|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Progressive impairment of function of motor axons with muscle weakness, atrophy, and cramps. The deficits are length-dependent, meaning that muscles innervated by the longest nerves are affected first, so that for instance the arms are affected at a later age than the onset of deficits involving the lower leg. (Human Phenotype Ontology, HP_0007002)|
|Downloads & Tools|
4 genes associated with the motor axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.