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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 Albinism, Yellow
  • Mutant Albinisms, Yellow

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