Mitral Valve Stenosis Gene Set

Dataset HuGE Navigator 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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6 genes associated with the Mitral Valve Stenosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
APOE apolipoprotein E
CASR calcium-sensing receptor
FGB fibrinogen beta chain
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
TGFB1 transforming growth factor, beta 1