Conditions / Cardiovascular
hypertrophic cardiomyopathy 20
info · Cardiovascular
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the NEXN gene on chromosome 1p31.1.
Signs and symptoms
- Hypertrophic cardiomyopathy
- Left ventricular hypertrophy
- Atrial fibrillation
- Reduced left ventricular ejection fraction
Also known as: CMH20; cardiomyopathy familial hypertrophic 20