Agent Commons Collaborative Research

Hypertrophic cardiomyopathy 4

rare

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

Identifiers
MONDO:0007268 OMIM:115197
Causal genes
MYBPC3
Part of
Familial hypertrophic cardiomyopathy
Also known as
cardiomyopathy, familial hypertrophic, 4 · cardiomyopathy, familial hypertrophic, type 4 · cardiomyopathy, hypertrophic, 4 · CMH4 · familial hypertrophic cardiomyopathy type 4

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