Table 1.
Classification of haematuric diseases by histopathological findings
| Glomerular endothelial cell layer | GBM disorders | Mesangial deposits | Podocytary slit diaphragm disorders | Subendothelial/subepithelial deposit | Others |
| ANCA | Primary | IgAN | MYH9 disease | Primary GN | WRN |
| Endocapillary | Alport | HSP | Fabry disease | MBP | SCD |
| TBMD | Endocapillary | ||||
| HANAC | Crescentic | ||||
| ? LPHS | |||||
| Secondary GN | |||||
| Secondary | SLE | ||||
| Anti-GBM disease | Cryoglobulinemia | ||||
| C3 glomerulopathy | |||||
| CFHR5 nephropathy | Fibrillar deposit | ||||
| Fibronectin | |||||
| Fibrillary | |||||
| Immunotactoid |
GBM: Glomerular basement membrane; ANCA: Antineutrophil cytoplasmic antibodies; CFHR5: Complement factor H–related 5 nephropathy; GN: Glomerulonephritis; HANAC: Hereditary angiopathy, nephropathy, aneurysms, and muscle cramps syndrome; IgAN: IgA nephropathy; LPHS: Loin back pain syndrome; MBP: Membranoproliferative; SCD: Sickle cell disease; HSP: Henoch-Schönlein purpura; SLE: Systemic lupus erythematous; TBMD: Thin basement membrane disease; WRN: Warfarin related nephropathy.