Mitochondrial encephalopathy
Symptom Information:
Symptom ID: | HPO:0006789 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Morphological abnormality of the central nervous system(HPO:0002011) Encephalopathy(HPO:0001298) Mitochondrial encephalopathy(HPO:0006789) MedDRA: |
||
Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
Renal tubulopathy - encephalopathy - liver failure | (Orphanet:254902) |