Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 21

rare

A hypertrophic cardiomyopathy associated that has material basis in region 7p12.1-q21 variation.

Identifiers
MONDO:0013852 OMIM:614676
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 21 · cardiomyopathy, hypertrophic, 21 · CMH21 · hypertrophic cardiomyopathy type 21

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