SST gene related symptoms and diseases
All the information presented here about the SST gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to SST gene
Symptoms // Phenotype | % Cases |
---|---|
Dysphagia | Very Common - Between 80% and 100% cases |
Obesity | Very Common - Between 80% and 100% cases |
Gastroesophageal reflux | Very Common - Between 80% and 100% cases |
Feeding difficulties in infancy | Very Common - Between 80% and 100% cases |
Cough | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with SST gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Nausea and vomiting
- Lymphadenopathy
- Chest pain
- Esophagitis
- Clinodactyly of the 5th toe
- Barrett esophagus
- Esophageal ulceration
- Esophageal carcinoma
Rare diseases associated to SST gene
Here you will find a list of rare diseases related to the SST. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
ADENOCARCINOMA OF THE ESOPHAGUS
Alternate names
ADENOCARCINOMA OF THE ESOPHAGUS Is also known as esophageal adenocarcinoma, barrett metaplasia
Description
Esophageal adenocarcinoma (EAC) is a sub-type of esophageal carcinoma (EC; see this term) affecting the glandular cells of the lower esophagus at the junction with the stomach.
Most common symptoms of ADENOCARCINOMA OF THE ESOPHAGUS
- Dysphagia
- Obesity
- Gastroesophageal reflux
- Feeding difficulties in infancy
- Cough
More info about ADENOCARCINOMA OF THE ESOPHAGUS
Search interest in SST
Potential gene panels for SST gene
SST Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the SST 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 B3GAT3 F2 TBX4 ADGRV1 PDCD10 GNAO1 MIR3681HG