Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive 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:C564948
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Genes

1 genes/proteins associated with the disease Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CCT5 chaperonin containing TCP1, subunit 5 (epsilon) 2.88009