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
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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