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遗传性蛋白C缺乏所致严重遗传性血栓症

ORPHA:745· ICD-10 D68.5· Severe hereditary thrombophilia due to congenital protein C deficiency

患病率
1-9 / 1 000 000
遗传方式
Autosomal dominant, Autosomal recessive
发病年龄
Neonatal