|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A type of ALS with juvenile onset caused_by mutation located_in senataxin gene (SETX) located_in chromosome 9. (Human Disease Ontology, DOID_0060196)|
|Downloads & Tools|
1 genes/proteins associated with the disease Amyotrophic Lateral Sclerosis 4, Juvenile from the curated CTD Gene-Disease Associations dataset.