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Summary Literature (0)
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

Xenbase Genes : gck

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011236 - hyperinsulinism due to glucokinase deficiency


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), genetic disease (is_a), hyperinsulinemic hypoglycemia (is_a)