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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,
Echinobase Genes :
MIM: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)