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C3 glomerulonephritis

MONDO:0013892

Glomerulonephritis characterized by C3 accumulation with little or absent deposition of immunoglobulin, in the absence of ultrastructural electron-dense transformation seen in dense deposit disease.

Also known as: complement-mediated membranoproliferative glomerulonephritis, nephropathy due to CFHR5 deficiency, CFHR5 deficiency

11 clinical trials for this condition and its sub-types, 7 tagged with C3 glomerulonephritis itself.

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Where it sits in the disease tree

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