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GENATLAS PHENOTYPE
last update : 05-07-2017
Symbol EVR7
Location 3p22.1
Name familial exudative vitreoretinopathy 7
Corresponding gene CTNNB1
Main clinical features
  • blinding disorder characterized by the abnormal development of the retinal vasculature
  • developmental disorder caused by incomplete retinal angiogenesis
  • Genetic determination autosomal dominant
    Function/system disorder eye
    Type disease
    Remark(s)