loading...| Preferred Name |
Brugada syndrome |
| ID |
http://www.orpha.net/ORDO/Orphanet_130 |
| alternative_term |
Idiopathic ventricular fibrillation, Brugada type |
| definition |
A cardiac disorder characterized on electrocardiogram (ECG) by ST segment elevation with a coved aspect on the right precordial leads, and a clinical susceptibility to ventricular tachyarrhythmias and sudden death occurring in the absence of overt myocardial abnormalities. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=130 |
| has_age_of_onset |
Adult Childhood |
| has_inheritance |
Not applicable Autosomal dominant |
| hasDbXref |
OMIM:613123 OMIM:616399 OMIM:611777 OMIM:612838 OMIM:611875 MedDRA:10059027 OMIM:611876 MeSH:D053840 OMIM:601144 OMIM:613120 ICD-10:I49.8 ICD-11:BC65.1 OMIM:613119 UMLS:C1142166 |
| label |
Brugada syndrome |
| notation |
ORPHA:130 |
| part_of | |
| prefixIRI |
ORDO:Orphanet_130 |
| prefLabel |
Brugada syndrome |
| present_in |
South East Asia AND has_point_prevalence_average_value : 75.0 AND has_point_prevalence_range : 6-9 / 10 000 Europe AND has_point_prevalence_average_value : 20.0 AND has_point_prevalence_range : 1-5 / 10 000 |
| treeView | |
| subClassOf |