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Results 1 - 6 of 6 for Short QT syndrome 2
  1. KCNJ2 gene 
    ... can cause fainting or sudden death.At least two mutations in the KCNJ2 gene have been found to cause short QT syndrome in a small number of affected families. These ...
    https://medlineplus.gov/genetics/gene/kcnj2 - Genetics
  2. KCNQ1 gene 
    ... death. More About This Health Condition At least two mutations in the KCNQ1 gene can cause a heart condition called short QT syndrome. In people with this condition, the cardiac muscle ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  3. KCNH2 gene 
    ... Wolpert C, Gaita F, Giustetto C, Borggrefe M. Short QT syndrome. Cardiovasc Res. ... pathogenesis of long QT syndrome type 2. J Arrhythm. 2016 Oct;32(5):373-380. ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  4. CACNA1C gene 
    ... exon 8. The other 20 percent of CaV1.2 channels contain a slightly different version of this segment, known ... More About This Health Condition Variants (also known ...
    https://medlineplus.gov/genetics/gene/cacna1c - Genetics
  5. CDKN1C gene 
    ... Neri G. Mild Beckwith-Wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p. Eur J Hum Genet. 2013 ...
    https://medlineplus.gov/genetics/gene/cdkn1c - Genetics
  6. KCNQ1OT1 gene 
    ... part of a cluster of genes on the short (p) arm of chromosome 11 that undergo genomic imprinting. KCNQ1OT1 and several other genes in this cluster that are thought to help regulate growth are controlled by a nearby region of DNA known as imprinting center 2 (IC2) or KvDMR. The IC2 region undergoes a ...
    https://medlineplus.gov/genetics/gene/kcnq1ot1 - Genetics