mitral valve atresia Gene Set

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

Symbol Name
RXRA retinoid X receptor, alpha