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Summary Literature (0)
DOID:0110222 - Brugada syndrome 5


Disease Ontology Definition:A Brugada syndrome that has material basis in heterozygous mutation in the SCN1B gene on chromosome 19q13.

Synonyms: BRGDA5

Xenbase Genes : scn1b

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013015 - Brugada syndrome 5


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)