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fibronectin glomerulopathy

Disease Summary
Associated Targets (1)
Tchem

1


GARD Rare
Mondo Description Fibronectin glomerulopathy is 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.
Mondo Term and Equivalent IDs
MONDO:0007671:  fibronectin glomerulopathy
GARD:0009268: 
MESH:C536826: 
MESH:C562900: 
OMIMPS:137950: 
Orphanet:84090: 
SCTID:236535001: