Table 3.

List of native-kidney biopsy diagnoses that are used to identify patients eligible for registration in the BC GN Registry

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

This list may be updated in the future as histologic classifications change over time.