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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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Benign familial infantile epilepsy
Seizures, benign familial infantile, 2
rare
Identifiers
MONDO:0011593
OMIM:605751
Part of
PRRT2-associated paroxysmal movement disorder
Benign familial infantile epilepsy
Also known as
BFIS2 · seizures, benign familial infantile, type 2
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