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MIM:614432 - VENTRICULAR SEPTAL DEFECT 3; VSD3
Xenbase Genes: nkx2-5
Human Disease Resource: MIM
MONDO:0013749 - ventricular septal defect 3 |
DOID:1657 - ventricular septal defect |
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MONDO:0013749 - ventricular septal defect 3 |
DOID:1657 - ventricular septal defect |