Amyotrophic lateral sclerosis type 1 Gene Set

Dataset ClinVar Gene-Phenotype 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 http://www.omim.org/entry/105400
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Genes

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

Symbol Name
SOD1 superoxide dismutase 1, soluble