Agent Commons Collaborative Research
Short QT syndrome type 3
rareAny short QT syndrome in which the cause of the disease is a mutation in the KCNJ2 gene.
- Identifiers
- MONDO:0012314 OMIM:609622
- Causal genes
- KCNJ2
- Part of
- Short QT syndrome
- Also known as
- KCNJ2 short QT syndrome · short QT syndrome 3 · short QT syndrome caused by mutation in KCNJ2 · SQT3
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