NRXN3 gene related symptoms and diseases
All the information presented here about the NRXN3 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to NRXN3 gene
|Symptoms // Phenotype||% Cases|
|Sensorineural hearing impairment||Very Common - Between 80% and 100% cases|
|Myocarditis||Very Common - Between 80% and 100% cases|
|Cheilitis||Very Common - Between 80% and 100% cases|
|Elevated C-reactive protein level||Very Common - Between 80% and 100% cases|
|Inflammatory abnormality of the eye||Very Common - Between 80% and 100% cases|
Other less frequent symptoms and clinical featuresPatients with NRXN3 gene alterations may also develop some of the following symptoms and phenotypes:
Commonly - More than 50% cases
- Recurrent pharyngitis
- Abnormal myocardium morphology
- Tubulointerstitial nephritis
- Ascending tubular aorta aneurysm
- Aortic root aneurysm
- Acute kidney injury
And 58 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to NRXN3 gene
Here you will find a list of rare diseases related to the NRXN3. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
KAWASAKI DISEASE Is also known as kd, infantile polyarteritis, mucocutaneous lymph node syndrome
Kawasaki disease (KD) is a febrile, systemic, self-limiting vasculitis affecting children and characterized by inflammation in the medium sized vessels associated with coronary arterial aneurysms (CAA) that may be life threatening when untreated. KD is the most common cause of acquired heart disease in children in developed countries and is a risk factor for ischemic heart disease in adulthood.
Most common symptoms of KAWASAKI DISEASE
- Sensorineural hearing impairment
More info about KAWASAKI DISEASE
Search interest in NRXN3
Potential gene panels for NRXN3 gene
By Fulgent Genetics Fulgent Genetics
This panel specifically test the NRXN3 gene.More info about this panel
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