Orphanet: Autosomal dominant vitreoretinochoroidopathy
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Autosomal dominant vitreoretinochoroidopathy

Disease definition

A rare, genetic, vitreous-retinal disease characterized by ocular developmental anomalies such as microcornea, a shallow anterior chamber, glaucoma and cataract. Abnormal chorioretinal pigmentation is present, usually lying between the vortex veins and the ora serrata for 360 degrees.

ORPHA:3086

Classification level: Disorder
  • Synonym(s):
    • ADVIRC
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: All ages
  • ICD-10: H35.5
  • OMIM: 193220
  • UMLS: C3888099
  • MeSH: C536352
  • GARD: 5507
  • MedDRA: -

Detailed information

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