ZFIN Human Disease: long QT syndrome 13

OBO ID: DOID:0110654

OBO ID: DOID:0110654

Term Name:	long QT syndrome 13	Search Ontology:
Synonyms:	LQT13
Definition:	A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNJ5 gene on chromosome 11q24.3. https://www.ncbi.nlm.nih.gov/pubmed/20560207
References:	ICD10CM:I45.8 OMIM:613485
Ontology:	Human Disease ( DOID:0110654 )

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 13 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KCNJ5	kcnj5	Long QT syndrome 13	613485

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None