|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormality of the level of activity of circulating fibrinogen. (Human Phenotype Ontology, HP_0011898)|
|Downloads & Tools|
7 genes associated with the abnormality of circulating fibrinogen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.