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| Term | Dubin-Johnson syndrome | ID (Ontology) | DOID:12308 (Human Disease) |
| Definition | A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin without elevation of liver alanine transaminase and aspartate transaminase enzymes as a result of the deficient ability of hepatocytes to secrete conjugated bilirubin into the bile. | ||
| Also Known As | "chronic idiopathic jaundice" ; "Dubin Johnson syndrome" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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inherited metabolic disorder |__bilirubin metabolic disorder |__Dubin-Johnson syndrome 1 rec. |
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| Is a | bilirubin metabolic disorder | ||
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External Crossreferences & Linkouts
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GARD:6289 ICD10CM:E80.6 MESH:D007566 MIM:237500 NCI:C34741 SNOMEDCT_US_2023_03_01:44553005 UMLS_CUI:C0022350 |
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