Subsarcolemmal mitochondrial accumulation
Symptom Information:
| Symptom ID: | OMIM : No Id available | |
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MedDRA: |
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| Database Frequency: | 4 / 7739 | |
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All diseases associated with this symptom:
| Autosomal dominant limb-girdle muscular dystrophy type 1H | (Orphanet:238755) |
| Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
| Hereditary myopathy with lactic acidosis due to ISCU deficiency | (Orphanet:43115) |
| Recessive mitochondrial ataxia syndrome | (Orphanet:94125) |