JSON

familial hypertrophic cardiomyopathy

Go to external page 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 ]

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

This is just here as a test because I lose it

Term information

database cross reference
  • MESH:D024741 (MONDO:equivalentTo)
  • DOID:0080326 (MONDO:equivalentTo)
  • OMIMPS:192600 (MONDO:equivalentTo)
  • Orphanet:155 (MONDO:equivalentObsolete)
  • SCTID:471885006 (MONDO:equivalentTo)
  • UMLS:C0949658 (MONDO:equivalentTo)
  • MEDGEN:183649 (MONDO:equivalentTo)
  • NCIT:C84773 (MONDO:equivalentTo)
Subsets

otar, rare, inferred_rare

exactMatch

http://linkedlifedata.com/resource/umls/id/C0949658

http://purl.obolibrary.org/obo/DOID_0080326

http://identifiers.org/snomedct/471885006

http://identifiers.org/mesh/D024741

http://identifiers.org/medgen/183649

https://omim.org/phenotypicSeries/PS192600

http://purl.obolibrary.org/obo/NCIT_C84773

id

MONDO:0024573