Hereditary hyperbilirubinemia
MONDO:0002408An inherited disorder affecting the metabolism of bilirubin. It results in increased levels of bilirubin in the blood. Representative examples of this condition include Gilbert syndrome and Crigler-Najjar syndrome.
Also known as: bilirubin metabolic disorder, hyperbilirubinaemia, hyperbilirubinemia, hereditary hyperbilirubinemia
18 clinical trials for this condition and its sub-types, 0 tagged with Hereditary hyperbilirubinemia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Hereditary hyperbilirubinemia
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Crigler-Najjar syndrome 0 trials
2 sub-types
- Crigler-Najjar syndrome type 1 0 trials
- Crigler-Najjar syndrome type 2 0 trials
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Dubin-Johnson syndrome 0 trials
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Gilbert syndrome 0 trials
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Rotor syndrome 0 trials
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Hyperbilirubinemia, shunt, primary 0 trials
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Could a simple hat make jaundice treatment kinder for newborns?
Symptom relief By invitation onlyThis study tests whether a special hat with built-in goggles can make phototherapy more comfortable for full-term newborns with jaundice, compared to standard eye patches. Researchers will measure the babies' comfort levels, bilirubin changes, treatment duration, and parental sat…
Sponsor: Karamanoğlu Mehmetbey University • Aim: Symptom relief
Last updated Aug 07, 2026 00:00 UTC
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Tiny sensors could revolutionize jaundice treatment for newborns
Knowledge-focused OngoingThis study tests a new wireless sensor that continuously measures the light dose babies receive during phototherapy for jaundice. Currently, doctors check light levels only once a day with a handheld device, which can be inaccurate. The sensor aims to provide real-time data to en…
Sponsor: McGill University Health Centre/Research Institute of the McGill University Health Centre • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:30 UTC