CIM11 3B62.0
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Inherited qualitative platelet defects
- 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 genetically inherited mutations leading to abnormalities in platelets. This disease is characterised by abnormal platelet formation or function. Confirmation is by identification of mutations by genetic testing.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1410128892 ↗