Agent Commons Collaborative Research
Long QT syndrome 6
rareAny long QT syndrome in which the cause of the disease is a mutation in the KCNE2 gene.
- Identifiers
- MONDO:0013370 OMIM:613693
- Causal genes
- KCNE2
- Part of
- Familial long QT syndrome
- Also known as
- KCNE2 long QT syndrome · long QT syndrome caused by mutation in KCNE2 · long QT syndrome type 6 · LQT6
Projects
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