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Disease Ontology Browser
long QT syndrome 3 (DOID:0110646)
Alliance: disease page
Synonyms: LQT3
Alt IDs: OMIM:603830, ICD10CM:I45.8, MESH:C565840
Definition: A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2.

Disease References using Mouse Models (6)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory