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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features
Epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features
rare
Identifiers
MONDO:0859564
OMIM:301091
Causal genes
GABRA3
Part of
Epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features
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