TNFSF4 gene related symptoms and diseases

All the information presented here about the TNFSF4 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,HGNC,NCBIGENE,ORPHANET, Mendelian Rare Disease Search Engine.

Top 5 symptoms and clinical features associated to TNFSF4 gene

Symptoms // Phenotype % Cases
Neoplasm Uncommon - Between 30% and 50% cases
Increased antibody level in blood Uncommon - Between 30% and 50% cases
Hemolytic anemia Uncommon - Between 30% and 50% cases
Abnormality of the skin Uncommon - Between 30% and 50% cases
Memory impairment Uncommon - Between 30% and 50% cases

Other less frequent symptoms and clinical features

Patients with TNFSF4 gene alterations may also develop some of the following symptoms and phenotypes:
  • Not very common - Between 30% and 50% cases

  • Psychosis
  • Cutaneous photosensitivity
  • Inflammatory abnormality of the skin
  • Vasculitis
  • Purpura
  • Leukopenia
  • Systemic lupus erythematosus
  • Nephritis

And 54 more phenotypes, you can get all of them using our tools for rare diseases.

Rare diseases associated to TNFSF4 gene

Here you will find a list of rare diseases related to the TNFSF4. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


NARCOLEPSY TYPE 1

Alternate names

NARCOLEPSY TYPE 1 Is also known as gÉlineau disease, narcoleptic syndrome 1, narcolepsy-cataplexy

Description

Narcolepsy with cataplexy is a sleep disorder characterized by excessive day-time sleepiness associated with uncontrollable sleep urges and cataplexy (loss of muscle tone often triggered by pleasant emotions).

Most common symptoms of NARCOLEPSY TYPE 1

  • Neoplasm
  • Obesity
  • Hyperactivity
  • Abnormality of the eye
  • Paralysis


More info about NARCOLEPSY TYPE 1

SOURCES: ORPHANET OMIM

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

MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO


Potential gene panels for TNFSF4 gene

AllNeuro panel Panel

Germany.

By Centogene AG - the Rare Disease Company AllNeuro panel that also includes the following genes: BCS1L ROR2 RPL10 BDNF RPS6KA3 RTN2 RYR1 SACS BIN1 SBF1

More info about this panel
Germany.

TNFSF4 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the TNFSF4 gene.

More info about this panel
United States.

Immune Report Card Panel

United States.

By OmniSeq, Inc. Immune Report Card that also includes the following genes: CXCL10 STAT1 TBX21 TGFB1 TNF TNFRSF14 TNFRSF18 CD40 CD27 TNFRSF9

More info about this panel
United States.

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