ORPHA:93601
Xanthinuria type I
Also called XDH deficiency, XO deficiency, XOR deficiency, Xanthine dehydrogenase deficiency, Xanthine oxidase deficiency, Xanthine oxidoreductase 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:93601 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.