EMG: axonal abnormality
Symptom Information:
Symptom ID: | HPO:0003482 | ||||
Synonyms: |
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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: axonal abnormality(HPO:0003482) MedDRA: |
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Database Frequency: | 3 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Cerebrotendinous xanthomatosis | (Orphanet:909) |
X-linked Charcot-Marie-Tooth disease type 2 | (Orphanet:101076) |
X-linked Charcot-Marie-Tooth disease type 3 | (Orphanet:101077) |