|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A symmetric loss of myelin from the internode regions along myelinated nerve fibers of the peripheral nervous system. (Human Phenotype Ontology, HP_0007262)|
|Downloads & Tools|
2 genes associated with the symmetric peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.