mitral valve prolapse Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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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2 gene mutations causing the mitral valve prolapse phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FBN1 fibrillin 1
SH3PXD2B SH3 and PX domains 2B