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Ventricular septal defect 3
MONDO:0013749Any ventricular septal defect in which the cause of the disease is a mutation in the NKX2-5 gene.
Also known as: NKX2-5 ventricular septal defect (disease), ventricular septal defect (disease) caused by mutation in NKX2-5, ventricular septal defect 3, ventricular septal defect type 3, VSD3
73 clinical trials for this condition and its sub-types, 0 tagged with Ventricular septal defect 3 itself.
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