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MeSH 搜索器

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.
推出的年份: 1991
副标题
树号: 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 单一 ID: D016115
进入的组:
  • 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
早前的内容:
  • Albinism (1966-1990)

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