| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores 2025 |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Hereditary metabolic disorder characterized by recurrent acute arthritis, hyperuricemia and deposition of sodium urate in and around the joints, sometimes with formation of uric acid calculi. (Experimental Factor Ontology, EFO_0004274) |
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6 genes involed in the disease Gout from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| ABCG2 | ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group) | 5.0 |
| SLC2A9 | solute carrier family 2 (facilitated glucose transporter), member 9 | 5.0 |
| PRPS1 | phosphoribosyl pyrophosphate synthetase 1 | 4.0 |
| HPRT1 | hypoxanthine phosphoribosyltransferase 1 | 4.0 |
| SAA2 | serum amyloid A2 | 4.0 |
| SAA1 | serum amyloid A1 | 4.0 |