A hemostatic disorder characterized by a tendency to thrombosis that has X-linked recessive inheritance, and can be caused by a gain-of-function mutation in the gene encoding factor IX (F9).
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factor 5 excess with spontaneous thrombosis
MONDO:0007594
thrombophilia due to thrombin defect
MONDO:0008559
thrombophilia due to activated protein C resistance
MONDO:0008560
thrombophilia, familial, due to decreased release of tissue plasminogen activator
MONDO:0012872
heparin cofactor 2 deficiency
MONDO:0012876
hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
MONDO:0013143