Term info
database cross reference
- Orphanet:101957 (MONDO:equivalentTo)
- UMLS:C0020635 (Orphanet:101957)
- ICD10CM:E23.0 (Orphanet:101957/specific)
Subsets
disease_grouping, ordo_group_of_disorders
comment
Editor note: in ORDO, Orphanet:101957 is classified as genetic, yet has acquired subtypes
exactMatch
http://purl.obolibrary.org/obo/Orphanet_101957
excluded subClassOf
http://purl.obolibrary.org/obo/MONDO_0015968
id
MONDO:0015127