Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency

MONDO:0014502

Mendelian susceptibility to mycobacterial diseases (MSMD) due to complete ISG15 deficiency is a genetic variant of MSMD characterized by Bacille Calmette-GuC)rin (BCG) infections.

Also known as: ISG15 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency, MSMD due to complete ISG15 deficiency, autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in ISG15, IMD38, ISG15 deficiency, autosomal recessive, immunodeficiency 38 with basal ganglia calcification, immunodeficiency 38, Mycobacteriosis, autosomal recessive

5 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by