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Summary Literature (8)
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 : scn4b, kcne1, snta1, cav3.1, 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

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)