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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,
Xenbase Genes : prdx1, slc22a5, slc25a1, amt, opa3, aass, pepd, fh, pcca, gamt, ggt1, ahcy, psph, bckdhb, hpd,
MONDO:0004736 - inherited amino acid metabolic disorder |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
inherited metabolic disorder (is_a)