Muscle abnormality related to mitochondrial dysfunction
Symptom Information:
| Symptom ID: | HPO:0003800 | ||
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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) MedDRA: |
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| Database Frequency: | 3 / 7739 | ||
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All diseases associated with this symptom:
| Cardiomyopathy, familial hypertrophic, 8 | (OMIM:608751) |
| Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
| Lethal infantile mitochondrial myopathy | (Orphanet:254857) |