Gilbert Disease
Disease ID: disease_node_3450
Connections displayed (default: 10).
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| Dbxref | GARD:6507, ICD10CM:E80.4, MESH:D005878, MIM:143500, NCI:C84729, SNOMEDCT_US_2023_03_01:27503000, UMLS_CUI:C0017551 |
|---|---|
| Subclassof | DOID_2741 |
| Data Source | DOID, MESH |
| Synonyms | Constitutional hyperbilirubinemia, Gilbert's disease, Gilbert's syndrome, Gilbert-Meulengracht syndrome, hereditary nonhemolytic jaundice |
| Mesh Id | D005878 |
| Mesh Label | Gilbert Disease |
| Mesh Subclassof | D006933 |
| Doid Label | Gilbert syndrome |
| Doid 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. OMIM mapping confirmed by DO. [SN]. |
| Disease Node Id | disease_node_3450 |
| Doid Id | DOID_2739 |
| Label | Gilbert Disease |
- Outgoing r'ship
SUBCLASS_OFto/from Hyperbilirubinemia, Hereditary(ID:disease_node_4077) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hyperbilirubinemia(ID:disease_node_4076) (Disease)