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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02580 | Hereditary sensory neuropathy with spastic paraplegia | ... with a spastic paraplegia and a mutilating lower limb acropathy. It has been reported that mutations in CCT5 cause this disease. CCT5 gene encodes the epsilon subunit of the cytosolic chaperonin-containing ... | Nervous system disease | CCT5 [HSA:22948] [KO:K09497] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |