|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An abnormality characterized by chronic impairment of the normal functioning of the axons. (Human Phenotype Ontology, HP_0007267)|
|Downloads & Tools|
3 genes associated with the chronic axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.