Oculocutaneous Albinism Type 1 C0268494
An inherited condition affecting skin, hair, and eye color due to lack of melanin pigment. People have very pale skin, white hair, and significant vision problems from birth. Lifelong sun protection and vision support are essential.
Key facts at a glance
- ICD-10
- Q84.9
- ICD-11
- LA00.0
- Body system
- dermatologic
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(dermatologic)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Medication Comparisons
Compare medications used to treat Oculocutaneous Albinism Type 1 C0268494. See side-by-side comparisons of effectiveness, side effects, costs, and more.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy