A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN5A gene on chromosome 3p22. [ url:https://www.ncbi.nlm.nih.gov/pubmed/9521325 http://purl.obolibrary.org/obo/ECO_0007645 ]
This is just here as a test because I lose it
Term information
database
cross reference
- ICD10CM:I49.8
- OMIM:601144
definition
- A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN5A gene on chromosome 3p22.
has exact synonym
- BRGDA1
has obo namespace
- disease_ontology
id
- DOID:0110218