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Summary Literature (0)
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 Disease Ontology (on Monarch Initiative):
MONDO:0002070 - ventricular septal defect (disease)

OMIM:
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)