CIM11 5C56.33
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Mucopolysaccharidosis type 6
- chapitre
- 05 Endocrine, nutritional or metabolic diseases
- bloc
- Inborn errors of metabolism
- definition
- Mucopolysaccharidosis type 6 (MPS VI) is a lysosomal storage disease with progressive multisystem involvement, associated with a deficiency of arylsulfatase B (ASB) leading to the accumulation of dermatan sulfate. The disorder shows a wide spectrum of symptoms from slowly to rapidly progressing form
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1288379621 ↗