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hydroxyphenyluria

[ hī-drŏk′sē-fĕn′ə-lurē-ə, -fē′nə- ]
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n.
The presence of tyrosine and phenylalanine in the urine as a result of a deficiency of ascorbic acid.
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The American Heritage® Stedman's Medical Dictionary Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.
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