|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Congenital onset of a marked decrease in the number of granulocytes. (Human Phenotype Ontology, HP_0005541)|
|Downloads & Tools|
2 genes associated with the congenital agranulocytosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.