Conditions / Cardiovascular
hypertrophic cardiomyopathy 7
info · Cardiovascular
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the TNNI3 gene on chromosome 19q13.4.
Signs and symptoms
- Hypertrophic cardiomyopathy
- Wolff-Parkinson-White syndrome
- Apical hypertrophic cardiomyopathy
- Ventricular hypertrophy
- Atrial fibrillation
Also known as: CMH7; cardiomyopathy, familial hypertrophic 7