familial atrial fibrillation
Information
- Disease name
- familial atrial fibrillation
- Disease ID
- DOID:0050650
- Description
- "An atrial fibrillation that has_material_basis_in autosomal dominant inheritance of the familial atrial fibrillation (ATFB) genes." [url:http\://en.wikipedia.org/wiki/Familial_atrial_fibrillation]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT04075994 | Completed | N/A | Atrial Fibrillation Health Literacy and Information Technology Trial | January 2, 2020 | August 1, 2023 |
| NCT04076020 | Completed | N/A | Atrial Fibrillation Health Literacy and Information Technology Trial in Rural Pennsylvania Counties | January 8, 2020 | August 2, 2023 |
- Exact Synonym (Disease Ontology)
- ATFB
- Disase is a (Disease Ontology)
- DOID:0060224
- Cross Reference ID (Disease Ontology)
- GARD:9740
- Cross Reference ID (Disease Ontology)
- MIM:607554
- Cross Reference ID (Disease Ontology)
- MIM:608583
- Cross Reference ID (Disease Ontology)
- MIM:608988
- Cross Reference ID (Disease Ontology)
- MIM:611493
- Cross Reference ID (Disease Ontology)
- MIM:611494
- Cross Reference ID (Disease Ontology)
- MIM:612201
- Cross Reference ID (Disease Ontology)
- MIM:612240
- Cross Reference ID (Disease Ontology)
- MIM:613055
- Cross Reference ID (Disease Ontology)
- MIM:613980
- Cross Reference ID (Disease Ontology)
- MIM:614022
- Cross Reference ID (Disease Ontology)
- MIM:614049
- Cross Reference ID (Disease Ontology)
- MIM:614050
- Cross Reference ID (Disease Ontology)
- MIM:615377
- Cross Reference ID (Disease Ontology)
- MIM:615378
- Cross Reference ID (Disease Ontology)
- MIM:615770
- Cross Reference ID (Disease Ontology)
- MIM:PS608583
- Cross Reference ID (Disease Ontology)
- ORDO:334
- OrphaNumber from OrphaNet (Orphanet)
- 334