prolonged prothrombin time Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased time to coagulation in the prothrombin time test, which is a measure of the extrinsic pathway of coagulation. (Human Phenotype Ontology, HP_0008151)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008151
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Genes

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

Symbol Name
F10 coagulation factor X
F2 coagulation factor II (thrombin)
PMM2 phosphomannomutase 2
PRF1 perforin 1 (pore forming protein)