Overview
Oculomotor apraxia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Oculomotor apraxia - Cogan type(child)
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1(child)
AOA2 - ataxia oculomotor apraxia type 2(child)
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome(child)
Optic ataxia, gaze apraxia, simultanagnosia syndrome(child)
Cerebrorenal syndrome Perez type(child)
Acquired oculomotor apraxia(child)
AOA4 - ataxia, oculomotor apraxia type 4(child)
Strabismus(parent)
Quick Facts
- SNOMED CT
- 193662007
- UMLS CUI
- C3489733
- Fully Specified Name
- Oculomotor apraxia (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.