Terminology Service for NFDI4Health

familial restrictive cardiomyopathy

Go to external page http://purl.obolibrary.org/obo/MONDO_0016340


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

Term info

Label

familial restrictive cardiomyopathy

Synonyms
  • hereditary restrictive cardiomyopathy
database cross reference
Subsets

disease_grouping, ordo_group_of_disorders

exactMatch

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

id

MONDO:0016340