TNFSF15 gene related symptoms and diseases
All the information presented here about the TNFSF15 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,NCBIGENE,HGNC,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to TNFSF15 gene
Symptoms // Phenotype | % Cases |
---|---|
Hypertension | Very Common - Between 80% and 100% cases |
Conjugated hyperbilirubinemia | Very Common - Between 80% and 100% cases |
Celiac disease | Very Common - Between 80% and 100% cases |
Osteomalacia | 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 TNFSF15 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Abnormality of lipid metabolism
- Hepatocellular carcinoma
- Xerostomia
- Antinuclear antibody positivity
- Excessive daytime somnolence
- Allergy
- Cholangitis
- Abnormality of the thyroid gland
And 36 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to TNFSF15 gene
Here you will find a list of rare diseases related to the TNFSF15. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
PRIMARY BILIARY CHOLANGITIS
Alternate names
PRIMARY BILIARY CHOLANGITIS Is also known as pbc, hanot syndrome, primary biliary cirrhosis
Description
Primary biliary cholangitis (PBC) is a chronic and slowly progressive cholestatic liver disease of autoimmune etiology characterized by injury of the intrahepatic bile ducts that may eventually lead to liver failure.
Most common symptoms of PRIMARY BILIARY CHOLANGITIS
- Hypertension
- Fatigue
- Diarrhea
- Encephalopathy
- Osteoporosis
More info about PRIMARY BILIARY CHOLANGITIS
Search interest in TNFSF15
Potential gene panels for TNFSF15 gene
TNFSF15 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the TNFSF15 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 ITK CYP11B1 BGN JAK2 ADA2 CTNS ADCY5