atrial fibrillation, familial, 15
Findings
No curated finding names atrial fibrillation, familial, 15 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any familial atrial fibrillation in which the cause of the disease is a mutation in the NUP155 gene.
Definition from the Mondo Disease Ontology (MONDO:0014340), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Congenital onset · Third trimester onset
HPO, annotations 2026-09-02
Features
5 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Atrial fibrillationHPOHP:0005110
- 5 of 5 reported patients
- Supraventricular tachycardiaHPOHP:0004755
- 3 of 5 reported patients
- Atrial flutterHPOHP:0004749
- 2 of 5 reported patients
- Sudden cardiac deathHPOHP:0001645
- 2 of 5 reported patients
- Left atrial enlargementHPOHP:0031295
- 1 of 5 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- NUP155HGNC:8063
- Limited · Ambry Genetics · Autosomal recessive · 2018
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2019
Where it sits
- A kind of
Other names
4 names
Resolves to: atrial fibrillation, familial, 15
- Also called
- atrial fibrillation 15atrial fibrillation, familial, type 15familial atrial fibrillation caused by mutation in NUP155NUP155 familial atrial fibrillation