Brugada syndrome 4
Information
- Disease name
- Brugada syndrome 4
- Disease ID
- DOID:0110221
- Description
- "A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the beta-2 subunit of the voltage-dependent L-type calcium channel (CACNB2) on chromosome 10p12." [url:https\://www.ncbi.nlm.nih.gov/pubmed/17224476]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:0050451
- Cross Reference ID (Disease Ontology)
- GARD:10362
- Cross Reference ID (Disease Ontology)
- ICD10CM:I49.8
- Cross Reference ID (Disease Ontology)
- MESH:C567508
- Cross Reference ID (Disease Ontology)
- MIM:611876
- Exact Synonym (Disease Ontology)
- BRGDA4