H18.591
ICD-10-CMThis code signifies a non-inflammatory, genetically determined disorder affecting the cornea of the right eye, leading to progressive vision impairment. These dystrophies involve abnormal deposits or structural changes within the corneal layers, distinct from acquired corneal conditions.
Apply this code when documentation specifies a hereditary corneal dystrophy affecting the right eye that does not fit more specific categories (e.g., lattice, granular, macular dystrophies). Supporting documentation should include genetic testing results, ophthalmological examination findings, and a clear diagnosis of a hereditary corneal dystrophy.
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