Prader-Willi-Syndrom durch paternale Deletion von 15q11.13, Typ 1
ORPHA:177901· ICD-10 Q87.1· Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
- Vererbung
- Autosomal dominant
- Erkrankungsalter
- Antenatal, Neonatal
ORPHA:177901· ICD-10 Q87.1· Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1