FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term bilirubin metabolic disorder ID (Ontology) DOID:2741 (Human Disease)
Definition An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism.
Also Known As "hereditary hyperbilirubinemia" ; "hyperbilirubinemia"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship: 
disease of metabolism__
genetic disease________|
                       inherited metabolic disorder
                        |__bilirubin metabolic disorder  25 rec.
                            |__Crigler-Najjar syndrome 24 rec.
                            |__Dubin-Johnson syndrome 1 rec.
                            |__Gilbert syndrome 24 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a inherited metabolic disorder
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "hereditary hyperbilirubinemia" EXACT
    "hyperbilirubinaemia" RELATED
    "hyperbilirubinemia" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
MESH:D006932
MESH:D006933
NCI:C84761
SNOMEDCT_US_2023_03_01:154770008
UMLS_CUI:C0020433
UMLS_CUI:C0020435