A genetically heterogeneous condition characterized by complete or incomplete right bundle branch block accompanied by ST elevation in leads V1-V3. There is a high incidence of ventricular arrhythmia that may result in sudden death. [ NCIT:C142891 ]
Synonyms: sudden unexplained nocturnal death syndrome Brugada type idiopathic ventricular fibrillation right bundle branch block, ST segment elevation, and sudden death syndrome SUNDS Brugada syndrome Pokkuri death syndrome idiopathic ventricular fibrillation, Brugada type dream disease Bangungut
Term information
- Orphanet:130 (MONDO:equivalentTo)
- OMIMPS:601144 (MONDO:equivalentTo)
- DOID:0050451 (MONDO:equivalentTo)
- SCTID:418818005 (MONDO:equivalentTo)
- NCIT:C142891 (MONDO:equivalentTo)
- NORD:878 (MONDO:NORD)
- UMLS:C1142166 (Orphanet:130/e)
- GARD:1030 (Orphanet:130)
- MedDRA:10059027 (Orphanet:130/e)
- ICD9:746.89 (MONDO:relatedTo)
- MESH:D053840 (Orphanet:130/e)
gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen
http://identifiers.org/snomedct/418818005
http://identifiers.org/mesh/D053840
http://purl.obolibrary.org/obo/NCIT_C142891
http://linkedlifedata.com/resource/umls/id/C1142166
http://purl.obolibrary.org/obo/DOID_0050451
https://omim.org/phenotypicSeries/PS601144
http://www.orpha.net/ORDO/Orphanet_130