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6 OMIM references -
9 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
2 OMIM references -
5 associated genes
No signs/symptoms info
Isolated CoQ-cytochrome C reductase deficiency
Fatal infantile cytochrome C oxidase deficiency

BCS1L COX10
CYC1 COX15
LYRM7 SCO1
MT-CYB SCO2
TTC19 SURF1
UQCC2
UQCRB
UQCRC2
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
Fatal infantile cytochrome C oxidase deficiency
COX10 COX15 SCO1 SCO2 SURF1



Isolated CoQ-cytochrome C reductase deficiency
Fatal infantile cytochrome C oxidase deficiency

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

Synonym(s):
- Fatal infantile COX deficiency
- Fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic 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:
2 OMIM references -
No MeSH references

No signs/symptoms info available.