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
Search interest in COMMD10
Potential gene panels for COMMD10 gene
COMMD10 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the COMMD10 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 ROBO1 PRPH AARS2 CACNA1F GATA2 KDM2B ALDOB