H18.592
ICD-10-CMThis code signifies a non-inflammatory, genetically determined disorder affecting the left cornea, leading to progressive vision impairment. These dystrophies are characterized by abnormal deposits or structural changes within the corneal layers, distinct from acquired corneal opacities or degenerations.
Apply this code when documentation specifies a hereditary corneal dystrophy affecting the left eye, and a more specific ICD-10-CM code (e.g., for Fuchs' endothelial dystrophy, lattice dystrophy) is not available. Supporting documentation should include genetic testing results, slit-lamp examination findings, or a clear ophthalmic diagnosis of a hereditary corneal dystrophy.
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