FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term familial hyperinsulinemic hypoglycemia 3 ID (Ontology) DOID:0070216 (Human Disease)
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.
Also Known As "HHF3" ; "hyperinsulinemic hypoglycemia due to glucokinase deficiency" ; "hyperinsulinism due to glucokinase deficiency"
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 Genes
 familial hyperinsulinemic hypoglycemia 3       4
 for disease ribbon | familial hyperinsulinemic hypoglycemia 3       4
 model of | familial hyperinsulinemic hypoglycemia 3       4
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_____
hypoglycemia                       |
 |__hyperinsulinemic hypoglycemia__|
                                   familial hyperinsulinemic hypoglycemia 3  4 rec.
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Is a autosomal dominant disease
hyperinsulinemic hypoglycemia
Part of
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Synonyms
  • "HHF3" EXACT OMO:0003012
    "hyperinsulinemic hypoglycemia due to glucokinase deficiency" EXACT
    "hyperinsulinism due to glucokinase deficiency" EXACT
Secondary IDs
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GARD:2818
MIM:602485
ORDO:79299