GRIN2A-related complex neurodevelopmental disorder
MONDO:1060139A group of neurological and neurodevelopmental disorders caused by variants in the GRIN2A gene, characterized by a broad spectrum of symptoms including developmental delay or intellectual disability, epilepsy, speech and language impairments, movement disorders, and neuropsychiatric features.
1 clinical trial for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-types
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
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GRIN2A-related developmental and/or epileptic encephalopathy with spike-wave activation in sleep
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GRIN2A-related rolandic epilepsy-speech dyspraxia syndrome
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GRIN2A-related self-limited epilepsy with centrotemporal spikes
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Landau-Kleffner syndrome
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Broader categories
Disease
(717)
Nervous system disorder
(243)
Hereditary disease
(188)
Neurodevelopmental disorder
(154)
Human disease
(15)
Hereditary neurological disease
(6)
Complex neurodevelopmental disorder
(3)
Disease of genetic or genomic mechanism
(2)
GRIN-related complex neurodevelopmental disorder
(2)
Disease by body system or component
(0)