Any self-limited epilepsy with centrotemporal spikes in which the cause of the disease is a variation in GRIN2A gene.
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Landau-Kleffner syndrome
MONDO:0009509
early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
MONDO:0017325
GRIN2A-related developmental and/or epileptic encephalopathy with spike-wave activation in sleep
MONDO:1060140
GRIN2A-related rolandic epilepsy-speech dyspraxia syndrome
MONDO:1060141