遗传性抗凝血酶缺乏所致遗传性易栓症
ORPHA:82· ICD-10 D68.5· Hereditary thrombophilia due to congenital antithrombin deficiency
- 患病率
- 1-5 / 10 000
- 遗传方式
- Autosomal dominant
- 发病年龄
- Adolescent, Adult
ORPHA:82· ICD-10 D68.5· Hereditary thrombophilia due to congenital antithrombin deficiency