Medical Subject Headings / 医学主题词表

Last uploaded: September 7, 2023
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Preferred Name

Brugada Syndrome
Synonyms

Sudden Unexplained Nocturnal Death Syndrome
Definitions

An autosomal dominant defect of cardiac conduction that is characterized by an abnormal ST-segment in leads V1-V3 on the ELECTROCARDIOGRAM resembling a right BUNDLE-BRANCH BLOCK; high risk of VENTRICULAR TACHYCARDIA; or VENTRICULAR FIBRILLATION; SYNCOPAL EPISODE; and possible sudden death. This syndrome is linked to mutations of gene encoding the cardiac SODIUM CHANNEL alpha subunit.
ID

http://purl.bioontology.org/ontology/MESH/D053840
altLabel

Sudden Unexplained Nocturnal Death Syndrome

Sudden Unexplained Nocturnal Death Syndrome (SUNDS)

Brugada ECG Pattern

Brugada Syndrome 1

Right Bundle Branch Block, ST Segment Elevation, and Sudden Death Syndrome

Brugada Type ECG Pattern

Sudden Unexplained Death Syndrome

ECG Pattern, Brugada
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

C1721096

C4551804

C1142166
DC

1
definition

An autosomal dominant defect of cardiac conduction that is characterized by an abnormal ST-segment in leads V1-V3 on the ELECTROCARDIOGRAM resembling a right BUNDLE-BRANCH BLOCK; high risk of VENTRICULAR TACHYCARDIA; or VENTRICULAR FIBRILLATION; SYNCOPAL EPISODE; and possible sudden death. This syndrome is linked to mutations of gene encoding the cardiac SODIUM CHANNEL alpha subunit.
DX

20070101
HN

2007
Inverse of AQ

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

http://purl.bioontology.org/ontology/MESH/Q000469
Inverse of RO

http://purl.bioontology.org/ontology/MESH/D062549

http://purl.bioontology.org/ontology/MESH/D062547
Machine permutation

2007
Mapped from

http://purl.bioontology.org/ontology/MESH/C567557

http://purl.bioontology.org/ontology/MESH/C567508

http://purl.bioontology.org/ontology/MESH/C567556

http://purl.bioontology.org/ontology/MESH/C567735

http://purl.bioontology.org/ontology/MESH/C567732

http://purl.bioontology.org/ontology/MESH/C567087

http://purl.bioontology.org/ontology/MESH/C531638

http://purl.bioontology.org/ontology/MESH/C567734

http://purl.bioontology.org/ontology/MESH/C567509
MDA

20060705
MMR

20190517
MN

C14.280.123.250

C16.320.100

C14.280.067.322
notation

D053840
prefLabel

Brugada Syndrome
TERMUI

T000905311

T670955

T670956

T841052

T812523

T670954

T812525

T681723
TH

NLM (2008)

NLM (2007)

ORD (2010)

OMIM (2013)

GHR (2014)
tui

T033

T047
subClassOf

http://purl.bioontology.org/ontology/MESH/D000075224

http://purl.bioontology.org/ontology/MESH/D030342

http://purl.bioontology.org/ontology/MESH/D001145
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/601144 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/601144 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/ICD10CM/I49.8 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类，第10版-临床修改 CUI
http://www.orpha.net/ORDO/Orphanet_130 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C142891 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.obolibrary.org/obo/DOID_0050451 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_0050451 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bioontology.org/ontology/OMIM/600163 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.obolibrary.org/obo/MONDO_0015263 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0015263 Experimental Factor Ontology / 实验性因素本体 LOOM