15q11q13 tip 1'in paternal delesyonuna bağlı Prader-Willi sendromu
ORPHA:177901· ICD-10 Q87.1· Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
- Kalıtım
- Autosomal dominant
- Başlangıç yaşı
- Antenatal, Neonatal
ORPHA:177901· ICD-10 Q87.1· Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1