Any congenital heart disease in which the cause of the disease is a mutation in the RBFOX2 gene.
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congenital heart defects, multiple types
MONDO:0000119
ventricular septal defect
MONDO:0002070
heart septal defect
MONDO:0002078
hypoplastic left heart syndrome
MONDO:0004933
familial cardiomyopathy
MONDO:0005217
atrial septal defect
MONDO:0006664