Lethal infantile mitochondrial myopathy
Symptom Information:
| Symptom ID: | HPO:0009069 | ||
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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) Mitochondrial myopathy(HPO:0003737) Lethal infantile mitochondrial myopathy(HPO:0009069) MedDRA: |
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| Database Frequency: | 2 / 7739 | ||
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All diseases associated with this symptom:
| Lethal infantile mitochondrial myopathy | (Orphanet:254857) |
| Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |