ZFIN Human Disease: long QT syndrome 2

OBO ID: DOID:0110645

Term Name:	long QT syndrome 2		Search Ontology:
Synonyms:	LQT2
Definition:	A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1. https://www.ncbi.nlm.nih.gov/pubmed/7889573
References:	GARD:3285 ICD10CM:I45.8 MESH:C563614 OMIM:613688
Ontology:	Human Disease ( DOID:0110645 )

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 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ALG10	alg10	{Long QT syndrome, acquired, reduced susceptibility to}	613688
ALG10	alg10	{Long QT syndrome, acquired, reduced susceptibility to}	613688
KCNH2	kcnh2a kcnh2b	Long QT syndrome 2	613688

ZEBRAFISH MODELS

Fish	Conditions	Citations
nkhspGFF3AEt + MO1-kcnh6a	standard conditions	Tanaka et al., 2018

PHENOTYPE No data available

CITATIONS (1)