NOS1 gene related symptoms and diseases
All the information presented here about the NOS1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,ORPHANET,NCBIGENE,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to NOS1 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Pain | Very Common - Between 80% and 100% cases |
| Hoarse voice | Very Common - Between 80% and 100% cases |
| Achalasia | Very Common - Between 80% and 100% cases |
| Xerostomia | Very Common - Between 80% and 100% cases |
| Keratoconjunctivitis sicca | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with NOS1 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Adrenal insufficiency
- Oral-pharyngeal dysphagia
- Rheumatoid arthritis
- Aspiration
- Dysphagia
- Asthma
- Chest pain
- Cough
And 5 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to NOS1 gene
Here you will find a list of rare diseases related to the NOS1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
IDIOPATHIC ACHALASIA
Alternate names
IDIOPATHIC ACHALASIA Is also known as idiopathic achalasia of esophagus, achalasia cardia, primary achalasia
Description
Idiopathic achalasia (IA) is a primary esophageal motor disorder characterized by loss of esophageal peristalsis and insufficient lower esophageal sphincter (LES) relaxation in response to deglutition.
Most common symptoms of IDIOPATHIC ACHALASIA
- Pain
- Dysphagia
- Vomiting
- Weight loss
- Gastroesophageal reflux
More info about IDIOPATHIC ACHALASIA
Search interest in NOS1
Potential gene panels for NOS1 gene
NOS1 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the NOS1 gene.
More info about this panel United States.
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