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.

Descriptor ID	D016115
MeSH Number(s)	C11.270.040.545 C16.320.290.040.100 C16.320.565.100.102.100 C16.320.850.080.100 C17.800.621.440.102.100 C17.800.827.080.100 C18.452.648.100.102.100
Concept/Terms	Albinism, Oculocutaneous Albinism, Oculocutaneous Oculocutaneous Albinism Albinism, Tyrosinase-Negative Albinism, Tyrosinase-Negative Albinism, Tyrosinase Negative Tyrosinase-Negative Albinism Albinism, Tyrosinase-Positive Albinism, Tyrosinase-Positive Albinism, Tyrosinase Positive Tyrosinase-Positive Albinism Albinism, Yellow-Mutant Albinism, Yellow-Mutant Albinism, Yellow Mutant Yellow-Mutant Albinism Yellow Mutant Albinism Mutant Albinism, Yellow Mutant Albinisms, Yellow

Below are MeSH descriptors whose meaning is more general than "Albinism, Oculocutaneous".

Below are MeSH descriptors whose meaning is related to "Albinism, Oculocutaneous".

Below are MeSH descriptors whose meaning is more specific than "Albinism, Oculocutaneous".