hereditary spastic paraplegia 62
ORPHA: 401785
Overview
hereditary spastic paraplegia that has material basis in mutation in the ERLIN1 gene on chromosome 10q24
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 62, sourced from HPO and Orphanet clinical annotations.
Lower limb spasticityDysarthriaGait disturbanceHyperreflexiaTip-toe gaitAreflexiaAbnormal cerebellum morphologySpastic gaitClonusThoracic scoliosisSkeletal muscle atrophyKnee flexion contractureLower limb pain
Classification & Codes
Orphanet Code
ORPHA:401785hereditary spastic paraplegia 62
| Orphanet | ORPHA:401785 |
| Treatments | 0 drug(s) |
| Symptoms on record | 13 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO