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Summary Literature (0)
MIM:613120 - BRUGADA SYNDROME 7; BRGDA7

Xenbase Genes: scn3b

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013146 - Brugada syndrome 7
MONDO:0015263 - Brugada syndrome
MONDO:0018054 - familial atrial fibrillation

Disease Ontology (DO):
DOID:0110224 - Brugada syndrome 7