hereditary spastic paraplegia 25
MeSH: C536861ORPHA: 101005
Overview
hereditary spastic paraplegia that has material basis in variation in the chromosome region 6q23-q24.1
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with hereditary spastic paraplegia 25, sourced from HPO and Orphanet clinical annotations.
ParaparesisHerniation of intervertebral nucleiSensory neuropathySpastic paraplegiaLower limb painNeck painDevelopmental cataractDevelopmental glaucomaAbnormality of peripheral nerve conductionSensorimotor neuropathyCervical spondylosisUpper limb painAbnormal lumbar spine morphology
Classification & Codes
MeSH Code
C536861Orphanet Code
ORPHA:101005hereditary spastic paraplegia 25
| MeSH | C536861 |
| Orphanet | ORPHA:101005 |
| Treatments | 0 drug(s) |
| Symptoms on record | 13 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO