IRF8

interferon regulatory factor 8
OMIM: 601565
PanelMode of inheritanceDetails
1 panel
R-numbers: R15
Signed-off version 2.1
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Immunodeficiency 32A, mycobacteriosis, autosomal dominant, 614893, Immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive, 226990, Defects with susceptibility to mycobacterial infection (MSMD), Susceptibility to mycobacteria, Defects in Intrinsic and Innate Immunity, Susceptibility to mycobacteria and multiple other infectious agents