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CIM11 3B62.01

CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09

Inherited giant platelet disorder

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. This disease is characterised by abnormally large platelets, low platelet count and a bleeding tendency. Confirmation is by identification of mutations through genetic testing.
type
category
navigateur oms (fr)
https://icd.who.int/browse/2026-01/mms/fr#2069754587 ↗