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.

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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.


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Hyperbiliverdinemia Recommended genes panels

Panel Name, Specifity and genes Tested/covered
BLVRA.

By Fulgent Genetics Fulgent Genetics (United States).

BLVRA
Specificity
100 %
Genes
100 %

We have -7 more panels available in our App

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Sources and references

You can check the following sources for additional information.

ORPHANET OMIM Rare Disease Search Engine

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