Brugada syndrome 4

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Summary

Literature (0)

DOID:0110221 - Brugada syndrome 4

Disease Ontology Definition:A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the beta-2 subunit of the voltage-dependent L-type calcium channel (CACNB2) on chromosome 10p12.

Synonyms: BRGDA4

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

: cacnb2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012743 - Brugada syndrome 4

MONDO:0012743 - Brugada syndrome 4

MIM:

MIM:611876 - BRUGADA SYNDROME 4; BRGDA4

MIM:611876 - BRUGADA SYNDROME 4; BRGDA4

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

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

Parent(s): Brugada syndrome (is_a)