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MIM:613485 - LONG QT SYNDROME 13; LQT13
Xenbase Genes: kcnj5
Human Disease Resource: MIM
| MONDO:0013279 - diaphysis of fibula |
| MONDO:0019171 - familial long QT syndrome |
| MONDO:0100316 - long QT syndrome 1 |
| DOID:0110654 - long QT syndrome 13 |
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| MONDO:0013279 - diaphysis of fibula |
| MONDO:0019171 - familial long QT syndrome |
| MONDO:0100316 - long QT syndrome 1 |
| DOID:0110654 - long QT syndrome 13 |