| Descriptor English: | Brugada Syndrome | ||||
| Descriptor Spanish: |
Síndrome de Brugada
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| Descriptor Portuguese: | Síndrome de Brugada | ||||
| Descriptor French: | Syndrome de Brugada | ||||
| Entry term(s): |
Brugada ECG Pattern Brugada Syndrome 1 Brugada Type ECG Pattern ECG Pattern, Brugada Right Bundle Branch Block, ST Segment Elevation, and Sudden Death Syndrome Sudden Unexplained Death Syndrome Sudden Unexplained Nocturnal Death Syndrome Sudden Unexplained Nocturnal Death Syndrome (SUNDS) |
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| Tree number(s): |
C14.280.067.322 C14.280.123.250 C16.320.100 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D053840 | ||||
| Scope note: | 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. |
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| 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 |
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| Previous Indexing: |
Arrhythmia (1996-2006) |
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| Public MeSH Note: | 2007 |
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| History Note: | 2007 |
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| DeCS ID: | 52136 | ||||
| Unique ID: | D053840 | ||||
| NLM Classification: | WG 330 | ||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
| Date Established: | 2007/01/01 | ||||
| Date of Entry: | 2006/07/05 | ||||
| Revision Date: | 2019/05/17 |
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Brugada Syndrome
- Preferred
Brugada ECG Pattern
- Related but not broader or narrower
Brugada Syndrome 1
- Narrower
| Concept UI |
M0496826 |
| Scope note | 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. |
| Preferred term | Brugada Syndrome |
| Entry term(s) |
Right Bundle Branch Block, ST Segment Elevation, and Sudden Death Syndrome Sudden Unexplained Death Syndrome Sudden Unexplained Nocturnal Death Syndrome Sudden Unexplained Nocturnal Death Syndrome (SUNDS) |
| Concept UI |
M0496827 |
| Preferred term | Brugada ECG Pattern |
| Entry term(s) |
Brugada Type ECG Pattern ECG Pattern, Brugada |
| Concept UI |
M000648999 |
| Preferred term | Brugada Syndrome 1 |
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