spinocerebellar ataxia
ICD-10: G11.1MeSH: D020754ORPHA: 98757
Overview
group of dominantly inherited, predominately late-onset, cerebellar ataxias. Neuro-developmental outcome and brain-derived neurotrophic factor level in relation to feeding practice in early infancy.
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 spinocerebellar ataxia, sourced from HPO and Orphanet clinical annotations.
ProptosisProgressive external ophthalmoplegiaNystagmusDiplopiaDelayed speech and language developmentDysarthriaDystoniaHyperreflexiaAbnormality of extrapyramidal motor functionProgressive cerebellar ataxiaClumsinessSkeletal muscle atrophyAbnormal pyramidal signVocal cord paralysisAbnormal vestibular functionAbnormality of temperature regulation
Classification & Codes
ICD-10 Code
G11.1MeSH Code
D020754Orphanet Code
ORPHA:98757spinocerebellar ataxia
| ICD-10 | G11.1 |
| MeSH | D020754 |
| Orphanet | ORPHA:98757 |
| Treatments | 0 drug(s) |
| Symptoms on record | 16 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO