alkaptonuria
homogentisic acid
alcapton
alkapton
tyrosinosis
phenylalaninase
metachromatic leukodystrophy
pretyrosine
PKU
prephenic acid
phenylketonuria
desaminotyrosine
fumarylacetoacetate
phosphotyrosine
maleylacetoacetate
phenylalkylamine
hawkinsinuria
tyrase
alcaptonuria
geranylgeranylase
naphthyridinone
monophenol monooxygenase
isochromenone
arabinosis
erythrosin
starvation acidosis
cyanoamino
carnosinemia
allantoinase
methylmalonic acidemia
interferase
lactate dehydrogenase
tyrosinylated
imidazolidone
aminostatic
high anion gap metabolic acidosis
myristone
pyrophosphorylase
phaeomelanogenesis
de-iodinase
phyloproteomic
pyomelanin
metabolic disorder
arginyl aminopeptidase
pheomelanogenic
ureohydrolase
hydrocytosis
chrysenone
koenoline
Edman's reagent
polytyrosine
hydroxyacylglutathione hydrolase
nucleophosphoprotein
phenoxyalkanoic
detyrosination
emethallicin
aryldialkylphosphatase
phylomitogenomic
phenylalkane
aminopolypeptidase
sialometabolism
dityrosine
phenanthridinone
nontasting
antityrosinase
phenylpyruvate
dephenylation
exometabolomics
antiphosphothreonine
arylamidase
catechol oxidase
desethylamiodarone
mucopolysaccharidosis
phenanthrenylene
Plicatoperipatus jamaicensis
deadenylase
phytocoenology
phosphinidene
aminergic
phosphoglucosamine mutase
ketoacidemia
phytomyxean
dehydrogenative
formamidase
kininogenolysis
benzopyrone
iododestannylation
oligoadenylase
phosphopentomutase
pyridylbenzene
dioleoylphosphatidylcholine
iodotyrosine
alkaline phosphatase
methylosome
nitrophenolate
guanosine monophosphate
exoenzymatic
propionylcholinesterase
dihydrobenzophenanthridine oxidase

English words for 'A rare inherited genetic disorder of phenylalanine and tyrosine metabolism, causing the accumulation and eventual excretion of alkapton.'

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