TREH gene related symptoms and diseases
All the information presented here about the TREH gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,ORPHANET,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to TREH gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Neoplasm | Very Common - Between 80% and 100% cases |
| Pain | Very Common - Between 80% and 100% cases |
| Vomiting | Very Common - Between 80% and 100% cases |
| Diarrhea | Very Common - Between 80% and 100% cases |
| Abdominal pain | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with TREH gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Irritability
- Malabsorption
- Abdominal distention
- Celiac disease
- Villous atrophy
- Peptic ulcer
- Decreased small intestinal mucosa lactase activity
Rare diseases associated to TREH gene
Here you will find a list of rare diseases related to the TREH. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
TREHALASE DEFICIENCY
Alternate names
TREHALASE DEFICIENCY Is also known as trehalose intolerance, isolated trehalose intolerance
Description
This syndrome is characterised by diarrhoea and vomiting after ingestion of trehalose, a disaccharide found mainly in mushrooms.
Most common symptoms of TREHALASE DEFICIENCY
- Neoplasm
- Pain
- Vomiting
- Diarrhea
- Abdominal pain
More info about TREHALASE DEFICIENCY
Search interest in TREH
Potential gene panels for TREH gene
TREH Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the TREH gene.
More info about this panel United States.
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