has material basis in germline mutation in IFNGR2 autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency https://www.malacards.org/card/autosomal_dominant_mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_ifngammar2_deficiency A genetic variant of mendelian susceptibility to mycobacterial diseases characterized by a partial deficiency in IFN-gammaR2, leading to impaired response to IFN-gamma and, consequently, to recurrent, moderately severe infections with bacillus Calmette-Guerin (BCG) and other environmental mycobacteria (EM). Orphanet:319589 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IFNGR2 autosomal dominant MSMD due to partial IFNgammaR2 deficiency autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 2 deficiency MEDGEN:1371829 MONDO:0017903 autosomal dominant MSMD due to partial interferon gamma receptor 2 deficiency UMLS:C4510875 IFNGR2 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency GARD:0021425 inherited susceptibility to mycobacterial diseases