hypertrophic cardiomyopathy 4

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the gene encoding cardiac myosin-binding protein C (MYBPC3) on chromosome 11p11.

Signs and symptoms

• Myofiber disarray
• Cardiomegaly
• Respiratory distress
• Hypertrophic cardiomyopathy
• Congestive heart failure
• Ventricular hypertrophy
• Cardiac arrest
• Myopathy
• Hepatomegaly
• Complete right bundle branch block

Also known as: CMH4; cardiomyopathy, familial hypertrophic, 4