Ocular albinism, unspecified

This code represents a congenital disorder characterized by hypopigmentation of the eyes, leading to visual impairment, nystagmus, and photophobia, without significant involvement of skin or hair pigmentation. It is a genetic condition affecting melanin production specifically in the ocular structures.

Assign this code when documentation indicates a diagnosis of ocular albinism without further specification of the type (e.g., Nettleship-Falls, Forsius-Eriksson). This code is appropriate when the provider has diagnosed ocular albinism but has not identified the specific genetic subtype.

• Do not use this code if the specific type of ocular albinism is documented; instead, use the more specific codes within E70.31.
• Distinguish from oculocutaneous albinism (E70.30) where both eyes and skin/hair are affected.
• Always review the physician's notes for any mention of the specific type of ocular albinism to ensure the highest level of specificity.