|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the neutrophil immunodeficiency syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
|RAC2||ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2)|