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Summary Literature (3)
DOID:0110645 - long QT syndrome 2


Disease Ontology Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1.

Synonyms: LQT2

Xenbase Genes : kcnh2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013367 - long QT syndrome 2


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)