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Up to: Familial cardiomyopathy · Dilated cardiomyopathy

Familial dilated cardiomyopathy

A a genetic form of heart disease that occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of the heart, causing the open area of the chamber to become enlarged (dilated). As a result, the heart is unable to pump blood as efficiently as usual. To compensate, the heart attempts to increase the amount of blood being pumped through the heart, leading to further thinning and weakening of the cardiac muscle. Over time, this condition results in heart failure.

7 trials tagged with this condition →

Leber hereditary optic neuropathy 18 trials Sub-types →
Familial isolated dilated cardiomyopathy 0 trials · 11 incl. sub-types Sub-types →
Barth syndrome 5 trials
Kearns-Sayre syndrome 5 trials
Autosomal recessive limb-girdle muscular dystrophy type 2E 5 trials
Autosomal recessive limb-girdle muscular dystrophy type 2C 4 trials
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers 4 trials
Autosomal recessive limb-girdle muscular dystrophy type 2D 3 trials
Histiocytoid cardiomyopathy 3 trials Sub-types →
Emery-Dreifuss muscular dystrophy 1 trial · 3 incl. sub-types Sub-types →
Autosomal recessive limb-girdle muscular dystrophy type 2F 2 trials
PGM1-congenital disorder of glycosylation 1 trial
Autosomal recessive limb-girdle muscular dystrophy type 2M 1 trial
Autosomal recessive limb-girdle muscular dystrophy type 2W 1 trial
Early-onset myopathy with fatal cardiomyopathy 1 trial
DK1-congenital disorder of glycosylation 0 trials
Cardiomyopathy, dilated, 100 0 trials
Cardiomyopathy, dilated, 1LL 0 trials
Cardiomyopathy, dilated, 1MM 0 trials
Cardiomyopathy, dilated, 1QQ 0 trials
Cardiomyopathy, dilated, 2I 0 trials
Cardiomyopathy, dilated, 2K 0 trials
Cardiomyopathy, dilated, 2M 0 trials
Cardiomyopathy, dilated, 2j 0 trials
Cardiomyopathy, dilated, 2l 0 trials
Cardiomyopathy, dilated, 3C 0 trials
Dilated cardiomyopathy 1J 0 trials
Hypertrophic cardiomyopathy 25 0 trials
Myofibrillar myopathy 1 0 trials