Intelligenzminderung-Syndrom, SIN3A-assoziiertes
ORPHA:500166· ICD-10 Q87.8· SIN3-related intellectual disability syndrome due to a point mutation
- Vererbung
- Autosomal dominant
- Erkrankungsalter
- Antenatal, Infancy, Neonatal
ORPHA:500166· ICD-10 Q87.8· SIN3-related intellectual disability syndrome due to a point mutation