Brugada syndrome 3
Information
- Disease name
- Brugada syndrome 3
- Disease ID
- DOID:0110220
- Description
- "A Brugada syndrome that has_material_basis_in heterozygous mutation in the gene encoding the alpha-1C subunit of the L-type voltage-dependent calcium channel (CACNA1C) on chromosome 12p13." [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:10361
- Cross Reference ID (Disease Ontology)
- ICD10CM:I49.8
- Cross Reference ID (Disease Ontology)
- MESH:C567509
- Cross Reference ID (Disease Ontology)
- MIM:611875
- Exact Synonym (Disease Ontology)
- BRGDA3