Olmsted syndrome
A hereditary palmoplantar keratoderma characterized by the combination of bilateral mutilating transgredient palmoplantar keratoderma and periorificial keratotic plaques. [ Orphanet:659 https://orcid.org/0000-0001-5208-3432 ]
Term info
- MedDRA:10068842 (Orphanet:659/e)
- UMLS:C2609071 (Orphanet:659/e)
- Orphanet:659 (OMIM:614594)
- GARD:0004075 (MONDO:equivalentTo)
- OMIMPS:614594 (MONDO:equivalentTo)
- DOID:0112011 (MONDO:equivalentTo)
http://identifiers.org/meddra/10068842
https://orcid.org/0000-0001-5208-3432
A hereditary palmoplantar keratoderma characterized by the combination of bilateral mutilating transgredient palmoplantar keratoderma and periorificial keratotic plaques.
http://linkedlifedata.com/resource/umls/id/C2609071, http://purl.obolibrary.org/obo/DOID_0112011, http://purl.obolibrary.org/obo/Orphanet_659, https://omim.org/phenotypicSeries/PS614594
mutilating palmoplantar hyperkeratosis with periorificial keratotic plaques, palmoplantar and periorificial keratoderma, palmoplantar keratoderma, mutilating, with periorificial keratotic plaques
MONDO:0031421