amyotrophic lateral sclerosis 12 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of ALS caused_by mutation located_in OPTN gene located_in chromosome 10. (Human Disease Ontology, DOID_0060203)
External Link
Similar Terms
Downloads & Tools


1 genes associated with the amyotrophic lateral sclerosis 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
OPTN optineurin