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