Other ocular albinism

This code signifies a rare, inherited genetic condition primarily affecting the eyes, resulting in reduced pigmentation of the iris, retina, and choroid. It leads to various visual impairments, including nystagmus, strabismus, photophobia, and reduced visual acuity, without significant involvement of the skin or hair. This specific code is used when the ocular albinism does not fit the criteria for X-linked ocular albinism (Nettleship-Falls type).

Use this code for patients diagnosed with a form of ocular albinism that is not X-linked, such as autosomal recessive ocular albinism, or other unspecified types. Documentation should clearly state the diagnosis of ocular albinism and specify that it is not the X-linked variant, often supported by genetic testing results or clinical presentation.

• Differentiate carefully from X-linked ocular albinism (E70.310) based on genetic testing or family history.
• Always code associated visual disturbances (e.g., nystagmus, strabismus, low vision) separately as secondary diagnoses.
• Ensure the medical record explicitly states "other ocular albinism" or provides sufficient detail to rule out the X-linked type.