DOID:0070216 - familial hyperinsulinemic hypoglycemia 3
Disease Ontology Definition:A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of a reduced threshold for insulin release and hypoglycemia induced by fasting or protein rich meals that has_material_basis_in activating mutations in the GCK gene on chromosome 7p13.
Synonyms: HHF3, hyperinsulinemic hypoglycemia due to glucokinase deficiency, hyperinsulinism due to glucokinase deficiency
|OMIM:602485 - HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 3; HHF3|
|MONDO:0011236 - hyperinsulinism due to glucokinase deficiency|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : gck
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD