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Hypertrophic cardiomyopathy 4

MONDO:0007268

An autosomal dominant condition caused by mutation(s) in the MYBPC3 gene, encoding MYBPC3 protein. It is characterized by severe neonatal hypertrophic cardiomyopathy.

Also known as: CMH4, MYBPC3 hypertrophic cardiomyopathy, cardiomyopathy, familial hypertrophic, 4, cardiomyopathy, familial hypertrophic, type 4, cardiomyopathy, hypertrophic, 4, familial hypertrophic cardiomyopathy type 4, hypertrophic cardiomyopathy 4, hypertrophic cardiomyopathy caused by mutation in MYBPC3

8 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic cardiomyopathy 4 itself.

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↑ Familial hypertrophic cardiomyopathy (86)

Including sub-types (8) Tagged with Hypertrophic cardiomyopathy 4 (0)

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