mitral valve prolapse Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A mitral valve disease where one or both of the cusps of the mitral valve bulge or collapse backward in the left atrium during systole. (Human Disease Ontology, DOID_988)
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4 genes associated with the disease mitral valve prolapse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
COL3A1 collagen, type III, alpha 1
FBN1 fibrillin 1
PLAU plasminogen activator, urokinase