| 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) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C536826 |
| Similar Terms | |
| Downloads & Tools |
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 |
