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MIM:613688 - LONG QT SYNDROME 2; LQT2
Xenbase Genes: kcnh2, alg10
Human Disease Resource: MIM
| MONDO:0013367 - long QT syndrome 2 |
| MONDO:0019171 - familial long QT syndrome |
| MONDO:0100316 - long QT syndrome 1 |
| DOID:0110645 - long QT syndrome 2 |
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| MONDO:0013367 - long QT syndrome 2 |
| MONDO:0019171 - familial long QT syndrome |
| MONDO:0100316 - long QT syndrome 1 |
| DOID:0110645 - long QT syndrome 2 |