- Concept UI
- M0012685
- Scope Note
- A form of long QT syndrome that is without congenital deafness. It is caused by mutation of the KCNQ1 gene which encodes a protein in the VOLTAGE-GATED POTASSIUM CHANNEL.
- Terms
-
Romano-Ward Syndrome
Preferred Term
Term UI
T024262
Date03/11/1985
LexicalTag
EPO
ThesaurusID
-
Long QT Syndrome 1
Term UI
T444045
Date04/24/2001
LexicalTag
NON
ThesaurusID
-
Ward-Romano Syndrome
Term UI
T444046
Date04/24/2001
LexicalTag
EPO
ThesaurusID
-
Long QT Syndrome Type 1
Term UI
T781531
Date12/02/2010
LexicalTag
NON
ThesaurusID
-
Ventricular Fibrillation with Prolonged QT Interval
Term UI
T781532
Date12/02/2010
LexicalTag
NON
ThesaurusID