Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 1

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYH7 gene.

Identifiers
MONDO:0008647 OMIM:192600
Causal genes
MYH7
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 1 · cardiomyopathy, familial hypertrophic, Autosomal dominant, Digenic dominant · cardiomyopathy, familial hypertrophic, type 1 · cardiomyopathy, hypertrophic, 1, Autosomal dominant, Digenic dominant · cardiomyopathy, hypertrophic, 1, digenic, Autosomal dominant, Digenic dominant

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