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Epidermolytic palmoplantar keratoderma, 1
rareA genetic skin disorder caused by mutations in the KRT9 gene. It is characterized by hyperkeratosis in the palms and soles resulting in abnormal thickening of the skin in these areas.
- Identifiers
- MONDO:0007758 OMIM:144200Orphanet:2199
- Causal genes
- KRT9
- Also known as
- diffuse erythrodermic palmoplantar keratoderma, VC6rner type · diffuse erythrodermic palmoplantar keratoderma, Voerner type · diffuse erythrodermic palmoplantar keratoderma, Vörner type · epidermolytic palmoplantar keratoderma of VC6rner · epidermolytic palmoplantar keratoderma of Voerner
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