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 (0)
DOID:0110222 - Brugada syndrome 5

Disease Ontology Definition:A Brugada syndrome that has material basis in heterozygous mutation in the SCN1B gene on chromosome 19q13.

Synonyms: BRGDA5

Xenbase Genes : scn1b

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013015 - Brugada syndrome 5

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

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