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.

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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

SOURCES: MESH OMIM ORPHANET

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


Potential gene panels for ADAM22 gene

ADAM22 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the ADAM22 gene.

More info about this panel


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