OBO ID: DOID:0110219
Term Name: Brugada syndrome 2 Search Ontology:
Synonyms:
  • BRGDA2
Definition: A Brugada syndrome that has_material_basis_in heterozygous mutation in the GPD1L gene on chromosome 3p22. https://www.ncbi.nlm.nih.gov/pubmed/17967977
References:
Ontology: Human Disease   ( DOID:0110219 )
Relationships
is a type of:
OTHER Brugada syndrome 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GPD1L Brugada syndrome 2 611777
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.