| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores 2025 |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A purine-pyrimidine metabolic disorder characterized by deficiency of xanthine oxidase, resulting in excretion of large amounts of xanthine in the urine and the formation of xanthine stones. (Human Disease Ontology, DOID_0060236) |
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2 genes involed in the disease Xanthinuria from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.