Amyotrophic lateral sclerosis type 11 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A type of ALS caused_by mutation located_in FIG4 gene located_in chromosome 6. (Human Disease Ontology, DOID_0060202)
External Link http://www.omim.org/entry/612577
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Genes

1 genes associated with the Amyotrophic lateral sclerosis type 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
FIG4 FIG4 phosphoinositide 5-phosphatase