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 (0)

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

MIM:

MIM:601144 - BRUGADA SYNDROME 1; BRGDA1

MIM:601144 - BRUGADA SYNDROME 1; BRGDA1

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

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

Parent(s): autosomal dominant disease (is_a), Brugada syndrome (is_a)