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Up to: Inborn disorder of purine metabolism · Xanthinuria
Hereditary xanthinuria
Hereditary xanthinuria is a purine metabolism disorder due to inherited deficiency of the xanthine dehydrogenase/oxidase enzyme and is characterized by very low (or undetectable) concentrations of uric acid in blood and urine and very high concentration of xanthine in urine, leading to urolithiasis.
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Xanthinuria type I 1 trial
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Xanthinuria type II 0 trials