OBO ID: DOID:0110222
Term Name: Brugada syndrome 5 Search Ontology:
Synonyms:
  • BRGDA5
Definition: A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN1B gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/18464934
References:
Ontology: Human Disease   (DOID:0110222)
OTHER Brugada syndrome 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SCN1B Cardiac conduction defect, nonspecific 612838
Brugada syndrome 5 612838
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None