aortic valve atresia Gene Set

Dataset MPO Gene-Phenotype 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)
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1 gene mutations causing the aortic valve atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CXCR4 chemokine (C-X-C motif) receptor 4