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Table 3 List of native-kidney biopsy diagnoses that are used to identify patients eligible for registration in the BC GN Registry

From: An overview of the British Columbia Glomerulonephritis network and registry: integrating knowledge generation and translation within a single framework

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

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