Spastic Paraplegia 38, 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:C567349
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease Spastic Paraplegia 38, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SPG38 spastic paraplegia 38 (autosomal dominant, Silver syndrome) 2.88009