IL32 gene related symptoms and diseases

All the information presented here about the IL32 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 IL32 gene

Symptoms // Phenotype % Cases
Neoplasm Very Common - Between 80% and 100% cases
Lymphadenopathy Very Common - Between 80% and 100% cases
Abnormal immunoglobulin level Very Common - Between 80% and 100% cases
Abnormal lymphocyte morphology Very Common - Between 80% and 100% cases
T-cell lymphoma Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with IL32 gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Lichenification
  • Abnormality of the pleura
  • Gangrene
  • Irregular hyperpigmentation
  • Erythroderma
  • Ectropion
  • Neoplasm of the skin
  • Thickened skin

And 21 more phenotypes, you can get all of them using our tools for rare diseases.


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Rare diseases associated to IL32 gene

Here you will find a list of rare diseases related to the IL32. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


Alternate names

SÉZARY SYNDROME Is also known as sÉzary lymphoma


Sézary syndrome (SS) is an aggressive form of cutaneous T-cell lymphoma characterized by a triad of erythroderma, lymphadenopathy and circulating atypical lymphocytes (Sézary cells).

Most common symptoms of SÉZARY SYNDROME

  • Neoplasm
  • Abnormal facial shape
  • Peripheral neuropathy
  • Hepatomegaly
  • Fever

More info about SÉZARY SYNDROME


Potential gene panels for IL32 gene

IL32 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the IL32 gene.

More info about this panel

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