| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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. (Human Disease Ontology, DOID_2739) |
| External Link | http://www.omim.org/entry/143500 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the [gilbert syndrome] phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| UGT1A1 | UDP glucuronosyltransferase 1 family, polypeptide A1 |
