Concept information
Preferred term
Keratoderma, Palmoplantar, Epidermolytic
Type
-
mesh:Descriptor
Definition
- 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.
Broader concept
Entry terms
- EPPK (Epidermolytic Palmoplantar Keratoderma)
- Hyperkeratosis, Localized Epidermolytic
- Keratoderma, Epidermolytic Palmoplantar
- Palmoplantar Keratoderma, Epidermolytic
- Thost-Unna Disease, Epidermolytic
- Unna-Thost Disease, Epidermolytic
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
Hyperkératose palmoplantaire acanthokératolytique
-
Hyperkératose palmoplantaire épidermolytique
-
Kératodermie palmo-plantaire épidermolytique
-
Kératodermie palmo-plantaire épidermolytique de type Thost-Unna
-
Kératodermie palmoplantaire épidermolytique de type Thost-Unna
URI
http://data.loterre.fr/ark:/67375/JVR-K6Q8MZZW-5
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