ventricular septal defect

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: tbx1, hand1, gdf1, gata6, nkx2-6, gata4, nkx2-5, cited2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0002070 - ventricular septal defect

MONDO:0002070 - ventricular septal defect

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)