CORO1A基因缺陷所致重症联合免疫缺陷
ORPHA:228003· ICD-10 D81.2· Severe combined immunodeficiency due to CORO1A deficiency
- 患病率
- <1 / 1 000 000
- 遗传方式
- Autosomal recessive
- 发病年龄
- Childhood, Infancy, Neonatal
ORPHA:228003· ICD-10 D81.2· Severe combined immunodeficiency due to CORO1A deficiency