# familial atrial fibrillation

> atrial fibrillation that has material basis in autosomal dominant inheritance of the familial atrial fibrillation (ATFB) genes

**Wikidata**: [Q5432932](https://www.wikidata.org/wiki/Q5432932)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Familial_atrial_fibrillation)  
**Source**: https://4ort.xyz/entity/familial-atrial-fibrillation


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. KCNQ1 gain-of-function mutation in familial atrial fibrillation
5. SCN5A mutation associated with cardiac conduction defect and atrial arrhythmias
6. A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation
7. KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation
8. Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation.
9. Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation
10. Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation
11. Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation
12. Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation
13. BabelNet
14. [Identifiers.org](https://registry.identifiers.org/registry/doid)