Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (2)
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

Xenbase Genes : kcnq3, kcnq2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0016027 - benign neonatal seizures

OMIM:
OMIM:121200 - SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1
OMIM:121201 - SEIZURES, BENIGN FAMILIAL NEONATAL, 2; BFNS2
OMIM:269720 - SEIZURES, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): neonatal period electroclinical syndrome (is_a)