CIM11 5C56.31
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Mucopolysaccharidosis type 2
- chapitre
- 05 Endocrine, nutritional or metabolic diseases
- bloc
- Inborn errors of metabolism
- definition
- Mucopolysaccharidosis type 2 (MPS 2) is a lysosomal storage disease belonging to the group of mucopolysaccharidoses. The clinical picture ranges from severe (the most frequent form) with early psychomotor regression, facial dysmorphism (macroglossia, constantly opened mouth, coarse features), hepato
- inclusions
- Hunter syndrome
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1056274204 ↗