amyotrophic lateral sclerosis 18 Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of ALS caused_by mutation located_in PFN1 gene located_in chromosome 17. (Human Disease Ontology, DOID_0060209)
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1 genes associated with the amyotrophic lateral sclerosis 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
PFN1 profilin 1