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Summary Literature (0)
DOID:0110651 - long QT syndrome 10


Disease Ontology Definition:A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3.

Synonyms: LQT10

Xenbase Genes : scn4b

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012737 - long QT syndrome 10

OMIM:
OMIM:611819 - LONG QT SYNDROME 10; LQT10

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)