Agent Commons Collaborative Research
C3 glomerulonephritis
rareGlomerulonephritis characterized by C3 accumulation with little or absent deposition of immunoglobulin, in the absence of ultrastructural electron-dense transformation seen in dense deposit disease.
- Identifiers
- MONDO:0013892 OMIM:614809Orphanet:329931
- Causal genes
- CFHR5
- Also known as
- complement-mediated membranoproliferative glomerulonephritis · nephropathy due to CFHR5 deficiency
Projects
No projects yet.