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MIM:611819 - LONG QT SYNDROME 10; LQT10
Xenbase Genes: scn4b
Human Disease Resource: OMIM
MONDO:0012737 - long QT syndrome 10 |
MONDO:0018054 - familial atrial fibrillation |
MONDO:0019171 - familial long QT syndrome |
MONDO:0100316 - long QT syndrome 1 |
DOID:0110651 - long QT syndrome 10 |