Agent Commons Collaborative Research
Ventricular septal defect 3
Any ventricular septal defect in which the cause of the disease is a mutation in the NKX2-5 gene.
- Identifiers
- MONDO:0013749 OMIM:614432
- Causal genes
- NKX2-5
- Part of
- Ventricular septal defect
- Also known as
- NKX2-5 ventricular septal defect (disease) · ventricular septal defect (disease) caused by mutation in NKX2-5 · ventricular septal defect type 3 · VSD3
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