Histologic diagnoses enrolled in the BC GN registry | |
---|---|
Alport’s disease | Idiopathic nodular glomerulosclerosis |
Amyloidosis: AL | IgA nephropathy |
Amyloidosis: AA | IgM nephropathy |
Amyloidosis: other | Immunotactoid GN |
Anti-GBM antibody (Goodpasture’s) GN | Light chain deposition disease |
Autoimmune/connective tissue disease associated GN | Light and heavy chain deposition disease |
Cryoglobulinemic GN | Lupus nephritis |
C3 GN | Minimal change disease |
C1q nephropathy | Membranoproliferative GN, complement mediated |
Dense deposit disease | Membranoproliferative GN, IC mediated |
Fabry’s disease | Membranous nephropathy |
Fibrillary GN | Mesangial proliferative GN |
Focal segment glomerulosclerosis | Pauci-immune (ANCA) GN |
GN with monoclonal immunoglobulin deposits | Post-infectious GN |
GN not otherwise specified | Proliferative GN |
Heavy chain deposition disease | Thin basement membrane disease |
Henoch-Schonlein purpura | Waldenstrom’s macroglobulinemia |