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Keratoderma, Palmoplantar, Epidermolytic MeSH Descriptor Data 2023


MeSH Heading
Keratoderma, Palmoplantar, Epidermolytic
Tree Number(s)
C16.320.850.475.440.500
C17.800.428.435.440.500
C17.800.827.475.440.500
Unique ID
D053546
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D053546
Scope Note
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 Term(s)
EPPK (Epidermolytic Palmoplantar Keratoderma)
Epidermolytic Palmoplantar Keratoderma Vorner Type
Hyperkeratosis, Localized Epidermolytic
Keratoderma, Epidermolytic Palmoplantar
Keratosis of Greither
Palmoplantar Keratoderma, Epidermolytic
Thost-Unna Disease, Epidermolytic
Unna-Thost Disease, Epidermolytic
Previous Indexing
Keratoderma, Palmoplantar, Diffuse (1989-2006)
Public MeSH Note
2007
History Note
2007
Date Established
2007/01/01
Date of Entry
2006/07/05
Revision Date
2015/06/18
Keratoderma, Palmoplantar, Epidermolytic Preferred
Keratosis of Greither Related
Epidermolytic Palmoplantar Keratoderma Vorner Type Related
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