phenylketonuria
dihydropyrimidine dehydrogenase
hydroxyacylglutathione hydrolase
methylmalonic acidemia
histidinemia
metabolopathy
syndrome X
metabolic disorder
nitrophenylphosphatase
pyrophosphorylytic
acylphosphatase
cystathioninuria
pyrophosphokinase
phenylketonuric
phosphorolytic
colloxylin
phosphoesterase
phosphohydrolytic
serum glutamic oxaloacetic transaminase
fulmicotton
homocystinuria
dephosphatase
ketoacidemia
phytoregulator
metachromatic leukodystrophy
dysmetabolism
phagolytic
exophosphatase
phosphopentomutase
diesterase
carnosinemia
phosphometabolomic
metabasis
phaeohyphomycotic
ureohydrolase
enzymuria
tetrahydrodipicolinic acid
phosphomimicry
Zellweger syndrome
pyrophosphorolytic
metaboloepigenetic
inborn error of metabolism
enzymopathic
immunoalkaline
phospholipidomic
phosphonatase
phosphorylative
citrullinemia
hepatosteatosis
hypophosphatasia
PKU
phosphospecificity
trimethylaminuria
Hunter syndrome
phosphohydrolase
aryldialkylphosphatase
phosphoprotein
phosphoamidase
phosphomannomutase
phosphotriesterase
kryptopyrrole
phosphodefective
monoamine oxidase
MAO
phenylalanine
metabolize
tyrosinemia
beta-hydroxybutyric acid
hyperphosphatasemia
mitoxosome
interferase
phytolithological
dyshepatia
phosphoacetylglucosamine mutase
xanthine
epietiocholanolone
phosphofructaldolase
pyorrheal
creatine-phosphoric acid
thyroid
hyperthyroidization
phosphoenzyme
phosphometabolomics
acylphosphatidylethanolamine
phagomyxean
phosphoanhydridic
hyperthyreosis
phosphatase
adenase
phosphorylytic
phytopathogenicity
phosphoselectivity
plurimetabolic
paedopsychological
hepatitic
phytomyxean
polyphosphatase
kolloxylin

English words for 'A metabolic disorder in which individuals lack the liver enzyme phenylalanine hydroxylase (PAH) which is needed to metabolize the amino acid phenylalanine.'

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