Term info
database cross reference
- ICD9:692.75 (DOID:3805)
- MedDRA:10036175 (Orphanet:79358/e)
- OMIMPS:175800 (MONDO:equivalentTo)
- DOID:3805 (MONDO:equivalentTo)
- HP:0200044 (MONDO:otherHierarchy)
- SCTID:400080004 (MONDO:equivalentTo)
- MESH:D017499 (https://orcid.org/0000-0003-1967-3726)
- ICD9:757.39 (MONDO:relatedTo)
- UMLS:C0162839 (Orphanet:79358/e)
- NCIT:C85019 (MONDO:equivalentTo)
- Wikipedia:Porokeratosis (EFO:1000757)
- EFO:1000757 (MONDO:equivalentTo)
- Orphanet:79358 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
IAO 0000589
porokeratosis (disease)
closeMatch
http://identifiers.org/meddra/10036175
definition
A clonal proliferation of abnormal keratinocytes characterized by the development of localized or multiple atrophic skin patches surrounded by an annular keratotic ring called cornoid lamella.
exactMatch
http://identifiers.org/mesh/D017499, http://purl.obolibrary.org/obo/NCIT_C85019, http://linkedlifedata.com/resource/umls/id/C0162839, http://purl.obolibrary.org/obo/Orphanet_79358, http://purl.obolibrary.org/obo/DOID_3805, https://omim.org/phenotypicSeries/PS175800, http://identifiers.org/snomedct/400080004
has exact synonym
porokeratosis, porokeratosis (disease)
id
MONDO:0006602