FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term benign familial infantile seizures 5 ID (Ontology) DOID:0081118 (Human Disease)
Definition A benign familial infantile epilepsy that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae and that has_material_basis_in mutation in the SCN8A gene on chromosome 12q13.
Also Known As "Benign Familial Infantile Seizures, 5"
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 benign familial infantile seizures 5       1
 for disease ribbon | benign familial infantile seizures 5       1
 model of | benign familial infantile seizures 5       1
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infancy electroclinical syndrome
 |__benign familial infantile epilepsy__
autosomal genetic disease               |
 |__autosomal dominant disease__________|
                                        benign familial infantile seizures 5  1 rec.
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Is a autosomal dominant disease
benign familial infantile epilepsy
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Synonyms
  • "Benign Familial Infantile Seizures, 5" EXACT
Secondary IDs
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MIM:617080