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Disease Ontology Browser
benign familial infantile seizures 6 (DOID:0081119)
Alliance: disease page
Synonyms: Autosomal dominant nocturnal frontal lobe epilepsy; Benign Familial Infantile Seizures, 6; nocturnal frontal lobe epilepsy-4
Alt IDs: OMIM:610353
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 CHRNA2 gene on chromosome 8p21.


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
01/31/2023
MGI 6.22
The Jackson Laboratory