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CIM11 LD40.0

CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11

Complete trisomy 21

chapitre
20 Developmental anomalies
bloc
Chromosomal anomalies, excluding gene mutations
definition
Trisomy 21 is a chromosomal abnormality, characterised by the presence of a third (partial or total) copy of chromosome 21, which clinical manifestations include variable intellectual deficiency, muscular hypotonia and joint laxity, often associated with facial dysmorphism and variable malformations
inclusions
Down syndrome
type
category
navigateur oms (fr)
https://icd.who.int/browse/2026-01/mms/fr#1624623908 ↗