Leber congenital amaurosis (Q1811132)

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retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness
  • AMAUROSIS CONGENITA OF LEBER I
  • LCA
  • Leber congenital amaurosis type 13
  • Leber congenital amaurosis type 14
  • Leber's amaurosis (disorder)
  • Leber's congenital amaurosis
  • Leber's disease
  • Leber's amaurosis
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English
Leber congenital amaurosis
retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness
  • AMAUROSIS CONGENITA OF LEBER I
  • LCA
  • Leber congenital amaurosis type 13
  • Leber congenital amaurosis type 14
  • Leber's amaurosis (disorder)
  • Leber's congenital amaurosis
  • Leber's disease
  • Leber's amaurosis

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