Term info
database cross reference
- ICD9:425.4 (MONDO:relatedTo)
- SCTID:35728003 (MONDO:equivalentTo)
- EFO:0002945 (MONDO:equivalentTo)
- UMLS:C0264789 (MONDO:equivalentTo)
definition
An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome.
exactMatch
http://linkedlifedata.com/resource/umls/id/C0264789, http://identifiers.org/snomedct/35728003
has exact synonym
hereditary cardiomyopathy
id
MONDO:0005217