DSCAS gene related symptoms and diseases

All the information presented here about the DSCAS 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 DSCAS gene

Symptoms // Phenotype % Cases
Hypertension Very Common - Between 80% and 100% cases
Palmoplantar hyperkeratosis Very Common - Between 80% and 100% cases
Diffuse palmoplantar hyperkeratosis Very Common - Between 80% and 100% cases
Right ventricular dilatation Very Common - Between 80% and 100% cases
Abnormal T-wave Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with DSCAS gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Abnormal echocardiogram
  • Right ventricular cardiomyopathy
  • T-wave inversion
  • Reduced ejection fraction
  • Woolly hair
  • Left bundle branch block
  • Abnormal EKG
  • Right bundle branch block

And 18 more phenotypes, you can get all of them using our tools for rare diseases.

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Rare diseases associated to DSCAS gene

Here you will find a list of rare diseases related to the DSCAS. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11


Alternate names

ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11 Is also known as arvc11, arrhythmogenic right ventricular cardiomyopathy 11

Most common symptoms of ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11

  • Hypertension
  • Cardiomyopathy
  • Dilatation
  • Arrhythmia
  • Hyperkeratosis


More info about ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11

SOURCES: MESH OMIM




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