autosomal recessive spastic paraplegia type 69
ORPHA: 401830
Overview
human disease
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 autosomal recessive spastic paraplegia type 69, sourced from HPO and Orphanet clinical annotations.
Hearing impairmentCataractMild intellectual disabilityGlobal developmental delayAgenesis of corpus callosumLower limb spasticityCerebral cortical atrophyHand tremorSpastic dysarthriaAplasia/Hypoplasia of the cerebellar vermisProgressive spastic paraplegiaAbnormal myelinationAbnormality of movement
Classification & Codes
Orphanet Code
ORPHA:401830autosomal recessive spastic paraplegia type 69
| Orphanet | ORPHA:401830 |
| Treatments | 0 drug(s) |
| Symptoms on record | 13 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO