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Oroticaciduria 1: A rare metabolic disorder where deficiency of two enzymes (orotidylic pyrophosphorylase and orotidylic decarboxylase) which impairs the body's ability to break down orotic acid which then builds up in the body where it can cause damage. More detailed information about the symptoms, causes, and treatments of Oroticaciduria 1 is available below.
Home medical testing related to Oroticaciduria 1:
Read more about causes of Oroticaciduria 1.
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Prognosis for Oroticaciduria 1: remission with treatment
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Oroticaciduria 1 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Oroticaciduria 1, or a subtype of Oroticaciduria 1,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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