Hyperbilirubinemia, Hereditary
Disease ID: disease_node_4077
Connections displayed (default: 10).
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| Dbxref | MESH:D006932, MESH:D006933, NCI:C84761, SNOMEDCT_US_2023_03_01:154770008, UMLS_CUI:C0020433, UMLS_CUI:C0020435 |
|---|---|
| Subclassof | DOID_655 |
| Data Source | DOID, MESH |
| Synonyms | hereditary hyperbilirubinemia, hyperbilirubinemia, hyperbilirubinaemia |
| Mesh Id | D006933 |
| Mesh Label | Hyperbilirubinemia, Hereditary |
| Mesh Subclassof | D008661 |
| Doid Label | bilirubin metabolic disorder |
| Doid Description | An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism. |
| Disease Node Id | disease_node_4077 |
| Doid Id | DOID_2741 |
| Label | Hyperbilirubinemia, Hereditary |
| Doid Alternate Ids | DOID_2740 |
- Incoming r'ship
SUBCLASS_OFto/from Jaundice, Chronic Idiopathic(ID:disease_node_4363) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Metabolism, Inborn Errors(ID:disease_node_5171) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Gilbert Disease(ID:disease_node_3450) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Crigler-Najjar Syndrome(ID:disease_node_2312) (Disease)