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Inherited susceptibility to mycobacterial diseases

A rare immunodeficiency syndrome, characterized by a narrow vulnerability to poorly virulent mycobacteria, such as bacillus Calmette-Guerin (BCG) vaccines and environmental mycobacteria (EM), and defined by severe, recurrent infections, either disseminated or localized.

1 trial tagged with this condition →

Mendelian susceptibility to mycobacterial diseases due to a complete deficiency 0 trials
Mendelian susceptibility to mycobacterial diseases due to a partial deficiency 0 trials
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency 0 trials
Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency 0 trials
Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency 0 trials
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency 0 trials
Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency 0 trials
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency 0 trials
X-linked Mendelian susceptibility to mycobacterial diseases 0 trials Sub-types →
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency 0 trials
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency 0 trials
Autosomal recessive Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency 0 trials
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency 0 trials
Immunodeficiency 27A 0 trials