|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Defective structure and function of myelin sheaths of the white matter of the brain. (Human Phenotype Ontology, HP_0007266)|
|Downloads & Tools|
7 genes associated with the cerebral dysmyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.