CIM11 5C51.3
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Glycogen storage disease
- chapitre
- 05 Endocrine, nutritional or metabolic diseases
- bloc
- Inborn errors of metabolism
- definition
- The term Glycogen storage disease characterises a group of heterogeneous diseases resulting from defects in the process of glycogen synthesis or breakdown within muscles, liver, and other cell types.
- inclusions
- Glycogen storage disease due to LAMP-2 deficiency | Glycogen storage disease due to glycogen debranching enzyme deficiency | Glycogen storage disease due to muscle glycogen phosphorylase deficiency | Glycogen storage disease due to liver glycogen phosphorylase deficiency | Glycogen storage disease due to GLUT2 deficiency | Glycogen storage disease due to aldolase A deficiency | Glycogen storage disease due to muscle beta-enolase deficiency | Glycogen storage disease due to phosphoglucomutase deficiency | Glycogen storage disease due to glycogenin deficiency | Glycogen storage disease due to phosphoglycerate kinase 1 deficiency | Glycogen storage disease due to lactate dehydrogenase deficiency | Glycogen storage disease due to muscle pyruvate kinase deficiency | Dilated cardiomyopathy due to glycogen branching enzyme deficiency
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1187107383 ↗