Mitochondrial myopathy
Symptom Information:
| Symptom ID: | HPO:0003737 | ||||
| Synonyms: |
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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) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Cytoplasmic disorders congenital(MedDRA:10052635) Genetic mitochondrial abnormalities NEC(MedDRA:10052637) Mitochondrial myopathy(HPO:0003737) |
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| Database Frequency: | 18 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
| Barth syndrome | (Orphanet:111) |
| Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
| Hereditary myopathy with lactic acidosis due to ISCU deficiency | (Orphanet:43115) |
| MELAS | (Orphanet:550) |
| MERRF | (Orphanet:551) |
| MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) | (OMIM:603041) |
| MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) | (OMIM:613662) |
| MITOCHONDRIAL MYOPATHY | (OMIM:251900) |
| MITOCHONDRIAL MYOPATHY WITH A DEFECT IN MITOCHONDRIAL-PROTEIN TRANSPORT | (OMIM:251945) |
| Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
| Mitochondrial myopathy - lactic acidosis - deafness | (Orphanet:2597) |
| Mitochondrial neurogastrointestinal encephalomyopathy | (Orphanet:298) |
| Myopathy and diabetes mellitus | (Orphanet:2596) |
| Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
| Myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2 | (OMIM:613561) |
| NARP syndrome | (Orphanet:644) |
| [DEL] SENGERS SYNDROME | (OMIM:212350) |