Amyotrophic Lateral Sclerosis 11 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of ALS caused_by mutation located_in FIG4 gene located_in chromosome 6. (Human Disease Ontology, DOID_0060202)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C567244
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1 genes/proteins associated with the disease Amyotrophic Lateral Sclerosis 11 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
FIG4 FIG4 phosphoinositide 5-phosphatase 2.88009