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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
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Juvenile myoclonic epilepsy
Myoclonic epilepsy, juvenile, 2
rare
Identifiers
MONDO:0800330
Part of
Juvenile myoclonic epilepsy
Also known as
EJM2
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