Orphanet: Autosomal dominant rhegmatogenous retinal detachment
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Autosomal dominant rhegmatogenous retinal detachment

Disease definition

A rare, hereditary, non-syndromic form of vitreoretinopathy characterized by retinal tears due to abnormal vitreous, and commonly present refractive errors. No other signs or symptoms of Stickler syndrome is present.

ORPHA:209867

Classification level: Disorder
  • Synonym(s): -
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Adult
  • ICD-10: H33.0
  • OMIM: 609508
  • UMLS: C1836081
  • MeSH: -
  • GARD: -
  • MedDRA: -
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