Hyperinsulinismus durch Kir6.2-Mangel, autosomal-rezessiver
ORPHA:79644· ICD-10 E16.1· Autosomal recessive hyperinsulinism due to Kir6.2 deficiency
- Prävalenz
- Unknown
- Vererbung
- Autosomal recessive
- Erkrankungsalter
- Neonatal
ORPHA:79644· ICD-10 E16.1· Autosomal recessive hyperinsulinism due to Kir6.2 deficiency