Medical Definition of Hydroxyphenyluria

1. Urinary excretion of tyrosine and phenylalanine, as a result of ascorbic acid deficiency; occurs notably in those premature infants who lack this vitamin. (05 Mar 2000)

Lexicographical Neighbors of Hydroxyphenyluria

hydroxymethylglutaryl-CoA synthase
hydroxymethylglutaryl CoA reductases
hydroxymethylgutaryl-CoA hydrolase
hydroxymethylpyrimidine kinase
hydroxymethyls
hydroxymethyluracil DNA glycosylase
hydroxynaphthoquinone
hydroxynaphthoquinones
hydroxynervone
hydroxynervonic acid
hydroxyneurosporene desaturase
hydroxypethidine
hydroxyphenamate
hydroxyphenyl
hydroxyphenylazouracil
hydroxyphenyluria (current term)
hydroxypiperidine
hydroxypiperidines
hydroxypregnenolone
hydroxyprolinaemia
hydroxyproline
hydroxyproline oxidase
hydroxyproline rich glycoprotein
hydroxyprolines
hydroxypropiophenone
hydroxypropyl
hydroxyprostaglandin dehydrogenases
hydroxypyruvate decarboxylase
hydroxypyruvate isomerase

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