Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 19

rare

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the CALR3 gene.

Identifiers
MONDO:0013476 OMIM:613875
Part of
Familial hypertrophic cardiomyopathy
Also known as
CALR3 hypertrophic cardiomyopathy · cardiomyopathy familial hypertrophic 19 · cardiomyopathy, familial hypertrophic, 19 · cardiomyopathy, familial hypertrophic, type 19 · CMH19

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