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Diseases groups

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