| General Information | |||
|---|---|---|---|
| Term | Gilbert syndrome | ID (Ontology) | DOID:2739 (Human Disease) |
| 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. | ||
| Also Known As | "Constitutional hyperbilirubinemia" ; "Gilbert's disease" ; "Gilbert's syndrome" (for all, see Synonyms field below) | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| 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
|
|||
|
||||||
inherited metabolic disorder |__bilirubin metabolic disorder |__Gilbert syndrome 24 rec. |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | bilirubin metabolic disorder | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
GARD:6507 ICD10CM:E80.4 MESH:D005878 MIM:143500 NCI:C84729 SNOMEDCT_US_2023_03_01:27503000 UMLS_CUI:C0017551 |
|||