Postural Orthostatic Tachycardia Syndrome Due To Net Deficiency

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.

Clinical Features

Top most frequent phenotypes and symptoms related to Postural Orthostatic Tachycardia Syndrome Due To Net Deficiency

  • Fatigue
  • Anxiety
  • Irritability
  • Vertigo
  • Nausea
  • Hypotension
  • Mitral valve prolapse
  • Orthostatic hypotension
  • Chronic fatigue
  • Asthenia

And another 1 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative 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.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.


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Postural Orthostatic Tachycardia Syndrome Due To Net Deficiency Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Orthostatic intolerance (sequence analysis of SLC6A2 gene).

By CGC Genetics (Portugal).

SLC6A2
Specificity
100 %
Genes
100 %
Hyperekplexia panel.

By Centogene AG - the Rare Disease Company (Germany).

SLC6A2, ARHGEF9, GPHN, GLRA1, GLRB
Specificity
20 %
Genes
100 %
Orthostatic intolerance.

By Centogene AG - the Rare Disease Company (Germany).

SLC6A2
Specificity
100 %
Genes
100 %
SLC6A2.

By Fulgent Genetics Fulgent Genetics (United States).

SLC6A2
Specificity
100 %
Genes
100 %

We have -4 more panels available in our App

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Sources and references

You can check the following sources for additional information.

OMIM ORPHANET Rare Disease Search Engine

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