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Collagen type III glomerulopathy

MONDO:0019396

A rare glomerular disease characterized by abnormal accumulation of type III collagen within the mesangium and subendothelial space of the glomerulus. Clinically it usually manifests with proteinuria (often in the nephrotic range), microscopic hematuria, peripheral edema and/or hypertension. In some cases progression to end-stage renal failure is observed.

Also known as: Collagenofibrotic glomerulopathy

0 clinical trials for this condition and its sub-types, 0 tagged with Collagen type III glomerulopathy itself.

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