CIM11 3B64.01
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Hereditary thrombocytopenia
- 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 a genetically inherited mutation leading to decreased platelet count. This disease is characterised by decreased levels of platelets within the blood. This disease may present with increased bruising or haemorrhaging. Confirmation is by identification of decreased platelet count
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#827950289 ↗