CCR6 gene related symptoms and diseases
All the information presented here about the CCR6 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 CCR6 gene
Symptoms // Phenotype | % Cases |
---|---|
Dysphagia | Very Common - Between 80% and 100% cases |
Autoimmunity | Very Common - Between 80% and 100% cases |
Nausea and vomiting | Very Common - Between 80% and 100% cases |
Abnormality of the skin | Very Common - Between 80% and 100% cases |
Pulmonary arterial hypertension | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with CCR6 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Skin ulcer
- Gastroesophageal reflux
- Pulmonary fibrosis
- Telangiectasia of the skin
- Narrow foramen obturatorium
Not very common - Between 30% and 50% cases
- Scleroderma
- Arthritis
- Carious teeth
And 29 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to CCR6 gene
Here you will find a list of rare diseases related to the CCR6. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
LIMITED CUTANEOUS SYSTEMIC SCLEROSIS
Alternate names
LIMITED CUTANEOUS SYSTEMIC SCLEROSIS Is also known as limited cutaneous systemic scleroderma
Description
Limited cutaneous systemic sclerosis (lcSSc) is a subtype of systemic sclerosis (SSc; see this term) characterized by the association of Raynaud's phenomenon with skin fibrosis limited to the hands, face, feet and forearms.
Most common symptoms of LIMITED CUTANEOUS SYSTEMIC SCLEROSIS
- Dysphagia
- Gastroesophageal reflux
- Autoimmunity
- Nausea and vomiting
- Abnormality of skin pigmentation
More info about LIMITED CUTANEOUS SYSTEMIC SCLEROSIS
SOURCES: ORPHANET
DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS
Alternate names
DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS Is also known as progressive cutaneous systemic scleroderma, diffuse cutaneous systemic scleroderma, progressive cutaneous systemic sclerosis
Description
Diffuse cutaneous systemic sclerosis (dcSSc) is a subtype of Systemic Sclerosis (SSc; see this term) characterized by truncal and acral skin fibrosis with an early and significant incidence of diffuse involvement (interstitial lung disease, oliguric renal failure, diffuse gastrointestinal disease, and myocardial involvement).
Most common symptoms of DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS
- Muscle weakness
- Pain
- Flexion contracture
- Hypertension
- Dysphagia
More info about DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS
SOURCES: ORPHANET
Search interest in CCR6
Potential gene panels for CCR6 gene
CCR6 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the CCR6 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 KCNA5 TGFBI KANK2 NKX2-1 KAT6B COL6A1 MVK