aortic valve atresia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congenital disorder of the aortic valve in which the orifice of the valve fails to develop. (Human Phenotype Ontology, HP_0010883)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010883
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Genes

1 genes associated with the aortic valve atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NKX2-5 NK2 homeobox 5