MeSH 搜索器

Cone-Rod Dystrophies

Genetically heterogeneous and sometimes syndromic (e.g., BARDET BIEDL SYNDROME; and SPINOCEREBELLAR ATAXIA TYPE 7) retinopathies with initial RETINAL CONE involvement. They are characterized by decreased VISUAL ACUITY; COLOR VISION DEFECTS; progressive loss of peripheral vision and night blindness.
推出的年份: 2017
副标题
树号: C11.270.152, C11.768.585.658.250, C16.320.290.152
MeSH 单一 ID: D000071700
进入的组:
  • Cone Rod Dystrophies
  • Retinal Cone-Rod Dystrophy
  • Cone-Rod Dystrophies, Retinal
  • Cone-Rod Dystrophy, Retinal
  • Retinal Cone Rod Dystrophy
  • Retinal Cone-Rod Dystrophies
  • Cone-Rod Retinal Dystrophy
  • Cone Rod Retinal Dystrophy
  • Cone-Rod Retinal Dystrophies
  • Retinal Dystrophies, Cone-Rod
  • Retinal Dystrophy, Cone-Rod
  • Cone-Rod Dystrophy
  • Cone Rod Dystrophy
  • Cone-Rod Degenerations
  • Cone Rod Degenerations
  • Cone-Rod Degeneration
  • Cone-Rod Dystrophy 2
  • Cone Rod Dystrophy 2
  • Rod-Cone Dystrophy
  • Rod-Cone Dystrophies
  • Rod Cone Dystrophies
  • Rod Cone Dystrophy
早前的内容:
  • Retinal Degeneration (1975-2016)
  • Retinitis Pigmentosa (1981-2016)

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