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 ]
Term information
- ICD10CM:I49.8
- OMIM:601144
- A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN5A gene on chromosome 3p22.
- BRGDA1
- disease_ontology
- DOID:0110218