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 )
Relationships
is a type of:
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
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.