Term information
- UMLS:C5680786 (MONDO:equivalentTo)
- GARD:21069 (MONDO:GARD)
- Orphanet:279928 (MONDO:equivalentTo)
- MEDGEN:1830109 (MONDO:equivalentTo)
gard_rare, ordo_disorder, rare, nord_rare, orphanet_rare
https://github.com/monarch-initiative/mondo/issues/6748
https://github.com/monarch-initiative/mondo/issues/6745
https://github.com/monarch-initiative/mondo/issues/6744
https://github.com/monarch-initiative/mondo/issues/6740
This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'cardiovascular disorder' (MONDO:0004995) ontology branch (https://orcid.org/0000-0001-9310-0163, https://orcid.org/0000-0001-6718-3559) and was determined to be excluded from the 'inflammatory disease' (MONDO:0021166) ontology branch (https://orcid.org/0000-0003-4830-7530, https://orcid.org/0000-0001-9310-0163)
http://linkedlifedata.com/resource/umls/id/C5680786
http://identifiers.org/medgen/1830109
http://www.orpha.net/ORDO/Orphanet_279928