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CIM11 LD55

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

Fragile X chromosome

chapitre
20 Developmental anomalies
bloc
Sex chromosome anomalies
definition
Fragile X syndrome is a rare genetic disease associated with mild to severe intellectual deficit that may be associated with behavioural disorders and characteristic physical features.
inclusions
Fragile X syndrome
type
category
navigateur oms (fr)
https://icd.who.int/browse/2026-01/mms/fr#1524287677 ↗