Corneal dystrophy
ORPHA:34533· ICD-10 H18.5
Definition
A heterogeneous group of bilateral, genetically determined, non-inflammatory eye diseases that are usually restricted to the cornea. The designation is imprecise but remains in use because of its clinical value.
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant, Autosomal recessive, Mitochondrial inheritance, Not applicable, X-linked recessive
- Age of onset
- All ages