SLC6A2 gene related symptoms and diseases
All the information presented here about the SLC6A2 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE,OMIM,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to SLC6A2 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Fatigue | Very Common - Between 80% and 100% cases |
| Anxiety | Very Common - Between 80% and 100% cases |
| Irritability | Very Common - Between 80% and 100% cases |
| Vertigo | Very Common - Between 80% and 100% cases |
| Nausea | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with SLC6A2 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Hypotension
- Mitral valve prolapse
- Orthostatic hypotension
- Chronic fatigue
- Asthenia
- Orthostatic tachycardia
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Rare diseases associated to SLC6A2 gene
Here you will find a list of rare diseases related to the SLC6A2. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME DUE TO NET DEFICIENCY
Alternate names
POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME DUE TO NET DEFICIENCY Is also known as pots due to net deficiency, orthostatic intolerance due to net deficiency, neurocirculatory asthenia, mitral valve prolapse syndrome, familial orthostatic tachycardia due to norepinephrine transporter deficiency, soldiers heart, irritable heart
Description
A condition characterized by development of symptoms while standing. It is an autonomic nervous system disorder and the symptoms are relieved once the person sits back down. Symptoms include heart palpitations, sweating, anxiety, lightheadedness, hyperpnea, anxiety, and blurred vision.
Most common symptoms of POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME DUE TO NET DEFICIENCY
- Fatigue
- Anxiety
- Irritability
- Vertigo
- Nausea
More info about POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME DUE TO NET DEFICIENCY
Search interest in SLC6A2
Potential gene panels for SLC6A2 gene
Orthostatic intolerance (sequence analysis of SLC6A2 gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the SLC6A2 gene.
More info about this panelHyperekplexia panel Panel
Germany.
By Centogene AG - the Rare Disease Company Hyperekplexia panel that also includes the following genes: SLC6A2 ARHGEF9 GPHN GLRA1 GLRB
More info about this panelOrthostatic intolerance Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the SLC6A2 gene.
More info about this panelSLC6A2 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the SLC6A2 gene.
More info about this panelIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like CAPN3 SERPINA6 TBL1XR1
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