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Disease Ontology Browser
familial hyperinsulinemic hypoglycemia 3 (DOID:0070216)
Alliance: disease page
Synonyms: HHF3; hyperinsulinemic hypoglycemia due to glucokinase deficiency; hyperinsulinism due to glucokinase deficiency
Alt IDs: OMIM:602485, ORDO:79299
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.

Disease References using Mouse Models (1)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory