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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 |
|---|---|---|---|
| 1312 | COMT | catechol-O-methyltransferase | |
| 1463 | NCAN | neurocan | |
| 1558 | CYP2C8 | cytochrome P450 family 2 subfamily C member 8 | |
| 1577 | CYP3A5 | cytochrome P450 family 3 subfamily A member 5 | |
| 1586 | CYP17A1 | cytochrome P450 family 17 subfamily A member 1 | |
| 1588 | CYP19A1 | cytochrome P450 family 19 subfamily A member 1 | |
| 1604 | CD55 | CD55 molecule (Cromer blood group) | |
| 1605 | DAG1 | dystroglycan 1 | |
| 1636 | ACE | angiotensin I converting enzyme | |
| 1890 | TYMP | thymidine phosphorylase |
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 |
