collagen type III glomerulopathy https://www.malacards.org/card/collagen_type_iii_glomerulopathy 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. MONDO:0019396 GARD:0019048 SCTID:708127008 UMLS:C3872695 Collagenofibrotic glomerulopathy ICD9:583.89 MEDGEN:836996 Orphanet:84087 glomerular disorder obsolete secondary glomerular disease