Mitochondrial encephalomyopathy
Symptom Information:
| Symptom ID: | MedDRA:10058799 | ||
| Synonyms: |
|
||
| Quality: | |||
| Cross references: |
|
||
| Is a (Direct Parents): |
|
||
| Is a (Whole tree): |
HPO:
MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Cytoplasmic disorders congenital(MedDRA:10052635) Genetic mitochondrial abnormalities NEC(MedDRA:10052637) Mitochondrial encephalomyopathy(MedDRA:10058799) |
||
| Database Frequency: | 5 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Combined oxidative phosphorylation defect type 13 | (Orphanet:319514) |
| Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
| MELAS | (Orphanet:550) |
| Maternally-inherited cardiomyopathy and hearing loss | (Orphanet:1349) |
| Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |