Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
DOID:0110646 - long QT syndrome 3


Disease Ontology Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2.

Synonyms: LQT3,

Echinobase Genes :


OMIM:
MIM:603830 - long qt syndrome 3; lqt3 long qt syndrome 3, acquired, susceptibility to, included;; long qt syndrome 2/3, digenic, included; lqt2/3, digenic, included;; long qt syndrome 3/6, digenic, included; lqt3/6, digenic, included

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): long QT syndrome (is_a)