CIM11 4A01.00
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Hereditary agammaglobulinaemia with profoundly reduced or absent B cells
- chapitre
- 04 Diseases of the immune system
- bloc
- Primary immunodeficiencies
- definition
- This refers to a hereditary type of primary immune deficiency disease characterised by a reduction in all types of gamma globulins, and rare X-linked genetic disorder that affects the body's ability to fight infection.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#393046642 ↗