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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

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