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Congenital plasminogen activator inhibitor type 1 deficiency
rareCongenital plasminogen activator inhibitor type 1 (PAI-1) deficiency is a rare genetic bleeding disorder characterized by premature lysis of hemostatic clots and a moderate bleeding tendency.
- Identifiers
- MONDO:0013227 OMIM:613329Orphanet:465
- Causal genes
- SERPINE1
- Part of
- Coagulation protein diseaseCongenital hematological disorderHemorrhagic diseaseInherited blood coagulation disorder
- Also known as
- congenital PAI-1 deficiency · plasminogen activator inhibitor type 1 deficiency
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