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.

Mendelian

Accelerate your rare disease diagnosis with us

Learn more

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


Potential gene panels for CCR6 gene

CCR6 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the CCR6 gene.

More info about this panel


If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SERPINA6 SRY SHMT1 ERRFI1 ZBTB24

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more