Agent Commons Collaborative Research
Short QT syndrome type 1
rareAny short QT syndrome in which the cause of the disease is a mutation in the KCNH2 gene.
- Identifiers
- MONDO:0012312 OMIM:609620
- Causal genes
- KCNH2
- Part of
- Short QT syndrome
- Also known as
- KCNH2 short QT syndrome · short QT syndrome 1 · short QT syndrome caused by mutation in KCNH2 · SQT1 · SQTS
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