Rare hemorrhagic disease due to constitutional coagulation factors defects (Other than Hemophilia and Von Willebrand disease)
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Diseases covered
- Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
- Congenital factor V deficiency
- Congenital fibrinogen deficiency
- Congenital alpha2-antiplasmin deficiency
- Congenital factor XIII deficiency
- Congenital factor XI deficiency
- Congenital plasminogen activator inhibitor type 1 deficiency
- Congenital high-molecular-weight kininogen deficiency
- Congenital prekallikrein deficiency
- Combined deficiency of factor V and factor VIII
- Congenital vitamin K-dependent coagulation factors deficiency
- Congenital factor VII deficiency
- Congenital factor II deficiency
- Congenital factor X deficiency
- Hereditary combined deficiency of vitamin K-dependent clotting factors
- Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation
- East Texas bleeding disorder
- Thrombomodulin-related bleeding disorder
- Acquired prothrombin deficiency