Term Name:	familial hyperinsulinemic hypoglycemia 6
Synonyms:	HHF6, HI/HA syndrome, hyperinsulinism-hyperammonemia syndrome
Definition:	A hyperinsulinemic hypoglycemia characterized by autosomal dominant inheritance of excessive insulin secretion, asymptomatic hyperammonemia and episodes of hypoglycemia induced by fasting or protein rich meals that has_material_basis_in mutation in the GLUD1 gene on chromosome 10q23.3.
Ontology:	Human Disease [DOID:0070217]   ( DOID:0070217 )