Multiple mitochondrial DNA (mtDNA) deletions seen on muscle biopsy
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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HPO:
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Database Frequency: | 3 / 7739 | |
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All diseases associated with this symptom:
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) | (OMIM:603041) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) | (OMIM:613662) |