CIM11 5C56.30
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Mucopolysaccharidosis type 1
- chapitre
- 05 Endocrine, nutritional or metabolic diseases
- bloc
- Inborn errors of metabolism
- definition
- Mucopolysaccharidosis type 1 (MPS 1) is a rare lysosomal storage disease belonging to the group of mucopolysaccharidoses. There are three variants, differing widely in their severity, with Hurler syndrome (57% of cases) being the most severe, Scheie syndrome (20% of cases) the mildest and Hurler-Sch
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1539226250 ↗