Depletion of mitochondrial DNA in muscle tissue
Symptom Information:
| Symptom ID: | HPO:0009141 | ||
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Muscle abnormality related to mitochondrial dysfunction(HPO:0003800) Depletion of mitochondrial DNA in muscle tissue(HPO:0009141) MedDRA: |
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| Database Frequency: | 5 / 7739 | ||
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All diseases associated with this symptom:
| Alpers syndrome | (Orphanet:726) |
| Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
| Mitochondrial DNA depletion syndrome, myopathic form | (Orphanet:254875) |
| Navajo neurohepatopathy | (Orphanet:255229) |
| Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |