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.

Table of contents:

Main symptoms and clinical features
Other symptoms and clinical features
Related Diseases
Current trends
Suitable testing panels

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

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.