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hydroxyphenyluria

(hī-drŏk′sē-fĕn′ə-lurē-ə, -fē′nə-)
n.
  1. 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.