FCGR3B gene related symptoms and diseases
All the information presented here about the FCGR3B gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,OMIM,NCBIGENE,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to FCGR3B gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Seizures | Common - Between 50% and 80% cases |
| Arthritis | Common - Between 50% and 80% cases |
| Pericarditis | Common - Between 50% and 80% cases |
| Glomerulonephritis | Common - Between 50% and 80% cases |
| Purpura | Common - Between 50% and 80% cases |
Other less frequent symptoms and clinical features
Patients with FCGR3B gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Vasculitis
- Pleuritis
- Skin rash
- Autoimmunity
- Gangrene
- Fatigue
Not very common - Between 30% and 50% cases
- Aseptic necrosis
- Elevated C-reactive protein level
And 118 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to FCGR3B gene
Here you will find a list of rare diseases related to the FCGR3B. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
GRANULOMATOSIS WITH POLYANGIITIS
Alternate names
GRANULOMATOSIS WITH POLYANGIITIS Is also known as wegener granulomatosis, formerly, gpa, wg, formerly
Description
Granulomatosis with polyangiitis is a small-vessel necrotizing vasculitis characterised by the association of inflammation of the vessel wall and peri- and extravascular granulomatosis.
Most common symptoms of GRANULOMATOSIS WITH POLYANGIITIS
- Seizures
- Hearing impairment
- Sensorineural hearing impairment
- Pain
- Visual impairment
More info about GRANULOMATOSIS WITH POLYANGIITIS
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).
Most common symptoms of SYSTEMIC LUPUS ERYTHEMATOSUS
- Seizures
- Short stature
- Cognitive impairment
- Anemia
- Fatigue
More info about SYSTEMIC LUPUS ERYTHEMATOSUS
NEONATAL ALLOIMMUNE NEUTROPENIA
Search interest in FCGR3B
Potential gene panels for FCGR3B gene
Defects of phagocytosis Panel Panel
Germany.
By CeGaT GmbH Defects of phagocytosis Panel that also includes the following genes: STAT1 TAZ TCIRG1 TCN2 TERT WAS WIPF1 ACTB VPS45 HPS3
More info about this panel Germany.
Neutrophil Antigen Genotyping Panel (includes HNA-1, 3, 4, 5) Panel
United States.
By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti Neutrophil Antigen Genotyping Panel (includes HNA-1, 3, 4, 5) that also includes the following genes: SLC44A2 CD177 FCGR3B ITGAL ITGAM
More info about this panel United States.
FCGR3B Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the FCGR3B gene.
More info about this panel United States.
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