Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (5)
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


In Mondo Disease Ontology:
MONDO:0004736 - inherited amino acid metabolic disorder

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : prdx1, slc22a5, slc25a1, amt, opa3, aass, pepd, fh, pcca, gamt, ggt1, ahcy, psph, bckdhb, hpd, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): inherited metabolic disorder (is_a)