Brugada syndrome 1

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 (1)

DOID:0110218 - Brugada syndrome 1

Disease Ontology Definition:A Brugada syndrome that has material basis in heterozygous mutation in the SCN5A gene on chromosome 3p22.

Synonyms: BRGDA1,

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

: scn5a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011001 - Brugada syndrome 1

MONDO:0011001 - Brugada syndrome 1

OMIM:

OMIM:601144 - BRUGADA SYNDROME 1; BRGDA1

OMIM:601144 - BRUGADA SYNDROME 1; BRGDA1

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)