CIM11 LD2D.10
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11
Neurofibromatosis type 1
- chapitre
- 20 Developmental anomalies
- bloc
- Multiple developmental anomalies or syndromes
- definition
- Neurofibromatosis type 1 (NF1) is an inherited, multi-system, neurocutaneous disorder that predisposes to the development of benign and malignant tumours. Two of the following criteria are required to diagnose NF1: six or more café au lait patches, neurofibromas, i.e. peripheral nerve sheath tumours
- inclusions
- von Recklinghausen disease
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#337970533 ↗