UGT1A9 gene related symptoms and diseases
All the information presented here about the UGT1A9 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,OMIM, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to UGT1A9 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 features
Patients with UGT1A9 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Myeloid leukemia
- Wheezing
- Iron deficiency anemia
- Poor appetite
- Aseptic necrosis
- Reticulocytosis
- Thrombocytosis
- Abnormality of the vasculature
And 57 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to UGT1A9 gene
Here you will find a list of rare diseases related to the UGT1A9. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
SICKLE CELL ANEMIA
Alternate names
SICKLE CELL ANEMIA Is also known as sickle cell disease
Description
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
- Pain
- Anemia
- Hypertension
- Hepatomegaly
More info about SICKLE CELL ANEMIA
Search interest in UGT1A9
Potential gene panels for UGT1A9 gene
UGT1A9 Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the UGT1A9 gene.
More info about this panelTempus xT assay Panel
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 panelIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like ZNF674 TNFRSF11A COL4A2 SMPD1 SMC1A ANO3 MYOM1