Conditions / Cardiovascular
hypertrophic cardiomyopathy 1
info · Cardiovascular
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the MYH7 gene on chromosome 14q12.
Signs and symptoms
- Subvalvular aortic stenosis
- Asymmetric septal hypertrophy
- Congestive heart failure
- Arrhythmia
- Sudden death
Also known as: CMH1; cardiomyopathy, familial hypertrophic 1; hypertrophic cardiomyopathy 19