methylmalonic acidemia
Hartnup disease
histidinemia
lysine intolerance
ketoacidemia
aminoacidopathy
Niemann-Pick disease
syndrome X
tyrosinemia
abetalipoproteinemia
metachromatic leukodystrophy
dysmetabolism
mucopolysaccharidosis
lysinemia
galactosemia
Morquio syndrome
aminoacylating
gargoylism
Hurler's syndrome
hawkinsinuria
dysostosis multiplex
phosphoglucosamine mutase
lipochondrodystrophy
Hurler's disease
phenylketonuria
metabolic disorder
saccharidosis
plurimetabolic
McArdle's disease
glutamine
homocysteinase
glycogenosis
hyperpipecolatemia
hippuricase
peptidogenomic
alanine
iminoglycinuria
Gaucher's disease
metabolopathy
Zellweger syndrome
homocystinuria
inborn error of metabolism
carnosinemia
peptidyltransferase
metabolostat
aspartylglucosaminuria
Chédiak-Higashi syndrome
deformylase
aminoaciduria
antisynthetase
aminoacyltransferase
glutamylase
metaboloepigenetics
arylamidase
aminopolypeptidase
aminolytic
cheese syndrome
phylometabolic
desaminotyrosine
homeostasis
degron
aminomethyltransferase
Gilbert's syndrome
aminomutase
Carpenter syndrome
aminohydrolase
threonine
interferase
phenylalanine
Alagille syndrome
metabolize
phosphosilent
alkaptonuria
arabinosis
archease
analphalipoproteinemia
carboxypeptidase
high anion gap metabolic acidosis
aceturic acid
halogenase
aminoalcoholic
saccharopine
azymia
carboxydipeptidase
Hurler syndrome
acetylaminopeptidase
autosomal recessive defect
nonessential amino acid
PKU
autosomal recessive disease
Wolman disease
metabolisis
lipidosis
metabolically
thermitase