ICD-11 classes
03 Diseases of the blood or blood-forming organs
Coagulation defects, purpura or other haemorrhagic or...
3B61 — Thrombophilia
3B61.0 — Hereditary thrombophilia
ICD-11 3B61.0 — Hereditary thrombophilia
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.
It includes 1 item.
- antithrombin deficiency
The diagnosis excludes nothing.
Diagnosis with code 3B61.0 contains 2 clarifying diagnoses:
- 3B61.00 — Hyperhomocysteinaemia
- 3B61.0Y — Other specified hereditary thrombophilia