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Long QT syndrome 12

MONDO:0013062

Any long QT syndrome in which the cause of the disease is a mutation in the SNTA1 gene.

Also known as: LQT12, SNTA1 long QT syndrome, long QT syndrome 12, long QT syndrome caused by mutation in SNTA1, long QT syndrome type 12

0 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Syndromic disease (24) Long QT syndrome (18) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0) Familial long QT syndrome (0)

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