ADAM22 gene related symptoms and diseases
All the information presented here about the ADAM22 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to ADAM22 gene
Symptoms // Phenotype | % Cases |
---|---|
Anemia | Uncommon - Between 30% and 50% cases |
Dyspareunia | Uncommon - Between 30% and 50% cases |
Acute hepatic failure | Uncommon - Between 30% and 50% cases |
Dysuria | Uncommon - Between 30% and 50% cases |
Abnormal myocardium morphology | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with ADAM22 gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Entropion
- Excessive salivation
- Abnormality of the pleura
- Esophageal stricture
- Acantholysis
- Abnormality of neutrophils
- Abnormality of the urethra
- Hypokalemic metabolic alkalosis
And 44 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to ADAM22 gene
Here you will find a list of rare diseases related to the ADAM22. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
STEVENS-JOHNSON SYNDROME
Alternate names
STEVENS-JOHNSON SYNDROME Is also known as dermatostomatitis, stevens johnson type
Description
Stevens-Johnson syndrome is a limited form of toxic epidermal necrolysis (see this term) characterized by destruction and detachment of the skin epithelium and mucous membranes involving less than 10% of the body surface area.
Most common symptoms of STEVENS-JOHNSON SYNDROME
- Anemia
- Visual impairment
- Fever
- Fatigue
- Dysphagia
More info about STEVENS-JOHNSON SYNDROME
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61; EIEE61
Most common symptoms of EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61; EIEE61
- Intellectual disability
- Seizures
- Generalized hypotonia
- Microcephaly
- Spasticity
More info about EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 61; EIEE61
SOURCES: OMIM
Search interest in ADAM22
Potential gene panels for ADAM22 gene
ADAM22 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the ADAM22 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 PGM3 ESPN SGCB AGPS TRAPPC9 SMPD1 ALDH5A1