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Disease Ontology Browser
long QT syndrome 15 (DOID:0110656)
Alliance: disease page
Synonyms: LQT15
Alt IDs: OMIM:616249, ICD10CM:I45.8
Definition: A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the CALM2 gene on chromosome 2p21.


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
07/02/2024
MGI 6.13
The Jackson Laboratory