320.850.475.440.500 C17.800.428.435.440.500 C17.800.827.475.440.500
|
| Concept/Terms |
Keratoderma, Palmoplantar, Epidermolytic- Keratoderma, Palmoplantar, Epidermolytic
- 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
|
Below are MeSH descriptors whose meaning is more general than "Keratoderma, Palmoplantar, Epidermolytic".
- Diseases [C]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Skin Diseases, Genetic [C16.320.850]
- Keratoderma, Palmoplantar [C16.320.850.475]
- Keratoderma, Palmoplantar, Diffuse [C16.320.850.475.440]
- Keratoderma, Palmoplantar, Epidermolytic [C16.320.850.475.440.500]
- Skin and Connective Tissue Diseases [C17]
- Skin Diseases [C17.800]
- Keratosis [C17.800.428]
- Keratoderma, Palmoplantar [C17.800.428.435]
- Keratoderma, Palmoplantar, Diffuse [C17.800.428.435.440]
- Keratoderma, Palmoplantar, Epidermolytic [C17.800.428.435.440.500]
- Skin Diseases, Genetic [C17.800.827]
- Keratoderma, Palmoplantar [C17.800.827.475]
- Keratoderma, Palmoplantar, Diffuse [C17.800.827.475.440]
- Keratoderma, Palmoplantar, Epidermolytic [C17.800.827.475.440.500]
Below are MeSH descriptors whose meaning is more specific than "Keratoderma, Palmoplantar, Epidermolytic".
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Below are the most recent publications written about "Keratoderma, Palmoplantar, Epidermolytic" by people in Profiles.