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.
|MONDO:0006504 - acquired metabolic disease|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : slc5a1.2, mapk8ip1, irs1, fga, app, nr0b2, ttr, il6, stat3.1, hnf4a, fgf23.2, ctla4, pparg, pdx1, pomc,
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): disease of metabolism (is_a)