DOID:0060158 - acquired metabolic disease
Disease Ontology Definition:A disease of metabolism that has _material_basis_in enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to an endocrine organ disease, organ malfunction, inadequate intake, dietary deficiency, or malabsorption.
Echinobase Genes : mttp, Tcf/Lef, gck, neurod1, hnf1a, glis3, mtnr1b, ptpn1, hnf4a
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): disease of metabolism (is_a)