|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A severe loss of myelin from nerve fibers in the central nervous system. (Human Phenotype Ontology, HP_0007258)|
|Downloads & Tools|
1 genes associated with the severe demyelination of the white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.