Brugada Syndrome 1
Disease ID: disease_node_19138
Connections displayed (default: 10).
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| Dbxref | ICD10CM:I49.8, MIM:601144 |
|---|---|
| Subclassof | DOID_0050736, DOID_0050451 |
| Data Source | DOID |
| Synonyms | BRGDA1 |
| Doid Label | Brugada syndrome 1 |
| Doid Description | A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN5A gene on chromosome 3p22. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_19138 |
| Doid Id | DOID_0110218 |
| Label | Brugada Syndrome 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Brugada Syndrome(ID:disease_node_11785) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)