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Summary Literature (0)
MIM:611819 - LONG QT SYNDROME 10; LQT10

Xenbase Genes: scn4b

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012737 - long QT syndrome 10
MONDO:0018054 - familial atrial fibrillation
MONDO:0019171 - familial long QT syndrome
MONDO:0100316 - long QT syndrome 1

Disease Ontology (DO):
DOID:0110651 - long QT syndrome 10