| Panel | Mode of inheritance | Details | 
|---|---|---|
1 panel  | ||
R-numbers: R15 Signed-off version 8.0  | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Chronic granulomatous disease due to deficiency of NCF-2 233710, Chronic granulomatous disease (CGD), Infections, autoinflammatory phenotype, Congenital defects of phagocyte number or function  |