mitral atresia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congenital defect with failure to open of the mitral valve orifice. (Human Phenotype Ontology, HP_0011560)
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1 genes associated with the mitral atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NKX2-5 NK2 homeobox 5