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Disease Ontology Browser
long QT syndrome 2 (DOID:0110645)
Alliance: disease page
Synonyms: LQT2
Alt IDs: OMIM:613688, ICD10CM:I45.8
Definition: A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1.

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 6.14
The Jackson Laboratory