Inherited blood coagulation disorder

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Sub-types of Inherited blood coagulation disorder

• Hemophilia A 180 trials
  5 sub-types

  • Severe hemophilia A 50 trials
  • Moderately severe hemophilia A 4 trials
  • Mild hemophilia A 2 trials
  • Hemophilia A with vascular abnormality 0 trials
  • Symptomatic form of hemophilia A in female carriers 0 trials
• Hemophilia B 84 trials · 91 incl. sub-types
  4 sub-types

  • Severe hemophilia B 9 trials
  • Moderately severe hemophilia B 2 trials
  • Mild hemophilia B 1 trial
  • Symptomatic form of hemophilia B in female carriers 0 trials
• Hereditary von Willebrand disease 18 trials · 29 incl. sub-types
  5 sub-types

  • Von Willebrand disease 3 9 trials
  • Von Willebrand disease 2 4 trials · 5 incl. sub-types Sub-types →
  • Von Willebrand disease 1 3 trials
  • Von Willebrand disease, X-linked form 0 trials
  • Platelet-type von Willebrand disease 0 trials
• Inherited thrombophilia 0 trials · 28 incl. sub-types
  12 sub-types

  • Thrombophilia due to thrombin defect 19 trials
  • Thrombophilia due to activated protein C resistance 5 trials
  • Hereditary antithrombin deficiency 3 trials
  • Hereditary thrombophilia due to congenital protein C deficiency 1 trial Sub-types →
  • Factor 5 excess with spontaneous thrombosis 0 trials
  • Heparin cofactor 2 deficiency 0 trials
  • Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency 0 trials
  • Hereditary thrombophilia due to congenital protein S deficiency 0 trials Sub-types →
  • Thrombomodulin-related bleeding disorder 0 trials
  • Thrombophilia, X-linked, due to factor 8 defect 0 trials
  • Thrombophilia, X-linked, due to factor 9 defect 0 trials
  • Thrombophilia, familial, due to decreased release of tissue plasminogen activator 0 trials
• Hereditary hemolytic uremic syndrome 0 trials · 19 incl. sub-types
  2 sub-types

  • Atypical hemolytic-uremic syndrome 19 trials Sub-types →
  • Hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature 0 trials
• Wiskott-Aldrich syndrome 10 trials
• Glanzmann thrombasthenia 8 trials
  2 sub-types

  • Glanzmann thrombasthenia 1 7 trials
  • Glanzmann thrombasthenia 2 0 trials
• Platelet-type bleeding disorder 10 8 trials
• Congenital thrombotic thrombocytopenic purpura 5 trials
• Hereditary thrombocytopenia and hematologic cancer predisposition syndrome 1 trial · 5 incl. sub-types
  2 sub-types

  • Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 5 trials
  • Thrombocytopenia 5 0 trials
• Hermansky-Pudlak syndrome 4 trials
  9 sub-types

  • Hermansky-Pudlak syndrome with pulmonary fibrosis 0 trials · 1 incl. sub-types Sub-types →
  • Hermansky-Pudlak syndrome 10 0 trials
  • Hermansky-Pudlak syndrome 11 0 trials
  • Hermansky-Pudlak syndrome 2 0 trials
  • Hermansky-Pudlak syndrome 7 0 trials
  • Hermansky-Pudlak syndrome 8 0 trials
  • Hermansky-Pudlak syndrome 9 0 trials
  • Hermansky-Pudlak syndrome without pulmonary fibrosis 0 trials Sub-types →
  • Kotzot-Richter syndrome 0 trials
• Congenital vitamin K-dependent coagulation factors deficiency 0 trials · 4 incl. sub-types
  5 sub-types

  • Congenital factor VII deficiency 3 trials
  • Vitamin K-dependent clotting factors, combined deficiency of, type 1 1 trial
  • Congenital factor X deficiency 0 trials
  • Congenital prothrombin deficiency 0 trials
  • Vitamin K-dependent clotting factors, combined deficiency of, type 2 0 trials
• Congenital factor XII deficiency 1 trial
• Congenital plasminogen activator inhibitor type 1 deficiency 1 trial
• Hypoplasminogenemia 1 trial
• Ehlers-Danlos syndrome, fibronectinemic type 0 trials
• Scott syndrome 0 trials
• Tatsumi factor deficiency 0 trials
• Alpha-2-plasmin inhibitor deficiency 0 trials
• Congenital factor V deficiency 0 trials
• Congenital factor XI deficiency 0 trials
• Congenital high-molecular-weight kininogen deficiency 0 trials
• Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder 0 trials
• Dysplasminogenemia 0 trials
• Factor 5 and Factor VIII, combined deficiency of, 2 0 trials
• Factor V and factor VIII, combined deficiency of, type 1 0 trials
• Factor VII and Factor VIII, combined deficiency of 0 trials
• Factor XIII, A subunit, deficiency of 0 trials
• Factor XIII, b subunit, deficiency of 0 trials
• Familial thrombomodulin anomalies 0 trials
• Hereditary thrombocytosis with transverse limb defect 0 trials
• Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency 0 trials
• Inherited prekallikrein deficiency 0 trials
• Plasminogen deficiency, type II 0 trials
• Platelet-type bleeding disorder 12 0 trials
• Platelet-type bleeding disorder 14 0 trials
• Platelet-type bleeding disorder 16 0 trials
• Platelet-type bleeding disorder 18 0 trials
• Platelet-type bleeding disorder 8 0 trials