mitral valve stenosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A mitral valve disease that is characterized by the narrowing of the orifice of the mitral valve of the heart. (Human Disease Ontology, DOID_1754)
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2 gene mutations causing the mitral valve stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GJA5 gap junction protein, alpha 5, 40kDa
RXRA retinoid X receptor, alpha