ZFIN Human Disease: Brugada syndrome 7

OBO ID: DOID:0110224

OBO ID: DOID:0110224

Term Name:	Brugada syndrome 7	Search Ontology:
Synonyms:	BRGDA7
Definition:	A Brugada syndrome that has_material_basis_in heterozygous mutation in the SCN3B gene on chromosome 11q24. https://www.ncbi.nlm.nih.gov/pubmed/20031595
References:	ICD10CM:I49.8 MESH:C567734 OMIM:613120
Ontology:	Human Disease ( DOID:0110224 )

Relationships

is a type of:	autosomal dominant disease Brugada syndrome autosomal dominant disease Brugada syndrome Show first 5 Terms

OTHER Brugada syndrome 7 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SCN3B	scn3b	Brugada syndrome 7	613120
		Atrial fibrillation, familial, 16	613120

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None