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Disease Ontology Browser
xanthinuria (DOID:0060236)
Alliance: disease page
Synonyms: classic xanthinuria; hereditary xanthinuria; xanthine dehydrogenase deficiency; xanthine oxidase deficiency
Alt IDs: ICD10CM:E79.8, OMIM:PS278300, ORDO:3467, UMLS_CUI:C0220988
Definition: 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.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory