Overview
Neuromyotonia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Anti-CASPR2
Frequent (30-79%)HP:5000005
Electroencephalogram abnormal
Frequent (30-79%)HP:0002353
EMG: myokymic discharges
Frequent (30-79%)HP:0100288
Increased size of calf muscles
Frequent (30-79%)HP:0008981
Muscle fasciculation
Frequent (30-79%)HP:0002380
Muscle fibrillation
Frequent (30-79%)HP:0010546
Muscle spasm
Frequent (30-79%)HP:0003394
Muscle stiffness
Frequent (30-79%)HP:0003552
Myokymia
Frequent (30-79%)HP:0002411
Sweating
Frequent (30-79%)HP:0000975
Weight loss
Frequent (30-79%)HP:0001824
Loss of distal sensation
Occasional (5-29%)HP:0002936
Muscle weakness
Very rare (1-4%)HP:0001324
Abnormal hands
HP:0001155
Blurred vision
HP:0000622
Difficulty articulating speech
HP:0001260
Dizziness
HP:0002321
Elevated circulating creatine phosphokinase
HP:0003236
Extensor plantar responses
HP:0003487
Headache
HP:0002315
Incoordination
HP:0002311
Increased reflexes
HP:0001347
Muscular abnormality
HP:0003011
Paroxysmal ataxia
HP:0002131
Slurred speech
HP:0001350
Spastic walk
HP:0002064
Tremor
HP:0001337
Quick Facts
- SNOMED CT
- 305719002
- UMLS CUI
- C0242287
- Fully Specified Name
- Neuromyotonia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 27
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.