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

hydroxymethylbilane synthase
hydroxymethyldeoxyuridinemonophosphate kinase
hydroxymethyldihydropterin pyrophosphokinase
hydroxymethylglutaryl-CoA reductase inhibitors
hydroxymethylglutaryl-CoA synthase
hydroxymethylglutaryl CoA reductases
hydroxymethylgutaryl-CoA hydrolase
hydroxymethylpyrimidine kinase
hydroxymethyluracil DNA glycosylase
hydroxymethyl and formyl transferases
hydroxynervone
hydroxynervonic acid
hydroxyneurosporene desaturase
hydroxyphenamate
hydroxyphenylazouracil
hydroxyphenyluria (current term)
hydroxypregnenolone
hydroxyprolinaemia
hydroxyproline
hydroxyproline
hydroxyprolines
hydroxyproline oxidase
hydroxyproline rich glycoprotein
hydroxypropiophenone
hydroxyprostaglandin dehydrogenases
hydroxypyruvate decarboxylase
hydroxypyruvate isomerase
hydroxyquinolines
hydroxysteroids
hydroxysteroid dehydrogenases

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