H18.523
ICD-10-CMThis code signifies a genetic disorder affecting the epithelial layer of the cornea, specifically a juvenile form that presents bilaterally. It involves abnormal development or function of the corneal epithelium, leading to visual impairment and discomfort.
Use this code when documentation specifies epithelial corneal dystrophy, explicitly noting its juvenile onset and bilateral involvement. This diagnosis is typically made by an ophthalmologist based on slit-lamp examination findings characteristic of epithelial dystrophies.
AI-generated reference. Verify against official guidelines.
+5 more in this category
Code History
Change History