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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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Epilepsy, familial adult myoclonic
Epilepsy, familial adult myoclonic, 1
rare
Identifiers
MONDO:0010985
OMIM:601068
Causal genes
SAMD12
Part of
Epilepsy, familial adult myoclonic
Also known as
FAME1
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