A complex neurodevelopmental disorder caused by a variation in the GRIN2B gene
Comprehensive, easy-to-understand information about this condition
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intellectual disability, autosomal dominant 6
MONDO:0013509
developmental and epileptic encephalopathy, 27
MONDO:0014505
developmental and epileptic encephalopathy, 46
MONDO:0014947
GRIN1-related complex neurodevelopmental disorder
MONDO:1060123
GRIN2A-related complex neurodevelopmental disorder
MONDO:1060139