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.
Year introduced: 1991
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Subheadings:
Tree 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
MeSH Unique ID: D016115
Entry Terms:
- Oculocutaneous Albinism
- Albinism, Tyrosinase-Negative
- Albinism, Tyrosinase Negative
- Tyrosinase-Negative Albinism
- Albinism, Tyrosinase-Positive
- Albinism, Tyrosinase Positive
- Tyrosinase-Positive Albinism
- Albinism, Yellow-Mutant
- Albinism, Yellow Mutant
- Yellow-Mutant Albinism
- Yellow Mutant Albinism
- Mutant Albinisms, Yellow
- Mutant Albinism, Yellow
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