CIM11 LD27.1
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11
Xeroderma pigmentosum
- chapitre
- 20 Developmental anomalies
- bloc
- Multiple developmental anomalies or syndromes
- definition
- Xeroderma pigmentosum (XP) is a rare genodermatosis characterised by extreme sensitivity to ultraviolet (UV)-induced changes in the skin and eyes, and multiple skin cancers. It is subdivided into 8 complementation groups, according to the affected gene: XPA to XPG, and XP variant (XPV). The severity
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1243068849 ↗