CIM11 8A03.13
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-09
Ataxia due to abetalipoproteinemia
- chapitre
- 08 Diseases of the nervous system
- bloc
- Movement disorders
- definition
- Ataxia in the setting of abetalipoproteinemia, a rare autosomal recessive disorder caused by a mutation of the MTP gene coding for microsomal triglyceride transfer protein which impairs the ability to produce very low density lipoprotein. All patients have fat malabsorption, acanthocytosis, hypochol
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#203890331 ↗