CIM11 5C64.00
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Wilson disease
- chapitre
- 05 Endocrine, nutritional or metabolic diseases
- bloc
- Disorders of metabolite absorption or transport
- definition
- Wilson disease is an autosomal recessive disorder of copper metabolism characterised by the toxic accumulation of copper, mainly in the liver and central nervous system that may present as hepatic, neurologic or psychiatric forms.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#468161208 ↗