Jump to:
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. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_0110218 |
|
| database_cross_reference |
MIM:601144 ICD10CM:I49.8 |
|
| 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 |
|
| prefLabel |
Brugada syndrome 1 |
|
| subClassOf |
Create mapping