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Disease Ontology Browser
Gilbert syndrome (DOID:2739)
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Synonyms: Constitutional hyperbilirubinemia; Gilbert's disease; Gilbert's syndrome; Gilbert-Meulengracht syndrome; hereditary nonhemolytic jaundice
Alt IDs: OMIM:143500, ICD10CM:E80.4, MESH:D005878, NCI:C84729, UMLS_CUI:C0017551
Definition: A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin as bilirubin is not being conjugated as a result of reduced glucuronyltransferase activity.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.13
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