Hypertrophic cardiomyopathy 3

MONDO:0007267

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

Also known as: CMH3, TPM1 hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, type 3, cardiomyopathy, hypertrophic, 3, hypertrophic cardiomyopathy 3, hypertrophic cardiomyopathy caused by mutation in TPM1, hypertrophic cardiomyopathy type 3, cardiomyopathy, familial hypertrophic, 3

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 3 itself.

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Part of

↑ Familial hypertrophic cardiomyopathy (86)

Including sub-types (8) Tagged with Hypertrophic cardiomyopathy 3 (0)

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