has characteristic has characteristic inborn disorder of amino acid metabolism https://www.malacards.org/card/amino_acid_metabolic_disorder rare inborn error of cellular amino acid metabolic process GARD:0006770 UMLS:C5886841 SCTID:42930003 inborn cellular amino acid metabolic process disorder ICD9:270 inherited amino acid metabolic disorder MEDGEN:1857273 NCIT:C97090 An inherited disorder that affects the metabolism of the amino acids. Representative examples include alkaptonuria, homocystinuria, tyrosinemia, and phenylketonuria. ICD9:270.9 amino acid metabolism, inborn errors MONDO:0004736 MESH:D000592 inborn error of cellular amino acid metabolic process inborn error of amino acid metabolism DOID:9252 inborn amino acid metabolism disorder inborn disorder of amino acid and other organic acid metabolism inherited amino acid metabolism disease