Prader-Willi-Syndrom durch Imprinting-Mutation
ORPHA:177910· ICD-10 Q87.1· Prader-Willi syndrome due to imprinting mutation
- Vererbung
- Not applicable
- Erkrankungsalter
- Antenatal, Neonatal
ORPHA:177910· ICD-10 Q87.1· Prader-Willi syndrome due to imprinting mutation