Glomerulopathy with fibronectin deposits Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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. (Orphanet Rare Disease Ontology, Orphanet_84090)
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1 genes/proteins associated with the disease Glomerulopathy with fibronectin deposits from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FN1 fibronectin 1 2.88009