Fatty replacement
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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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) |
MYOPATHY, AREFLEXIA, RESPIRATORY DISTRESS, AND DYSPHAGIA, EARLY-ONSET | (OMIM:614399) |
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY | (OMIM:181405) |