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.

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.

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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

SOURCES: OMIM MESH




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