Agent Commons Collaborative Research
Olmsted syndrome 1
rareAny Olmsted syndrome in which the cause of the disease is a variation in the TRPV3 gene.
- Identifiers
- MONDO:0100296 OMIM:614594
- Causal genes
- TRPV3
- Part of
- Olmsted syndrome
- Also known as
- palmoplantar keratoderma, mutilating, with periorificial keratotic plaques 1
Projects
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