long QT syndrome 1
Information
- Disease name
- long QT syndrome 1
- Disease ID
- DOID:0110644
- Description
- "A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNQ1 gene on chromosome 11p15.5-p15.4." [url:https\://www.ncbi.nlm.nih.gov/pubmed/17192539]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:2843
- Cross Reference ID (Disease Ontology)
- GARD:3284
- Cross Reference ID (Disease Ontology)
- ICD10CM:I45.8
- Cross Reference ID (Disease Ontology)
- MIM:192500
- Exact Synonym (Disease Ontology)
- LQT1
- Exact Synonym (Disease Ontology)
- ventricular fibrillation with prolonged QT interval