Summary Literature (0)

DOID:14264 - benign neonatal seizures

Disease Ontology Definition:A neonatal period electroclinical syndrome that is characterized by tonic-clonic seizures in newborns occurring within the first seven days of life and ceasing within the first 15 weeks of life and has_material_basis_in autosomal dominant inheritance of voltage-gated potassium channels or a chromosomal inversion.

Synonyms: benign familial neonatal seizures, benign neonatal convulsions,

Echinobase Genes :


OMIM:

MIM:121200 - seizures, benign familial neonatal, 1; bfns1 epilepsy, benign neonatal, 1, and/or myokymia, included;; seizures, benign familial neonatal, 1, and/or myokymia, included

MIM:121201 - seizures, benign familial neonatal, 2; bfns2

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

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