3B61.0 Hereditary thrombophilia
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
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.
sections/codes in this section (3B61.0-3B61.0)
- Hyperhomocysteinaemia (3B61.00)
- Other specified hereditary thrombophilia (3B61.0Y)
- Hereditary thrombophilia, unspecified (3B61.0Z)
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