amyotrophic lateral sclerosis 1 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The most common type of familial ALS caused_by mutation located_in SOD1 gene located in chromosome 21. (Human Disease Ontology, DOID_0060193)
External Link
Similar Terms
Downloads & Tools


1 genes associated with the amyotrophic lateral sclerosis 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SOD1 superoxide dismutase 1, soluble