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Disease Ontology Browser
xanthinuria type II (DOID:0070453)
Alliance: disease page
Synonyms: XAN2
Alt IDs: OMIM:603592, MESH:C566358, ORDO:93602, UMLS_CUI:C1863688
Definition: A xanthinuria characterized by deficiency of xanthine dehydrogenase and aldehyde oxidase that has_material_basis_in homozygous or compound heterozygous mutation in the MOCOS gene on chromosome 18q12.

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