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Repository for lectin-assisted multimodality data
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long QT syndrome 10
Summary
- Synonym
-
- LQT10
- Definition
- A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN4B gene on chromosome 11q23.3.
- Super Class
- autosomal dominant disease long QT syndrome
External Links
- Disease Ontology
- DOID:0110651
- Mondo Disease Ontology
- MeSH
- GARD
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q8IWT1 | Sodium channel regulatory subunit beta-4 |
