Conditions / Cardiovascular
hypertrophic cardiomyopathy 3
info · Cardiovascular
A familial hypertrophic cardiomyopathy that has_material_basis_in heterozygous mutation in the alpha-tropomyosin gene (TPM1) on chromosome 15q22.
Signs and symptoms
- Hypertrophic cardiomyopathy
- Sudden cardiac death
Also known as: CMH3; cardiomyopathy familial hypertrophic 3