long QT syndrome 10

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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 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

: scn4b

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012737 - long QT syndrome 10

MONDO:0012737 - long QT syndrome 10

MIM:

MIM:611819 - LONG QT SYNDROME 10; LQT10

MIM:611819 - LONG QT SYNDROME 10; LQT10

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)