|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An anomaly in the number of monocytes, which are myeloid mononuclear recirculating leukocyte that can act as a precursor of tissue macrophages, osteoclasts and some populations of tissue dendritic cells. (Human Phenotype Ontology, HP_0012310)|
|Downloads & Tools|
4 genes associated with the abnormal monocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.