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Echinobase
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,

Echinobase Genes :


OMIM:
MIM:611819 - long qt syndrome 10; lqt10 atrial fibrillation, familial, 17, included; atfb17, included

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)