Polycystic Kidney, Autosomal Recessive
Disease ID: disease_node_9012
Connections displayed (default: 10).
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| Dbxref | GARD:8378, ICD10CM:Q61.1, ICD9CM:753.14, MESH:D017044, NCI:C84579, ORDO:731, SNOMEDCT_US_2023_03_01:28770003, UMLS_CUI:C0085548 |
|---|---|
| Subclassof | DOID_0080322, DOID_0050737 |
| Data Source | DOID, MESH |
| Synonyms | AR-PKD |
| Mesh Id | D017044 |
| Mesh Label | Polycystic Kidney, Autosomal Recessive |
| Mesh Subclassof | D007690 |
| Doid Label | autosomal recessive 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 recessive fashion. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_9012 |
| Doid Id | DOID_0110861 |
| Label | Polycystic Kidney, Autosomal Recessive |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Polycystic Kidney Disease 4(ID:disease_node_13257) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Polycystic Kidney Disease 5(ID:disease_node_13258) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Polycystic Kidney Disease(ID:disease_node_13256) (Disease)