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Dilated cardiomyopathy 1E

MONDO:0011003

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the SCN5A gene.

Also known as: CDCD2, CMD1E, SCN5A familial isolated dilated cardiomyopathy, cardiomyopathy dilated with conduction defect type 2, cardiomyopathy, dilated, 1E, cardiomyopathy, dilated, type 1E, cardiomyopathy, dilated, with conduction defect 2, cardiomyopathy, dilated, with conduction disorder and arrhythmia

8 clinical trials for this condition and its sub-types, 0 tagged with Dilated cardiomyopathy 1E itself.

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