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Xanthinuria: A hereditary condition that is characterised by a disorder of purine metabolism. More detailed information about the symptoms, causes, and treatments of Xanthinuria is available below.
See full list of 11 symptoms of Xanthinuria
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Read more about causes of Xanthinuria.
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Xanthinuria as a "rare disease".
Source - Orphanet
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