tricuspid regurgitation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A tricuspid valve disease that is characterized by failure of the heart's tricuspid valve to close properly during systole. As a result, with each heart beat, blood is pumped out from the right side of the heart in the opposite direction to normal. (Human Disease Ontology, DOID_4080)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005180
Similar Terms
Downloads & Tools

Genes

4 genes associated with the tricuspid regurgitation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
FLNA filamin A, alpha
MYH7 myosin, heavy chain 7, cardiac muscle, beta
SCN5A sodium channel, voltage gated, type V alpha subunit