ETS1 gene related symptoms and diseases

All the information presented here about the ETS1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,OMIM,HGNC,ORPHANET, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to ETS1 gene

Symptoms // Phenotype % Cases
Seizures Very Common - Between 80% and 100% cases
Aseptic necrosis Very Common - Between 80% and 100% cases
Abnormality of coagulation Very Common - Between 80% and 100% cases
Increased antibody level in blood Very Common - Between 80% and 100% cases
Abnormality of the thyroid gland Very Common - Between 80% and 100% cases

Other less frequent symptoms and clinical features

Patients with ETS1 gene alterations may also develop some of the following symptoms and phenotypes:
  • Commonly - More than 50% cases

  • Autoimmune hemolytic anemia
  • Pericarditis
  • Thyroiditis
  • Autoimmune thrombocytopenia
  • Epiphyseal stippling
  • Glomerulonephritis
  • Hashimoto thyroiditis
  • Gangrene

And 29 more phenotypes, you can get all of them using our tools for rare diseases.

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Rare diseases associated to ETS1 gene

Here you will find a list of rare diseases related to the ETS1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


SYSTEMIC LUPUS ERYTHEMATOSUS


Alternate names

SYSTEMIC LUPUS ERYTHEMATOSUS Is also known as disseminated lupus erythematosus, sle

Description

Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by production of autoantibodies against nuclear, cytoplasmic, and cell surface molecules that transcend organ-specific boundaries. Tissue deposition of antibodies or immune complexes induces inflammation and subsequent injury of multiple organs and finally results in clinical manifestations of SLE, including glomerulonephritis, dermatitis, thrombosis, vasculitis, seizures, and arthritis. Evidence strongly suggests the involvement of genetic components in SLE susceptibility (summary by Oishi et al., 2008). Genetic Heterogeneity of Systemic Lupus ErythematosusAn autosomal recessive form of systemic lupus erythematosus (SLEB16 ) is caused by mutation in the DNASE1L3 gene (OMIM ) on chromosome 3p14.3.See MAPPING and MOLECULAR GENETICS sections for a discussion of genetic heterogeneity of susceptibility to SLE.

Most common symptoms of SYSTEMIC LUPUS ERYTHEMATOSUS

  • Seizures
  • Short stature
  • Cognitive impairment
  • Anemia
  • Fatigue


More info about SYSTEMIC LUPUS ERYTHEMATOSUS

SOURCES: OMIM ORPHANET


Potential gene panels for ETS1 gene

ETS1 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the ETS1 gene.

More info about this panel

FoundationOne® Heme Panel

United States.

By Foundation Medicine, Inc. FoundationOne® Heme that also includes the following genes: BCL6 BCL7A ROS1 RUNX1 BLM SDHA SDHB SDHC SDHD SF3B1

More info about this panel

Tempus xT assay Panel

United States.

By Tempus Labs, Inc. Tempus xT assay that also includes the following genes: BCL6 RIT1 BCL7A BCR ROS1 RPL5 RPS15 RPS6KB1 RUNX1 RXRA

More info about this panel

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


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