congenital agranulocytosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Congenital onset of a marked decrease in the number of granulocytes. (Human Phenotype Ontology, HP_0005541)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005541
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Genes

2 genes associated with the congenital agranulocytosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AK2 adenylate kinase 2
ELANE elastase, neutrophil expressed