Hyperbiliverdinemia
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.
Clinical Features
Top most frequent phenotypes and symptoms related to Hyperbiliverdinemia
- Fatigue
- Encephalopathy
- Jaundice
- Elevated hepatic transaminase
- Nausea
- Hepatic failure
- Ascites
- Cholestasis
- Decreased liver function
- Cholelithiasis
And another 4 symptoms. If you need more information about this disease we can help you.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Hyperbiliverdinemia Is also known as green jaundice.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Hyperbiliverdinemia Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 BLVRA.
By Fulgent Genetics Fulgent Genetics (United States).
BLVRA
Specificity
100 %
Genes
100 % |
You can get up to -7 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
ORPHANET OMIM Rare Disease Search EngineIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like MULTIPLE FIBROADENOMAS OF THE BREAST; MFAB MICROCEPHALY-LYMPHEDEMA-CHORIORETINOPATHY SYNDROME OPSISMODYSPLASIA; OPSMD OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE; OSMEDB KOOLEN-DE VRIES SYNDROME; KDVS