CARMIL2基因缺陷诱导的重症联合型免疫缺陷病
ORPHA:542301· ICD-10 D82.3· EBV-induced lymphoproliferative disease due to CARMIL2 deficiency
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal recessive
- 发病年龄
- Childhood
ORPHA:542301· ICD-10 D82.3· EBV-induced lymphoproliferative disease due to CARMIL2 deficiency