Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 3

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TPM1 gene.

Identifiers
MONDO:0007267 OMIM:115196
Causal genes
TPM1
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 3 · cardiomyopathy, familial hypertrophic, type 3 · cardiomyopathy, hypertrophic, 3 · CMH3 · hypertrophic cardiomyopathy caused by mutation in TPM1

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