Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency

Any autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency in which the cause of the disease is a mutation in the IL12B gene.

Also known as: IL12B autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency, MSMD due to complete IL12B deficiency, MSMD due to complete interleukin 12B deficiency, Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency, autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in IL12B, immunodeficiency type 29, IL12B deficiency, IMD29

0 clinical trials for this condition and its sub-types, 0 tagged with Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency itself.