long QT syndrome 12 Disease Ontology Browser

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Disease Ontology Browser

long QT syndrome 12 (DOID:0110653)
Alliance: disease page
Synonyms: LQT12
Alt IDs: OMIM:612955, ICD10CM:I45.8, MESH:C567842
Definition: A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SNTA1 gene on chromosome 20q11.21.

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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