|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||The most common type of familial ALS caused_by mutation located_in SOD1 gene located in chromosome 21. (Human Disease Ontology, DOID_0060193)|
|Downloads & Tools|
1 genes associated with the amyotrophic lateral sclerosis 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
|SOD1||superoxide dismutase 1, soluble|