Overview
Muscle fibrillation is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Japanese encephalitis virus disease
Occasional (5-29%)
Isaacs syndrome
Frequent (30-79%)
Nemaline myopathy, late onset type
Occasional (5-29%)
Neuromyotonia
Frequent (30-79%)
MEMSA - myoclonic epilepsy myopathy sensory ataxia
Occasional (5-29%)
Hereditary motor and sensory neuropathy Okinawa type
Frequent (30-79%)
Autosomal dominant centronuclear myopathy
Frequent (30-79%)
Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome
Occasional (5-29%)
Spinocerebellar ataxia type 18
Frequent (30-79%)
Charcot-Marie-Tooth disease type 4B3
Always present (100%)
Amyotrophic lateral sclerosis type 4
Familial infantile myoclonus epilepsy
Occasional (5-29%)
Polyglucosan body myopathy type 2
Frequent (30-79%)
Quick Facts
- SNOMED CT
- 41405005
- UMLS CUI
- C0231531
- Fully Specified Name
- Muscle fibrillation (finding)
- Associated Conditions
- 13
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.