An inborn error of metabolism with the urinary excretion of alpha-hydroxy-butyric acid and phenylpyruvic acid.
D002087:Butyrates; D006801:Humans; D007657:Ketone Bodies / Q000652:urine*; D010661:Phenylketonurias / Q000652:urine*; D010667:Phenylpyruvic Acids
D002087:Butyrates; D007657:Ketone Bodies; D010667:Phenylpyruvic Acids; C031606:phenylpyruvic acid
KETONE BODIES/in urine; PHENYLPYRUVIC OLIGOPHRENIA/urine in