A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina. [ https://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)
  • UMLS:CN236383 (MONDO:equivalentTo)
Subsets

ordo_group_of_disorders

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/specific_disease_by_dysfunctional_structure.yaml

definition

A rare genetic disorder caused by mutations in genes encoding proteins of the nuclear lamina.

exactMatch

http://linkedlifedata.com/resource/umls/id/CN236383

http://www.orpha.net/ORDO/Orphanet_98301

id

MONDO:0021106