/hypertrophic cardiomyopathy 4

hypertrophic cardiomyopathy 4

Rare Disease

MONDO:0007268

Also Known As

CMH4MYBPC3 hypertrophic cardiomyopathycardiomyopathy, familial hypertrophic, 4cardiomyopathy, familial hypertrophic, type 4cardiomyopathy, hypertrophic, 4familial hypertrophic cardiomyopathy type 4hypertrophic cardiomyopathy 4hypertrophic cardiomyopathy caused by mutation in MYBPC3hypertrophic cardiomyopathy type 4cardiomyopathy, familial hypertrophic, 4, susceptibility to

Definition

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