ZFIN Human Disease: long QT syndrome 1

OBO ID: DOID:0110644

Term Name:	long QT syndrome 1		Search Ontology:
Synonyms:	LQT1 ventricular fibrillation with prolonged QT interval
Definition:	A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4. https://www.ncbi.nlm.nih.gov/pubmed/17192539
References:	GARD:3284 ICD10CM:I45.8 OMIM:192500
Ontology:	Human Disease ( DOID:0110644 )

Relationships

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

OTHER long QT syndrome 1 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KCNQ1	kcnq1.1	{Long QT syndrome 1, acquired, susceptibility to}	192500
		Long QT syndrome 1	192500

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None