long QT syndrome 1

Summary

DOID:0110644 - long QT syndrome 1

Disease Ontology Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4.

Synonyms: LQT1, ventricular fibrillation with prolonged QT interval

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: scn4b, kcne1, snta1, cav3, calm1, kcnh2, ank2, calm2, cav3.2, kcnj5, kcnq1, akap9, scn5a, kcne2, trdn

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0008646 - obsolete long QT syndrome 1

MONDO:0008646 - obsolete long QT syndrome 1

MIM:

MIM:192500 - LONG QT SYNDROME 1; LQT1

MIM:192500 - LONG QT SYNDROME 1; LQT1

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), long QT syndrome (is_a)