Orphanet: Oguchi disease

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Oguchi disease

Disease definition

Oguchi disease is an autosomal recessive retinal disorder characterized by congenital stationary night blindness (see this term) and the Mizuo-Nakamura phenomenon.


Classification level: Disorder
  • Synonym(s):
    • Congenital stationary night blindness, Oguchi type
    • Oguchi syndrome
  • Prevalence: Unknown
  • Inheritance: Autosomal recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: H53.6
  • OMIM: 258100  613411
  • UMLS: C1306122
  • MeSH: C537743
  • GARD: 10118
  • MedDRA: -

Detailed information


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