Conditions / Genetic
dilated cardiomyopathy 2A
info · Genetic · ICD-10: I42.0
A dilated cardiomyopathy that has_material_basis_in mutation in the TNNI3 gene on chromosome 19q13.
Signs and symptoms
- Cardiomyocyte hypertrophy
- Congestive heart failure
- Dilated cardiomyopathy
- Increased left ventricular end-diastolic volume
- Myofiber disarray
Also known as: CMD2A