Brugada syndrome 3

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Summary

Literature (0)

DOID:0110220 - Brugada syndrome 3

Disease Ontology Definition:A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the alpha-1C subunit of the L-type voltage-dependent calcium channel (CACNA1C) on chromosome 12p13.

Synonyms: BRGDA3

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

: cacna1c

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012742 - Brugada syndrome 3

MONDO:0012742 - Brugada syndrome 3

MIM:

MIM:611875 - BRUGADA SYNDROME 3; BRGDA3

MIM:611875 - BRUGADA SYNDROME 3; BRGDA3

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)