Medical Subject Headings

Last uploaded: January 31, 2024
Preferred Name

Romano-Ward Syndrome

Synonyms

Ward Romano Syndrome

Definitions

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.

ID

http://purl.bioontology.org/ontology/MESH/D029597

altLabel

Ward Romano Syndrome

Syndrome, Romano-Ward

Romano Ward Syndrome

Syndrome, Ward-Romano

Ventricular Fibrillation with Prolonged QT Interval

Long QT Syndrome 1

Ward-Romano Syndrome

Long QT Syndrome Type 1

AQL

BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C4551647

DC

1

definition

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.

DX

20020101

HN

2002; use LONG QT SYNDROME 1986-2001

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000469

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000401

Machine permutation

2002; see LONG QT SYNDROME 1986-2001

Mapped from

http://purl.bioontology.org/ontology/MESH/C566006

MDA

20010725

MMR

20170620

MN

C16.131.240.400.715.720

C14.280.123.625.720

C23.550.073.547.720

C14.280.067.565.720

notation

D029597

prefLabel

Romano-Ward Syndrome

TERMUI

T444046

T781532

T444045

T024262

T781531

TH

OMIM (2013)

NLM (2002)

NLM (2012)

UNK (19XX)

GHR (2014)

ORD (2010)

tui

T047

subClassOf

http://purl.bioontology.org/ontology/MESH/D008133

Delete Subject Author Type Created
No notes to display
Create mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MEDDRA/10039211 MEDDRA CUI
http://purl.bioontology.org/ontology/SCTSPA/20852007 SCTSPA CUI
http://purl.bioontology.org/ontology/MDRGER/10039211 MDRGER CUI
http://purl.bioontology.org/ontology/MSHFRE/D029597 MSHFRE CUI
http://purl.bioontology.org/ontology/RCD/G56y2 RCD CUI
http://purl.bioontology.org/ontology/OMIM/607542 OMIM CUI
http://purl.bioontology.org/ontology/SNMI/D3-31832 SNMI CUI
http://purl.bioontology.org/ontology/SNOMEDCT/20852007 SNOMEDCT CUI
http://purl.bioontology.org/ontology/MDRFRE/10039211 MDRFRE CUI
http://purl.bioontology.org/ontology/OMIM/192500 OMIM CUI
http://www.orpha.net/ORDO/Orphanet_101016 EFO LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_4069 NATPRO LOOM
http://purl.bioontology.org/ontology/MEDDRA/10039211 MEDDRA LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C14.280.067.565.720 RH-MESH LOOM
http://id.nlm.nih.gov/mesh/D029597 MDM LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#10936 OCHV LOOM
http://www.orpha.net/ORDO/Orphanet_101016 ORDO LOOM
http://purl.bioontology.org/ontology/RCTV2/G56y200 RCTV2 LOOM
http://purl.obolibrary.org/obo/OMIT_0021576 OMIT LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Romano-Ward_Syndrome CSEO LOOM
http://purl.jp/bio/4/id/200906088761501012 IOBC LOOM
http://purl.bioontology.org/ontology/RCD/G56y2 RCD LOOM
http://www.co-ode.org/ontologies/galen#RomanoWardSyndrome GALEN LOOM
http://purl.bioontology.org/ontology/SNMI/D3-31832 SNMI LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/20852007 SNOMEDCT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C23.550.073.547.720 RH-MESH LOOM
http://www.phoc.org.cn/pmo/class/PMO_00036200 PMAPP-PMO LOOM
http://www.gamuts.net/entity#Romano_Ward_syndrome GAMUTS LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.240.400.715.720 RH-MESH LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0035828 OCHV LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D029597 RH-MESH LOOM
http://www.limics.org/hrdo/rdfns#pat_id_14727 HRDO LOOM