Mitochondrial encephalopathy

Symptom Information:

Symptom ID: HPO:0006789
Synonyms:
Mitochondrial encephalopathy [OMIM:Mitochondrial encephalopathy]
Quality:
Cross references:
OMIM: "Mitochondrial encephalopathy" [OMIM:Mitochondrial encephalopathy]
Is a (Direct Parents):
HPO         Encephalopathy
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)