Mild muscle weakness
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Database Frequency: | 4 / 7739 | ||
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All diseases associated with this symptom:
ARTHROGRYPOSIS, DISTAL, TYPE 2A | (OMIM:193700) |
Autosomal dominant myoglobinuria | (Orphanet:99846) |
Intellectual deficit - myopathy - short stature - endocrine defect | (Orphanet:3068) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII | (OMIM:615548) |