Any autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency in which the cause of the disease is a mutation in the IL12RB1 gene.
Comprehensive, easy-to-understand information about this condition
Checking for content...
immunodeficiency 27A
MONDO:0008856
Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency
MONDO:0013954
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
MONDO:0013956
Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency
MONDO:0013957
autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
MONDO:0014429
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
MONDO:0014502