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familial hypertrophic cardiomyopathy

^ http://purl.obolibrary.org/obo/MONDO_0024573

Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions. [ NCIT:C84773 ]

Term info

database cross reference
  • MESH:D024741 (MONDO:equivalentTo)
  • OMIMPS:192600 (MONDO:equivalentTo)
  • DOID:0080326 (MONDO:equivalentTo)
  • GARD:0007229 (MONDO:equivalentTo)
  • SCTID:471885006 (MONDO:equivalentTo)
  • NCIT:C84773 (MONDO:equivalentTo)
  • Orphanet:155 (MONDO:equivalentTo)
definition

Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions.

exactMatch

http://purl.obolibrary.org/obo/DOID_0080326, http://identifiers.org/snomedct/471885006, http://identifiers.org/mesh/D024741, http://purl.obolibrary.org/obo/Orphanet_155, https://omim.org/phenotypicSeries/PS192600, http://purl.obolibrary.org/obo/NCIT_C84773

has exact synonym

hereditary hypertrophic cardiomyopathy, hypertrophic familial cardiomyopathy, cardiomyopathy, familial hypertrophic, familial hypertrophic cardiomyopathy, familila or idiopathic hypertrophic obstructive cardiomyopathy

id

MONDO:0024573