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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, BFIE
Xenbase Genes
:
kcnq3,
scn8a,
chrna2,
prrt2,
kcnq2,
scn2a
| MONDO:0017615 - vomerine dentition |
| MIM:607745 - SEIZURES, BENIGN FAMILIAL INFANTILE, 3; BFIS3 |
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)