FCGR2A gene related symptoms and diseases
All the information presented here about the FCGR2A 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 FCGR2A gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Respiratory distress | Uncommon - Between 30% and 50% cases |
| Allergy | Uncommon - Between 30% and 50% cases |
| Acute kidney injury | Uncommon - Between 30% and 50% cases |
| Elevated C-reactive protein level | Uncommon - Between 30% and 50% cases |
| Nausea and vomiting | Uncommon - Between 30% and 50% cases |
Other less frequent symptoms and clinical features
Patients with FCGR2A gene alterations may also develop some of the following symptoms and phenotypes:Not very common - Between 30% and 50% cases
- Skin rash
- Vasculitis
- Respiratory tract infection
- Pericarditis
- Arthritis
- Thrombocytopenia
- Abdominal pain
- Anemia
And 178 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to FCGR2A gene
Here you will find a list of rare diseases related to the FCGR2A. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
KAWASAKI DISEASE
Alternate names
KAWASAKI DISEASE Is also known as kd, infantile polyarteritis, mucocutaneous lymph node syndrome
Description
Kawasaki disease (KD) is a febrile, systemic, self-limiting vasculitis affecting children and characterized by inflammation in the medium sized vessels associated with coronary arterial aneurysms (CAA) that may be life threatening when untreated. KD is the most common cause of acquired heart disease in children in developed countries and is a risk factor for ischemic heart disease in adulthood.
Most common symptoms of KAWASAKI DISEASE
- Sensorineural hearing impairment
- Ptosis
- Fever
- Fatigue
- Edema
More info about KAWASAKI DISEASE
CYSTIC FIBROSIS
Alternate names
CYSTIC FIBROSIS Is also known as mucoviscidosis, cf
Description
Cystic fibrosis (CF) is a genetic disorder characterized by the production of sweat with a high salt content and mucus secretions with an abnormal viscosity.
Most common symptoms of CYSTIC FIBROSIS
- Growth delay
- Neoplasm
- Failure to thrive
- Pain
- Hypertension
More info about CYSTIC FIBROSIS
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
MALARIA
Description
Malaria is a preventable life-threatening parasitic disease caused by Plasmodium (P. ) parasites that are transmitted by Anophles mosquito bites to humans and is typically clinically characterized by attacks of fever, headache, chills and vomiting.
Most common symptoms of MALARIA
- Cognitive impairment
- Anemia
- Fever
- Respiratory distress
- Headache
More info about MALARIA
Search interest in FCGR2A
Potential gene panels for FCGR2A gene
Cobalamin/Propionate/Homocysteine Metabolism Related Disorders Panel, Sequencing and Deletion/Duplication Panel
United States.
By ARUP Laboratories, Molecular Genetics and Genomics Cobalamin/Propionate/Homocysteine Metabolism Related Disorders Panel, Sequencing and Deletion/Duplication that also includes the following genes: SUCLA2 SUCLG1 TCN1 TCN2 AMN CBS MCEE MMAA MMAB LMBRD1
More info about this panel United States.
FCGR2A Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the FCGR2A gene.
More info about this panel United States.
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 United States.
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like DLG3 SLC16A1 PMM2 TWNK SLC4A1 AUTS2 A4GALT