CIM11 LD45.1
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11
Uniparental disomies of paternal origin
- chapitre
- 20 Developmental anomalies
- bloc
- Chromosomal anomalies, excluding gene mutations
- definition
- Any disease caused by the inheritance of two homologous copies of a chromosome from the father, and none from the mother. Confirmation is by observation of identical chromosome pairs, and matching to a paternal chromosome, by genetic testing.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#2028476598 ↗