prolonged whole-blood clotting time Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal prolongation (delay) in the time required by whole blood to produce a visible clot. (Human Phenotype Ontology, HP_0005542)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005542
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Genes

4 genes associated with the prolonged whole-blood clotting time phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
F12 coagulation factor XII (Hageman factor)
F5 coagulation factor V (proaccelerin, labile factor)
F9 coagulation factor IX
VWF von Willebrand factor