Prader-Willi-Syndrom durch paternale Deletion 15q11.13
ORPHA:98793· ICD-10 Q87.1· Prader-Willi syndrome due to paternal 15q11q13 deletion
- Vererbung
- Autosomal dominant
- Erkrankungsalter
- Antenatal, Neonatal
ORPHA:98793· ICD-10 Q87.1· Prader-Willi syndrome due to paternal 15q11q13 deletion