Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0110112 - atrial heart septal defect 7


Disease Ontology Definition:An atrial heart septal defect that has material basis in heterozygous mutation in the NKX2-5 gene on chromosome 5q35.

Synonyms: ASD with or without atrioventricular conduction defects, atrial septal defect 7, with or without AV conduction defects , atrial septal defect-atrioventricular conduction defects syndrome

Xenbase Genes : nkx2-5

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007173 - atrial septal defect 7

OMIM:
OMIM:108900 - ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS; ASD7

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): atrial heart septal defect (is_a)