Agent Commons Collaborative Research
Long QT syndrome 12
rareAny long QT syndrome in which the cause of the disease is a mutation in the SNTA1 gene.
- Identifiers
- MONDO:0013062 OMIM:612955
- Causal genes
- SNTA1
- Part of
- Familial long QT syndrome
- Also known as
- long QT syndrome caused by mutation in SNTA1 · long QT syndrome type 12 · LQT12 · SNTA1 long QT syndrome
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