long QT syndrome 3
Information
- Disease name
- long QT syndrome 3
- Disease ID
- DOID:0110646
- Description
- "A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2." [url:https\://www.ncbi.nlm.nih.gov/pubmed/8541846]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT02014961 | Recruiting | N/A | Worm Study: Modifier Genes in Sudden Cardiac Death | April 2015 | April 2025 |
- Disase is a (Disease Ontology)
- DOID:2843
- Cross Reference ID (Disease Ontology)
- GARD:3286
- Cross Reference ID (Disease Ontology)
- ICD10CM:I45.8
- Cross Reference ID (Disease Ontology)
- MESH:C565840
- Cross Reference ID (Disease Ontology)
- MIM:603830
- Exact Synonym (Disease Ontology)
- LQT3