hypertrophic cardiomyopathy 18

A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the gene encoding phospholamban (PLN) on chromosome 6q22.1.

Signs and symptoms

• Hypertrophic cardiomyopathy
• Left ventricular hypertrophy
• Paroxysmal atrial fibrillation
• Atrial fibrillation
• Chest pain

Also known as: CMH18; cardiomyopathy familial hypertrophic 18