has material basis in germline mutation in IFNGR1 autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/immunodeficiency_27b immunodeficiency 27B, Mycobacteriosis, autosomal dominant UMLS:C4014863 autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency DOID:0111956 A genetic variant of Mendelian susceptibility to mycobacterial disease characterized by a partial deficiency leading to impaired IFN-gamma immunity and, consequently, recurrent, moderately severe infections with bacillus Calmette-Guerin (BCG) and other environmental mycobacteria (EM). MEDGEN:863300 immunodeficiency type 27B autosomal dominant MSMD due to partial IFNgammaR1 deficiency IFNGR1 deficiency, autosomal dominant autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in IFNGR1 Orphanet:319581 immunodeficiency 27B, mycobacteriosis, AD MONDO:0014429 OMIM:615978 IMD27B autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency GARD:0017461 immunodeficiency 27B IFNGR1 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency inherited susceptibility to mycobacterial diseases