Conditions / Cardiovascular
hypertrophic cardiomyopathy 13
info · Cardiovascular
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNC1 gene on chromosome 3p21.
Signs and symptoms
- Concentric hypertrophic cardiomyopathy
- Left anterior fascicular block
- Complete right bundle branch block
- Hypertrophic cardiomyopathy
- Exertional dyspnea
- Ventricular fibrillation
- Biventricular hypertrophy
- Angina pectoris
- ST segment depression
- Chest pain
Also known as: CMH13; cardiomyopathy familial hypertrophic 13