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Descriptor English: Romano-Ward Syndrome
Descriptor Spanish: Síndrome de Romano-Ward
Descriptor síndrome de Romano-Ward
Entry term(s) síndrome de QT largo de tipo 1
síndrome de QT largo tipo 1
síndrome de Ward-Romano
Scope note: Forma de síndrome de QT largo que no se acompaña de sordera congénita. Está causado por mutación del gen KCNQ1 que codifica una proteína del CANAL DE POSTASIO DEPENDIENTE DEL VOLTAJE.
Descriptor Portuguese: Síndrome de Romano-Ward
Descriptor French: Syndrome de Romano-Ward
Entry term(s): Long QT Syndrome 1
Long QT Syndrome Type 1
Romano Ward Syndrome
Syndrome, Romano-Ward
Syndrome, Ward-Romano
Ventricular Fibrillation with Prolonged QT Interval
Ward Romano Syndrome
Ward-Romano 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
RDF Unique Identifier: https://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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
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
DeCS ID: 36018
Unique ID: D029597
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2002/01/01
Date of Entry: 2001/07/25
Revision Date: 2017/06/20
Romano-Ward Syndrome - Preferred
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.
Preferred term Romano-Ward Syndrome
Entry term(s) Long QT Syndrome 1
Long QT Syndrome Type 1
Romano Ward Syndrome
Syndrome, Romano-Ward
Syndrome, Ward-Romano
Ventricular Fibrillation with Prolonged QT Interval
Ward Romano Syndrome
Ward-Romano Syndrome



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