|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Glomerulopathy with fibronectin deposits from the curated CTD Gene-Disease Associations dataset.