autosomal recessive limb-girdle muscular dystrophy type 2D
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts
Cardiomyopathy Associated with Myopathy and Sudden Death
Cardiomyopathy Hypogonadism Collagenoma Syndrome
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods
Chagas Cardiomyopathy
Danon disease
Diabetic Cardiomyopathies
Early-Onset Myopathy with Fatal Cardiomyopathy
endocardial fibroelastosis +
A condition characterized by the thickening of ENDOCARDIUM due to proliferation of fibrous and elastic tissue, usually in the left ventricle leading to impaired cardiac function (CARDIOMYOPATHY, RESTRICTIVE). It is most commonly seen in young children and rarely in adults. It is often associated with congenital heart anomalies (HEART DEFECTS CONGENITAL;) INFECTION; or gene mutation. Defects in the tafazzin protein, encoded by TAZ gene, result in a form of autosomal dominant familial endocardial fibroelastosis.
endocarditis +
endocardium cancer
endomyocardial fibrosis
extrinsic cardiomyopathy +
Familial Cardiac Lipidosis
Fatal Fetal Cardiomyopathy due to Myocardial Calcification
Hypertaurinuric Cardiomyopathy
intrinsic cardiomyopathy +
Kearns-Sayre syndrome
Keshan disease
linear skin defects with multiple congenital anomalies 3