Left ventricular noncompaction 8

MONDO:0014152

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the PRDM16 gene.

Also known as: PRDM16 familial isolated dilated cardiomyopathy, familial isolated dilated cardiomyopathy caused by mutation in PRDM16, left ventricular noncompaction 8, left ventricular noncompaction type 8, LVNC8, cardiomyopathy, dilated, 1Ll

83 clinical trials for this condition and its sub-types, 0 tagged with Left ventricular noncompaction 8 itself.

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↑ Familial isolated dilated cardiomyopathy (11) ↑ Left ventricular noncompaction (4)

Including sub-types (83) Tagged with Left ventricular noncompaction 8 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.