benign familial infantile epilepsy

Summary

DOID:0060169 - benign familial infantile epilepsy

Disease Ontology Definition:An infancy electroclinical syndrome 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.

Synonyms: benign familial infantile convulsion, benign familial infantile seizures, BFIC, BFIE

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: kcnq3, scn8a, chrna2, prrt2, kcnq2, scn2a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0017615 - benign familial infantile epilepsy

MONDO:0017615 - benign familial infantile epilepsy

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): infancy electroclinical syndrome (is_a)