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DOID:1657 - ventricular septal defect
Disease Ontology Definition:A heart septal defect characterized by an opening in the interventricular septum, causing a shunt between ventricles.
Synonyms: Interventricular septal defect, Ventricular septal abnormality,
Xenbase Genes
:
tbx1,
gdf1,
gata6,
nkx2-6,
gata4,
nkx2-5,
cited2
| MONDO:0002070 - ventricular septal defect |
| OMIM:614429 - VENTRICULAR SEPTAL DEFECT 1; VSD1 |
| OMIM:614431 - VENTRICULAR SEPTAL DEFECT 2; VSD2 |
| OMIM:614432 - VENTRICULAR SEPTAL DEFECT 3; VSD3 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
heart septal defect (is_a)