DYRK1A点突变相关的智力障碍
ORPHA:464311· ICD-10 Q87.8· Intellectual disability syndrome due to a DYRK1A point mutation
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal dominant
- 发病年龄
- Infancy, Neonatal
ORPHA:464311· ICD-10 Q87.8· Intellectual disability syndrome due to a DYRK1A point mutation