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polyneuropathy
Summary
- Definition
- A peripheral system disease that is characterized by damage affecting peripheral nerves (peripheral neuropathy) in roughly the same areas on both sides of the body, featuring weakness, numbness, pins-and-needles, and burning pain.
- Super Class
- peripheral nervous system disease
External Links
- Disease Ontology
- DOID:1389
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 6342 | SCP2 | sterol carrier protein 2 | |
| 6484 | ST3GAL4 | ST3 beta-galactoside alpha-2,3-sialyltransferase 4 | |
| 6517 | SLC2A4 | solute carrier family 2 member 4 | |
| 7086 | TKT | transketolase | |
| 7167 | TPI1 | triosephosphate isomerase 1 | |
| 8560 | DEGS1 | delta 4-desaturase, sphingolipid 1 | |
| 8879 | SGPL1 | sphingosine-1-phosphate lyase 1 | |
| 8898 | MTMR2 | myotubularin related protein 2 | |
| 9104 | RGN | regucalcin | |
| 9420 | CYP7B1 | cytochrome P450 family 7 subfamily B member 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O95394 | Phosphoacetylglucosamine mutase | |
| O95470 | Sphingosine-1-phosphate lyase 1 | |
| P00491 | Purine nucleoside phosphorylase | |
| P04040 | Catalase | |
| P04066 | Tissue alpha-L-fucosidase | |
| P04156 | Major prion protein | |
| P05093 | Steroid 17-alpha-hydroxylase/17,20 lyase | |
| P06280 | Alpha-galactosidase A | |
| P07203 | Glutathione peroxidase 1 | |
| P07602 | Prosaposin |
