Brugada Syndrome
Disease ID: disease_node_11785
Connections displayed (default: 10).
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| Dbxref | GARD:1030, ICD10CM:I49.8, MESH:D053840, MIM:PS601144, NCI:C142891, ORDO:130, SNOMEDCT_US_2023_03_01:418818005, UMLS_CUI:C1142166, UMLS_CUI:C1721096 |
|---|---|
| Subclassof | DOID_10273, DOID_0050177 |
| Data Source | DOID, MESH |
| Synonyms | Bangungut, Brugada type idiopathic ventricular fibrillation, Dream disease, Pokkuri death syndrome, SUNDS, sudden unexplained nocturnal death syndrome |
| Mesh Id | D053840 |
| Mesh Label | Brugada Syndrome |
| Mesh Subclassof | D030342, D001145, D000075224 |
| Doid Label | Brugada syndrome |
| Doid Description | A heart conduction disease that is characterized by abnormal electrocardiogram (ECG) findings and an increased risk of sudden cardiac death. OMIM mapping confirmed by DO. [SN]. |
| Disease Node Id | disease_node_11785 |
| Doid Id | DOID_0050451 |
| Disease Has Basis In | SO_0000704 |
| Label | Brugada Syndrome |
- Incoming r'ship
SUBCLASS_OFto/from Brugada Syndrome 1(ID:disease_node_19138) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Monogenic Disease(ID:disease_node_13650) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Brugada Syndrome 9(ID:disease_node_19137) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Heart Conduction Disease(ID:disease_node_13164) (Disease)