ZFIN Human Disease: long QT syndrome 10

OBO ID: DOID:0110651

Term Name:	long QT syndrome 10		Search Ontology:
Synonyms:	LQT10
Definition:	A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3. https://www.ncbi.nlm.nih.gov/pubmed/17592081
References:	GARD:10436 ICD10CM:I45.8 MESH:C567514 OMIM:611819
Ontology:	Human Disease ( DOID:0110651 )

Relationships

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

OTHER long QT syndrome 10 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SCN4B	scn4ba scn4bb	Atrial fibrillation, familial, 17	611819
		Long QT syndrome 10	611819

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None