Brugada syndrome 7

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Summary

Literature (0)

DOID:0110224 - Brugada syndrome 7

Disease Ontology Definition:A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN3B gene on chromosome 11q24.

Synonyms: BRGDA7

Echinobase 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

MIM:

MIM:613120 - brugada syndrome 7; brgda7 atrial fibrillation, familial, 16, included; atfb16, included

MIM:613120 - brugada syndrome 7; brgda7 atrial fibrillation, familial, 16, included; atfb16, included

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)