CIM11 LD44.N0
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11
CATCH 22 phenotype
- chapitre
- 20 Developmental anomalies
- bloc
- Chromosomal anomalies, excluding gene mutations
- definition
- Monosomy 22q11 (DiGeorge Velocardiofacial syndrome, DGS/VCF) syndrome is a chromosomal anomaly characterised by the association of several variable malformations: hypoplastic thymus and parathyroid glands, congenital conotruncal heart defects, a subtle but characteristic facial dysmorphism, cleft pa
- inclusions
- DiGeorge syndrome | Pharyngeal pouch syndrome | Velocardiofacial syndrome
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1868156761 ↗