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.
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
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