H18.543
ICD-10-CMThis code signifies a bilateral inherited corneal disorder characterized by the deposition of amyloid protein in the corneal stroma, leading to a lattice-like pattern. This progressive dystrophy can cause recurrent corneal erosions, pain, and significant vision impairment in both eyes.
Apply this code when documentation confirms the diagnosis of lattice corneal dystrophy affecting both the right and left eyes. This diagnosis is typically made through slit-lamp examination revealing the characteristic refractile lines and opacities in the corneal stroma.
AI-generated reference. Verify against official guidelines.
+5 more in this category
Code History
Change History