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GENATLAS PHENOTYPE
last update : 6/07/2006
Symbol CACD2
Location 6p21.1
Name choroidal dystrophy, central, areolar 2
Corresponding gene PRPH2
Main clinical features
  • zone of atrophy developing in the macula of the eye and involving the retinal pigment epithelium and the choriocapillaris
  • Genetic determination autosomal dominant
    Function/system disorder
    Type disease
    Gene product
    Name retinal degeneration, slow
    Remark(s)