ISG15

ISG15 ubiquitin-like modifier
OMIM: 147571
PanelMode of inheritanceDetails
1 panel
R-numbers: R15
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Immunodeficiency 38, 616126, Defects with susceptibility to mycobacterial infection (MSMD), idiopathic basal ganglia calcification, Susceptibility to mycobacteria, brain calcifications, Defects in Intrinsic and Innate Immunity