Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency

A rare genetic variant of Mendelian susceptibility to mycobacterial diseases characterized by a selective susceptibility to relatively mild infections with bacillus Calmette-Guerin (BCG).

Also known as: IRF8 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency, MSMD due to partial IRF8 deficiency, MSMD due to partial interferon regulatory factor 8 deficiency, Mendelian susceptibility to mycobacterial diseases due to partial interferon regulatory factor 8 deficiency, autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IRF8, immunodeficiency type 32A, CD11c-positive/CD1c-positive Dendritic cell deficiency, autosomal dominant, IMD32A

0 clinical trials for this condition and its sub-types, 0 tagged with Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency itself.