|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing. (Human Disease Ontology, DOID_332)|
|Downloads & Tools|
9 genes associated with the amyotrophic lateral sclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.