A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina. [ http://en.wikipedia.org/wiki/Laminopathy ]
This is just here as a test because I lose it
Term information
database
cross reference
- Orphanet:98301 (MONDO:equivalentTo)
- MEDGEN:1716073 (MONDO:equivalentTo)
- UMLS:C5392094 (MONDO:equivalentTo)
- MESH:D000083083 (MONDO:equivalentTo)
- GARD:19444 (MONDO:GARD)
Subsets
gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders
exactMatch
http://identifiers.org/medgen/1716073
http://identifiers.org/mesh/D000083083
http://linkedlifedata.com/resource/umls/id/C5392094
http://www.orpha.net/ORDO/Orphanet_98301