has material basis in germline mutation in
CFHR5
hereditary nephritis
C3 glomerulonephritis
https://github.com/monarch-initiative/mondo/issues/4521
GARD:16487
NCIT:C123043
CFHR5 deficiency
nephropathy due to CFHR5 deficiency
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.
UMLS:C4055342
OMIM:614809
MONDO:0013892
non-immunoglobulin-mediated membranoproliferative glomerulonephritis