Concept information
Término preferido
Keratoderma, Palmoplantar, Epidermolytic
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Tipo
-
mesh:Descriptor
Definición
- 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.
Concepto genérico
Etiquetas alternativas
- EPPK (Epidermolytic Palmoplantar Keratoderma)
- Hyperkeratosis, Localized Epidermolytic
- Keratoderma, Epidermolytic Palmoplantar
- Palmoplantar Keratoderma, Epidermolytic
- Thost-Unna Disease, Epidermolytic
- Unna-Thost Disease, Epidermolytic
En otras lenguas
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francés
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Hyperkératose palmoplantaire acanthokératolytique
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Hyperkératose palmoplantaire épidermolytique
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Kératodermie palmo-plantaire épidermolytique
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Kératodermie palmo-plantaire épidermolytique de type Thost-Unna
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Kératodermie palmoplantaire épidermolytique de type Thost-Unna
URI
http://data.loterre.fr/ark:/67375/JVR-K6Q8MZZW-5
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