Spastic Paraplegia 37, 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:C567931
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Genes

1 genes/proteins associated with the disease Spastic Paraplegia 37, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SPG37 spastic paraplegia 37 (autosomal dominant) 2.88009