OBO ID: DOID:0070216
Term Name: familial hyperinsulinemic hypoglycemia 3 Search Ontology:
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. (2)
References:
Ontology: Human Disease   ( DOID:0070216 )
Relationships
is a type of:
OTHER familial hyperinsulinemic hypoglycemia 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GCK Hyperinsulinemic hypoglycemia, familial, 3 602485
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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