An umbrella term for a group of rare genetic skin disorders characterized by well-demarcated plaques of reddened, dry and thickened skin. Typically, these lesions are distributed symmetrically on the body and tend to slowly expand and progress over time. [ https://rarediseases.org/rare-diseases/https-rarediseases-org-rare-diseases-erythrokeratoderma/ https://orcid.org/0000-0001-5208-3432 ]
Term information
- Orphanet:79355 (MONDO:equivalentTo)
- MedDRA:10015280 (Orphanet:79355/e)
- UMLS:C0432330 (MONDO:equivalentTo)
- ICD9:757.39 (MONDO:relatedTo)
- GARD:18986 (MONDO:GARD)
- MEDGEN:609461 (MONDO:equivalentTo)
- SCTID:254215005 (MONDO:equivalentTo)
gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders
http://identifiers.org/medgen/609461
http://linkedlifedata.com/resource/umls/id/C0432330
http://www.orpha.net/ORDO/Orphanet_79355
http://identifiers.org/snomedct/254215005