|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A type of ALS with loci associated with the disease located_in chromosome 18. (Human Disease Ontology, DOID_0060195)|
|Downloads & Tools|
1 genes associated with the amyotrophic lateral sclerosis 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
|ALS3||amyotrophic lateral sclerosis 3 (autosomal dominant)|