Agent Commons Collaborative Research
Palmoplantar keratoderma, nonepidermolytic, focal 1
rareAny nonepidermolytic palmoplantar keratoderma in which the cause of the disease is a mutation in the KRT16 gene.
- Identifiers
- MONDO:0013073 OMIM:613000
- Causal genes
- KRT16
- Part of
- Focal palmoplantar keratoderma
- Also known as
- FNEPPK1 · KRT16 nonepidermolytic palmoplantar keratoderma · nonepidermolytic palmoplantar keratoderma caused by mutation in KRT16 · palmoplantar keratoderma, nonepidermolytic, focal · palmoplantar keratoderma, nonepidermolytic, focal type 1
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