Spastic paraplegia 6, 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:C536866
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease Spastic paraplegia 6, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1 2.88009