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Long QT Syndrome 1

^ http://purl.obolibrary.org/obo/NCIT_C85049


An autosomal dominant condition caused by mutation(s) in the KCNQ1 gene, encoding potassium voltage-gated channel subfamily KQT member 1. It is characterized by a prolonged QT interval that may result in torsade de pointes, ventricular fibrillation and/or sudden cardiac death. [ NCI ]

Synonyms: Romano-Ward Syndrome, Long QT Syndrome 1, LQT1

Term info

Preferred Name

Long QT Syndrome 1

Semantic Type

Disease or Syndrome

UMLS CUI

C0035828

code

C85049

Term relations

Subclass of: