Depletion of mitochondrial DNA in liver
Symptom Information:
| Symptom ID: | HPO:0006581 | ||
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abnormality of the abdominal organs(HPO:0002012) Abnormality of the liver(HPO:0001392) Depletion of mitochondrial DNA in liver(HPO:0006581) MedDRA: |
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| Database Frequency: | 3 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Alpers syndrome | (Orphanet:726) |
| Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
| Navajo neurohepatopathy | (Orphanet:255229) |