ICD-9-CM 377.16 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 377.16 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (optic atrophy, autosomal dominant) and leber hereditary optic atrophy (optic atrophy, hereditary, leber)