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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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Hereditary generalized epilepsy
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Idiopathic generalized epilepsy
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Variable-age onset idiopathic generalized epilepsy syndrome
Epilepsy, idiopathic generalized 20
rare
Identifiers
MONDO:0980988
OMIM:621500
Causal genes
ZFHX3
Part of
Variable-age onset idiopathic generalized epilepsy syndrome
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