Catalog
Hereditary thrombophilia
Link to WHO Definition
Hereditary thrombophilia – http://id.who.int/icd/entity/535489185
A disease caused by hereditary factors leading to abnormalities in blood. This disease is characterised by abnormality of blood coagulation that increases the risk of thrombosis, clots in blood vessels. This disease may present with deep vein thrombosis or pulmonary embolism. Confirmation is identification of abnormal blood coagulation in a blood sample.
Parents
Children
- Heparin co-factor II deficiency
- Hereditary thrombophilia due to activated protein C resistance
- Hereditary thrombophilia due to congenital protein S deficiency
- Hereditary thrombophilia due to other inherited factor V defects
- Hereditary thrombophilia due to other prothrombotic prothrombin gene mutations
- Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
- Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
- Hereditary thrombophilia due to prothrombin gene
- Hereditary thrombophilia due to thrombomodulin deficiency
- Hereditary thrombophilia due to congenital antithrombin deficiency
- 3B61.00 Hyperhomocysteinaemia
- Hereditary thrombophilia due to congenital protein C deficiency