CXCL8 gene related symptoms and diseases
All the information presented here about the CXCL8 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,OMIM,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to CXCL8 gene
Symptoms // Phenotype | % Cases |
---|---|
Nausea and vomiting | Common - Between 50% and 80% cases |
Neoplasm | Common - Between 50% and 80% cases |
Chest pain | Uncommon - Between 30% and 50% cases |
Dementia | Uncommon - Between 30% and 50% cases |
Abnormality of blood and blood-forming tissues | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with CXCL8 gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Anemia
- Developmental regression
- Dysphagia
- Obesity
- Cough
- Thrombocytopenia
- Weight loss
- Paresthesia
And 291 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to CXCL8 gene
Here you will find a list of rare diseases related to the CXCL8. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
BEHÇET DISEASE
Alternate names
BEHÇET DISEASE Is also known as bd, behcet disease
Description
Behçet's disease (BD) is a chronic, relapsing, multisystemic vasculitis characterized by mucocutaneous lesions, as well as articular, vascular, ocular and central nervous system manifestations.
Most common symptoms of BEHÇET DISEASE
- Seizures
- Ataxia
- Neoplasm
- Pain
- Cataract
More info about BEHÇET DISEASE
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
DOWN SYNDROME
Alternate names
DOWN SYNDROME Is also known as trisomy 21
Description
Down syndrome is a chromosomal abnormality caused by the presence of a third (partial or total) copy of chromosome 21 and that is characterized by variable intellectual disability, muscular hypotonia, and joint laxity, often associated with a characteristic facial dysmorphism and various anomalies such as cardiac, gastrointestinal, or endocrine defects.
Most common symptoms of DOWN SYNDROME
- Intellectual disability
- Global developmental delay
- Short stature
- Generalized hypotonia
- Hearing impairment
More info about DOWN SYNDROME
WILSON DISEASE
Alternate names
WILSON DISEASE Is also known as wd, hepatolenticular degeneration, wnd
Description
Wilson disease is a very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.
Most common symptoms of WILSON DISEASE
- Intellectual disability
- Growth delay
- Neoplasm
- Failure to thrive
- Spasticity
More info about WILSON DISEASE
Search interest in CXCL8
Potential gene panels for CXCL8 gene
CXCL8 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the CXCL8 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 PDSS2 MALT1 NCF2 ANLN SCN11A JUN SLC6A19