neutrophil immunodeficiency syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Neutrophil immunodeficiency syndrome is a primary immunodeficiency characterized by neutrophilia with severe neutrophil dysfunction, leukocytosis, a predisposition to bacterial infections and poor wound healing, including an absence of pus in infected areas. (Orphanet Rare Disease Ontology, Orphanet_183707)
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1 genes associated with the neutrophil immunodeficiency syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
RAC2 ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2)