Hypertrophic cardiomyopathy 7

MONDO:0013369

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNI3 gene.

Also known as: CMH7, TNNI3 hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, type 7, cardiomyopathy, hypertrophic, 7, hypertrophic cardiomyopathy 7, hypertrophic cardiomyopathy caused by mutation in TNNI3, hypertrophic cardiomyopathy type 7, cardiomyopathy, familial hypertrophic, 7

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 7 itself.

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Part of

↑ Familial hypertrophic cardiomyopathy (86)

Including sub-types (8) Tagged with Hypertrophic cardiomyopathy 7 (0)

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