MeSH 搜索器

Gyrate Atrophy

Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
推出的年份: 1990
副标题
树号: C11.270.468, C11.941.160.578, C16.320.290.468
MeSH 单一 ID: D015799
进入的组:
  • Atrophy, Gyrate
  • Ornithinemia with Gyrate Atrophy
  • Hyperornithinemia with Gyrate Atrophy of Choroid and Retina
  • Gyrate Atrophy of Choroid and Retina
  • Gyrate Atrophy of the Choroid and Retina
  • Ornithine Aminotransferase Deficiency
  • Deficiency, Ornithine Aminotransferase
  • Ornithine-Delta-Aminotransferase Deficiency
  • Deficiency, Ornithine-Delta-Aminotransferase
  • Ornithine Delta Aminotransferase Deficiency
  • Ornithine Keto Acid Aminotransferase Deficiency
  • Ornithine Ketoacid Aminotransferase Deficiency
  • OAT Deficiency
  • Deficiency, OAT
  • OKT Deficiency
  • Deficiency, OKT
早前的内容:
  • Atrophy (1970-1989)
  • Choroid (1970-1989)
  • Retinal Degeneration (1970-1989)

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