← All indications

Albinism, Oculocutaneous

Heterogeneous group of autosomal recessive disorders comprising at least four recognized types, all having in common varying degrees of hypopigmentation of the skin, hair, and eyes. The two most common are the tyrosinase-positive and tyrosinase-negative types.

Subtype terms (1)

More specific conditions that are subtypes of Albinism, Oculocutaneous in the MeSH hierarchy.

Drugs by status

Organizations

ICD-10 crosswalk