Search Ontology:
Human Disease
Brugada syndrome 4
- Term ID
- DOID:0110221
- Synonyms
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- BRGDA4
- Definition
- 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. https://www.ncbi.nlm.nih.gov/pubmed/17224476
- References
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- GARD:10362
- ICD10CM:I49.8
- MESH:C567508
- MIM:611876
- Ontology
- Human Disease ( DOID:0110221 )
- is a type of
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Genes Involved
Zebrafish Models