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ENCongenital Alpha2-Antiplasmin Deficiency
Alias:
Congenital Alpha2 Antiplasmin Deficiency
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Congenital Alpha2-Antiplasmin Deficiency, is also known as congenital alpha2 antiplasmin deficiency. An important gene associated with Congenital Alpha2-Antiplasmin Deficiency is SERPINF2 (Serpin Family F Member 2). Affiliated tissues include bone, and related phenotypes are persistent bleeding after trauma and joint hemorrhage
Related ID：
ICD11：688627594
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MALACARDS
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