Polycystic Kidney Diseases
Disease ID: disease_node_4502
Connections displayed (default: 10).
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| Dbxref | GARD:10413, ICD10CM:Q61.3, ICD9CM:753.12, MESH:D007690, NCI:C75464, ORDO:730, SNOMEDCT_US_2023_03_01:204955006, UMLS_CUI:C0022680 |
|---|---|
| Subclassof | DOID_0080322, DOID_0050736 |
| Data Source | DOID, MESH |
| Synonyms | ADPKD, Congenital biliary ectasias, POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1 |
| Mesh Id | D007690 |
| Mesh Label | Polycystic Kidney Diseases |
| Mesh Subclassof | D052177, D000015, D000072661 |
| Doid Label | autosomal domit polycystic kidney disease |
| Doid Description | A polycystic kidney disease characterized by the presence of multiple cysts located_in the kidney resulting from ciliopathy that disrupts the function of primary cilium, inherited in an autosomal domit fashion. Xref MGI. OMIM mapping confirmed by DO. [SN]. Updating outdated UMLS CUI. Removing Caroli disease as a synonym as this is a distinct disease. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_4502 |
| Doid Id | DOID_898 |
| Label | Polycystic Kidney Diseases |
- Incoming r'ship
SUBCLASS_OFto/from Polycystic Kidney Disease 1(ID:disease_node_19894) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Polycystic Kidney Disease 2(ID:disease_node_19893) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Polycystic Kidney Disease 6(ID:disease_node_19896) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Polycystic Kidney Disease 7(ID:disease_node_19895) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Polycystic Kidney Disease 3(ID:disease_node_19892) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Polycystic Kidney Disease(ID:disease_node_13256) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)