CIM11 LD50.2
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11
Mosaicism, lines with various numbers of X chromosomes
- chapitre
- 20 Developmental anomalies
- bloc
- Sex chromosome anomalies
- definition
- A disease caused by embryonic fusion or gain or loss of X chromosomes early in embryonic development, resulting in a subset of cells in the body having an abnormal number of X chromosomes. This disease may present with abnormal height, genitourinary abnormalities, or may be asymptomatic.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#145150850 ↗