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MIRAGE
bilirubin metabolic disorder
Summary
- Synonym
-
- hereditary hyperbilirubinemia
- hyperbilirubinemia
- Definition
- An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism.
- Super Class
- inherited metabolic disorder
External Links
- Disease Ontology
- DOID:2741
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1244 | ABCC2 | ATP binding cassette subfamily C member 2 | |
| 3082 | HGF | hepatocyte growth factor | |
| 6648 | SOD2 | superoxide dismutase 2 | |
| 10599 | SLCO1B1 | solute carrier organic anion transporter family member 1B1 | |
| 28234 | SLCO1B3 | solute carrier organic anion transporter family member 1B3 | |
| 54658 | UGT1A1 | UDP glucuronosyltransferase family 1 member A1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q63120 | ATP-binding cassette sub-family C member 2 | |
| Q64550 | UDP-glucuronosyltransferase 1A1 | |
| Q9QZX8 | Solute carrier organic anion transporter family member 1B2 |
