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loading...| Preferred Name |
Brugada syndrome 5 |
| Synonyms |
BRGDA5 |
| Definitions |
A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN1B gene on chromosome 19q13. |
| ID |
http://purl.obolibrary.org/obo/DOID_0110222 |
| database_cross_reference |
MESH:C567556 OMIM:612838 ICD10CM:I49.8 |
| definition |
A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN1B gene on chromosome 19q13. |
| has exact synonym |
BRGDA5 |
| has_obo_namespace |
disease_ontology |
| id |
DOID:0110222 |
| label |
Brugada syndrome 5 |
| notation |
DOID:0110222 |
| prefLabel |
Brugada syndrome 5 |
| subClassOf |
Create New Mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/MESH/C567556 | Medical Subject Headings | LOOM | |
| http://purl.bioontology.org/ontology/OMIM/612838 | Online Mendelian Inheritance in Man | LOOM |