congenital neutropenia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of neutropenia with congenital onset. (Human Phenotype Ontology, HP_0005549)
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2 genes associated with the congenital neutropenia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GFI1 growth factor independent 1 transcription repressor
WAS Wiskott-Aldrich syndrome