Hypertrophic cardiomyopathy 8

MONDO:0012111

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL3 gene.

Also known as: MYL3 hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, 8, cardiomyopathy, familial hypertrophic, type 8, cardiomyopathy, hypertrophic, 8, hypertrophic cardiomyopathy 8, hypertrophic cardiomyopathy caused by mutation in MYL3, hypertrophic cardiomyopathy type 8, CMH8

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

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Part of

↑ Familial hypertrophic cardiomyopathy (86)

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

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