H18.542
ICD-10-CMThis code signifies a genetic, progressive corneal disorder characterized by the accumulation of amyloid deposits within the corneal stroma of the left eye. These deposits form lattice-like patterns, leading to recurrent corneal erosions, pain, and progressive vision impairment.
Apply this code when documentation confirms a diagnosis of lattice corneal dystrophy affecting the patient's left eye. This diagnosis is typically made through slit-lamp examination revealing the characteristic lattice-like opacities and may be supported by genetic testing.
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