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Metadata
ID DOID:0060236
Name xanthinuria
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.
http://en.wikipedia.org/wiki/Xanthinuria, https://medlineplus.gov/genetics/condition/hereditary-xanthinuria/, https://www.ncbi.nlm.nih.gov/pubmed/4369449
Xrefs

ICD10CM:E79.8

MIM:PS278300

ORDO:3467

SNOMEDCT_US_2023_03_01:190919008

UMLS_CUI:C0220988

Subsets

DO_FlyBase_slim

DO_rare_slim

Synonyms

classic xanthinuria [EXACT]

hereditary xanthinuria [EXACT]

xanthine dehydrogenase deficiency [EXACT]

xanthine oxidase deficiency [EXACT]

Parent Relationships

is_a purine-pyrimidine metabolic disorder

is_a autosomal recessive disease

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