DRI	dietary reference intakes
EAA	essential amino acid
FAD	flavin adenine dinucleotide
FAOD	fatty acid oxidation disorder
FMN	flavin mononucleotide
GALT	galactose 1-phosphate urydyltransferase
GLUT1-DS	glucose transporter type 1 deficiency syndrome
GMP	glycomacropeptides
GSD	glycogen storage disorder
HF	hereditary fructosemia
IMD	inherited metabolic disorder
KD	ketogenic diet
LCFAOD	long-chain fatty acid oxidation disorder
MCT	medium-chain triglyceride
MCV	mean corpuscular volume
MMA	methylmalonic acidemia
MSUD	maple syrup urine disease
NE	niacin equivalents
OA	organic acidosis
PA	propionic acidemia
DHA	docosahexaenoic acid
PAH	phenylalanine hydroxylase
PDHc	pyruvate dehydrogenase complex
PKU	phenylketonuria
PLP	pyridoxal 5′-phosphate
RDA	recommended dietary allowances
UCD	urea cycle disorder
VLCADD	very-long-chain Acyl CoA dehydrogenase deficiency
WHO	World Health Organization