SIN3A点突变导致的智力障碍综合征
ORPHA:500166· ICD-10 Q87.8· SIN3-related intellectual disability syndrome due to a point mutation
- 遗传方式
- Autosomal dominant
- 发病年龄
- Antenatal, Infancy, Neonatal
ORPHA:500166· ICD-10 Q87.8· SIN3-related intellectual disability syndrome due to a point mutation