GABRD-related neurodevelopmental disorder with epilepsy
MONDO:0700359A 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.
0 clinical trials for this condition and its sub-types, 0 tagged with GABRD-related neurodevelopmental disorder with epilepsy itself.
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