JSON

familial restrictive cardiomyopathy

^ http://purl.obolibrary.org/obo/MONDO_0016340

An instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]

Term info

database cross reference
  • SCTID:233878008 (MONDO:equivalentTo)
  • OMIMPS:115210 (MONDO:equivalentTo)
  • ICD9:425.4 (MONDO:relatedTo)
  • Orphanet:217635 (MONDO:equivalentTo)
Subsets

disease_grouping, ordo_group_of_disorders

definition

An instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome.

exactMatch

http://identifiers.org/snomedct/233878008, https://omim.org/phenotypicSeries/PS115210, http://purl.obolibrary.org/obo/Orphanet_217635

has exact synonym

hereditary restrictive cardiomyopathy

id

MONDO:0016340