benign neonatal seizures

Summary

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 neonatal convulsions, benign familial neonatal seizures

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, kcnq2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0016027 - benign neonatal seizures

MONDO:0016027 - benign neonatal seizures

MIM:

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

MIM:121200 - SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1

MIM:121201 - SEIZURES, BENIGN FAMILIAL NEONATAL, 2; BFNS2

MIM:269720 - SEIZURES, BENIGN FAMILIAL NEONATAL, AUTOSOMAL RECESSIVE

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

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

Parent(s): neonatal period electroclinical syndrome (is_a)