CIM11 3B61.0
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Hereditary thrombophilia
- chapitre
- 03 Diseases of the blood or blood-forming organs
- bloc
- Coagulation defects, purpura or other haemorrhagic or related conditions
- definition
- 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 identif
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#535489185 ↗