H18.521
ICD-10-CMThis code describes a genetic disorder affecting the outermost layer of the cornea (epithelium) in the right eye, typically presenting in childhood or adolescence. It involves abnormal deposits or structural changes within the corneal epithelium, leading to recurrent erosions, pain, and vision impairment. This specific dystrophy is often referred to as Meesmann corneal dystrophy or juvenile epithelial dystrophy.
Use this code when documentation specifies a diagnosis of epithelial (juvenile) corneal dystrophy affecting the right eye. This diagnosis is typically made by an ophthalmologist based on slit-lamp examination findings characteristic of the condition. Supporting documentation should detail the specific type of dystrophy and laterality.
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