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6 OMIM references -
9 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
7 OMIM references -
9 associated genes
No signs/symptoms info
Isolated CoQ-cytochrome C reductase deficiency
Immunodeficiency due to an early component of complement deficiency

BCS1L C1QA
CYC1 C1QB
LYRM7 C1QC
MT-CYB C1R
TTC19 C1S
UQCC2 C2
UQCRB C4A
UQCRC2 C4B
UQCRQ SERPING1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CYC1
(0.63)
C4A



Citations in the biomedical literature:


Isolated CoQ-cytochrome C reductase deficiency
BCS1L CYC1 LYRM7 MT-CYB TTC19 UQCC2
UQCRB UQCRC2 UQCRQ
Immunodeficiency due to an early component of complement deficiency
C1QA C1QB C1QC C1R C1S C2
C4A C4B SERPING1



Isolated CoQ-cytochrome C reductase deficiency
Immunodeficiency due to an early component of complement 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):
- Immunodeficiency due to a C1, C4, or C2 component complement deficiency

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

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:
7 OMIM references -
No MeSH references

No signs/symptoms info available.