ZFIN Human Disease: Brugada syndrome 9

OBO ID: DOID:0110226

Term Name:	Brugada syndrome 9		Search Ontology:
Synonyms:	BRGDA9
Definition:	A Brugada syndrome that has_material_basis_in heterozygous mutation in the KCND3 gene on chromosome 1p13. https://www.ncbi.nlm.nih.gov/pubmed/21349352
References:	ICD10CM:I49.8 OMIM:616399
Ontology:	Human Disease ( DOID:0110226 )

Relationships

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

OTHER Brugada syndrome 9 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KCND3	kcnd3	Brugada syndrome 9	616399

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None