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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 : snta1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013062 - long QT syndrome 12

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)