autosomal recessive spinocerebellar ataxia 12
ORPHA: 284282
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 spinocerebellar ataxia 12, sourced from HPO and Orphanet clinical annotations.
NystagmusDelayed speech and language developmentDysarthriaHyporeflexiaMotor delayGait ataxiaLimb ataxiaUrinary bladder sphincter dysfunction
Classification & Codes
Orphanet Code
ORPHA:284282autosomal recessive spinocerebellar ataxia 12
| Orphanet | ORPHA:284282 |
| Treatments | 0 drug(s) |
| Symptoms on record | 8 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO