Alport综合征-智力障碍-面中部发育不全-椭圆形红细胞增多症综合征
ORPHA:86818· ICD-10 Q87.8· Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
- 患病率
- <1 / 1 000 000
- 遗传方式
- X-linked recessive
- 发病年龄
- Antenatal, Infancy, Neonatal
ORPHA:86818· ICD-10 Q87.8· Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome