Search Ontology:
Human Disease

xanthinuria type II

Term ID
DOID:0070453
Synonyms
  • XAN2
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. (2)
References
Ontology
Human Disease   ( DOID:0070453 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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