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Summary Literature (0)
DOID:9252 - amino acid metabolic disorder

Disease Ontology Definition:An inherited metabolic disorder that is characterized by impaired synthesis and degradation of amino acids.

Synonyms: inborn errors of amino acid metabolism

Echinobase Genes : ppm1k, adk, pcca, mccc1, pccb, lmbrd1, abat, serac1, d2hgdh, phgdh, mmut, mmadhc, mmab, asl, hpd, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): inherited metabolic disorder (is_a)