hawkinsinuria
fumarylacetoacetate
maleylacetoacetate
tyrosinosis
monophenol monooxygenase
alkapton
metirosine
alcapton
homogentisic acid
tyrosinemia
tyrase
cheese syndrome
tyrphostin
phenylalaninase
apotyrosinase
prephenic acid
phosphotyrosine
iodotyrosine
pretyrosine
detyrosination
tyrosinamide
catechol oxidase
paroxypropione
phosphoglucosamine mutase
methylmalonic acidemia
anlotinib
phenylketonuria
oligoadenylase
acylphosphatase
dihydropyrimidinase
dityrosine
hypotyrosinemia
PKU
monoiodotyrosine
meta-
methyltyrosine
lestaurtinib
telatinib
hydroxyprotein
antityrosinase
methoxyhydroxyphenylglycol
syndrome X
guanidinobutyrase
morforex
diazobenzol
lanostane
succinylacetone
propionylcholinesterase
nutrimetabolomics
alkaptonuria
tyrotoxine
dibutyltin
adenosine diphosphate
nicotinamide adenine dinucleotide phosphate
metabolic disorder
tyrosinylated
tandutinib
tetrahydrobiopterin
monophosphothiamine
phosphopentomutase
levothyroxine
epoxysqualene
fructanohydrolase
osteotesticular
desaminotyrosine
phosphoacetylglucosamine mutase
dimethyloxalylglycine
glyA
tyrosinated
stigmastane
thyroxine
metachromatic leukodystrophy
tyrosinemic
deoxythymine
sialometabolism
thyronamine
histidinemia
fructanase
ketohydroxyestrin
preprothyrotropin
metabolisis
liarozole
adenylyl
fructofuranosidase
maculosin
phosphohydrolase
androstenetriol
codehydrogenase
Plicatoperipatus jamaicensis
hypophosphatasia
dextrinase
nitrotyrosine
Hashitoxicosis
metabolically
epiandrosterone
oligopeptidase
oligomerase
prasterone

English words for '4-alpha-hydroxyphenylpyruvate hydroxylase deficiency, an autosomal dominant metabolic disorder affecting the metabolism of tyrosine.'

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