| Dataset | DisGeNET Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A symmetric loss of myelin from the internode regions along myelinated nerve fibers of the peripheral nervous system. (Human Phenotype Ontology, HP_0007262) |
| External Link | https://www.disgenet.org/browser/0/1/0/C4024914 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the disease Symmetric Peripheral Demyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| LMNB1 | lamin B1 |
