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Romano-Ward Syndrome MeSH Descriptor Data 2022


MeSH Heading
Romano-Ward Syndrome
Tree Number(s)
C14.280.067.565.720
C14.280.123.625.720
C16.131.240.400.715.720
C23.550.073.547.720
Unique ID
D029597
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D029597
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.
Entry Term(s)
Long QT Syndrome 1
Long QT Syndrome Type 1
Ventricular Fibrillation with Prolonged QT Interval
Ward-Romano Syndrome
Previous Indexing
Long QT Syndrome (1985-2001)
Public MeSH Note
2002; see LONG QT SYNDROME 1986-2001
History Note
2002; use LONG QT SYNDROME 1986-2001
Date Established
2002/01/01
Date of Entry
2001/07/25
Revision Date
2017/06/20
Romano-Ward Syndrome Preferred
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