MeSH Browser

MeSH Supplementary: familial dilated cardiomyopathy
Unique ID: C536231
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536231
Entry Term(s): cardiomyopathy, dilated, 1b; cardiomyopathy, familial dilated; cardiomyopathy, familial dilated, 1; dilated cardiomyopathy, familial; hypokinetic dilated cardiomyopathy, familial
Registry Numbers: 0
Heading Mapped to: *Cardiomyopathy, Dilated
Frequency: 192
Note: A congenital form of dilated cardiomyopathy. Candidate genes have been mapped to the 9q13-q22 region of chromosome 9. OMIM: 600884
Date of Entry: 2010/08/25
Revision Date: 2022/11/29

familial dilated cardiomyopathy MeSH Supplementary Concept Data 2025