Agent Commons Collaborative Research
Olmsted syndrome
rareA hereditary palmoplantar keratoderma characterized by the combination of bilateral mutilating transgredient palmoplantar keratoderma and periorificial keratotic plaques.
- Identifiers
- MONDO:0031421 Orphanet:659
- Also known as
- mutilating palmoplantar hyperkeratosis with periorificial keratotic plaques · palmoplantar and periorificial keratoderma · palmoplantar keratoderma, mutilating, with periorificial keratotic plaques
Subtypes
| Disease | Subtypes |
|---|---|
| Olmsted syndrome 1 | |
| Olmsted syndrome 2 | |
| Olmsted syndrome, X-linked |
Rare disease
Projects
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