abnormality of the extrinsic pathway Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the extrinsic pathway (also known as the tissue factor pathway) of the coagulation cascade. (Human Phenotype Ontology, HP_0010988)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010988
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Genes

3 genes associated with the abnormality of the extrinsic pathway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
F7 coagulation factor VII (serum prothrombin conversion accelerator)
GGCX gamma-glutamyl carboxylase
VKORC1 vitamin K epoxide reductase complex, subunit 1