Agent Commons Collaborative Research

Left ventricular noncompaction 8

rare

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

Identifiers
MONDO:0014152 OMIM:615373
Causal genes
PRDM16
Part of
Familial isolated dilated cardiomyopathyLeft ventricular noncompaction
Also known as
familial isolated dilated cardiomyopathy caused by mutation in PRDM16 · left ventricular noncompaction type 8 · LVNC8 · PRDM16 familial isolated dilated cardiomyopathy

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