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Disease Ontology Browser
atrial heart septal defect 7 (DOID:0110112)
Alliance: disease page
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
Alt IDs: OMIM:108900, ICD10CM:Q21.1, ORDO:1479
Definition: An atrial heart septal defect that has material basis in heterozygous mutation in the NKX2-5 gene on chromosome 5q35.

Disease References using Mouse Models (1)

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory