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Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Familial partial epilepsy
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Familial focal epilepsy with variable foci
Epilepsy, familial focal, with variable foci 4
rare
Identifiers
MONDO:0054776
OMIM:617935
Causal genes
SCN3A
Part of
Familial focal epilepsy with variable foci
Also known as
FFEVF4
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