Alpers' disease
Symptom Information:
| Symptom ID: | MedDRA:10062943 | ||
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HPO:
MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Cytoplasmic disorders congenital(MedDRA:10052635) Genetic mitochondrial abnormalities NEC(MedDRA:10052637) Alpers' disease(MedDRA:10062943) |
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| Database Frequency: | 1 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |