BLVRA gene related symptoms and diseases
All the information presented here about the BLVRA gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: NCBIGENE,HGNC,OMIM,ORPHANET, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to BLVRA gene
Symptoms // Phenotype | % Cases |
---|---|
Fatigue | Very Common - Between 80% and 100% cases |
Encephalopathy | Very Common - Between 80% and 100% cases |
Jaundice | Very Common - Between 80% and 100% cases |
Elevated hepatic transaminase | Very Common - Between 80% and 100% cases |
Nausea | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with BLVRA gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Hepatic failure
- Ascites
- Cholestasis
- Decreased liver function
- Cholelithiasis
- Malnutrition
- Esophageal varix
- Biliary atresia
And 1 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to BLVRA gene
Here you will find a list of rare diseases related to the BLVRA. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
HYPERBILIVERDINEMIA
Alternate names
HYPERBILIVERDINEMIA Is also known as green jaundice
Description
Hyperbiliverdinemia is a rare, genetic hepatic disease characterized by the presence of green coloration of the skin, urine, plasma and other body fluids (ascites, breastmilk) or parts (sclerae) due to increased serum levels of biliverdin in association with biliary obstruction and/or liver failure. Association with malnutrition, medication, and congenital biliary atresia has also been reported.
Most common symptoms of HYPERBILIVERDINEMIA
- Fatigue
- Encephalopathy
- Jaundice
- Elevated hepatic transaminase
- Nausea
More info about HYPERBILIVERDINEMIA
Search interest in BLVRA
Potential gene panels for BLVRA gene
BLVRA Panel
By Fulgent Genetics Fulgent Genetics
This panel specifically test the BLVRA gene.
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 NPHP3-ACAD11 PIK3CA CD96 ALX1 AXL WIPF1 ARMC9