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Disease Ontology Browser
benign familial infantile seizures 3 (DOID:0081116)
Alliance: disease page
Synonyms: Benign Familial Infantile Seizures, 3; benign familial neonatal-infantile seizures
Alt IDs: OMIM:607745
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 mutations in the SCN2A gene on chromosome 2q24.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory