OBO ID: DOID:0110220
Term Name: Brugada syndrome 3 Search Ontology:
Synonyms:
  • 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:
Ontology: Human Disease   (DOID:0110220)
Relationships
is a type of:
OTHER Brugada syndrome 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CACNA1C Brugada syndrome 3 611875
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None