COMMD10 gene related symptoms and diseases

All the information presented here about the COMMD10 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 COMMD10 gene

Symptoms // Phenotype % Cases
Seizures Very Common - Between 80% and 100% cases
Petechiae Very Common - Between 80% and 100% cases
Tracheal stenosis Very Common - Between 80% and 100% cases
Myositis Very Common - Between 80% and 100% cases
Gangrene Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with COMMD10 gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Pulmonary infiltrates
  • Hemoptysis
  • Wheezing
  • Pericarditis
  • Glomerulopathy
  • Elevated erythrocyte sedimentation rate
  • Restrictive ventilatory defect
  • Angina pectoris

And 87 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to COMMD10 gene

Here you will find a list of rare diseases related to the COMMD10. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


GRANULOMATOSIS WITH POLYANGIITIS

Alternate names

GRANULOMATOSIS WITH POLYANGIITIS Is also known as wegener granulomatosis, formerly, gpa, wg, formerly

Description

Granulomatosis with polyangiitis is a small-vessel necrotizing vasculitis characterised by the association of inflammation of the vessel wall and peri- and extravascular granulomatosis.

Most common symptoms of GRANULOMATOSIS WITH POLYANGIITIS

  • Seizures
  • Hearing impairment
  • Sensorineural hearing impairment
  • Pain
  • Visual impairment


More info about GRANULOMATOSIS WITH POLYANGIITIS

SOURCES: ORPHANET OMIM MESH


Potential gene panels for COMMD10 gene

COMMD10 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the COMMD10 gene.

More info about this panel
United States.

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like ROBO1 PRPH AARS2 CACNA1F GATA2 KDM2B ALDOB