ICD-10 Code E70.32 – Oculocutaneous albinism (2026): Diagnosis, Symptoms & Billing Guide
2026 ICD-10-CM Diagnosis Code E70.32 – Oculocutaneous albinism
What it is
Oculocutaneous albinism is an inherited disorder of melanin production affecting the skin, hair, and eyes. It causes reduced pigment from birth and is coded when the diagnosis is documented.
Clinical signs
Typical findings include very light skin and hair, reduced iris pigment, and visual problems such as nystagmus or reduced acuity. Clinical features vary; refer to documentation.
When to use this code
Use E70.32 when the provider documents oculocutaneous albinism, including confirmed subtype descriptions that still map to this diagnosis. Apply it for visits focused on congenital hypopigmentation with eye involvement when the record supports this condition.
Do not code it for temporary pigment loss, acquired depigmentation, or unspecified “albinism” without further detail if another code is documented. Check documentation when the record is unclear.
Do not use for
Do not use this code for vitiligo, piebaldism, or other acquired or localized pigment disorders. It is also wrong for isolated ocular albinism unless the record specifically supports oculocutaneous involvement.
Coding tip
Confirm that the documentation names oculocutaneous albinism, not just “albinism” or a pigment change, before assigning E70.32.