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Up to: Hereditary nephritis · Primary membranoproliferative glomerulonephritis · Familial nephrotic syndrome
Immunoglobulin-mediated membranoproliferative glomerulonephritis
Glomerulonephritis characterized by mesangial proliferation, endocapillary proliferation, and glomerular capillary wall remodeling with immune complex deposits from classical complement pathway activation.
This condition has no sub-types.