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)