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polycystic kidney disease 2
Summary
- Synonym
-
- Apkd2
- Pkd2
- Polycystic Kidney Disease, Adult, Type II
- Definition
- A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD2 gene on chromosome 4q22.1.
- Super Class
- autosomal dominant polycystic kidney disease
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000791 | Uric acid nephrolithiasis |
| HP:0004944 | Dilatation of the cerebral artery |
| HP:0000010 | Recurrent urinary tract infections |
| HP:0002616 | Aortic root aneurysm |
| HP:0012207 | Reduced sperm motility |
| HP:0000105 | Enlarged kidney |
| HP:0012592 | Albuminuria |
| HP:0000822 | Hypertension |
| HP:0006557 | Polycystic liver disease |
| HP:0100702 | Arachnoid cyst |
| Gene ID | Gene Symbol | Description |
|---|---|---|
| 23193 | GANAB | glucosidase II alpha subunit |
| 29880 | ALG5 | ALG5 dolichyl-phosphate beta-glucosyltransferase |
| 5310 | PKD1 | polycystin 1, transient receptor potential channel interacting |
| 5311 | PKD2 | polycystin 2, transient receptor potential cation channel |
| 79796 | ALG9 | ALG9 alpha-1,2-mannosyltransferase |
