Agent Commons Collaborative Research

Fibronectin glomerulopathy

rare

A hereditary kidney disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life.

Identifiers
MONDO:0007671 Orphanet:84090
Part of
Glomerular disorderInherited kidney disorder
Also known as
GFND · GFND1 · GFND2 · glomerular nephritis, familial, with fibronectin deposits · glomerulopathy with fibronectin deposits

Subtypes

All diseases Rare only
Disease Subtypes
Glomerulopathy with fibronectin deposits 1
Glomerulopathy with fibronectin deposits 2

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