JSON

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. [ MONDO:patterns/hereditary ]

Synonyms: hereditary restrictive cardiomyopathy

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:425.4 (MONDO:relatedTo)
  • OMIMPS:115210 (MONDO:equivalentTo)
  • GARD:20532 (Orphanet:217635)
  • Orphanet:217635 (MONDO:equivalentTo)
  • SCTID:233878008 (MONDO:equivalentTo)
Subsets

gard_rare, disease_grouping, rare, nord_rare, orphanet_rare, ordo_group_of_disorders

exactMatch

http://identifiers.org/snomedct/233878008

http://www.orpha.net/ORDO/Orphanet_217635

https://omim.org/phenotypicSeries/PS115210

id

MONDO:0016340