3B61.0Y Other specified hereditary thrombophilia

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

inclusions

• Hereditary thrombophilia due to activated protein C resistance
• Hereditary thrombophilia due to congenital antithrombin deficiency
• Hereditary thrombophilia due to congenital protein S deficiency
• Hereditary thrombophilia due to congenital protein C deficiency
• Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency

synonyms

• Other specified hereditary thrombophilia
• Hereditary thrombophilia due to activated protein C resistance
• Hereditary thrombophilia due to activated protein C resistance, factor V Leiden
• Hereditary thrombophilia due to other inherited factor V defects
• Hereditary thrombophilia due to factor V Hong Kong defects
• Hereditary thrombophilia due to factor V Cambridge defects
• Hereditary thrombophilia due to congenital antithrombin deficiency
• hereditary thrombophilia due to congenital antithrombin 3 deficiency
• hereditary thrombophilia due to congenital antithrombin III deficiency
• antithrombin deficiency NOS
• Hereditary thrombophilia due to congenital protein S deficiency
• Hereditary thrombophilia due to congenital protein C deficiency
• Hereditary thrombophilia due to thrombomodulin deficiency
• Hereditary thrombophilia due to prothrombin gene
• hereditary thrombophilia due to prothrombin G20210A mutation
• hereditary thrombophilia due to prothrombin gene mutation
• Hereditary thrombophilia due to other prothrombotic prothrombin gene mutations
• Prothrombin gene mutation
• Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
• Hereditary thrombophilia due to congenital HRG - [histidine-rich (poly-L) glycoprotein] deficiency
• Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency
• Heparin co-factor II deficiency

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