DISEASES

Disease-gene associations mined from literature

Human genes for familial hyperinsulinemic hypoglycemia 3

Familial hyperinsulinemic hypoglycemia 3 [DOID:0070216]

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:  familial hyperinsulinemic hypoglycemia 3,  DOID:0070216,  hereditary hyperinsulinemic hypoglycemia 3,  HHF3,  hyperinsulinemic hypoglycemia due to glucokinase deficiency ...