autosomal semi-dominant severe lipodystrophic laminopathy
Go to external page http://purl.obolibrary.org/obo/MONDO_0017230
This is just here as a test because I lose it
Term information
database
cross reference
- GARD:21080 (MONDO:GARD)
- UMLS:C5680783 (MONDO:equivalentTo)
- MEDGEN:1808090 (MONDO:equivalentTo)
- Orphanet:280365 (MONDO:equivalentTo)
Subsets
ordo_disorder, gard_rare, otar, rare, nord_rare, orphanet_rare
exactMatch
http://identifiers.org/medgen/1808090
http://www.orpha.net/ORDO/Orphanet_280365
http://linkedlifedata.com/resource/umls/id/C5680783