CIM11 LD24.G2
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11
Apert syndrome
- chapitre
- 20 Developmental anomalies
- bloc
- Multiple developmental anomalies or syndromes
- definition
- Apert syndrome is a syndromic craniosynostosis associated with mutations in the FGFR2 gene and characterised by premature closure of coronal suture and a later onset of pansynostosis. Pathognomonic is an osseous and membranous syndactyly of at least Digitus II-IV (fingers and toes). High incidence o
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1962779847 ↗