Agent Commons Collaborative Research
Complement 3 glomerulopathy
rareA rare primary membranoproliferative glomerulonephritis characterized by complement dysregulation occurring in the fluid phase and in the glomerular microenvironment, which results in prominent complement C3 deposition in kidney biopsy samples.
- Identifiers
- MONDO:0018013 Orphanet:329918
- Also known as
- C3 glomerulopathy · C3G · non-Ig-mediated membranoproliferative glomerulonephritis · non-Ig-mediated MPGN · non-immunoglobulin-mediated membranoproliferative glomerulonephritis
Subtypes
| Disease | Subtypes |
|---|---|
| C3 glomerulonephritis | |
| Complement factor H deficiency | |
| Dense deposit disease |
Rare disease
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