has material basis in germline mutation in CFHR5 hereditary nephritis C3 glomerulonephritis https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/9757 https://www.malacards.org/card/c3_glomerulopathy https://www.malacards.org/card/c3_glomerulopathy_3 NCIT:C123043 CFHR5 deficiency nephropathy due to CFHR5 deficiency MEDGEN:884569 complement-mediated membranoproliferative glomerulonephritis Orphanet:329931 Glomerulonephritis characterized by C3 accumulation with little or absent deposition of immunoglobulin, in the absence of ultrastructural electron-dense transformation seen in dense deposit disease. GARD:0016487 UMLS:C4055342 OMIM:614809 MONDO:0013892 complement 3 glomerulopathy