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Inherited thrombophilia

MONDO:0100240

An instance of thrombophilia that is inherited.

Also known as: hereditary hypercoagulable disorder, hereditary thrombophilia, thrombophilia, hereditary

31 clinical trials for this condition and its sub-types.

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Sub-types

Thrombophilia due to thrombin defect (18) Thrombophilia due to activated protein C resistance (5) Hereditary antithrombin deficiency (3) Hereditary thrombophilia due to congenital protein C deficiency (1) Factor 5 excess with spontaneous thrombosis (0) Heparin cofactor 2 deficiency (0) Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency (0) Hereditary thrombophilia due to congenital protein S deficiency (0) Thrombomodulin-related bleeding disorder (0) Thrombophilia due to protein C deficiency, autosomal dominant (0) Thrombophilia due to protein C deficiency, autosomal recessive (0) Thrombophilia due to protein S deficiency, autosomal dominant (0) Thrombophilia due to protein S deficiency, autosomal recessive (0) Thrombophilia, familial, due to decreased release of tissue plasminogen activator (0) Thrombophilia, X-linked, due to factor 8 defect (0) Thrombophilia, X-linked, due to factor 9 defect (0)

Broader categories

Disease (680) Hereditary disease (176) Hematologic disorder (170) Blood coagulation disease (53) Human disease (14) Thrombophilia (12) Inherited blood coagulation disorder (8) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)

Trials to join now! 13 Not yet recruiting 3 Not yet finished but already full! 4 Completed 10 Terminated 1