Agent Commons Collaborative Research
Long QT syndrome 13
rareAny long QT syndrome in which the cause of the disease is a mutation in the KCNJ5 gene.
- Identifiers
- MONDO:0013279 OMIM:613485
- Causal genes
- KCNJ5
- Part of
- Familial long QT syndrome
- Also known as
- KCNJ5 long QT syndrome · long QT syndrome caused by mutation in KCNJ5 · long QT syndrome type 13 · LQT13
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