Conditions / Cardiovascular
hypertrophic cardiomyopathy 16
info · Cardiovascular
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYOZ2 gene on chromosome 4q26.
Signs and symptoms
- Hypertrophic cardiomyopathy
- Left ventricular hypertrophy
- Palpitations
- Asymmetric septal hypertrophy
- Atrial fibrillation
- Dyspnea
- Left bundle branch block
- Orthopnea
- Syncope
- Ventricular tachycardia
Also known as: CMH16; cardiomyopathy familial hypertrophic 16