Hydroxyphenyluria



hydroxyphenyluria hy·drox·y·phen·yl·u·ri·a (hī-drŏk’sē-fěn’ə-lur’ē-ə, əl-yur’-, -fē’nə-)
n.
The presence of tyrosine and phenylalanine in the urine as a result of a deficiency of ascorbic acid.

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