IL12A-AS1 gene related symptoms and diseases
All the information presented here about the IL12A-AS1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,HGNC,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to IL12A-AS1 gene
Symptoms // Phenotype | % Cases |
---|---|
Seizures | Very Common - Between 80% and 100% cases |
Glomerulopathy | Very Common - Between 80% and 100% cases |
Raynaud phenomenon | Very Common - Between 80% and 100% cases |
Gangrene | Very Common - Between 80% and 100% cases |
Pulmonary infiltrates | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with IL12A-AS1 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Pustule
- Uveitis
- Aseptic necrosis
- Pulmonary embolism
- Hemoptysis
- Pericarditis
- Keratoconjunctivitis sicca
- Blurred vision
And 94 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to IL12A-AS1 gene
Here you will find a list of rare diseases related to the IL12A-AS1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
BEHÇET DISEASE
Alternate names
BEHÇET DISEASE Is also known as bd, behcet disease
Description
Behçet's disease (BD) is a chronic, relapsing, multisystemic vasculitis characterized by mucocutaneous lesions, as well as articular, vascular, ocular and central nervous system manifestations.
Most common symptoms of BEHÇET DISEASE
- Seizures
- Ataxia
- Neoplasm
- Pain
- Cataract
More info about BEHÇET DISEASE
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