laminopathy
http://purl.obolibrary.org/obo/MONDO_0021106
A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina. [ Wikipedia:Laminopathy ]
Term info
database cross reference
- Orphanet:98301 (MONDO:equivalentTo)
- MESH:D000083083 (MONDO:equivalentTo)
- UMLS:CN236383 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina.
exactMatch
http://purl.obolibrary.org/obo/Orphanet_98301, http://linkedlifedata.com/resource/umls/id/CN236383, http://identifiers.org/mesh/D000083083
id
MONDO:0021106