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

OMIM:

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: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

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

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