Conditions / Cardiovascular
hypertrophic cardiomyopathy 17
info · Cardiovascular
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the junctophilin gene (JPH2) on chromosome 20q12.
Signs and symptoms
- Hypertrophic cardiomyopathy
- Dyspnea
- Left ventricular hypertrophy
- Myocardial fibrosis
- Angina pectoris
- Palpitations
- Ventricular tachycardia
- Atrial fibrillation
Also known as: CMH17; cardiomyopathy familial hypertrophic 17