Spastic Paraplegia 42, Autosomal Dominant Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C567262
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Genes

1 genes/proteins associated with the disease Spastic Paraplegia 42, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1 2.88009