Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
ORPHA:319552Autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency
ORPHA:319543Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
ORPHA:319581Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
ORPHA:319589Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency
ORPHA:319535Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency
ORPHA:319539Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
ORPHA:319569Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency
ORPHA:319574Combined immunodeficiency due to IL21R deficiency
ORPHA:357329Immunodeficiency due to CD25 deficiency
ORPHA:169100Mendelian susceptibility to mycobacterial diseases
ORPHA:748Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency
ORPHA:99898Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
ORPHA:319547Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency
ORPHA:319558Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
ORPHA:319563Mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency
ORPHA:477857Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency
ORPHA:319600Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
ORPHA:319595OBSOLETE: X-linked mendelian susceptibility to mycobacterial diseases due to CYBB deficiency
ORPHA:319623OBSOLETE: X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
ORPHA:319612Severe mendelian susceptibility to mycobacterial diseases due to complete IFNG deficiency
ORPHA:699618Severe mendelian susceptibility to mycobacterial diseases due to complete IRF1 deficiency
ORPHA:699615Sterile multifocal osteomyelitis with periostitis and pustulosis
ORPHA:210115Susceptibility to infection due to TYK2 deficiency
ORPHA:331226