Mesh term Albinism, Oculocutaneous
Browse to parent terms:Albinism
Description
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.Browse to child terms:
Hermanski-Pudlak Syndrome
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