Síndrome de Prader-Willi por una mutación de impronta
ORPHA:177910· ICD-10 Q87.1· Prader-Willi syndrome due to imprinting mutation
- Herencia
- Not applicable
- Edad de inicio
- Antenatal, Neonatal
ORPHA:177910· ICD-10 Q87.1· Prader-Willi syndrome due to imprinting mutation