遗传性持续性胎儿血红蛋白综合征复合β地中海贫血综合征
ORPHA:46532· ICD-10 D56.4· Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome
- 患病率
- Unknown
- 遗传方式
- Autosomal dominant
- 发病年龄
- Childhood
ORPHA:46532· ICD-10 D56.4· Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome