UGT1A5 gene related symptoms and diseases
All the information presented here about the UGT1A5 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: OMIM,NCBIGENE,HGNC, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to UGT1A5 gene
|Symptoms // Phenotype||% Cases|
|Intellectual disability||Very Common - Between 80% and 100% cases|
|Increased mean corpuscular volume||Very Common - Between 80% and 100% cases|
|Leukocytosis||Very Common - Between 80% and 100% cases|
|Osteomyelitis||Very Common - Between 80% and 100% cases|
|Microcytic anemia||Very Common - Between 80% and 100% cases|
Other less frequent symptoms and clinical featuresPatients with UGT1A5 gene alterations may also develop some of the following symptoms and phenotypes:
Commonly - More than 50% cases
- Myeloid leukemia
- Iron deficiency anemia
- Poor appetite
- Aseptic necrosis
- Abnormality of the vasculature
And 57 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to UGT1A5 gene
Here you will find a list of rare diseases related to the UGT1A5. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
SICKLE CELL ANEMIA
SICKLE CELL ANEMIA Is also known as sickle cell disease
Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: severe anemia, severe bacterial infections, and ischemic vasoocclusive accidents (VOA) caused by sickle-shaped red blood cells obstructing small blood vessels and capillaries. Many diverse complications can occur.
Most common symptoms of SICKLE CELL ANEMIA
- Intellectual disability
More info about SICKLE CELL ANEMIA
Search interest in UGT1A5
Potential gene panels for UGT1A5 gene
By Fulgent Genetics Fulgent Genetics
This panel specifically test the UGT1A5 gene.More info about this panel