ARRHYTHMOGENIC CARDIOMYOPATHY WITH VARIABLE ECTODERMAL ABNORMALITIES
This disease is characterized by severe dilated cardiomyopathy resulting in death or cardiac transplantation in childhood. Various ectodermal abnormalities may be present in patients.
Ataxia, Deafness, and Cardiomyopathy
Atrial Dilation and Standstill +
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
congenital myopathy 5
Danon disease
Diabetic Cardiomyopathies
endocardial fibroelastosis +
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
Mitochondrial Cardiomyopathy
mitochondrial DNA depletion syndrome 12a
mitochondrial DNA depletion syndrome 12b
Muscular Dystrophy, Cardiac Type
Myocardial Reperfusion Injury
myocarditis +
myofibrillar myopathy 2
neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities