Mitochondrial hepatopathy
Symptom Information:
| Symptom ID: | MedDRA:10062938 | ||
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| 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 hepatopathy(MedDRA:10062938) |
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| Database Frequency: | 2 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| MEGDEL syndrome | (Orphanet:352328) |
| Recessive mitochondrial ataxia syndrome | (Orphanet:94125) |