"autosomal recessive MSMD due to complete RORgamma receptor defiency"^^ . _:vb50945779 . _:vb50945779 . . "DOID:0111940"^^ . "disease_ontology"^^ . "autosomal recessive primary immunodeficiency due to RORC mutation"^^ . "A primary immunodeficiency disease characterized by onset in infancy of increased susceptibility to mycobacterial and candidal infections that has_material_basis_in homozygous or compound heterozygous mutation in RORC on chromosome 1q21.3."^^ . "ORDO:477857"^^ . "IMD42"^^ . . "OMIM:616622"^^ . . _:vb50945779 . . "autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency"^^ . _:vb50945779 . _:vb50945779 . "immunodeficiency 42"^^ .