3B61 Thrombophilia

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

A disease caused by determinants arising after birth or genetically inherited 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.

sections/codes in this section (3B61-3B61)

• Hereditary thrombophilia  (3B61.0)
• Acquired thrombophilia  (3B61.1)
• Other specified thrombophilia  (3B61.Y)
• Thrombophilia, unspecified  (3B61.Z)

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