long QT syndrome 2

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Summary

Literature (4)

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 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

: alg10, kcnh2

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013367 - long QT syndrome 2

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