Amyotrophic lateral sclerosis 18 Gene Set

Dataset ClinVar Gene-Phenotype 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)
External Link http://www.omim.org/entry/614808
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Genes

1 genes associated with the Amyotrophic lateral sclerosis 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
PFN1 profilin 1