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Summary Literature (0)
DOID:0070453 - xanthinuria type II

Disease Ontology 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.

Synonyms: XAN2,

Xenbase Genes : mocos



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): xanthinuria (is_a)