Xanthinuria Gene Set

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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Genes

2 genes involed in the disease Xanthinuria from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Symbol Name Standardized Value
XDH xanthine dehydrogenase 5.0
MOCOS molybdenum cofactor sulfurase 5.0