Vitreoretinal dystrophy

This code describes a group of inherited disorders characterized by progressive degeneration of both the vitreous and the retina. These conditions often lead to visual impairment due to structural and functional abnormalities in these ocular tissues.

Use this code when documentation specifies a diagnosis of vitreoretinal dystrophy, such as Wagner's syndrome, Stickler syndrome, or other similar genetic conditions affecting both the vitreous and retina. Supporting documentation should clearly indicate the diagnosis and often includes genetic testing results or ophthalmological examination findings.

• Ensure the documentation explicitly states "vitreoretinal dystrophy" or a specific syndrome classified under this umbrella.
• Do not confuse with isolated retinal dystrophies (H35.50) or vitreous disorders without retinal involvement.
• Consider sequencing this code as a primary diagnosis when it is the reason for the encounter, or as a secondary diagnosis if it is a co-morbidity affecting treatment.