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GENATLAS PHENOTYPE
last update : 12-05-2020
Symbol EVR8
Location 10q23.33
Name familial, exudative vitreoretinopathy 8
Corresponding gene KIF11
Main clinical features
  • retinal fold and chorioretinal atrophy uni or bilateral, associated with microcephaly
  • Genetic determination autosomal dominant
    Function/system disorder
    Type disease
    Remark(s)