Amyotrophic lateral sclerosis type 12 Gene Set

Dataset ClinVar Gene-Phenotype 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 http://www.omim.org/entry/613435
Similar Terms
Downloads & Tools

Genes

1 genes associated with the Amyotrophic lateral sclerosis type 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
OPTN optineurin