DSG2-AS1 gene related symptoms and diseases
All the information presented here about the DSG2-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.
Table of contents:
Top 5 symptoms and clinical features associated to DSG2-AS1 gene
Symptoms // Phenotype | % Cases |
---|---|
Congestive heart failure | Very Common - Between 80% and 100% cases |
Ventricular extrasystoles | Very Common - Between 80% and 100% cases |
Severely reduced ejection fraction | Very Common - Between 80% and 100% cases |
Right ventricular dilatation | Very Common - Between 80% and 100% cases |
Prolonged QRS complex | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with DSG2-AS1 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Abnormal T-wave
- Abnormal echocardiogram
- Right ventricular cardiomyopathy
- T-wave inversion
- Left bundle branch block
- Abnormal EKG
- Dilatation
- Right bundle branch block
And 8 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to DSG2-AS1 gene
Here you will find a list of rare diseases related to the DSG2-AS1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10
Alternate names
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10 Is also known as arrhythmogenic right ventricular cardiomyopathy 10, arvc10
Most common symptoms of ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10
- Congestive heart failure
- Dilatation
- Dyspnea
- Sudden cardiac death
- Chest pain
More info about ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10; ARVD10
Search interest in DSG2-AS1
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