Related Conditions
Early onset cerebellar ataxia(child)
Drug-induced cerebellar ataxia(child)
Varicella cerebellar ataxia(child)
Nothnagel's syndrome(child)
Sanger-Brown cerebellar ataxia(child)
Dyssynergia cerebellaris myoclonica(child)
Cerebellar ataxia associated with another disorder(child)
Cerebellar ataxia co-occurrent with ectodermal dysplasia(child)
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1(child)
Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome(child)
Cerebellar ataxia Cayman type(child)
Ataxia with deafness and intellectual disability syndrome(child)
Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome(child)
Non-progressive cerebellar ataxia with intellectual disability(child)
Autosomal recessive ataxia due to ubiquinone deficiency(child)
AOA2 - ataxia oculomotor apraxia type 2(child)
Myoclonus, cerebellar ataxia, deafness syndrome(child)
Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome(child)
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome(child)
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Quick Facts
- SNOMED CT
- 85102008
- UMLS CUI
- C0007758
- Fully Specified Name
- Cerebellar ataxia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.