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