Hyperinsulinismus durch Kir6.2-Mangel, autosomal-dominanter
ORPHA:276580· ICD-10 E16.1· Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
- Prävalenz
- Unknown
- Vererbung
- Autosomal dominant
- Erkrankungsalter
- Infancy, Neonatal
ORPHA:276580· ICD-10 E16.1· Autosomal dominant hyperinsulinism due to Kir6.2 deficiency