EMG shows neuropathic changes
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
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HPO:
MedDRA: |
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| Database Frequency: | 2 / 7739 | |
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All diseases associated with this symptom:
| Autosomal recessive intermediate Charcot-Marie-Tooth disease type B | (Orphanet:254334) |
| METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |