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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