EMG: decremental response of compound muscle action potential to repetitive nerve stimulation
Symptom Information:
| Symptom ID: | HPO:0003403 | ||
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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: decremental response of compound muscle action potential to repetitive nerve stimulation(HPO:0003403) MedDRA: |
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| Database Frequency: | 7 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Congenital myasthenic syndromes with glycosylation defect | (Orphanet:353327) |
| MYASTHENIC SYNDROME, CONGENITAL, 15 | (OMIM:616227) |
| MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL | (OMIM:605809) |
| MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:608931) |
| Myasthenia gravis | (Orphanet:589) |
| Presynaptic congenital myasthenic syndromes | (Orphanet:98914) |
| Synaptic congenital myasthenic syndromes | (Orphanet:98915) |