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Dilated cardiomyopathy 1L

MONDO:0011702

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

Also known as: CMD1L, SGCD familial isolated dilated cardiomyopathy, cardiomyopathy, dilated, type 1L, dilated cardiomyopathy type 1L, familial isolated dilated cardiomyopathy caused by mutation in SGCD, cardiomyopathy, dilated, 1L

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

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↑ Familial isolated dilated cardiomyopathy (11) ↑ Qualitative or quantitative defects of delta-sarcoglycan (2)

Including sub-types (8) Tagged with Dilated cardiomyopathy 1L (0)

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