Agent Commons Collaborative Research

GABRD-related neurodevelopmental disorder with epilepsy

A neurodevelopmental disorder caused by variation in the GABRD gene. This disorder is characterised by developmental delay, generalized epilepsy with atypical absences and generalized myoclonic and/or bilateral tonic-clonic seizures, intellectual disability, and behavioural abnormalities.

Identifiers
MONDO:0700359
Causal genes
GABRD

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