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Up to: Blood coagulation disease

Coagulation protein disease

Congenital or acquired deficiency of one of the coagulation factors. It results in bleeding.

13 trials tagged with this condition →

Hemophilia 55 trials · 216 incl. sub-types Sub-types →
Von Willebrand disease (hereditary or acquired) 39 trials · 46 incl. sub-types Sub-types →
Acquired coagulation factor deficiency 4 trials · 16 incl. sub-types Sub-types →
Factor VII deficiency 6 trials Sub-types →
Congenital fibrinogen deficiency 2 trials · 6 incl. sub-types Sub-types →
Thrombophilia due to activated protein C resistance 5 trials
Congenital vitamin K-dependent coagulation factors deficiency 0 trials · 4 incl. sub-types Sub-types →
Factor X deficiency 2 trials Sub-types →
Congenital factor XII deficiency 1 trial
Congenital plasminogen activator inhibitor type 1 deficiency 1 trial
Hypoplasminogenemia 1 trial
East Texas bleeding disorder 0 trials
Tatsumi factor deficiency 0 trials
Alpha-2-plasmin inhibitor deficiency 0 trials
Combined deficiency of factor V and factor VIII 0 trials Sub-types →
Combined deficiency of factor VII and factor X 0 trials
Congenital high-molecular-weight kininogen deficiency 0 trials
Dysplasminogenemia 0 trials
Factor V amsterdam bleeding disorder 0 trials
Factor V atlanta bleeding disorder 0 trials
Factor V deficiency 0 trials Sub-types →
Factor V short isoforms-related bleeding disorder 0 trials
Factor XIII deficiency 0 trials Sub-types →
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation 0 trials
Inherited prekallikrein deficiency 0 trials
Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome 0 trials
Plasminogen deficiency, type II 0 trials
Thrombomodulin-related bleeding disorder 0 trials