has material basis in germline mutation in IRF8 Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency https://www.malacards.org/card/immunodeficiency_32a MONDO:0013957 UMLS:C3808589 IMD32A MSMD due to partial interferon regulatory factor 8 deficiency IRF8 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency Mendelian susceptibility to mycobacterial diseases due to partial interferon regulatory factor 8 deficiency immunodeficiency type 32A GARD:0017463 immunodeficiency 32A DOID:0111986 MEDGEN:814919 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IRF8 Orphanet:319600 OMIM:614893 A rare genetic variant of Mendelian susceptibility to mycobacterial diseases characterized by a selective susceptibility to relatively mild infections with bacillus Calmette-Guerin (BCG). MSMD due to partial IRF8 deficiency inherited susceptibility to mycobacterial diseases