UBAC2 gene related symptoms and diseases
All the information presented here about the UBAC2 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,ORPHANET,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to UBAC2 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 UBAC2 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 UBAC2 gene
Here you will find a list of rare diseases related to the UBAC2. 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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