dilated cardiomyopathy 1D

A dilated cardiomyopathy that has_material_basis_in mutation in the TNNT2 gene on chromosome 1q32.

Signs and symptoms

• Left ventricular noncompaction
• Increased circulating brain natriuretic peptide concentration
• Increased left ventricular end-diastolic volume
• Dilated cardiomyopathy
• Reduced left ventricular ejection fraction
• Congestive heart failure
• Sudden cardiac death
• Left ventricular hypertrophy
• Prolonged QT interval
• Incomplete right bundle branch block

Also known as: CMD1D