ORPHA:93602
Xanthinuria type II
Also called XDH and AOX dual deficiency, Xanthine dehydrogenase and xanthine aldehyde oxidase dual deficiency
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:93602 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.