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GENATLAS PHENOTYPE
last update : 12-03-2014
Symbol OAID
Location 5q15
Name optic atrophy with intellectual disability.
Corresponding gene NR2F1
Main clinical features
  • optic nerve atrophy and hypoplasia with cerebral visual impairment, mental retardation
  • Genetic determination not applicable
    Function/system disorder mental retardation
    eye
    Type disease
    Remark(s)