MeSH Browser

MeSH Supplementary: Long Qt Syndrome 2
Unique ID: C563614
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563614
Registry Numbers: 0
Heading Mapped to: *Long QT Syndrome
Frequency: 100
Note: A congenital disorder characterized by a prolonged QT interval and TORSADE DE POINTES. These cardiac arrhythmias may result in recurrent SYNCOPE, seizure, or sudden death. Mutations in the KCNH2 gene have been identified. OMIM: 613688
Date of Entry: 2012/11/05
Revision Date: 2015/08/18

Long Qt Syndrome 2 MeSH Supplementary Concept Data 2025