Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency
ORPHA:99898Autosomal 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 combined immunodeficiency due to complete IL6ST deficiency
ORPHA:656283Autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency
ORPHA:319535Autosomal 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 with factor I anomaly
ORPHA:200418Mendelian 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 IL12RB1 deficiency
ORPHA:319552Mendelian 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:319600Obesity due to leptin receptor gene deficiency
ORPHA:179494Severe combined immunodeficiency due to complete RAG1/2 deficiency
ORPHA:331206Severe 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:210115