| Dataset | DisGeNET Gene-Disease Associations |
| 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) |
| External Link | https://www.disgenet.org/browser/0/1/0/C1863688 |
| Similar Terms | |
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7 genes associated with the disease Xanthinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
