A disorder of amino acid metabolism that has its basis in the disruption of the metabolism of lysine, hydroxylysine, and/or tryptophan.
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2-aminoadipic 2-oxoadipic aciduria
MONDO:0008774
encephalopathy due to hydroxykynureninuria
MONDO:0009372
seizures-intellectual disability due to hydroxylysinuria syndrome
MONDO:0009373
hyperlysinemia
MONDO:0009388
saccharopinuria
MONDO:0010005
familial hypertryptophanemia
MONDO:0010907