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Diseases / Nervous system disorder/ Neurodevelopmental disorder/ Complex neurodevelopmental disorder/ GRIN-related complex neurodevelopmental disorder/ GRIN2A-related complex neurodevelopmental disorder

GRIN2A-related rolandic epilepsy-speech dyspraxia syndrome

rare

Any rolandic epilepsy-speech dyspraxia syndrome in which the cause of the disease is a variation in GRIN2A gene.

Identifiers: MONDO:1060141
Part of: GRIN2A-related complex neurodevelopmental disorder Rolandic epilepsy-speech dyspraxia syndrome

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