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6 OMIM references -
9 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
8 associated genes
No signs/symptoms info
Isolated CoQ-cytochrome C reductase deficiency
Leigh syndrome with cardiomyopathy

BCS1L COA5
CYC1 COX10
LYRM7 COX15
MT-CYB COX6B1
TTC19 PDHA1
UQCC2 SCO2
UQCRB SURF1
UQCRC2 TACO1
UQCRQ


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CYC1
CYC1
(0.49)
(0.49)
COX15
SURF1



Citations in the biomedical literature:


Isolated CoQ-cytochrome C reductase deficiency
BCS1L CYC1 LYRM7 MT-CYB TTC19 UQCC2
UQCRB UQCRC2 UQCRQ
Leigh syndrome with cardiomyopathy
COA5 COX10 COX15 COX6B1 PDHA1 SCO2
SURF1 TACO1



Isolated CoQ-cytochrome C reductase deficiency
Leigh syndrome with cardiomyopathy

Synonym(s):
- Isolated coenzyme Q-cytochrome C reductase deficiency
- Isolated mitochondrial respiratory chain complex III deficiency
- Isolated ubiquinone-cytochrome C reductase deficiency

Synonym(s):
- Cardiomyopathy with hypotonia due to cytochrome C oxidase deficiency
- Cardiomyopathy with myopathy due to COX deficiency
- Leigh disease with myopathy

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

External references:
6 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.