PEX10基因缺乏所致常染色体隐性遗传性共济失调
ORPHA:247815· ICD-10 G11.8· Autosomal recessive ataxia due to PEX10 deficiency
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal recessive
- 发病年龄
- Adolescent, Childhood
ORPHA:247815· ICD-10 G11.8· Autosomal recessive ataxia due to PEX10 deficiency