Prader-Willi-Syndrom durch paternale Deletion von 15q11.13, Typ 2
ORPHA:177904· ICD-10 Q87.1· Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
- Vererbung
- Autosomal dominant
- Erkrankungsalter
- Antenatal, Neonatal
ORPHA:177904· ICD-10 Q87.1· Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2