Term info
database cross reference
- Orphanet:404584 (MONDO:obsoleteEquivalent)
- UMLS:CN227376 (MONDO:obsoleteEquivalent)
Subsets
disease_grouping, ordo_group_of_disorders
IAO 0000231
out of scope
IAO 0000233
https://github.com/monarch-initiative/mondo/issues/254, https://github.com/monarch-initiative/mondo/issues/2662
exactMatch
http://purl.obolibrary.org/obo/Orphanet_404584, http://linkedlifedata.com/resource/umls/id/CN227376
has exact synonym
rare genetic skeletal development disorder
id
MONDO:0018457