long QT syndrome 3 (Q32139750)
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A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2.
- LQT3
- Long Qt Syndrome 3, Acquired, Susceptibility to
- Long Qt Syndrome 3/6, Digenic
- LONG QT SYNDROME 3; LQT3
- Long Qt Syndrome type 3
- Long Qt Syndrome 2/3, Digenic
- LONG QT SYNDROME 3
Language | Label | Description | Also known as |
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English | long QT syndrome 3 |
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2. |
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C137959
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C137959
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