loading...| Preferred Name | Brugada Syndrome [Disease/Finding] | |
| Synonyms |
Brugada Syndrome Sudden Unexplained Nocturnal Death Syndrome Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome Brugada Syndrome 1 |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000181195 |
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| altLabel |
Brugada Syndrome Sudden Unexplained Nocturnal Death Syndrome Right Bundle Branch Block, St Segment Elevation, And Sudden Death Syndrome Brugada Syndrome 1 |
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| cui |
C1142166 |
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| MESH 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. |
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| MESH DUI |
D053840 |
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| MeSH name |
Brugada Syndrome |
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| MESH UI |
M0496826 |
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| NDFRT kind |
DISEASE_KIND |
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| notation |
N0000181195 |
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| NUI |
N0000181195 |
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| prefLabel |
Brugada Syndrome [Disease/Finding] |
|
| tui |
T047 |
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| subClassOf |