Kleefstra-Syndrom durch Punktmutationen
ORPHA:261652· ICD-10 Q87.8· Kleefstra syndrome due to a point mutation
- Prävalenz
- <1 / 1 000 000
- Vererbung
- Autosomal dominant
- Erkrankungsalter
- Neonatal
ORPHA:261652· ICD-10 Q87.8· Kleefstra syndrome due to a point mutation