|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Defective structure and function of myelin sheaths. Dysmyelination is distinguished from demyleination where there is destruction or damage of previously normal myelination. (Human Phenotype Ontology, HP_0003469)|
|Downloads & Tools|
2 genes associated with the peripheral dysmyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.