Gilbert syndrome
Information
- Disease name
- Gilbert syndrome
- Disease ID
- DOID:2739
- Description
- "A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin as bilirubin is not being conjugated as a result of reduced glucuronyltransferase activity." [url:http\://en.wikipedia.org/wiki/Gilbert%27s_syndrome]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT06336369 | Recruiting | Brown Adipose Tissue Activity in Gilbert's Syndrome | March 6, 2024 | January 15, 2027 |
- Disase is a (Disease Ontology)
- DOID:2741
- Cross Reference ID (Disease Ontology)
- GARD:6507
- Cross Reference ID (Disease Ontology)
- ICD10CM:E80.4
- Cross Reference ID (Disease Ontology)
- MESH:D005878
- Cross Reference ID (Disease Ontology)
- MIM:143500
- Cross Reference ID (Disease Ontology)
- NCI:C84729
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:27503000
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0017551
- Exact Synonym (Disease Ontology)
- Constitutional hyperbilirubinemia
- Exact Synonym (Disease Ontology)
- Gilbert's disease
- Exact Synonym (Disease Ontology)
- Gilbert's syndrome
- Exact Synonym (Disease Ontology)
- Gilbert-Meulengracht syndrome
- Exact Synonym (Disease Ontology)
- hereditary nonhemolytic jaundice
- ICD10 preferred id (Insert disease from ICD10)
- D0003925
- ICD10 class code (Insert disease from ICD10)
- E80.4