|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A symmetric and progressive loss of myelin from the internode regions along myelinated nerve fibers of the peripheral nervous system. (Human Phenotype Ontology, HP_0006873)|
|Downloads & Tools|
1 genes associated with the symmetrical progressive peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.