Disease association ontology term - MONDO:0011236 - hyperinsulinemic hypoglycemia, familial, 3
Term summary
- ID
- MONDO:0011236
- Name
- hyperinsulinemic hypoglycemia, familial, 3
- Ontology or CV name
- Disease association
- Definition
- A form of diffuse hyperinsulinism due to glucokinase hyperactivity associated with a variation in the GCK gene, and characterized by an excessive/ uncontrolled insulin secretion (inappropriate for the level of glycemia) and recurrent episodes of hypoglycemia induced by fasting and glucose rich meals.
