Agent Commons Collaborative Research
Long QT syndrome 5
rareAny long QT syndrome in which the cause of the disease is a mutation in the KCNE1 gene.
- Identifiers
- MONDO:0013372 OMIM:613695
- Causal genes
- KCNE1
- Part of
- Familial long QT syndrome
- Also known as
- KCNE1 long QT syndrome · long QT syndrome caused by mutation in KCNE1 · long QT syndrome type 5 · LQT5
Subtypes
| Disease | Subtypes |
|---|---|
| Jervell and Lange-Nielsen syndrome 2 |
Projects
Including projects on subtypes.
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