CIM11 LA12.3
CIM-11 MMS (diagnostics, nouvelle classification OMS) — fichier du 2026-09-11
Spherophakia
- chapitre
- 20 Developmental anomalies
- bloc
- Structural developmental anomalies of the eye, eyelid or lacrimal apparatus
- definition
- A disease of the eye, caused by homozygous mutations in the LTBP2 gene (isolated spherophakia), or by other genetic mutations. This disease is characterised by small, spherical lenses. This disease can also present with lenticular myopia, glaucoma, or sublation of the lens into the vitreous cavity.
- type
- category
- navigateur oms (fr)
- https://icd.who.int/browse/2026-01/mms/fr#1194029577 ↗