Amyotrophic Lateral Sclerosis 2, Juvenile Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of ALS with juvenile onset caused_by mutation located_in alsin gene located_in chromosome 2. (Human Disease Ontology, DOID_0060194)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C565957
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Genes

1 genes/proteins associated with the disease Amyotrophic Lateral Sclerosis 2, Juvenile from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ALS2 amyotrophic lateral sclerosis 2 (juvenile) 2.88009