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GENATLAS PHENOTYPE
last update : 26-10-2018
Symbol ARCC7
Location 9q22.33
Name congenital cataract, autosomal recessive 7
Other name(s)
  • cataract multiple type 36
  • Corresponding gene TDRD7
    Other symbol(s) CTRCT36
    Main clinical features
  • autosomal recessive congenital cataract
  • cataracts present at birth or developed in infancy
  • bilateral membranous cataracts accompanied by other ocular abnormalities, including corneal opacity, microcornea, and nystagmus
    Genetic determination autosomal recessive
    Function/system disorder eye
    Type disease
    Remark(s)