|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormal prolongation (delay) in the time required by whole blood to produce a visible clot. (Human Phenotype Ontology, HP_0005542)|
|Downloads & Tools|
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.