has material basis in germline mutation in RORC autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency https://www.malacards.org/card/immunodeficiency_42 immunodeficiency 42 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency caused by mutation in RORC IMD42 RORC autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency OMIM:616622 DOID:0111940 UMLS:C5567647 GARD:0017861 MEDGEN:1799070 MONDO:0014710 immunodeficiency type 42 Orphanet:477857 Any autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency in which the cause of the disease is a mutation in the RORC gene. inherited susceptibility to mycobacterial diseases