| LiverAtlas Disease ID | HuLDi00145 |
| Name | Gilbert syndrome |
| Description | | Xref: |
| Definition | 1.A benign familial disorder, transmitted as an autosomal dominant trait. It is characterized by low-grade chronic hyperbilirubinemia with considerable daily fluctuations of the bilirubin level. | Xref: MeSH2011_6_17:D005878 |
| 2.An autosomal recessive inherited disorder characterized by unconjugated hyperbilirubinemia, resulting in harmless intermittent jaundice. | Xref: UMLS2011AA:C0017551 |
|
| Synonym | Arias Type Hyperbilirubinemia | EXACT | Xref: MeSH2011_6_17:D005878 |
| Arias Type Hyperbilirubinemias | EXACT | Xref: MeSH2011_6_17:D005878 |
| Disease, Gilbert | EXACT | Xref: MeSH2011_6_17:D005878 |
| Disease, Gilbert's | EXACT | Xref: MeSH2011_6_17:D005878 |
| Gilbert Disease | EXACT | Xref: MeSH2011_6_17:D005878 |
| Gilbert Syndrome | EXACT | Xref: MeSH2011_6_17:D005878 |
| Gilbert syndrome | EXACT | Xref: HumanDO2011_6_18:DOID:2739 |
| Gilbert's Disease | EXACT | Xref: MeSH2011_6_17:D005878 |
| Gilbert's disease | EXACT | Xref: SNOMEDCT_2005_07_31:154770008 |
| Gilbert's Syndrome | EXACT | Xref: MeSH2011_6_17:D005878 |
| Gilberts Disease | EXACT | Xref: MeSH2011_6_17:D005878 |
| Gilberts Syndrome | EXACT | Xref: MeSH2011_6_17:D005878 |
| Hyperbilirubinemia 1 | EXACT | Xref: MeSH2011_6_17:D005878 |
| Hyperbilirubinemia 1s | EXACT | Xref: MeSH2011_6_17:D005878 |
| Hyperbilirubinemia, Arias Type | EXACT | Xref: MeSH2011_6_17:D005878 |
| Hyperbilirubinemias, Arias Type | EXACT | Xref: MeSH2011_6_17:D005878 |
| Syndrome, Gilbert | EXACT | Xref: MeSH2011_6_17:D005878 |
| Syndrome, Gilbert's | EXACT | Xref: MeSH2011_6_17:D005878 |
|
| Xref | Clinical Hepatology,2004.Page 581 |
| HumanDO2011_6_18:DOID:2739 |
| MeSH2011_6_17:D005878 |
| Schiff's Diseases of the LIVER,10ed:Page 229 |
| UMLS2011AA:C0017551 |
|
| Genetics Relation | Gene/Protein/Pathway |
| Gene:UGT1A1 |
| Protein: |
|
