This is just here as a test because I lose it

Term information

database cross reference
  • ICD10CM:E23.0 (Orphanet:101957/specific)
  • Orphanet:101957 (MONDO:equivalentTo)
  • GARD:19801 (Orphanet:101957)
  • UMLS:C0020635 (Orphanet:101957)
Subsets

gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders

comment

Editor note: in ORDO, Orphanet:101957 is classified as genetic, yet has acquired subtypes

exactMatch

http://www.orpha.net/ORDO/Orphanet_101957

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0015968

id

MONDO:0015127

Term relations