metachromatic leukodystrophy
inborn error of metabolism
enzymopathy
ARSA
histidinemia
ketoacidemia
Gaucher's disease
methylmalonic acidemia
metaboloepigenetics
metabolotyping
galactosemia
interferase
mucopolysaccharidosis
alkaptonuria
trimethylaminuria
Gilbert's syndrome
carnosinemia
plurimetabolic
glycomutant
aminoacidopathy
crossregulation
acetoacetic acid
metabolotype
abetalipoproteinemia
ureohydrolase
archease
erythroenzymopathy
acylphosphatase
metabolopathy
metabolic disorder
flavoprotein
phenylketonuria
alcaptonuria
lipomics
arylesterase
sitosterolemia
antienzyme
aryldialkylphosphatase
diabetes
saccharidosis
analbuminaemia
hawkinsinuria
analphalipoproteinemia
codehydrogenase
metaboloepigenetic
high anion gap metabolic acidosis
Niemann-Pick disease
pseudoenzyme
enzymotic
acetylase
azymia
activase
coproporphyria
Hurler's disease
aminoacyltransferase
lysine intolerance
catabolic
arabinosis
dysostosis multiplex
gargoylism
allantoinase
katabolic
Hurler's syndrome
creatinase
dehydrogenative
metametabolomics
neomorphic
syndrome X
dioxgyenase
lipochondrodystrophy
adenylase
homocystinuria
polysaccharase
hypophosphatasia
PKU
enzymologic
adipolin
epoxidase
calmodulinopathy
Wolman disease
acylphosphatidylethanolamine
urobilinoid
heteroallele
anhydrofructose
enzymelike
mutasynthetic
ornithine transcarbamylase deficiency
cardiometabolic
tyrosinemia
enzymopathic
glutamylase
procarboxysome
phosphoglucomutase
metabolon
tetramutant