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Summary Literature (7)
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

Referenced OMIM:
OMIM:192500 - LONG QT SYNDROME 1; LQT1

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : kcnq1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): long QT syndrome (is_a)


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Version: 4.14.0
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