Browse

Explore conditions, clinical trials, and the organisations running them.

Conditions By category Trials Sponsors

← All categories

Up to: Hereditary disease · Blood coagulation disease

Inherited blood coagulation disorder

Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation.

8 trials tagged with this condition →

Hemophilia A 178 trials Sub-types →
Hemophilia B 84 trials · 91 incl. sub-types Sub-types →
Hereditary von Willebrand disease 18 trials · 29 incl. sub-types Sub-types →
Inherited thrombophilia 0 trials · 28 incl. sub-types Sub-types →
Hereditary hemolytic uremic syndrome 0 trials · 19 incl. sub-types Sub-types →
Wiskott-Aldrich syndrome 10 trials
Glanzmann thrombasthenia 8 trials Sub-types →
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 Sub-types →
Hermansky-Pudlak syndrome 4 trials Sub-types →
Congenital vitamin K-dependent coagulation factors deficiency 0 trials · 4 incl. sub-types Sub-types →
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