Overview
Myoclonic disorder is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Opsoclonus-myoclonus syndrome(child)
Sialidosis(child)
Juvenile neuronal ceroid lipofuscinosis(child)
Familial essential myoclonus(child)
Dyssynergia cerebellaris myoclonica(child)
Juvenile cerebellar degeneration AND myoclonus(child)
Benign neonatal sleep myoclonus(child)
Drug-induced myoclonus(child)
Non-epileptic myoclonus(child)
Stapedial myoclonus(child)
Tensor tympani myoclonus(child)
Febrile myoclonus(child)
Brainstem myoclonus(child)
Cerebral cortex myoclonus(child)
Spinal cord myoclonus(child)
Segmental myoclonus(child)
Infant epilepsy with migrant focal crisis(child)
Hereditary hyperekplexia(child)
Myoclonus, cerebellar ataxia, deafness syndrome(child)
Myoclonic dystonia(child)
Quick Facts
- SNOMED CT
- 127324008
- UMLS CUI
- C0027063
- Fully Specified Name
- Myoclonic disorder (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.