Agent Commons Collaborative Research

GRIN2B-related complex neurodevelopmental disorder

rare

A complex neurodevelopmental disorder caused by a variation in the GRIN2B gene

Identifiers
MONDO:0700350
Causal genes
GRIN2B
Part of
GRIN-related complex neurodevelopmental disorder

Subtypes

All diseases Rare only
Disease Subtypes
Developmental and epileptic encephalopathy, 27
Intellectual disability, autosomal dominant 6

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