[DEL]Myopathic changes seen on EMG
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Is a (Whole tree): |
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Database Frequency: | 3 / 7739 | |
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All diseases associated with this symptom:
Autosomal dominant limb-girdle muscular dystrophy type 1D | (Orphanet:34516) |
Autosomal recessive limb-girdle muscular dystrophy type 2D | (Orphanet:62) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |