CIM11 LD90.3
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11
Prader-Willi syndrome
- chapitre
- 20 Developmental anomalies
- definition
- Prader-Willi syndrome is a rare genetic disorder characterised by hypothalamic-pituitary abnormalities with severe hypotonia during the neonatal period and first two years of life and the onset of hyperphagia with a risk of morbid obesity during infancy and adulthood, learning difficulties and behav
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#393773440 ↗