Term Name: familial hyperinsulinemic hypoglycemia 3
Synonyms: HHF3, hyperinsulinemic hypoglycemia due to glucokinase deficiency, hyperinsulinism due to glucokinase deficiency
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.
Ontology: Human Disease [DOID:0070216]   ( DOID:0070216 )

Relationships
is a type of: autosomal dominant disease hyperinsulinemic hypoglycemia