EMG: chronic denervation signs
Symptom Information:
Symptom ID: | HPO:0003444 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) EMG abnormality(HPO:0003457) EMG: neuropathic changes(HPO:0003445) EMG: chronic denervation signs(HPO:0003444) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Charcot-Marie-Tooth disease type 2L | (Orphanet:99945) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT | (OMIM:610100) |
Infantile neuroaxonal dystrophy | (Orphanet:35069) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |