Cytoscape Web
Click node...

Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
1 OMIM reference -
2 associated genes
No signs/symptoms info
COMMON GENES: 1
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
1 OMIM reference -
1 associated gene
No signs/symptoms info
Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins

MT-TE
(OMIM)
 TRMU
(UniProt - OMIM)
TRMU
(UniProt - OMIM)

COMMON
GENES 		TRMU


Citations in the biomedical literature:


Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
MT-TE TRMU
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins



Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins

Synonym(s):
- Benign COX deficiency
- Infantile reversible cytochrome c oxidase deficiency myopathy
- Mitochondrial myopathy with reversible COX deficiency
- Mitochondrial myopathy with reversible complex IV deficiency
- Reversible infantile cytochrome c oxidase deficiency
- Reversible infantile respiratory chain deficiency
Synonym(s):
- Acute infantile liver failure due to synthesis defect of mitochondrial DNA-encoded proteins
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hepatic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
Class of prevalence: -
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: mitochondrial inheritance
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.