Search Ontology:
Human Disease
Brugada syndrome 3
- Term ID
- DOID:0110220
- Synonyms
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- BRGDA3
- Definition
- 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. https://www.ncbi.nlm.nih.gov/pubmed/17224476
- References
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- GARD:10361
- ICD10CM:I49.8
- MESH:C567509
- MIM:611875
- Ontology
- Human Disease ( DOID:0110220 )
- is a type of
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Genes Involved
Zebrafish Models