ORPHA:276603
Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency
Also called Hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, diazoxide-resistant focal form
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:276603 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.