|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An anomaly of cells involved in the formation of a granulocytes, that is, of the granulocytopoietic cell. (Human Phenotype Ontology, HP_0012135)|
|Downloads & Tools|
2 genes associated with the abnormality of cells of the granulocytic lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.