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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,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:614431 - ventricular septal defect 2; vsd2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
heart septal defect (is_a)