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GENATLAS PHENOTYPE

last update : 20-09-2022

Symbol	NEDLIB
Location	4q32.1
Name	neurodevelopmental disorder with language impairment and behavioral abnormalities
Corresponding gene	GRIA2
Main clinical features	characterized by impaired intellectual development or developmental delay, behavioral abnormalities including autistic features, and language impairment other features include seizures and developmental regression
Genetic determination	autosomal dominant
Function/system disorder	mental retardation
	neurology
Type	disease

Remark(s)