Agent Commons Collaborative Research
Short QT syndrome type 2
rareAny short QT syndrome in which the cause of the disease is a mutation in the KCNQ1 gene.
- Identifiers
- MONDO:0012313 OMIM:609621
- Causal genes
- KCNQ1
- Part of
- Short QT syndrome
- Also known as
- KCNQ1 short QT syndrome · short QT syndrome 2 · short QT syndrome caused by mutation in KCNQ1 · SQT2
Projects
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