|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An anomaly of clotting factor II, which is known as prothrombin, a vitamin K-dependent proenzyme that functions in the blood coagulation cascade. (Human Phenotype Ontology, HP_0012200)|
|Downloads & Tools|
7 genes associated with the abnormality of prothrombin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.