LA11.5ICD-11 MMS 2026-01
Congenital corneal opacity
Description
A condition caused by failure of the cornea to correctly develop during the antenatal period. This condition is characterised by opacity of the cornea.
Index terms
- Congenital corneal opacity
- Congenital corneal opacity, unilateral
- Congenital corneal opacity, bilateral
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- Posterior polymorphous corneal dystrophy
- PPCD - [Posterior polymorphous corneal dystrophy] C1 or C2
- Congenital hereditary endothelial dystrophy type 1
- CHED - [Congenital hereditary endothelial dystrophy] C1
- Congenital leucoma
Exclusions from above levels
- http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism
Sibling codes
LA11.0– Blue scleraLA11.1– Structural developmental anomalies of corneaLA11.2– Anterior segment dysgenesisLA11.3– AniridiaLA11.4– Coloboma of irisLA11.6– Structural disorders of the pupilLA11.Y– Other specified structural developmental anomalies of the anterior segment of eyeLA11.Z– Structural developmental anomalies of the anterior segment of eye, unspecified
Foundation entity
Congenital corneal opacity – http://id.who.int/icd/entity/675096862
Allowed postcoordination axes
Part of: LA11: Structural developmental anomalies of the anterior segment of eye › 20: Developmental anomalies