RELB gene related symptoms and diseases

All the information presented here about the RELB 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 RELB gene

Symptoms // Phenotype % Cases
Immunodeficiency Very Common - Between 80% and 100% cases
Recurrent infections Very Common - Between 80% and 100% cases
Arthritis Very Common - Between 80% and 100% cases
Respiratory tract infection Very Common - Between 80% and 100% cases
Recurrent urinary tract infections Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

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

  • Joint swelling
  • Polyarticular arthritis
Mendelian

Accelerate your rare disease diagnosis with us

Learn more

Rare diseases associated to RELB gene

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


IMMUNODEFICIENCY 53; IMD53


Most common symptoms of IMMUNODEFICIENCY 53; IMD53

  • Immunodeficiency
  • Recurrent infections
  • Arthritis
  • Respiratory tract infection
  • Recurrent urinary tract infections


More info about IMMUNODEFICIENCY 53; IMD53

SOURCES: OMIM


Potential gene panels for RELB gene

Tempus xO assay Panel

United States.

By Tempus Labs, Inc. Tempus xO assay that also includes the following genes: BCL6 RHEB RIPK1 RIPK2 RIPK3 RIT1 BCL7A BCL9 BCR ROBO2

More info about this panel


If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like LRSAM1 DNAJC6 NONO NDUFS4 EFTUD2 NOS3 FOXC2

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more