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loading...| Preferred Name | Brugada syndrome 1 | |
| Synonyms |
BRGDA1 |
|
| Definitions |
A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN5A gene on chromosome 3p22. |
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| ID |
http://purl.obolibrary.org/obo/DOID_0110218 |
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| alternative label |
BRGDA1 |
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| database_cross_reference |
ICD10CM:I49.8 MIM:601144 |
|
| definition |
A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN5A gene on chromosome 3p22. |
|
| has exact synonym |
BRGDA1 |
|
| has material basis in | ||
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:0110218 |
|
| label |
Brugada syndrome 1 |
|
| notation |
DOID:0110218 |
|
| note |
A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN5A gene on chromosome 3p22. |
|
| preferred label |
Brugada syndrome 1 |
|
| prefLabel |
Brugada syndrome 1 |
|
| subClassOf |
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