Home Page
References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 26-10-2018
Symbol CCA3
Location 2q33.3
Name cataract, congenital, cerulean type 3
Other name(s)
  • cataract, congenital, "blue dot", type 3
  • cataract 4, multiple types
  • Corresponding gene CRYGD
    Other symbol(s) . CTRCT4
    Main clinical features moroccan family with early onset and fasting progression
    Genetic determination autosomal dominant
    Function/system disorder eye
    Type disease
    Gene product
    Name gamma D crystallin
    Remark(s)