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CIM11 4A00.14

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

Hereditary angioedema

chapitre
04 Diseases of the immune system
bloc
Primary immunodeficiencies
definition
Hereditary angioedema is caused in the majority of cases by genetically determined low absolute (type I) or functional (type II) levels of C1 inhibitor, a plasma proteinase inhibitor involved in regulation of complement activation. It is characterised clinically by recurrent subcutaneous and/or subm
type
category
navigateur oms (fr)
https://icd.who.int/browse/2026-01/mms/fr#795969334 ↗