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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
5 associated genes
No signs/symptoms info
Burkitt lymphoma
Fatal infantile cytochrome C oxidase deficiency

MYC COX10
COX15
SCO1
SCO2
SURF1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MYC
(0.72)
SCO2



Citations in the biomedical literature:


Burkitt lymphoma
MYC
Fatal infantile cytochrome C oxidase deficiency
COX10 COX15 SCO1 SCO2 SURF1



Burkitt lymphoma
Fatal infantile cytochrome C oxidase deficiency

Synonym(s):
- Small non-cleaved cell lymphoma

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

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: any age
Type of inheritance: sporadic
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
2 MeSH references: D002051 / D008228
External references:
2 OMIM references -
No MeSH references

No signs/symptoms info available.