long QT syndrome 10 (Q32139798)
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A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3.
- LQT10
- Atrial Fibrillation, Familial, 17
- LONG QT SYNDROME 10
- Long Qt Syndrome type 10
- LONG QT SYNDROME 10; LQT10
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | long QT syndrome 10 |
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3. |
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