has material basis in germline mutation in predisposes towards IFNGR2 immunodeficiency 28 autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency https://github.com/monarch-initiative/mondo/issues/4882 Orphanet:319574 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IFNGR2 MONDO:0017902 autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 2 deficiency IFNGR2 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency GARD:0017460 A genetic variant of Mendelian susceptibility to mycobacterial diseases characterized by a partial deficiency in IFN-gammaR2, leading to a residual response to IFN-gamma and consequently to recurrent, moderately severe infections with bacillus Calmette-Guerin (BCG) and other environmental mycobacteria (EM). autosomal recessive MSMD due to partial interferon gamma receptor 2 deficiency UMLS:C4511098 autosomal recessive MSMD due to partial IFNgammaR2 deficiency MEDGEN:1387677 inherited disease susceptibility mycobacterial infectious disease