Hartnup disease
methylmalonic acidemia
lysine intolerance
aminoacylating
aminoaciduric
abetalipoproteinemia
iminoglycinuria
aminoacidopathy
aminolytic
aminoaciduria
A.A.
ketoacidemia
a.a.
aminoalcoholic
proteolysis
glutamine
histidinemia
threonine
norvaline
nonaminoacylated
tridecapeptide
aminoglycosidic
deaminoacylation
peptidogenomic
hypoaminoacidemia
mutein
dopasensitivity
peptoprime
carboxyglutamic acid
aminoacidic
degron
hippuricase
dopasensitive
mistranslation
aminoacetylation
aminopeptidasic
tyrosine
preproalbumin
glycine
simple protein
peptidyltransferase
alanine
aminoacidemia
aminochronological
isoglutamine
beta-amino acid
interresidue
Niemann-Pick disease
aminoacyltransferase
glycosamine
lysinemia
decapeptide
tyrosinemia
homopeptide
monoaminylation
deaminoacylate
aminopolycarboxylate
hyperaminoacidemia
aminotransaminase
preprosequence
aminomutase
aminoamide
essential amino acid
elmiric acid
citrullination
missense mutation
acetylaminopeptidase
citrulline
lipopentapeptide
transpeptidation
butyrine
hyperaminoaciduria
octapeptide
telopeptide
aminocyclopropanecarboxylate
carboxypeptidase
monoaminosaccharide
hypoproteinemia
metaboloepigenetic
phosphoglucosamine mutase
hydroxy amino acid
aminohexanoate
hydroxy-amino acid
aminoarylated
amastatin
metaboloepigenetics
Edman degradation
allotype
rumination
eupeptide
aminobutyrate
nonessential amino acid
peptide bond
tyrosinosis
aminosteroidal
complete protein
aminoisobutyrate
aminoproteolytic
deamination
Morquio syndrome

English words for 'An autosomal-recessive metabolic disorder affecting the absorption of nonpolar amino acids.'

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