hereditary spastic paraplegia 16
MeSH: C536643ORPHA: 100997
Overview
hereditary spastic paraplegia that has material basis in variation in the chromosome region Xq11.2
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 16, sourced from HPO and Orphanet clinical annotations.
Functional abnormality of the bladderVisual lossNystagmusMild intellectual disabilityMotor delayAbnormal hallux morphologyExpressive aphasiaTetraplegiaFunctional abnormality of the gastrointestinal tract
Classification & Codes
MeSH Code
C536643Orphanet Code
ORPHA:100997hereditary spastic paraplegia 16
| MeSH | C536643 |
| Orphanet | ORPHA:100997 |
| Treatments | 0 drug(s) |
| Symptoms on record | 9 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO