先天性纤溶酶原激活物抑制剂1型缺乏症
ORPHA:465· ICD-10 D68.8· Congenital plasminogen activator inhibitor type 1 deficiency
- 患病率
- Unknown
- 遗传方式
- Autosomal recessive
- 发病年龄
- Adolescent, Adult, Childhood, Elderly
ORPHA:465· ICD-10 D68.8· Congenital plasminogen activator inhibitor type 1 deficiency