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Diseases
Hyperbilirubinemia, Hereditary
hyperbilirubinemia, hereditary
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
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Core Information
- Disease Name
- Hyperbilirubinemia, Hereditary
- Standard Disease Name
- hyperbilirubinemia, hereditary
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D006933
- OMIM ID
- No data
- UMLS ID
- C0020435
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:An 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.|MSH2017_2016_08_12:Inborn errors of bilirubin metabolism resulting in excessive amounts of bilirubin in the circulating blood, either because of increased bilirubin production or because of delayed clearance of bilirubin from the blood.|CSP2006:inborn errors of bilirubin metabolism resulting in excessive amounts of bilirubin in the circulating blood, either because of increased bilirubin production or because of delayed clearance of bilirubin from the blood.
Related
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Related Targets
target disease8 Targets
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