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| Term | Brugada syndrome 8 | ID (Ontology) | DOID:0110225 (Human Disease) |
| Definition | A Brugada syndrome that has_material_basis_in heterozygous mutation in the HCN4 gene on chromosome 15q24. | ||
| Also Known As | "BRGDA8" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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monogenic disease_________ heart conduction disease__| Brugada syndrome |__Brugada syndrome 8 1 rec. |
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| Is a | Brugada syndrome | ||
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External Crossreferences & Linkouts
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ICD10CM:I49.8 MESH:C567732 MIM:613123 |
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