NPPA-AS1 gene related symptoms and diseases
All the information presented here about the NPPA-AS1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to NPPA-AS1 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Hypertension | Very Common - Between 80% and 100% cases |
| Cardiomyopathy | Very Common - Between 80% and 100% cases |
| Stroke | Very Common - Between 80% and 100% cases |
| Vertigo | Very Common - Between 80% and 100% cases |
| Tachycardia | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with NPPA-AS1 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Atrial fibrillation
- Palpitations
- Thromboembolic stroke
- Sick sinus syndrome
Rare diseases associated to NPPA-AS1 gene
Here you will find a list of rare diseases related to the NPPA-AS1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
ATRIAL FIBRILLATION, FAMILIAL, 6; ATFB6
Description
Atrial fibrillation (AF) is the most common sustained cardiac rhythm disturbance, affecting more than 2 million Americans, with an overall prevalence of 0.89%. The prevalence increases rapidly with age, to 2.3% between the ages of 40 and 60 years, and to 5.9% over the age of 65. The most dreaded complication is thromboembolic stroke (Brugada et al., 1997).For a discussion of genetic heterogeneity of atrial fibrillation, see {608583}.
Most common symptoms of ATRIAL FIBRILLATION, FAMILIAL, 6; ATFB6
- Hypertension
- Cardiomyopathy
- Stroke
- Vertigo
- Tachycardia
More info about ATRIAL FIBRILLATION, FAMILIAL, 6; ATFB6
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