long QT syndrome 12

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Summary

Literature (0)

DOID:0110653 - long QT syndrome 12

Disease Ontology Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SNTA1 gene on chromosome 20q11.21.

Synonyms: LQT12

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

: snta1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013062 - long QT syndrome 12

MONDO:0013062 - long QT syndrome 12

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)