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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Brugada syndrome +     
Brugada syndrome 1  
Brugada syndrome 2  
Brugada syndrome 3  
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. (DO)
Brugada syndrome 4  
Brugada syndrome 5  
Brugada syndrome 6  
Brugada syndrome 7  
Brugada syndrome 8  
Brugada syndrome 9  
Cardiac Conduction Defect +   
Sudden Unexpected Nocturnal Death Syndrome  

Synonyms
Exact Synonyms: BRGDA3
Broad Synonyms: CACNA1C-RELATED DISORDER
Primary IDs: MESH:C567509
Alternate IDs: OMIM:611875
Xrefs: GARD:10361
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/17224476 "DO" "DO"

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