Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
MONDO:0014502Mendelian 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.
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