Caroli Syndrome
Disease ID: disease_node_15475
Connections displayed (default: 10).
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| Dbxref | GARD:6002 |
|---|---|
| Subclassof | DOID_272, DOID_225, DOID_0050737, DOID_866, DOID_4138 |
| Data Source | DOID |
| Disease Has Location | UBERON_0002017, UBERON_0002107, UBERON_0002394 |
| Doid Label | Caroli syndrome |
| Doid Description | A syndrome that is characterized by the presence of associated congenital hepatic fibrosis and that is associated with autosomal recessive polycystic kidney disease. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15475 |
| Doid Id | DOID_0081394 |
| Label | Caroli Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hepatic Vascular Disease(ID:disease_node_15427) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Vein Disease(ID:disease_node_13127) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Bile Duct Diseases(ID:disease_node_1523) (Disease)