Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/256840
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Genes

1 genes associated with the Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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